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11 matches for
Hu S.
The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study
Winkler TW,
Justice AE,
Graff M,
Barata L,
Feitosa MF,
Chu S,
Czajkowski J,
Esko T,
Fall T,
Kilpeläinen TO,
Lu Y,
Mägi R
and 427 more — show all
Mihailov E,
Pers TH,
Rüeger S,
Teumer A,
Ehret GB,
Ferreira T,
Heard-Costa NL,
Karjalainen J,
Lagou V,
Mahajan A,
Neinast MD,
Prokopenko I,
Simino J,
Teslovich TM,
Jansen R,
Westra HJ,
White CC,
Absher D,
Ahluwalia TS,
Ahmad S,
Albrecht E,
Alves AC,
Bragg-Gresham JL,
de Craen AJ,
Bis JC,
Bonnefond A,
Boucher G,
Cadby G,
Cheng YC,
Chiang CW,
Delgado G,
Demirkan A,
Dueker N,
Eklund N,
Eiriksdottir G,
Eriksson J,
Feenstra B,
Fischer K,
Frau F,
Galesloot TE,
Geller F,
Goel A,
Gorski M,
Grammer TB,
Gustafsson S,
Haitjema S,
Hottenga JJ,
Huffman JE,
Jackson AU,
Jacobs KB,
Johansson Å,
Kaakinen M,
Kleber ME,
Lahti J,
Mateo Leach I,
Lehne B,
Liu Y,
Lo KS,
Lorentzon M,
Luan J,
Madden PA,
Mangino M,
McKnight B,
Medina-Gomez C,
Monda KL,
Montasser ME,
Müller G,
Müller-Nurasyid M,
Nolte IM,
Panoutsopoulou K,
Pascoe L,
Paternoster L,
Rayner NW,
Renström F,
Rizzi F,
Rose LM,
Ryan KA,
Salo P,
Sanna S,
Scharnagl H,
Shi J,
Smith AV,
Southam L,
Stančáková A,
Steinthorsdottir V,
Strawbridge RJ,
Sung YJ,
Tachmazidou I,
Tanaka T,
Thorleifsson G,
Trompet S,
Pervjakova N,
Tyrer JP,
Vandenput L,
van der Laan SW,
van der Velde N,
van Setten J,
van Vliet-Ostaptchouk JV,
Verweij N,
Vlachopoulou E,
Waite LL,
Wang SR,
Wang Z,
Wild SH,
Willenborg C,
Wilson JF,
Wong A,
Yang J,
Yengo L,
Yerges-Armstrong LM,
Yu L,
Zhang W,
Zhao JH,
Andersson EA,
Bakker SJ,
Baldassarre D,
Banasik K,
Barcella M,
Barlassina C,
Bellis C,
Benaglio P,
Blangero J,
Blüher M,
Bonnet F,
Bonnycastle LL,
Boyd HA,
Bruinenberg M,
Buchman AS,
Campbell H,
Chen YD,
Chines PS,
Claudi-Boehm S,
Cole J,
Collins FS,
de Geus EJ,
de Groot LC,
Dimitriou M,
Duan J,
Enroth S,
Eury E,
Farmaki AE,
Forouhi NG,
Friedrich N,
Gejman PV,
Gigante B,
Glorioso N,
Go AS,
Gottesman O,
Gräßler J,
Grallert H,
Grarup N,
Gu YM,
Broer L,
Ham AC,
Hansen T,
Harris TB,
Hartman CA,
Hassinen M,
Hastie N,
Hattersley AT,
Heath AC,
Henders AK,
Hernandez D,
Hillege H,
Holmen O,
Hovingh KG,
Hui J,
Husemoen LL,
Hutri-Kähönen N,
Hysi PG,
Illig T,
De Jager PL,
Jalilzadeh S,
Jørgensen T,
Jukema JW,
Juonala M,
Kanoni S,
Karaleftheri M,
Khaw KT,
Kinnunen L,
Kittner SJ,
Koenig W,
Kolcic I,
Kovacs P,
Krarup NT,
Kratzer W,
Krüger J,
Kuh D,
Kumari M,
Kyriakou T,
Langenberg C,
Lannfelt L,
Lanzani C,
Lotay V,
Launer LJ,
Leander K,
Lindström J,
Linneberg A,
Liu YP,
Lobbens S,
Luben R,
Lyssenko V,
Männistö S,
Magnusson PK,
McArdle WL,
Menni C,
Merger S,
Milani L,
Montgomery GW,
Morris AP,
Narisu N,
Nelis M,
Ong KK,
Palotie A,
Pérusse L,
Pichler I,
Pilia MG,
Pouta A,
Rheinberger M,
Ribel-Madsen R,
Richards M,
Rice KM,
Rice TK,
Rivolta C,
Salomaa V,
Sanders AR,
Sarzynski MA,
Scholtens S,
Scott RA,
Scott WR,
Sebert S,
Sengupta S,
Sennblad B,
Seufferlein T,
Silveira A,
Slagboom PE,
