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성함이나 학술지명, PMID로 찾아보십시오.
Stefansson H에 대해
39건, 그중 20건 표시.
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls MA,
Pankratz N,
Lill CM,
Do CB,
Hernandez DG,
Saad M,
DeStefano AL,
Kara E,
Bras J,
Sharma M,
Schulte C,
Keller MF
외 35명 — 모두 보기
Arepalli S,
Letson C,
Edsall C,
Stefansson H,
Liu X,
Pliner H,
Lee JH,
Cheng R,
Ikram MA,
Ioannidis JP,
Hadjigeorgiou GM,
Bis JC,
Martinez M,
Perlmutter JS,
Goate A,
Marder K,
Fiske B,
Sutherland M,
Xiromerisiou G,
Myers RH,
Clark LN,
Stefansson K,
Hardy JA,
Heutink P,
Chen H,
Wood NW,
Houlden H,
Payami H,
Brice A,
Scott WK,
Gasser T,
Bertram L,
Eriksson N,
Foroud T,
Singleton AB
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) 외 컨소시엄 10곳
Nature genetics · 2014 · PMID 25064009 · open access
페이지 12개+
Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits
Hammerschlag AR,
Stringer S,
de Leeuw CA,
Sniekers S,
Taskesen E,
Watanabe K,
Blanken TF,
Dekker K,
Te Lindert BHW,
Wassing R,
Jonsdottir I,
Thorleifsson G
외 10명 — 모두 보기
Nature genetics · 2017 · PMID 28604731 · open access
페이지 12개+
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk
Jansen IE,
Savage JE,
Watanabe K,
Bryois J,
Williams DM,
Steinberg S,
Sealock J,
Karlsson IK,
Hägg S,
Athanasiu L,
Voyle N,
Proitsi P
외 41명 — 모두 보기
Witoelar A,
Stringer S,
Aarsland D,
Almdahl IS,
Andersen F,
Bergh S,
Bettella F,
Bjornsson S,
Brækhus A,
Bråthen G,
de Leeuw C,
Desikan RS,
Djurovic S,
Dumitrescu L,
Fladby T,
Hohman TJ,
Jonsson PV,
Kiddle SJ,
Rongve A,
Saltvedt I,
Sando SB,
Selbæk G,
Shoai M,
Skene NG,
Snaedal J,
Stordal E,
Ulstein ID,
Wang Y,
White LR,
Hardy J,
Hjerling-Leffler J,
Sullivan PF,
van der Flier WM,
Dobson R,
Davis LK,
Stefansson H,
Stefansson K,
Pedersen NL,
Ripke S,
Andreassen OA,
Posthuma D
Nature genetics · 2019 · PMID 30617256
페이지 12개+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
외 111명 — 모두 보기
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
페이지 12개+
Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Mullins N,
Forstner AJ,
O'Connell KS,
Coombes B,
Coleman JRI,
Qiao Z,
Als TD,
Bigdeli TB,
Børte S,
Bryois J,
Charney AW,
Drange OK
외 305명 — 모두 보기
Gandal MJ,
Hagenaars SP,
Ikeda M,
Kamitaki N,
Kim M,
Krebs K,
Panagiotaropoulou G,
Schilder BM,
Sloofman LG,
Steinberg S,
Trubetskoy V,
Winsvold BS,
Won HH,
Abramova L,
Adorjan K,
Agerbo E,
Al Eissa M,
Albani D,
Alliey-Rodriguez N,
Anjorin A,
Antilla V,
Antoniou A,
Awasthi S,
Baek JH,
Bækvad-Hansen M,
Bass N,
Bauer M,
Beins EC,
Bergen SE,
Birner A,
Bøcker Pedersen C,
Bøen E,
Boks MP,
Bosch R,
Brum M,
Brumpton BM,
Brunkhorst-Kanaan N,
Budde M,
Bybjerg-Grauholm J,
Byerley W,
Cairns M,
Casas M,
Cervantes P,
Clarke TK,
Cruceanu C,
Cuellar-Barboza A,
Cunningham J,
Curtis D,
Czerski PM,
Dale AM,
Dalkner N,
David FS,
Degenhardt F,
Djurovic S,
Dobbyn AL,
Douzenis A,
Elvsåshagen T,
Escott-Price V,
Ferrier IN,
Fiorentino A,
Foroud TM,
Forty L,
Frank J,
Frei O,
Freimer NB,
Frisén L,
Gade K,
Garnham J,
Gelernter J,
Giørtz Pedersen M,
Gizer IR,
Gordon SD,
Gordon-Smith K,
Greenwood TA,
Grove J,
Guzman-Parra J,
Ha K,
Haraldsson M,
Hautzinger M,
Heilbronner U,
Hellgren D,
Herms S,
Hoffmann P,
Holmans PA,
Huckins L,
Jamain S,
Johnson JS,
Kalman JL,
Kamatani Y,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koromina M,
Kranz TM,
Kranzler HR,
Kubo M,
