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Is your paper here?
2,660 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.
7 matches for
Ko A.
Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2
Hernandez Cordero AI,
Gonzales NM,
Parker CC,
Sokolof G,
Vandenbergh DJ,
Cheng R,
Abney M,
Sko A,
Douglas A,
Palmer AA,
Gregory JS,
Lionikas A
American journal of human genetics · 2019 · PMID 31761296
12 pages+
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos
Ko A,
Cantor RM,
Weissglas-Volkov D,
Nikkola E,
Reddy PM,
Sinsheimer JS,
Pasaniuc B,
Brown R,
Alvarez M,
Rodriguez A,
Rodriguez-Guillen R,
Bautista IC
and 19 more — show all
Arellano-Campos O,
Muñoz-Hernández LL,
Salomaa V,
Kaprio J,
Jula A,
Jauhiainen M,
Heliövaara M,
Raitakari O,
Lehtimäki T,
Eriksson JG,
Perola M,
Lohmueller KE,
Matikainen N,
Taskinen MR,
Rodriguez-Torres M,
Riba L,
Tusie-Luna T,
Aguilar-Salinas CA,
Pajukanta P
Nature communications · 2014 · PMID 24886709 · open access
5 pages
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
Barnes DR,
Tyrer JP,
Dennis J,
Leslie G,
Bolla MK,
Lush M,
Aeilts AM,
Aittomäki K,
Andrieu N,
Andrulis IL,
Anton-Culver H,
Arason A
and 156 more — show all
Arun BK,
Balmaña J,
Bandera EV,
Barkardottir RB,
Berger LPV,
Berrington de Gonzalez A,
Berthet P,
Białkowska K,
Bjørge L,
Blanco AM,
Blok MJ,
Bobolis KA,
Bogdanova NV,
Brenton JD,
Butz H,
Buys SS,
Caligo MA,
Campbell I,
Castillo C,
Claes KBM,
Colonna SV,
Cook LS,
Daly MB,
Dansonka-Mieszkowska A,
de la Hoya M,
deFazio A,
DePersia A,
Ding YC,
Doherty JA,
Domchek SM,
Dörk T,
Einbeigi Z,
Engel C,
Evans DG,
Foretova L,
Fortner RT,
Fostira F,
Foti MC,
Friedman E,
Frone MN,
Ganz PA,
Gentry-Maharaj A,
Glendon G,
Godwin AK,
González-Neira A,
Greene MH,
Gronwald J,
Guerrieri-Gonzaga A,
Hamann U,
Hansen TVO,
Harris HR,
Hauke J,
Heitz F,
Hogervorst FBL,
Hooning MJ,
Hopper JL,
Huff CD,
Huntsman DG,
Imyanitov EN,
Izatt L,
Jakubowska A,
James PA,
Janavicius R,
John EM,
Kar S,
Karlan BY,
Kennedy CJ,
Kiemeney LALM,
Konstantopoulou I,
Kupryjanczyk J,
Laitman Y,
Lavie O,
Lawrenson K,
Lester J,
Lesueur F,
Lopez-Pleguezuelos C,
Mai PL,
Manoukian S,
May T,
McNeish IA,
Menon U,
Milne RL,
Modugno F,
Mongiovi JM,
Montagna M,
Moysich KB,
Neuhausen SL,
Nielsen FC,
Noguès C,
Oláh E,
Olopade OI,
Osorio A,
Papi L,
Pathak H,
Pearce CL,
Pedersen IS,
Peixoto A,
Pejovic T,
Peng PC,
Peshkin BN,
Peterlongo P,
Powell CB,
Prokofyeva D,
Pujana MA,
Radice P,
Rashid MU,
Rennert G,
Richenberg G,
Sandler DP,
Sasamoto N,
Setiawan VW,
Sharma P,
Sieh W,
Singer CF,
Snape K,
Sokolenko AP,
Soucy P,
Southey MC,
Stoppa-Lyonnet D,
Sutphen R,
Sutter C,
Tan YY,
Teixeira MR,
Terry KL,
Thomsen LCV,
Tischkowitz M,
Toland AE,
Van Gorp T,
Vega A,
Velez Edwards DR,
Webb PM,
Weitzel JN,
Wentzensen N,
Whittemore AS,
Winham SJ,
Wu AH,
Yadav S,
Yu Y,
Ziogas A,
Berchuck A,
Couch FJ,
Goode EL,
Goodman MT,
Monteiro AN,
Offit K,
Ramus SJ,
Risch HA,
Schildkraut JM,
Thomassen M,
Simard J,
Easton DF,
Jones MR,
Chenevix-Trench G,
Gayther SA,
Antoniou AC,
Pharoah PDP
NPJ genomic medicine · 2025 · PMID 41266372 · open access
4 pages
Genetic determinants of circulating sphingolipid concentrations in European populations
Hicks AA,
Pramstaller PP,
Johansson A,
Vitart V,
Rudan I,
Ugocsai P,
Aulchenko Y,
Franklin CS,
Liebisch G,
Erdmann J,
Jonasson I,
Zorkoltseva IV
and 34 more — show all
Pattaro C,
Hayward C,
Isaacs A,
Hengstenberg C,
Campbell S,
Gnewuch C,
Janssens AC,
Kirichenko AV,
König IR,
Marroni F,
Polasek O,
Demirkan A,
Kolcic I,
Schwienbacher C,
Igl W,
Biloglav Z,
Witteman JC,
Pichler I,
Zaboli G,
Axenovich TI,
Peters A,
Schreiber S,
Wichmann HE,
Schunkert H,
Hastie N,
Oostra BA,
Wild SH,
Meitinger T,
Gyllensten U,
van Duijn CM,
Wilson JF,
Wright A,
Schmitz G,
Campbell H
PLoS genetics · 2009 · PMID 19798445 · open access
2 pages
T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection
Lee RJ,
Xiong G,
Kofonow JM,
Chen B,
Lysenko A,
Jiang P,
Abraham V,
Doghramji L,
Adappa ND,
Palmer JN,
Kennedy DW,
Beauchamp GK
and 5 more — show all
The Journal of clinical investigation · 2012 · PMID 23041624
2 pages
A SNP in the ABCC11 gene is the determinant of human earwax type
Yoshiura K,
Kinoshita A,
Ishida T,
Ninokata A,
Ishikawa T,
Kaname T,
Bannai M,
Tokunaga K,
Sonoda S,
Komaki R,
Ihara M,
Saenko VA
and 27 more — show all
Alipov GK,
Sekine I,
Komatsu K,
Takahashi H,
Nakashima M,
Sosonkina N,
Mapendano CK,
Ghadami M,
Nomura M,
Liang DS,
Miwa N,
Kim DK,
Garidkhuu A,
Natsume N,
Ohta T,
Tomita H,
Kaneko A,
Kikuchi M,
Russomando G,
Hirayama K,
Ishibashi M,
Takahashi A,
Saitou N,
Murray JC,
Saito S,
Nakamura Y,
Niikawa N
Nature genetics · 2006 · PMID 16444273
1 page
Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci
Thio CHL,
Reznichenko A,
van der Most PJ,
Kamali Z,
Vaez A,
Smit JH,
Penninx BWJH,
Haller T,
Mihailov E,
Metspalu A,
Damman J,
de Borst MH
and 6 more — show all
Lifelines Cohort Study group
American journal of nephrology · 2019 · PMID 30808845
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.