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성함이나 학술지명, PMID로 찾아보십시오.
Chang KM에 대해
21건, 그중 20건 표시.
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program
Klarin D,
Damrauer SM,
Cho K,
Sun YV,
Teslovich TM,
Honerlaw J,
Gagnon DR,
DuVall SL,
Li J,
Peloso GM,
Chaffin M,
Small AM
외 33명 — 모두 보기
Huang J,
Tang H,
Lynch JA,
Ho YL,
Liu DJ,
Emdin CA,
Li AH,
Huffman JE,
Lee JS,
Natarajan P,
Chowdhury R,
Saleheen D,
Vujkovic M,
Baras A,
Pyarajan S,
Di Angelantonio E,
Neale BM,
Naheed A,
Khera AV,
Danesh J,
Chang KM,
Abecasis G,
Willer C,
Dewey FE,
Carey DJ,
Concato J,
Gaziano JM,
O'Donnell CJ,
Tsao PS,
Kathiresan S,
Rader DJ,
Wilson PWF,
Assimes TL
Global Lipids Genetics Consortium · Myocardial Infarction Genetics (MIGen) Consortium 외 컨소시엄 2곳
Nature genetics · 2018 · PMID 30275531 · open access
페이지 12개+
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis
Vujkovic M,
Keaton JM,
Lynch JA,
Miller DR,
Zhou J,
Tcheandjieu C,
Huffman JE,
Assimes TL,
Lorenz K,
Zhu X,
Hilliard AT,
Judy RL
외 35명 — 모두 보기
Huang J,
Lee KM,
Klarin D,
Pyarajan S,
Danesh J,
Melander O,
Rasheed A,
Mallick NH,
Hameed S,
Qureshi IH,
Afzal MN,
Malik U,
Jalal A,
Abbas S,
Sheng X,
Gao L,
Kaestner KH,
Susztak K,
Sun YV,
DuVall SL,
Cho K,
Lee JS,
Gaziano JM,
Phillips LS,
Meigs JB,
Reaven PD,
Wilson PW,
Edwards TL,
Rader DJ,
Damrauer SM,
O'Donnell CJ,
Tsao PS,
Chang KM,
Voight BF,
Saleheen D
HPAP Consortium · Regeneron Genetics Center 외 컨소시엄 1곳
Nature genetics · 2020 · PMID 32541925 · open access
페이지 12개+
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Pazoki R,
Vujkovic M,
Elliott J,
Evangelou E,
Gill D,
Ghanbari M,
van der Most PJ,
Pinto RC,
Wielscher M,
Farlik M,
Zuber V,
de Knegt RJ
외 23명 — 모두 보기
Snieder H,
Uitterlinden AG,
Lynch JA,
Jiang X,
Said S,
Kaplan DE,
Lee KM,
Serper M,
Carr RM,
Tsao PS,
Atkinson SR,
Dehghan A,
Tzoulaki I,
Ikram MA,
Herzig KH,
Järvelin MR,
Alizadeh BZ,
O'Donnell CJ,
Saleheen D,
Voight BF,
Chang KM,
Thursz MR,
Elliott P
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
페이지 12개+
The power of genetic diversity in genome-wide association studies of lipids
Graham SE,
Clarke SL,
Wu KH,
Kanoni S,
Zajac GJM,
Ramdas S,
Surakka I,
Ntalla I,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
외 523명 — 모두 보기
Hwang MY,
Han S,
Narita A,
Choudhury A,
Bentley AR,
Ekoru K,
Verma A,
Trivedi B,
Martin HC,
Hunt KA,
Hui Q,
Klarin D,
Zhu X,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Ruotsalainen SE,
Havulinna AS,
Veturi Y,
Feng Q,
Rosenthal EA,
Lingren T,
Pacheco JA,
Pendergrass SA,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
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Hindy G,
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Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
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Pitsillides A,
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Willemsen G,
Wood AR,
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Chai JF,
Aadahl M,
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Manichaikul A,
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Kårhus LL,
Goel A,
Sabater-Lleal M,
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Sidore C,
Fiorillo E,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Thuesen BH,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Daw EW,
Zmuda JM,
Mitchell JS,
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Lyssenko V,
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Pitkänen N,
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Lee J,
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Chitrala KN,
Weiss S,
Zimmermann ME,
Lee JY,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
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Wang CA,
Lin SY,
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Couture C,
Lyytikäinen LP,
Nikus K,
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Vestergaard H,
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Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Schwander K,
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Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Highland HM,
Young KL,
Kawaguchi T,
Thiery J,
Bis JC,
Nadkarni GN,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
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Campbell H,
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Nabika T,
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Kolcic I,
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Giardoglou T,
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Bhatti KF,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
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Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
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Kähönen M,
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Chen YI,
Pennell CE,
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Lieb W,
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Cho YS,
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Koh WP,
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Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
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de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
den Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
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Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
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Hunt SC,
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Yajnik CS,
Mercader JM,
Tusié-Luna T,
Aguilar-Salinas CA,
Villalpando CG,
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Fornage M,
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van Dam RM,
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Liu J,
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Palmer CNA,
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Lin X,
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Parra EJ,
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Cruz M,
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Tardif JC,
Lettre G,
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Damrauer SM,
Kumari M,
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Psaty BM,
Brandslund I,
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Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
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Gu D,
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Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Cucca F,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Rotter JI,
Dantoft TM,
Karpe F,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
de Geus EJC,
Cupples LA,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
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Baras A,
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Ridker PM,
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Kooperberg C,
Wei WQ,
Jarvik GP,
Namjou B,
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Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Thorsteinsdottir U,