Kupka R,
Kushner SA,
Lavebratt C,
Lawrence J,
Leber M,
Lee HJ,
Lee PH,
Levy SE,
Lewis C,
Liao C,
Lucae S,
Lundberg M,
MacIntyre DJ,
Magnusson SH,
Maier W,
Maihofer A,
Malaspina D,
Maratou E,
Martinsson L,
Mattheisen M,
McCarroll SA,
McGregor NW,
McGuffin P,
McKay JD,
Medeiros H,
Medland SE,
Millischer V,
Montgomery GW,
Moran JL,
Morris DW,
Mühleisen TW,
O'Brien N,
O'Donovan C,
Olde Loohuis LM,
Oruc L,
Papiol S,
Pardiñas AF,
Perry A,
Pfennig A,
Porichi E,
Potash JB,
Quested D,
Raj T,
Rapaport MH,
DePaulo JR,
Regeer EJ,
Rice JP,
Rivas F,
Rivera M,
Roth J,
Roussos P,
Ruderfer DM,
Sánchez-Mora C,
Schulte EC,
Senner F,
Sharp S,
Shilling PD,
Sigurdsson E,
Sirignano L,
Slaney C,
Smeland OB,
Smith DJ,
Sobell JL,
Søholm Hansen C,
Soler Artigas M,
Spijker AT,
Stein DJ,
Strauss JS,
Świątkowska B,
Terao C,
Thorgeirsson TE,
Toma C,
Tooney P,
Tsermpini EE,
Vawter MP,
Vedder H,
Walters JTR,
Witt SH,
Xi S,
Xu W,
Yang JMK,
Young AH,
Young H,
Zandi PP,
Zhou H,
Zillich L,
Adolfsson R,
Agartz I,
Alda M,
Alfredsson L,
Babadjanova G,
Backlund L,
Baune BT,
Bellivier F,
Bengesser S,
Berrettini WH,
Blackwood DHR,
Boehnke M,
Børglum AD,
Breen G,
Carr VJ,
Catts S,
Corvin A,
Craddock N,
Dannlowski U,
Dikeos D,
Esko T,
Etain B,
Ferentinos P,
Frye M,
Fullerton JM,
Gawlik M,
Gershon ES,
Goes FS,
Green MJ,
Grigoroiu-Serbanescu M,
Hauser J,
Henskens F,
Hillert J,
Hong KS,
Hougaard DM,
Hultman CM,
Hveem K,
Iwata N,
Jablensky AV,
Jones I,
Jones LA,
Kahn RS,
Kelsoe JR,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Lochner C,
Loughland C,
Martin NG,
Mathews CA,
Mayoral F,
McElroy SL,
McIntosh AM,
McMahon FJ,
Melle I,
Michie P,
Milani L,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Mowry B,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nievergelt CM,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Olsson T,
Owen MJ,
Paciga SA,
Pantelis C,
Pato C,
Pato MT,
Patrinos GP,
Perlis RH,
Posthuma D,
Ramos-Quiroga JA,
Reif A,
Reininghaus EZ,
Ribasés M,
Rietschel M,
Ripke S,
Rouleau GA,
Saito T,
Schall U,
Schalling M,
Schofield PR,
Schulze TG,
Scott LJ,
Scott RJ,
Serretti A,
Shannon Weickert C,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Streit F,
Sullivan PF,
Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Waldman ID,
Weickert TW,
Werge T,
Wray NR,
Zwart JA,
Biernacka JM,
Nurnberger JI,
Cichon S,
Edenberg HJ,
Stahl EA,
McQuillin A,
Di Florio A,
Ophoff RA,
Andreassen OA
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
페이지 12개+
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
Skuladottir AT,
Bjornsdottir G,
Ferkingstad E,
Einarsson G,
Stefansdottir L,
Nawaz MS,
Oddsson A,
Olafsdottir TA,
Saevarsdottir S,
Walters GB,
Magnusson SH,
Bjornsdottir A
외 18명 — 모두 보기
Sveinsson OA,
Vikingsson A,
Hansen TF,
Jacobsen RL,
Erikstrup C,
Schwinn M,
Brunak S,
Banasik K,
Ostrowski SR,
Troelsen A,
Henkel C,
Pedersen OB,
Jonsdottir I,
Gudbjartsson DF,
Sulem P,
Thorgeirsson TE,
Stefansson H,
Stefansson K
DBDS Genetic Consortium
Nature communications · 2022 · PMID 35332129 · open access
페이지 12개+
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
Akiyama M
외 205명 — 모두 보기
Albert CM,
Aliev F,
Alonso A,
Arnett DK,
Ashley-Koch AE,
Ashrani AA,
Barnes KC,
Barr RG,
Bartz TM,
Becker DM,
Bielak LF,
Benjamin EJ,
Bis JC,
Bjornsdottir G,
Blangero J,
Bleecker ER,
Boardman JD,
