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Ann Nordgren

Ann Nordgren

Adjungerad Professor
E-postadress: ann.nordgren@ki.se
µþ±ð²õö°ì²õ²¹»å°ù±ð²õ²õ: ̽»¨¾«Ñ¡, BioClinicum J10:20, Visionsgatan 4, 17164 Solna
Postadress: K1 Molekylär medicin och kirurgi, K1 MMK Sällsynta diagnoser, 171 76 Stockholm

Om mig


  • Adjungerad professor i klinisk genetik
    Forskargruppsledare för gruppen Sällsynta diagnoser, Institutionen för
    molekylär medicin och kirurgi [1]
    [1] /mmk/sallsynta-diagnoser

    Professor i klinisk genetik, Sahlgrenska Akademin/Sahlgrenska Unic´versitetssjukhuset

Forskningsbeskrivning

  • Sällsynta diagnoser

    Barncancerpredisposition

    Intellektuell funktionsnedsättning

    Missbildningar

    Syndromutredning

    Fenotypning

    Cytogenetik

    Genomik

    Epigenetik

Undervisning

  • Ämnesföreträdare - Klinisk genetik pÃ¥ läkarprogrammet i Göteborg

    Föreläser på grundutbildningen för läkare om Sällsynta diagnoser och Syndromutredning

    Utformat ST-kurs Sällsynta diagnoser som ges med jämna mellanrum.

    Föreläser regelbundet för ST-läkare och specialister inom pediatrik om syndromdiagnostik och barncancer predisposition samt om specifika genetiska syndrom

    Föreläser regelbundet på familjevistelser och patientträffar.

    Skrivit kapitel om syndromdiagnostik i läroboken "Genetiska sjukdomar" samt kapitel om specifika diagnoser i Socialstyrelsens databas för Sällsynta Hälsotillstånd

Utvalda publikationer

  • Letter: NATURE MEDICINE. 2025;31(6):1730-1732
    Kampe A; Gudmundsson S; Walsh CP; Lindblad-Toh K; Johansson A; Clareborn A; Ameur A; Edsjo A; Fioretos T; Ehrencrona H; Eriksson D; Fall T; Franks PW; Gyllensten U; Haag M; Hagwall A; Johansson Soller M; Lehtio J; Lu Y; Magnusson PKE; Melen E; Melin B; Michaelsson K; Nordgren A; Nordlund J; Saal LH; Schwenk JM; Sikora P; Sundstrom J; Taylan F; Van Guelpen B; Wadelius M; Wedell A; Wirta V; Ostling P; Jacobsson B; Sjoblom T; Persson B; Rosenquist R; Lindstrand A; Lappalainen T
  • Article: JOURNAL OF INTERNAL MEDICINE. 2025;297(6):683-692
    Pedersen A; Nordenvall AS; Tettamanti G; Nordgren A
  • Editorial comment: NATURE GENETICS. 2024;56(11):2287-2294
    Delgado-Vega AM; Cederroth H; Taylan F; Ekholm K; Ek M; Thonberg H; Jemt A; Nilsson D; Eisfeldt J; Saether KB; Hoijer I; Akgun-Dogan O; Asano Y; Barakat TS; Batkovskyte D; Baynam G; Bodamer O; Chetruengchai W; Corcoran P; Couse M; Danis D; Demidov G; Dohi E; Erhardsson M; Fernandez-Luna L; Fujiwara T; Garg N; Giugliani R; Gonzaga-Jauregui C; Grigelioniene G; Groza T; Gunnarsson C; Hammarsjo A; Hammond CK; Ng OH; Hesketh S; Hettiarachchi D; Soller MJ; Kirmani UA; Kjellberg M; Kvarnung M; Kvlividze O; Lagerstedt-Robinson K; Lasko P; Lassmann T; Lau LYS; Laurie S; Lim WK; Liu Z; Wiklander ML; Makay P; Maiga AB; Maya-Gonzalez C; Meyn MS; Neethiraj R; Nigro V; Nordgren F; Nordlund J; Orrsjo S; Ottosson J; Ozbek U; Ozdemir O; Partin C; Pearce DA; Peck R; Pedersen A; Pettersson M; Pongpanich M; de la Paz MP; Ramani A; Romero JA; Romero VI; Rosenquist R; Saw AM; Spencer M; Stattin E-L; Srichomthong C; Tapia-Paez I; Taruscio D; Taylor JP; Tkemaladze T; Tully I; Tumer Z; van Zelst-Stams WAG; Verloes A; Vasterviga E; Wang S; Yang R; Yamamoto S; Yepez VA; Zhang Q; Shotelersuk V; Wiafe SA; Alanay Y; Botto LD; Kirmani S; Lumaka A; Palmer EE; Puri RD; Wirta V; Lindstrand A; Buske OJ; Cederroth M; Nordgren A
  • Article: NEUROLOGY. 2024;103(8):e209883
    Maya-Gonzalez C; Tettamanti G; Taylan F; Nordenvall AS; Sejersen T; Nordgren A
  • Article: BRITISH JOURNAL OF CANCER. 2024;131(4):755-762
    Wachtmeister A; Tettamanti G; Nordgren I; Norrby C; Laurell T; Lu Y; Nordenvall AS; Nordgren A
  • Review: NPJ GENOMIC MEDICINE. 2024;9(1):37
    Palmer EE; Cederroth H; Cederroth M; Delgado-Vega AM; Roberts N; Taylan F; Nordgren A; Botto LD
  • Article: LANCET REGIONAL HEALTH-EUROPE. 2024;39:100881
    Tesi B; Robinson KL; Abel F; Stahl TDD; Orrsjoe S; Poluha A; Hellberg M; Wessman S; Samuelsson S; Frisk T; Vogt H; Henning K; Sabel M; Ek T; Pal N; Nyman P; Giraud G; Wille J; Pronk CJ; Noren-Nystroem U; Borssen M; Fili M; Stalhammar G; Herold N; Tettamanti G; Maya-Gonzalez C; Arvidsson L; Rosen A; Ekholm K; Kuchinskaya E; Hallbeck A-L; Nordling M; Palmebaeck P; Kogner P; Smoler GK; Laehteenmaeki P; Fransso S; Martinsson T; Shamik A; Mertens F; Rosenquist R; Wirta V; Tham E; Grillner P; Sandgren J; Ljungman G; Gisselsson D; Taylan F; Nordgren A
  • Review: ORPHANET JOURNAL OF RARE DISEASES. 2023;18(1):348
    Curic E; Ewans L; Pysar R; Taylan F; Botto LD; Nordgren A; Gahl W; Palmer EE
  • Article: FRONTIERS IN MEDICINE. 2023;10:1172565
    Maya-Gonzalez C; Wessman S; Lagerstedt-Robinson K; Taylan F; Tesi B; Kuchinskaya E; McCluggage WG; Poluha A; Holm S; Nergardh R; De Stahl TD; Hoybye C; Tettamanti G; Delgado-Vega AM; Skarin Nordenvall A; Nordgren A
  • Article: JCO PRECISION ONCOLOGY. 2023;7:e2300039
    Wadensten E; Wessman S; Abel F; De Stahl TD; Tesi B; Pietras CO; Arvidsson L; Taylan F; Fransson S; Vogt H; Poluha A; Pradhananga S; Hellberg M; Lagerstedt-Robinson K; Raj Somarajan P; Samuelsson S; Orrsjo S; Maqbool K; Henning K; Strid T; Ek T; Fagman H; Bontell TO; Martinsson T; Puls F; Kogner P; Wirta V; Pronk CJ; Wille J; Rosenquist R; Nister M; Mertens F; Sabel M; Noren-Nystrom U; Grillner P; Nordgren A; Ljungman G; Sandgren J; Gisselsson D
  • Journal article: PATHOLOGY. 2023;55:s19-s20
