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Is your paper here?
2,657 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
Xu X.
Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes
Liu N,
Zhang L,
Tian T,
Cheng J,
Zhang B,
Qiu S,
Geng Z,
Cui G,
Zhang Q,
Liao W,
Yu Y,
Zhang H
and 32 more — show all
Gao B,
Xu X,
Han T,
Yao Z,
Qin W,
Liu F,
Liang M,
Xu Q,
Fu J,
Xu J,
Zhu W,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Li J,
Zhang J,
Wang D,
Shen W,
Miao Y,
Xian J,
Gao JH,
Zhang X,
Li MJ,
Xu K,
Zuo XN,
Wang M,
Ye Z,
Yu C
CHIMGEN Consortium
Nature genetics · 2023 · PMID 37337106
12 pages+
Cross-ancestry genome-wide association studies of brain imaging phenotypes
Fu J,
Zhang Q,
Wang J,
Wang M,
Zhang B,
Zhu W,
Qiu S,
Geng Z,
Cui G,
Yu Y,
Liao W,
Zhang H
and 32 more — show all
Gao B,
Xu X,
Han T,
Yao Z,
Qin W,
Liu F,
Liang M,
Wang S,
Xu Q,
Xu J,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Zhang J,
Li J,
Shen W,
Miao Y,
Wang D,
Xian J,
Gao JH,
Zhang X,
Xu K,
Zuo XN,
Zhang L,
Ye Z,
Cheng J,
Li MJ,
Yu C
CHIMGEN Consortium
Nature genetics · 2024 · PMID 38811844
12 pages+
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy
Tadros R,
Zheng SL,
Grace C,
Jordà P,
Francis C,
West DM,
Jurgens SJ,
Thomson KL,
Harper AR,
Ormondroyd E,
Xu X,
Theotokis PI
and 50 more — show all
Buchan RJ,
McGurk KA,
Mazzarotto F,
Boschi B,
Pelo E,
Lee M,
Noseda M,
Varnava A,
Vermeer AMC,
Walsh R,
Amin AS,
van Slegtenhorst MA,
Roslin NM,
Strug LJ,
Salvi E,
Lanzani C,
de Marvao A,
Roberts JD,
Tremblay-Gravel M,
Giraldeau G,
Cadrin-Tourigny J,
L'Allier PL,
Garceau P,
Talajic M,
Gagliano Taliun SA,
Pinto YM,
Rakowski H,
Pantazis A,
Bai W,
Baksi J,
Halliday BP,
Prasad SK,
Barton PJR,
O'Regan DP,
Cook SA,
de Boer RA,
Christiaans I,
Michels M,
Kramer CM,
Ho CY,
Neubauer S,
Matthews PM,
Wilde AAM,
Tardif JC,
Olivotto I,
Adler A,
Goel A,
Ware JS,
Bezzina CR,
Watkins H
Hypergenes InterOmics Collaborators · HCMR Investigators
Nature genetics · 2025 · PMID 39966646 · open access
12 pages+
Cross-ancestry and sex-stratified genome-wide association analyses of amygdala and subnucleus volumes
Ji Y,
Liu N,
Yang Y,
Wang M,
Cheng J,
Zhu W,
Qiu S,
Geng Z,
Cui G,
Yu Y,
Liao W,
Zhang H
and 33 more — show all
Gao B,
Xu X,
Han T,
Yao Z,
Zhang Q,
Qin W,
Liu F,
Liang M,
Wang S,
Xu Q,
Xu J,
Fu J,
Zhang P,
Li W,
Shi D,
Wang C,
Lui S,
Yan Z,
Chen F,
Zhang J,
Shen W,
Miao Y,
Wang D,
Gao JH,
Zhang X,
Xu K,
Zuo XN,
Zhang L,
Ye Z,
Li MJ,
Xian J,
Zhang B,
Yu C
CHIMGEN Consortium
Nature genetics · 2025 · PMID 40097784
12 pages+
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Tadros R,
Francis C,
Xu X,
