For researchers
Is your paper here?
3,086 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.
8 matches for
Wojcik G.
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study
Hu Y,
Bien SA,
Nishimura KK,
Haessler J,
Hodonsky CJ,
Baldassari AR,
Highland HM,
Wang Z,
Preuss M,
Sitlani CM,
Wojcik GL,
Tao R
and 22 more — show all
Graff M,
Huckins LM,
Sun Q,
Chen MH,
Mousas A,
Auer PL,
Lettre G,
Tang W,
Qi L,
Thyagarajan B,
Buyske S,
Fornage M,
Hindorff LA,
Li Y,
Lin D,
Reiner AP,
North KE,
Loos RJF,
Raffield LM,
Peters U,
Avery CL,
Kooperberg C
Blood Cell Consortium
BMC genomics · 2021 · PMID 34107879 · open access
12 pages+
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
Tcheandjieu C,
Zhu X,
Hilliard AT,
Clarke SL,
Napolioni V,
Ma S,
Lee KM,
Fang H,
Chen F,
Lu Y,
Tsao NL,
Raghavan S
and 70 more — show all
Koyama S,
Gorman BR,
Vujkovic M,
Klarin D,
Levin MG,
Sinnott-Armstrong N,
Wojcik GL,
Plomondon ME,
Maddox TM,
Waldo SW,
Bick AG,
Pyarajan S,
Huang J,
Song R,
Ho YL,
Buyske S,
Kooperberg C,
Haessler J,
Loos RJF,
Do R,
Verbanck M,
Chaudhary K,
North KE,
Avery CL,
Graff M,
Haiman CA,
Le Marchand L,
Wilkens LR,
Bis JC,
Leonard H,
Shen B,
Lange LA,
Giri A,
Dikilitas O,
Kullo IJ,
Stanaway IB,
Jarvik GP,
Gordon AS,
Hebbring S,
Namjou B,
Kaufman KM,
Ito K,
Ishigaki K,
Kamatani Y,
Verma SS,
Ritchie MD,
Kember RL,
Baras A,
Lotta LA,
Kathiresan S,
Hauser ER,
Miller DR,
Lee JS,
Saleheen D,
Reaven PD,
Cho K,
Gaziano JM,
Natarajan P,
Huffman JE,
Voight BF,
Rader DJ,
Chang KM,
Lynch JA,
Damrauer SM,
Wilson PWF,
Tang H,
Sun YV,
Tsao PS,
O'Donnell CJ,
Assimes TL
Regeneron Genetics Center · CARDIoGRAMplusC4D Consortium and 2 more consortia
Nature medicine · 2022 · PMID 35915156
12 pages+
Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits
Baldassari AR,
Sitlani CM,
Highland HM,
Arking DE,
Buyske S,
Darbar D,
Gondalia R,
Graff M,
Guo X,
Heckbert SR,
Hindorff LA,
Hodonsky CJ
and 20 more — show all
Ida Chen YD,
Kaplan RC,
Peters U,
Post W,
Reiner AP,
Rotter JI,
Shohet RV,
Seyerle AA,
Sotoodehnia N,
Tao R,
Taylor KD,
Wojcik GL,
Yao J,
Kenny EE,
Lin HJ,
Soliman EZ,
Whitsel EA,
North KE,
Kooperberg C,
Avery CL
Circulation. Genomic and precision medicine · 2020 · PMID 32602732
2 pages
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study
Downie CG,
Dimos SF,
Bien SA,
Hu Y,
Darst BF,
Polfus LM,
Wang Y,
Wojcik GL,
Tao R,
Raffield LM,
Armstrong ND,
Polikowsky HG
and 19 more — show all
Below JE,
Correa A,
Irvin MR,
Rasmussen-Torvik LJF,
Carlson CS,
Phillips LS,
Liu S,
Pankow JS,
Rich SS,
Rotter JI,
Buyske S,
Matise TC,
North KE,
Avery CL,
Haiman CA,
Loos RJF,
Kooperberg C,
Graff M,
Highland HM
Diabetologia · 2022 · PMID 34951656
2 pages
Mexican Biobank advances population and medical genomics of diverse ancestries
Sohail M,
Palma-Martínez MJ,
Chong AY,
