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6 matches for
Cheng I.
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
and 205 more — show all
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
12 pages+
Tissue-specific genetic variation suggests distinct molecular pathways between body shape phenotypes and colorectal cancer
Peruchet-Noray L,
Sedlmeier AM,
Dimou N,
Baurecht H,
Fervers B,
Fontvieille E,
Konzok J,
Tsilidis KK,
Christakoudi S,
Jansana A,
Cordova R,
Bohmann P
and 18 more — show all
Stein MJ,
Weber A,
Bézieau S,
Brenner H,
Chan AT,
Cheng I,
Figueiredo JC,
Garcia-Etxebarria K,
Moreno V,
Newton CC,
Schmit SL,
Song M,
Ulrich CM,
Ferrari P,
Viallon V,
Carreras-Torres R,
Gunter MJ,
Freisling H
Science advances · 2024 · PMID 38640244 · open access
12 pages+
Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population
Shi J,
Shiraishi K,
Choi J,
Matsuo K,
Chen TY,
Dai J,
Hung RJ,
Chen K,
Shu XO,
Kim YT,
Landi MT,
Lin D
and 210 more — show all
Zheng W,
Yin Z,
Zhou B,
Song B,
Wang J,
Seow WJ,
Song L,
Chang IS,
Hu W,
Chien LH,
Cai Q,
Hong YC,
Kim HN,
Wu YL,
Wong MP,
Richardson BD,
Funderburk KM,
Li S,
Zhang T,
Breeze C,
Wang Z,
Blechter B,
Bassig BA,
Kim JH,
Albanes D,
Wong JYY,
Shin MH,
Chung LP,
Yang Y,
An SJ,
Zheng H,
Yatabe Y,
Zhang XC,
Kim YC,
Caporaso NE,
Chang J,
Ho JCM,
Kubo M,
Daigo Y,
Song M,
Momozawa Y,
Kamatani Y,
Kobayashi M,
Okubo K,
Honda T,
Hosgood DH,
Kunitoh H,
Patel H,
Watanabe SI,
Miyagi Y,
Nakayama H,
Matsumoto S,
Horinouchi H,
Tsuboi M,
Hamamoto R,
Goto K,
Ohe Y,
Takahashi A,
Goto A,
Minamiya Y,
Hara M,
Nishida Y,
Takeuchi K,
Wakai K,
Matsuda K,
Murakami Y,
Shimizu K,
Suzuki H,
Saito M,
Ohtaki Y,
Tanaka K,
Wu T,
Wei F,
Dai H,
Machiela MJ,
Su J,
Kim YH,
Oh IJ,
Lee VHF,
Chang GC,
Tsai YH,
Chen KY,
Huang MS,
Su WC,
Chen YM,
Seow A,
Park JY,
Kweon SS,
Chen KC,
Gao YT,
Qian B,
Wu C,
Lu D,
Liu J,
Schwartz AG,
Houlston R,
Spitz MR,
Gorlov IP,
Wu X,
Yang P,
Lam S,
Tardon A,
Chen C,
Bojesen SE,
Johansson M,
Risch A,
Bickeböller H,
Ji BT,
Wichmann HE,
Christiani DC,
Rennert G,
Arnold S,
Brennan P,
McKay J,
Field JK,
Shete SS,
Le Marchand L,
Liu G,
Andrew A,
Kiemeney LA,
Zienolddiny-Narui S,
Grankvist K,
Johansson M,
Cox A,
Taylor F,
Yuan JM,
Lazarus P,
Schabath MB,
Aldrich MC,
Jeon HS,
Jiang SS,
Sung JS,
Chen CH,
Hsiao CF,
Jung YJ,
Guo H,
Hu Z,
Burdett L,
Yeager M,
Hutchinson A,
Hicks B,
Liu J,
Zhu B,
Berndt SI,
Wu W,
Wang J,
Li Y,
Choi JE,
Park KH,
Sung SW,
Liu L,
Kang CH,
Wang WC,
Xu J,
Guan P,
Tan W,
Yu CJ,
Yang G,
Sihoe ADL,
Chen Y,
Choi YY,
Kim JS,
Yoon HI,
Park IK,
Xu P,
He Q,
Wang CL,
Hung HH,
Vermeulen RCH,
Cheng I,
Wu J,
Lim WY,
Tsai FY,
Chan JKC,
Li J,
Chen H,
Lin HC,
Jin L,
Liu J,
Sawada N,
Yamaji T,
Wyatt K,
Li SA,
Ma H,
Zhu M,
Wang Z,
Cheng S,
Li X,
Ren Y,
Chao A,
Iwasaki M,
Zhu J,
Jiang G,
Fei K,
Wu G,
Chen CY,
Chen CJ,
Yang PC,
Yu J,
Stevens VL,
Fraumeni JF Jr,
Chatterjee N,
Gorlova OY,
Hsiung CA,
Amos CI,
Shen H,
Chanock SJ,
Rothman N,
Kohno T,
Lan Q
Nature communications · 2023 · PMID 37236969 · open access
5 pages
Novel Common Genetic Susceptibility Loci for Colorectal Cancer
Schmit SL,
Edlund CK,
Schumacher FR,
Gong J,
Harrison TA,
Huyghe JR,
Qu C,
Melas M,
Van Den Berg DJ,
Wang H,
Tring S,
Plummer SJ
and 171 more — show all
Albanes D,
Alonso MH,
Amos CI,
Anton K,
Aragaki AK,
Arndt V,
Barry EL,
Berndt SI,
Bezieau S,
Bien S,
Bloomer A,
Boehm J,
Boutron-Ruault MC,
Brenner H,
Brezina S,