Vermeer AMC,
Harper AR,
Huurman R,
Kelu Bisabu K,
Walsh R,
Hoorntje ET,
Te Rijdt WP,
Buchan RJ,
van Velzen HG
and 58 more — show all
van Slegtenhorst MA,
Vermeulen JM,
Offerhaus JA,
Bai W,
de Marvao A,
Lahrouchi N,
Beekman L,
Karper JC,
Veldink JH,
Kayvanpour E,
Pantazis A,
Baksi AJ,
Whiffin N,
Mazzarotto F,
Sloane G,
Suzuki H,
Schneider-Luftman D,
Elliott P,
Richard P,
Ader F,
Villard E,
Lichtner P,
Meitinger T,
Tanck MWT,
van Tintelen JP,
Thain A,
McCarty D,
Hegele RA,
Roberts JD,
Amyot J,
Dubé MP,
Cadrin-Tourigny J,
Giraldeau G,
L'Allier PL,
Garceau P,
Tardif JC,
Boekholdt SM,
Lumbers RT,
Asselbergs FW,
Barton PJR,
Cook SA,
Prasad SK,
O'Regan DP,
van der Velden J,
Verweij KJH,
Talajic M,
Lettre G,
Pinto YM,
Meder B,
Charron P,
de Boer RA,
Christiaans I,
Michels M,
Wilde AAM,
Watkins H,
Matthews PM,
Ware JS,
Bezzina CR
Nature genetics · 2021 · PMID 33495596 · open access
10 pages
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity
Harper AR,
Goel A,
Grace C,
Thomson KL,
Petersen SE,
Xu X,
Waring A,
Ormondroyd E,
Kramer CM,
Ho CY,
Neubauer S,
Tadros R
and 4 more — show all
HCMR Investigators
Nature genetics · 2021 · PMID 33495597
7 pages
Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas
Hughes O,
Bentley AR,
Breeze CE,
Aguet F,
Xu X,
Nadkarni G,
Sun Q,
Lin BM,
Gilliland T,
Meyer MC,
Du J,
Raffield LM
and 62 more — show all
Kramer H,
Morton RW,
Gouveia MH,
Atkinson EG,
Valladares-Salgado A,
Wacher-Rodarte N,
Dueker ND,
Guo X,
Hai Y,
Adeyemo A,
Best LG,
Cai J,
Chen G,
Chong M,
Doumatey A,
Eales J,
Goodarzi MO,
Ipp E,
Irvin MR,
Jiang M,
Jones AC,
Kooperberg C,
Krieger JE,
Lange EM,
Lanktree MB,
Lash JP,
Lotufo PA,
Loos RJF,
Ha My VT,
Peralta-Romero J,
Qi L,
Raffel LJ,
Rich SS,
Rodriquez EJ,
Tarazona-Santos E,
Taylor KD,
Umans JG,
Wen J,
Young BA,
Yu Z,
Zhang Y,
Ida Chen YD,
Rundek T,
Rotter JI,
Cruz M,
Fornage M,
Lima-Costa MF,
Pereira AC,
Paré G,
Natarajan P,
Cole SA,
Carson AP,
Lange LA,
Li Y,
Perez-Stable EJ,
Do R,
Charchar FJ,
Tomaszewski M,
Mychaleckyj JC,
Rotimi C,
Morris AP,
Franceschini N
Cell genomics · 2024 · PMID 38190104 · open access
5 pages
Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome
Liu X,
Tong X,
Zhu J,
Tian L,
Jie Z,
Zou Y,
Lin X,
Liang H,
Li W,
Ju Y,
Qin Y,
Zou L
and 11 more — show all
Lu H,
Zhu S,
Jin X,
Xu X,
Yang H,
Wang J,
Zong Y,
Liu W,
Hou Y,
Jia H,
Zhang T
Cell discovery · 2021 · PMID 34873157 · open access
3 pages
The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay
Cheng S,
Xu Z,
Bian S,
Chen X,
Shi Y,
Li Y,
Duan Y,
Liu Y,
Lin J,
Jiang Y,
Jing J,
Li Z
and 11 more — show all
Wang Y,
Meng X,
Liu Y,
Fang M,
Jin X,
