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55 matches for
Ho K,
showing the first 15.
A genome-wide association study of polycystic ovary syndrome identified from electronic health records
Zhang Y,
Ho K,
Keaton JM,
Hartzel DN,
Day F,
Justice AE,
Josyula NS,
Pendergrass SA,
Actkins K,
Davis LK,
Velez Edwards DR,
Holohan B
and 8 more — show all
American journal of obstetrics and gynecology · 2020 · PMID 32289280
2 pages
Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline
Gorski M,
Jung B,
Li Y,
Matias-Garcia PR,
Wuttke M,
Coassin S,
Thio CHL,
Kleber ME,
Winkler TW,
Wanner V,
Chai JF,
Chu AY
and 119 more — show all
Cocca M,
Feitosa MF,
Ghasemi S,
Hoppmann A,
Horn K,
Li M,
Nutile T,
Scholz M,
Sieber KB,
Teumer A,
Tin A,
Wang J,
Tayo BO,
Ahluwalia TS,
Almgren P,
Bakker SJL,
Banas B,
Bansal N,
Biggs ML,
Boerwinkle E,
Bottinger EP,
Brenner H,
Carroll RJ,
Chalmers J,
Chee ML,
Chee ML,
Cheng CY,
Coresh J,
de Borst MH,
Degenhardt F,
Eckardt KU,
Endlich K,
Franke A,
Freitag-Wolf S,
Gampawar P,
Gansevoort RT,
Ghanbari M,
Gieger C,
Hamet P,
Ho K,
Hofer E,
Holleczek B,
Xian Foo VH,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Josyula NS,
Kähönen M,
Khor CC,
Koenig W,
Kramer H,
Krämer BK,
Kühnel B,
Lange LA,
Lehtimäki T,
Lieb W,
Loos RJF,
Lukas MA,
Lyytikäinen LP,
Meisinger C,
Meitinger T,
Melander O,
Milaneschi Y,
Mishra PP,
Mononen N,
Mychaleckyj JC,
Nadkarni GN,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
O'Donoghue ML,
Orho-Melander M,
Pendergrass SA,
Penninx BWJH,
Preuss MH,
Psaty BM,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rosenkranz AR,
Rossing P,
Rotter JI,
Sabanayagam C,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Sedaghat S,
Shaffer CM,
Strauch K,
Szymczak S,
Taylor KD,
Tremblay J,
Chaker L,
van der Harst P,
van der Most PJ,
Verweij N,
Völker U,
Waldenberger M,
Wallentin L,
Waterworth DM,
White HD,
Wilson JG,
Wong TY,
Woodward M,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang Y,
Snieder H,
Wanner C,
Böger CA,
Köttgen A,
Kronenberg F,
Pattaro C,
Heid IM
Lifelines Cohort Study · Regeneron Genetics Center
Kidney international · 2021 · PMID 33137338
2 pages
Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure
Rasooly D,
Peloso GM,
Pereira AC,
Dashti H,
Giambartolomei C,
Wheeler E,
Aung N,
Ferolito BR,
Pietzner M,
Farber-Eger EH,
Wells QS,
Kosik NM
and 22 more — show all
Gaziano L,
Posner DC,
Bento AP,
Hui Q,
Liu C,
Aragam K,
Wang Z,
Charest B,
Huffman JE,
Wilson PWF,
Phillips LS,
Whittaker J,
Munroe PB,
Petersen SE,
Cho K,
Leach AR,
Magariños MP,
Gaziano JM,
Langenberg C,
Sun YV,
Joseph J,
Casas JP
VA Million Veteran Program
Nature communications · 2023 · PMID 37429843 · open access
2 pages
Identification of common variants associated with human hippocampal and intracranial volumes
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Senstad RE,
Winkler AM,
Toro R,
Appel K,
Bartecek R,
Bergmann Ø,
Bernard M,
Brown AA
and 190 more — show all
Cannon DM,
Chakravarty MM,
Christoforou A,
Domin M,
Grimm O,
Hollinshead M,
Holmes AJ,
Homuth G,
Hottenga JJ,
Langan C,
Lopez LM,
Hansell NK,
Hwang KS,
Kim S,
Laje G,
Lee PH,
Liu X,
Loth E,
Lourdusamy A,
Mattingsdal M,
Mohnke S,
Maniega SM,
Nho K,
Nugent AC,
O'Brien C,
Papmeyer M,
Pütz B,
Ramasamy A,
Rasmussen J,
Rijpkema M,
Risacher SL,
Roddey JC,
Rose EJ,
Ryten M,
Shen L,
Sprooten E,
