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.
111 matches for
Lee J,
showing the first 11.
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
A coding variant in <i>FTO</i> confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD
Kim HS,
Cheon JH,
Jung ES,
Park J,
Aum S,
Park SJ,
Eun S,
Lee J,
Rüther U,
Yeo GSH,
Ma M,
Park KS
and 5 more — show all
Gut · 2017 · PMID 27558924
1 page
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
and 55 more — show all
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease
Lee JC,
Biasci D,
Roberts R,
Gearry RB,
Mansfield JC,
Ahmad T,
Prescott NJ,
Satsangi J,
Wilson DC,
Jostins L,
Anderson CA,
Traherne JA
and 3 more — show all
UK IBD Genetics Consortium
Nature genetics · 2017 · PMID 28067912
1 page
BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts
Lee JY,
Kim J,
Kim SW,
Park SK,
Ahn SH,
Lee MH,
Suh YJ,
Noh DY,
Son BH,
Cho YU,
Lee SB,
Lee JW
and 2 more — show all
Scientific reports · 2018 · PMID 30323354 · open access
1 page
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke
Keene KL,
Hyacinth HI,
Bis JC,
Kittner SJ,
Mitchell BD,
Cheng YC,
Pare G,
Chong M,
O'Donnell M,
Meschia JF,
Chen WM,
Sale MM
and 35 more — show all
Rich SS,
Nalls MA,
Zonderman AB,
Evans MK,
Wilson JG,
Correa A,
Markus HS,
Traylor M,
Lewis CM,
Carty CL,
Reiner A,
Haessler J,
Langefeld CD,
Gottesman R,
Mosley TH,
Woo D,
Yaffe K,
Liu Y,
Longstreth WT,
Psaty BM,
Kooperberg C,
Lange LA,
Sacco R,
Rundek T,
Lee JM,
Cruchaga C,
Furie KL,
Arnett DK,
Benavente OR,
Grewal RP,
Peddareddygari LR,
Dichgans M,
Malik R,
Worrall BB,
Fornage M
COMPASS, SiGN, and METASTROKE Consortia
Stroke · 2020 · PMID 32693751
1 page
Association of genetic variants in migraineurs with and without restless legs syndrome
Lin GY,
Lin YK,
Liang CS,
Lee JT,
Tsai CL,
Hung KS,
Luo WJ,
Tsai CK,
Hsu YW,
Ho TH,
Yang FC
Annals of clinical and translational neurology · 2020 · PMID 32918390 · open access
1 page
Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program
Cade BE,
Lee J,
Sofer T,
Wang H,
Zhang M,
Chen H,
Gharib SA,
Gottlieb DJ,
Guo X,
Lane JM,
Liang J,
Lin X
and 27 more — show all
Mei H,
Patel SR,
Purcell SM,
Saxena R,
Shah NA,
Evans DS,
Hanis CL,
Hillman DR,
Mukherjee S,
Palmer LJ,
Stone KL,
Tranah GJ,
Abecasis GR,
Boerwinkle EA,
Correa A,
Cupples LA,
Kaplan RC,
Nickerson DA,
North KE,
Psaty BM,
Rotter JI,
Rich SS,
Tracy RP,
Vasan RS,
Wilson JG,
Zhu X,
Redline S
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Sleep Working Group
Genome medicine · 2021 · PMID 34446064 · open access
1 page
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages
Park JY,
Lee D,
Lee JJ,
Gim J,
Gunasekaran TI,
Choi KY,
Kang S,
Do AR,
Jo J,
Park J,
Park K,
Li D
and 21 more — show all
Lee S,
Kim H,
Dhanasingh I,
Ghosh S,
Keum S,
Choi JH,
Song GJ,
Sael L,
Rhee S,
Lovestone S,
Kim E,
Moon SH,
Kim BC,
Kim S,
Saykin AJ,
Nho K,
Lee SH,
Farrer LA,
Jun GR,
Won S,
Lee KH
Alzheimer’s Disease Neuroimaging Initiative
Translational psychiatry · 2021 · PMID 34785643 · 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.