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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.
373 matches for
An P,
showing the first 13.
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
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes
Berndt SI,
Vijai J,
Benavente Y,
Camp NJ,
Nieters A,
Wang Z,
Smedby KE,
Kleinstern G,
Hjalgrim H,
Besson C,
Skibola CF,
Morton LM
and 128 more — show all
Brooks-Wilson AR,
Teras LR,
Breeze C,
Arias J,
Adami HO,
Albanes D,
Anderson KC,
Ansell SM,
Bassig B,
Becker N,
Bhatti P,
Birmann BM,
Boffetta P,
Bracci PM,
Brennan P,
Brown EE,
Burdett L,
Cannon-Albright LA,
Chang ET,
Chiu BCH,
Chung CC,
Clavel J,
Cocco P,
Colditz G,
Conde L,
Conti DV,
Cox DG,
Curtin K,
Casabonne D,
De Vivo I,
Diepstra A,
Diver WR,
Dogan A,
Edlund CK,
Foretova L,
Fraumeni JF Jr,
Gabbas A,
Ghesquières H,
Giles GG,
Glaser S,
Glenn M,
Glimelius B,
Gu J,
Habermann TM,
Haiman CA,
Haioun C,
Hofmann JN,
Holford TR,
Holly EA,
Hutchinson A,
Izhar A,
Jackson RD,
Jarrett RF,
Kaaks R,
Kane E,
Kolonel LN,
Kong Y,
Kraft P,
Kricker A,
Lake A,
Lan Q,
Lawrence C,
Li D,
Liebow M,
Link BK,
Magnani C,
Maynadie M,
McKay J,
Melbye M,
Miligi L,
Milne RL,
Molina TJ,
Monnereau A,
Montalvan R,
North KE,
Novak AJ,
Onel K,
Purdue MP,
Rand KA,
Riboli E,
Riby J,
Roman E,
Salles G,
Sborov DW,
Severson RK,
Shanafelt TD,
Smith MT,
Smith A,
Song KW,
Song L,
Southey MC,
Spinelli JJ,
Staines A,
Stephens D,
Sutherland HJ,
Tkachuk K,
Thompson CA,
Tilly H,
Tinker LF,
Travis RC,
Turner J,
Vachon CM,
Vajdic CM,
Van Den Berg A,
Van Den Berg DJ,
Vermeulen RCH,
Vineis P,
Wang SS,
Weiderpass E,
Weiner GJ,
Weinstein S,
Doo NW,
Ye Y,
Yeager M,
Yu K,
Zeleniuch-Jacquotte A,
Zhang Y,
Zheng T,
Ziv E,
Sampson J,
Chatterjee N,
Offit K,
Cozen W,
Wu X,
Cerhan JR,
Chanock SJ,
Slager SL,
Rothman N
Leukemia · 2022 · PMID 36273105
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
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
Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions
Lindström S,
Wang L,
Feng H,
Majumdar A,
Huo S,
Macdonald J,
Harrison T,
Turman C,
Chen H,
Mancuso N,
Bammler T,
Gallinger S
and 49 more — show all
Gruber SB,
Gunter MJ,
Le Marchand L,
Moreno V,
Offit K,
De Vivo I,
O'Mara TA,
Spurdle AB,
Tomlinson I,
Fitzgerald R,
Gharahkhani P,
Gockel I,
Jankowski J,
Macgregor S,
Schumacher J,
Barnholtz-Sloan J,
Bondy ML,
Houlston RS,
Jenkins RB,
Melin B,
Wrensch M,
Brennan P,
Christiani DC,
Johansson M,
Mckay J,
Aldrich MC,
Amos CI,
Landi MT,
Tardon A,
Bishop DT,
Demenais F,
Goldstein AM,
Iles MM,
Kanetsky PA,
Law MH,
Amundadottir LT,
Stolzenberg-Solomon R,
Wolpin BM,
Klein A,
Petersen G,
Risch H,
Chanock SJ,
Purdue MP,
Scelo G,
Pharoah P,
Kar S,
Hung RJ,
Pasaniuc B,
Kraft P
Breast Cancer Association Consortium (BCAC) · Colorectal Transdisciplinary Study (CORECT), Colon Cancer Family Registry Study (CCFR), Genetics And Epidemiology Of Colorectal Cancer Consortium (GECCO) and 5 more consortia
Journal of the National Cancer Institute · 2023 · PMID 36929942
1 page
Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population
Bai H,
Song M,
Lei S,
Jiao L,
Hu X,
Wu T,
Song J,
Liu T,
Peng W,
Zhao Z,
Meng Z,
Ying B
MedComm · 2023 · PMID 37009413 · open access
1 page
Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry
Brandenburg JT,
Chen WC,
Boua PR,
Govender MA,
Agongo G,
Micklesfield LK,
Sorgho H,
Tollman S,
Asiki G,
Mashinya F,
Hazelhurst S,
Morris AP
and 2 more — show all
Frontiers in genetics · 2024 · PMID 38812969 · 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.