Boerwinkle E,
Boomsma DI,
Boorgula MP,
Bowden DW,
Brody JA,
Cade BE,
Chasman DI,
Chavan S,
Chen YI,
Chen Z,
Cheng I,
Cho MH,
Choquet H,
Cole JW,
Cornelis MC,
Cucca F,
Curran JE,
de Andrade M,
Dick DM,
Docherty AR,
Duggirala R,
Eaton CB,
Ehringer MA,
Esko T,
Faul JD,
Fernandes Silva L,
Fiorillo E,
Fornage M,
Freedman BI,
Gabrielsen ME,
Garrett ME,
Gharib SA,
Gieger C,
Gillespie N,
Glahn DC,
Gordon SD,
Gu CC,
Gu D,
Gudbjartsson DF,
Guo X,
Haessler J,
Hall ME,
Haller T,
Harris KM,
He J,
Herd P,
Hewitt JK,
Hickie I,
Hidalgo B,
Hokanson JE,
Hopfer C,
Hottenga J,
Hou L,
Huang H,
Hung YJ,
Hunter DJ,
Hveem K,
Hwang SJ,
Hwu CM,
Iacono W,
Irvin MR,
Jee YH,
Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
Kaprio J,
Kardia SLR,
Keller MC,
Kelly TN,
Kooperberg C,
Korhonen T,
Kraft P,
Krauter K,
Kuusisto J,
Laakso M,
Lasky-Su J,
Lee WJ,
Lee JJ,
Levy D,
Li L,
Li K,
Li Y,
Lin K,
Lind PA,
Liu C,
Lloyd-Jones DM,
Lutz SM,
Ma J,
Mägi R,
Manichaikul A,
Martin NG,
Mathur R,
Matoba N,
McArdle PF,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Meyers DA,
Millwood IY,
Mitchell BD,
Mohlke KL,
Moll M,
Montasser ME,
Morrison AC,
Mulas A,
Nielsen JB,
North KE,
Oelsner EC,
Okada Y,
Orrù V,
Palmer ND,
Palviainen T,
Pandit A,
Park SL,
Peters U,
Peters A,
Peyser PA,
Polderman TJC,
Rafaels N,
Redline S,
Reed RM,
Reiner AP,
Rice JP,
Rich SS,
Richmond NE,
Roan C,
Rotter JI,
Rueschman MN,
Runarsdottir V,
Saccone NL,
Schwartz DA,
Shadyab AH,
Shi J,
Shringarpure SS,
Sicinski K,
Skogholt AH,
Smith JA,
Smith NL,
Sotoodehnia N,
Stallings MC,
Stefansson H,
Stefansson K,
Stitzel JA,
Sun X,
Syed M,
Tal-Singer R,
Taylor AE,
Taylor KD,
Telen MJ,
Thai KK,
Tiwari H,
Turman C,
Tyrfingsson T,
Wall TL,
Walters RG,
Weir DR,
Weiss ST,
White WB,
Whitfield JB,
Wiggins KL,
Willemsen G,
Willer CJ,
Winsvold BS,
Xu H,
Yanek LR,
Yin J,
Young KL,
Young KA,
Yu B,
Zhao W,
Zhou W,
Zöllner S,
Zuccolo L,
Batini C,
Bergen AW,
Bierut LJ,
David SP,
Gagliano Taliun SA,
Hancock DB,
Jiang B,
Munafò MR,
Thorgeirsson TE,
Liu DJ,
Vrieze S
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
페이지 12개+
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Schormair B,
Zhao C,
Bell S,
Didriksen M,
Nawaz MS,
Schandra N,
Stefani A,
Högl B,
Dauvilliers Y,
Bachmann CG,
Kemlink D,
Sonka K
외 55명 — 모두 보기
Paulus W,
Trenkwalder C,
Oertel WH,
Hornyak M,
Teder-Laving M,
Metspalu A,
Hadjigeorgiou GM,
Polo O,
Fietze I,
Ross OA,
Wszolek ZK,
Ibrahim A,
Bergmann M,
Kittke V,
Harrer P,
Dowsett J,
Chenini S,
Ostrowski SR,
Sørensen E,
Erikstrup C,
Pedersen OB,
Topholm Bruun M,
Nielsen KR,
Butterworth AS,
Soranzo N,
Ouwehand WH,
Roberts DJ,
Danesh J,
Burchell B,
Furlotte NA,
Nandakumar P,
Earley CJ,
Ondo WG,
Xiong L,
Desautels A,
Perola M,
Vodicka P,
Dina C,
Stoll M,
Franke A,
Lieb W,
Stewart AFR,
Shah SH,
Gieger C,
Peters A,
Rye DB,
Rouleau GA,
Berger K,
Stefansson H,
Ullum H,
Stefansson K,
Hinds DA,
Di Angelantonio E,
Oexle K,
Winkelmann J
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
페이지 12개+
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Ripke S,
O'Dushlaine C,
Chambert K,
Moran JL,
Kähler AK,
Akterin S,
Bergen SE,
Collins AL,
Crowley JJ,
Fromer M,
Kim Y,
Lee SH
외 176명 — 모두 보기
Lee SH,
Magnusson PK,
Sanchez N,
Stahl EA,
Williams S,
Wray NR,
Xia K,
Bettella F,
Borglum AD,
Bulik-Sullivan BK,
Cormican P,
Craddock N,
de Leeuw C,