Smit JH,
Sparsø TH,
Stirrups K,
Stolk RP,
Stringham HM,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Thorand B,
Tönjes A,
Tremblay A,
Tsafantakis E,
van der Most PJ,
Völker U,
Vohl MC,
Vonk JM,
Waldenberger M,
Walker RW,
Wennauer R,
Widén E,
Willemsen G,
Wilsgaard T,
Wright AF,
Zillikens MC,
van Dijk SC,
van Schoor NM,
Asselbergs FW,
de Bakker PI,
Beckmann JS,
Beilby J,
Bennett DA,
Bergman RN,
Bergmann S,
Böger CA,
Boehm BO,
Boerwinkle E,
Boomsma DI,
Bornstein SR,
Bottinger EP,
Bouchard C,
Chambers JC,
Chanock SJ,
Chasman DI,
Cucca F,
Cusi D,
Dedoussis G,
Erdmann J,
Eriksson JG,
Evans DA,
de Faire U,
Farrall M,
Ferrucci L,
Ford I,
Franke L,
Franks PW,
Froguel P,
Gansevoort RT,
Gieger C,
Grönberg H,
Gudnason V,
Gyllensten U,
Hall P,
Hamsten A,
van der Harst P,
Hayward C,
Heliövaara M,
Hengstenberg C,
Hicks AA,
Hingorani A,
Hofman A,
Hu F,
Huikuri HV,
Hveem K,
James AL,
Jordan JM,
Jula A,
Kähönen M,
Kajantie E,
Kathiresan S,
Kiemeney LA,
Kivimaki M,
Knekt PB,
Koistinen HA,
Kooner JS,
Koskinen S,
Kuusisto J,
Maerz W,
Martin NG,
Laakso M,
Lakka TA,
Lehtimäki T,
Lettre G,
Levinson DF,
Lind L,
Lokki ML,
Mäntyselkä P,
Melbye M,
Metspalu A,
Mitchell BD,
Moll FL,
Murray JC,
Musk AW,
Nieminen MS,
Njølstad I,
Ohlsson C,
Oldehinkel AJ,
Oostra BA,
Palmer LJ,
Pankow JS,
Pasterkamp G,
Pedersen NL,
Pedersen O,
Penninx BW,
Perola M,
Peters A,
Polašek O,
Pramstaller PP,
Psaty BM,
Qi L,
Quertermous T,
Raitakari OT,
Rankinen T,
Rauramaa R,
Ridker PM,
Rioux JD,
Rivadeneira F,
Rotter JI,
Rudan I,
den Ruijter HM,
Saltevo J,
Sattar N,
Schunkert H,
Schwarz PE,
Shuldiner AR,
Sinisalo J,
Snieder H,
Sørensen TI,
Spector TD,
Staessen JA,
Stefania B,
Thorsteinsdottir U,
Stumvoll M,
Tardif JC,
Tremoli E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
Verbeek AL,
Vermeulen SH,
Viikari JS,
Vitart V,
Völzke H,
Vollenweider P,
Waeber G,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Zeggini E,
Chakravarti A,
Clegg DJ,
Cupples LA,
Gordon-Larsen P,
Jaquish CE,
Rao DC,
Abecasis GR,
Assimes TL,
Barroso I,
Berndt SI,
Boehnke M,
Deloukas P,
Fox CS,
Groop LC,
Hunter DJ,
Ingelsson E,
Kaplan RC,
McCarthy MI,
Mohlke KL,
O'Connell JR,
Schlessinger D,
Strachan DP,
Stefansson K,
van Duijn CM,
Hirschhorn JN,
Lindgren CM,
Heid IM,
North KE,
Borecki IB,
Kutalik Z,
Loos RJ
CHARGE Consortium · DIAGRAM Consortium and 4 more consortia
PLoS genetics · 2015 · PMID 26426971 · open access
12 pages+
Deciphering tissue-specific protein regulation for insights into cardiometabolic disease
Hartley AE,
Sukhavasi K,
Hu S,
Traylor M,
Gonzalez-Ramirez M,
Hanghøj KE,
Talukdar H,
Ruusalepp A,
Björkegren E,
Björkegren JL,
Howson JM,
Jamshidi Y
Molecular metabolism · 2026 · PMID 41456820 · open access
10 pages
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study
Shrine N,
Portelli MA,
John C,
Soler Artigas M,
Bennett N,
Hall R,
Lewis J,
Henry AP,
Billington CK,
Ahmad A,
Packer RJ,
Shaw D
and 31 more — show all
Pogson ZEK,
Fogarty A,
McKeever TM,
Singapuri A,
Heaney LG,
Mansur AH,
