For researchers

Is your paper here?

2,682 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.

19 matches for Liu H.

Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease

Liu H, Doke T, Guo D, Sheng X, Ma Z, Park J, Vy HMT, Nadkarni GN, Abedini A, Miao Z, Palmer M, Voight BF

and 5 more — show all

Li H, Brown CD, Ritchie MD, Shu Y, Susztak K

Nature genetics · 2022 · PMID 35710981

12 pages+

rs9295131 rs10462068 rs12222671 rs1274653 rs17512836 rs62088028

A genome-wide association analysis reveals new pathogenic pathways in gout

Major TJ, Takei R, Matsuo H, Leask MP, Sumpter NA, Topless RK, Shirai Y, Wang W, Cadzow MJ, Phipps-Green AJ, Li Z, Ji A

and 86 more — show all

Merriman ME, Morice E, Kelley EE, Wei WH, McCormick SPA, Bixley MJ, Reynolds RJ, Saag KG, Fadason T, Golovina E, O'Sullivan JM, Stamp LK, Dalbeth N, Abhishek A, Doherty M, Roddy E, Jacobsson LTH, Kapetanovic MC, Melander O, Andrés M, Pérez-Ruiz F, Torres RJ, Radstake T, Jansen TL, Janssen M, Joosten LAB, Liu R, Gaal OI, Crişan TO, Rednic S, Kurreeman F, Huizinga TWJ, Toes R, Lioté F, Richette P, Bardin T, Ea HK, Pascart T, McCarthy GM, Helbert L, Stibůrková B, Tausche AK, Uhlig T, Vitart V, Boutin TS, Hayward C, Riches PL, Ralston SH, Campbell A, MacDonald TM, Nakayama A, Takada T, Nakatochi M, Shimizu S, Kawamura Y, Toyoda Y, Nakaoka H, Yamamoto K, Matsuo K, Shinomiya N, Ichida K, Lee C, Bradbury LA, Brown MA, Robinson PC, Buchanan RRC, Hill CL, Lester S, Smith MD, Rischmueller M, Choi HK, Stahl EA, Miner JN, Solomon DH, Cui J, Giacomini KM, Brackman DJ, Jorgenson EM, Liu H, Susztak K, Shringarpure S, So A, Okada Y, Li C, Shi Y, Merriman TR

FAST Study Group · Japan Gout Genomics Consortium and 3 more consortia

Nature genetics · 2024 · PMID 39406924

12 pages+

rs12846379 rs17003845 rs2808387 rs6946898 rs7562348 rs11446

Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women

Fan W, Kan H, Liu HY, Wang TL, He YN, Zhang M, Li YX, Li YJ, Meng W, Li Q, Hu AQ, Zheng YJ

mSystems · 2021 · PMID 34282934 · open access

11 pages

rs75042393 rs78166340 rs58520434 rs117290187 rs12204265 rs12205331

A genome-wide association study of neonatal metabolites

He Q, Liu H, Lu L, Zhang Q, Wang Q, Wang B, Wu X, Guan L, Mao J, Xue Y, Zhang C, Cao X

and 9 more — show all

He Y, Peng X, Peng H, Zhao K, Li H, Jin X, Zhao L, Zhang J, Wang T

Cell genomics · 2024 · PMID 39389019 · open access

9 pages

rs1859000 rs10988200 rs1075650 rs695948 rs35525135 rs12401729

Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy

Liu H, Irwanto A, Fu X, Yu G, Yu Y, Sun Y, Wang C, Wang Z, Okada Y, Low H, Li Y, Liany H

and 20 more — show all

Chen M, Bao F, Li J, You J, Zhang Q, Liu J, Chu T, Andiappan AK, Wang N, Niu G, Liu D, Yu X, Zhang L, Tian H, Zhou G, Rotzschke O, Chen S, Zhang X, Liu J, Zhang F

Nature genetics · 2015 · PMID 25642632

5 pages

rs13220141 rs10817758 rs58600253 rs10414149 Leprosy

Genomewide association study of leprosy

Zhang FR, Huang W, Chen SM, Sun LD, Liu H, Li Y, Cui Y, Yan XX, Yang HT, Yang RD, Chu TS, Zhang C

and 55 more — show all

Zhang L, Han JW, Yu GQ, Quan C, Yu YX, Zhang Z, Shi BQ, Zhang LH, Cheng H, Wang CY, Lin Y, Zheng HF, Fu XA, Zuo XB, Wang Q, Long H, Sun YP, Cheng YL, Tian HQ, Zhou FS, Liu HX, Lu WS, He SM, Du WL, Shen M, Jin QY, Wang Y, Low HQ, Erwin T, Yang NH, Li JY, Zhao X, Jiao YL, Mao LG, Yin G, Jiang ZX, Wang XD, Yu JP, Hu ZH, Gong CH, Liu YQ, Liu RY, Wang DM, Wei D, Liu JX, Cao WK, Cao HZ, Li YP, Yan WG, Wei SY, Wang KJ, Hibberd ML, Yang S, Zhang XJ, Liu JJ

The New England journal of medicine · 2009 · PMID 20018961

4 pages

rs602875 rs40457 rs42490 Leprosy

Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy

Zhang F, Liu H, Chen S, Low H, Sun L, Cui Y, Chu T, Li Y, Fu X, Yu Y, Yu G, Shi B

and 25 more — show all

Tian H, Liu D, Yu X, Li J, Lu N, Bao F, Yuan C, Liu J, Liu H, Zhang L, Sun Y, Chen M, Yang Q, Yang H, Yang R, Zhang L, Wang Q, Liu H, Zuo F, Zhang H, Khor CC, Hibberd ML, Yang S, Liu J, Zhang X

