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2,657 papers hold this site up. Every variant and condition page names
the research it was written from, and this is that list, gathered from the pages themselves.
Search your name, your journal, or a PMID.
14 matches for
Huang S.
Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels
Spracklen CN,
Chen P,
Kim YJ,
Wang X,
Cai H,
Li S,
Long J,
Wu Y,
Wang YX,
Takeuchi F,
Wu JY,
Jung KJ
and 103 more — show all
Hu C,
Akiyama K,
Zhang Y,
Moon S,
Johnson TA,
Li H,
Dorajoo R,
He M,
Cannon ME,
Roman TS,
Salfati E,
Lin KH,
Guo X,
Sheu WHH,
Absher D,
Adair LS,
Assimes TL,
Aung T,
Cai Q,
Chang LC,
Chen CH,
Chien LH,
Chuang LM,
Chuang SC,
Du S,
Fan Q,
Fann CSJ,
Feranil AB,
Friedlander Y,
Gordon-Larsen P,
Gu D,
Gui L,
Guo Z,
Heng CK,
Hixson J,
Hou X,
Hsiung CA,
Hu Y,
Hwang MY,
Hwu CM,
Isono M,
Juang JJ,
Khor CC,
Kim YK,
Koh WP,
Kubo M,
Lee IT,
Lee SJ,
Lee WJ,
Liang KW,
Lim B,
Lim SH,
Liu J,
Nabika T,
Pan WH,
Peng H,
Quertermous T,
Sabanayagam C,
Sandow K,
Shi J,
Sun L,
Tan PC,
Tan SP,
Taylor KD,
Teo YY,
Toh SA,
Tsunoda T,
van Dam RM,
Wang A,
Wang F,
Wang J,
Wei WB,
Xiang YB,
Yao J,
Yuan JM,
Zhang R,
Zhao W,
Chen YI,
Rich SS,
Rotter JI,
Wang TD,
Wu T,
Lin X,
Han BG,
Tanaka T,
Cho YS,
Katsuya T,
Jia W,
Jee SH,
Chen YT,
Kato N,
Jonas JB,
Cheng CY,
Shu XO,
He J,
Zheng W,
Zheng W,
Wong TY,
Huang W,
Kim BJ,
Tai ES,
Mohlke KL,
Sim X
Human molecular genetics · 2017 · PMID 28334899
12 pages+
Interpreting type 1 diabetes risk with genetics and single-cell epigenomics
Chiou J,
Geusz RJ,
Okino ML,
Han JY,
Miller M,
Melton R,
Beebe E,
Benaglio P,
Huang S,
Korgaonkar K,
Heller S,
Kleger A
and 4 more — show all
Nature · 2021 · PMID 34012112
12 pages+
Your height affects your health: genetic determinants and health-related outcomes in Taiwan
Chiou JS,
Cheng CF,
Liang WM,
Chou CH,
Wang CH,
Lin WD,
Chiu ML,
Cheng WC,
Lin CW,
Lin TH,
Liao CC,
Huang SM
and 3 more — show all
BMC medicine · 2022 · PMID 35831902 · open access
12 pages+
Genetic basis of pregnancy-associated decreased platelet counts and gestational thrombocytopenia
Yang Z,
Hu L,
Zhen J,
Gu Y,
Liu Y,
Huang S,
Wei Y,
Zheng H,
Guo X,
Chen GB,
Yang Y,
Xiong L
and 2 more — show all
Blood · 2024 · PMID 38064665 · open access
12 pages+
The X chromosome's influences on the human brain
Jiang Z,
Sullivan PF,
Li T,
Zhao B,
Wang X,
Luo T,
Huang S,
Guan PY,
Chen J,
Yang Y,
Stein JL,
Li Y
and 3 more — show all
Science advances · 2025 · PMID 39854466 · open access
12 pages+
Genome-wide association analyses of gestational phenotypes identify context-specific genetic effects
Liu S,
Zheng H,
Gu Y,
Yang Z,
Zhen J,
Wei Y,
Liu Y,
Chen Y,
Wan Z,
Guo X,
Hu L,
Chen X
and 11 more — show all
Li X,
Qiu X,
Huang S,
Chen GB,
Hu Z,
Namba S,
Kanai M,
Matsuda K,
Okada Y,
Zhang Q,
Wei F
Nature genetics · 2026 · PMID 42509370
12 pages+
Genome-wide association study of colorectal cancer identifies six new susceptibility loci
Schumacher FR,
Schmit SL,
Jiao S,
Edlund CK,
Wang H,
Zhang B,
Hsu L,
Huang SC,
Fischer CP,
Harju JF,
Idos GE,
Lejbkowicz F
and 93 more — show all
Manion FJ,
McDonnell K,
McNeil CE,
Melas M,
Rennert HS,
Shi W,
Thomas DC,
Van Den Berg DJ,
Hutter CM,
Aragaki AK,
