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성함이나 학술지명, PMID로 찾아보십시오.
Dudbridge F에 대해
11건.
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Shrine N,
Guyatt AL,
Erzurumluoglu AM,
Jackson VE,
Hobbs BD,
Melbourne CA,
Batini C,
Fawcett KA,
Song K,
Sakornsakolpat P,
Li X,
Boxall R
외 99명 — 모두 보기
Reeve NF,
Obeidat M,
Zhao JH,
Wielscher M,
Weiss S,
Kentistou KA,
Kentistou KA,
Cook JP,
Sun BB,
Zhou J,
Hui J,
Karrasch S,
Imboden M,
Harris SE,
Marten J,
Enroth S,
Kerr SM,
Surakka I,
Vitart V,
Lehtimäki T,
Allen RJ,
Bakke PS,
Beaty TH,
Bleecker ER,
Bossé Y,
Brandsma CA,
Chen Z,
Crapo JD,
Danesh J,
DeMeo DL,
Dudbridge F,
Ewert R,
Gieger C,
Gulsvik A,
Hansell AL,
Hao K,
Hoffman JD,
Hokanson JE,
Homuth G,
Joshi PK,
Joubert P,
Langenberg C,
Li X,
Li L,
Lin K,
Lind L,
Locantore N,
Luan J,
Mahajan A,
Maranville JC,
Murray A,
Nickle DC,
Packer R,
Parker MM,
Paynton ML,
Porteous DJ,
Porteous DJ,
Prokopenko D,
Qiao D,
Rawal R,
Runz H,
Sayers I,
Sin DD,
Smith BH,
Soler Artigas M,
Sparrow D,
Tal-Singer R,
Timmers PRHJ,
Van den Berge M,
Whittaker JC,
Woodruff PG,
Yerges-Armstrong LM,
Troyanskaya OG,
Raitakari OT,
Kähönen M,
Polašek O,
Gyllensten U,
Rudan I,
Deary IJ,
Probst-Hensch NM,
Schulz H,
James AL,
Wilson JF,
Stubbe B,
Zeggini E,
Jarvelin MR,
Wareham N,
Silverman EK,
Hayward C,
Morris AP,
Butterworth AS,
Scott RA,
Walters RG,
Meyers DA,
Cho MH,
Strachan DP,
Hall IP,
Tobin MD,
Wain LV
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
페이지 12개+
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
Trubetskoy V,
Pardiñas AF,
Qi T,
Panagiotaropoulou G,
Awasthi S,
Bigdeli TB,
Bryois J,
Chen CY,
Dennison CA,
Hall LS,
Lam M,
Watanabe K
외 422명 — 모두 보기
Frei O,
Ge T,
Harwood JC,
Koopmans F,
Magnusson S,
Richards AL,
Sidorenko J,
Wu Y,
Zeng J,
Grove J,
Kim M,
Li Z,
Voloudakis G,
Zhang W,
Adams M,
Agartz I,
Atkinson EG,
Agerbo E,
Al Eissa M,
Albus M,
Alexander M,
Alizadeh BZ,
Alptekin K,
Als TD,
Amin F,
Arolt V,
Arrojo M,
Athanasiu L,
Azevedo MH,
Bacanu SA,
Bass NJ,
Begemann M,
Belliveau RA,
Bene J,
Benyamin B,
Bergen SE,
Blasi G,
Bobes J,
Bonassi S,
Braun A,
Bressan RA,
Bromet EJ,
Bruggeman R,
Buckley PF,
Buckner RL,
Bybjerg-Grauholm J,
Cahn W,
Cairns MJ,
Calkins ME,
Carr VJ,
Castle D,
Catts SV,
Chambert KD,
Chan RCK,
Chaumette B,
Cheng W,
Cheung EFC,
Chong SA,
Cohen D,
Consoli A,
Cordeiro Q,
Costas J,
Curtis C,
Davidson M,
Davis KL,
de Haan L,
Degenhardt F,
DeLisi LE,
Demontis D,
Dickerson F,
Dikeos D,
Dinan T,
Djurovic S,
Duan J,
Ducci G,
Dudbridge F,
Eriksson JG,
Fañanás L,
Faraone SV,
Fiorentino A,
Forstner A,
Frank J,
Freimer NB,
Fromer M,
Frustaci A,
Gadelha A,
Genovese G,
Gershon ES,
Giannitelli M,
Giegling I,
Giusti-Rodríguez P,
Godard S,
Goldstein JI,
González Peñas J,
González-Pinto A,
Gopal S,
Gratten J,
Green MF,
Greenwood TA,
Guillin O,
Gülöksüz S,
Gur RE,
Gur RC,
Gutiérrez B,
Hahn E,
Hakonarson H,
Haroutunian V,
Hartmann AM,
Harvey C,
Hayward C,
Henskens FA,
Herms S,
Hoffmann P,
Howrigan DP,
Ikeda M,
Iyegbe C,
Joa I,
Julià A,
Kähler AK,
Kam-Thong T,
Kamatani Y,
Karachanak-Yankova S,
Kebir O,
Keller MC,
Kelly BJ,
Khrunin A,
Kim SW,
Klovins J,
Kondratiev N,
Konte B,
Kraft J,
Kubo M,
Kučinskas V,
Kučinskiene ZA,
Kusumawardhani A,
Kuzelova-Ptackova H,
Landi S,
Lazzeroni LC,
Lee PH,
Legge SE,
Lehrer DS,
Lencer R,
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Li M,
Lieberman J,
Light GA,
Limborska S,
Liu CM,
Lönnqvist J,
Loughland CM,
Lubinski J,
Luykx JJ,
Lynham A,
Macek M Jr,
Mackinnon A,
Magnusson PKE,
Maher BS,
Maier W,
Malaspina D,
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Mattheisen M,
McCarley RW,
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Mondelli V,
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Myin-Germeys I,
Nenadić I,
Nestadt G,
Nikitina-Zake L,
