For researchers
Is your paper here?
2,663 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.
10 matches for
Ye C.
Variants in tubule epithelial regulatory elements mediate most heritable differences in human kidney function
Loeb GB,
Kathail P,
Shuai RW,
Chung R,
Grona RJ,
Peddada S,
Sevim V,
Federman S,
Mader K,
Chu AY,
Davitte J,
Du J
and 7 more — show all
Nature genetics · 2024 · PMID 39256582
12 pages+
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color
Simcoe M,
Valdes A,
Liu F,
Furlotte NA,
Evans DM,
Hemani G,
Ring SM,
Smith GD,
Duffy DL,
Zhu G,
Gordon SD,
Medland SE
and 32 more — show all
Vuckovic D,
Girotto G,
Sala C,
Catamo E,
Concas MP,
Brumat M,
Gasparini P,
Toniolo D,
Cocca M,
Robino A,
Yazar S,
Hewitt A,
Wu W,
Kraft P,
Hammond CJ,
Shi Y,
Chen Y,
Zeng C,
Klaver CCW,
Uitterlinden AG,
Ikram MA,
Hamer MA,
van Duijn CM,
Nijsten T,
Han J,
Mackey DA,
Martin NG,
Cheng CY,
Hinds DA,
Spector TD,
Kayser M,
Hysi PG
23andMe Research Team · International Visible Trait Genetics Consortium
Science advances · 2021 · PMID 33692100 · open access
5 pages
Genome-wide association study of tanning phenotype in a population of European ancestry
Nan H,
Kraft P,
Qureshi AA,
Guo Q,
Chen C,
Hankinson SE,
Hu FB,
Thomas G,
Hoover RN,
Chanock S,
Hunter DJ,
Han J
The Journal of investigative dermatology · 2009 · PMID 19340012
2 pages
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
Song H,
Ramus SJ,
Tyrer J,
Bolton KL,
Gentry-Maharaj A,
Wozniak E,
Anton-Culver H,
Chang-Claude J,
Cramer DW,
DiCioccio R,
Dörk T,
Goode EL
and 73 more — show all
Goodman MT,
Schildkraut JM,
Sellers T,
Baglietto L,
Beckmann MW,
Beesley J,
Blaakaer J,
Carney ME,
Chanock S,
Chen Z,
Cunningham JM,
Dicks E,
Doherty JA,
Dürst M,
Ekici AB,
Fenstermacher D,
Fridley BL,
Giles G,
Gore ME,
De Vivo I,
Hillemanns P,
Hogdall C,
Hogdall E,
Iversen ES,
Jacobs IJ,
Jakubowska A,
Li D,
Lissowska J,
Lubiński J,
Lurie G,
McGuire V,
McLaughlin J,
Medrek K,
Moorman PG,
Moysich K,
Narod S,
Phelan C,
Pye C,
Risch H,
Runnebaum IB,
Severi G,
Southey M,
Stram DO,
Thiel FC,
Terry KL,
Tsai YY,
Tworoger SS,
Van Den Berg DJ,
Vierkant RA,
Wang-Gohrke S,
Webb PM,
Wilkens LR,
Wu AH,
Yang H,
Brewster W,
Ziogas A,
Houlston R,
Tomlinson I,
Whittemore AS,
Rossing MA,
Ponder BA,
Pearce CL,
Ness RB,
Menon U,
Kjaer SK,
Gronwald J,
Garcia-Closas M,
Fasching PA,
Easton DF,
Chenevix-Trench G,
Berchuck A,
Pharoah PD,
Gayther SA
Australian Cancer (Ovarian) Study · Australian Ovarian Cancer Study Group and 1 more consortia
Nature genetics · 2009 · PMID 19648919
2 pages
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Ollila HM,
Sharon E,
Lin L,
Sinnott-Armstrong N,
Ambati A,
Yogeshwar SM,
Hillary RP,
Jolanki O,
Faraco J,
Einen M,
Luo G,
Zhang J
and 78 more — show all
Han F,
Yan H,
Dong XS,
Li J,
Zhang J,
Hong SC,
Kim TW,
Dauvilliers Y,
Barateau L,
Lammers GJ,
Fronczek R,
Mayer G,
Santamaria J,
Arnulf I,
Knudsen-Heier S,
Bredahl MKL,
Thorsby PM,
Plazzi G,
Pizza F,
Moresco M,
Crowe C,
Van den Eeden SK,
Lecendreux M,
Bourgin P,
Kanbayashi T,
Martínez-Orozco FJ,
Peraita-Adrados R,
Benetó A,
Montplaisir J,
Desautels A,
Huang YS,
Jennum P,
Nevsimalova S,
Kemlink D,
Iranzo A,
Overeem S,
Wierzbicka A,
Geisler P,
Sonka K,
Honda M,
Högl B,
Stefani A,
Coelho FM,
Mantovani V,
Feketeova E,
Wadelius M,
Eriksson N,
Smedje H,
Hallberg P,
Hesla PE,
Rye D,
Pelin Z,
Ferini-Strambi L,
Bassetti CL,
Mathis J,
Khatami R,
Aran A,
Nampoothiri S,
Olsson T,
Kockum I,
Partinen M,
Perola M,
Kornum BR,
Rueger S,
Winkelmann J,
Miyagawa T,
Toyoda H,
Khor SS,
Shimada M,
Tokunaga K,
Rivas M,
Pritchard JK,
Risch N,
Kutalik Z,
O'Hara R,
Hallmayer J,
Ye CJ,
Mignot EJ
FinnGen
Nature communications · 2023 · PMID 37188663 · open access
2 pages
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
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.