Durmishi N,
Gill M,
Golimbet V,
Hamshere ML,
Holmans P,
Hougaard DM,
Kendler KS,
Lin K,
Morris DW,
Mors O,
Mortensen PB,
Neale BM,
O'Neill FA,
Owen MJ,
Milovancevic MP,
Posthuma D,
Powell J,
Richards AL,
Riley BP,
Ruderfer D,
Rujescu D,
Sigurdsson E,
Silagadze T,
Smit AB,
Stefansson H,
Steinberg S,
Suvisaari J,
Tosato S,
Verhage M,
Walters JT,
Levinson DF,
Gejman PV,
Kendler KS,
Laurent C,
Mowry BJ,
O'Donovan MC,
Owen MJ,
Pulver AE,
Riley BP,
Schwab SG,
Wildenauer DB,
Dudbridge F,
Holmans P,
Shi J,
Albus M,
Alexander M,
Campion D,
Cohen D,
Dikeos D,
Duan J,
Eichhammer P,
Godard S,
Hansen M,
Lerer FB,
Liang KY,
Maier W,
Mallet J,
Nertney DA,
Nestadt G,
Norton N,
O'Neill FA,
Papadimitriou GN,
Ribble R,
Sanders AR,
Silverman JM,
Walsh D,
Williams NM,
Wormley B,
Arranz MJ,
Bakker S,
Bender S,
Bramon E,
Collier D,
Crespo-Facorro B,
Hall J,
Iyegbe C,
Jablensky A,
Kahn RS,
Kalaydjieva L,
Lawrie S,
Lewis CM,
Lin K,
Linszen DH,
Mata I,
McIntosh A,
Murray RM,
Ophoff RA,
Powell J,
Rujescu D,
Van Os J,
Walshe M,
Weisbrod M,
Wiersma D,
Donnelly P,
Barroso I,
Blackwell JM,
Bramon E,
Brown MA,
Casas JP,
Corvin AP,
Deloukas P,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
Wood NW,
Spencer CC,
Band G,
Bellenguez C,
Freeman C,
Hellenthal G,
Giannoulatou E,
Pirinen M,
Pearson RD,
Strange A,
Su Z,
Vukcevic D,
Donnelly P,
Langford C,
Hunt SE,
Edkins S,
Gwilliam R,
Blackburn H,
Bumpstead SJ,
Dronov S,
Gillman M,
Gray E,
Hammond N,
Jayakumar A,
McCann OT,
Liddle J,
Potter SC,
Ravindrarajah R,
Ricketts M,
Tashakkori-Ghanbaria A,
Waller MJ,
Weston P,
Widaa S,
Whittaker P,
Barroso I,
Deloukas P,
Mathew CG,
Blackwell JM,
Brown MA,
Corvin AP,
McCarthy MI,
Spencer CC,
Bramon E,
Corvin AP,
O'Donovan MC,
Stefansson K,
Scolnick E,
Purcell S,
McCarroll SA,
Sklar P,
Hultman CM,
Sullivan PF
Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 23974872 · open access
페이지 10개
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Wray NR,
Ripke S,
Mattheisen M,
Trzaskowski M,
Byrne EM,
Abdellaoui A,
Adams MJ,
Agerbo E,
Air TM,
Andlauer TMF,
Bacanu SA,
Bækvad-Hansen M
외 205명 — 모두 보기
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
Christensen JH,
Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
Craddock N,
Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
Dunn EC,
Eley TC,
Eriksson N,
Escott-Price V,
Kiadeh FHF,
Finucane HK,
Forstner AJ,
Frank J,
Gaspar HA,
Gill M,
Giusti-Rodríguez P,
Goes FS,
Gordon SD,
Grove J,
Hall LS,
Hannon E,
Hansen CS,
Hansen TF,
Herms S,
Hickie IB,
Hoffmann P,
Homuth G,
Horn C,
Hottenga JJ,
Hougaard DM,
Hu M,
Hyde CL,
Ising M,
Jansen R,
Jansen R,
Jin F,
Jorgenson E,
Knowles JA,
Kohane IS,
Kraft J,
Kretzschmar WW,
Krogh J,
Kutalik Z,
Lane JM,
Li Y,
Li Y,
Lind PA,
Liu X,
Lu L,
MacIntyre DJ,
MacKinnon DF,
Maier RM,
Maier W,
Marchini J,
Mbarek H,
McGrath P,
McGuffin P,
Medland SE,
Mehta D,
Middeldorp CM,
Mihailov E,
Milaneschi Y,
Milani L,
Mill J,
Mondimore FM,
Montgomery GW,
Mostafavi S,
Mullins N,
Nauck M,
Ng B,
Nivard MG,
Nyholt DR,
O'Reilly PF,
Oskarsson H,
Owen MJ,
Painter JN,
Pedersen CB,
Pedersen MG,
Peterson RE,
Pettersson E,
Peyrot WJ,
Pistis G,
Posthuma D,
Purcell SM,
Quiroz JA,
Qvist P,
Rice JP,
Riley BP,
Rivera M,
Saeed Mirza S,
Saxena R,
Schoevers R,
Schulte EC,
Shen L,
Shi J,
Shyn SI,
Sigurdsson E,
Sinnamon GBC,
Smit JH,
Smith DJ,
