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.
Genetic and functional analysis of Raynaud's syndrome implicates loci in vasculature and immunity
Tervi A,
Ramste M,
Abner E,
Cheng P,
Lane JM,
Maher M,
Valliere J,
Lammi V,
Strausz S,
Riikonen J,
Nguyen T,
Martyn GE
and 17 more — show all
Sheth MU,
Xia F,
Docampo ML,
Gu W,
Esko T,
Saxena R,
Pirinen M,
Palotie A,
Ripatti S,
Sinnott-Armstrong N,
Daly M,
Engreitz JM,
Rabinovitch M,
Heckman CA,
Quertermous T,
Jones SE,
Ollila HM
FinnGen, Estonian Biobank research team
Cell genomics · 2024 · PMID 39142284 · open access
1 page
Meta-analysis of genome-wide association studies of stable warfarin dose in patients of African ancestry
Asiimwe IG,
Blockman M,
Cavallari LH,
Cohen K,
Cupido C,
Dandara C,
Davis BH,
Jacobson B,
Johnson JA,
Lamorde M,
Limdi NA,
Morgan J
and 15 more — show all
Mouton JP,
Muyambo S,
Nakagaayi D,
Ndadza A,
Okello E,
Perera MA,
Schapkaitz E,
Sekaggya-Wiltshire C,
Semakula JR,
Tatz G,
Waitt C,
Yang G,
Zhang EJ,
Jorgensen AL,
Pirmohamed M
Blood advances · 2024 · PMID 39163621 · open access
1 page
Optimizing Nav1.7-Targeted Analgesics: Revealing Off-Target Effects of Spider Venom-Derived Peptide Toxins and Engineering Strategies for Improvement
Luo S,
Zhou X,
Wu M,
Wang G,
Wang L,
Feng X,
Wu H,
Luo R,
Lu M,
Ju J,
Wang W,
Yuan L
and 10 more — show all
Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024 · PMID 39248322 · open access
1 page
Genetic, transcriptomic, histological, and biochemical analysis of progressive supranuclear palsy implicates glial activation and novel risk genes
Farrell K,
Humphrey J,
Chang T,
Zhao Y,
Leung YY,
Kuksa PP,
Patil V,
Lee WP,
Kuzma AB,
Valladares O,
Cantwell LB,
Wang H
and 37 more — show all
Ravi A,
De Sanctis C,
Han N,
Christie TD,
Afzal R,
Kandoi S,
Whitney K,
Krassner MM,
Ressler H,
Kim S,
Dangoor D,
Iida MA,
Casella A,
Walker RH,
Nirenberg MJ,
Renton AE,
Babrowicz B,
Coppola G,
Raj T,
Höglinger GU,
Müller U,
Golbe LI,
Morris HR,
Hardy J,
Revesz T,
Warner TT,
Jaunmuktane Z,
Mok KY,
Rademakers R,
Dickson DW,
Ross OA,
Wang LS,
Goate A,
Schellenberg G,
Geschwind DH,
Crary JF,
Naj A
PSP Genetics Study Group
Nature communications · 2024 · PMID 39251599 · open access
1 page
Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration
Ahmad S,
Imtiaz MA,
Mishra A,
Wang R,
Herrera-Rivero M,
Bis JC,
Fornage M,
Roshchupkin G,
Hofer E,
Logue M,
Longstreth WT Jr,
Xia R
and 22 more — show all
Bouteloup V,
Mosley T,
Launer LJ,
Khalil M,
Kuhle J,
Rissman RA,
Chene G,
Dufouil C,
Djoussé L,
Lyons MJ,
Mukamal KJ,
Kremen WS,
Franz CE,
Schmidt R,
Debette S,
Breteler MMB,
Berger K,
Yang Q,
Seshadri S,
Aziz NA,
Ghanbari M,
Ikram MA
Communications biology · 2024 · PMID 39251807 · open access
1 page
Treatment of restless legs syndrome and periodic limb movement disorder: an American Academy of Sleep Medicine clinical practice guideline
Winkelman JW,
Berkowski JA,
DelRosso LM,
Koo BB,
Scharf MT,
Sharon D,
Zak RS,
Kazmi U,
Falck-Ytter Y,
Shelgikar AV,
Trotti LM,
Walters AS
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2025 · PMID 39324694
1 page
Identification of susceptibility loci and relevant cell type for IgA nephropathy in Han Chinese by integrative genome-wide analysis
Li M,
Hao X,
Shi D,
Cheng S,
Zhong Z,
Cai L,
Jiang M,
Ding L,
Ding L,
Wang C,
Yu X
Frontiers of medicine · 2024 · PMID 39343836
1 page
Whole exome sequencing identified six novel genes for depressive symptoms
Li ZY,
Fei CJ,
Yin RY,
Kang JJ,
Ma Q,
He XY,
Wu XR,
Zhao YJ,
Zhang W,
Liu WS,
Wu BS,
Yang L
and 4 more — show all
Molecular psychiatry · 2025 · PMID 39472661
1 page
A genome-wide association study identifies eight loci associated with intraductal papillary mucinous neoplasm progression toward malignancy
Gentiluomo M,
Corradi C,
Apadula L,
Comandatore A,
Lauri G,
Rossi G,
Peduzzi G,
Crippa S,
Rizzato C,
Falconi M,
Arcidiacono PG,
Morelli L
and 2 more — show all
Cancer · 2025 · PMID 39639588 · open access
1 page
A genome-wide association study of imaging-defined atherosclerosis
Gummesson A,
Lundmark P,
Chen QS,
Björnson E,
Dekkers KF,
Hammar U,
Adiels M,
Wang Y,
Andersson T,
Bergström G,
Carlhäll CJ,
Erlinge D
and 13 more — show all
Jernberg T,
Landfors F,
Lind L,
Mannila M,
Melander O,
Pirazzi C,
Sundström J,
Östgren CJ,
Gunnarsson C,
Orho-Melander M,
Söderberg S,
Fall T,
Gigante B
Nature communications · 2025 · PMID 40164586 · open access
1 page
Cross-ancestry genome-wide association study identifies implications of SORL1 in cerebral beta-amyloid deposition
Kim JP,
Jung SH,
Jang B,
Cho M,
Song M,
Kim J,
Kim B,
Lee H,
Shin D,
Lee EH,
Jang H,
Kim BH
and 8 more — show all
Nature communications · 2025 · PMID 40175353 · open access
1 page
Meta-analysis of uveal melanoma genome-wide association studies identifies novel risk loci and population effect size heterogeneity
Mies G,
Tsao NL,
Houy A,
Coupland SE,
Kalirai H,
Försti A,
Hemminki K,
Thomsen H,
Stern MH,
Shields CL,
Damrauer SM,
Ewens KG
and 2 more — show all
HGG advances · 2025 · PMID 40495383 · open access
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.