    Lindstrand A; Ek M; Kvarnung M; Anderlid B-M; Björck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjö A; Helgadottir HT; Hellström-Pigg M; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-Å; Lieden A; Lindelöf H; Malmgren H; Nilsson D; Svensson E; Paucar M; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Soller MJ; Pettersson M; Nordgren A
  • Article: GENETICS IN MEDICINE. 2022;24(11):2296-2307
    Lindstrand A; Ek M; Kvarnung M; Anderlid B-M; Bjoerck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjoe A; Helgadottir HT; Hellstroem-Pigg M; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-A; Lieden A; Lindeloef H; Malmgren H; Nilsson D; Svensson E; Paucar M; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Soller MJ; Pettersson M; Nordgren A
  • Letter: NATURE MEDICINE. 2022;28(10):1980-1982
    Fioretos T; Wirta V; Cavelier L; Berglund E; Friedman M; Akhras M; Botling J; Ehrencrona H; Engstrand L; Helenius G; Fagerqvist T; Gisselsson D; Gruvberger-Saal S; Gyllensten U; Heidenblad M; Hoglund K; Jacobsson B; Johansson M; Johansson A; Soller MJ; Landstrom M; Larsson P; Levin L-A; Lindstrand A; Lovmar L; Lyander A; Melin M; Nordgren A; Nordmark G; Molling P; Palmqvist L; Palmqvist R; Repsilber D; Sikora P; Stenmark B; Soderkvist P; Stranneheim H; Strid T; Wheelock CE; Wadelius M; Wedell A; Edsjo A; Rosenquist R
  • Article: BLOOD ADVANCES. 2022;6(7):2275-2289
    Bang B; Eisfeldt J; Barbany G; Harila-Saari A; Heyman M; Zachariadis V; Taylan F; Nordgren A
  • Article: MOLECULAR GENETICS & GENOMIC MEDICINE. 2022;10(4):e1880
    Frisk S; Wachtmeister A; Laurell T; Lindstrand A; Jantti N; Malmgren H; Lagerstedt-Robinson K; Tesi B; Taylan F; Nordgren A
  • Article: JOURNAL OF MEDICAL GENETICS. 2022;59(2):141-146
    Ponten E; Frisk S; Taylan F; Vaz R; Wessman S; de Kock L; Pal N; Foulkes WD; Lagerstedt-Robinson K; Nordgren A
  • Article: ORPHANET JOURNAL OF RARE DISEASES. 2021;16(1):472
    Willfors C; Riby DM; van der Poll M; Ekholm K; Bjorlin HA; Kleberg JL; Nordgren A
  • Article: CELL DEATH & DISEASE. 2020;11(4):238
    Bergstrand S; Bohm S; Malmgren H; Norberg A; Sundin M; Nordgren A; Farnebo M
  • Editorial comment: NATURE GENETICS. 2020;52(1):21-26
    Baynam GS; Groft S; van der Westhuizen FH; Gassman SD; du Plessis K; Coles EP; Selebatso E; Selebatso M; Gaobinelwe B; Selebatso T; Joel D; Llera VA; Vorster BC; Wuebbels B; Djoudalbaye B; Austin CP; Kumuthini J; Forman J; Kaufmann P; Chipeta J; Gavhed D; Larsson A; Stojiljkovic M; Nordgren A; Roldan EJA; Taruscio D; Wong-Rieger D; Nowak K; Bilkey GA; Easteal S; Bowdin S; Reichardt JKV; Beltran S; Kosaki K; van Karnebeek CDM; Gong M; Zhang S; Mehrian-Shai R; Adams DR; Puri RD; Zhang F; Pachter N; Muenke M; Nellaker C; Gahl WA; Cederroth H; Broley S; Schoonen M; Boycott KM; Posada M
  • Article: BLOOD ADVANCES. 2019;3(18):2722-2731
    Jarviaho T; Bang B; Zachariadis V; Taylan F; Moilanen J; Mottonen M; Smith CIE; Harila-Saari A; Niinimaki R; Nordgren A
  • Article: CLINICAL GENETICS. 2019;96(2):118-125
    Frisk S; Taylan F; Blaszczyk I; Nennesmo I; Anneren G; Herm B; Stattin E-L; Zachariadis V; Lindstrand A; Tesi B; Laurell T; Nordgren A
  • Letter: BRITISH JOURNAL OF HAEMATOLOGY. 2019;185(2):354-357
    Jarviaho T; Zachariadis V; Tesi B; Chiang S; Bryceson YT; Mottonen M; Niinimaki R; Bang B; Rahikkala E; Taylan F; Uusimaa J; Harila-Saari A; Nordgren A
  • Letter: CLINICAL CHEMISTRY. 2019;65(2):345-347
    Taylan F; Bang B; Ofverholm II; Anh-Nhi T; Heyman M; Barbany G; Zachariadis V; Nordgren A
  • Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2016;98(2):373-381
    Reijnders MRF; Zachariadis V; Latour B; Jolly L; Mancini GM; Pfundt R; Wu KM; van Ravenswaaij-Arts CMA; Veenstra-Knol HE; Anderlid B-MM; Wood SA; Cheung SW; Barnicoat A; Probst F; Magoulas P; Brooks AS; Malmgren H; Harila-Saari A; Marcelis CM; Vreeburg M; Hobson E; Sutton VR; Stark Z; Vogt J; Cooper N; Lim JY; Price S; Lai AHM; Domingo D; Reversade B; Gecz J; Gilissen C; Brunner HG; Kini U; Roepman R; Nordgren A; Kleefstra T
  • Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2015;96(3):507-513
    Tham E; Lindstrand A; Santani A; Malmgren H; Nesbitt A; Dubbs HA; Zackai EH; Parker MJ; Millan F; Rosenbaum K; Wilson GN; Nordgren A
  • Letter: LEUKEMIA. 2014;28(1):196-198
    Zachariadis V; Schoumans J; Ofverholm I; Barbany G; Halvardsson E; Forestier E; Johansson B; Nordenskjold M; Nordgren A
  • Article: JOURNAL OF MEDICAL GENETICS. 2014;51(1):45-54
    Lindstrand A; Grigelioniene G; Nilsson D; Pettersson M; Hofmeister W; Anderlid B-M; Kant SG; Ruivenkamp CAL; Gustavsson P; Valta H; Geiberger S; Topa A; Lagerstedt-Robinson K; Taylan F; Wincent J; Laurell T; Pekkinen M; Nordenskjold M; Makitie O; Nordgren A
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2013;21(10):1085-1092
    Laurell T; Lundin J; Anderlid B-M; Gorski JL; Grigelioniene G; Knight SJL; Krepischi ACV; Nordenskjold A; Price SM; Rosenberg C; Turnpenny PD; Vianna-Morgante AM; Nordgren A
  • Article: JOURNAL OF MEDICAL GENETICS. 2013;50(8):521-528
    Kvarnung M; Nilsson D; Lindstrand A; Korenke GC; Chiang SCC; Blennow E; Bergmann M; Stodberg T; Makitie O; Anderlid B-M; Bryceson YT; Nordenskjold M; Nordgren A
  • Letter: BRITISH JOURNAL OF HAEMATOLOGY. 2012;159(4):488-491
    Zachariadis V; Schoumans J; Barbany G; Heyman M; Forestier E; Johansson B; Nordenskjold M; Nordgren A
  • Article: LEUKEMIA. 2011;25(4):622-628
    Zachariadis V; Gauffin F; Kuchinskaya E; Heyman M; Schoumans J; Blennow E; Gustafsson B; Barbany G; Golovleva I; Ehrencrona H; Cavelier L; Palmqvist L; Lonnerholm G; Nordenskjold M; Johansson B; Forestier E; Nordgren A
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Artiklar

