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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.
30 matches for
Arnett DK,
showing the first 10.
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia
Berndt SI,
Camp NJ,
Skibola CF,
Vijai J,
Wang Z,
Gu J,
Nieters A,
Kelly RS,
Smedby KE,
Monnereau A,
Cozen W,
Cox A
and 115 more — show all
Wang SS,
Lan Q,
Teras LR,
Machado M,
Yeager M,
Brooks-Wilson AR,
Hartge P,
Purdue MP,
Birmann BM,
Vajdic CM,
Cocco P,
Zhang Y,
Giles GG,
Zeleniuch-Jacquotte A,
Lawrence C,
Montalvan R,
Burdett L,
Hutchinson A,
Ye Y,
Call TG,
Shanafelt TD,
Novak AJ,
Kay NE,
Liebow M,
Cunningham JM,
Allmer C,
Hjalgrim H,
Adami HO,
Melbye M,
Glimelius B,
Chang ET,
Glenn M,
Curtin K,
Cannon-Albright LA,
Diver WR,
Link BK,
Weiner GJ,
Conde L,
Bracci PM,
Riby J,
Arnett DK,
Zhi D,
Leach JM,
Holly EA,
Jackson RD,
Tinker LF,
Benavente Y,
Sala N,
Casabonne D,
Becker N,
Boffetta P,
Brennan P,
Foretova L,
Maynadie M,
McKay J,
Staines A,
Chaffee KG,
Achenbach SJ,
Vachon CM,
Goldin LR,
Strom SS,
Leis JF,
Weinberg JB,
Caporaso NE,
Norman AD,
De Roos AJ,
Morton LM,
Severson RK,
Riboli E,
Vineis P,
Kaaks R,
Masala G,
Weiderpass E,
Chirlaque MD,
Vermeulen RCH,
Travis RC,
Southey MC,
Milne RL,
Albanes D,
Virtamo J,
Weinstein S,
Clavel J,
Zheng T,
Holford TR,
Villano DJ,
Maria A,
Spinelli JJ,
Gascoyne RD,
Connors JM,
Bertrand KA,
Giovannucci E,
Kraft P,
Kricker A,
Turner J,
Ennas MG,
Ferri GM,
Miligi L,
Liang L,
Ma B,
Huang J,
Huang J,
Crouch S,
Park JH,
Chatterjee N,
North KE,
Snowden JA,
Wright J,
Fraumeni JF,
Offit K,
Wu X,
de Sanjose S,
Cerhan JR,
Chanock SJ,
Rothman N,
Slager SL
Nature communications · 2016 · PMID 26956414 · open access
2 pages
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele
Zhang X,
Brody JA,
Graff M,
Highland HM,
Chami N,
Xu H,
Wang Z,
Ferrier KR,
Chittoor G,
Josyula NS,
Meyer M,
Gupta S
and 113 more — show all
Li X,
Li Z,
Allison MA,
Becker DM,
Bielak LF,
Bis JC,
Boorgula MP,
Bowden DW,
Broome JG,
Buth EJ,
Carlson CS,
Chang KM,
Chavan S,
Chiu YF,
Chuang LM,
Conomos MP,
DeMeo DL,
Du M,
Duggirala R,
Eng C,
Fohner AE,
Freedman BI,
Garrett ME,
Guo X,
Haiman C,
Heavner BD,
Hidalgo B,
Hixson JE,
Ho YL,
Hobbs BD,
Hu D,
Hui Q,
Hwu CM,
Jackson RD,
Jain D,
Kalyani RR,
Kardia SLR,
Kelly TN,
Lange EM,
LeNoir M,
Li C,
Le Marchand L,
McDonald MN,
McHugh CP,
Morrison AC,
Naseri T,
O'Connell J,
O'Donnell CJ,
Palmer ND,
Pankow JS,
Perry JA,
Peters U,
Preuss MH,
Rao DC,
Regan EA,
Reupena SM,
Roden DM,
Rodriguez-Santana J,
Sitlani CM,
Smith JA,
Tiwari HK,
Vasan RS,
Wang Z,
Weeks DE,
Wessel J,
Wiggins KL,
Wilkens LR,
Wilson PWF,
Yanek LR,
Yoneda ZT,
Zhao W,
Zhao W,
Zöllner S,
Arnett DK,
Ashley-Koch AE,
Barnes KC,
Blangero J,
