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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.
12 matches for
Xiao X.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
McKay JD,
Hung RJ,
Han Y,
Zong X,
Carreras-Torres R,
Christiani DC,
Caporaso NE,
Johansson M,
Xiao X,
Li Y,
Byun J,
Dunning A
and 128 more — show all
Pooley KA,
Qian DC,
Ji X,
Liu G,
Timofeeva MN,
Bojesen SE,
Wu X,
Le Marchand L,
Albanes D,
Bickeböller H,
Aldrich MC,
Bush WS,
Tardon A,
Rennert G,
Teare MD,
Field JK,
Kiemeney LA,
Lazarus P,
Haugen A,
Lam S,
Schabath MB,
Andrew AS,
Shen H,
Hong YC,
Yuan JM,
Bertazzi PA,
Pesatori AC,
Ye Y,
Diao N,
Su L,
Zhang R,
Brhane Y,
Leighl N,
Johansen JS,
Mellemgaard A,
Saliba W,
Haiman CA,
Wilkens LR,
Fernandez-Somoano A,
Fernandez-Tardon G,
van der Heijden HFM,
Kim JH,
Dai J,
Hu Z,
Davies MPA,
Marcus MW,
Brunnström H,
Manjer J,
Melander O,
Muller DC,
Overvad K,
Trichopoulou A,
Tumino R,
Doherty JA,
Barnett MP,
Chen C,
Goodman GE,
Cox A,
Taylor F,
Woll P,
Brüske I,
Wichmann HE,
Manz J,
Muley TR,
Risch A,
Rosenberger A,
Grankvist K,
Johansson M,
Shepherd FA,
Tsao MS,
Arnold SM,
Haura EB,
Bolca C,
Holcatova I,
Janout V,
Kontic M,
Lissowska J,
Mukeria A,
Ognjanovic S,
Orlowski TM,
Scelo G,
Swiatkowska B,
Zaridze D,
Bakke P,
Skaug V,
Zienolddiny S,
Duell EJ,
Butler LM,
Koh WP,
Gao YT,
Houlston RS,
McLaughlin J,
Stevens VL,
Joubert P,
Lamontagne M,
Nickle DC,
Obeidat M,
Timens W,
Zhu B,
Song L,
Kachuri L,
Artigas MS,
Tobin MD,
Wain LV,
Rafnar T,
Thorgeirsson TE,
Reginsson GW,
Stefansson K,
Hancock DB,
Bierut LJ,
Spitz MR,
Gaddis NC,
Lutz SM,
Gu F,
Johnson EO,
Kamal A,
Pikielny C,
Zhu D,
Lindströem S,
Jiang X,
Tyndale RF,
Chenevix-Trench G,
Beesley J,
Bossé Y,
Chanock S,
Brennan P,
Landi MT,
Amos CI
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · open access
12 pages+
Multi-ancestry GWAS meta-analyses of lung cancer reveal susceptibility loci and elucidate smoking-independent genetic risk
Gorman BR,
Ji SG,
Francis M,
Sendamarai AK,
Shi Y,
Devineni P,
Saxena U,
Partan E,
DeVito AK,
Byun J,
Han Y,
Xiao X
and 11 more — show all
Sin DD,
Timens W,
Moser J,
Muralidhar S,
Ramoni R,
Hung RJ,
McKay JD,
Bossé Y,
Sun R,
Amos CI,
Pyarajan S
VA Million Veteran Program
Nature communications · 2024 · PMID 39366959 · open access
12 pages+
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Dehghan A,
Dupuis J,
Barbalic M,
Bis JC,
Eiriksdottir G,
Lu C,
Pellikka N,
Wallaschofski H,
Kettunen J,
Henneman P,
Baumert J,
Strachan DP
and 102 more — show all
Fuchsberger C,
Vitart V,
Wilson JF,
Paré G,
Naitza S,
Rudock ME,
Surakka I,
de Geus EJ,
Alizadeh BZ,
Guralnik J,
Shuldiner A,
Tanaka T,
Zee RY,
Schnabel RB,
Nambi V,
Kavousi M,
Ripatti S,
Nauck M,
Smith NL,
Smith AV,
Sundvall J,
Scheet P,
Liu Y,
Ruokonen A,
Rose LM,
Larson MG,
Hoogeveen RC,
Freimer NB,
Teumer A,
Tracy RP,
Launer LJ,
Buring JE,
Yamamoto JF,
Folsom AR,
Sijbrands EJ,
Pankow J,
Elliott P,
Keaney JF,
Sun W,
Sarin AP,