  • Journal article: JOURNAL OF MEDICAL GENETICS. 2025;62(10):656-663
    Bouhatous Y-M; Bredrup C; Maurer A; Mirakovska L; Foster A; Kosaki K; Jost C; Demoulin J-B; Luu M; Vabres P; Kurtz J-E; Schaefer E; Guimier A; Cormier-Daire V; Lim D; Thompson S; Olson L; Kwon HR; Aguirre-Rodriguez C; Hernandez-Dorronsoro U; Martinez-Soroa I; Iznardo H; Mascaro J-MJ; Baselga E; Kalantari S; Mussa A; Gazzin A; Carli D; Svinvik I; Mutlu-Albayrak H; Bluefeather S; Zarate Y; Takenouchi T; Naicker T; Chateau A; Gokhul A; Dube-Pule A; Haniffa M; Ong Peitee W; Nordgren A; Carpentier M; Binquet C; Briffaut A-S; Bal L; Pond D; Rustad CF; Bardou M; Faivre L
  • Article: FRONTIERS IN GENETICS. 2025;16:1624306
    Onder G; Ozdemir O; Taylan F; Canpolat C; Yalcin K; Erbey F; Sozmen BO; Asarcikli F; Bayhan T; Akcabelen YM; Yarali N; Ozbek NY; Bozkaya IO; Kacar D; Ergun B; Akkus A; Albayrak D; Ince E; Demirsoy U; Ozdemir GN; Dogru O; Aras S; Aydin E; Unal B; Amanvermez U; Dogan OA; Akyoney S; Sayitoglu M; Nordgren A; Bugra Agaoglu N; Ozbek U; Ng OH
  • Journal article: JOURNAL OF CLINICAL INVESTIGATION. 2025;135(17):e193099
    He M; Ding M; Chocholouskova M; Chin CF; Engvall M; Malmgren H; Wagner M; Lauffer MC; Heisinger J; Malicdan MCV; Allamand V; Durbeej M; Delgado Vega A; Sejersen T; Nordgren A; Torta F; Silver DL
  • Journal article: JOURNAL OF NEURODEVELOPMENTAL DISORDERS. 2025;17(1):48
    Hallman A; Willfors C; Fawcett C; Frick MA; Nordgren A; Kleberg JL
  • Article: CLINICAL GENETICS. 2025;108(2):199-205
    Stavren-Eriksson E; Hammarsjo A; Lindstrand A; Nordgren A; Grigelioniene G; Pigg MH
  • Article: UROLOGY PRACTICE. 2025;12(6):101097upj0000000000000860-742
    Phillips L; Tettamanti G; Nordgren A; Skarin Nordenvall A; Nordenskjöld A
  • Article: FRONTIERS IN GENETICS. 2025;16:1580879
    Malmgren H; Kvarnung M; Gustafsson P; Anderlid B-M; Arthur C; Carlsten J; De Geer K; Ehn E; Grigelioniene G; Hammarsjo A; Helgadottir HT; Hellstrom-Pigg M; Iwarsson E; Kuchinskaya E; Lindelof H; Mannila M; Nilsson D; Pettersson M; Rudd E; Sahlin E; Tesi B; Tham E; Thonberg H; Westenius E; Winberg J; Winerdal M; Nordenskjold M; Johansson-Soller M; Wirta V; Nordgren A; Lindstrand A; Lagerstedt-Robinson K
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2025;:1-10
    Lindelof H; Hammarsjo A; Voss U; Piticchio SG; Conner P; Papadogiannakis N; Batkovskyte D; Orellana L; Kvarnung M; Malmgren H; Robinson KL; Nordgren A; Lindstrand A; Nishimura G; Grigelioniene G
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2025;33(5):580-587
    Kvarnung M; Pettersson M; Chun-on P; Rafati M; Mcreynolds LJ; Norberg A; Moura PL; Pesonen I; Chaireti R; Soderholm BG; Burlin J; Ryden J; Lindberg EH; Giri N; Savage SA; Agarwal S; Nordgren A; Tesi B
  • Article: MOVEMENT DISORDERS. 2025;40(4):672-682
    Paucar M; Li T; Bergendal A; Savitcheva I; Pourhamidi K; Laffita-Mesa JM; Nordgren A; Engvall M; Uhlen P; Lagerstedt-Robinson K; Svenningsson P
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2025;197(3):e63935
    Batkovskyte D; Swolin-Eide D; Hammarsjo A; Saether KB; Thunstrom S; Lundin J; Eisfeldt J; Lindstrand A; Nordgren A; Astrom E; Grigelioniene G
  • Article: JOURNAL OF CLINICAL MEDICINE. 2025;14(4):1307
    Giesecke J; Oskarsson A; Petersson M; Nordenvall AS; Tettamanti G; Nordgren A; Hoybye C
  • Article: HGG ADVANCES. 2025;6(1):100380
    van der Laan L; Silva A; Kleinendorst L; Rooney K; Haghshenas S; Lauffer P; Alanay Y; Bhai P; Brusco A; de Munnik S; de Vries BBA; Vega AD; Engelen M; Herkert JC; Hochstenbach R; Hopman S; Kant SG; Kira R; Kato M; Keren B; Kroes HY; Levy MA; Lock-Hock N; Maas SM; Mancini GMS; Marcelis C; Matsumoto N; Mizuguchi T; Mussa A; Mignot C; Narhi A; Nordgren A; Pfundt R; Polstra AM; Trajkova S; van Bever Y; van den Boogaard MJ; van der Smagt JJ; Barakat TS; Alders M; Mannens MMAM; Sadikovic B; van Haelst MM; Henneman P
  • Journal article: FRONTIERS IN GENETICS. 2025;16
    Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical setting
    Malmgren H; Kvarnung M; Gustafsson P; Anderlid B-M; Arthur C; Carlsten J; De Geer K; Ehn E; Grigelioniené G; Hammarsjö A; Helgadottir HT; Hellström-Pigg M; Iwarsson E; Kuchinskaya E; Lindelöf H; Mannila M; Nilsson D; Pettersson M; Rudd E; Sahlin E; Tesi B; Tham E; Thonberg H; Westenius E; Winberg J; Winerdal M; Nordenskjöld M; Johansson-Soller M; Wirta V; Nordgren A; Lindstrand A; Lagerstedt-Robinson K
  • Article: AMERICAN JOURNAL OF CASE REPORTS. 2024;25:e945715
    Maya-Gonzalez C; De Stahl TD; Wessman S; Taylan F; Tesi B; Lagerstedt-Robinson K; Tettamanti G; Dukic M; Poluha A; Ljungman G; Nordgren A
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2024;194(12):e63812
    Maya-Gonzalez C; Delgado-Vega AM; Taylan F; Robinson KL; Hansson L; Pal N; Fagman H; Puls F; Wessman S; Stenman J; Georgantzi K; Fransson S; De Stahl TD; Ek T; Palmer R; Tesi B; Kogner P; Martinsson T; Nordgren A
  • Article: GENOME RESEARCH. 2024;34(11):1785-1797
    Bilgrav Saether K; Eisfeldt J; Bengtsson JD; Lun MY; Grochowski CM; Mahmoud M; Chao H-T; Rosenfeld JA; Liu P; Ek M; Schuy J; Ameur A; Dai H; Hwang JP; Sedlazeck FJ; Bi W; Marom R; Wincent J; Nordgren A; Carvalho CMB; Lindstrand A
  • Article: COGNITIVE SYSTEMS RESEARCH. 2024;86:101235
    Strannegard C; Engsner N; Ulfsbacker S; Andreasson S; Endler J; Nordgren A
  • Article: SCIENTIFIC REPORTS. 2024;14(1):17583
    Willfors C; Borg J; Kleberg JL; Hallman A; Van Der Poll M; Remnelius KL; Avdic HB; Bolte S; Nordgren A
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2024;32(3):333-341
    Johansson J; Lideus S; Frykholm C; Gunnarsson C; Mihalic F; Gudmundsson S; Ekvall S; Molin A-M; Pham M; Vihinen M; Lagerstedt-Robinson K; Nordgren A; Jemth P; Ameur A; Anneren G; Wilbe M; Bondeson M-L
  • Article: OPHTHALMIC GENETICS. 2024;45(1):95-102
    Pechhacker MKG; Molnar A; Pekkola Pacheco N; Thonberg H; Querat L; Birkeldh U; Nordgren A; Lindstrand A
  • Article: NPJ PRECISION ONCOLOGY. 2023;7(1):131
    Krali O; Marincevic-Zuniga Y; Arvidsson G; Enblad AP; Lundmark A; Sayyab S; Zachariadis V; Heinaniemi M; Suhonen J; Oksa L; Vepsaelaeinen K; Ofverholm I; Barbany G; Nordgren A; Lilljebjorn H; Fioretos T; Madsen HO; Marquart HV; Flaegstad T; Forestier E; Jonsson OG; Kanerva J; Lohi O; Noren-Nystrom U; Schmiegelow K; Harila A; Heyman M; Lonnerholm G; Syvanen A-C; Nordlund J
  • Article: NPJ GENOMIC MEDICINE. 2023;8(1):39
    Jacob P; Lindelof H; Rustad CF; Sutton VR; Moosa S; Udupa P; Hammarsjo A; Bhavani GS; Batkovskyte D; Tveten K; Dalal A; Horemuzova E; Nordgren A; Tham E; Shah H; Merckoll E; Orellana L; Nishimura G; Girisha KM; Grigelioniene G
  • Article: SCIENTIFIC REPORTS. 2023;13(1):18397
    Kleberg JL; Hallman AEZ; Galazka MA; Riby DM; Bolte S; Willfors C; Fawcett C; Nordgren A
  • Article: SCIENTIFIC REPORTS. 2023;13(1):15858
    Avdic HB; Strannegard C; Engberg H; Willfors C; Nordgren I; Frisen L; Hirschberg AL; Guath M; Nordgren A; Kleberg JL
  • Article: GENETICS IN MEDICINE. 2023;25(8):100856
    Caron V; Chassaing N; Ragge N; Boschann F; Ngu AM-H; Meloche E; Chor S; Lakhani SA; Ji W; Steiner L; Marcadier J; Jansen PR; van de Pol LA; van Hagen JM; Russi AS; Le Guyader G; Nordenskjold M; Nordgren A; Anderlid B-M; Plaisancie J; Stoltenburg C; Horn D; Drenckhahn A; Hamdan FF; Lefebvre M; Attie-Bitach T; Forey P; Smirnov V; Ernould F; Jacquemont M-L; Grotto S; Alcantud A; Coret A; Ferrer-Avargues R; Srivastava S; Vincent-Delorme C; Romoser S; Safina N; Saade D; Lupski JR; Calame DG; Genevieve D; Chatron N; Schluth-Bolard C; Myers KA; Dobyns WB; Calvas P; Salmon C; Holt R; Elmslie F; Allaire M; Prigozhin DM; Tremblay A; Michaud JL
  • Article: JAMA NETWORK OPEN. 2023;6(7):e2325482
    Kampitsi C-E; Nordgren A; Mogensen H; Ponten E; Feychting M; Tettamanti G
  • Article: JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS. 2023;53(7):2786-2797
    Kleberg JL; Riby D; Fawcett C; Bjorlin Avdic H; Frick MA; Brocki KC; Hogstrom J; Serlachius E; Nordgren A; Willfors C
  • Article: COGNITIVE NEUROPSYCHIATRY. 2023;28(3):207-225
    Avdic HB; Kleberg JL; van der Poll M; Frisen L; Hutley M; Sarjanen M; Nordgren I; Ekholm K; Hirschberg AL; Nordgren A; Willfors C
  • Article: SCIENTIFIC REPORTS. 2023;13(1):6904
    Runheim H; Pettersson M; Hammarsjo A; Nordgren A; Henriksson M; Lindstrand A; Levin L-A; Soller MJ
  • Article: JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY. 2023;29(3):306-315
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    Ofverholm II; Anh NT; Olsson L; Zachariadis V; Heyman M; Rudd E; Lundberg ES; Nordenskjold M; Johansson B; Nordgren A; Barbany G
  • Article: CANCER EPIDEMIOLOGY. 2016;41:57-62
