For researchers

Is your paper here?

2,663 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.

29 matches for Huang H, showing the first 9.

Genome-wide association study identifies novel loci association with fasting insulin and insulin resistance in African Americans

Chen G, Bentley A, Adeyemo A, Shriner D, Zhou J, Doumatey A, Huang H, Ramos E, Erdos M, Gerry N, Herbert A, Christman M

and 1 more — show all

Rotimi C

Human molecular genetics · 2012 · PMID 22791750

2 pages

rs17046216 rs10829848

New susceptibility loci associated with kidney disease in type 1 diabetes

Sandholm N, Salem RM, McKnight AJ, Brennan EP, Forsblom C, Isakova T, McKay GJ, Williams WW, Sadlier DM, Mäkinen VP, Swan EJ, Palmer C

and 80 more — show all

Boright AP, Ahlqvist E, Deshmukh HA, Keller BJ, Huang H, Ahola AJ, Fagerholm E, Gordin D, Harjutsalo V, He B, Heikkilä O, Hietala K, Kytö J, Lahermo P, Lehto M, Lithovius R, Osterholm AM, Parkkonen M, Pitkäniemi J, Rosengård-Bärlund M, Saraheimo M, Sarti C, Söderlund J, Soro-Paavonen A, Syreeni A, Thorn LM, Tikkanen H, Tolonen N, Tryggvason K, Tuomilehto J, Wadén J, Gill GV, Prior S, Guiducci C, Mirel DB, Taylor A, Hosseini SM, Parving HH, Rossing P, Tarnow L, Ladenvall C, Alhenc-Gelas F, Lefebvre P, Rigalleau V, Roussel R, Tregouet DA, Maestroni A, Maestroni S, Falhammar H, Gu T, Möllsten A, Cimponeriu D, Ioana M, Mota M, Mota E, Serafinceanu C, Stavarachi M, Hanson RL, Nelson RG, Kretzler M, Colhoun HM, Panduru NM, Gu HF, Brismar K, Zerbini G, Hadjadj S, Marre M, Groop L, Lajer M, Bull SB, Waggott D, Paterson AD, Savage DA, Bain SC, Martin F, Hirschhorn JN, Godson C, Florez JC, Groop PH, Maxwell AP

DCCT/EDIC Research Group

PLoS genetics · 2012 · PMID 23028342 · open access

2 pages

rs12437854 rs7583877

Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B

Jiang DK, Ma XP, Yu H, Cao G, Ding DL, Chen H, Huang HX, Gao YZ, Wu XP, Long XD, Zhang H, Zhang Y

and 29 more — show all

Gao Y, Chen TY, Ren WH, Zhang P, Shi Z, Jiang W, Wan B, Saiyin H, Yin J, Zhou YF, Zhai Y, Lu PX, Zhang H, Gu X, Tan A, Wang JB, Zuo XB, Sun LD, Liu JO, Yi Q, Mo Z, Zhou G, Liu Y, Sun J, Shugart YY, Zheng SL, Zhang XJ, Xu J, Yu L

Hepatology (Baltimore, Md.) · 2015 · PMID 25802187

2 pages

rs2853953 rs2856718

Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome

Dai Y, Chen Y, Huang H, Zhou W, Niu Y, Zhang M, Bin P, Dong H, Jia Q, Huang J, Yi J, Liao Q

and 26 more — show all

Li H, Teng Y, Zang D, Zhai Q, Duan H, Shen J, He J, Meng T, Sha Y, Shen M, Ye M, Jia X, Xiang Y, Huang H, Wu Q, Shi M, Huang X, Yang H, Luo L, Li S, Li L, Zhao J, Li L, Wang J, Wang J, Zheng Y

Scientific reports · 2015 · PMID 26190474 · open access

2 pages

rs2857281 Trichloroethylene-Induced Hypersensitivity Syndrome

Genome-wide association analysis of insomnia using data from Partners Biobank

Song W, Torous J, Kossowsky J, Chen CY, Huang H, Wright A

Scientific reports · 2020 · PMID 32332799 · open access

2 pages

rs9894577 Insomnia

Genome-wide and phenome-wide studies provided insights into brain glymphatic system function and its clinical associations

Ran L, Fang Y, Cheng C, He Y, Shao Z, Kong Y, Huang H, Xu S, Luo X, Wang W, Hao X, Wang M

Science advances · 2025 · PMID 39823331 · open access

2 pages

rs9961058 rs1845561

Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility

Chen H, Chen G, Li G, Zhang S, Chen H, Chen Y, Duggan D, Hu Z, Chen J, Zhao Y, Zhao Y, Huang H

and 11 more — show all

Zheng SL, Trent JM, Yu L, Jiang D, Mo Z, Wang H, Mou Y, Jiang T, Mao Y, Xu J, Lu D

International journal of cancer · 2019 · PMID 30714141

1 page

rs10842893

Genome-wide association analysis of opioid use disorder: A novel approach using clinical data

Song W, Kossowsky J, Torous J, Chen CY, Huang H, Mukamal KJ, Berde CB, Bates DW, Wright A

Drug and alcohol dependence · 2020 · PMID 32961455

1 page

rs10014685

Colorectal Polyp Occurrence Associated With the ZMIZ1-AS1 rs704017 Variant and Hypertension Among Taiwan Biobank Participants

Shiu BH, Huang HC, Nfor ON, Hsu SY, Liaw YP

Cancer medicine · 2026 · PMID 42706660

1 page

Research roundup — September 2026

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.