Quinto-Cortés CD,
Barberena-Jonas C,
Medina-Muñoz SG,
Ragsdale A,
Delgado-Sánchez G,
Cruz-Hervert LP,
Ferreyra-Reyes L,
Ferreira-Guerrero E,
Mongua-Rodríguez N
and 17 more — show all
Canizales-Quintero S,
Jimenez-Kaufmann A,
Moreno-Macías H,
Aguilar-Salinas CA,
Auckland K,
Cortés A,
Acuña-Alonzo V,
Gignoux CR,
Wojcik GL,
Ioannidis AG,
Fernández-Valverde SL,
Hill AVS,
Tusié-Luna MT,
Mentzer AJ,
Novembre J,
García-García L,
Moreno-Estrada A
Nature · 2023 · PMID 37821706 · open access
2 pages
Genome-wide association study of hepatitis C virus- and cryoglobulin-related vasculitis
Zignego AL,
Wojcik GL,
Cacoub P,
Visentini M,
Casato M,
Mangia A,
Latanich R,
Charles ED,
Gragnani L,
Terrier B,
Piazzola V,
Dustin LB
and 7 more — show all
Genes and immunity · 2014 · PMID 25030430
1 page
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations
Daya M,
Rafaels N,
Brunetti TM,
Chavan S,
Levin AM,
Shetty A,
Gignoux CR,
Boorgula MP,
Wojcik G,
Campbell M,
Vergara C,
Torgerson DG
and 53 more — show all
Ortega VE,
Doumatey A,
Johnston HR,
Acevedo N,
Araujo MI,
Avila PC,
Belbin G,
Bleecker E,
Bustamante C,
Caraballo L,
Cruz A,
Dunston GM,
Eng C,
Faruque MU,
Ferguson TS,
Figueiredo C,
Ford JG,
Gan W,
Gourraud PA,
Hansel NN,
Hernandez RD,
Herrera-Paz EF,
Jiménez S,
Kenny EE,
Knight-Madden J,
Kumar R,
Lange LA,
Lange EM,
Lizee A,
Maul P,
Maul T,
Mayorga A,
Meyers D,
Nicolae DL,
O'Connor TD,
Oliveira RR,
Olopade CO,
Olopade O,
Qin ZS,
Rotimi C,
Vince N,
Watson H,
Wilks RJ,
Wilson JG,
Salzberg S,
Ober C,
Burchard EG,
Williams LK,
Beaty TH,
Taub MA,
Ruczinski I,
Mathias RA,
Barnes KC
CAAPA
Nature communications · 2019 · PMID 30787307 · open access
1 page
Genetic analyses of diverse populations improves discovery for complex traits
Wojcik GL,
Graff M,
Nishimura KK,
Tao R,
Haessler J,
Gignoux CR,
Highland HM,
Patel YM,
Sorokin EP,
Avery CL,
Belbin GM,
Bien SA
and 74 more — show all
Cheng I,
Cullina S,
Hodonsky CJ,
Hu Y,
Huckins LM,
Jeff J,
Justice AE,
Kocarnik JM,
Lim U,
Lin BM,
Lu Y,
Nelson SC,
Park SL,
Poisner H,
Preuss MH,
Richard MA,
Schurmann C,
Setiawan VW,
Sockell A,
Vahi K,
Verbanck M,
Vishnu A,
Walker RW,
Young KL,
Zubair N,
Acuña-Alonso V,
Ambite JL,
Barnes KC,
Boerwinkle E,
Bottinger EP,
Bustamante CD,
Caberto C,
Canizales-Quinteros S,
Conomos MP,
Deelman E,
Do R,
Doheny K,
Fernández-Rhodes L,
Fornage M,
Hailu B,
Heiss G,
Henn BM,
Hindorff LA,
Jackson RD,
Laurie CA,
Laurie CC,
Li Y,
Lin DY,
Moreno-Estrada A,
Nadkarni G,
Norman PJ,
Pooler LC,
Reiner AP,
Romm J,
Sabatti C,
Sandoval K,
Sheng X,
Stahl EA,
Stram DO,
Thornton TA,
Wassel CL,
Wilkens LR,
Winkler CA,
Yoneyama S,
Buyske S,
Haiman CA,
Kooperberg C,
Le Marchand L,
Loos RJF,
Matise TC,
North KE,
Peters U,
Kenny EE,
Carlson CS
Nature · 2019 · PMID 31217584
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.