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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.
13 matches for
Sun X.
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
Akiyama M
and 205 more — show all
Albert CM,
Aliev F,
Alonso A,
Arnett DK,
Ashley-Koch AE,
Ashrani AA,
Barnes KC,
Barr RG,
Bartz TM,
Becker DM,
Bielak LF,
Benjamin EJ,
Bis JC,
Bjornsdottir G,
Blangero J,
Bleecker ER,
Boardman JD,
Boerwinkle E,
Boomsma DI,
Boorgula MP,
Bowden DW,
Brody JA,
Cade BE,
Chasman DI,
Chavan S,
Chen YI,
Chen Z,
Cheng I,
Cho MH,
Choquet H,
Cole JW,
Cornelis MC,
Cucca F,
Curran JE,
de Andrade M,
Dick DM,
Docherty AR,
Duggirala R,
Eaton CB,
Ehringer MA,
Esko T,
Faul JD,
Fernandes Silva L,
Fiorillo E,
Fornage M,
Freedman BI,
Gabrielsen ME,
Garrett ME,
Gharib SA,
Gieger C,
Gillespie N,
Glahn DC,
Gordon SD,
Gu CC,
Gu D,
Gudbjartsson DF,
Guo X,
Haessler J,
Hall ME,
Haller T,
Harris KM,
He J,
Herd P,
Hewitt JK,
Hickie I,
Hidalgo B,
Hokanson JE,
Hopfer C,
Hottenga J,
Hou L,
Huang H,
Hung YJ,
Hunter DJ,
Hveem K,
Hwang SJ,
Hwu CM,
Iacono W,
Irvin MR,
Jee YH,
Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
Kaprio J,
Kardia SLR,
Keller MC,
Kelly TN,
Kooperberg C,
Korhonen T,
Kraft P,
Krauter K,
Kuusisto J,
Laakso M,
Lasky-Su J,
Lee WJ,
Lee JJ,
Levy D,
Li L,
Li K,
Li Y,
Lin K,
Lind PA,
Liu C,
Lloyd-Jones DM,
Lutz SM,
Ma J,
Mägi R,
Manichaikul A,
Martin NG,
Mathur R,
Matoba N,
McArdle PF,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Meyers DA,
Millwood IY,
Mitchell BD,
Mohlke KL,
Moll M,
Montasser ME,
Morrison AC,
Mulas A,
Nielsen JB,
North KE,
Oelsner EC,
Okada Y,
Orrù V,
Palmer ND,
Palviainen T,
Pandit A,
Park SL,
Peters U,
Peters A,
Peyser PA,
Polderman TJC,
Rafaels N,
Redline S,
Reed RM,
Reiner AP,
Rice JP,
Rich SS,
Richmond NE,
Roan C,
Rotter JI,
Rueschman MN,
Runarsdottir V,
Saccone NL,
Schwartz DA,
Shadyab AH,
Shi J,
Shringarpure SS,
Sicinski K,
Skogholt AH,
Smith JA,
Smith NL,
Sotoodehnia N,
Stallings MC,
Stefansson H,
Stefansson K,
Stitzel JA,
Sun X,
Syed M,
Tal-Singer R,
Taylor AE,
Taylor KD,
Telen MJ,
Thai KK,
Tiwari H,
Turman C,
Tyrfingsson T,
Wall TL,
Walters RG,
Weir DR,
Weiss ST,
White WB,
Whitfield JB,
Wiggins KL,
Willemsen G,
Willer CJ,
Winsvold BS,
Xu H,
Yanek LR,
Yin J,
Young KL,
Young KA,
Yu B,
Zhao W,
Zhou W,
Zöllner S,
Zuccolo L,
Batini C,
Bergen AW,
Bierut LJ,
David SP,
Gagliano Taliun SA,
Hancock DB,
Jiang B,
Munafò MR,
Thorgeirsson TE,
Liu DJ,
Vrieze S
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
12 pages+
Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population
Huang L,
Chen Y,
Lin Y,
Tam POS,
Cheng Y,
Shi Y,
Gong B,
Lu F,
Yang J,
Wang H,
Yin Y,
Cao Y
and 9 more — show all
Science China. Life sciences · 2019 · PMID 30591961
5 pages
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
Chen ZJ,
Zhao H,
He L,
Shi Y,
Qin Y,
Shi Y,
Li Z,
You L,
Zhao J,
Liu J,
Liang X,
Zhao X
and 22 more — show all
Zhao J,
Sun Y,
Zhang B,
Jiang H,
Zhao D,
Bian Y,
Gao X,
Geng L,
Li Y,
Zhu D,
Sun X,
Xu JE,
Hao C,
Ren CE,
Zhang Y,
Chen S,
Zhang W,
Yang A,
Yan J,
Li Y,
Ma J,
Zhao Y
Nature genetics · 2011 · PMID 21151128
4 pages
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus
Gateva V,
Sandling JK,
Hom G,
Taylor KE,
