For researchers

Is your paper here?

2,673 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.

22 matches for Yang Z, showing the first 20.

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

Wei F, Liu S

Blood · 2024 · PMID 38064665 · open access

12 pages+

rs145450404 rs4741744 rs77649000 rs2040571 rs79647915 rs394772

Genome-wide association studies of thyroid-related hormones, dysfunction, and autoimmunity among 85,421 Chinese pregnancies

Wei Y, Zhen J, Hu L, Gu Y, Liu Y, Guo X, Yang Z, Zheng H, Cheng S, Wei F, Xiong L, Liu S

Nature communications · 2024 · PMID 39266554 · open access

12 pages+

rs10901251 rs9378805 rs12321067 rs74868707 rs76569227 rs17020123

Genetic architecture and risk prediction of gestational diabetes mellitus in Chinese pregnancies

Gu Y, Zheng H, Wang P, Liu Y, Guo X, Wei Y, Yang Z, Cheng S, Chen Y, Hu L, Chen X, Zhang Q

and 4 more — show all

Chen G, Wei F, Zhen J, Liu S

Nature communications · 2025 · PMID 40325049 · open access

12 pages+

rs4716672 rs76154673 rs72554664 rs182573065 rs61160304 rs146844151

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+

rs544856801 rs2961667 rs2965188 rs142065151 rs75633704 rs9654412

Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population

Huang L, Chen Y, Lin Y, Tam POS, Cheng Y, Shi Y, Gong B, Lu F, Yang J, Wang H, Yin Y, Cao Y

and 9 more — show all

Jiang D, Zhong L, Xue B, Wang J, Hao F, Lee DY, Pang CP, Sun X, Yang Z

Science China. Life sciences · 2019 · PMID 30591961

6 pages

rs11078446 rs17737857 rs4467035 rs201143466 rs12504231 rs7047871

Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension

Lu X, Wang L, Lin X, Huang J, Charles Gu C, He M, Shen H, He J, Zhu J, Li H, Hixson JE, Wu T

and 37 more — show all

Dai J, Lu L, Shen C, Chen S, He L, Mo Z, Hao Y, Mo X, Yang X, Li J, Cao J, Chen J, Fan Z, Li Y, Zhao L, Li H, Lu F, Yao C, Yu L, Xu L, Mu J, Wu X, Deng Y, Hu D, Zhang W, Ji X, Guo D, Guo Z, Zhou Z, Yang Z, Wang R, Yang J, Zhou X, Yan W, Sun N, Gao P, Gu D

Human molecular genetics · 2015 · PMID 25249183

5 pages

rs9810888 rs2021783 rs1902859 rs13143871 rs4409766

Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft

Huang L, Jia Z, Shi Y, Du Q, Shi J, Wang Z, Mou Y, Wang Q, Zhang B, Wang Q, Ma S, Lin H

and 15 more — show all

Duan S, Yin B, Lin Y, Wang Y, Jiang D, Hao F, Zhang L, Wang H, Jiang S, Xu H, Yang C, Li C, Li J, Shi B, Yang Z

PLoS genetics · 2019 · PMID 31609978 · open access

5 pages

rs4646211 rs6791526 rs730570 rs17820943 rs730643

Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations

Lu X, Huang J, Mo Z, He J, Wang L, Yang X, Tan A, Chen S, Chen J, Gu CC, Chen J, Li Y

and 26 more — show all

Zhao L, Li H, Hao Y, Li J, Hixson JE, Li Y, Cheng M, Liu X, Cao J, Liu F, Huang C, Shen C, Shen J, Yu L, Xu L, Mu J, Wu X, Ji X, Guo D, Zhou Z, Yang Z, Wang R, Yang J, Yan W, Peng X, Gu D