Noto C,
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Olincy A,
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Pantelis C,
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Parellada M,
Paunio T,
Pellegrino R,
Periyasamy S,
Perkins DO,
Pfuhlmann B,
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Porteous D,
Powell J,
Quattrone D,
Quested D,
Radant AD,
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Rapaport MH,
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Salomaa V,
Sanjuan J,
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Savitz A,
Schall U,
Scott RJ,
Seidman LJ,
Sharp SI,
Shi J,
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Sigurdsson E,
Sim K,
Skarabis N,
Slominsky P,
So HC,
Sobell JL,
Söderman E,
Stain HJ,
Steen NE,
Steixner-Kumar AA,
Stögmann E,
Stone WS,
Straub RE,
Streit F,
Strengman E,
Stroup TS,
Subramaniam M,
Sugar CA,
Suvisaari J,
Svrakic DM,
Swerdlow NR,
Szatkiewicz JP,
Ta TMT,
Takahashi A,
Terao C,
Thibaut F,
Toncheva D,
Tooney PA,
Torretta S,
Tosato S,
Tura GB,
Turetsky BI,
Üçok A,
Vaaler A,
van Amelsvoort T,
van Winkel R,
Veijola J,
Waddington J,
Walter H,
Waterreus A,
Webb BT,
Weiser M,
Williams NM,
Witt SH,
Wormley BK,
Wu JQ,
Xu Z,
Yolken R,
Zai CC,
Zhou W,
Zhu F,
Zimprich F,
Atbaşoğlu EC,
Ayub M,
Benner C,
Bertolino A,
Black DW,
Bray NJ,
Breen G,
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Byerley WF,
Chen WJ,
Cloninger CR,
Crespo-Facorro B,
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Jablensky AV,
McCarroll SA,
Moran JL,
Mors O,
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Müller-Myhsok B,
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Nordentoft M,
Pato MT,
Petryshen TL,
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Escott-Price V,
Esko T,
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Gejman PV,
Gill M,
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Golimbet V,
Hong KS,
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Iwata N,
Jönsson EG,
Kahn RS,
Kennedy JL,
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Kirov G,
Knowles JA,
Krebs MO,
Laurent-Levinson C,
Lee J,
Lencz T,
Levinson DF,
Li QS,
Liu J,
Malhotra AK,
Malhotra D,
McIntosh A,
McQuillin A,
Menezes PR,
Morgan VA,
Morris DW,
Mowry BJ,
Murray RM,
Nimgaonkar V,
Nöthen MM,
Ophoff RA,
Paciga SA,
Palotie A,
Pato CN,
Qin S,
Rietschel M,
Riley BP,
Rivera M,
Rujescu D,
Saka MC,
Sanders AR,
Schwab SG,
Serretti A,
Sham PC,
Shi Y,
St Clair D,
Stefánsson H,
Stefansson K,
Tsuang MT,
van Os J,
Vawter MP,
Weinberger DR,
Werge T,
Wildenauer DB,
Yu X,
Yue W,
Holmans PA,
Pocklington AJ,
Roussos P,
Vassos E,
Verhage M,
Visscher PM,
Yang J,
Posthuma D,
Andreassen OA,
Kendler KS,
Owen MJ,
Wray NR,
Daly MJ,
Huang H,
Neale BM,
Sullivan PF,
Ripke S,
Walters JTR,
O'Donovan MC
Indonesia Schizophrenia Consortium · PsychENCODE 외 컨소시엄 3곳
Nature · 2022 · PMID 35396580
페이지 12개+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
외 136명 — 모두 보기
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
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Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
페이지 12개+
Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease
Williams AT,
Chen J,
Coley K,
Batini C,
Izquierdo A,
Packer R,
Abner E,
Kanoni S,
Shepherd DJ,
Free RC,
Hollox EJ,
Brunskill NJ
외 20명 — 모두 보기
Ntalla I,
Reeve N,
Brightling CE,
Venn L,
Adams E,
Bee C,
Wallace SE,
Pareek M,
Hansell AL,
Esko T,
Stow D,
Jacobs BM,
van Heel DA,
Hennah W,
Rao BS,
Dudbridge F,
Wain LV,
Shrine N,
Tobin MD,
John C
Estonian Biobank Research Team · Genes & Health Research Team
Nature communications · 2023 · PMID 37872160 · 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,
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Brown MA,