Stefansson H,
Steinberg S,
Stockmeier CA,
Streit F,
Strohmaier J,
Tansey KE,
Teismann H,
Teumer A,
Thompson W,
Thomson PA,
Thorgeirsson TE,
Tian C,
Traylor M,
Treutlein J,
Trubetskoy V,
Uitterlinden AG,
Umbricht D,
Van der Auwera S,
van Hemert AM,
Viktorin A,
Visscher PM,
Wang Y,
Webb BT,
Weinsheimer SM,
Wellmann J,
Willemsen G,
Witt SH,
Wu Y,
Xi HS,
Yang J,
Zhang F,
Arolt V,
Baune BT,
Berger K,
Boomsma DI,
Cichon S,
Dannlowski U,
de Geus ECJ,
DePaulo JR,
Domenici E,
Domschke K,
Esko T,
Grabe HJ,
Hamilton SP,
Hayward C,
Heath AC,
Hinds DA,
Kendler KS,
Kloiber S,
Lewis G,
Li QS,
Lucae S,
Madden PFA,
Magnusson PK,
Martin NG,
McIntosh AM,
Metspalu A,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Paciga SA,
Pedersen NL,
Penninx BWJH,
Perlis RH,
Porteous DJ,
Potash JB,
Preisig M,
Rietschel M,
Schaefer C,
Schulze TG,
Smoller JW,
Stefansson K,
Tiemeier H,
Uher R,
Völzke H,
Weissman MM,
Werge T,
Winslow AR,
Lewis CM,
Levinson DF,
Breen G,
Børglum AD,
Sullivan PF
eQTLGen · 23andMe 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29700475 · open access
페이지 10개
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
Gormley P,
Anttila V,
Winsvold BS,
Palta P,
Esko T,
Pers TH,
Farh KH,
Cuenca-Leon E,
Muona M,
Furlotte NA,
Kurth T,
Ingason A
외 95명 — 모두 보기
McMahon G,
Ligthart L,
Terwindt GM,
Kallela M,
Freilinger TM,
Ran C,
Gordon SG,
Stam AH,
Steinberg S,
Borck G,
Koiranen M,
Quaye L,
Adams HH,
Lehtimäki T,
Sarin AP,
Wedenoja J,
Hinds DA,
Buring JE,
Schürks M,
Ridker PM,
Hrafnsdottir MG,
Stefansson H,
Ring SM,
Hottenga JJ,
Penninx BW,
Färkkilä M,
Artto V,
Kaunisto M,
Vepsäläinen S,
Malik R,
Heath AC,
Madden PA,
Martin NG,
Montgomery GW,
Kurki MI,
Kals M,
Mägi R,
Pärn K,
Hämäläinen E,
Huang H,
Byrnes AE,
Franke L,
Huang J,
Stergiakouli E,
Lee PH,
Sandor C,
Webber C,
Cader Z,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Eriksson JG,
Salomaa V,
Heikkilä K,
Loehrer E,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Cherkas L,
Pedersen LM,
Stubhaug A,
Nielsen CS,
Männikkö M,
Mihailov E,
Milani L,
Göbel H,
Esserlind AL,
Christensen AF,
Hansen TF,
Werge T,
Kaprio J,
Aromaa AJ,
Raitakari O,
Ikram MA,
Spector T,
Järvelin MR,
Metspalu A,
Kubisch C,
Strachan DP,
Ferrari MD,
Belin AC,
Dichgans M,
Wessman M,
van den Maagdenberg AM,
Zwart JA,
Boomsma DI,
Smith GD,
Stefansson K,
Eriksson N,
Daly MJ,
Neale BM,
Olesen J,
Chasman DI,
Nyholt DR,
Palotie A
International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
페이지 9개
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Demontis D,
Walters RK,
Martin J,
Mattheisen M,
Als TD,
Agerbo E,
Baldursson G,
Belliveau R,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Cerrato F,
Chambert K
외 69명 — 모두 보기
Churchhouse C,
Dumont A,
Eriksson N,
Gandal M,
Goldstein JI,
Grasby KL,
Grove J,
Gudmundsson OO,
Hansen CS,
Hauberg ME,
Hollegaard MV,
Howrigan DP,
Huang H,
Maller JB,
Martin AR,
Martin NG,
Moran J,
Pallesen J,
Palmer DS,
Pedersen CB,
Pedersen MG,
Poterba T,
Poulsen JB,
Ripke S,
Robinson EB,
Satterstrom FK,
Stefansson H,
Stevens C,
Turley P,
Walters GB,
Won H,
Wright MJ,
Andreassen OA,
Asherson P,
Burton CL,
Boomsma DI,
Cormand B,
Dalsgaard S,
Franke B,
Gelernter J,
Geschwind D,
Hakonarson H,
Haavik J,
Kranzler HR,
Kuntsi J,
Langley K,
Lesch KP,
Middeldorp C,
Reif A,
Rohde LA,
Roussos P,
Schachar R,
Sklar P,
