For researchers
Is your paper here?
2,661 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.
14 matches for
Pei Y.
Joint Genome-Wide Association Analyses Identified 49 Novel Loci For Age at Natural Menopause
Zhang L,
Wei XT,
Niu JJ,
Lin ZX,
Xu Q,
Ni JJ,
Zhang WL,
Han BX,
Yan SS,
Feng GJ,
Zhang H,
Yang XL
and 5 more — show all
The Journal of clinical endocrinology and metabolism · 2021 · PMID 34050765
12 pages+
Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis
Zhang H,
Liu L,
Ni JJ,
Wei XT,
Feng GJ,
Yang XL,
Xu Q,
Zhang ZJ,
Hai R,
Tian Q,
Shen H,
Deng HW
and 2 more — show all
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2020 · PMID 32314116
11 pages
Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density
Pei YF,
Hu WZ,
Yan MW,
Li CW,
Liu L,
Yang XL,
Hai R,
Wang XY,
Shen H,
Tian Q,
Deng HW,
Zhang L
Bone · 2018 · PMID 29499414
10 pages
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Kiryluk K,
Sanchez-Rodriguez E,
Zhou XJ,
Zanoni F,
Liu L,
Mladkova N,
Khan A,
Marasa M,
Zhang JY,
Balderes O,
Sanna-Cherchi S,
Bomback AS
and 177 more — show all
Canetta PA,
Appel GB,
Radhakrishnan J,
Trimarchi H,
Sprangers B,
Cattran DC,
Reich H,
Pei Y,
Ravani P,
Galesic K,
Maixnerova D,
Tesar V,
Stengel B,
Metzger M,
Canaud G,
Maillard N,
Berthoux F,
Berthelot L,
Pillebout E,
Monteiro R,
Nelson R,
Wyatt RJ,
Smoyer W,
Mahan J,
Samhar AA,
Hidalgo G,
Quiroga A,
Weng P,
Sreedharan R,
Selewski D,
Davis K,
Kallash M,
Vasylyeva TL,
Rheault M,
Chishti A,
Ranch D,
Wenderfer SE,
Samsonov D,
Claes DJ,
Akchurin O,
Goumenos D,
Stangou M,
Nagy J,
Kovacs T,
Fiaccadori E,
Amoroso A,
Barlassina C,
Cusi D,
Del Vecchio L,
Battaglia GG,
Bodria M,
Boer E,
Bono L,
Boscutti G,
Caridi G,
Lugani F,
Ghiggeri G,
Coppo R,
Peruzzi L,
Esposito V,
Esposito C,
Feriozzi S,
Polci R,
Frasca G,
Galliani M,
Garozzo M,
Mitrotti A,
Gesualdo L,
Granata S,
Zaza G,
Londrino F,
Magistroni R,
Pisani I,
Magnano A,
Marcantoni C,
Messa P,
Mignani R,
Pani A,
Ponticelli C,
Roccatello D,
Salvadori M,
Salvi E,
Santoro D,
Gembillo G,
Savoldi S,
Spotti D,
Zamboli P,
Izzi C,
Alberici F,
Delbarba E,
Florczak M,
Krata N,
Mucha K,
Pączek L,
Niemczyk S,
Moszczuk B,
Pańczyk-Tomaszewska M,
Mizerska-Wasiak M,
Perkowska-Ptasińska A,
Bączkowska T,
Durlik M,
Pawlaczyk K,
Sikora P,
Zaniew M,
Kaminska D,
Krajewska M,
Kuzmiuk-Glembin I,
Heleniak Z,
Bullo-Piontecka B,
Liberek T,
Dębska-Slizien A,
Hryszko T,
Materna-Kiryluk A,
Miklaszewska M,
Szczepańska M,
Szczepańska M,
Dyga K,
Machura E,
Siniewicz-Luzeńczyk K,
Pawlak-Bratkowska M,
Tkaczyk M,
Runowski D,
Kwella N,
Drożdż D,
Habura I,
Kronenberg F,
Prikhodina L,
van Heel D,
Fontaine B,
Cotsapas C,
Wijmenga C,
Franke A,
Annese V,
Gregersen PK,
Parameswaran S,
Weirauch M,
Kottyan L,
Harley JB,
Suzuki H,
Narita I,
Goto S,
Lee H,
Kim DK,
Kim YS,
Park JH,
Cho B,
Choi M,
Van Wijk A,
Huerta A,
Ars E,
Ballarin J,
Lundberg S,
Vogt B,
Mani LY,
Caliskan Y,
Barratt J,
Abeygunaratne T,
Kalra PA,
Gale DP,
Panzer U,
Rauen T,
Floege J,
Schlosser P,
Ekici AB,
Eckardt KU,
Chen N,
Xie J,
Lifton RP,
Loos RJF,
Kenny EE,
Ionita-Laza I,
Köttgen A,
Julian BA,
Novak J,
Scolari F,
Zhang H,
Gharavi AG
Nature genetics · 2023 · PMID 37337107
3 pages
Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene
Choi HJ,
Park H,
Zhang L,
Kim JH,
Kim YA,
Yang JY,
Pei YF,
Tian Q,
Shen H,
Hwang JY,
Deng HW,
Cho NH
and 1 more — show all
Bone · 2016 · PMID 27424934
2 pages
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity
Pei YF,
Zhang L,
Liu Y,
Li J,
Shen H,
Liu YZ,
Tian Q,
He H,
Wu S,
Ran S,
Han Y,
Hai R
and 5 more — show all
Human molecular genetics · 2014 · PMID 24064335
1 page
Association of 3q13.32 variants with hip trochanter and intertrochanter bone mineral density identified by a genome-wide association study
Pei YF,
Xie ZG,
Wang XY,
Hu WZ,
Li LB,
Ran S,
Lin Y,
Hai R,
Shen H,
Tian Q,
Zhang YH,
Lei SF
and 3 more — show all
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016 · PMID 27311723
1 page
Two novel pleiotropic loci associated with osteoporosis and abdominal obesity
Liu L,
Yang XL,
Zhang H,
Zhang ZJ,
Wei XT,
Feng GJ,
Liu J,
Peng HP,
Hai R,
Shen H,
Tian Q,
Deng HW
and 2 more — show all
Human genetics · 2020 · PMID 32239398
1 page
Four pleiotropic loci associated with fat mass and lean mass
Liu Y,
Ran S,
Lin Y,
Zhang YX,
Yang XL,
Wei XT,
Jiang ZX,
He X,
Zhang H,
Feng GJ,
Shen H,
Tian Q
and 3 more — show all
International journal of obesity (2005) · 2020 · PMID 32719433
1 page
Integrative exome sequencing and multi-omics analysis elucidates the regulatory role of rare variants in metabolic syndrome
Wu CX,
Sang J,
Xu Q,
Zhan Y,
Yuan SJ,
Ge YY,
Yu XJ,
Zheng X,
Wang XF,
He XM,
Liu CJ,
Luo Y
and 2 more — show all
Functional & integrative genomics · 2026 · PMID 42472903
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.