Chaudhuri R,
Thomson NC,
Holloway JW,
Lockett GA,
Howarth PH,
Djukanovic R,
Hankinson J,
Niven R,
Simpson A,
Chung KF,
Sterk PJ,
Blakey JD,
Adcock IM,
Hu S,
Guo Y,
Obeidat M,
Sin DD,
van den Berge M,
Nickle DC,
Bossé Y,
Tobin MD,
Hall IP,
Brightling CE,
Wain LV,
Sayers I
The Lancet. Respiratory medicine · 2019 · PMID 30552067 · open access
7 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
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
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis
Lin Z,
Bei JX,
Shen M,
Li Q,
Liao Z,
Zhang Y,
Lv Q,
Wei Q,
Low HQ,
Guo YM,
Cao S,
Yang M
and 39 more — show all
Hu Z,
Xu M,
Wang X,
Wei Y,
Li L,
Li C,
Li T,
Huang J,
Pan Y,
Jin O,
Wu Y,
Wu J,
Guo Z,
He P,
Hu S,
Wu H,
Song H,
Zhan F,
Liu S,
Gao G,
Liu Z,
Li Y,
Xiao C,
Li J,
Ye Z,
He W,
Liu D,
Shen L,
Huang A,
Wu H,
Tao Y,
Pan X,
Yu B,
Tai ES,
Zeng YX,
Ren EC,
Shen Y,
Liu J,
Gu J
Nature genetics · 2011 · PMID 22138694
2 pages
Genetic Associations and Architecture of Asthma-COPD Overlap
John C,
Guyatt AL,
Shrine N,
Packer R,
Olafsdottir TA,
Liu J,
Hayden LP,
Chu SH,
Koskela JT,
Luan J,
Li X,
Terzikhan N
and 42 more — show all
Xu H,
Bartz TM,
Petersen H,
Leng S,
Belinsky SA,
Cepelis A,
Hernández Cordero AI,
Obeidat M,
Thorleifsson G,
Meyers DA,
Bleecker ER,
Sakoda LC,
Iribarren C,
Tesfaigzi Y,
Gharib SA,
Dupuis J,
Brusselle G,
Lahousse L,
Ortega VE,
Jonsdottir I,
Sin DD,
Bossé Y,
van den Berge M,
Nickle D,
Quint JK,
Sayers I,
Hall IP,
Langenberg C,
Ripatti S,
Laitinen T,
Wu AC,
Lasky-Su J,
Bakke P,
Gulsvik A,
Hersh CP,
Hayward C,
Langhammer A,
Brumpton B,
Stefansson K,
Cho MH,
Wain LV,
Tobin MD
Chest · 2022 · PMID 35104449 · open access
2 pages
Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project
Lopera-Maya EA,
Kurilshikov A,
van der Graaf A,
Hu S,
Andreu-Sánchez S,
Chen L,
Vila AV,
Gacesa R,
Sinha T,
Collij V,
Klaassen MAY,
Bolte LA
and 9 more — show all
LifeLines Cohort Study
Nature genetics · 2022 · PMID 35115690
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 provides insights into the genetic basis of Lewy body dementia
Zhu P,
Jin Z,
Wu S,
Gao S,
He Y,
Hu S,
Liu F,
Chen Y,
Wang M,
Wang K,
Liu G
Molecular psychiatry · 2025 · PMID 41068259
2 pages
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23
Li Y,
Zhang K,
Chen H,
Sun F,
Xu J,
Wu Z,
Li P,
Zhang L,
Du Y,
Luan H,
Li X,
Wu L
and 64 more — show all
Li H,
Wu H,
Li X,
Li X,
Zhang X,
Gong L,
Dai L,
Sun L,
Zuo X,
Xu J,
Gong H,
Li Z,
Tong S,
Wu M,
Li X,
Xiao W,
Wang G,
Zhu P,
Shen M,
Liu S,
Zhao D,
Liu W,
Wang Y,
Huang C,
Jiang Q,
Liu G,
Liu B,
Hu S,
Zhang W,
Zhang Z,
You X,
Li M,
Hao W,
Zhao C,
Leng X,
Bi L,
Wang Y,
Zhang F,
Shi Q,
Qi W,
Zhang X,
Jia Y,
Su J,
Li Q,
Hou Y,
Wu Q,
Xu D,
Zheng W,
Zhang M,
Wang Q,
Fei Y,
Zhang X,
Li J,
Jiang Y,
Tian X,
Zhao L,
Wang L,
Zhou B,
Li Y,
Zhao Y,
Zeng X,
Ott J,
Wang J,
Zhang F
Nature genetics · 2013 · PMID 24097066
1 page
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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.