Sonuga-Barke EJS,
Sullivan PF,
Thapar A,
Tung JY,
Waldman ID,
Medland SE,
Stefansson K,
Nordentoft M,
Hougaard DM,
Werge T,
Mors O,
Mortensen PB,
Daly MJ,
Faraone SV,
Børglum AD,
Neale BM
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) · Early Lifecourse & Genetic Epidemiology (EAGLE) Consortium 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 30478444
페이지 8개
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
Bjornsdottir G,
Stefansdottir L,
Thorleifsson G,
Sulem P,
Norland K,
Ferkingstad E,
Oddsson A,
Zink F,
Lund SH,
Nawaz MS,
Bragi Walters G,
Skuladottir AT
외 32명 — 모두 보기
Gudjonsson SA,
Einarsson G,
Halldorsson GH,
Bjarnadottir V,
Sveinbjornsson G,
Helgadottir A,
Styrkarsdottir U,
Gudmundsson LJ,
Pedersen OB,
Hansen TF,
Werge T,
Banasik K,
Troelsen A,
Skou ST,
Thørner LW,
Erikstrup C,
Nielsen KR,
Mikkelsen S,
Jonsdottir I,
Bjornsson A,
Olafsson IH,
Ulfarsson E,
Blondal J,
Vikingsson A,
Brunak S,
Ostrowski SR,
Ullum H,
Thorsteinsdottir U,
Stefansson H,
Gudbjartsson DF,
Thorgeirsson TE,
Stefansson K
DBDS Genetic Consortium · GO Consortium
Nature communications · 2022 · PMID 35110524 · open access
페이지 8개
Seven new loci associated with age-related macular degeneration
Fritsche LG,
Chen W,
Schu M,
Yaspan BL,
Yu Y,
Thorleifsson G,
Zack DJ,
Arakawa S,
Cipriani V,
Ripke S,
Igo RP Jr,
Buitendijk GH
외 144명 — 모두 보기
Sim X,
Weeks DE,
Guymer RH,
Merriam JE,
Francis PJ,
Hannum G,
Agarwal A,
Armbrecht AM,
Audo I,
Aung T,
Barile GR,
Benchaboune M,
Bird AC,
Bishop PN,
Branham KE,
Brooks M,
Brucker AJ,
Cade WH,
Cain MS,
Campochiaro PA,
Chan CC,
Cheng CY,
Chew EY,
Chin KA,
Chowers I,
Clayton DG,
Cojocaru R,
Conley YP,
Cornes BK,
Daly MJ,
Dhillon B,
Edwards AO,
Evangelou E,
Fagerness J,
Ferreyra HA,
Friedman JS,
Geirsdottir A,
George RJ,
Gieger C,
Gupta N,
Hagstrom SA,
Harding SP,
Haritoglou C,
Heckenlively JR,
Holz FG,
Hughes G,
Ioannidis JP,
Ishibashi T,
Joseph P,
Jun G,
Kamatani Y,
Katsanis N,
N Keilhauer C,
Khan JC,
Kim IK,
Kiyohara Y,
Klein BE,
Klein R,
Kovach JL,
Kozak I,
Lee CJ,
Lee KE,
Lichtner P,
Lotery AJ,
Meitinger T,
Mitchell P,
Mohand-Saïd S,
Moore AT,
Morgan DJ,
Morrison MA,
Myers CE,
Naj AC,
Nakamura Y,
Okada Y,
Orlin A,
Ortube MC,
Othman MI,
Pappas C,
Park KH,
Pauer GJ,
Peachey NS,
Poch O,
Priya RR,
Reynolds R,
Richardson AJ,
Ripp R,
Rudolph G,
Ryu E,
Sahel JA,
Schaumberg DA,
Scholl HP,
Schwartz SG,
Scott WK,
Shahid H,
Sigurdsson H,
Silvestri G,
Sivakumaran TA,
Smith RT,
Sobrin L,
Souied EH,
Stambolian DE,
Stefansson H,
Sturgill-Short GM,
Takahashi A,
Tosakulwong N,
Truitt BJ,
Tsironi EE,
Uitterlinden AG,
van Duijn CM,
Vijaya L,
Vingerling JR,
Vithana EN,
Webster AR,
Wichmann HE,
Winkler TW,
Wong TY,
Wright AF,
Zelenika D,
Zhang M,
Zhao L,
Zhang K,
Klein ML,
Hageman GS,
Lathrop GM,
Stefansson K,
Allikmets R,
Baird PN,
Gorin MB,
Wang JJ,
Klaver CC,
Seddon JM,
Pericak-Vance MA,
Iyengar SK,
Yates JR,
Swaroop A,
Weber BH,
Kubo M,
Deangelis MM,
Léveillard T,
Thorsteinsdottir U,
Haines JL,
Farrer LA,
Heid IM,
Abecasis GR
AMD Gene Consortium
Nature genetics · 2013 · PMID 23455636 · open access
페이지 7개
New basal cell carcinoma susceptibility loci
Stacey SN,
Helgason H,
Gudjonsson SA,
Thorleifsson G,
Zink F,
Sigurdsson A,
Kehr B,
Gudmundsson J,
Sulem P,
Sigurgeirsson B,
Benediktsdottir KR,
Thorisdottir K
외 31명 — 모두 보기
Ragnarsson R,
Fuentelsaz V,
