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2,673 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.
193 matches for
O D,
showing the first 13.
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Xie J,
Liu L,
Mladkova N,
Li Y,
Ren H,
Wang W,
Cui Z,
Lin L,
Hu X,
Yu X,
Xu J,
Liu G
and 108 more — show all
Caliskan Y,
Sidore C,
Balderes O,
Rosen RJ,
Bodria M,
Zanoni F,
Zhang JY,
Krithivasan P,
Mehl K,
Marasa M,
Khan A,
Ozay F,
Canetta PA,
Bomback AS,
Appel GB,
Sanna-Cherchi S,
Sampson MG,
Mariani LH,
Perkowska-Ptasinska A,
Durlik M,
Mucha K,
Moszczuk B,
Foroncewicz B,
Pączek L,
Habura I,
Ars E,
Ballarin J,
Mani LY,
Vogt B,
Ozturk S,
Yildiz A,
Seyahi N,
Arikan H,
Koc M,
Basturk T,
Karahan G,
Akgul SU,
Sever MS,
Zhang D,
Santoro D,
Bonomini M,
Londrino F,
Gesualdo L,
Reiterova J,
Tesar V,
Izzi C,
Savoldi S,
Spotti D,
Marcantoni C,
Messa P,
Galliani M,
Roccatello D,
Granata S,
Zaza G,
Lugani F,
Ghiggeri G,
Pisani I,
Allegri L,
Sprangers B,
Park JH,
Cho B,
Kim YS,
Kim DK,
Suzuki H,
Amoroso A,
Cattran DC,
Fervenza FC,
Pani A,
Hamilton P,
Harris S,
Gupta S,
Cheshire C,
Dufek S,
Issler N,
Pepper RJ,
Connolly J,
Powis S,
Bockenhauer D,
Stanescu HC,
Ashman N,
Loos RJF,
Kenny EE,
Wuttke M,
Eckardt KU,
Köttgen A,
Hofstra JM,
Coenen MJH,
Kiemeney LA,
Akilesh S,
Kretzler M,
Beck LH,
Stengel B,
Debiec H,
Ronco P,
Wetzels JFM,
Zoledziewska M,
Cucca F,
Ionita-Laza I,
Lee H,
Hoxha E,
Stahl RAK,
Brenchley P,
Scolari F,
Zhao MH,
Gharavi AG,
Kleta R,
Chen N,
Kiryluk K
Nature communications · 2020 · PMID 32231244 · open access
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 of phenotypes based on clustering patterns of hand osteoarthritis identify <i>WNT9A</i> as novel osteoarthritis gene
Boer CG,
Yau MS,
Rice SJ,
Coutinho de Almeida R,
Cheung K,
Styrkarsdottir U,
Southam L,
Broer L,
Wilkinson JM,
Uitterlinden AG,
Zeggini E,
Felson D
and 5 more — show all
Annals of the rheumatic diseases · 2021 · PMID 33055079 · open access
1 page
Genome-Wide Association Study Identifies Risk Loci for Cluster Headache
O'Connor E,
Fourier C,
Ran C,
Sivakumar P,
Liesecke F,
Southgate L,
Harder AVE,
Vijfhuizen LS,
Yip J,
Giffin N,
Silver N,
Ahmed F
and 28 more — show all
Hostettler IC,
Davies B,
Cader MZ,
Simpson BS,
Sullivan R,
Efthymiou S,
Adebimpe J,
Quinn O,
Campbell C,
Cavalleri GL,
Vikelis M,
Kelderman T,
Paemeleire K,
Kilbride E,
Grangeon L,
Lagrata S,
Danno D,
Trembath R,
Wood NW,
Kockum I,
Winsvold BS,
Steinberg A,
Sjöstrand C,
Waldenlind E,
Vandrovcova J,
Houlden H,
Matharu M,
Belin AC
Annals of neurology · 2021 · PMID 34184781 · 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
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
A genome-wide association study on adherence to low-carbohydrate diets in Japanese
Nakamura Y,
Tamura T,
Narita A,
Shimizu A,
Sutoh Y,
Takashima N,
Matsui K,
Miyagawa N,
Kadota A,
Miura K,
Otonari J,
Ikezaki H
and 24 more — show all
Hishida A,
Nagayoshi M,
Okada R,
Kubo Y,
Tanaka K,
Shimanoe C,
Ibusuki R,
Nishimoto D,
Oze I,
Ito H,
Ozaki E,
Matsui D,
Mikami H,
Kusakabe M,
Suzuki S,
Watanabe M,
Arisawa K,
Katsuura-Kamano S,
Kuriki K,
Nakatochi M,
Momozawa Y,
Kubo M,
Takeuchi K,
Wakai K
J-MICC Research Group Consortium
European journal of clinical nutrition · 2022 · PMID 35132194
1 page
Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population
Pan H,
Liu Z,
Ma J,
Li Y,
Zhao Y,
Zhou X,
Xiang Y,
Wang Y,
Zhou X,
He R,
Xie Y,
Zhou Q
and 48 more — show all
Yuan K,
Xu Q,
Sun Q,
Wang J,
Yan X,
Zhang H,
Wang C,
Lei L,
Liu W,
Wang X,
Ding X,
Wang T,
Xue Z,
Zhang Z,
Chen L,
Wang Q,
Liu Y,
Tang J,
Zhang X,
Peng S,
Wang C,
Ding J,
Liu C,
Wang L,
Chen H,
Shen L,
Jiang H,
Wu X,
Tan H,
Luo D,
Xiao S,
Chen X,
Tan J,
Hu Z,
Chen C,
Xia K,
Zhang Z,
Foo JN,
Blauwendraat C,
Nalls MA,
Singleton AB,
Liu J,
Chan P,
Zheng H,
Li J,
Guo J,
Yang J,
Tang B
Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC)
NPJ Parkinson's disease · 2023 · PMID 36759515 · open access
1 page
Case-Case Genome-Wide Analyses Identify Subtype-Informative Variants That Confer Risk for Breast Cancer
Sun X,
Verma SP,
Jia G,
Wang X,
Ping J,
Guo X,
Shu XO,
Chen J,
Derkach A,
Cai Q,
Liang X,
Long J
and 34 more — show all
Offit K,
Oh JH,
Reiner AS,
Watt GP,
Woods M,
Yang Y,
Ambrosone CB,
Ambs S,
Chen Y,
Concannon P,
Garcia-Closas M,
Gu J,
Haiman CA,
Hu JJ,
Huo D,
John EM,
Knight JA,
Li CI,
Lynch CF,
Mellemkjær L,
Nathanson KL,
Nemesure B,
Olopade OI,
Olshan AF,
Pal T,
Palmer JR,
Press MF,
Sanderson M,
Sandler DP,
Troester MA,
Zheng W,
Bernstein JL,
Buas MF,
Shu X
Cancer research · 2024 · PMID 38832928
1 page
Convergent imaging and genetic signatures of gray matter atrophy in Parkinson's disease
Xie Y,
Dong Z,
Jiang Y,
Lin S,
Wang X,
Sun J,
Zhang N,
Zhang Z,
Du J,
Liu H,
Cao D
NeuroImage · 2026 · PMID 42336304
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.