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.
44 matches for
Smith NL,
showing the first 4.
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
Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
Suri P,
Palmer MR,
Tsepilov YA,
Freidin MB,
Boer CG,
Yau MS,
Evans DS,
Gelemanovic A,
Bartz TM,
Nethander M,
Arbeeva L,
Karssen L
and 25 more — show all
Neogi T,
Campbell A,
Mellstrom D,
Ohlsson C,
Marshall LM,
Orwoll E,
Uitterlinden A,
Rotter JI,
Lauc G,
Psaty BM,
Karlsson MK,
Lane NE,
Jarvik GP,
Polasek O,
Hochberg M,
Jordan JM,
Van Meurs JBJ,
Jackson R,
Nielson CM,
Mitchell BD,
Smith BH,
Hayward C,
Smith NL,
Aulchenko YS,
Williams FMK
PLoS genetics · 2018 · PMID 30261039 · open access
1 page
Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program
Mikhaylova AV,
McHugh CP,
Polfus LM,
Raffield LM,
Boorgula MP,
Blackwell TW,
Brody JA,
Broome J,
Chami N,
Chen MH,
Conomos MP,
Cox C
and 81 more — show all
Curran JE,
Daya M,
Ekunwe L,
Glahn DC,
Heard-Costa N,
Highland HM,
Hobbs BD,
Ilboudo Y,
Jain D,
Lange LA,
Miller-Fleming TW,
Min N,
Moon JY,
Preuss MH,
Rosen J,
Ryan K,
Smith AV,
Sun Q,
Surendran P,
de Vries PS,
Walter K,
Wang Z,
Wheeler M,
Yanek LR,
Zhong X,
Abecasis GR,
Almasy L,
Barnes KC,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Chavan S,
Cho MH,
Choquet H,
Correa A,
Cox N,
DeMeo DL,
Faraday N,
Fornage M,
Gerszten RE,
Hou L,
Johnson AD,
Jorgenson E,
Kaplan R,
Kooperberg C,
Kundu K,
Laurie CA,
Lettre G,
Lewis JP,
Li B,
Li Y,
Lloyd-Jones DM,
Loos RJF,
Manichaikul A,
Meyers DA,
Mitchell BD,
Morrison AC,
Ngo D,
Nickerson DA,
Nongmaithem S,
North KE,
O'Connell JR,
Ortega VE,
Pankratz N,
Perry JA,
Psaty BM,
Rich SS,
Soranzo N,
Rotter JI,
Silverman EK,
Smith NL,
Tang H,
Tracy RP,
Thornton TA,
Vasan RS,
Zein J,
Mathias RA,
Reiner AP,
Auer PL
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 34582791
1 page
Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism
Iglesias MJ,
Sanchez-Rivera L,
Ibrahim-Kosta M,
Naudin C,
Munsch G,
Goumidi L,
Farm M,
Smith PM,
Thibord F,
Kral-Pointner JB,
Hong MG,
Suchon P
and 31 more — show all
Germain M,
Schrottmaier W,
Dusart P,
Boland A,
Kotol D,
Edfors F,
Koprulu M,
Pietzner M,
Langenberg C,
Damrauer SM,
Johnson AD,
Klarin DM,
Smith NL,
Smadja DM,
Holmström M,
Magnusson M,
Silveira A,
Uhlén M,
Renné T,
Martinez-Perez A,
Emmerich J,
Deleuze JF,
Antovic J,
Soria Fernandez JM,
Assinger A,
Schwenk JM,
Souto Andres JC,
Morange PE,
Butler LM,
Trégouët DA,
Odeberg J
Nature communications · 2023 · PMID 37286573 · 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.