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Wright MJ에 대해
23건, 그중 20건 표시.
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
Perry JR,
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Elks CE,
Sulem P,
Thompson DJ,
Ferreira T,
He C,
Chasman DI,
Esko T,
Thorleifsson G,
Albrecht E,
Ang WQ
외 186명 — 모두 보기
Corre T,
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Feenstra B,
Franceschini N,
Ganna A,
Johnson AD,
Kjellqvist S,
Lunetta KL,
McMahon G,
Nolte IM,
Paternoster L,
Porcu E,
Smith AV,
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Hottenga JJ,
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Pers TH,
Yerges-Armstrong LM,
Zhao JH,
Andrulis IL,
Anton-Culver H,
Atsma F,
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Beckmann MW,
Benitez J,
Blomqvist C,
Bojesen SE,
Bolla MK,
Bonanni B,
Brauch H,
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Buring JE,
Chang-Claude J,
Chanock S,
Chen J,
Chenevix-Trench G,
Collée JM,
Couch FJ,
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Coveillo AD,
Cox A,
Czene K,
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Smith GD,
De Vivo I,
Demerath EW,
Dennis J,
Devilee P,
Dieffenbach AK,
Dunning AM,
Eiriksdottir G,
Eriksson JG,
Fasching PA,
Ferrucci L,
Flesch-Janys D,
Flyger H,
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García-Closas M,
Geller F,
de Geus EE,
Giles GG,
Gudbjartsson DF,
Gudnason V,
Guénel P,
Guo S,
Hall P,
Hamann U,
Haring R,
Hartman CA,
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Hofman A,
Hooning MJ,
Hopper JL,
Hu FB,
Hunter DJ,
Karasik D,
Kiel DP,
Knight JA,
Kosma VM,
Kutalik Z,
Lai S,
Lambrechts D,
Lindblom A,
Mägi R,
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Mannermaa A,
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Milani L,
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Nevanlinna H,
Neven P,
Nohr EA,
Oldehinkel AJ,
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Palotie A,
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Peterlongo P,
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Postma DS,
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Boomsma DI,
Econs MJ,
Khaw KT,
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McCarthy MI,
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Thorsteinsdottir U,
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Australian Ovarian Cancer Study · GENICA Network 외 컨소시엄 4곳
Nature · 2014 · PMID 25231870 · open access
페이지 12개+
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Davies G,
Lam M,
Harris SE,
Trampush JW,
Luciano M,
Hill WD,
Hagenaars SP,
Ritchie SJ,
Marioni RE,
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Liewald DCM,
Okely JA
외 212명 — 모두 보기
Ahola-Olli AV,
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Bertram L,
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Christoforou A,
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Hayward C,
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Li S,
Mather KA,
Melle I,
Morris D,
Oldmeadow C,
Palviainen T,
Payton A,
Pazoki R,
Petrovic K,
Reynolds CA,
Sargurupremraj M,
Scholz M,
Smith JA,
Smith AV,
Terzikhan N,
Thalamuthu A,
Trompet S,
van der Lee SJ,
Ware EB,
Windham BG,
Wright MJ,
Yang J,
Yu J,
Ames D,
Amin N,
Amouyel P,
Andreassen OA,
Armstrong NJ,
Assareh AA,
Attia JR,
Attix D,
Avramopoulos D,
Bennett DA,
Böhmer AC,
Boyle PA,
Brodaty H,
Campbell H,
Cannon TD,
Cirulli ET,
Congdon E,
Conley ED,
Corley J,
Cox SR,
Dale AM,
Dehghan A,
Dick D,
Dickinson D,
Eriksson JG,
Evangelou E,
Faul JD,
Ford I,
Freimer NA,
Gao H,
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Gordon SD,
Gottesman RF,
Griswold ME,
Gudnason V,
Harris TB,
Hartmann AM,
Hatzimanolis A,
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Holliday EG,
Joshi PK,
Kähönen M,
Kardia SLR,
Karlsson I,
Kleineidam L,
Knopman DS,
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Le Hellard S,
Lee T,
Lehtimäki T,
Li SC,
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Koini M,
London E,
Longstreth WT Jr,
Lopez OL,
Loukola A,
Luck T,
Lundervold AJ,
Lundquist A,
Lyytikäinen LP,
Martin NG,
Montgomery GW,
Murray AD,
Need AC,
Noordam R,
Nyberg L,
Ollier W,
Papenberg G,
Pattie A,
Polasek O,
Poldrack RA,
Psaty BM,