Butterbach K,
Caan BJ,
Carlson CS,
Chanock SJ,
Curtis KR,
Fuchs CS,
Gala M,
Giovannucci EL,
Gogarten SM,
Hayes RB,
Henderson B,
Hunter DJ,
Jackson RD,
Kolonel LN,
Kooperberg C,
Küry S,
LaCroix A,
Laurie CC,
Laurie CA,
Lemire M,
Levine D,
Ma J,
Makar KW,
Qu C,
Taverna D,
Ulrich CM,
Wu K,
Kono S,
West DW,
Berndt SI,
Bezieau S,
Brenner H,
Campbell PT,
Chan AT,
Chang-Claude J,
Coetzee GA,
Conti DV,
Duggan D,
Figueiredo JC,
Fortini BK,
Gallinger SJ,
Gauderman WJ,
Giles G,
Green R,
Haile R,
Harrison TA,
Hoffmeister M,
Hopper JL,
Hudson TJ,
Hudson TJ,
Jacobs E,
Jacobs E,
Iwasaki M,
Jee SH,
Jenkins M,
Jia WH,
Joshi A,
Li L,
Lindor NM,
Matsuo K,
Moreno V,
Mukherjee B,
Newcomb PA,
Potter JD,
Potter JD,
Raskin L,
Rennert G,
Rosse S,
Severi G,
Schoen RE,
Seminara D,
Shu XO,
Slattery ML,
Tsugane S,
White E,
Xiang YB,
Zanke BW,
Zheng W,
Zheng W,
Le Marchand L,
Casey G,
Gruber SB,
Peters U
Nature communications · 2015 · PMID 26151821
4 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
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans
Jiang L,
Yin J,
Ye L,
Yang J,
Hemani G,
Liu AJ,
Zou H,
He D,
Sun L,
Zeng X,
Li Z,
Zheng Y
and 61 more — show all
Lin Y,
Liu Y,
Fang Y,
Xu J,
Li Y,
Dai S,
Guan J,
Jiang L,
Wei Q,
Wang Y,
Li Y,
Huang C,
Zuo X,
Liu Y,
Wu X,
Zhang L,
Zhou L,
Zhang Q,
Li T,
Chen L,
Xu Z,
Yang X,
Qian F,
Xie W,
Liu W,
Guo Q,
Huang S,
Zhao J,
Li M,
Jin Y,
Gao J,
Lv Y,
Wang Y,
Lin L,
Guo A,
Danoy P,
Willner D,
Cremin C,
Hadler J,
Zhang F,
Zhao Y,
Li M,
Yue T,
Fan X,
Guo J,
Mu R,
Li J,
Wu C,
Zeng M,
Wang J,
Li S,
Jin L,
Wang B,
Wang J,
Ma X,
Sun L,
Zhang X,
Brown MA,
Visscher PM,
Su DF,
Xu H
Arthritis & rheumatology (Hoboken, N.J.) · 2014 · PMID 24782177
2 pages
Genome-Wide Association and Functional Studies Identify <i>SCML4</i> and <i>THSD7A</i> as Novel Susceptibility Genes for Coronary Artery Disease
Li Y,
Wang DW,
Chen Y,
Chen C,
Guo J,
Zhang S,
Sun Z,
Ding H,
Yao Y,
Zhou L,
Xu K,
Song C
and 30 more — show all
Yang F,
Zhao B,
Yan H,
Wang WJ,
Wu C,
Lu X,
Yang X,
Dong J,
Zheng G,
Tian S,
Cui Y,
Jin L,
Liu G,
Cui H,
Wang S,
Jiang F,
Wang C,
Erdmann J,
Zeng L,
Huang S,
Zhong J,
Ma Y,
Chen W,
Sun J,
Lei W,
Chen S,
Rao S,
Gu D,
Schunkert H,
Tian XL
Arteriosclerosis, thrombosis, and vascular biology · 2018 · PMID 29472232
2 pages
A genome wide association study identifies common variants associated with lipid levels in the Chinese population
Zhou L,
He M,
Mo Z,
Wu C,
Yang H,
Yu D,
Yang X,
Zhang X,
Wang Y,
Sun J,
Gao Y,
Tan A
and 31 more — show all
He Y,
Zhang H,
Qin X,
Zhu J,
Li H,
Lin X,
Zhu J,
Min X,
Lang M,
Li D,
Zhai K,
Chang J,
Tan W,
Yuan J,
Chen W,
Wang Y,
Wei S,
Miao X,
Wang F,
Fang W,
Liang Y,
Deng Q,
Dai X,
Lin D,
Huang S,
Guo H,
Lilly Zheng S,
Xu J,
Lin D,
Hu FB,
Wu T
PloS one · 2013 · PMID 24386095 · open access
1 page
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population
Yang B,
Mo Z,
Wu C,
Yang H,
Yang X,
He Y,
Gui L,
Zhou L,
Guo H,
Zhang X,
Yuan J,
Dai X
and 17 more — show all
Li J,
Qiu G,
Huang S,
Deng Q,
Feng Y,
Guan L,
Hu D,
Zhang X,
Wang T,
Zhu J,
Min X,
Lang M,
Li D,
Hu FB,
Lin D,
Wu T,
He M
BMC medical genomics · 2014 · PMID 24513273 · open access
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.