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.
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
Genome-wide association study meta-analysis uncovers novel genetic variants associated with olfactory dysfunction
Imtiaz MA,
Melas K,
Tin A,
Talevi V,
Chen H,
Fornage M,
Shrestha S,
Gögele M,
Emmert D,
Pattaro C,
Pramstaller P,
Förster F
and 6 more — show all
BMC genomic data · 2025 · PMID 40963118 · open access
1 page
Genome-wide association study reveals genetic architecture and evolution of human retinal pigmentation
Yuan J,
Zhang Y,
Yao Y,
Li S,
Liang J,
Dai W,
Yang J,
Liu M,
Zhang Q,
Zhou Y,
Li J,
Liu H
and 5 more — show all
Myopia Associated Genetics and Intervention Consortium
Science advances · 2026 · PMID 41477839 · open access
1 page
Trans-ancestry GWAS of hot flashes reveals potent treatment target and overlap with psychiatric disorders
Werwath KE,
Lawn RB,
Salem MT,
Li T,
Mitchell BL,
Shen H,
Gordon SD,
Kung B,
Stafford C,
Vemuri M,
Ratanatharathorn A,
Meijsen J
and 6 more — show all
Communications medicine · 2026 · PMID 41495267 · open access
1 page
Genetic dissection of serum pro-neurotensin suggests potential causal impact on brain structure
Breitfeld J,
Horn K,
Velluva A,
Beyer F,
Pott J,
Baber R,
Stumvoll M,
Le Duc D,
Witte V,
Giontella A,
Melander O,
Kovacs P
and 2 more — show all
EBioMedicine · 2026 · PMID 41520650 · open access
1 page
A Genome-Wide Association Study Reveals <i>Desmoglein-2</i> Predominance in Japanese Arrhythmogenic Cardiomyopathy
Ishikawa T,
Sonehara K,
Sonoda K,
Hayashi K,
Kato K,
Nagase S,
Kusano K,
Aiba T,
Horie M,
Ohno S,
Okada Y,
Makita N
Journal of arrhythmia · 2026 · PMID 41607864 · open access
1 page
A genome-wide association meta-analysis of cholesterol synthesis intermediates identifies three associations for lanosterol
Förster F,
Horn K,
Pott J,
Delgado GE,
Kleber ME,
März W,
Moissl-Blanke AP,
Silbernagel G,
Waldenberger M,
Grallert H,
Peters A,
Gieger C
and 15 more — show all
Baber R,
Kirsten H,
Loeffler M,
Isermann B,
Thiery J,
Kovacs P,
Tönjes A,
Stumvoll M,
Gylling H,
Kähönen M,
Lehtimäki T,
Mishra PP,
Raitakari O,
Ceglarek U,
Scholz M
EBioMedicine · 2026 · PMID 41619350 · open access
1 page
Whole-genome sequencing analysis of anthropometric traits in 672,976 individuals reveals convergence between rare and common genetic associations
Hawkes G,
Wright HIW,
Beaumont RN,
Chundru K,
Hanson A,
Jackson L,
Murray A,
Patel K,
Frayling TM,
Wright CF,
Wood AR,
Weedon MN
Nature communications · 2026 · PMID 41651857 · open access
1 page
The HUNT study identifies host genetic factors reproducibly associated with human gut microbiota composition
Moksnes MR,
Coward E,
Nethander M,
Dekkers K,
Grahnemo L,
Törnqvist AE,
Li L,
Lundmark P,
Pertiwi K,
Baldanzi G,
Mjelle R,
Moll JM
and 15 more — show all
Eklund AC,
Nielsen HB,
Svensson J,
Langhammer A,
Giskeødegård GF,
Brumpton B,
Hjort R,
Ness-Jensen E,
Engström G,
Pelaseyed T,
Michaëlsson K,
Orho-Melander M,
Fall T,
Hveem K,
Ohlsson C
Nature genetics · 2026 · PMID 41688637 · open access
1 page
Genome-wide association analyses highlight the role of the intestinal molecular environment in human gut microbiota variation
Dekkers KF,
Pertiwi K,
Baldanzi G,
Lundmark P,
Hammar U,
Moksnes MR,
Coward E,
Nethander M,
Salih GA,
Miari M,
Nguyen D,
Sayols-Baixeras S
and 23 more — show all
Eklund AC,
Holm JB,
Nielsen HB,
Volpiano CG,
Méric G,
Thangam M,
Hakaste L,
Tuomi T,
Ahlqvist E,
Smith CA,
Allen M,
Reimann F,
Gribble FM,
Ohlsson C,
Hveem K,
Melander O,
Nilsson PM,
Engström G,
Smith JG,
Michaëlsson K,
Ärnlöv J,
Orho-Melander M,
Fall T
Nature genetics · 2026 · PMID 41688638 · open access
1 page
Oculocutaneous albinism variants in 28 consanguineous families and functional classification of a pathogenic deep intron variant in TYR
Farooq M,
Bruun GH,
Sarusie MVK,
Kessel L,
Akhtar H,
Abdullah U,
Ali Z,
Shah SA,
Ali N,
Anjum I,
Doktor TK,
Andresen BS
and 3 more — show all
European journal of human genetics : EJHG · 2026 · PMID 41807736 · open access
1 page
Genome-wide meta-analysis in lichen sclerosus identifies 14 genomic risk loci
Dand N,
Rayinda T,
Silz E,
Thomas LF,
Saklatvala JR,
McSweeney SM,
Ung CY,
Christou E,
Lewis F,
Kettunen J,
Huilaja L,
Brumpton BM
and 6 more — show all
The British journal of dermatology · 2026 · PMID 41850335 · open access
1 page
Convergent imaging and genetic signatures of gray matter atrophy in Parkinson's disease
Xie Y,
Dong Z,
Jiang Y,
Lin S,
Wang X,
Sun J,
Zhang N,
Zhang Z,
Du J,
Liu H,
Cao D
NeuroImage · 2026 · PMID 42336304
1 page
Integrative exome sequencing and multi-omics analysis elucidates the regulatory role of rare variants in metabolic syndrome
Wu CX,
Sang J,
Xu Q,
Zhan Y,
Yuan SJ,
Ge YY,
Yu XJ,
Zheng X,
Wang XF,
He XM,
Liu CJ,
Luo Y
and 2 more — show all
Functional & integrative genomics · 2026 · PMID 42472903
1 page
Showing the most-cited first. The list is rebuilt from the pages every hour, so a paper
appears here the moment a page starts resting on it — and disappears if that page stops.
Not finding yours is not a judgement. This catalogue is assembled from what a small team
could read, and it is thinnest outside European-ancestry cohorts — which we say on the
pages themselves, in the
graph and in each
condition's open questions.
Tell us what we are missing →
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.