Reppermund S,
Riedel-Heller SG,
Rose RJ,
Rotter JI,
Roussos P,
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Saba Y,
Sabb FW,
Sachdev PS,
Satizabal CL,
Satizabal CL,
Schmid M,
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Smyrnis N,
Soumaré A,
Stefanis NC,
Stott DJ,
Straub RE,
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Taylor AM,
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Tzoulaki I,
Tzourio C,
Uitterlinden A,
Vitart V,
Voineskos AN,
Kaprio J,
Wagner M,
Wagner H,
Weinhold L,
Wen KH,
Widen E,
Yang Q,
Zhao W,
Adams HHH,
Arking DE,
Bilder RM,
Bitsios P,
Boerwinkle E,
Chiba-Falek O,
Corvin A,
De Jager PL,
Debette S,
Donohoe G,
Elliott P,
Fitzpatrick AL,
Gill M,
Glahn DC,
Hägg S,
Hansell NK,
Hariri AR,
Ikram MK,
Jukema JW,
Jukema JW,
Vuoksimaa E,
Keller MC,
Kremen WS,
Launer L,
Lindenberger U,
Palotie A,
Pedersen NL,
Pendleton N,
Porteous DJ,
Räikkönen K,
Raitakari OT,
Ramirez A,
Reinvang I,
Rudan I,
Dan Rujescu,
Schmidt R,
Schmidt H,
Schofield PW,
Schofield PR,
Starr JM,
Steen VM,
Trollor JN,
Turner ST,
Van Duijn CM,
Villringer A,
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Mosley TH Jr,
Bressler J,
Lencz T,
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Nature communications · 2018 · PMID 29844566 · open access
페이지 12개+
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence
Savage JE,
Jansen PR,
Stringer S,
Watanabe K,
Bryois J,
de Leeuw CA,
Nagel M,
Awasthi S,
Barr PB,
Coleman JRI,
Grasby KL,
Hammerschlag AR
외 105명 — 모두 보기
Kaminski JA,
Karlsson R,
Krapohl E,
Lam M,
Nygaard M,
Reynolds CA,
Trampush JW,
Young H,
Zabaneh D,
Hägg S,
Hansell NK,
Karlsson IK,
Linnarsson S,
Montgomery GW,
Muñoz-Manchado AB,
Quinlan EB,
Schumann G,
Skene NG,
Webb BT,
White T,
Arking DE,
Avramopoulos D,
Bilder RM,
Bitsios P,
Burdick KE,
Cannon TD,
Chiba-Falek O,
Christoforou A,
Cirulli ET,
Congdon E,
Corvin A,
Davies G,
Deary IJ,
DeRosse P,
Dickinson D,
Djurovic S,
Donohoe G,
Conley ED,
Eriksson JG,
Espeseth T,
Freimer NA,
Giakoumaki S,
Giegling I,
Gill M,
Glahn DC,
Hariri AR,
Hatzimanolis A,
Keller MC,
Knowles E,
Koltai D,
Konte B,
Lahti J,
Le Hellard S,
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Melle I,
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Payton A,
Pendleton N,
Poldrack RA,
Räikkönen K,
Reinvang I,
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Sabb FW,
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Posthuma D
Nature genetics · 2018 · PMID 29942086
페이지 12개+
The genetic architecture of the human cerebral cortex
Grasby KL,
Jahanshad N,
Painter JN,
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Hibar DP,
Lind PA,
Pizzagalli F,
Ching CRK,
McMahon MAB,
Shatokhina N,
Zsembik LCP
외 348명 — 모두 보기
Thomopoulos SI,
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Chen Q,
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de Zwarte SMC,
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Kaufmann T,
Kelly S,
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Verhoef E,
Walton E,
Wang M,
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Whelan CD,
Witt SH,
Wittfeld K,
Wolf C,
Wolfers T,
Wu JQ,
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Kahn RS,
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Alzheimer’s Disease Neuroimaging Initiative · CHARGE Consortium 외 컨소시엄 5곳
Science (New York, N.Y.) · 2020 · PMID 32193296
페이지 12개+
Cerebral small vessel disease genomics and its implications across the lifespan
Sargurupremraj M,
Suzuki H,
Jian X,
Sarnowski C,
Evans TE,
Bis JC,
Eiriksdottir G,
Sakaue S,
Terzikhan N,
Habes M,
Zhao W,
Zhao W
외 105명 — 모두 보기
Armstrong NJ,
Hofer E,
Yanek LR,
Hagenaars SP,
Kumar RB,
van den Akker EB,
McWhirter RE,
Trompet S,
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Sigurdsson S,
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Lewis CE,
Aggarwal NT,
Lopez OL,
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Wright MJ,
Knol MJ,
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Thomson RJ,
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Le Grand Q,
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Schreiner PJ,
Evans DA,
Rotter JI,
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Maniega SM,
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Trollor J,
