For researchers
Is your paper here?
2,676 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.
145 matches for
He J,
showing the first 20.
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Flanagan J,
Liu X,
Ortega-Reyes D,
Tomizuka K,
Matoba N,
Akiyama M,
Koido M,
Ishigaki K,
Ashikawa K,
Takata S,
Shi M,
Aoi T
and 8 more — show all
Biobank Japan Project
Communications biology · 2024 · PMID 39702642 · open access
2 pages
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
and 113 more — show all
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
2 pages
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population
Takeuchi F,
Serizawa M,
Yamamoto K,
Fujisawa T,
Nakashima E,
Ohnaka K,
Ikegami H,
Sugiyama T,
Katsuya T,
Miyagishi M,
Nakashima N,
Nawata H
and 4 more — show all
Diabetes · 2009 · PMID 19401414 · open access
1 page
A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population
Asano K,
Matsushita T,
Umeno J,
Hosono N,
Takahashi A,
Kawaguchi T,
Matsumoto T,
Matsui T,
Kakuta Y,
Kinouchi Y,
Shimosegawa T,
Hosokawa M
and 8 more — show all
Nature genetics · 2009 · PMID 19915573
1 page
Genome-wide association study of the age of onset of childhood asthma
Forno E,
Lasky-Su J,
Himes B,
Howrylak J,
Ramsey C,
Brehm J,
Klanderman B,
Ziniti J,
Melén E,
Pershagen G,
Wickman M,
Martinez F
and 6 more — show all
The Journal of allergy and clinical immunology · 2012 · PMID 22560479
1 page
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion
Huyghe JR,
Jackson AU,
Fogarty MP,
Buchkovich ML,
Stančáková A,
Stringham HM,
Sim X,
Yang L,
Fuchsberger C,
Cederberg H,
Chines PS,
Teslovich TM
and 17 more — show all
Romm JM,
Ling H,
McMullen I,
Ingersoll R,
Pugh EW,
Doheny KF,
Neale BM,
Daly MJ,
Kuusisto J,
Scott LJ,
Kang HM,
Collins FS,
Abecasis GR,
Watanabe RM,
Boehnke M,
Laakso M,
Mohlke KL
Nature genetics · 2013 · PMID 23263489
1 page
Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics
Wu AC,
Himes BE,
Lasky-Su J,
Litonjua A,
Peters SP,
Lima J,
Kubo M,
Tamari M,
Nakamura Y,
Qiu W,
Weiss ST,
Tantisira K
The Journal of allergy and clinical immunology · 2014 · PMID 24280104
1 page
Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries
Futema M,
Shah S,
Cooper JA,
Li K,
Whittall RA,
Sharifi M,
Goldberg O,
Drogari E,
Mollaki V,
Wiegman A,
Defesche J,
D'Agostino MN
and 14 more — show all
D'Angelo A,
Rubba P,
Fortunato G,
Waluś-Miarka M,
Hegele RA,
Aderayo Bamimore M,
Durst R,
Leitersdorf E,
Mulder MT,
Roeters van Lennep JE,
Sijbrands EJ,
Whittaker JC,
Talmud PJ,
Humphries SE
Clinical chemistry · 2015 · PMID 25414277
1 page
Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study
Musani SK,
Fox ER,
Kraja A,
Bidulescu A,
Lieb W,
Lin H,
Beecham A,
Chen MH,
Felix JF,
Fox CS,
Kao WH,
Kardia SL
and 11 more — show all
Liu CT,
Nalls MA,
Rundek T,
Sacco RL,
Smith J,
Sun YV,
Wilson G,
Zhang Z,
Mosley TH,
Taylor HA,
Vasan RS
Circulation. Cardiovascular genetics · 2015 · PMID 25561047
1 page
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference
Wen W,
Kato N,
Hwang JY,
Guo X,
Tabara Y,
Li H,
Dorajoo R,
Yang X,
Tsai FJ,
Li S,
Wu Y,
Wu T
and 64 more — show all
Kim S,
Guo X,
Liang J,
Shungin D,
Adair LS,
Akiyama K,
Allison M,
Cai Q,
Chang LC,
Chen CH,
Chen YT,
Cho YS,
Choi BY,
Gao Y,
Go MJ,
Gu D,
Han BG,
He M,
Hixson JE,
Hu Y,
Huang T,
Isono M,
Jung KJ,
Kang D,
Kim YJ,
Kita Y,
Lee J,
Lee NR,
Lee J,
Wang Y,
Liu JJ,
Long J,
Moon S,
Nakamura Y,
Nakatochi M,
Ohnaka K,
Rao D,
Shi J,
Sull JW,
Tan A,
Ueshima H,
Wu C,
Xiang YB,
Yamamoto K,
Yao J,
Ye X,
Yokota M,
Zhang X,
Zheng Y,
Qi L,
Rotter JI,
Jee SH,
Lin D,
Mohlke KL,
He J,
Mo Z,
Wu JY,
Tai ES,
Lin X,
Miki T,
Kim BJ,
Takeuchi F,
Zheng W,
Shu XO
Scientific reports · 2016 · PMID 26785701 · 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.