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2,677 papers hold this site up. Every variant and condition page names
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11 matches for
McHugh C.
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Hu Y,
Stilp AM,
McHugh CP,
Rao S,
Jain D,
Zheng X,
Lane J,
Méric de Bellefon S,
Raffield LM,
Chen MH,
Yanek LR,
Wheeler M
and 67 more — show all
Yao Y,
Ren C,
Broome J,
Moon JY,
de Vries PS,
Hobbs BD,
Sun Q,
Surendran P,
Brody JA,
Blackwell TW,
Choquet H,
Ryan K,
Duggirala R,
Heard-Costa N,
Wang Z,
Chami N,
Preuss MH,
Min N,
Ekunwe L,
Lange LA,
Cushman M,
Faraday N,
Curran JE,
Almasy L,
Kundu K,
Smith AV,
Gabriel S,
Rotter JI,
Fornage M,
Lloyd-Jones DM,
Vasan RS,
Smith NL,
North KE,
Boerwinkle E,
Becker LC,
Lewis JP,
Abecasis GR,
Hou L,
O'Connell JR,
Morrison AC,
Beaty TH,
Kaplan R,
Correa A,
Blangero J,
Jorgenson E,
Psaty BM,
Kooperberg C,
Walton RT,
Kleinstiver BP,
Tang H,
Loos RJF,
Soranzo N,
Butterworth AS,
Nickerson D,
Rich SS,
Mitchell BD,
Johnson AD,
Auer PL,
Li Y,
Mathias RA,
Lettre G,
Pankratz N,
Laurie CC,
Laurie CA,
Bauer DE,
Conomos MP,
Reiner AP
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
American journal of human genetics · 2021 · PMID 33887194
12 pages+
Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos
Hodonsky CJ,
Jain D,
Schick UM,
Morrison JV,
Brown L,
McHugh CP,
Schurmann C,
Chen DD,
Liu YM,
Auer PL,
Laurie CA,
Taylor KD
and 15 more — show all
Browning BL,
Li Y,
Papanicolaou G,
Rotter JI,
Kurita R,
Nakamura Y,
Browning SR,
Loos RJF,
North KE,
Laurie CC,
Thornton TA,
Pankratz N,
Bauer DE,
Sofer T,
Reiner AP
PLoS genetics · 2017 · PMID 28453575 · open access
4 pages
Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations
Kowalski MH,
Qian H,
Hou Z,
Rosen JD,
Tapia AL,
Shan Y,
Jain D,
Argos M,
Arnett DK,
Avery C,
Barnes KC,
Becker LC
and 66 more — show all
Bien SA,
Bis JC,
Blangero J,
Boerwinkle E,
Bowden DW,
Buyske S,
Cai J,
Cho MH,
Choi SH,
Choquet H,
Cupples LA,
Cushman M,
Daya M,
de Vries PS,
Ellinor PT,
Faraday N,
Fornage M,
Gabriel S,
Ganesh SK,
Graff M,
Gupta N,
He J,
Heckbert SR,
Hidalgo B,
Hodonsky CJ,
Irvin MR,
Johnson AD,
Jorgenson E,
Kaplan R,
Kardia SLR,
Kelly TN,
Kooperberg C,
Lasky-Su JA,
Loos RJF,
Lubitz SA,
Mathias RA,
McHugh CP,
Montgomery C,
Moon JY,
Morrison AC,
Palmer ND,
Pankratz N,
Papanicolaou GJ,
Peralta JM,
Peyser PA,
Rich SS,
Rotter JI,
Silverman EK,
Smith JA,
Smith NL,
Taylor KD,
Thornton TA,
Tiwari HK,
Tracy RP,
Wang T,
Weiss ST,
Weng LC,
Wiggins KL,
Wilson JG,
Yanek LR,
Zöllner S,
North KE,
Auer PL,
Raffield LM,
Reiner AP,
Li Y
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium · TOPMed Hematology & Hemostasis Working Group
PLoS genetics · 2019 · PMID 31869403 · open access
3 pages
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies
Hayes MG,
Urbanek M,
Hivert MF,
Armstrong LL,
Morrison J,
Guo C,
Lowe LP,
Scheftner DA,
Pluzhnikov A,
Levine DM,
McHugh CP,
Ackerman CM
and 12 more — show all
Bouchard L,
Brisson D,
Layden BT,
Mirel D,
Doheny KF,
Leya MV,
Lown-Hecht RN,
Dyer AR,
Metzger BE,
Reddy TE,
Cox NJ,
Lowe WL Jr
HAPO Study Cooperative Research Group
Diabetes · 2013 · PMID 23903356 · open access
2 pages
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
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Desch KC,
Ozel AB,
Siemieniak D,
Kalish Y,
Shavit JA,
Thornburg CD,
Sharathkumar AA,
McHugh CP,
Laurie CC,
Crenshaw A,
Mirel DB,
Kim Y
and 10 more — show all
Proceedings of the National Academy of Sciences of the United States of America · 2013 · PMID 23267103
1 page
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study
Urbanek M,
Hayes MG,
Armstrong LL,
Morrison J,
Lowe LP,
Badon SE,
Scheftner D,
Pluzhnikov A,
Levine D,
Laurie CC,
McHugh C,
Ackerman CM
and 9 more — show all
HAPO Study Cooperative Research Group
Human molecular genetics · 2013 · PMID 23575227
1 page
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans
Schick UM,
Jain D,
Hodonsky CJ,
Morrison JV,
Davis JP,
Brown L,
Sofer T,
Conomos MP,
Schurmann C,
McHugh CP,
Nelson SC,
Vadlamudi S
and 26 more — show all
Stilp A,
Plantinga A,
Baier L,
Bien SA,
Gogarten SM,
Laurie CA,
Taylor KD,
Liu Y,
Auer PL,
Franceschini N,
Szpiro A,
Rice K,
Kerr KF,
Rotter JI,
Hanson RL,
Papanicolaou G,
Rich SS,
Loos RJ,
Browning BL,
Browning SR,
Weir BS,
Laurie CC,
Mohlke KL,
North KE,
Thornton TA,
Reiner AP
American journal of human genetics · 2016 · PMID 26805783
1 page
Multiethnic genome-wide and HLA association study of total serum IgE level
Daya M,
Cox C,
Acevedo N,
Boorgula MP,
Campbell M,
Chavan S,
Cho MH,
David GL,
Kachroo P,
Lasky-Su J,
Li X,
McHugh CP
and 35 more — show all
Qiao D,
Rafaels N,
Beck LA,
Bleecker ER,
Caraballo L,
Cupples AL,
Figueiredo CA,
Gallo RL,
Hanifin J,
Hansel NN,
Hata TR,
Hersh CP,
Knight-Madden J,
Leung DYM,
Guttman-Yassky E,
Meyers DA,
O'Connor G,
Ober C,
Ong PY,
Ortega VE,
Paller AS,
Putcha N,
Reed RM,
Schneider LC,
Silverman EK,
Slifka MK,
Spergel JM,
Vasan RS,
Viaud-Martinez KA,
Watson H,
Weiss ST,
Ruczinski I,
Beaty TH,
Mathias RA,
Barnes KC
NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
The Journal of allergy and clinical immunology · 2021 · PMID 34536413
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
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.