For researchers
Is your paper here?
2,665 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.
26 matches for
Andrade M,
showing the first 6.
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium
Tang W,
Teichert M,
Chasman DI,
Heit JA,
Morange PE,
Li G,
Pankratz N,
Leebeek FW,
Paré G,
de Andrade M,
Tzourio C,
Psaty BM
and 28 more — show all
Basu S,
Ruiter R,
Rose L,
Armasu SM,
Lumley T,
Heckbert SR,
Uitterlinden AG,
Lathrop M,
Rice KM,
Cushman M,
Hofman A,
Lambert JC,
Glazer NL,
Pankow JS,
Witteman JC,
Amouyel P,
Bis JC,
Bovill EG,
Kong X,
Tracy RP,
Boerwinkle E,
Rotter JI,
Trégouët DA,
Loth DW,
Stricker BHC,
Ridker PM,
Folsom AR,
Smith NL
Genetic epidemiology · 2013 · PMID 23650146
1 page
Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study
Ding K,
de Andrade M,
Manolio TA,
Crawford DC,
Rasmussen-Torvik LJ,
Ritchie MD,
Denny JC,
Masys DR,
Jouni H,
Pachecho JA,
Kho AN,
Roden DM
and 2 more — show all
G3 (Bethesda, Md.) · 2013 · PMID 23696099 · open access
1 page
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects
Shameer K,
Denny JC,
Ding K,
Jouni H,
Crosslin DR,
de Andrade M,
Chute CG,
Peissig P,
Pacheco JA,
Li R,
Bastarache L,
Kho AN
and 8 more — show all
Human genetics · 2014 · PMID 24026423
1 page
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk
Lindström S,
Thompson DJ,
Paterson AD,
Li J,
Gierach GL,
Scott C,
Stone J,
Douglas JA,
dos-Santos-Silva I,
Fernandez-Navarro P,
Verghase J,
Smith P
and 33 more — show all
Brown J,
Luben R,
Wareham NJ,
Loos RJ,
Heit JA,
Pankratz VS,
Norman A,
Goode EL,
Cunningham JM,
deAndrade M,
Vierkant RA,
Czene K,
Fasching PA,
Baglietto L,
Southey MC,
Giles GG,
Shah KP,
Chan HP,
Helvie MA,
Beck AH,
Knoblauch NW,
Hazra A,
Hunter DJ,
Kraft P,
Pollan M,
Figueroa JD,
Couch FJ,
Hopper JL,
Hall P,
Easton DF,
Boyd NF,
Vachon CM,
Tamimi RM
Nature communications · 2014 · PMID 25342443 · open access
1 page
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
van 't Hof FN,
Ruigrok YM,
Lee CH,
Ripke S,
Anderson G,
de Andrade M,
Baas AF,
Blankensteijn JD,
Böttinger EP,
Bown MJ,
Broderick J,
Bijlenga P
and 59 more — show all
Carrell DS,
Crawford DC,
Crosslin DR,
Ebeling C,
Eriksson JG,
Eriksson JG,
Fornage M,
Foroud T,
von Und Zu Fraunberg M,
Friedrich CM,
Gaál EI,
Gottesman O,
Guo DC,
Harrison SC,
Hernesniemi J,
Hofman A,
Inoue I,
Jääskeläinen JE,
Jones GT,
Kiemeney LA,
Kivisaari R,
Ko N,
Koskinen S,
Kubo M,
Kullo IJ,
Kuivaniemi H,
Kurki MI,
Laakso A,
Lai D,
Leal SM,
Lehto H,
LeMaire SA,
Low SK,
Malinowski J,
McCarty CA,
Milewicz DM,
Mosley TH,
Nakamura Y,
Nakaoka H,
Niemelä M,
Pacheco J,
Peissig PL,
Pera J,
Rasmussen-Torvik L,
Ritchie MD,
Rivadeneira F,
van Rij AM,
Santos-Cortez RL,
Saratzis A,
Slowik A,
Takahashi A,
Tromp G,
Uitterlinden AG,
Verma SS,
Vermeulen SH,
Wang GT,
Han B,
Rinkel GJ,
de Bakker PI
Aneurysm Consortium; Vascular Research Consortium of New Zealand
Journal of the American Heart Association · 2016 · PMID 27418160 · open access
1 page
Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm
Joo YY,
Pacheco JA,
Thompson WK,
Rasmussen-Torvik LJ,
Rasmussen LV,
Lin FTJ,
Andrade M,
Borthwick KM,
Bottinger E,
Cagan A,
Carrell DS,
Denny JC
and 13 more — show all
Ellis SB,
Gottesman O,
Linneman JG,
Pathak J,
Peissig PL,
Shang N,
Tromp G,
Veerappan A,
Smith ME,
Chisholm RL,
Gawron AJ,
Hayes MG,
Kho AN
PloS one · 2023 · PMID 37196047 · 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.