    Lu Y; Segelman J; Nordgren A; Lindstrom L; Frisell J; Martling A
  • Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2016;98(2):363-372
    Kasher PR; Schertz KE; Thomas M; Jackson A; Annunziata S; Ballesta-Martinez MJ; Campeau PM; Clayton PE; Eaton JL; Granata T; Guillen-Navarro E; Hernando C; Laverriere CE; Lieden A; Villa-Marcos O; McEntagart M; Nordgren A; Pantaleoni C; Pebrel-Richard C; Sarret C; Sciacca FL; Wright R; Kerr B; Glasgow E; Banka S
  • Article: NEUROLOGY-GENETICS. 2016;2(1):e49
    Paucar M; Malmgren H; Taylor M; Reynolds JJ; Svenningsson P; Press R; Nordgren A
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2016;24(2):198-207
    Tham E; Eklund EA; Hammarsjo A; Bengtson P; Geiberger S; Lagerstedt-Robinson K; Malmgren H; Nilsson D; Grigelionis G; Conner P; Lindgren P; Lindstrand A; Wedell A; Albage M; Zielinska K; Nordgren A; Papadogiannakis N; Nishimura G; Grigelioniene G
  • Article: MOLECULAR GENETICS & GENOMIC MEDICINE. 2016;4(1):39-45
    Wincent J; Luthman A; van Belzen M; van der Lans C; Albert J; Nordgren A; Anderlid B-M
  • Article: CLINICAL GENETICS. 2016;89(1):99-103
    Kvarnung M; Taylan F; Nilsson D; Albage M; Nordenskjold M; Anderlid BM; Nordgren A; Lundberg ES
  • Article: JAMA PSYCHIATRY. 2016;73(1):20-30
    D'Angelo D; Lebon S; Chen Q; Martin-Brevet S; Snyder LG; Hippolyte L; Hanson E; Maillard AM; Faucett WA; Mace A; Pain A; Bernier R; Chawner SJRA; David A; Andrieux J; Aylward E; Baujat G; Caldeira I; Conus P; Ferrari C; Forzano F; Gerard M; Goin-Kochel RP; Grant E; Hunter JV; Isidor B; Jacquette A; Jonch AE; Keren B; Lacombe D; Le Caignec C; Martin CL; Maennik K; Metspalu A; Mignot C; Mukherjee P; Owen MJ; Passeggeri M; Rooryck-Thambo C; Rosenfeld JA; Spence SJ; Steinman KJ; Tjernagel J; Van Haelst M; Shen Y; Draganski B; Sherr EH; Ledbetter DH; van den Bree MBM; Beckmann JS; Spiro JE; Reymond A; Jacquemont S; Chung WK
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2015;170(6):847-858
    Olsson L; Oefverholm II; Noren-Nystroem U; Zachariadis V; Nordlund J; Sjoegren H; Golovleva I; Nordgren A; Paulsson K; Heyman M; Barbany G; Johansson B
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(9):1176-1185
    Ockeloen CW; Willemsen MH; de Munnik S; van Bon BWM; de Leeuw N; Verrips A; Kant SG; Jones EA; Brunner HG; van Loon RLE; Smeets EEJ; van Haelst MM; van Haaften G; Nordgren A; Malmgren H; Grigelioniene G; Vermeer S; Louro P; Ramos L; Maal TJJ; van Heumen CC; Yntema HG; Carels CEL; Kleefstra T
  • Article: NATURE GENETICS. 2015;47(6):672-676
    Paulsson K; Lilljebjorn H; Biloglav A; Olsson L; Rissler M; Castor A; Barbany G; Fogelstrand L; Nordgren A; Sjogren H; Fioretos T; Johansson B
  • Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2015;96(5):784-796
    Migliavacca E; Golzio C; Maennik K; Blumenthal I; Oh EC; Harewood L; Kosmicki JA; Loviglio MN; Giannuzzi G; Hippolyte L; Maillard AM; Alfaiz AA; van Haelst MM; Andrieux J; Gusella JF; Daly MJ; Beckmann JS; Jacquemont S; Talkowski ME; Katsanis N; Reymond A
  • Article: CLINICAL GENETICS. 2015;87(3):273-278
    Makitie O; Geiberger S; Horemuzova E; Hagenas L; Mostrom E; Nordenskjold M; Grigelioniene G; Nordgren A
  • Article: EUROPEAN JOURNAL OF MEDICAL GENETICS. 2015;58(3):129-133
    Winberg J; Berggren H; Malm T; Johansson S; Ramgren JJ; Nilsson B; Lieden A; Nordenskjold A; Gustavsson P; Nordgren A
  • Article: CLINICAL EPIGENETICS. 2015;7(1):11
    Nordlund J; Backlin CL; Zachariadis V; Cavelier L; Dahlberg J; Ofverholm I; Barbany G; Nordgren A; Overnas E; Abrahamsson J; Flaegstad T; Heyman MM; Jonsson OG; Kanerva J; Larsson R; Palle J; Schmiegelow K; Gustafsson MG; Lonnerholm G; Forestier E; Syvanen A-C
  • Article: HORMONE RESEARCH IN PAEDIATRICS. 2015;83(5):361-364
    Reynaert N; Ockeloen CW; Savendahl L; Beckers D; Devriendt K; Kleefstra T; Carels CEL; Grigelioniene G; Nordgren A; Francois I; de Zegher F; Casteels K
  • Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2014;95(3):285-293
    Acuna-Hidalgo R; Schanze D; Kariminejad A; Nordgren A; Kariminejad MH; Conner P; Grigelioniene G; Nilsson D; Nordenskjold M; Wedell A; Freyer C; Wredenberg A; Wieczorek D; Gillessen-Kaesbach G; Kayserili H; Elcioglu N; Ghaderi-Sohi S; Goodarzi P; Setayesh H; van de Vorst M; Steehouwer M; Pfundt R; Krabichler B; Curry C; MacKenzie MG; Boycott KM; Gilissen C; Janecke AR; Hoischen A; Zenker M
  • Article: MOLECULAR GENETICS & GENOMIC MEDICINE. 2014;2(5):402-411
    Laurell T; Nilsson D; Hofmeister W; Lindstrand A; Ahituv N; Vandermeer J; Amilon A; Anneren G; Arner M; Pettersson M; Jantti N; Rosberg H-E; Cattini PA; Nordenskjold A; Makitie O; Grigelioniene G; Nordgren A
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS. 2014;166(3):315-326
    Vandeweyer G; Helsmoortel C; Van Dijck A; Vulto-van Silfhout AT; Coe BP; Bernier R; Gerdts J; Rooms L; van den Ende J; Bakshi M; Wilson M; Nordgren A; Hendon LG; Abdulrahman OA; Romano C; de Vries BBA; Kleefstra T; Eichler EE; Van der Aa N; Kooy RF
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2014;164(7):1635-1641
    Grigelioniene G; Geiberger S; Horemuzova E; Mostrom E; Jantti N; Neumeyer L; Astrom E; Nordenskjold M; Nordgren A; Makitie O
  • Article: TWIN RESEARCH AND HUMAN GENETICS. 2014;17(3):164-176
    Bölte S; Willfors C; Berggren S; Norberg J; Poltrago L; Mevel K; Coco C; Fransson P; Borg J; Sitnikov R; Toro R; Tammimies K; Anderlid B-M; Nordgren A; Falk A; Meyer U; Kere J; Landén M; Dalman C; Ronald A; Anckarsäter H; Lichtenstein P
  • Article: JOURNAL OF HEMATOLOGY & ONCOLOGY. 2014;7:32
    Lundin C; Forestier E; Andersen MK; Autio K; Barbany G; Cavelier L; Golovleva I; Heim S; Heinonen K; Hovland R; Johannsson JH; Kjeldsen E; Nordgren A; Palmqvist L; Johansson B
  • Article: NATURE GENETICS. 2014;46(4):380-384
    Helsmoortel C; Vulto-van Silfhout AT; Coe BP; Vandeweyer G; Rooms L; van den Ende J; Schuurs-Hoeijmakers JHM; Marcelis CL; Willemsen MH; Vissers LELM; Yntema HG; Bakshi M; Wilson M; Witherspoon KT; Malmgren H; Nordgren A; Anneren G; Fichera M; Bosco P; Romano C; de Vries BBA; Kleefstra T; Kooy RF; Eichler EE; Van der Aa N
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2014;164(2):425-431
    Anderlid B-M; Lundin J; Malmgren H; Lehtihet M; Nordgren A
  • Article: PLOS ONE. 2014;9(1):e85313
    Winberg J; Gustavsson P; Papadogiannakis N; Sahlin E; Bradley F; Nordenskjold E; Svensson P-J; Anneren G; Iwarsson E; Nordgren A; Nordenskjold A
  • Article: CLINICAL GENETICS. 2013;84(6):539-545
    Makrythanasis P; van Bon BW; Steehouwer M; Rodriguez-Santiago B; Simpson M; Dias P; Anderlid BM; Arts P; Bhat M; Augello B; Biamino E; Bongers EMHF; del Campo M; Cordeiro I; Cueto-Gonzalez AM; Cusco I; Deshpande C; Frysira E; Izatt L; Flores R; Galan E; Gener B; Gilissen C; Granneman SM; Hoyer J; Yntema HG; Kets CM; Koolen DA; Marcelis CL; Medeira A; Micale L; Mohammed S; de Munnik SA; Nordgren A; Psoni S; Reardon W; Revencu N; Roscioli T; Ruiterkamp-Versteeg M; Santos HG; Schoumans J; Schuurs-Hoeijmakers JHM; Silengo MC; Toledo L; Vendrell T; van der Burgt I; van Lier B; Zweier C; Reymond A; Trembath RC; Perez-Jurado L; Dupont J; de Vries BBA; Brunner HG; Veltman JA; Merla G; Antonarakis SE; Hoischen A
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2013;161(10):2554-2558
    Grigelioniene G; Geiberger S; Papadogiannakis N; Makitie O; Nishimura G; Nordgren A; Conner P
  • Article: HAEMATOLOGICA. 2013;98(9):1424-1432
    Paulsson K; Forestier E; Andersen MK; Autio K; Barbany G; Borgstrom G; Cavelier L; Golovleva I; Heim S; Heinonen K; Hovland R; Johannsson JH; Kjeldsen E; Nordgren A; Palmqvist L; Johansson B
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2013;161A(6):1284-1290
    Winberg J; Robinson KL; Naess K; Lesko N; Wibom R; Lieden A; Anderlid B-M; Graff C; Nordenskjoeld A; Nordgren A; Gustavsson P
  • Article: LEUKEMIA RESEARCH. 2012;36(7):936-938
    Barbany G; Andersen MK; Autio K; Borgstrom G; Franco LC; Golovleva I; Heim S; Heinonen K; Hovland R; Johansson B; Johannsson JH; Kjeldsen E; Nordgren A; Palmqvist L; Forestier E
  • Article: HUMAN MUTATION. 2012;33(7):1063-1066
    Laurell T; VanderMeer JE; Wenger AM; Grigelioniene G; Nordenskjold A; Arner M; Ekblom AG; Bejerano G; Ahituv N; Nordgren A
  • Article: GENES CHROMOSOMES & CANCER. 2012;51(2):196-206
    Lundin C; Hjorth L; Behrendtz M; Nordgren A; Palmqvist L; Andersen MK; Biloglav A; Forestier E; Paulsson K; Johansson B
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2011;155(2):235-243
    Andersen MK; Autio K; Barbany G; Borgstroem G; Cavelier L; Golovleva I; Heim S; Heinonen K; Hovland R; Johannsson JH; Johansson B; Kjeldsen E; Nordgren A; Palmqvist L; Forestier E