Boerwinkle E,
Burchard EG,
Carson AP,
Chasman DI,
Ida Chen YD,
Curran JE,
Fornage M,
Gordeuk VR,
He J,
Heckbert SR,
Hou L,
Irvin MR,
Kooperberg C,
Minster RL,
Mitchell BD,
Nouraie M,
Psaty BM,
Raffield LM,
Reiner AP,
Rich SS,
Rotter JI,
Benjamin Shoemaker M,
Smith NL,
Taylor KD,
Telen MJ,
Weiss ST,
Zhang Y,
Heard-Costa N,
Sun YV,
Lin X,
Cupples LA,
Lange LA,
Liu CT,
Loos RJF,
North KE,
Justice AE
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Nature communications · 2025 · PMID 40216759 · open access
2 pages
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits
Zheng JS,
Arnett DK,
Lee YC,
Shen J,
Parnell LD,
Smith CE,
Richardson K,
Li D,
Borecki IB,
Ordovás JM,
Lai CQ
PloS one · 2013 · PMID 24204828 · open access
1 page
Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium
Mozaffarian D,
Kabagambe EK,
Johnson CO,
Lemaitre RN,
Manichaikul A,
Sun Q,
Foy M,
Wang L,
Wiener H,
Irvin MR,
Rich SS,
Wu H
and 17 more — show all
Jensen MK,
Chasman DI,
Chu AY,
Fornage M,
Steffen L,
King IB,
McKnight B,
Psaty BM,
Djoussé L,
Chen IY,
Wu JH,
Siscovick DS,
Ridker PM,
Tsai MY,
Rimm EB,
Hu FB,
Arnett DK
The American journal of clinical nutrition · 2015 · PMID 25646338
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
Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations
Hu Y,
Tanaka T,
Zhu J,
Guan W,
Wu JHY,
Psaty BM,
McKnight B,
King IB,
Sun Q,
Richard M,
Manichaikul A,
Frazier-Wood AC
and 21 more — show all
Kabagambe EK,
Hopkins PN,
Ordovas JM,
Ferrucci L,
Bandinelli S,
Arnett DK,
Chen YI,
Liang S,
Siscovick DS,
Tsai MY,
Rich SS,
Fornage M,
Hu FB,
Rimm EB,
Jensen MK,
Lemaitre RN,
Mozaffarian D,
Steffen LM,
Morris AP,
Li H,
Lin X
Journal of lipid research · 2017 · PMID 28298293 · open access
1 page
Genome-Wide Association Study of Apparent Treatment-Resistant Hypertension in the CHARGE Consortium: The CHARGE Pharmacogenetics Working Group
Irvin MR,
Sitlani CM,
Floyd JS,
Psaty BM,
Bis JC,
Wiggins KL,
Whitsel EA,
Sturmer T,
Stewart J,
Raffield L,
Sun F,
Liu CT
and 32 more — show all
Xu H,
Cupples AL,
Tanner RM,
Rossing P,
Smith A,
Zilhão NR,
Launer LJ,
Noordam R,
Rotter JI,
Yao J,
Li X,
Guo X,
Limdi N,
Sundaresan A,
Lange L,
Correa A,
Stott DJ,
Ford I,
Jukema JW,
Gudnason V,
Mook-Kanamori DO,
Trompet S,
Palmas W,
Warren HR,
Hellwege JN,
Giri A,
O'donnell C,
Hung AM,
Edwards TL,
Ahluwalia TS,
Arnett DK,
Avery CL
American journal of hypertension · 2019 · PMID 31545351
1 page
Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke
Keene KL,
Hyacinth HI,
Bis JC,
Kittner SJ,
Mitchell BD,
Cheng YC,
Pare G,
Chong M,
O'Donnell M,
Meschia JF,
Chen WM,
Sale MM
and 35 more — show all
Rich SS,
Nalls MA,
Zonderman AB,
Evans MK,
Wilson JG,
Correa A,
