For researchers
Is your paper here?
2,661 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.
37 matches for
He F,
showing the first 17.
Genetic and functional insights into the fractal structure of the heart
Meyer HV,
Dawes TJW,
Serrani M,
Bai W,
Tokarczuk P,
Cai J,
de Marvao A,
Henry A,
Lumbers RT,
Gierten J,
Thumberger T,
Wittbrodt J
and 8 more — show all
Nature · 2020 · PMID 32814899
2 pages
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
Suetsugu H,
Kim K,
Yamamoto T,
Bang SY,
Sakamoto Y,
Shin JM,
Sugano N,
Kim JS,
Mukai M,
Lee YK,
Ohmura K,
Park DJ
and 43 more — show all
Takahashi D,
Ahn GY,
Karino K,
Kwon YC,
Miyamura T,
Kim J,
Nakamura J,
Motomura G,
Kuroda T,
Niiro H,
Miyamoto T,
Takeuchi T,
Ikari K,
Amano K,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Seki T,
Tanaka Y,
Kubo T,
Hisada R,
Yoshioka T,
Yamazaki M,
Kabata T,
Kajino T,
Ohta Y,
Okawa T,
Naito Y,
Kaneuji A,
Yasunaga Y,
Ohzono K,
Tomizuka K,
Koido M,
Matsuda K,
Okada Y,
Suzuki A,
Kim BJ,
Kochi Y,
Lee HS,
Ikegawa S,
Bae SC,
Terao C
Human molecular genetics · 2022 · PMID 34850884
2 pages
Genome-Wide Association Study Identifies the First Germline Genetic Variant Associated With Erdheim-Chester Disease
Martínez-López J,
Márquez A,
Pegoraro F,
Ortiz-Fernández L,
Acosta-Herrera M,
Kerick M,
Gelain E,
Diamond EL,
Durham BH,
Abdel-Wahab O,
Go RS,
Koster MJ
and 12 more — show all
Dagna L,
Campochiaro C,
Collin M,
Milne P,
Estrada-Veras JI,
O'Brien K,
Papo M,
Cohen-Aubar F,
Amoura Z,
Haroche J,
Martín J,
Vaglio A
Arthritis & rheumatology (Hoboken, N.J.) · 2024 · PMID 37561109
2 pages
Risk Variants Associated With Normal Pressure Hydrocephalus: Genome-Wide Association Study in the FinnGen Cohort
Räsänen J,
Heikkinen S,
Mäklin K,
Lipponen A,
Kuulasmaa T,
Mehtonen J,
Korhonen VE,
Junkkari A,
Grenier-Boley B,
Bellenguez C,
Oinas M,
Avellan C
and 22 more — show all
Frantzén J,
Kotkansalo A,
Rinne J,
Ronkainen A,
Kauppinen M,
von Und Zu Fraunberg M,
Lönnrot K,
Satopää J,
Perola M,
Koivisto AM,
Julkunen V,
Portaankorva AM,
Mannermaa A,
Soininen H,
Helisalmi S,
Jääskeläinen JE,
Lambert JC,
Eide PK,
Palotie A,
Kurki MI,
Hiltunen M,
Leinonen V
for FinnGen
Neurology · 2024 · PMID 39141892 · open access
2 pages
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
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity
Frayling TM,
Timpson NJ,
Weedon MN,
Zeggini E,
Freathy RM,
Lindgren CM,
Perry JR,
Elliott KS,
Lango H,
Rayner NW,
Shields B,
Harries LW
and 29 more — show all
Barrett JC,
Ellard S,
Groves CJ,
Knight B,
Patch AM,
Ness AR,
Ebrahim S,
Lawlor DA,
Ring SM,
Ben-Shlomo Y,
Jarvelin MR,
Sovio U,
Bennett AJ,
Melzer D,
Ferrucci L,
Loos RJ,
Barroso I,
Wareham NJ,
Karpe F,
Owen KR,
Cardon LR,
Walker M,
Hitman GA,
Palmer CN,
Doney AS,
Morris AD,
Smith GD,
Hattersley AT,
McCarthy MI
Science (New York, N.Y.) · 2007 · PMID 17434869
1 page
A genome-wide association study of pulmonary function measures in the Framingham Heart Study
Wilk JB,
Chen TH,
Gottlieb DJ,
Walter RE,
Nagle MW,
Brandler BJ,
Myers RH,
Borecki IB,
Silverman EK,
Weiss ST,
O'Connor GT
PLoS genetics · 2009 · PMID 19300500 · open access
1 page
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
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese
Li Y,
Si L,
Zhai Y,
Hu Y,
Hu Z,
Bei JX,
Xie B,
Ren Q,
Cao P,
Yang F,
Song Q,
Bao Z
and 38 more — show all
Zhang H,
Han Y,
Wang Z,
Chen X,
Xia X,
Yan H,
Wang R,
Zhang Y,
Gao C,
Meng J,
Tu X,
Liang X,
Cui Y,
Liu Y,
Wu X,
Li Z,
Wang H,
Li Z,
Hu B,
He M,
Gao Z,
Xu X,
Ji H,
Yu C,
Sun Y,
Xing B,
Yang X,
Zhang H,
Tan A,
Wu C,
Jia W,
Li S,
Zeng YX,
Shen H,
He F,
Mo Z,
Zhang H,
Zhou G
Nature communications · 2016 · PMID 27244555 · open access
1 page
Genome-wide analyses of psychological resilience in U.S. Army soldiers
Stein MB,
Choi KW,
Jain S,
Campbell-Sills L,
Chen CY,
Gelernter J,
He F,
Heeringa SG,
Maihofer AX,
Nievergelt C,
Nock MK,
Ripke S
and 4 more — show all
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2019 · PMID 31081985
1 page
Genetic variation in the FMO and GSTO gene clusters impacts arsenic metabolism in humans
Tamayo LI,
Tong L,
Davydiuk T,
Vander Griend D,
Haque SE,
Islam T,
Jasmine F,
Kibriya MG,
Graziano J,
Chen L,
Le XC,
Ahsan H
and 2 more — show all
PLoS genetics · 2025 · PMID 40892834 · open access
1 page
Pharmacogenomic diversity in Amazonian Indigenous populations: implications for Berlin-Frankfurt-Münster acute lymphoblastic leukemia therapy
Leitão LPC,
Monte N,
Marcellino JCR,
Ribeiro-Dos-Santos AM,
Wanderley AV,
de Souza SJ,
de Santana Souza JE,
Ribeiro-Dos-Santos Â,
Santos S,
Guerreiro JF,
Dos Santos NPC
Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026 · PMID 42704601
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.