  • Article: NATURE. 2011;478(7367):97-U111
    Jacquemont S; Reymond A; Zufferey F; Harewood L; Walters RG; Kutalik Z; Martinet D; Shen Y; Valsesia A; Beckmann ND; Thorleifsson G; Belfiore M; Bouquillon S; Campion D; de Leeuw N; de Vries BBA; Esko T; Fernandez BA; Fernandez-Aranda F; Manuel Fernandez-Real J; Gratacos M; Guilmatre A; Hoyer J; Jarvelin M-R; Kooy RF; Kurg A; Le Caignec C; Maennik K; Platt OS; Sanlaville D; Van Haelst MM; Villatoro Gomez S; Walha F; Wu B-L; Yu Y; Aboura A; Addor M-C; Alembik Y; Antonarakis SE; Arveiler B; Barth M; Bednarek N; Bena F; Bergmann S; Beri M; Bernardini L; Blaumeiser B; Bonneau D; Bottani A; Boute O; Brunner HG; Cailley D; Callier P; Chiesa J; Chrast J; Coin L; Coutton C; Cuisset J-M; Cuvellier J-C; David A; de Freminville B; Delobel B; Delrue M-A; Demeer B; Descamps D; Didelot G; Dieterich K; Disciglio V; Doco-Fenzy M; Drunat S; Duban-Bedu B; Dubourg C; Moustafa JSE-S; Elliott P; Faas BHW; Faivre L; Faudet A; Fellmann F; Ferrarini A; Fisher R; Flori E; Forer L; Gaillard D; Gerard M; Gieger C; Gimelli S; Gimelli G; Grabe HJ; Guichet A; Guillin O; Hartikainen A-L; Heron D; Hippolyte L; Holder M; Homuth G; Isidor B; Jaillard S; Jaros Z; Jimenez-Murcia S; Helas GJ; Jonveaux P; Kaksonen S; Keren B; Kloss-Brandstaetter A; Knoers NVAM; Koolen DA; Kroisel PM; Kronenberg F; Labalme A; Landais E; Lapi E; Layet V; Legallic S; Leheup B; Leube B; Lewis S; Lucas J; MacDermot KD; Magnusson P; Marshall C; Mathieu-Dramard M; McCarthy MI; Meitinger T; Mencarelli MA; Merla G; Moerman A; Mooser V; Morice-Picard F; Mucciolo M; Nauck M; Ndiaye NC; Nordgren A; Pasquier L; Petit F; Pfundt R; Plessis G; Rajcan-Separovic E; Ramelli GP; Rauch A; Ravazzolo R; Reis A; Renieri A; Richart C; Ried JS; Rieubland C; Roberts W; Roetzer KM; Rooryck C; Rossi M; Saemundsen E; Satre V; Schurmann C; Sigurdsson E; Stavropoulos DJ; Stefansson H; Tengstrom C; Thorsteinsdottir U; Tinahones FJ; Touraine R; Vallee L; van Binsbergen E; Van der Aa N; Vincent-Delorme C; Visvikis-Siest S; Vollenweider P; Voelzke H; Vulto-van Silfhout AT; Waeber G; Wallgren-Pettersson C; Witwicki RM; Zwolinksi S; Andrieux J; Estivill X; Gusella JF; Gustafsson O; Metspalu A; Scherer SW; Stefansson K; Blakemore AIF; Beckmann JS; Froguel P
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2011;156B(2):115-124
    Bremer A; Giacobini M; Eriksson M; Gustavsson P; Nordin V; Fernell E; Gillberg C; Nordgren A; Uppstromer A; Anderlid B-M; Nordenskjold M; Schoumans J
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2011;152(5):615-622
    Kuchinskaya E; Heyman M; Nordgren A; Soderhall S; Forestier E; Wehner P; Vettenranta K; Jonsson O; Wesenberg F; Sahlen S; Nordenskjold M; Blennow E
  • Article: CURRENT GENOMICS. 2010;11(6):409-419
    Hulten MA; Jonasson J; Nordgren A; Iwarsson E
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2010;152A(9):2277-2286
    Winberg J; Gustavsson P; Lagerstedt-Robinson K; Blennow E; Lundin J; Iwarsson E; Nordenstrom A; Anderlid B-M; Bondeson M-L; Nordenskjold A; Nordgren A
  • Article: LEUKEMIA. 2010;24(5):924-931
    Davidsson J; Paulsson K; Lindgren D; Lilljebjorn H; Chaplin T; Forestier E; Andersen MK; Nordgren A; Rosenquist R; Fioretos T; Young BD; Johansson B
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2010;152A(5):1233-1243
    Lindstrand A; Malmgren H; Verri A; Benetti E; Eriksson M; Nordgren A; Anderlid B-M; Golovleva I; Schoumans J; Blennow E
  • Article: CLINICAL GENETICS. 2010;77(2):145-154
    Lindstrand A; Malmgren H; Sahlen S; Schoumans J; Nordgren A; Ergander U; Holm E; Anderlid BM; Blennow E
  • Journal article: BLOOD. 2009;114(22):2591
    Davidsson J; Paulsson K; Lindgren D; Lilljebjörn H; Chaplin T; Forestier E; Andersen MK; Nordgren A; Rosenquist R; Fioretos T; Young BD; Johansson B
  • Article: HAEMATOLOGICA. 2009;94(9):1301-1306
    Akagi T; Shih L-Y; Ogawa S; Gerss J; Moore SR; Schreck R; Kawamata N; Liang D-C; Sanada M; Nannya Y; Deneberg S; Zachariadis V; Nordgren A; Song JH; Dugas M; Lehmann S; Koeffler HP
  • Article: JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY. 2009;31(9):696-701
    Diffner E; Gauffin F; Anagnostaki L; Nordgren A; Gustafsson B; Sander B; Gustafsson B; Persson JL
  • Article: GENES CHROMOSOMES & CANCER. 2009;48(9):795-805
    Karrman K; Forestier E; Heyman M; Andersen MK; Autio K; Blennow E; Borgstrom G; Ehrencrona H; Golovleva I; Heim S; Heinonen K; Hovland R; Johannsson JH; Kerndrup G; Nordgren A; Palmqvist L; Johansson B
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2009;149A(8):1706-1711
    Iwarsson E; Sahlen S; Nordgren A
  • Article: CLINICAL CHEMISTRY AND LABORATORY MEDICINE. 2009;47(12):1467-1469
    Gauffin F; Nordgren A; Barbany G; Gustafsson B; Karlsson H
  • Article: PEDIATRIC HEMATOLOGY AND ONCOLOGY. 2009;26(1):48-56
    Gauffin F; Diffner E; Gustafsson B; Nordgren A; Wingren AG; Sander B; Persson JL; Gustafsson B
  • Article: EUROPEAN JOURNAL OF HAEMATOLOGY. 2008;81(3):218-225
    Bostrom H; Leuchowius K-J; Hallbook H; Nordgren A; Thorn I; Thorselius M; Rosenquist R; Soderberg O; Sundstrom C
  • Article: LEUKEMIA & LYMPHOMA. 2008;49(3):477-487
    Thelander EF; Ichimura K; Corcoran M; Barbany G; Nordgren A; Heyman M; Berglund M; Mungall A; Rosenquist R; Collins VP; Grander D; Larsson C; Lagercrantz S
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2008;140(5):572-577
    Kuchinskaya E; Heyman M; Nordgren A; Schoumans J; Staaf J; Borg A; Soderhall S; Grander D; Nordenskjold M; Blennow E
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2008;140(6):665-672
    Forestier E; Heyman M; Andersen MK; Autio K; Blennow E; Borgstrom G; Golovleva I; Heim S; Heinonen K; Hovland R; Johannsson JH; Kerndrup G; Nordgren A; Rosenquist R; Swolin B; Johansson B
  • Article: BRITISH JOURNAL OF CANCER. 2007;97(7):992-994
    Gustafsson B; Huang W; Bogdanovic G; Gauffin F; Nordgren A; Talekar G; Ornelles DA; Gooding LR
  • Article: HUMAN MOLECULAR GENETICS. 2007;16(14):1773-1782
    Hilton EN; Manson FDC; Urquhart JE; Johnston JJ; Slavotinek AM; Hedera P; Stattin E-L; Nordgren A; Biesecker LG; Black GCM
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2007;15(2):143-149
    Schoumans J; Wincent J; Barbaro M; Djureinovic T; Maguire P; Forsberg L; Staaf J; Thuresson AC; Borg A; Nordgren A; Malm G; Anderlid BM
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2006;135(4):492-499
    Schoumans J; Johansson B; Corcoran M; Kuchinskaya E; Golovleva I; Grander D; Forestier E; Staaf J; Borg A; Gustafsson B; Blennow E; Nordgren A
  • Journal article: EUROPEAN JOURNAL OF MEDICAL GENETICS. 2005;48(4):447-448
    Schoumans J; Maguire P; Staaf J; Jönsson G; Ruivenkamp C; Thuresson A-C; Nordgren A; Malm G; Borg Å; Blennow E; Anderlid B-M; Nordenskjöld M
  • Article: EUROPEAN JOURNAL OF HAEMATOLOGY. 2005;74(6):466-480
    Kuchinskaya E; Heyman M; Grandér D; Linderholm M; Söderhäll S; Zaritskey A; Nordgren A; Porwit-MacDonald A; Zueva E; Pawitan Y; Corcoran M; Nordenskjöld M; Blennow E
  • Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2005;13(2):260-263
    Schoumans J; Nordgren A; Ruivenkamp C; Brondum-Nielsen K; Teh BT; Annéren G; Holmberg E; Nordenskjöld M; Anderlid BM
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2003;121(4):566-577
    Forestier E; Heim S; Blennow E; Borgström G; Holmgren G; Heinonen K; Johannsson J; Kerndrup G; Andersen MK; Lundin C; Nordgren A; Rosenquist R; Swolin B; Johansson B
  • Article: EUROPEAN JOURNAL OF HAEMATOLOGY. 2002;68(1):31-41
    Nordgren A; Heyman M; Sahlén S; Schoumans J; Söderhäll S; Nordenskjöld M; Blennow E
  • Article: BRITISH JOURNAL OF HAEMATOLOGY. 2001;114(4):786-793
    Nordgren A; Schoumans J; Söderhäll S; Nordenskjöld M; Blennow E
  • Article: EUROPEAN JOURNAL OF HAEMATOLOGY. 2001;66(5):297-304
    Nordgren A; Farnebo F; Johansson B; Holmgren G; Forestier E; Larsson C; Söderhäll S; Nordenskjöld M; Blennow E
  • Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2001;68(4):1043-1047
    Lee C; Gisselsson D; Jin C; Nordgren A; Ferguson DO; Blennow E; Fletcher JA; Morton CC
  • Article: GENES CHROMOSOMES & CANCER. 2000;28(3):308-317
    Kytölä S; Rummukainen J; Nordgren A; Karhu R; Farnebo F; Isola J; Larsson C
  • Article: INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE. 2000;5(5):485-492
    Nordgren A; Sorensen AG; Tinggaard-Pedersen N; Blennow E; Larsson C; Lagercrantz S
  • Article: HEMATOLOGY JOURNAL. 2000;1(2):95-101
    Nordgren A; Farnebo F; Björkholm M; Sahlén S; Porwit-MacDonald A; Osby E; Kytölä S; Larsson C; Nordenskjöld M; Blennow E
  • Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 1997;73(3):351-355
