For researchers
Is your paper here?
2,673 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.
28 matches for
Denny J,
showing the first 8.
Identification of unique venous thromboembolism-susceptibility variants in African-Americans
Heit JA,
Armasu SM,
McCauley BM,
Kullo IJ,
Sicotte H,
Pathak J,
Chute CG,
Gottesman O,
Bottinger EP,
Denny JC,
Roden DM,
Li R
and 2 more — show all
Thrombosis and haemostasis · 2017 · PMID 28203683
3 pages
Medical Records-Based Genetic Studies of the Complement System
Khan A,
Shang N,
Petukhova L,
Zhang J,
Shen Y,
Hebbring SJ,
Moncrieffe H,
Kottyan LC,
Namjou-Khales B,
Knevel R,
Raychaudhuri S,
Karlson EW
and 9 more — show all
Journal of the American Society of Nephrology : JASN · 2021 · PMID 33941608
3 pages
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
Warren HR,
Trompet S,
Arsenault BJ,
Avery CL,
Bis JC,
Chasman DI,
de Keyser CE,
Deshmukh HA,
Evans DS,
Feng Q,
Li X
and 76 more — show all
Smit RA,
Smith AV,
Sun F,
Taylor KD,
Arnold AM,
Barnes MR,
Barratt BJ,
Betteridge J,
Boekholdt SM,
Boerwinkle E,
Buckley BM,
Chen YI,
de Craen AJ,
Cummings SR,
Denny JC,
Dubé MP,
Durrington PN,
Eiriksdottir G,
Ford I,
Guo X,
Harris TB,
Heckbert SR,
Hofman A,
Hovingh GK,
Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
Neil A,
Nickerson DA,
Nyberg F,
O'Brien E,
O'Donnell CJ,
Post W,
Poulter N,
Vasan RS,
Rice K,
Rich SS,
Rivadeneira F,
Sattar N,
Sever P,
Shaw-Hawkins S,
Shields DC,
Slagboom PE,
Smith NL,
Smith JD,
Sotoodehnia N,
Stanton A,
Stott DJ,
Stricker BH,
Stürmer T,
Uitterlinden AG,
Wei WQ,
Westendorp RG,
Whitsel EA,
Wiggins KL,
Wilke RA,
Ballantyne CM,
Colhoun HM,
Cupples LA,
Franco OH,
Gudnason V,
Hitman G,
Palmer CN,
Psaty BM,
Ridker PM,
Stafford JM,
Stein CM,
Tardif JC,
Caulfield MJ,
Jukema JW,
Rotter JI,
Krauss RM
Journal of medical genetics · 2016 · PMID 27587472
2 pages
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
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia
Karol SE,
Yang W,
Van Driest SL,
Chang TY,
Kaste S,
Bowton E,
Basford M,
Bastarache L,
Roden DM,
Denny JC,
Larsen E,
Winick N
and 16 more — show all
Carroll WL,
Cheng C,
Pei D,
Fernandez CA,
Liu C,
Smith C,
Loh ML,
Raetz EA,
Hunger SP,
Scheet P,
Jeha S,
Pui CH,
Evans WE,
Devidas M,
Mattano LA Jr,
Relling MV
Blood · 2015 · PMID 26265699
1 page
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
Zhou W,
Nielsen JB,
Fritsche LG,
Dey R,
Gabrielsen ME,
Wolford BN,
LeFaive J,
VandeHaar P,
Gagliano SA,
Gifford A,
Bastarache LA,
Wei WQ
and 7 more — show all
Nature genetics · 2018 · PMID 30104761 · 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.