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2,675 papers hold this site up. Every variant and condition page names
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27 matches for
Heard-Costa N,
showing the first 7.
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Little A,
Hu Y,
Sun Q,
Jain D,
Broome J,
Chen MH,
Thibord F,
McHugh C,
Surendran P,
Blackwell TW,
Brody JA,
Bhan A
and 55 more — show all
Chami N,
de Vries PS,
Ekunwe L,
Heard-Costa N,
Hobbs BD,
Manichaikul A,
Moon JY,
Preuss MH,
Ryan K,
Wang Z,
Wheeler M,
Yanek LR,
Abecasis GR,
Almasy L,
Beaty TH,
Becker LC,
Blangero J,
Boerwinkle E,
Butterworth AS,
Choquet H,
Correa A,
Curran JE,
Faraday N,
Fornage M,
Glahn DC,
Hou L,
Jorgenson E,
Kooperberg C,
Lewis JP,
Lloyd-Jones DM,
Loos RJF,
Min YI,
Mitchell BD,
Morrison AC,
Nickerson DA,
North KE,
O'Connell JR,
Pankratz N,
Psaty BM,
Vasan RS,
Rich SS,
Rotter JI,
Smith AV,
Smith NL,
Tang H,
Tracy RP,
Conomos MP,
Laurie CA,
Mathias RA,
Li Y,
Auer PL,
Thornton T,
Reiner AP,
Johnson AD,
Raffield LM
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Human molecular genetics · 2022 · PMID 34553764
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
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
Heard-Costa NL,
Zillikens MC,
Monda KL,
Johansson A,
Harris TB,
Fu M,
Haritunians T,
Feitosa MF,
Aspelund T,
Eiriksdottir G,
Garcia M,
Launer LJ
and 49 more — show all
Smith AV,
Mitchell BD,
McArdle PF,
Shuldiner AR,
Bielinski SJ,
Boerwinkle E,
Brancati F,
Demerath EW,
Pankow JS,
Arnold AM,
Chen YD,
Glazer NL,
McKnight B,
Psaty BM,
Rotter JI,
Amin N,
Campbell H,
Gyllensten U,
Pattaro C,
Pramstaller PP,
Rudan I,
Struchalin M,
Vitart V,
Gao X,
Kraja A,
Province MA,
Zhang Q,
Atwood LD,
Dupuis J,
Hirschhorn JN,
Jaquish CE,
O'Donnell CJ,
Vasan RS,
White CC,
Aulchenko YS,
Estrada K,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Witteman JC,
Oostra BA,
Kaplan RC,
Gudnason V,
O'Connell JR,
Borecki IB,
van Duijn CM,
Cupples LA,
Fox CS,
North KE
PLoS genetics · 2009 · PMID 19557197 · open access
1 page
FTO genotype is associated with phenotypic variability of body mass index
Yang J,
Loos RJ,
Powell JE,
Medland SE,
Speliotes EK,
Chasman DI,
Rose LM,
Thorleifsson G,
Steinthorsdottir V,
Mägi R,
Waite L,
Smith AV
and 160 more — show all
Yerges-Armstrong LM,
Monda KL,
Hadley D,
Mahajan A,
Li G,
Kapur K,
Vitart V,
Huffman JE,
Wang SR,
Palmer C,
Esko T,
Fischer K,
Zhao JH,
Demirkan A,
Isaacs A,
Feitosa MF,
Luan J,
Heard-Costa NL,
White C,
Jackson AU,
Preuss M,
Ziegler A,
Eriksson J,
Kutalik Z,
Frau F,
Nolte IM,
Van Vliet-Ostaptchouk JV,
Hottenga JJ,
Jacobs KB,
Verweij N,
Goel A,
Medina-Gomez C,
Estrada K,
Bragg-Gresham JL,
Sanna S,
Sidore C,
Tyrer J,
Teumer A,
Prokopenko I,
Mangino M,
Lindgren CM,
Assimes TL,
Shuldiner AR,
Hui J,
Beilby JP,
McArdle WL,
Hall P,
Haritunians T,
Zgaga L,