    Nordgren A; Arver S; Kvist U; Carter N; Blennow E
  • Article: CANCER GENETICS. 1997;99(2):93-96
    Nordgren A; Nordenskjold M; Soderhall S; PorwitMacDonald A; Blennow E
  • Article: LEUKEMIA. 1996;10(5):909-917
    Heyman M; Nordgren A; JeddiTehrani M; Rasool O; Liu Y; Grander D; Ost A; Wallberg B; Johansson B; Einhorn S
  • Article: LEUKEMIA. 1996;10(4):662-668
    Bernell P; Jacobsson B; Nordgren A; Hast R
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    Bilgrav Saether K; Eisfeldt J; Bengtsson J; Lun MY; Grochowski CM; Mahmoud M; Chao H-T; Rosenfeld JA; Liu P; Schuy J; Ameur A; Undiagnosed Diseases Network; Hwang JP; Sedlazeck FJ; Bi W; Marom R; Nordgren A; Carvalho CMB; Lindstrand A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2024;32:52
    Tesi B; Taylan F; Lagerstedt-Robinson K; Abel F; Hellberg M; de Stahl TD; Wessman S; Samuelsson S; Henning K; Frisk T; Sabel M; Vogt H; Nyman P; Giraud G; Wille J; Pronk CJ; Nystrom UN; Borssen M; Fili M; Stalhammar G; Herold N; Orrsjo S; Poluha A; Gonzalez CM; Arvidsson L; Rosen A; Ekholm K; Kuchinskaya E; Hallbeck A-L; Shamikh A; Mertens F; Brandell RR; Tham E; Grillner P; Sandgren J; Ljungman G; Nord DG; Nordgren A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2024;32:545-546
    Gonzalez CM; Taylan F; Tesi B; Lagerstedt-Robinson K; Wessman S; Stenman J; Fagman H; Olsen TK; Georgantzi K; de Stahl TD; Ek T; Palmer R; Forsberg S; Martinsson T; Kogner P; Nordgren A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2024;32:528-529
    Bouhatous Y-M; Bredrup C; Rustad C; Bardou M; Maurer A; Luu M; Vabres P; Kurtz JE; Schaefer E; Guimier A; Cormier-Daire V; Demoulin J-B; Lim D; Nordgren A; Aguirre-Rodriguez C; Hernandez-Dorronsoro U; Martinez-Soroa I; Iznardo H; Kalantari S; Mussa A; Carli D; Gawlinski P; Svinvik I; Mutlu H; Bluefeather S; Pond D; Zarate Y; Wenger T; Biesecker L; Kosaki K; Binquet C; Foster A; Faivre L
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2024;32:1461-1462
    de Boer ETB; Shahsavani M; Eisfeldt J; Nordgren A; Lindstrand A
  • Review: JOURNAL OF INTERNAL MEDICINE. 2023;294(4):397-412
    Tesi B; Boileau C; Boycott KM; Canaud G; Caulfield M; Choukair D; Hill S; Spielmann M; Wedell A; Wirta V; Nordgren A; Lindstrand A
  • Preprint: PSYARXIV. 2023
    Kleberg JL; Hallman AEZ; Galazka M; Riby D; Bölte S; Willfors C; Fawcett C; Nordgren A
  • Other: JOURNAL OF PEDIATRIC UROLOGY. 2023;19(3):335-338
    Nordgren A; Lindstrand A; Wu H-Y; Fossum M
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:524-525
    Gonzalez CM; Wessman S; Tesi B; Taylan F; McCluggage G; Kuchinskaya E; Poluha A; Holm S; Nargard R; de Stahl TD; Nord DG; Lagerstedt K; Nordgren A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:326-327
    Le Dref M; Avela K; Bartuli A; Bedeschi MF; Dan D; Demirdas S; Houge SD; Dufke A; Faivre L; Genevieve D; Guerrini R; Hadzsiev K; Hennekam R; Hugon A; Huning I; Jouannic J-M; Kaiser FJ; Kleefstra T; Lacombe D; Macek M; Matuleviciene A; Mazzanti L; Menke L; Meuwissen M; Mosiello G; Nordgren A; Odent S; Petit F; Puiu M; Ramos L; Renieri A; Rossi M; Salviati L; Sigaudy S; Stumpel C; Szeto N; Tanteles G; Tartaglia M; Tumer Z; Tumiene B; van Eeghen A; Van Esch H; Van Ierland Y; Vilain C; Vissers L; Vyshka K; Wieczorek D; Zampino G; Verloes A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:395-396
    Lindelof H; Horemuzova E; Nordgren A; Voss U; Hammarsjo A; Grigelioniene G
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:512-513
    Taylan F; Gonzalez CM; Khoshnood B; Campbell T; Bobeck J; Bryceson Y; Nordenskjold M; Nordgren A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:451
    Lindstrand A; Ek M; Kvarnung M; Anderlid BM; Bjorck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjo A; Helgadottir H; Pigg MH; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-A; Lieden A; Lindelof H; Malmgren H; Nilsson D; Svensson E; Arce MP; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Soller MJ; Pettersson M; Nordgren A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:632
    Soller M; Runheim H; Nordgren A; Petters-Son M; Hammarsjo A; Henriksson M; Levin L-A; Lindstrand A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:590-591
    Lindstrand A; Stranneheim H; Lagerstedt-Robinson K; Lesko N; Nilsson D; Vonlanthen S; Eisfeldt J; Kvarnung M; Engvall M; Malmgren H; Anderlid B-M; Rasi C; Jemt A; Marits P; Soller MJ; Nordgren A; Wirta V; Wedell A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2023;31:444
    Frisk S; Wachtmeister A; Laurell T; Lindstrand A; Jantti N; Malmgren H; Lagerstedt-Robinson K; Tesi B; Taylan F; Nordgren A
  • Preprint: MEDRXIV. 2023
    Krali O; Marincevic-Zuniga Y; Arvidsson G; Enblad AP; Lundmark A; Sayyab S; Zachariadis V; Heinäniemi M; Suhonen J; Oksa L; Vepsäläinen K; Öfverholm I; Barbany G; Nordgren A; Lilljebjörn H; Fioretos T; Madsen H; Marquart HV; Flaegstad T; Forestier E; Jónsson Ó; Kanerva J; Lohi O; Norén-Nyström U; Schmiegelow K; Harila A; Heyman M; Lönnerholm G; Syvänen A-C; Nordlund J
  • Preprint: MEDRXIV. 2023
    Bychkov G; Bang B; Engsner N; Heyman MM; Nordenvall AS; Tettamanti G; Herold N; Taylan F; Pontén E; Albert J; Jörnsten R; Strannegård C; Nordgren A
  • Conference publication: 2022 34TH WORKSHOP OF THE SWEDISH ARTIFICIAL INTELLIGENCE SOCIETY (SAIS 2022). 2022;:1-9
    Strannegard C; Engsner N; Eisfeldt J; Endler J; Hansson A; Lindgren R; Mostad P; Olsson S; Perini I; Reese H; Taylan F; Ulfsbacker S; Nordgren A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2022;30(SUPPL 1):41-42
    Batkovskyte D; McKenzie F; Taylan F; Simsek-Kiper PO; Nikkel SM; Ohashi H; Miyahara H; Eriksson G; Ha T; Utine GE; Chiu T; Shimizu K; Hammarsjo A; Boduroglu K; Arts P; Babic M; Jackson MR; Papadogiannakis N; Lindstrand A; Nordgren A; Barnett CP; Scott HS; Chagin AS; Nishimura G; Grigelioniene G
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2022;30(SUPPL 1):558-559
    Luu M; Foster A; Aguirre Rodriguez C; Westergren H; Hernandez Dorronsor U; Martinez Soroa I; Lim D; Thompson S; Nordgren A; Bluefeather S; Schaefer E; Bardou M; Vabres P; Kurtz J-E; Faivre L
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2022;30(SUPPL 1):236-237
    Denomme-Pichon A-S; de Boer E; Jackson A; Benetti E; Banka S; Casari G; Ciolfi A; Clayton-Smith J; Dallapiccola B; Ellwanger K; Faivre L; Gilissen C; Graessner H; Haack TB; Hammarsjo A; Havlovicova M; Hoischen A; Hugon A; Kleefstra T; Lindstrand A; Lopez-Martin E; Macek MJ; Matalonga L; Morleo M; Nigro V; Nordgren A; Pettersson M; Pinelli M; Pizzi S; Posada M; Radio FC; Renieri A; Rooryck C; Ryba L; Schwarz M; Tartaglia M; Thauvin C; Torella A; Trimouille A; Votypka P; Vyshka K; Zurek B; Verloes A; Vitobello A; Vissers L
  • Conference publication: JOURNAL OF INTELLECTUAL DISABILITY RESEARCH. 2021;65(9):811
    Willfors C; Riby D; Kleberg JL; Nordgren A
  • Corrigendum: EUROPEAN JOURNAL OF HUMAN GENETICS. 2021;29(9):1470-1471
    de Boer E; Ockeloen CW; Matalonga L; Horvath R; Rodenburg RJ; Coenen MJH; Janssen M; Henssen D; Gilissen C; Steyaert W; Trimouille A; Kleefstra T; Verloes A; Vissers LELM
  • Other: LAKARTIDNINGEN. 2021;118:21015
    Johansson Soller M; Nordgren A; Ehrencrona H; Lovmar L; Wedell A; Lindstrand A
  • Preprint: PSYARXIV. 2020
    Kleberg JL; Riby D; Fawcett C; Avdic HB; Frick M; Brocki K; Högström J; Serlachius E; Nordgren A; Willfors C
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020;28(SUPPL 1):254
    Hammarsjo A; Pettersson M; Chitayat D; Handa A; Taylan F; Batkovskyte D; Anderlid B; Lin AE; Shimizu K; Beleza-Meireles A; Chung B; Voss U; Nordgren A; Nishimura G; Lindstrand A; Grigelioniene G
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020;28(SUPPL 1):3-4
    Kvarnung M; Wang T; Hoekzema K; Vecchio D; Wu H; Sulovari A; Coe BP; Gillentine MA; Wilfert AB; Lindstrand A; Nordgren A; Anderlid B; Rosenfeld JA; Liu P; Scheffer IE; Brunetti-Perri N; Rommelse N; Amaral DG; Santen GWE; Trabetti E; Sedlacek Z; Michaelson JJ; Pierce K; Courchesne E; Kooy FR; Romano C; Peeters H; Bernier RA; Gecz J; Xia K; Eichler EE; Nordenskjold M
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020;28(SUPPL 1):52-53
    Lindstrand A; Stranneheim H; Lagerstedt-Robinson K; Kvarnung M; Lesko N; Nilsson D; Anderlid B; Arnell H; Johansson CB; Barbaro M; Bjorck E; Bruhn H; Eisfeldt J; Engvall M; Freyer C; Grigelioniene G; Gustavsson P; Hammarsjo A; Hellstrom-Pigg M; Jemt A; Laaksonen M; Enoksson SL; Magnusson M; Malmgren H; Naess K; Nordenskjold M; Oscarson M; Pettersson M; Rasi C; Rosenbaum A; Sahlin E; Stodberg T; Tesi B; Tham E; Thonberg H; von Dobeln U; Vonlanthen S; Wikstrom A; Wincent J; Winqvist O; Wredenberg A; Ygberg S; Zetterstrom RH; Marits P; Johansson-Soller M; Soller MJ; Nordgren A; Wirta V; Wedell A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2020;28(SUPPL 1):462-463
