For researchers
Is your paper here?
2,662 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.
3 matches for
Thomas A.
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21
Teerlink CC,
Leongamornlert D,
Dadaev T,
Thomas A,
Farnham J,
Stephenson RA,
Riska S,
McDonnell SK,
Schaid DJ,
Catalona WJ,
Zheng SL,
Cooney KA
and 29 more — show all
Ray AM,
Zuhlke KA,
Lange EM,
Giles GG,
Southey MC,
Fitzgerald LM,
Rinckleb A,
Luedeke M,
Maier C,
Stanford JL,
Ostrander EA,
Kaikkonen EM,
Sipeky C,
Tammela T,
Schleutker J,
Wiley KE,
Isaacs SD,
Walsh PC,
Isaacs WB,
Xu J,
Cancel-Tassin G,
Cussenot O,
Mandal D,
Laurie C,
Laurie C,
Thibodeau SN,
Eeles RA,
Kote-Jarai Z,
Cannon-Albright L
PRACTICAL consortium · International Consortium for Prostate Cancer Genetics
Human genetics · 2016 · PMID 27262462
3 pages
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
Fernández-Rhodes L,
Graff M,
Buchanan VL,
Justice AE,
Highland HM,
Guo X,
Zhu W,
Chen HH,
Young KL,
Adhikari K,
Palmer ND,
Below JE
and 104 more — show all
Bradfield J,
Pereira AC,
Glover L,
Kim D,
Lilly AG,
Shrestha P,
Thomas AG,
Zhang X,
Chen M,
Chiang CWK,
Pulit S,
Horimoto A,
Krieger JE,
Guindo-Martínez M,
Preuss M,
Schumann C,
Smit RAJ,
Torres-Mejía G,
Acuña-Alonzo V,
Bedoya G,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
González-José R,
Poletti G,
Rothhammer F,
Hakonarson H,
Igo R,
Adler SG,
Iyengar SK,
Nicholas SB,
Gogarten SM,
Isasi CR,
Papnicolaou G,
Stilp AM,
Qi Q,
Kho M,
Smith JA,
Langefeld CD,
Wagenknecht L,
Mckean-Cowdin R,
Gao XR,
Nousome D,
Conti DV,
Feng Y,
Allison MA,
Arzumanyan Z,
Buchanan TA,
Ida Chen YD,
Genter PM,
Goodarzi MO,
Hai Y,
Hsueh W,
Ipp E,
Kandeel FR,
Lam K,
Li X,
Nadler JL,
Raffel LJ,
Roll K,
Sandow K,
Tan J,
Taylor KD,
Xiang AH,
Yao J,
Audirac-Chalifour A,
de Jesus Peralta Romero J,
Hartwig F,
Horta B,
Blangero J,
Curran JE,
Duggirala R,
Lehman DE,
Puppala S,
Fejerman L,
John EM,
Aguilar-Salinas C,
Burtt NP,
Florez JC,
García-Ortíz H,
González-Villalpando C,
Mercader J,
Orozco L,
Tusié-Luna T,
Blanco E,
Gahagan S,
Cox NJ,
Hanis C,
Butte NF,
Cole SA,
Comuzzie AG,
Voruganti VS,
Rohde R,
Wang Y,
Sofer T,
Ziv E,
Grant SFA,
Ruiz-Linares A,
Rotter JI,
Haiman CA,
Parra EJ,
Cruz M,
Loos RJF,
North KE
HGG advances · 2022 · PMID 35399580 · open access
3 pages
Genetic determinants of zinc homeostasis and its role in cardiometabolic diseases
Sadler MC,
Ghobril JP,
Borisov O,
Perrais M,
Schiano G,
Petrovic D,
Ha E,
Ponte B,
Li Y,
Rodriguez-Hernandez Z,
Pruijm M,
Ackermann D
and 20 more — show all
Guessous I,
Stringhini S,
Ehret G,
Corre T,
Vogt B,
Martin PY,
Ongen H,
Dermitzakis E,
Williams JE,
Murdoch BM,
McGuire MK,
Meehan CL,
Lenglet S,
Susztak K,
Vaucher J,
Thomas A,
Devuyst O,
Köttgen A,
Bochud M,
Kutalik Z
INSPIRE Consortium
PLoS genetics · 2025 · PMID 41325371 · open access
3 pages
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.