Buchanan DD,
Butterbach K,
Caan BJ,
Campbell PT,
Carlson CS,
Castelao JE,
Chan AT,
Chang-Claude J,
Chanock SJ,
Cheng I,
Cheng YW,
Chin LS,
Church JM,
Church T,
Coetzee GA,
Cotterchio M,
Cruz Correa M,
Curtis KR,
Duggan D,
Easton DF,
English D,
Feskens EJM,
Fischer R,
FitzGerald LM,
Fortini BK,
Fritsche LG,
Fuchs CS,
Gago-Dominguez M,
Gala M,
Gallinger SJ,
Gauderman WJ,
Giles GG,
Giovannucci EL,
Gogarten SM,
Gonzalez-Villalpando C,
Gonzalez-Villalpando EM,
Grady WM,
Greenson JK,
Gsur A,
Gunter M,
Haiman CA,
Hampe J,
Harlid S,
Harju JF,
Hayes RB,
Hofer P,
Hoffmeister M,
Hopper JL,
Huang SC,
Huerta JM,
Hudson TJ,
Hunter DJ,
Idos GE,
Iwasaki M,
Jackson RD,
Jacobs EJ,
Jee SH,
Jenkins MA,
Jia WH,
Jiao S,
Joshi AD,
Kolonel LN,
Kono S,
Kooperberg C,
Krogh V,
Kuehn T,
Küry S,
LaCroix A,
Laurie CA,
Lejbkowicz F,
Lemire M,
Lenz HJ,
Levine D,
Li CI,
Li L,
Lieb W,
Lin Y,
Lindor NM,
Liu YR,
Loupakis F,
Lu Y,
Luh F,
Ma J,
Mancao C,
Manion FJ,
Markowitz SD,
Martin V,
Matsuda K,
Matsuo K,
McDonnell KJ,
McNeil CE,
Milne R,
Molina AJ,
Mukherjee B,
Murphy N,
Newcomb PA,
Offit K,
Omichessan H,
Palli D,
Cotoré JPP,
Pérez-Mayoral J,
Pharoah PD,
Potter JD,
Qu C,
Raskin L,
Rennert G,
Rennert HS,
Riggs BM,
Schafmayer C,
Schoen RE,
Sellers TA,
Seminara D,
Severi G,
Shi W,
Shibata D,
Shu XO,
Siegel EM,
Slattery ML,
Southey M,
Stadler ZK,
Stern MC,
Stintzing S,
Taverna D,
Thibodeau SN,
Thomas DC,
Trichopoulou A,
Tsugane S,
Ulrich CM,
van Duijnhoven FJB,
van Guelpan B,
Vijai J,
Virtamo J,
Weinstein SJ,
White E,
Win AK,
Wolk A,
Woods M,
Wu AH,
Wu K,
Xiang YB,
Yen Y,
Zanke BW,
Zeng YX,
Zhang B,
Zubair N,
Kweon SS,
Figueiredo JC,
Zheng W,
Marchand LL,
Lindblom A,
Moreno V,
Peters U,
Casey G,
Hsu L,
Conti DV,
Gruber SB
Journal of the National Cancer Institute · 2019 · PMID 29917119
3 pages
Evaluating genetic risk for prostate cancer among Japanese and Latinos
Cheng I,
Chen GK,
Nakagawa H,
He J,
Wan P,
Laurie CC,
Shen J,
Sheng X,
Pooler LC,
Crenshaw AT,
Mirel DB,
Takahashi A
and 19 more — show all
Kubo M,
Nakamura Y,
Al Olama AA,
Benlloch S,
Donovan JL,
Guy M,
Hamdy FC,
Kote-Jarai Z,
Neal DE,
Wilkens LR,
Monroe KR,
Stram DO,
Muir K,
Eeles RA,
Easton DF,
Kolonel LN,
Henderson BE,
Le Marchand L,
Haiman CA
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2012 · PMID 22923026
2 pages
Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL,
Graff M,
Nishimura KK,
Tao R,
Haessler J,
Gignoux CR,
Highland HM,
Patel YM,
Sorokin EP,
Avery CL,
Belbin GM,
Bien SA
and 74 more — show all
Cheng I,
Cullina S,
Hodonsky CJ,
Hu Y,
Huckins LM,
Jeff J,
Justice AE,
Kocarnik JM,
Lim U,
Lin BM,
Lu Y,
Nelson SC,
Park SL,
Poisner H,
Preuss MH,
Richard MA,
Schurmann C,
Setiawan VW,
Sockell A,
Vahi K,
Verbanck M,
Vishnu A,
Walker RW,
Young KL,
Zubair N,
Acuña-Alonso V,
Ambite JL,
Barnes KC,
Boerwinkle E,
Bottinger EP,
Bustamante CD,
Caberto C,
Canizales-Quinteros S,
Conomos MP,
Deelman E,
Do R,
Doheny K,
Fernández-Rhodes L,
Fornage M,
Hailu B,
Heiss G,
Henn BM,
Hindorff LA,
Jackson RD,
Laurie CA,
Laurie CC,
Li Y,
Lin DY,
Moreno-Estrada A,
Nadkarni G,
Norman PJ,
Pooler LC,
Reiner AP,
Romm J,
Sabatti C,
Sandoval K,
Sheng X,
Stahl EA,
Stram DO,
Thornton TA,
Wassel CL,
Wilkens LR,
Winkler CA,
Yoneyama S,
Buyske S,
Haiman CA,
Kooperberg C,
Le Marchand L,
Loos RJF,
Matise TC,
North KE,
Peters U,
Kenny EE,
Carlson CS
Nature · 2019 · PMID 31217584
1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.