    Frisk SA; Ponten E; Lagerstedt-Robinson K; Vaz R; Taylan F; Nordgren A
  • Other: NATURE COMMUNICATIONS. 2020;11(1):5398
    Wang T; Hoekzema K; Vecchio D; Wu H; Sulovari A; Coe BP; Gillentine MA; Wilfert AB; Perez-Jurado LA; Kvarnung M; Sleyp Y; Earl RK; Rosenfeld JA; Geisheker MR; Han L; Du B; Barnett C; Thompson E; Shaw M; Carroll R; Friend K; Catford R; Palmer EE; Zou X; Ou J; Li H; Guo H; Gerdts J; Avola E; Calabrese G; Elia M; Greco D; Lindstrand A; Nordgren A; Anderlid B-M; Vandeweyer G; Van Dijck A; Van der Aa N; McKenna B; Hancarova M; Bendova S; Havlovicova M; Malerba G; Bernardina BD; Muglia P; van Haeringen A; Hoffer MJV; Franke B; Cappuccio G; Delatycki M; Lockhart PJ; Manning MA; Liu P; Scheffer IE; Brunetti-Pierri N; Rommelse N; Amaral DG; Santen GWE; Trabetti E; Sedlacek Z; Michaelson JJ; Pierce K; Courchesne E; Kooy RF; Nordenskjold M; Romano C; Peeters H; Bernier RA; Gecz J; Xia K; Eichler EE
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27:1666-1667
    Nilsson D; Eisfeldt J; Lundin J; Pettersson M; Kvarnung M; Lieden A; Sahlin E; Lagerstedt K; Martin M; Ygberg S; Bjerin O; Stranneheim H; Wedell A; Nordenskjold M; Soller MJ; Nordgren A; Wirta V; Lindstrand A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27:1533
    Lagerstedt-Robinson K; Anderlid B; Nordgren A; Grigelioniene G; Kvarnung M; Gustavsson P; Tham E; Nilsson D; Soller MJ; Nordenskjold M; Lindstrand A; Malmgren H
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27:1143
    Kvarnung M; Shahsavani M; Taylan F; Breeuwsma N; Laan L; Schuster J; Jin Z; Nilsson D; Lieden A; Anderlid B; Nordenskjold M; Lundberg ES; Birnir B; Dahl N; Nordgren A; Lindstrand A; Falk A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27:1519-1520
    Taylan F; Frisk S; Blaszczyk I; Nennesmo I; Anneren G; Stattin E; Zachariadis V; Lindstrand A; Tesi B; Laurell T; Nordgren A
  • Conference publication: 2019
    G G; HI S; F T; F M; ZU B; UM A; S T; E H; A L; MA W; G G; A H; E M; A N; M N; DR E; ML W; G N; PA S; T K
  • Editorial comment: STEM CELL RESEARCH. 2019;39:101518
    Schuster J; Sobol M; Fatima A; Khalfallah A; Laan L; Anderlid B-M; Nordgren A; Dahl N
  • Conference publication: MOLECULAR CYTOGENETICS. 2019;12
    Eisfeldt J; Lundin J; Pettersson M; Kvarnung M; Lieden A; Sahlin E; Lagerstedt K; Martin M; Ygberg S; Bjerin O; Stranneheim H; Wedell A; Nordenskjold M; Soller MJ; Nordgren A; Wirta V; Nilsson D; Lindstrand A
  • Review: CLINICAL GENETICS. 2019;95(4):462-478
    Zollino M; Zweier C; Van Balkom ID; Sweetser DA; Alaimo J; Bijlsma EK; Cody J; Elsea SH; Giurgea I; Macchiaiolo M; Smigiel R; Thibert RL; Benoist I; Clayton-Smith J; De Winter CF; Deckers S; Gandhi A; Huisman S; Kempink D; Kruisinga F; Lamacchia V; Marangi G; Menke L; Mulder P; Nordgren A; Renieri A; Routledge S; Saunders CJ; Stembalska A; Van Balkom H; Whalen S; Hennekam RC
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2018;26:677
    Nilsson D; Robinson KL; Malmgren H; Karlsson M; Gustavsson P; Hammarsjo A; Grigelioniene G; Arce MP; Tham E; Pigg MH; Anderlid B; Nordgren A; Jorholt J; Kvarnung M; Sejersen T; Lieden A; Lundin J; Eisfeldt J; Lindstrand A; Wirta V; Nordenskjold M
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2018;26:675
    Lagerstedt-Robinson K; Anderlid B; Nordgren A; Kvarnung M; Lindstrand A; Grigelioniene G; Tham E; Gustavsson P; Nilsson D; Nordenskjold M; Malmgren H
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2018;26:548-549
    Bang B; Jarviaho T; Zachariadis V; Taylan F; Niinimaki R; Moilanen J; Harila-Saari A; Nordgren A
  • Conference publication: EUROPEAN JOURNAL OF HUMAN GENETICS. 2018;26:644-645
    Taylan F; Zachariadis V; Bang B; Ofverholm I; Harila-Saari A; Heyman M; Tran A; Barbany G; Nordgren A
  • Preprint: BIORXIV. 2017
    Stamouli S; Anderlid B-M; Willfors C; Thiruvahindrapuram B; Wei J; Berggren S; Nordgren A; Scherer S; Lichtenstein P; Tammimies K; Bölte S
  • Review: LAKARTIDNINGEN. 2017;114:ELYP
    Björlin Avdic H; Giacobini M; Anderlid B-M; Nordgren A; Frisén L
  • Other: MOLECULAR GENETICS & GENOMIC MEDICINE. 2016;4(3):367
    Wincent J; Luthman A; van Belzen M; van der Lans C; Albert J; Nordgren A; Anderlid B-M
  • Letter: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2016;170(1):266-269
    Hammarsjo A; Nordgren A; Lagerstedt-Robinson K; Malmgren H; Nilsson D; Wedren S; Nordenskjold M; Nishimura G; Grigelioniene G
  • Letter: HAEMATOLOGICA. 2016;101(1):e20-e23
    Marincevic-Zuniga Y; Zachariadis V; Cavelier L; Castor A; Barbany G; Forestier E; Fogelstrand L; Heyman M; Abrahamsson J; Lonnerholm G; Nordgren A; Syvanen A-C; Nordlund J
  • Corrigendum: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(9):1270
    Ockeloen CW; Willemsen MH; de Munnik S; van Bon BWM; de Leeuw N; Verrips A; Kant SG; Jones EA; Brunner HG; van Loon RLE; Smeets EEJ; van Haelst MM; van Haaften G; Nordgren A; Malmgren H; Grigelioniene G; Vermeer S; Louro P; Ramos L; Maal TJJ; van Heumen CC; Yntema HG; Carels CEL; Kleefstra T
  • Letter: CLINICAL GENETICS. 2015;87(5):496-498
    Tham E; Nishimura G; Geiberger S; Horemuzova E; Nilsson D; Lindstrand A; Hammarsjo A; Armenio M; Makitie O; Zabel B; Nordgren A; Nordenskjold M; Grigelioniene G
  • Conference publication: BLOOD. 2014;124(21):1085
    Ofverholm II; Anh NT; Zachariadis V; Heyman M; Rudd E; Lundberg ES; Nordenskjold M; Nordgren A; Barbany G
  • Conference publication: BLOOD. 2014;124(21):490
    Nordlund J; Backlin C; Zachariadis V; Cavelier L; Dahlberg J; Ofverholm I; Barbany G; Nordgren A; Overnas E; Abrahamsson J; Flaegstad T; Heyman M; Jonsson OG; Kanerva JA; Larsson R; Palle J; Schmiegelow K; Gustafsson MG; Lonnerholm G; Forestier E; Syvanen A-C
  • Conference publication: HAEMATOLOGICA. 2014;99:9
    Ofverholm II; Olsson L; Noren-Nystrom U; Forestier E; Nordlund J; Sjogren H; Golovleva I; Heyman M; Zachariadis V; Nordgren A; Johansson B; Barbany G
  • Letter: LEUKEMIA & LYMPHOMA. 2013;54(12):2742-2744
    Barbany G; Gauffin F; Ofverholm I; Karlsson H; Thorn I; Arvidson J; Heyman M; Gustafsson B; Nordgren A
  • Letter: LEUKEMIA. 2013;27(9):1936-1939
    Ofverholm I; Tran AN; Heyman M; Zachariadis V; Nordenskjold M; Nordgren A; Barbany G
  • Conference publication: CHROMOSOME RESEARCH. 2013;21:S16
    Blennow E; Kouru KH; Kvarnung M; Nordgren A; Malmgren H
  • Letter: LEUKEMIA. 2013;27(4):974-977
    Paulsson K; Harrison CJ; Andersen MK; Chilton L; Nordgren A; Moorman AV; Johansson B
  • Review: LAKARTIDNINGEN. 2010;107(17):1144-1149
    Anderlid B-M; Blennow E; Giacobini M; Nordgren A; Wincent J; Schoumans J; Nordenskjöld M
  • Review: EUROPEAN JOURNAL OF HAEMATOLOGY. 2010;84(1):17-25
    Nordgren A; Corcoran M; Saaf A; Bremer A; Kluin-Nelemans HC; Schoumans J; Grander D
  • Conference publication: BLOOD. 2009;114(22):1017
    Davidsson J; Paulsson K; Lindgren D; Lilljebjorn H; Chaplin T; Forestier E; Andersen MK; Nordgren A; Rosenquist R; Fioretos T; Young BD; Johansson B
  • Conference publication: CHROMOSOME RESEARCH. 2009;17:80-81
    Nordgren A; Lundin J; Malmgren H; Lehtihet M; Anderlid B
  • Letter: LEUKEMIA. 2009;23(1):209-212
    Lonnerholm G; Nordgren A; Frost B-M; Jonsson OG; Kanerva J; Nygaard R; Schmiegelow K; Larsson R; Forestier E
  • Review: GENES CHROMOSOMES & CANCER. 2008;47(2):149-158
    Forestier E; Gauffin F; Andersen MK; Autio K; Borgstrom G; Golovleva I; Gustafsson B; Heim S; Heinonen K; Heyman M; Hovland R; Johannsson JH; Kerndrup G; Rosenquist R; Schoumans J; Swolin B; Johansson B; Nordgren A
  • Letter: LEUKEMIA. 2007;21(6):1327-1330
    Kuchinskaya E; Nordgren A; Heyman M; Schoumans J; Corcoran M; Staaf J; Borg A; Soderhall S; Grander D; Nordenskjold M; Blennow E
  • Review: GENES CHROMOSOMES & CANCER. 2007;46(5):440-450
    Forestier E; Andersen MK; Autio K; Blennow E; Borgstrom G; Golovleva I; Heim S; Heinonen K; Hovland R; Johannsson JH; Kerndrup G; Nordgren A; Rosenquist R; Swolin B; Johansson B
  • Conference publication: CELLULAR ONCOLOGY. 2007;29(2):118-119
    Kuchinskaya E; Nordgren A; Heyman M; Schoumans J; Corcoran M; Staaf J; Borg A; Soderhall S; Grander D; Nordenskjold M
  • Review: LEUKEMIA & LYMPHOMA. 2003;44(12):2039-2053
    Nordgren A
  • Doctoral thesis: 2001
    Nordgren A
  • Meeting abstract: PEDIATRIC RESEARCH. 1999;45(4):144A
    Blennow E; Nordgren A; Farnebo F; Soderhall S; Nordenskjold M
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Forskningsbidrag

