For researchers
Is your paper here?
2,671 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.
95 matches for
He C,
showing the first 15.
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
Irvin MR,
Sitlani CM,
Floyd JS,
Psaty BM,
Bis JC,
Wiggins KL,
Whitsel EA,
Sturmer T,
Stewart J,
Raffield L,
Sun F,
Liu CT
and 32 more — show all
Xu H,
Cupples AL,
Tanner RM,
Rossing P,
Smith A,
Zilhão NR,
Launer LJ,
Noordam R,
Rotter JI,
Yao J,
Li X,
Guo X,
Limdi N,
Sundaresan A,
Lange L,
Correa A,
Stott DJ,
Ford I,
Jukema JW,
Gudnason V,
Mook-Kanamori DO,
Trompet S,
Palmas W,
Warren HR,
Hellwege JN,
Giri A,
O'donnell C,
Hung AM,
Edwards TL,
Ahluwalia TS,
Arnett DK,
Avery CL
American journal of hypertension · 2019 · PMID 31545351
1 page
Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort
Richard MA,
Brown AL,
Belmont JW,
Scheurer ME,
Arroyo VM,
Foster KL,
Kern KD,
Hudson MM,
Leisenring WM,
Okcu MF,
Sapkota Y,
Yasui Y
and 8 more — show all
Cancer · 2021 · PMID 33048379
1 page
Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder
Demontis D,
Walters RK,
Rajagopal VM,
Waldman ID,
Grove J,
Als TD,
Dalsgaard S,
Ribasés M,
Bybjerg-Grauholm J,
Bækvad-Hansen M,
Werge T,
Nordentoft M
and 8 more — show all
ADHD Working Group of the Psychiatric Genomics Consortium (PGC)
Nature communications · 2021 · PMID 33495439 · open access
1 page
TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study
Meijer AJM,
Diepstraten FA,
Langer T,
Broer L,
Domingo IK,
Clemens E,
Uitterlinden AG,
de Vries ACH,
van Grotel M,
Vermeij WP,
Ozinga RA,
Binder H
and 43 more — show all
Byrne J,
van Dulmen-den Broeder E,
Garrè ML,
Grabow D,
Kaatsch P,
Kaiser M,
Kenborg L,
Winther JF,
Rechnitzer C,
Hasle H,
Kepak T,
Kepakova K,
Tissing WJE,
van der Kooi ALF,
Kremer LCM,
Kruseova J,
Pluijm SMF,
Kuehni CE,
van der Pal HJH,
Parfitt R,
Spix C,
Tillmanns A,
Deuster D,
Matulat P,
Calaminus G,
Hoetink AE,
Elsner S,
Gebauer J,
Haupt R,
Lackner H,
Blattmann C,
Neggers SJCMM,
Rassekh SR,
Wright GEB,
Brooks B,
Nagtegaal AP,
Drögemöller BI,
Ross CJD,
Bhavsar AP,
Am Zehnhoff-Dinnesen AG,
Carleton BC,
Zolk O,
van den Heuvel-Eibrink MM
PanCareLIFE Consortium · and the CPNDS Consortium
NPJ precision oncology · 2021 · PMID 34262104 · open access
1 page
The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and Statin-Associated Musculoskeletal Symptoms
Cooper-DeHoff RM,
Niemi M,
Ramsey LB,
Luzum JA,
Tarkiainen EK,
Straka RJ,
Gong L,
Tuteja S,
Wilke RA,
Wadelius M,
Larson EA,
Roden DM
and 9 more — show all
Clinical pharmacology and therapeutics · 2022 · PMID 35152405
1 page
Pharmacogenomic study of heart failure and candesartan response from the CHARM programme
Dubé MP,
Chazara O,
Lemaçon A,
Asselin G,
Provost S,
Barhdadi A,
Lemieux Perreault LP,
Mongrain I,
Wang Q,
Carss K,
Paul DS,
Cunningham JW
and 8 more — show all
ESC heart failure · 2022 · PMID 35736394 · open access
1 page
Genome-wide analyses of 200,453 individuals yield new insights into the causes and consequences of clonal hematopoiesis
Kar SP,
Quiros PM,
Gu M,
Jiang T,
Mitchell J,
Langdon R,
Iyer V,
Barcena C,
Vijayabaskar MS,
Fabre MA,
Carter P,
Petrovski S
and 2 more — show all
Nature genetics · 2022 · PMID 35835912 · open access
1 page
Genotyping and population characteristics of the China Kadoorie Biobank
Walters RG,
Millwood IY,
Lin K,
Schmidt Valle D,
McDonnell P,
Hacker A,
Avery D,
Edris A,
Fry H,
Cai N,
Kretzschmar WW,
Ansari MA
and 15 more — show all
Lyons PA,
Collins R,
Donnelly P,
Hill M,
Peto R,
Shen H,
Jin X,
Nie C,
Xu X,
Guo Y,
Yu C,
Lv J,
Clarke RJ,
Li L,
Chen Z
China Kadoorie Biobank Collaborative Group
Cell genomics · 2023 · PMID 37601966 · open access
1 page
Resistance to HIV-1 infection in caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene
Samson M,
Libert F,
Doranz BJ,
Rucker J,
Liesnard C,
Farber CM,
Saragosti S,
Lapoumeroulie C,
Cognaux J,
Forceille C,
Muyldermans G,
Verhofstede C
and 10 more — show all
Nature · 1996 · PMID 8751444
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.