Circulation. Cardiovascular genetics · 2016 · PMID 26582766

4 pages

rs1260333 rs2575876 rs7525649 rs9357121

Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis

Li HJ, Zhang C, Hui L, Zhou DS, Li Y, Zhang CY, Wang C, Wang L, Li W, Yang Y, Qu N, Tang J

and 37 more — show all

He Y, Zhou J, Yang Z, Li X, Cai J, Yang L, Chen J, Fan W, Tang W, Tang W, Jia QF, Liu W, Zhuo C, Song X, Liu F, Bai Y, Zhong BL, Zhang SF, Chen J, Xia B, Lv L, Liu Z, Hu S, Li XY, Liu JW, Cai X, Yao YG, Zhang Y, Yan H, Chang S, Zhao JP, Yue WH, Luo XJ, Chen X, Xiao X, Fang Y, Li M

GeseDNA Research Team

JAMA psychiatry · 2021 · PMID 33263727

4 pages

rs11647445 rs3804640 rs6130764 rs11557713

A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans

Li H, Gan W, Lu L, Dong X, Han X, Hu C, Yang Z, Sun L, Bao W, Li P, He M, Sun L

and 26 more — show all

Wang Y, Zhu J, Ning Q, Tang Y, Zhang R, Wen J, Wang D, Zhu X, Guo K, Zuo X, Guo X, Yang H, Zhou X, Zhang X, Qi L, Loos RJ, Hu FB, Wu T, Liu Y, Liu L, Yang Z, Hu R, Jia W, Ji L, Li Y, Lin X

DIAGRAM Consortium · AGEN-T2D Consortium

Diabetes · 2013 · PMID 22961080 · open access

3 pages

rs10886471 rs10814916 rs12010175

A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12

Shi Y, Li L, Hu Z, Li S, Wang S, Liu J, Wu C, He L, Zhou J, Li Z, Hu T, Chen Y

and 72 more — show all

Jia Y, Wang S, Wu L, Cheng X, Yang Z, Yang R, Li X, Huang K, Zhang Q, Zhou H, Tang F, Chen Z, Shen J, Jiang J, Ding H, Xing H, Zhang S, Qu P, Song X, Lin Z, Deng D, Xi L, Lv W, Han X, Tao G, Yan L, Han Z, Li Z, Miao X, Pan S, Shen Y, Wang H, Liu D, Gong E, Li Z, Zhou L, Luan X, Wang C, Song Q, Wu S, Xu H, Shen J, Qiang F, Ma G, Liu L, Chen X, Liu J, Wu J, Shen Y, Wen Y, Chu M, Yu J, Hu X, Fan Y, He H, Jiang Y, Lei Z, Liu C, Chen J, Zhang Y, Yi C, Chen S, Li W, Wang D, Wang Z, Di W, Shen K, Lin D, Shen H, Feng Y, Xie X, Ma D

Nature genetics · 2013 · PMID 23817570

2 pages

rs13117307 Cervical Cancer

Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3

Hou S, Du L, Lei B, Pang CP, Zhang M, Zhuang W, Zhang M, Huang L, Gong B, Wang M, Zhang Q, Hu K

and 17 more — show all

Zhou Q, Qi J, Wang C, Tian Y, Ye Z, Liang L, Yu H, Li H, Zhou Y, Cao Q, Liu Y, Bai L, Liao D, Kijlstra A, Xu J, Yang Z, Yang P

Nature genetics · 2014 · PMID 25108386

2 pages

rs117633859 Vogt-Koyanagi-Harada Syndrome

Genetic mechanisms of critical illness in COVID-19

Pairo-Castineira E, Clohisey S, Klaric L, Bretherick AD, Rawlik K, Pasko D, Walker S, Parkinson N, Fourman MH, Russell CD, Furniss J, Richmond A

and 54 more — show all

GenOMICC Investigators · ISARIC4C Investigators and 4 more consortia

Nature · 2021 · PMID 33307546

2 pages

rs73064425 rs71325088

A genetic variant in IL-6 lowering its expression is protective for critical patients with COVID-19

Gong B, Huang L, He Y, Xie W, Yin Y, Shi Y, Xiao J, Zhong L, Zhang Y, Jiang Z, Hao F, Zhou Y

and 11 more — show all

Li H, Jiang L, Yang X, Song X, Kang Y, Tuo L, Huang Y, Shuai P, Liu Y, Zheng F, Yang Z