Stott DJ,
Vernooij MW,
Wittfeld K,
Niessen WJ,
Soumaré A,
Boerwinkle E,
Sidney S,
Turner ST,
Davies G,
Thalamuthu A,
Völker U,
van Buchem MA,
Bryan RN,
Dupuis J,
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Kamatani Y,
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Longstreth WT Jr,
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Tzourio C,
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Fornage M,
Debette S
International Network against Thrombosis (INVENT) Consortium · International Headache Genomics Consortium (IHGC)
Nature communications · 2020 · PMID 33293549 · open access
페이지 12개+
Genetic architecture of subcortical brain structures in 38,851 individuals
Satizabal CL,
Adams HHH,
Hibar DP,
White CC,
Knol MJ,
Stein JL,
Scholz M,
Sargurupremraj M,
Jahanshad N,
Roshchupkin GV,
Smith AV,
Bis JC
외 277명 — 모두 보기
Jian X,
Luciano M,
Hofer E,
Teumer A,
van der Lee SJ,
Yang J,
Yanek LR,
Lee TV,
Li S,
Hu Y,
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Desrivières S,
Arias-Vasquez A,
Chauhan G,
Athanasiu L,
Rentería ME,
Kim S,
Hoehn D,
Armstrong NJ,
Chen Q,
Holmes AJ,
den Braber A,
Kloszewska I,
Andersson M,
Espeseth T,
Grimm O,
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Jones HJ,
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Harris TB,
Filippi I,
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Becker JT,
Doan NT,
Hagenaars SP,
Saba Y,
Cuellar-Partida G,
Amin N,
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Goldman AL,
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페이지 10개
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
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외 69명 — 모두 보기
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페이지 8개
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외 106명 — 모두 보기
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페이지 7개
Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero
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외 18명 — 모두 보기
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Human molecular genetics · 2018 · PMID 29659830 · open access
페이지 5개
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
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외 48명 — 모두 보기
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Proceedings of the National Academy of Sciences of the United States of America · 2014 · PMID 25201988
페이지 4개
Discovery of 42 genome-wide significant loci associated with dyslexia
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외 15명 — 모두 보기
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페이지 3개
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외 76명 — 모두 보기
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페이지 3개
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development
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American journal of human genetics · 2011 · PMID 21835309
페이지 2개
Common variants at 12q14 and 12q24 are associated with hippocampal volume
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외 71명 — 모두 보기
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Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
페이지 2개
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
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외 142명 — 모두 보기
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Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) 외 컨소시엄 2곳
Molecular psychiatry · 2015 · PMID 25288136
페이지 2개
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
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외 74명 — 모두 보기
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페이지 2개
Sequence variants in three loci influence monocyte counts and erythrocyte volume
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외 11명 — 모두 보기
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American journal of human genetics · 2009 · PMID 19853236
페이지 1개
Common variants in the trichohyalin gene are associated with straight hair in Europeans
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외 6명 — 모두 보기
American journal of human genetics · 2009 · PMID 19896111
페이지 1개
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622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.