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성함이나 학술지명, PMID로 찾아보십시오.
Harris KM에 대해
10건.
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
Turcot V,
Lu Y,
Highland HM,
Schurmann C,
Justice AE,
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Bradfield JP,
Esko T,
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Hendricks AE
외 390명 — 모두 보기
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Abecasis G,
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Allison M,
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Bottinger EP,
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Brandslund I,
Breen G,
Brilliant MH,
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Chen YI,
Chowdhury R,
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Steinthorsdottir V,
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Wu Y,
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Yao J,
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Zhao JH,
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Zhao W,
Zhou W,
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Rotter JI,
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Loos RJF
CHD Exome+ Consortium · EPIC-CVD Consortium 외 컨소시엄 9곳
Nature genetics · 2018 · PMID 29273807 · open access
페이지 12개+
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Lee JJ,
Wedow R,
Okbay A,
Kong E,
Maghzian O,
Zacher M,
Nguyen-Viet TA,
Bowers P,
Sidorenko J,
Karlsson Linnér R,
Fontana MA,
Kundu T
외 65명 — 모두 보기
Lee C,
Li H,
Li R,
Royer R,
Timshel PN,
Walters RK,
Willoughby EA,
Yengo L,
Alver M,
Bao Y,
Clark DW,
Day FR,
Furlotte NA,
Joshi PK,
Kemper KE,
Kleinman A,
Langenberg C,
Mägi R,
Trampush JW,
Verma SS,
Wu Y,
Lam M,
Zhao JH,
Zheng Z,
Boardman JD,
Campbell H,
Freese J,
Harris KM,
Hayward C,
Herd P,
Kumari M,
Lencz T,
Luan J,
Malhotra AK,
Metspalu A,
Milani L,
Ong KK,
Perry JRB,
Porteous DJ,
Ritchie MD,
Smart MC,
Smith BH,
Tung JY,
Wareham NJ,
Wilson JF,
Beauchamp JP,
Conley DC,
Esko T,
Lehrer SF,
Magnusson PKE,
Oskarsson S,
Pers TH,
Robinson MR,
Thom K,
Watson C,
Chabris CF,
Meyer MN,
Laibson DI,
Yang J,
Johannesson M,
Koellinger PD,
Turley P,
Visscher PM,
Benjamin DJ,
Cesarini D
23andMe Research Team · COGENT (Cognitive Genomics Consortium) 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 30038396
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 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,
Fontanillas P,
Gonzalez JR,
Joshi PK,
Karhunen V,
Kleinman A,
Levin RZ,
Lill CM,
Meddens GA,
Muntané G,
Sanchez-Roige S,
Rooij FJV,
Taskesen E,
Wu Y,
Zhang F,
Auton A,
Boardman JD,
Clark DW,
Conlin A,
Dolan CC,
Fischbacher U,
Groenen PJF,
Harris KM,
Hasler G,
Hofman A,
Ikram MA,
Jain S,
Karlsson R,
Kessler RC,
Kooyman M,
MacKillop J,
Männikkö M,
Morcillo-Suarez C,
McQueen MB,
Schmidt KM,
Smart MC,
Sutter M,
Thurik AR,
Uitterlinden AG,
White J,
Wit H,
Yang J,
Bertram L,
Boomsma DI,
Esko T,
Fehr E,
Hinds DA,
Johannesson M,
Kumari M,
Laibson D,
Magnusson PKE,
Meyer MN,
Navarro A,
Palmer AA,
Pers TH,
Posthuma D,
Schunk D,
Stein MB,
Svento R,
Tiemeier H,
Timmers PRHJ,
Turley P,
Ursano RJ,
Wagner GG,
Wilson JF,
Gratten J,
Lee JJ,
Cesarini D,
Benjamin DJ,
Koellinger PD,
Beauchamp JP
23and Me Research Team · eQTLgen Consortium 외 컨소시엄 2곳
Nature genetics · 2019 · PMID 30643258
페이지 12개+
Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction
Demange PA,
Malanchini M,
Mallard TT,
Biroli P,
Cox SR,
Grotzinger AD,
Tucker-Drob EM,
Abdellaoui A,
Arseneault L,
van Bergen E,
Boomsma DI,
Caspi A
외 15명 — 모두 보기
Corcoran DL,
Domingue BW,
Harris KM,
Ip HF,
Mitchell C,
Moffitt TE,
Poulton R,
Prinz JA,
Sugden K,
Wertz J,
Williams BS,
de Zeeuw EL,
Belsky DW,
Harden KP,
Nivard MG
Nature genetics · 2021 · PMID 33414549 · open access
페이지 12개+
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
Karlsson Linnér R,
Mallard TT,
Barr PB,
Sanchez-Roige S,
Madole JW,
Driver MN,
Poore HE,
de Vlaming R,
Grotzinger AD,
Tielbeek JJ,
Johnson EC,
Liu M
외 17명 — 모두 보기
Rosenthal SB,
Ideker T,
Zhou H,
Kember RL,
Pasman JA,
Verweij KJH,
Liu DJ,
Vrieze S,
Kranzler HR,
Gelernter J,
Harris KM,
Tucker-Drob EM,
Waldman ID,
Palmer AA,
Harden KP,
Koellinger PD,
Dick DM
COGA Collaborators
Nature neuroscience · 2021 · PMID 34446935 · 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+
Large-scale genome-wide analyses of stuttering
Polikowsky HG,
Scartozzi AC,
Shaw DM,
Pruett DG,
Chen HH,
Petty LE,
Petty AS,
Lowther EJ,
Cho SH,
Yu Y,
Mozaffari S,
Avery CL
외 9명 — 모두 보기
23andMe Research Team
Nature genetics · 2025 · PMID 40721530 · open access
페이지 12개+
Genomic loci and molecular genetic mechanisms for hidradenitis suppurativa
Broadaway KA,
Sun Q,
Edmiston SN,
Currin KW,
Vadlamudi S,
Miller-Fleming TW,
Shi Y,
Fajgenbaum K,
Melendez-Gonzalez M,
Bui H,
Blum FR,
Westerkam L
외 16명 — 모두 보기
Shams R,
Mallela T,
Levitt B,
Lin L,
Hao H,
Memili A,
Straub P,
Zhou W,
Harris KM,
Martin A,
Cox NJ,
Liu Z,
Thomas NE,
Li Y,
Mohlke KL,
Sayed CJ
The British journal of dermatology · 2025 · PMID 40650879 · open access
페이지 4개
Genetic Variants Associated With Hidradenitis Suppurativa
Sun Q,
Broadaway KA,
Edmiston SN,
Fajgenbaum K,
Miller-Fleming T,
Westerkam LL,
Melendez-Gonzalez M,
Bui H,
Blum FR,
Levitt B,
Lin L,
Hao H
외 7명 — 모두 보기
JAMA dermatology · 2023 · PMID 37494057
페이지 1개
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가져옵니다.
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.