Strengman E,
Teumer A,
Trabzuni D,
Turner J,
van Eijk K,
van Erp TG,
van Tol MJ,
Wittfeld K,
Wolf C,
Woudstra S,
Aleman A,
Alhusaini S,
Almasy L,
Binder EB,
Brohawn DG,
Cantor RM,
Carless MA,
Corvin A,
Czisch M,
Curran JE,
Davies G,
de Almeida MA,
Delanty N,
Depondt C,
Duggirala R,
Dyer TD,
Erk S,
Fagerness J,
Fox PT,
Freimer NB,
Gill M,
Göring HH,
Hagler DJ,
Hoehn D,
Holsboer F,
Hoogman M,
Hosten N,
Jahanshad N,
Johnson MP,
Kasperaviciute D,
Kent JW Jr,
Kochunov P,
Lancaster JL,
Lawrie SM,
Liewald DC,
Mandl R,
Matarin M,
Mattheisen M,
Meisenzahl E,
Melle I,
Moses EK,
Mühleisen TW,
Nauck M,
Nöthen MM,
Olvera RL,
Pandolfo M,
Pike GB,
Puls R,
Reinvang I,
Rentería ME,
Rietschel M,
Roffman JL,
Royle NA,
Rujescu D,
Savitz J,
Schnack HG,
Schnell K,
Seiferth N,
Smith C,
Steen VM,
Valdés Hernández MC,
Van den Heuvel M,
van der Wee NJ,
Van Haren NE,
Veltman JA,
Völzke H,
Walker R,
Westlye LT,
Whelan CD,
Agartz I,
Boomsma DI,
Cavalleri GL,
Dale AM,
Djurovic S,
Drevets WC,
Hagoort P,
Hall J,
Heinz A,
Jack CR Jr,
Foroud TM,
Le Hellard S,
Macciardi F,
Montgomery GW,
Poline JB,
Porteous DJ,
Sisodiya SM,
Starr JM,
Sussmann J,
Toga AW,
Veltman DJ,
Walter H,
Weiner MW,
Bis JC,
Ikram MA,
Smith AV,
Gudnason V,
Tzourio C,
Vernooij MW,
Launer LJ,
DeCarli C,
Seshadri S,
Andreassen OA,
Apostolova LG,
Bastin ME,
Blangero J,
Brunner HG,
Buckner RL,
Cichon S,
Coppola G,
de Zubicaray GI,
Deary IJ,
Donohoe G,
de Geus EJ,
Espeseth T,
Fernández G,
Glahn DC,
Grabe HJ,
Hardy J,
Hulshoff Pol HE,
Jenkinson M,
Kahn RS,
McDonald C,
McIntosh AM,
McMahon FJ,
McMahon KL,
Meyer-Lindenberg A,
Morris DW,
Müller-Myhsok B,
Nichols TE,
Ophoff RA,
Paus T,
Pausova Z,
Penninx BW,
Potkin SG,
Sämann PG,
Saykin AJ,
Schumann G,
Smoller JW,
Wardlaw JM,
Weale ME,
Martin NG,
Franke B,
Wright MJ,
Thompson PM
Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium and 4 more consortia
Nature genetics · 2012 · PMID 22504417
1 page
Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies
Fang H,
Hui Q,
Lynch J,
Honerlaw J,
Assimes TL,
Huang J,
Vujkovic M,
Damrauer SM,
Pyarajan S,
Gaziano JM,
DuVall SL,
O'Donnell CJ
and 6 more — show all
VA Million Veteran Program
American journal of human genetics · 2019 · PMID 31564439
1 page
A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages
Park JY,
Lee D,
Lee JJ,
Gim J,
Gunasekaran TI,
Choi KY,
Kang S,
Do AR,
Jo J,
Park J,
Park K,
Li D
and 21 more — show all
Lee S,
Kim H,
Dhanasingh I,
Ghosh S,
Keum S,
Choi JH,
Song GJ,
Sael L,
Rhee S,
Lovestone S,
Kim E,
Moon SH,
Kim BC,
Kim S,
Saykin AJ,
Nho K,
Lee SH,
Farrer LA,
Jun GR,
Won S,
Lee KH
Alzheimer’s Disease Neuroimaging Initiative
Translational psychiatry · 2021 · PMID 34785643 · open access
1 page
Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci
Bellomo TR,
Bone WP,
Chen BY,
Gawronski KAB,
Zhang D,
Park J,
Levin M,
Tsao N,
Klarin D,
Lynch J,
Assimes TL,
Gaziano JM
and 10 more — show all
Frontiers in genetics · 2021 · PMID 35186008 · open access
1 page
Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program
Huang RDL,
Nguyen XT,
Peloso GM,
Trinder M,
Posner DC,
Aragam KG,
Ho YL,
Lynch JA,
Damrauer SM,
Chang KM,
Tsao PS,
Natarajan P
and 7 more — show all
Veterans Affairs’ Million Veteran Program
PloS one · 2022 · PMID 35613103 · open access
1 page
Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning
Lahti J,
Tuominen S,
Yang Q,