Markus HS,
Traylor M,
Lewis CM,
Carty CL,
Reiner A,
Haessler J,
Langefeld CD,
Gottesman R,
Mosley TH,
Woo D,
Yaffe K,
Liu Y,
Longstreth WT,
Psaty BM,
Kooperberg C,
Lange LA,
Sacco R,
Rundek T,
Lee JM,
Cruchaga C,
Furie KL,
Arnett DK,
Benavente OR,
Grewal RP,
Peddareddygari LR,
Dichgans M,
Malik R,
Worrall BB,
Fornage M
COMPASS, SiGN, and METASTROKE Consortia
Stroke · 2020 · PMID 32693751
1 page
Genome-wide association study of circulating interleukin 6 levels identifies novel loci
Ahluwalia TS,
Prins BP,
Abdollahi M,
Armstrong NJ,
Aslibekyan S,
Bain L,
Jefferis B,
Baumert J,
Beekman M,
Ben-Shlomo Y,
Bis JC,
Mitchell BD
and 114 more — show all
de Geus E,
Delgado GE,
Marek D,
Eriksson J,
Kajantie E,
Kanoni S,
Kemp JP,
Lu C,
Marioni RE,
McLachlan S,
Milaneschi Y,
Nolte IM,
Petrelis AM,
Porcu E,
Sabater-Lleal M,
Naderi E,
Seppälä I,
Shah T,
Singhal G,
Standl M,
Teumer A,
Thalamuthu A,
Thiering E,
Trompet S,
Ballantyne CM,
Benjamin EJ,
Casas JP,
Toben C,
Dedoussis G,
Deelen J,
Durda P,
Engmann J,
Feitosa MF,
Grallert H,
Hammarstedt A,
Harris SE,
Homuth G,
Hottenga JJ,
Jalkanen S,
Jamshidi Y,
Jawahar MC,
Jess T,
Kivimaki M,
Kleber ME,
Lahti J,
Liu Y,
Marques-Vidal P,
Mellström D,
Mooijaart SP,
Müller-Nurasyid M,
Penninx B,
Revez JA,
Rossing P,
Räikkönen K,
Sattar N,
Scharnagl H,
Sennblad B,
Silveira A,
Pourcain BS,
Timpson NJ,
Trollor J,
van Dongen J,
Van Heemst D,
Visvikis-Siest S,
Vollenweider P,
Völker U,
Waldenberger M,
Willemsen G,
Zabaneh D,
Morris RW,
Arnett DK,
Baune BT,
Boomsma DI,
Chang YC,
Deary IJ,
Deloukas P,
Eriksson JG,
Evans DM,
Ferreira MA,
Gaunt T,
Gudnason V,
Hamsten A,
Heinrich J,
Hingorani A,
Humphries SE,
Jukema JW,
Koenig W,
Kumari M,
Kutalik Z,
Lawlor DA,
Lehtimäki T,
März W,
Mather KA,
Naitza S,
Nauck M,
Ohlsson C,
Price JF,
Raitakari O,
Rice K,
Sachdev PS,
Slagboom E,
Sørensen TIA,
Spector T,
Stacey D,
Stathopoulou MG,
Tanaka T,
Wannamethee SG,
Whincup P,
Rotter JI,
Dehghan A,
Boerwinkle E,
Psaty BM,
Snieder H,
Alizadeh BZ
CHARGE Inflammation Working Group
Human molecular genetics · 2021 · PMID 33517400 · open access
1 page
Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program
Sarnowski C,
Chen H,
Biggs ML,
Wassertheil-Smoller S,
Bressler J,
Irvin MR,
Ryan KA,
Karasik D,
Arnett DK,
Cupples LA,
Fardo DW,
Gogarten SM
and 16 more — show all
Heavner BD,
Jain D,
Kang HM,
Kooperberg C,
Mainous AG,
Mitchell BD,
Morrison AC,
O'Connell JR,
Psaty BM,
Rice K,
Smith AV,
Vasan RS,
Windham BG,
Kiel DP,
Murabito JM,
Lunetta KL
TOPMed Longevity and Healthy Aging Working Group · from the NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
PloS one · 2021 · PMID 34214102 · 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.