Kolcic I,
Polasek O,
Zemunik T,
Oostra BA,
Junttila MJ,
Grönberg H,
Schreiber S,
Peters A,
Hicks AA,
Stephens J,
Foad NS,
Laitinen J,
Pouta A,
Kaakinen M,
Willemsen G,
Vink JM,
Wild SH,
Navis G,
Asselbergs FW,
Homuth G,
John U,
Iribarren C,
Harris T,
Launer L,
Gudnason V,
O'Connell JR,
Boerwinkle E,
Cadby G,
Palmer LJ,
James AL,
Musk AW,
Ingelsson E,
Psaty BM,
Beckmann JS,
Waeber G,
Vollenweider P,
Hayward C,
Wright AF,
Rudan I,
Groop LC,
Metspalu A,
Khaw KT,
van Duijn CM,
Borecki IB,
Province MA,
Wareham NJ,
Tardif JC,
Huikuri HV,
Cupples LA,
Atwood LD,
Fox CS,
Boehnke M,
Collins FS,
Mohlke KL,
Erdmann J,
Schunkert H,
Hengstenberg C,
Stark K,
Lorentzon M,
Ohlsson C,
Cusi D,
Staessen JA,
Van der Klauw MM,
Pramstaller PP,
Kathiresan S,
Jolley JD,
Ripatti S,
Jarvelin MR,
de Geus EJ,
Boomsma DI,
Penninx B,
Wilson JF,
Campbell H,
Chanock SJ,
van der Harst P,
Hamsten A,
Watkins H,
Hofman A,
Witteman JC,
Zillikens MC,
Uitterlinden AG,
Rivadeneira F,
Zillikens MC,
Kiemeney LA,
Vermeulen SH,
Abecasis GR,
Schlessinger D,
Schipf S,
Stumvoll M,
Tönjes A,
Spector TD,
North KE,
Lettre G,
McCarthy MI,
Berndt SI,
Heath AC,
Madden PA,
Nyholt DR,
Montgomery GW,
Martin NG,
McKnight B,
Strachan DP,
Hill WG,
Snieder H,
Ridker PM,
Thorsteinsdottir U,
Stefansson K,
Frayling TM,
Hirschhorn JN,
Goddard ME,
Visscher PM
Nature · 2012 · PMID 22982992
1 page
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course
Graff M,
Ngwa JS,
Workalemahu T,
Homuth G,
Schipf S,
Teumer A,
Völzke H,
Wallaschofski H,
Abecasis GR,
Edward L,
Francesco C,
Sanna S
and 37 more — show all
Scheet P,
Schlessinger D,
Sidore C,
Xiao X,
Wang Z,
Chanock SJ,
Jacobs KB,
Hayes RB,
Hu F,
Van Dam RM,
Crout RJ,
Marazita ML,
Shaffer JR,
Atwood LD,
Fox CS,
Heard-Costa NL,
White C,
Choh AC,
Czerwinski SA,
Demerath EW,
Dyer TD,
Towne B,
Amin N,
Oostra BA,
Van Duijn CM,
Zillikens MC,
Esko T,
Nelis M,
Nikopensius T,
Metspalu A,
Strachan DP,
Monda K,
Qi L,
North KE,
Cupples LA,
Gordon-Larsen P,
Berndt SI
GIANT Consortium
Human molecular genetics · 2013 · PMID 23669352
1 page
Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment
Nagtegaal AP,
Broer L,
Zilhao NR,
Jakobsdottir J,
Bishop CE,
Brumat M,
Christiansen MW,
Cocca M,
Gao Y,
Heard-Costa NL,
Evans DS,
Pankratz N
and 30 more — show all
Pratt SR,
Price TR,
Spankovich C,
Stimson MR,
Valle K,
Vuckovic D,
Wells H,
Eiriksdottir G,
Fransen E,
Ikram MA,
Li CM,
Longstreth WT Jr,
Steves C,
Van Camp G,
Correa A,
Cruickshanks KJ,
Gasparini P,
Girotto G,
Kaplan RC,
Nalls M,
Schweinfurth JM,
Seshadri S,
Sotoodehnia N,
Tranah GJ,
Uitterlinden AG,
Wilson JG,
Gudnason V,
Hoffman HJ,
Williams FMK,
Goedegebure A
Scientific reports · 2019 · PMID 31645637 · 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
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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.