Pergola G,
Ahmad S,
Amin N,
Armstrong NJ,
Beiser A,
Bey K,
Bis JC,
Boerwinkle E,
Bressler J
and 112 more — show all
Campbell A,
Campbell H,
Chen Q,
Corley J,
Cox SR,
Davies G,
De Jager PL,
Derks EM,
Faul JD,
Fitzpatrick AL,
Fohner AE,
Ford I,
Fornage M,
Gerring Z,
Grabe HJ,
Grodstein F,
Gudnason V,
Simonsick E,
Holliday EG,
Joshi PK,
Kajantie E,
Kaprio J,
Karell P,
Kleineidam L,
Knol MJ,
Kochan NA,
Kwok JB,
Leber M,
Lam M,
Lee T,
Li S,
Loukola A,
Luck T,
Marioni RE,
Mather KA,
Medland S,
Mirza SS,
Nalls MA,
Nho K,
O'Donnell A,
Oldmeadow C,
Painter J,
Pattie A,
Reppermund S,
Risacher SL,
Rose RJ,
Sadashivaiah V,
Scholz M,
Satizabal CL,
Schofield PW,
Schraut KE,
Scott RJ,
Simino J,
Smith AV,
Smith JA,
Stott DJ,
Surakka I,
Teumer A,
Thalamuthu A,
Trompet S,
Turner ST,
van der Lee SJ,
Villringer A,
Völker U,
Wilson RS,
Wittfeld K,
Vuoksimaa E,
Xia R,
Yaffe K,
Yu L,
Zare H,
Zhao W,
Zhao W,
Ames D,
Attia J,
Bennett DA,
Brodaty H,
Chasman DI,
Goldman AL,
Hayward C,
Ikram MA,
Jukema JW,
Kardia SLR,
Lencz T,
Loeffler M,
Mattay VS,
Palotie A,
Psaty BM,
Ramirez A,
Ridker PM,
Riedel-Heller SG,
Sachdev PS,
Saykin AJ,
Scherer M,
Schofield PR,
Sidney S,
Starr JM,
Trollor J,
Ulrich W,
Wagner M,
Weir DR,
Wilson JF,
Wright MJ,
Weinberger DR,
Debette S,
Eriksson JG,
Mosley TH Jr,
Launer LJ,
van Duijn CM,
Deary IJ,
Seshadri S,
Räikkönen K
Molecular psychiatry · 2022 · PMID 35974141 · open access
1 page
African ancestry GWAS of dementia in a large military cohort identifies significant risk loci
Sherva R,
Zhang R,
Sahelijo N,
Jun G,
Anglin T,
Chanfreau C,
Cho K,
Fonda JR,
Gaziano JM,
Harrington KM,
Ho YL,
Kremen WS
and 16 more — show all
Litkowski E,
Lynch J,
Neale Z,
Roussos P,
Marra D,
Mez J,
Miller MW,
Salat DH,
Tsuang D,
Wolf E,
Zeng Q,
Panizzon MS,
Merritt VC,
Farrer LA,
Hauger RL,
Logue MW
Molecular psychiatry · 2023 · PMID 36543923
1 page
Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry
Chen F,
Madduri RK,
Rodriguez AA,
Darst BF,
Chou A,
Sheng X,
Wang A,
Shen J,
Saunders EJ,
Rhie SK,
Bensen JT,
Ingles SA
and 106 more — show all
Kittles RA,
Strom SS,
Rybicki BA,
Nemesure B,
Isaacs WB,
Stanford JL,
Zheng W,
Sanderson M,
John EM,
Park JY,
Xu J,
Wang Y,
Berndt SI,
Huff CD,
Yeboah ED,
Tettey Y,
Lachance J,
Tang W,
Rentsch CT,
Cho K,
Mcmahon BH,
Biritwum RB,
Adjei AA,
Tay E,
Truelove A,
Niwa S,
Sellers TA,
Yamoah K,
Murphy AB,
Crawford DC,
Patel AV,
Bush WS,
Aldrich MC,
Cussenot O,
Petrovics G,
Cullen J,
Neslund-Dudas CM,
Stern MC,
Kote-Jarai Z,
Govindasami K,
Cook MB,
Chokkalingam AP,
Hsing AW,
Goodman PJ,
Hoffmann TJ,
Drake BF,
Hu JJ,
Keaton JM,
Hellwege JN,
Clark PE,
Jalloh M,
Gueye SM,
Niang L,
Ogunbiyi O,
Idowu MO,
Popoola O,
Adebiyi AO,
Aisuodionoe-Shadrach OI,
Ajibola HO,
Jamda MA,
Oluwole OP,
Nwegbu M,
Adusei B,
Mante S,
Darkwa-Abrahams A,
Mensah JE,
Diop H,
Van Den Eeden SK,
Blanchet P,
Fowke JH,
Casey G,
Hennis AJ,
Lubwama A,
Thompson IM Jr,
Leach R,
Easton DF,
Preuss MH,
Loos RJ,
Gundell SM,
Wan P,
Mohler JL,
Fontham ET,
Smith GJ,
Taylor JA,
Srivastava S,
Eeles RA,
Carpten JD,
Kibel AS,
Multigner L,
Parent MÉ,
Menegaux F,
Cancel-Tassin G,
Klein EA,
Andrews C,
Rebbeck TR,
Brureau L,
Ambs S,
Edwards TL,
Watya S,
Chanock SJ,
Witte JS,
Blot WJ,
Michael Gaziano J,
Justice AC,
Conti DV,
Haiman CA
European urology · 2023 · PMID 36872133
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.