Casas JP,
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Deloukas P,
Duncanson A,
Jankowski J,
Markus HS,
Mathew CG,
Palmer CN,
Plomin R,
Rautanen A,
Sawcer SJ,
Trembath RC,
Viswanathan AC,
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Spencer CC,
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McCarroll SA,
Sklar P,
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Multicenter Genetic Studies of Schizophrenia Consortium · Psychosis Endophenotypes International Consortium 외 컨소시엄 1곳
Nature genetics · 2013 · PMID 23974872 · open access
페이지 10개
Whole-genome sequence-based analysis of thyroid function
Taylor PN,
Porcu E,
Chew S,
Campbell PJ,
Traglia M,
Brown SJ,
Mullin BH,
Shihab HA,
Min J,
Walter K,
Memari Y,
Huang J
외 38명 — 모두 보기
Barnes MR,
Beilby JP,
Charoen P,
Danecek P,
Dudbridge F,
Forgetta V,
Greenwood C,
Grundberg E,
Johnson AD,
Hui J,
Lim EM,
McCarthy S,
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Panicker V,
Perry JR,
Bell JT,
Yuan W,
Relton C,
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Schlessinger D,
Abecasis G,
Cucca F,
Surdulescu GL,
Woltersdorf W,
Zeggini E,
Zheng HF,
Toniolo D,
Dayan CM,
Naitza S,
Walsh JP,
Spector T,
Davey Smith G,
Durbin R,
Richards JB,
Sanna S,
Soranzo N,
Timpson NJ,
Wilson SG
UK0K Consortium
Nature communications · 2015 · PMID 25743335 · open access
페이지 7개
Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry
Gui A,
Hollowell A,
Wigdor EM,
Morgan MJ,
Hannigan LJ,
Corfield EC,
Odintsova V,
Hottenga JJ,
Wong A,
Pool R,
Cullen H,
Wilson S
외 16명 — 모두 보기
Warrier V,
Eilertsen EM,
Andreassen OA,
Middeldorp CM,
St Pourcain B,
Bartels M,
Boomsma DI,
Hartman CA,
Robinson EB,
Arichi T,
Edwards AD,
Johnson MH,
Dudbridge F,
Sanders SJ,
Havdahl A,
Ronald A
Nature human behaviour · 2025 · PMID 40335706 · open access
페이지 2개
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
Steinthorsdottir V,
McGinnis R,
Williams NO,
Stefansdottir L,
Thorleifsson G,
Shooter S,
Fadista J,
Sigurdsson JK,
Auro KM,
Berezina G,
Borges MC,
Bumpstead S
외 63명 — 모두 보기
Bybjerg-Grauholm J,
Colgiu I,
Dolby VA,
Dudbridge F,
Engel SM,
Franklin CS,
Frigge ML,
Frisbaek Y,
Geirsson RT,
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Gudbjartsson DF,
Harmon Q,
Hougaard DM,
Hegay T,
Helgadottir A,
Hjartardottir S,
Jääskeläinen T,
Johannsdottir H,
Jonsdottir I,
Juliusdottir T,
Kalsheker N,
Kasimov A,
Kemp JP,
Kivinen K,
Klungsøyr K,
Lee WK,
Melbye M,
Miedzybrodska Z,
Moffett A,
Najmutdinova D,
Nishanova F,
Olafsdottir T,
Perola M,
Pipkin FB,
Poston L,
Prescott G,
Saevarsdottir S,
Salimbayeva D,
Scaife PJ,
Skotte L,
Staines-Urias E,
Stefansson OA,
Sørensen KM,
Thomsen LCV,
Tragante V,
Trogstad L,
Simpson NAB,
Aripova T,
Casas JP,
Dominiczak AF,
Walker JJ,
Thorsteinsdottir U,
Iversen AC,
Feenstra B,
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Zakhidova N,
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Stefansson K,
Morgan L
FINNPEC Consortium · GOPEC Consortium
Nature communications · 2020 · PMID 33239696 · open access
페이지 1개
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3
Nolan J,
Campbell PJ,
Brown SJ,
Zhu G,
Gordon S,
Lim EM,
Joseph J,
Cross SM,
Panicker V,
Medland SE,
Melton PE,
Beilin LJ
외 8명 — 모두 보기
European journal of endocrinology · 2021 · PMID 34524976
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Body mass index stratified meta-analysis of genome-wide association studies of polycystic ovary syndrome in women of European ancestry
Burns K,
Mullin BH,
Moolhuijsen LME,
Laisk T,
Tyrmi JS,
Cui J,
Actkins KV,
Louwers YV,
Davis LK,
Dudbridge F,
Azziz R,
Goodarzi MO
외 7명 — 모두 보기
Estonian Biobank Research Team · FinnGen 외 컨소시엄 1곳
BMC genomics · 2024 · PMID 38408933 · open access
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