  • Swedish Research Council
    1 January 2024 - 31 December 2026
    Pediatric Acute Lymphoblastic Leukemia (ALL) arises from lymphocyte progenitors and is known to present a hierarchy of cell differentiation, making it a suitable model disease for studying differentiation state instability and cancer stem cells. We will analyze ALL samples during treatment and at relapsed from the same patient using a novel method that allows RNA sequencing and genomic sequencing in jointly in the same single cells. Using this method, we will characterize the clonal structure of the leukemia and analyze clonal leukemic cell types in the primary sample of patients which later relapse. Since we obtain data on both the genotype (genomic sequencing) and gene expression profile (RNA-seq) of each cell, we can trace clonal expansions that are mainly driven by epigenetic factors as well as those driven by genetic alterations. Based on this map of treatment escape, we will 1) Determine molecular targets for therapy using a gene editing screen and 2) Test the added value of single-cell genomics for diagnostic tests (in collaboration with clinical genetics). The ultimate goal of the project is to gain a deep understanding of the cancer stem cell population in pediatric ALL tumors in a way that will have a direct impact on the treatment and prevention of ALL recurrence. To ensure that potential discoveries will have clinical diagnostic adaptation, we have partnered with experienced clinicians in genetics and hematopathology.
  • Barncancerfonden
    1 January 2024 - 31 December 2024
  • Barncancerfonden
    1 January 2024 - 31 December 2024
  • Swedish Cancer Society
    1 January 2023
    Research has in recent years shown that between 10-15% of all children with cancer have a congenital genetic change. This applies above all to children with adult tumors, various forms of cancer, close relatives affected by childhood cancer, children who have reacted with severe side effects of cancer treatment and children with malformations, overgrowth syndrome or other rare diseases. Congenital genetic changes can negatively affect prognosis by affecting treatment response and increasing the risk of therapy-related severe side effects. Such complications may in turn be possible to avoid if the congenital diagnosis is detected in time. All different forms of childhood cancer are studied using genetic analyzes with whole genome sequencing and epidemiological studies where we also use AI and machine learning. The project is about improving genetic diagnostics and introducing whole genome sequencing regarding congenital genetic changes in clinical routine. The project affects both diagnostics, treatment and prevention and will lead to more children being offered precision medicine with targeted treatments and that treatment complications can be avoided and new treatment targets can be identified. In addition, preventive screening programs can be offered to relatives at risk of cancer. We want to understand why children get cancer and understand the mechanisms of its occurrence and find ways to improve survival and quality of life for survivors of childhood cancer and their relatives. We want to try to answer the following questions. Is the incidence of childhood cancer higher in specific genetic syndromes? Is cancer more common in families with a child with cancer and how big is the risk for relatives? Are congenital genetic abnormalities detected in cancer cells at diagnosis correlated to prognosis, treatment outcome, infectious diseases, seasons and geographic locations? Can we find new disease and cancer associations?
  • Barncancerfonden
    1 January 2022 - 31 December 2022
  • Molecular and Epidemiological studies of Childhood Cancer predisposition
    Cancerföreningen i Stockholm
    1 January 2022 - 31 December 2024
  • Swedish Research Council
    1 December 2021 - 31 December 2025
    Our overall ambition is to study childhood cancer etiology through genetic, epidemiological and machine learning studies based on a novel machine learning algorithm in order to discover novel genes, pathways and molecular mechanisms as well as environmental factors critical in the development of childhood cancer. Our aim is to discover novel targets for therapy and situations where treatment should be modified to avoid toxicity or therapy resistance and when genetic counselling should be offered the family. We also want to identify risk factors for cancer development and contribute to the development of surveillance protocols, increase awareness of genetic predisposition and investigate the benefits of integrating germline sequencing into clinical practice in pediatric oncology. The long-term objective is to identify risk factors and to translate rare phenotypes into gene discoveries and to improve diagnostics and precision medicine in order to reduce morbidity and mortality of cancer in children.
  • Swedish Research Council
    1 January 2021 - 31 December 2023
  • Swedish Cancer Society
    1 January 2020
    In recent years, research has shown that more than 10% of all children affected by cancer have congenital genetic changes as a contributing cause of their disease. This is especially true for children with rare tumors that normally only occur in adults, children who suffer from several different cancers, children with several close relatives who suffered from cancer at an early age, children who suffer from abnormally severe side effects of cancer treatment and children with cancer and malformations, overgrowth syndrome, epilepsy, intellectual disability, autism, or other rare disease. It is important to find these patients as it can save lives. We want to introduce diagnostics into clinical routine to look for known and new congenital genetic abnormalities and then compare them with genetic abnormalities in cancer cells in people with cancer, children whose cancer type or side effect profile gives strong suspicion of congenital genetic causes and people who included in families where more than one child has been affected by cancer. We want to use new DNA and RNA based methods that are based on sequencing of the entire human genome. In cases where we find new suspected cancer-associated genes, we will proceed with various functional studies in animal models and cells from patients. I want to identify patients who need a tailored treatment and understand the mechanisms of emergence and find new disease genes behind the syndrome and cancer. Increased knowledge about familial cancer and why certain syndromes are associated with cancer risk and increased sensitivity to cytotoxic drugs and radiation is important and will lead to improved care, tailored therapies and opportunities to implement preventive measures in the affected individual and his family. . The research also leads to increased knowledge about childhood cancer in general, which can lead to improved diagnostics and treatment and improved survival.
  • Constitutional genetic aberrations behind childhood cancer predisposition
    Swedish Cancer Society
    1 January 2019
    In recent years, research has shown that more than 10% of all children affected by cancer have congenital genetic changes as a contributing cause of their disease. This is especially true for children with rare tumors that normally only occur in adults, children who suffer from several different cancers, children with several close relatives who suffered from cancer at an early age, children who suffer from abnormally severe side effects of cancer treatment and children with cancer and malformations, overgrowth syndrome, epilepsy, intellectual disability, autism, or other rare disease. It is important to find these patients as it can save lives. We want to introduce diagnostics into clinical routine to look for known and new congenital genetic abnormalities and then compare them with genetic abnormalities in cancer cells in people with cancer, children whose cancer type or side effect profile gives strong suspicion of congenital genetic causes and people who included in families where more than one child has been affected by cancer. We want to use new DNA and RNA based methods that are based on sequencing of the entire human genome. In cases where we find new suspected cancer-associated genes, we will proceed with various functional studies in animal models and cells from patients. I want to identify patients who need a tailored treatment and understand the mechanisms of emergence and find new disease genes behind the syndrome and cancer. Increased knowledge about familial cancer and why certain syndromes are associated with cancer risk and increased sensitivity to cytotoxic drugs and radiation is important and will lead to improved care, tailored therapies and opportunities to implement preventive measures in the affected individual and his family. . The research also leads to increased knowledge about childhood cancer in general, which can lead to improved diagnostics and treatment and improved survival.
  • Barncancerfonden
    1 January 2019 - 31 December 2019
  • Swedish Research Council
    1 January 2019 - 31 December 2021
  • Swedish Research Council
    1 January 2019 - 31 December 2021
  • The importance of innate genetic factors for childhood cancer
    Swedish Cancer Society
    1 January 2018
    Little is known about the importance of congenital changes in childhood cancer. Previously, it has been said that congenital syndrome and cancer are two completely different things. In recent years, research has shown that there are often the same genes and signal pathways that are involved in the different conditions. Most cases occur sporadically and it is very rare for several children within the same family to suffer. However, there are rare families where several close relatives suffered from childhood cancer. These families are very interesting from a research point of view because they allow the identification of cancer-associated genes. There are also congenital syndromes that increase the risk of cancer. The purpose is to understand emergence mechanisms and find new disease genes behind syndrome and childhood cancer. We want to use modern technology with sequencing of all human genes to characterize innate genetic abnormalities and compare with genetic abnormalities in cancer cells in people with syndrome and in families where more than one child affected by childhood cancer. We have also collected 380,000 people with various rare genetic diagnoses in a unique registry study to investigate cancer incidence and risk in specific rare diagnoses. Identification of new disease genes and mechanisms behind syndrome and cancer development and familial cancer will give increased knowledge of childhood cancer as a whole and that this can eventually lead to opportunities for preventive measures and new therapies. If cancer cells can be detected already in PKU samples, this can lead to a new understanding of the growth of cancer cells. The registry study is the first of its kind and will lead to new insights on cancer risk in relatives and other associated symptoms in various congenital rare diseases and childhood cancer.
  • Swedish Research Council
    1 January 2018 - 31 December 2020
  • The importance of innate genetic factors for childhood cancer
    Swedish Cancer Society
    1 January 2017
    Little is known about the importance of congenital changes in childhood cancer. Previously, it has been said that congenital syndrome and cancer are two completely different things. In recent years, research has shown that there are often the same genes and signal pathways that are involved in the different conditions. Most cases occur sporadically and it is very rare for several children within the same family to suffer. However, there are rare families where several close relatives suffered from childhood cancer. These families are very interesting from a research point of view because they allow the identification of cancer-associated genes. There are also congenital syndromes that increase the risk of cancer. The purpose is to understand emergence mechanisms and find new disease genes behind syndrome and childhood cancer. We want to use modern technology with sequencing of all human genes to characterize innate genetic abnormalities and compare with genetic abnormalities in cancer cells in people with syndrome and in families where more than one child affected by childhood cancer. We have also collected 380,000 people with various rare genetic diagnoses in a unique registry study to investigate cancer incidence and risk in specific rare diagnoses. Identification of new disease genes and mechanisms behind syndrome and cancer development and familial cancer will give increased knowledge of childhood cancer as a whole and that this can eventually lead to opportunities for preventive measures and new therapies. If cancer cells can be detected already in PKU samples, this can lead to a new understanding of the growth of cancer cells. The registry study is the first of its kind and will lead to new insights on cancer risk in relatives and other associated symptoms in various congenital rare diseases and childhood cancer.
  • The importance of innate genetic factors for childhood cancer
    Swedish Cancer Society
    1 January 2016
    Little is known about the importance of congenital changes in childhood cancer. Previously, it has been said that congenital syndrome and cancer are two completely different things. In recent years, research has shown that there are often the same genes and signal pathways that are involved in the different conditions. Most cases occur sporadically and it is very rare for several children within the same family to suffer. However, there are rare families where several close relatives suffered from childhood cancer. These families are very interesting from a research point of view because they allow the identification of cancer-associated genes. There are also congenital syndromes that increase the risk of cancer. The purpose is to understand emergence mechanisms and find new disease genes behind syndrome and childhood cancer. We want to use modern technology with sequencing of all human genes to characterize innate genetic abnormalities and compare with genetic abnormalities in cancer cells in people with syndrome and in families where more than one child affected by childhood cancer. We have also collected 380,000 people with various rare genetic diagnoses in a unique registry study to investigate cancer incidence and risk in specific rare diagnoses. Identification of new disease genes and mechanisms behind syndrome and cancer development and familial cancer will give increased knowledge of childhood cancer as a whole and that this can eventually lead to opportunities for preventive measures and new therapies. If cancer cells can be detected already in PKU samples, this can lead to a new understanding of the growth of cancer cells. The registry study is the first of its kind and will lead to new insights on cancer risk in relatives and other associated symptoms in various congenital rare diseases and childhood cancer.
  • Swedish Research Council
    1 January 2016 - 31 December 2018
  • Swedish Research Council
    1 January 2012 - 31 December 2014

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  • Adjungerad Professor, Molekylär medicin och kirurgi, ̽»¨¾«Ñ¡, 2019-2027

Examina och utbildning

  • Docent, Medicinsk genetik, ̽»¨¾«Ñ¡, 2010
  • MEDICINE DOKTORSEXAMEN, Institutionen för molekylär medicin och kirurgi, ̽»¨¾«Ñ¡, 2001

Handledning

  • Handledning till doktorsexamen

    • Hillevi Lindelöf, 2020-
    • Emeli Pontén, 2018-
    • Dominyka Batkovskyte, Genetic studies of rare skeletal disorders : to solve the unsolved, , 2024
    • Anders Kämpe, Genetic causes and underlying disease mechanisms in early-onset osteoporosis, , 2020
    • Anna Hammarsjö, EXPANDING THE GENETIC AND PHENOTYPIC SPECTRUM OF SKELETAL DYSPLASIAS, 2018
    • Carolina Maya Gonzalez
    • Benedicte Bang
    • Sofia Frisk, Studies of Genetic Mosaicism in Rare Diseases, 2022

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