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Gratten J에 대해
5건.
Genome-wide association study identifies 74 loci associated with educational attainment
Okbay A,
Beauchamp JP,
Fontana MA,
Lee JJ,
Pers TH,
Rietveld CA,
Turley P,
Chen GB,
Emilsson V,
Meddens SF,
Oskarsson S,
Pickrell JK
외 243명 — 모두 보기
Thom K,
Timshel P,
de Vlaming R,
Abdellaoui A,
Ahluwalia TS,
Bacelis J,
Baumbach C,
Bjornsdottir G,
Brandsma JH,
Pina Concas M,
Derringer J,
Furlotte NA,
Galesloot TE,
Girotto G,
Gupta R,
Hall LM,
Harris SE,
Hofer E,
Horikoshi M,
Huffman JE,
Kaasik K,
Kalafati IP,
Karlsson R,
Kong A,
Lahti J,
van der Lee SJ,
deLeeuw C,
Lind PA,
Lindgren KO,
Liu T,
Mangino M,
Marten J,
Mihailov E,
Miller MB,
van der Most PJ,
Oldmeadow C,
Payton A,
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Peyrot WJ,
Qian Y,
Raitakari O,
Rueedi R,
Salvi E,
Schmidt B,
Schraut KE,
Shi J,
Smith AV,
Poot RA,
St Pourcain B,
Teumer A,
Thorleifsson G,
Verweij N,
Vuckovic D,
Wellmann J,
Westra HJ,
Yang J,
Zhao W,
Zhu Z,
Alizadeh BZ,
Amin N,
Bakshi A,
Baumeister SE,
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Boyle PA,
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Halldórsson BV,
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Heath AC,
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Homuth G,
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Hottenga JJ,
de Jager PL,
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Spector TD,
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Thorsteinsdottir U,
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Visscher PM,
Esko T,
Koellinger PD,
Cesarini D,
Benjamin DJ
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
페이지 12개+
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Karlsson Linnér R,
Biroli P,
Kong E,
Meddens SFW,
Wedow R,
Fontana MA,
Lebreton M,
Tino SP,
Abdellaoui A,
Hammerschlag AR,
Nivard MG,
Okbay A
외 80명 — 모두 보기
Rietveld CA,
Timshel PN,
Trzaskowski M,
Vlaming R,
Zünd CL,
Bao Y,
Buzdugan L,
Caplin AH,
Chen CY,
Eibich P,
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Joshi PK,
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Beauchamp JP
23and Me Research Team · eQTLgen Consortium 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30643258
페이지 12개+
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
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Xue A,
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Young E
외 39명 — 모두 보기
von Coelln R,
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23andMe Research Team · System Genomics of Parkinson's Disease Consortium 외 컨소시엄 1곳
The Lancet. Neurology · 2019 · PMID 31701892
페이지 12개+
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
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외 422명 — 모두 보기
Frei O,
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McIntosh A,
McQuillin A,
Menezes PR,
Morgan VA,
Morris DW,
Mowry BJ,
Murray RM,
Nimgaonkar V,
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Riley BP,
Rivera M,
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Saka MC,
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Schwab SG,
Serretti A,
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Shi Y,
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Indonesia Schizophrenia Consortium · PsychENCODE 외 컨소시엄 3곳
Nature · 2022 · PMID 35396580
페이지 12개+
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Okbay A,
Baselmans BM,
De Neve JE,
Turley P,
Nivard MG,
Fontana MA,
Meddens SF,
Linnér RK,
Rietveld CA,
Derringer J,
Gratten J,
Lee JJ
외 180명 — 모두 보기
Liu JZ,
de Vlaming R,
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LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
페이지 10개
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왜 "외 몇 명"이 아니라 저자를 다 적습니까?
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.