Fontes JD,
Badola S,
Astor BC,
Hofman A,
Pouta A,
Werdan K,
Greiser KH,
Kuss O,
Meyer zu Schwabedissen HE,
Thiery J,
Jamshidi Y,
Nolte IM,
Soranzo N,
Spector TD,
Völzke H,
Parker AN,
Aspelund T,
Bates D,
Young L,
Tsui K,
Siscovick DS,
Guo X,
Rotter JI,
Uda M,
Schlessinger D,
Rudan I,
Hicks AA,
Penninx BW,
Thorand B,
Gieger C,
Coresh J,
Willemsen G,
Harris TB,
Uitterlinden AG,
Järvelin MR,
Rice K,
Radke D,
Salomaa V,
Willems van Dijk K,
Boerwinkle E,
Vasan RS,
Ferrucci L,
Gibson QD,
Bandinelli S,
Snieder H,
Boomsma DI,
Xiao X,
Campbell H,
Hayward C,
Pramstaller PP,
van Duijn CM,
Peltonen L,
Psaty BM,
Gudnason V,
Ridker PM,
Homuth G,
Koenig W,
Ballantyne CM,
Witteman JC,
Benjamin EJ,
Perola M,
Chasman DI
Circulation · 2011 · PMID 21300955
9 pages
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study
Yu H,
Yan H,
Wang L,
Li J,
Tan L,
Deng W,
Chen Q,
Yang G,
Zhang F,
Lu T,
Yang J,
Li K
and 12 more — show all
Lv L,
Tan Q,
Zhang H,
Xiao X,
Li M,
Ma X,
Yang F,
Li L,
Wang C,
Li T,
Zhang D,
Yue W
Chinese Antipsychotics Pharmacogenomics Consortium
The lancet. Psychiatry · 2018 · PMID 29503163
4 pages
Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis
Li HJ,
Zhang C,
Hui L,
Zhou DS,
Li Y,
Zhang CY,
Wang C,
Wang L,
Li W,
Yang Y,
Qu N,
Tang J
and 37 more — show all
He Y,
Zhou J,
Yang Z,
Li X,
Cai J,
Yang L,
Chen J,
Fan W,
Tang W,
Tang W,
Jia QF,
Liu W,
Zhuo C,
Song X,
Liu F,
Bai Y,
Zhong BL,
Zhang SF,
Chen J,
Xia B,
Lv L,
Liu Z,
Hu S,
Li XY,
Liu JW,
Cai X,
Yao YG,
Zhang Y,
Yan H,
Chang S,
Zhao JP,
Yue WH,
Luo XJ,
Chen X,
Xiao X,
Fang Y,
Li M
GeseDNA Research Team
JAMA psychiatry · 2021 · PMID 33263727
4 pages
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
Byun J,
Han Y,
Li Y,
Xia J,
Long E,
Choi J,
Xiao X,
Zhu M,
Zhou W,
Sun R,
Bossé Y,
Song Z
and 73 more — show all
Schwartz A,
Lusk C,
Rafnar T,
Stefansson K,
Zhang T,
Zhao W,
Pettit RW,
Liu Y,
Li X,
Zhou H,
Walsh KM,
Gorlov I,
Gorlova O,
Zhu D,
Rosenberg SM,
Pinney S,
Bailey-Wilson JE,
Mandal D,
de Andrade M,
Gaba C,
Willey JC,
You M,
Anderson M,
Wiencke JK,
Albanes D,
Lam S,
Tardon A,
Chen C,
Goodman G,
Bojeson S,
Brenner H,
Landi MT,
Chanock SJ,
Johansson M,
Muley T,
Risch A,
Wichmann HE,
Bickeböller H,
Christiani DC,
Rennert G,
Arnold S,
Field JK,
Shete S,
Le Marchand L,
Melander O,
Brunnstrom H,
Liu G,
Andrew AS,
Kiemeney LA,
Shen H,
Zienolddiny S,
Grankvist K,
Johansson M,
Caporaso N,
Cox A,
Hong YC,
Yuan JM,
Lazarus P,
Schabath MB,
Aldrich MC,
Patel A,
Lan Q,
Rothman N,
Taylor F,
Kachuri L,
Witte JS,
Sakoda LC,
Spitz M,
Brennan P,
Lin X,
McKay J,
Hung RJ,
Amos CI
Nature genetics · 2022 · PMID 35915169
3 pages
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis
Qiu F,
Tang R,
Zuo X,
Shi X,
Wei Y,
Zheng X,
Dai Y,
Gong Y,
Wang L,
Xu P,
Zhu X,
Wu J
and 78 more — show all
Han C,
Gao Y,
Zhang K,
Jiang Y,
Zhou J,
Shao Y,
Hu Z,
Tian Y,
Zhang H,
Dai N,
Liu L,
Wu X,
Zhao W,
Zhang X,
Zang Z,
Nie J,
Sun W,
Zhao Y,
Mao Y,