Xu X,
Wang J,
Wang C,
Li H,
Liu S,
Wang Y
Cell discovery · 2023 · PMID 37479695 · open access
3 pages
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis
Guo Y,
Tan LJ,
Lei SF,
Yang TL,
Chen XD,
Zhang F,
Chen Y,
Pan F,
Yan H,
Liu X,
Tian Q,
Zhang ZX
and 21 more — show all
Zhou Q,
Qiu C,
Dong SS,
Xu XH,
Guo YF,
Zhu XZ,
Liu SL,
Wang XL,
Li X,
Luo Y,
Zhang LS,
Li M,
Wang JT,
Wen T,
Drees B,
Hamilton J,
Papasian CJ,
Recker RR,
Song XP,
Cheng J,
Deng HW
PLoS genetics · 2010 · PMID 20072603 · open access
2 pages
Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population
Zhang Z,
Li H,
Weng H,
Zhou G,
Chen H,
Yang G,
Zhang P,
Zhang X,
Ji Y,
Ying K,
Liu B,
Xu Q
and 36 more — show all
Tang Y,
Zhu G,
Liu Z,
Xia S,
Yang X,
Dong L,
Zhu L,
Zeng M,
Yuan Y,
Yang Y,
Zhang N,
Xu X,
Pang W,
Zhang M,
Zhang Y,
Zhen K,
Wang D,
Lei J,
Wu S,
Shu S,
Zhang Y,
Zhang S,
Gao Q,
Huang Q,
Deng C,
Fu X,
Chen G,
Duan W,
Wan J,
Xie W,
Zhang P,
Wang S,
Yang P,
Zuo X,
Zhai Z,
Wang C
China pUlmonary Thromboembolism REgistry Study (CURES) investigators
BMC medicine · 2023 · PMID 37076872 · open access
2 pages
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese
Li Y,
Si L,
Zhai Y,
Hu Y,
Hu Z,
Bei JX,
Xie B,
Ren Q,
Cao P,
Yang F,
Song Q,
Bao Z
and 38 more — show all
Zhang H,
Han Y,
Wang Z,
Chen X,
Xia X,
Yan H,
Wang R,
Zhang Y,
Gao C,
Meng J,
Tu X,
Liang X,
Cui Y,
Liu Y,
Wu X,
Li Z,
Wang H,
Li Z,
Hu B,
He M,
Gao Z,
Xu X,
Ji H,
Yu C,
Sun Y,
Xing B,
Yang X,
Zhang H,
Tan A,
Wu C,
Jia W,
Li S,
Zeng YX,
Shen H,
He F,
Mo Z,
Zhang H,
Zhou G
Nature communications · 2016 · PMID 27244555 · open access
1 page
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study
Zhu M,
Xu K,
Chen Y,
Gu Y,
Zhang M,
Luo F,
Liu Y,
Gu W,
Hu J,
Xu H,
Xie Z,
Sun C
and 42 more — show all
Li Y,
Sun M,
Xu X,
Hsu HT,
Chen H,
Fu Q,
Shi Y,
Xu J,
Ji L,
Liu J,
Bian L,
Zhu J,
Chen S,
Xiao L,
Li X,
Jiang H,
Shen M,
Huang Q,
Fang C,
Li X,
Huang G,
Fan J,
Jiang Z,
Jiang Y,
Dai J,
Ma H,
Zheng S,
Cai Y,
Dai H,
Zheng X,
Zhou H,
Ni S,
Jin G,
She JX,
Yu L,
Polychronakos C,
Hu Z,
Zhou Z,
Weng J,
Weng J,
Shen H,
Yang T
Diabetes care · 2019 · PMID 31152121
1 page
Genotyping and population characteristics of the China Kadoorie Biobank
Walters RG,
Millwood IY,
Lin K,
Schmidt Valle D,
McDonnell P,
Hacker A,
Avery D,
Edris A,
Fry H,
Cai N,
Kretzschmar WW,
Ansari MA
and 15 more — show all
Lyons PA,
Collins R,
Donnelly P,
Hill M,
Peto R,
Shen H,
Jin X,
Nie C,
Xu X,
Guo Y,
Yu C,
Lv J,
Clarke RJ,
Li L,
Chen Z
China Kadoorie Biobank Collaborative Group
Cell genomics · 2023 · PMID 37601966 · 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.