Chung SA,
Sun X,
Ortmann W,
Kosoy R,
Ferreira RC,
Nordmark G,
Gunnarsson I,
Svenungsson E
and 24 more — show all
Padyukov L,
Sturfelt G,
Jönsen A,
Bengtsson AA,
Rantapää-Dahlqvist S,
Baechler EC,
Brown EE,
Alarcón GS,
Edberg JC,
Ramsey-Goldman R,
McGwin G Jr,
Reveille JD,
Vilá LM,
Kimberly RP,
Manzi S,
Petri MA,
Lee A,
Gregersen PK,
Seldin MF,
Rönnblom L,
Criswell LA,
Syvänen AC,
Behrens TW,
Graham RR
Nature genetics · 2009 · PMID 19838195
3 pages
Genome-wide analysis of insomnia disorder
Stein MB,
McCarthy MJ,
Chen CY,
Jain S,
Gelernter J,
He F,
Heeringa SG,
Kessler RC,
Nock MK,
Ripke S,
Sun X,
Wynn GH
and 2 more — show all
Molecular psychiatry · 2018 · PMID 29520036 · open access
3 pages
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease
Garcia-Barcelo MM,
Tang CS,
Ngan ES,
Lui VC,
Chen Y,
So MT,
Leon TY,
Miao XP,
Shum CK,
Liu FQ,
Yeung MY,
Yuan ZW
and 12 more — show all
Guo WH,
Liu L,
Sun XB,
Huang LM,
Tou JF,
Song YQ,
Chan D,
Cheung KM,
Wong KK,
Cherny SS,
Sham PC,
Tam PK
Proceedings of the National Academy of Sciences of the United States of America · 2009 · PMID 19196962
2 pages
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Garcia-Barceló MM,
Yeung MY,
Miao XP,
Tang CS,
Cheng G,
So MT,
Ngan ES,
Lui VC,
Chen Y,
Liu XL,
Hui KJ,
Li L
and 13 more — show all
Guo WH,
Sun XB,
Tou JF,
Chan KW,
Wu XZ,
Song YQ,
Chan D,
Cheung K,
Chung PH,
Wong KK,
Sham PC,
Cherny SS,
Tam PK
Human molecular genetics · 2010 · PMID 20460270
2 pages
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls
Zhu Z,
Tang NL,
Xu L,
Qin X,
Mao S,
Song Y,
Liu L,
Li F,
Liu P,
Yi L,
Chang J,
Jiang L
and 25 more — show all
Ng BK,
Shi B,
Zhang W,
Qiao J,
Sun X,
Qiu X,
Wang Z,
Wang F,
Xie D,
Chen L,
Chen Z,
Jin M,
Han X,
Hu Z,
Zhang Z,
Liu Z,
Zhu F,
Qian BP,
Yu Y,
Wang B,
Lee KM,
Lee WYW,
Lam TP,
Qiu Y,
Cheng JC
Nature communications · 2015 · PMID 26394188 · open access
2 pages
Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma
Chen C,
Song N,
Dong Q,
Sun X,
Mulder HL,
Easton J,
Zhang J,
Yasui Y,
Bhatia S,
Armstrong GT,
Wang H,
Ness KK
and 3 more — show all
JAMA network open · 2022 · PMID 35939300 · open access
2 pages
Genome-wide analyses of psychological resilience in U.S. Army soldiers
Stein MB,
Choi KW,
Jain S,
Campbell-Sills L,
Chen CY,
Gelernter J,
He F,
Heeringa SG,
Maihofer AX,
Nievergelt C,
Nock MK,
Ripke S
and 4 more — show all
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2019 · PMID 31081985
1 page
Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer
Dong Q,
Song N,
Qin N,
Chen C,
Li Z,
Sun X,
Easton J,
Mulder H,
Plyler E,
Neale G,
Walker E,
Li Q
and 9 more — show all
Genome medicine · 2022 · PMID 35313970 · open access
1 page
Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women
Chung J,
Das A,
Sun X,
Sobreira DR,
Leung YY,
Igartua C,
Mozaffari S,
Chou YF,
Thiagalingam S,
Mez J,
Zhang X,
Jun GR
and 13 more — show all
Stein TD,
Kunkle BW,
Martin ER,
Pericak-Vance MA,
Mayeux R,
Haines JL,
Schellenberg GD,
Nobrega MA,
Lunetta KL,
Pinto JM,
Wang LS,
Ober C,
Farrer LA
Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023 · PMID 35770850
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
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.