Nature genetics · 2011 · PMID 22019778

4 pages

rs16948876 rs2275606 rs3762318 Leprosy

A large-scale genome-wide association and meta-analysis identified four novel susceptibility loci for leprosy

Wang Z, Sun Y, Fu X, Yu G, Wang C, Bao F, Yue Z, Li J, Sun L, Irwanto A, Yu Y, Chen M

and 21 more — show all

Mi Z, Wang H, Huai P, Li Y, Du T, Yu W, Xia Y, Xiao H, You J, Li J, Yang Q, Wang N, Shang P, Niu G, Chi X, Wang X, Cao J, Cheng X, Liu H, Liu J, Zhang F

Nature communications · 2016 · PMID 27976721 · open access

3 pages

rs10100465 rs6807915 Leprosy

A prospective study of the associations among fine particulate matter, genetic variants, and the risk of colorectal cancer

Chu H, Xin J, Yuan Q, Wu Y, Du M, Zheng R, Liu H, Wu S, Zhang Z, Wang M

Environment international · 2021 · PMID 33338681

3 pages

rs4971775 rs9313579 rs6950598

Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese

Zheng R, Li Z, He F, Liu H, Chen J, Chen J, Xie X, Zhou J, Chen H, Wu X, Wu J, Chen B

and 21 more — show all

Liu Y, Cui H, Fan L, Sha W, Liu Y, Wang J, Huang X, Zhang L, Xu F, Wang J, Feng Y, Qin L, Yang H, Liu Z, Cui Z, Liu F, Chen X, Gao S, Sun S, Shi Y, Ge B

Nature communications · 2018 · PMID 30287856 · open access

2 pages

rs6114027 Tuberculosis

A Genome-Wide Association Study Identifies Two Novel Susceptible Regions for Squamous Cell Carcinoma of the Head and Neck

Shete S, Liu H, Wang J, Yu R, Sturgis EM, Li G, Dahlstrom KR, Liu Z, Amos CI, Wei Q

Cancer research · 2020 · PMID 32276964

2 pages

rs1265081 rs13211972

Identification of shared loci associated with both Crohn's disease and leprosy in East Asians

Jung S, Park D, Lee HS, Kim Y, Baek J, Hwang SW, Park SH, Yang SK, Ye BD, Han B, Sun Y, Liu H

and 3 more — show all

Zhang F, Liu J, Song K

Human molecular genetics · 2022 · PMID 35512355

2 pages

rs10817678 rs9271011

Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease

Sandholm N, Cole JB, Nair V, Sheng X, Liu H, Ahlqvist E, van Zuydam N, Dahlström EH, Fermin D, Smyth LJ, Salem RM, Forsblom C

and 19 more — show all

Valo E, Harjutsalo V, Brennan EP, McKay GJ, Andrews D, Doyle R, Looker HC, Nelson RG, Palmer C, McKnight AJ, Godson C, Maxwell AP, Groop L, McCarthy MI, Kretzler M, Susztak K, Hirschhorn JN, Florez JC, Groop PH

GENIE Consortium

Diabetologia · 2022 · PMID 35763030 · open access

2 pages

rs116216059 rs185299109

Genome-wide association study of HBV-related hepatocellular carcinoma identifies a functional variant at the FAM114A1 locus

Yu HP, Xiang BD, Qian J, Liu H, Li YF, Lin Q, Liu S, Wei J, Zhan S, Jiang B, Dai J, Ma L

and 20 more — show all

Zhang L, Liu Y, Wen Q, Gong W, Li S, Jiang Y, Zheng J, Zhu T, Zhou Z, Zeng X, Wang Z, Wang JA, Guo R, Yang Y, Wei Q, Zhou G, Qiu XQ, Tang W, Wang M, Zhang R

Journal of genetics and genomics = Yi chuan xue bao · 2026 · PMID 41241147

2 pages

rs55718051 HBV-Related Hepatocellular Carcinoma

Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans

Zhang M, Song F, Liang L, Nan H, Zhang J, Liu H, Wang LE, Wei Q, Lee JE, Amos CI, Kraft P, Qureshi AA

and 1 more — show all

Han J

Human molecular genetics · 2013 · PMID 23548203

1 page

rs1126809

A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3

American journal of human genetics · 2016 · PMID 27018472

1 page

rs41268753

Identification of the BTN3A3 Gene as a Molecule Implicated in Generalized Pustular Psoriasis in a Chinese Population

Zhang Q, Shi P, Wang Z, Sun L, Li W, Zhao Q, Liu T, Pan Q, Sun Y, Jia F, Chen W, Fu X

and 10 more — show all

Yu G, Bao F, Mi Z, Wang C, Sun Y, Li B, Liu J, Liu H, Gu H, Zhang F

The Journal of investigative dermatology · 2023 · PMID 36804966

1 page

rs148755083

Genome-wide association study reveals genetic architecture and evolution of human retinal pigmentation

Yuan J, Zhang Y, Yao Y, Li S, Liang J, Dai W, Yang J, Liu M, Zhang Q, Zhou Y, Li J, Liu H

and 5 more — show all

Chen ZJ, MacGregor S, Qu J, Han X, Su J

Myopia Associated Genetics and Intervention Consortium

Science advances · 2026 · PMID 41477839 · open access

1 page

rs77915629

Convergent imaging and genetic signatures of gray matter atrophy in Parkinson's disease

Xie Y, Dong Z, Jiang Y, Lin S, Wang X, Sun J, Zhang N, Zhang Z, Du J, Liu H, Cao D

NeuroImage · 2026 · PMID 42336304

1 page

rs470934

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.