For researchers
Is your paper here?
2,676 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.
49 matches for
Le P,
showing the first 9.
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia
Hillmer AM,
Hanneken S,
Ritzmann S,
Becker T,
Freudenberg J,
Brockschmidt FF,
Flaquer A,
Freudenberg-Hua Y,
Jamra RA,
Metzen C,
Heyn U,
Schweiger N
and 13 more — show all
Betz RC,
Blaumeiser B,
Hampe J,
Schreiber S,
Schulze TG,
Hennies HC,
Schumacher J,
Propping P,
Ruzicka T,
Cichon S,
Wienker TF,
Kruse R,
Nothen MM
American journal of human genetics · 2005 · PMID 15902657
1 page
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia
Sanna S,
Busonero F,
Maschio A,
McArdle PF,
Usala G,
Dei M,
Lai S,
Mulas A,
Piras MG,
Perseu L,
Masala M,
Marongiu M
and 8 more — show all
Human molecular genetics · 2009 · PMID 19419973
1 page
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
Heard-Costa NL,
Zillikens MC,
Monda KL,
Johansson A,
Harris TB,
Fu M,
Haritunians T,
Feitosa MF,
Aspelund T,
Eiriksdottir G,
Garcia M,
Launer LJ
and 49 more — show all
Smith AV,
Mitchell BD,
McArdle PF,
Shuldiner AR,
Bielinski SJ,
Boerwinkle E,
Brancati F,
Demerath EW,
Pankow JS,
Arnold AM,
Chen YD,
Glazer NL,
McKnight B,
Psaty BM,
Rotter JI,
Amin N,
Campbell H,
Gyllensten U,
Pattaro C,
Pramstaller PP,
Rudan I,
Struchalin M,
Vitart V,
Gao X,
Kraja A,
Province MA,
Zhang Q,
Atwood LD,
Dupuis J,
Hirschhorn JN,
Jaquish CE,
O'Donnell CJ,
Vasan RS,
White CC,
Aulchenko YS,
Estrada K,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Witteman JC,
Oostra BA,
Kaplan RC,
Gudnason V,
O'Connell JR,
Borecki IB,
van Duijn CM,
Cupples LA,
Fox CS,
North KE
PLoS genetics · 2009 · PMID 19557197 · open access
1 page
Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population
Liao M,
Ye F,
Zhang B,
Huang L,
Xiao Q,
Qin M,
Mo L,
Tan A,
Gao Y,
Lu Z,
Wu C,
Zhang Y
and 5 more — show all
Genes and immunity · 2012 · PMID 22673310
1 page
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder
Song J,
Bergen SE,
Di Florio A,
Karlsson R,
Charney A,
Ruderfer DM,
Stahl EA,
Chambert KD,
Moran JL,
Gordon-Smith K,
Forty L,
Green EK
and 39 more — show all
Jones I,
Jones L,
Scolnick EM,
Sklar P,
Smoller JW,
Lichtenstein P,
Hultman C,
Craddock N,
Landén M,
Smoller JW,
Perlis RH,
Lee PH,
Castro VM,
Hoffnagle AG,
Sklar P,
Stahl EA,
Purcell SM,
Ruderfer DM,
Charney AW,
Roussos P,
Michele Pato CP,
Medeiros H,
Sobel J,
Craddock N,
Jones I,
Forty L,
Florio AD,
Green E,
Jones L,
Gordon-Smith K,
Landen M,
Hultman C,
Jureus A,
Bergen S,
McCarroll S,
Moran J,
Smoller JW,
Chambert K,
Belliveau RA
Members of the International Cohort Collection for Bipolar Disorder (ICCBD)
Molecular psychiatry · 2016 · PMID 26503763 · open access
1 page
Genetic variation at 16q24.2 is associated with small vessel stroke
Traylor M,
Malik R,
Nalls MA,
Cotlarciuc I,
Radmanesh F,
Thorleifsson G,
Hanscombe KB,
Langefeld C,
Saleheen D,
Rost NS,
Yet I,
Spector TD
and 55 more — show all
Bell JT,
Hannon E,
Mill J,
Chauhan G,
Debette S,
Bis JC,
Longstreth WT Jr,
Ikram MA,
Launer LJ,
Seshadri S,
Hamilton-Bruce MA,
Jimenez-Conde J,
Cole JW,
Schmidt R,
Słowik A,
Lemmens R,
Lindgren A,
Melander O,
Grewal RP,
Sacco RL,
Rundek T,
Rexrode K,
Arnett DK,
Johnson JA,
Benavente OR,
Wasssertheil-Smoller S,
Lee JM,
Pulit SL,
Wong Q,
Rich SS,
de Bakker PI,
McArdle PF,
Woo D,
Anderson CD,
Xu H,
Heitsch L,
Fornage M,
Jern C,
Stefansson K,
Thorsteinsdottir U,
Gretarsdottir S,
Lewis CM,
Sharma P,
Sudlow CL,
Rothwell PM,
Boncoraglio GB,
Thijs V,
Levi C,
Meschia JF,
Rosand J,
Kittner SJ,
Mitchell BD,
Dichgans M,
Worrall BB,
Markus HS
METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium · International Stroke Genetics Consortium
Annals of neurology · 2017 · PMID 27997041 · open access
1 page
Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry
Rawofi L,
Edwards M,
Krithika S,
Le P,
Cha D,
Yang Z,
Ma Y,
Wang J,
Su B,
Jin L,
Norton HL,
Parra EJ
PeerJ · 2017 · PMID 29109912 · open access
1 page
A meta-analysis of genome-wide association studies identifies multiple longevity genes
Deelen J,
Evans DS,
Arking DE,
Tesi N,
Nygaard M,
Liu X,
Wojczynski MK,
Biggs ML,
van der Spek A,
Atzmon G,
Ware EB,
Sarnowski C
and 72 more — show all
Smith AV,
Seppälä I,
Cordell HJ,
Dose J,
Amin N,
Arnold AM,
Ayers KL,
Barzilai N,
Becker EJ,
Beekman M,
Blanché H,
Christensen K,
Christiansen L,
Collerton JC,
Cubaynes S,
Cummings SR,
Davies K,
Debrabant B,
Deleuze JF,
Duncan R,
Faul JD,
Franceschi C,
Galan P,
Gudnason V,
Harris TB,
Huisman M,
Hurme MA,
Jagger C,
Jansen I,
Jylhä M,
Kähönen M,
Karasik D,
Kardia SLR,
Kingston A,
Kirkwood TBL,
Launer LJ,
Lehtimäki T,
Lieb W,
Lyytikäinen LP,
Martin-Ruiz C,
Min J,
Nebel A,
Newman AB,
Nie C,
Nohr EA,
Orwoll ES,
Perls TT,
Province MA,
Psaty BM,
Raitakari OT,
Reinders MJT,
Robine JM,
Rotter JI,
Sebastiani P,
Smith J,
Sørensen TIA,
Taylor KD,
Uitterlinden AG,
van der Flier W,
van der Lee SJ,
van Duijn CM,
van Heemst D,
Vaupel JW,
Weir D,
Ye K,
Zeng Y,
Zheng W,
Holstege H,
Kiel DP,
Lunetta KL,
Slagboom PE,
Murabito JM
Nature communications · 2019 · PMID 31413261 · 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.