Corredera C,
Gilaberte Y,
Grasa M,
Planelles D,
Sanmartin O,
Rudnai P,
Gurzau E,
Koppova K,
Nexø BA,
Tjønneland A,
Overvad K,
Jonasson JG,
Tryggvadottir L,
Johannsdottir H,
Kristinsdottir AM,
Stefansson H,
Masson G,
Magnusson OT,
Halldorsson BV,
Kong A,
Rafnar T,
Thorsteinsdottir U,
Vogel U,
Kumar R,
Nagore E,
Mayordomo JI,
Gudbjartsson DF,
Olafsson JH,
Stefansson K
Nature communications · 2015 · PMID 25855136 · open access
페이지 7개
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
Skuladottir AT,
Stefansdottir L,
Halldorsson GH,
Stefansson OA,
Bjornsdottir A,
Jonsson P,
Palmadottir V,
Thorgeirsson TE,
Walters GB,
Gisladottir RS,
Bjornsdottir G,
Jonsdottir GA
외 20명 — 모두 보기
Sulem P,
Gudbjartsson DF,
Knowlton KU,
Jones DA,
Ottas A,
Pedersen OB,
Didriksen M,
Brunak S,
Banasik K,
Hansen TF,
Erikstrup C,
Haavik J,
Andreassen OA,
Rye D,
Igland J,
Ostrowski SR,
Milani LA,
Nadauld LD,
Stefansson H,
Stefansson K
Estonian Biobank · DBDS Genomic Consortium
Communications biology · 2024 · PMID 38671141 · open access
페이지 7개
Genome-wide association study identifies 30 loci associated with bipolar disorder
Stahl EA,
Breen G,
Forstner AJ,
McQuillin A,
Ripke S,
Trubetskoy V,
Mattheisen M,
Wang Y,
Coleman JRI,
Gaspar HA,
de Leeuw CA,
Steinberg S
외 265명 — 모두 보기
Pavlides JMW,
Trzaskowski M,
Byrne EM,
Pers TH,
Holmans PA,
Richards AL,
Abbott L,
Agerbo E,
Akil H,
Albani D,
Alliey-Rodriguez N,
Als TD,
Anjorin A,
Antilla V,
Awasthi S,
Badner JA,
Bækvad-Hansen M,
Barchas JD,
Bass N,
Bauer M,
Belliveau R,
Bergen SE,
Pedersen CB,
Bøen E,
Boks MP,
Boocock J,
Budde M,
Bunney W,
Burmeister M,
Bybjerg-Grauholm J,
Byerley W,
Casas M,
Cerrato F,
Cervantes P,
Chambert K,
Charney AW,
Chen D,
Churchhouse C,
Clarke TK,
Coryell W,
Craig DW,
Cruceanu C,
Curtis D,
Czerski PM,
Dale AM,
de Jong S,
Degenhardt F,
Del-Favero J,
DePaulo JR,
Djurovic S,
Dobbyn AL,
Dumont A,
Elvsåshagen T,
Escott-Price V,
Fan CC,
Fischer SB,
Flickinger M,
Foroud TM,
Forty L,
Frank J,
Fraser C,
Freimer NB,
Frisén L,
Gade K,
Gage D,
Garnham J,
Giambartolomei C,
Pedersen MG,
Goldstein J,
Gordon SD,
Gordon-Smith K,
Green EK,
Green MJ,
Greenwood TA,
Grove J,
Guan W,
Guzman-Parra J,
Hamshere ML,
Hautzinger M,
Heilbronner U,
Herms S,
Hipolito M,
Hoffmann P,
Holland D,
Huckins L,
Jamain S,
Johnson JS,
Juréus A,
Kandaswamy R,
Karlsson R,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koller AC,
Kupka R,
Lavebratt C,
Lawrence J,
Lawson WB,
Leber M,
Lee PH,
Levy SE,
Li JZ,
Liu C,
Lucae S,
Maaser A,
MacIntyre DJ,
Mahon PB,
Maier W,
Martinsson L,
McCarroll S,
McGuffin P,
McInnis MG,
McKay JD,
Medeiros H,
Medland SE,
Meng F,
Milani L,
Montgomery GW,
Morris DW,
Mühleisen TW,
Mullins N,
Nguyen H,
Nievergelt CM,
Adolfsson AN,
Nwulia EA,
O'Donovan C,
Loohuis LMO,
Ori APS,
Oruc L,
Ösby U,
Perlis RH,
Perry A,
Pfennig A,
Potash JB,
Purcell SM,
Regeer EJ,
Reif A,
Reinbold CS,
Rice JP,
Rivas F,
Rivera M,
Roussos P,
Ruderfer DM,
Ryu E,
Sánchez-Mora C,
Schatzberg AF,
Scheftner WA,
Schork NJ,
Shannon Weickert C,
Shehktman T,
Shilling PD,
Sigurdsson E,
Slaney C,
Smeland OB,
Sobell JL,
Søholm Hansen C,
Spijker AT,
St Clair D,
Steffens M,
Strauss JS,
Streit F,
Strohmaier J,
Szelinger S,
Thompson RC,
Thorgeirsson TE,
Treutlein J,
Vedder H,
Wang W,
Watson SJ,
Weickert TW,
Witt SH,
Xi S,
Xu W,
Young AH,
Zandi P,
Zhang P,
Zöllner S,