Jiang P,
Ji H,
Dong Q,
Li J,
Li Z,
Bai X,
Li L,
Lin M,
Dong M,
Li J,
Zhu P,
Wang C,
Zhang Y,
Jiang P,
Wang Y,
Jawed R,
Xu J,
Zhang Y,
Wang Q,
Yang Y,
Yang F,
Lian M,
Jiang X,
Xiao X,
Li Y,
Fang J,
Qiu D,
Zhu Z,
Qiu H,
Zhang J,
Tian W,
Chen S,
Jiang L,
Ji B,
Li P,
Chen G,
Wu T,
Sun Y,
Yu J,
Tang H,
He M,
Xia M,
Pei H,
Huang L,
Qing Z,
Wu J,
Huang Q,
Han J,
Xie W,
Sun Z,
Guo J,
He G,
Eric Gershwin M,
Lian Z,
Liu X,
Seldin MF,
Liu X,
Chen W,
Ma X
Nature communications · 2017 · PMID 28425483 · open access
2 pages
GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21
Wiemels JL,
Walsh KM,
de Smith AJ,
Metayer C,
Gonseth S,
Hansen HM,
Francis SS,
Ojha J,
Smirnov I,
Barcellos L,
Xiao X,
Morimoto L
and 6 more — show all
Nature communications · 2018 · PMID 29348612 · open access
2 pages
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population
Shi Y,
Qu J,
Zhang D,
Zhao P,
Zhang Q,
Tam POS,
Sun L,
Zuo X,
Zhou X,
Xiao X,
Hu J,
Li Y
and 30 more — show all
Cai L,
Liu X,
Lu F,
Liao S,
Chen B,
He F,
Gong B,
Lin H,
Ma S,
Cheng J,
Zhang J,
Chen Y,
Zhao F,
Yang X,
Chen Y,
Yang C,
Lam DSC,
Li X,
Shi F,
Wu Z,
Lin Y,
Yang J,
Li S,
Ren Y,
Xue A,
Fan Y,
Li D,
Pang CP,
Zhang X,
Yang Z
American journal of human genetics · 2011 · PMID 21640322
1 page
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course
Graff M,
Ngwa JS,
Workalemahu T,
Homuth G,
Schipf S,
Teumer A,
Völzke H,
Wallaschofski H,
Abecasis GR,
Edward L,
Francesco C,
Sanna S
and 37 more — show all
Scheet P,
Schlessinger D,
Sidore C,
Xiao X,
Wang Z,
Chanock SJ,
Jacobs KB,
Hayes RB,
Hu F,
Van Dam RM,
Crout RJ,
Marazita ML,
Shaffer JR,
Atwood LD,
Fox CS,
Heard-Costa NL,
White C,
Choh AC,
Czerwinski SA,
Demerath EW,
Dyer TD,
Towne B,
Amin N,
Oostra BA,
Van Duijn CM,
Zillikens MC,
Esko T,
Nelis M,
Nikopensius T,
Metspalu A,
Strachan DP,
Monda K,
Qi L,
North KE,
Cupples LA,
Gordon-Larsen P,
Berndt SI
GIANT Consortium
Human molecular genetics · 2013 · PMID 23669352
1 page
Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers
Lesseur C,
Ferreiro-Iglesias A,
McKay JD,
Bossé Y,
Johansson M,
Gaborieau V,
Landi MT,
Christiani DC,
Caporaso NC,
Bojesen SE,
Amos CI,
Shete S
and 41 more — show all
Liu G,
Rennert G,
Albanes D,
Aldrich MC,
Tardon A,
Chen C,
Triantafillos L,
Field JK,
Teare MD,
Kiemeney LA,
Diergaarde B,
Ferris RL,
Zienolddiny S,
Lam S,
Olshan AF,
Weissler MC,
Lacko M,
Risch A,
Bickeböller H,
Ness AR,
Thomas S,
Le Marchand L,
Schabath MB,
Wünsch-Filho V,
Tajara EH,
Andrew AS,
Clifford GM,
Lazarus P,
Grankvist K,
Johansson M,
Arnold S,
Melander O,
Brunnström H,
Boccia S,
Cadoni G,
Timens W,
Obeidat M,
Xiao X,
Houlston RS,
Hung RJ,
Brennan P
PLoS genetics · 2021 · PMID 33667223 · open access
1 page
Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia
Liu J,
Li S,
Li X,
Li W,
Yang Y,
Guo S,
Lv L,
Xiao X,
Yao YG,
Guan F,
Li M,
Luo XJ
BMC medicine · 2021 · PMID 34380480 · 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.