Signal transduction and targeted therapy · 2022 · PMID 35368020 · open access

2 pages

rs7598285 rs7422259

Genetic Landscape of the ACE2 Coronavirus Receptor

Yang Z, Macdonald-Dunlop E, Chen J, Zhai R, Li T, Richmond A, Klarić L, Pirastu N, Ning Z, Zheng C, Wang Y, Huang T

and 57 more — show all

GenOMICC Consortium† · IMI-DIRECT Consortium†

Circulation · 2022 · PMID 35387486 · open access

2 pages

rs5992134 rs3094087

Genetic determinants of IgG antibody response to COVID-19 vaccination

Bian S, Guo X, Yang X, Wei Y, Yang Z, Cheng S, Yan J, Chen Y, Chen GB, Du X, Francis SS, Shu Y

and 1 more — show all

Liu S

American journal of human genetics · 2024 · PMID 38181733 · open access

2 pages

rs35986240 rs10947290

Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population

Shi Y, Qu J, Zhang D, Zhao P, Zhang Q, Tam POS, Sun L, Zuo X, Zhou X, Xiao X, Hu J, Li Y

and 30 more — show all

Cai L, Liu X, Lu F, Liao S, Chen B, He F, Gong B, Lin H, Ma S, Cheng J, Zhang J, Chen Y, Zhao F, Yang X, Chen Y, Yang C, Lam DSC, Li X, Shi F, Wu Z, Lin Y, Yang J, Li S, Ren Y, Xue A, Fan Y, Li D, Pang CP, Zhang X, Yang Z

American journal of human genetics · 2011 · PMID 21640322

1 page

rs9318086

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease

Lu X, Wang L, Chen S, He L, Yang X, Shi Y, Cheng J, Zhang L, Gu CC, Huang J, Wu T, Ma Y

and 68 more — show all

Li J, Cao J, Chen J, Ge D, Fan Z, Li Y, Zhao L, Li H, Zhou X, Chen L, Liu D, Chen J, Duan X, Hao Y, Wang L, Lu F, Liu Z, Yao C, Shen C, Pu X, Yu L, Fang X, Xu L, Mu J, Wu X, Zheng R, Wu N, Zhao Q, Li Y, Liu X, Wang M, Yu D, Hu D, Ji X, Guo D, Sun D, Wang Q, Yang Y, Liu F, Mao Q, Liang X, Ji J, Chen P, Mo X, Li D, Chai G, Tang Y, Li X, Du Z, Liu X, Dou C, Yang Z, Meng Q, Wang D, Wang R, Yang J, Schunkert H, Samani NJ, Kathiresan S, Reilly MP, Erdmann J, Peng X, Wu X, Liu D, Yang Y, Chen R, Qiang B, Gu D

Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium

Nature genetics · 2012 · PMID 22751097

1 page

rs9268402

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population

Shi Y, Gong B, Chen L, Zuo X, Liu X, Tam PO, Zhou X, Zhao P, Lu F, Qu J, Sun L, Zhao F

and 13 more — show all

Chen H, Zhang Y, Zhang D, Lin Y, Lin H, Ma S, Cheng J, Yang J, Huang L, Zhang M, Zhang X, Pang CP, Yang Z

Human molecular genetics · 2013 · PMID 23406873

1 page

rs4455882

Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

Khor CC, Miyake M, Chen LJ, Shi Y, Barathi VA, Qiao F, Nakata I, Yamashiro K, Zhou X, Tam PO, Cheng CY, Tai ES

and 14 more — show all

Vithana EN, Aung T, Teo YY, Wong TY, Moriyama M, Ohno-Matsui K, Mochizuki M, Matsuda F, Yong RY, Yap EP, Yang Z, Pang CP, Saw SM, Yoshimura N

Nagahama Study Group

Human molecular genetics · 2013 · PMID 23933737

1 page

rs6469937

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.