Adolfsson R,
Agartz I,
Alda M,
Backlund L,
Baune BT,
Bellivier F,
Berrettini WH,
Biernacka JM,
Blackwood DHR,
Boehnke M,
Børglum AD,
Corvin A,
Craddock N,
Daly MJ,
Dannlowski U,
Esko T,
Etain B,
Frye M,
Fullerton JM,
Gershon ES,
Gill M,
Goes F,
Grigoroiu-Serbanescu M,
Hauser J,
Hougaard DM,
Hultman CM,
Jones I,
Jones LA,
Kahn RS,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Martin NG,
Mayoral F,
McElroy SL,
McIntosh AM,
McMahon FJ,
Melle I,
Metspalu A,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nimgaonkar V,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Owen MJ,
Paciga SA,
Pato C,
Pato MT,
Posthuma D,
Ramos-Quiroga JA,
Ribasés M,
Rietschel M,
Rouleau GA,
Schalling M,
Schofield PR,
Schulze TG,
Serretti A,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Sullivan PF,
Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Werge T,
Nurnberger JI,
Wray NR,
Di Florio A,
Edenberg HJ,
Cichon S,
Ophoff RA,
Scott LJ,
Andreassen OA,
Kelsoe J,
Sklar P
eQTLGen Consortium · BIOS Consortium 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31043756 · open access
페이지 6개
Rare and Common Variants Conferring Risk of Tooth Agenesis
Jonsson L,
Magnusson TE,
Thordarson A,
Jonsson T,
Geller F,
Feenstra B,
Melbye M,
Nohr EA,
Vucic S,
Vucic S,
Dhamo B,
Rivadeneira F
외 25명 — 모두 보기
Ongkosuwito EM,
Wolvius EB,
Leslie EJ,
Marazita ML,
Howe BJ,
Moreno Uribe LM,
Alonso I,
Santos M,
Pinho T,
Jonsson R,
Audolfsson G,
Gudmundsson L,
Nawaz MS,
Olafsson S,
Gustafsson O,
Ingason A,
Unnsteinsdottir U,
Bjornsdottir G,
Walters GB,
Zervas M,
Oddsson A,
Gudbjartsson DF,
Steinberg S,
Stefansson H,
Stefansson K
Journal of dental research · 2018 · PMID 29364747
페이지 4개
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Demontis D,
Walters GB,
Athanasiadis G,
Walters R,
Therrien K,
Nielsen TT,
Farajzadeh L,
Voloudakis G,
Bendl J,
Zeng B,
Zhang W,
Grove J
외 35명 — 모두 보기
Als TD,
Duan J,
Satterstrom FK,
Bybjerg-Grauholm J,
Bækved-Hansen M,
Gudmundsson OO,
Magnusson SH,
Baldursson G,
Davidsdottir K,
Haraldsdottir GS,
Agerbo E,
Hoffman GE,
Dalsgaard S,
Martin J,
Ribasés M,
Boomsma DI,
Soler Artigas M,
Roth Mota N,
Howrigan D,
Medland SE,
Zayats T,
Rajagopal VM,
Nordentoft M,
Mors O,
Hougaard DM,
Mortensen PB,
Daly MJ,
Faraone SV,
Stefansson H,
Roussos P,
Franke B,
Werge T,
Neale BM,
Stefansson K,
Børglum AD
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
페이지 4개
The genetic architecture of fibromyalgia across 2.5 million individuals
Kerrebijn I,
Bjornsdottir G,
Arbabi K,
Urpa L,
Haapaniemi H,
Thorleifsson G,
Stefansdottir L,
Frangakis S,
Valliere J,
Kunorozva L,
Abner E,
Ji C
외 41명 — 모두 보기
Kangur M,
Aagaard B,
Bliddal H,
Brunak S,
Bruun MT,
Didriksen M,
Erikstrup C,
Finer S,
Geirsson AJ,
Gudbjartsson DF,
Hansen TF,
van Heel D,
Jonsdottir I,
Knight S,
Knowlton KU,
Mikkelsen C,
Nadauld LD,
Olafsdottir TA,
Ostrowski SR,
Pedersen OBV,
Saevarsdottir S,
Skuladottir AT,
Sørensen E,
Stefansson H,
Sulem P,
Sveinsson OA,
Thorlacius GE,
Thorsteinsdottir U,
Ullum H,
Vikingsson A,
Werge TM,
Saxena R,
Stefansson K,
Brummett CM,
Glintborg B,
Clauw DJ,
Thorgeirsson TE,
Williams FMK,
Sinnott-Armstrong N,
Ollila HM,
Wainberg M
Chronic Pain Genomics Consortium · FinnGen 외 컨소시엄 3곳
Nature medicine · 2026 · PMID 42521817 · open access
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