Stefansson K,
Ho YL,
Lynch JA,
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Tsao PS,
Chang KM,
Cho K,
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Gaziano JM,
Wilson P,
Rotimi CN,
Hazelhurst S,
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Kim BJ,
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Kathiresan S,
Boehnke M,
Natarajan P,
Peloso GM,
Brown CD,
Morris AP,
Assimes TL,
Deloukas P,
Sun YV,
Willer CJ
VA Million Veteran Program · Global Lipids Genetics Consortium*
Nature · 2021 · PMID 34887591
페이지 12개+
Genomics and phenomics of body mass index reveals a complex disease network
Huang J,
Huffman JE,
Huang Y,
Do Valle Í,
Assimes TL,
Raghavan S,
Voight BF,
Liu C,
Barabási AL,
Huang RDL,
Hui Q,
Nguyen XT
외 26명 — 모두 보기
Ho YL,
Djousse L,
Lynch JA,
Vujkovic M,
Tcheandjieu C,
Tang H,
Damrauer SM,
Reaven PD,
Miller D,
Phillips LS,
Ng MCY,
Graff M,
Haiman CA,
Loos RJF,
North KE,
Yengo L,
Smith GD,
Saleheen D,
Gaziano JM,
Rader DJ,
Tsao PS,
Cho K,
Chang KM,
Wilson PWF,
Sun YV,
O'Donnell CJ
VA Million Veteran Program
Nature communications · 2022 · PMID 36581621 · open access
페이지 12개+
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Suzuki K,
Hatzikotoulas K,
Southam L,
Taylor HJ,
Yin X,
Lorenz KM,
Mandla R,
Huerta-Chagoya A,
Melloni GEM,
Kanoni S,
Rayner NW,
Bocher O
외 351명 — 모두 보기
Arruda AL,
Sonehara K,
Namba S,
Lee SSK,
Preuss MH,
Petty LE,
Schroeder P,
Vanderwerff B,
Kals M,
Bragg F,
Lin K,
Guo X,
Zhang W,
Yao J,
Kim YJ,
Graff M,
Takeuchi F,
Nano J,
Lamri A,
Nakatochi M,
Moon S,
Scott RA,
Cook JP,
Lee JJ,
Pan I,
Taliun D,
Parra EJ,
Chai JF,
Bielak LF,
Tabara Y,
Hai Y,
Thorleifsson G,
Grarup N,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Kwak SH,
Long J,
Sun M,
Tong L,
Chen WM,
Nongmaithem SS,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Brody JA,
Kabagambe E,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Broadaway KA,
Williamson A,
Kamali Z,
Cui J,
Thangam M,
Adair LS,
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Aguilar-Salinas CA,
Ahluwalia TS,
Anand SS,
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Brandslund I,
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Burant CF,
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Canouil M,
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Chuang LM,
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Das SK,
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Huang W,
Hung YJ,
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Hwu CM,
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Ikram MA,
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Islam MT,
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Jang HM,
Jasmine F,
Jiang G,
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Mahajan A,
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Vujkovic M,
Voight BF,
Morris AP,
Zeggini E
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
페이지 12개+
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
Ghouse J,
Sveinbjörnsson G,
Vujkovic M,
Seidelin AS,
Gellert-Kristensen H,
Ahlberg G,
Tragante V,
Rand SA,
Brancale J,
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Lundegaard PR,
Sørensen E
외 39명 — 모두 보기
Erikstrup C,
Bruun MT,
Jensen BA,
Brunak S,
Banasik K,
Ullum H,
Verweij N,
Lotta L,
Baras A,
Mirshahi T,
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Dochtermann DR,
Pyarajan S,
Tsao PS,
Laisk T,
Mägi R,
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페이지 12개+
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외 18명 — 모두 보기
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Cell · 2025 · PMID 40049164
페이지 12개+
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외 78명 — 모두 보기
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Regeneron Genetics Center · Geisinger-Regeneron DiscovEHR Collaboration 외 컨소시엄 2곳
Nature genetics · 2022 · PMID 35654975
페이지 8개
Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease
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외 30명 — 모두 보기
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INVENT Consortium · Veterans Affairs’ Million Veteran Program
Nature genetics · 2019 · PMID 31676865 · open access
페이지 7개
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
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외 527명 — 모두 보기
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Genome biology · 2022 · PMID 36575460 · open access
페이지 7개
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Klarin D,
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외 41명 — 모두 보기
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Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
페이지 6개
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
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외 70명 — 모두 보기
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Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium 외 컨소시엄 2곳
Nature medicine · 2022 · PMID 35915156
페이지 6개
A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program
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외 12명 — 모두 보기
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VA Million Veteran Program
PLoS genetics · 2022 · PMID 35653334 · open access
페이지 5개
Genetic variants affect diurnal glucose levels throughout the day
Sinnott-Armstrong N,
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외 4명 — 모두 보기
FinnGen · Estonian Biobank Research Team 외 컨소시엄 1곳
Nature communications · 2026 · PMID 42173832 · open access
페이지 4개
Genome-wide association study of peripheral artery disease in the Million Veteran Program
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외 24명 — 모두 보기
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VA Million Veteran Program
Nature medicine · 2019 · PMID 31285632 · open access
페이지 3개
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience
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외 46명 — 모두 보기
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FinnGen · VA Million Veteran Program 외 컨소시엄 1곳
Nature genetics · 2024 · PMID 39572784 · open access
페이지 3개
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
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외 6명 — 모두 보기
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
페이지 1개
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
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외 10명 — 모두 보기
Frontiers in genetics · 2021 · PMID 35186008 · open access
페이지 1개
Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
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외 7명 — 모두 보기
Veterans Affairs’ Million Veteran Program
PloS one · 2022 · PMID 35613103 · open access
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인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
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
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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
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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
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