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145 matches for
He G,
showing the first 20.
The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders
Ou YN,
Ge YJ,
Wu BS,
Zhang Y,
Jiang YC,
Kuo K,
Yang L,
Tan L,
Feng JF,
Cheng W,
Yu JT
Translational psychiatry · 2023 · PMID 37236919 · open access
7 pages
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
Wain LV,
Shrine N,
Miller S,
Jackson VE,
Ntalla I,
Soler Artigas M,
Billington CK,
Kheirallah AK,
Allen R,
Cook JP,
Probert K,
Obeidat M
and 27 more — show all
Bossé Y,
Hao K,
Postma DS,
Paré PD,
Ramasamy A,
Mägi R,
Mihailov E,
Reinmaa E,
Melén E,
O'Connell J,
Frangou E,
Delaneau O,
Freeman C,
Petkova D,
McCarthy M,
Sayers I,
Deloukas P,
Hubbard R,
Pavord I,
Hansell AL,
Thomson NC,
Zeggini E,
Morris AP,
Marchini J,
Strachan DP,
Tobin MD,
Hall IP
UK Brain Expression Consortium (UKBEC) · OxGSK Consortium
The Lancet. Respiratory medicine · 2015 · PMID 26423011 · open access
6 pages
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
Hong J,
Hatchell KE,
Bradfield JP,
Bjonnes A,
Chesi A,
Lai CQ,
Langefeld CD,
Lu L,
Lu Y,
Lutsey PL,
Musani SK,
Nalls MA
and 48 more — show all
Robinson-Cohen C,
Roizen JD,
Saxena R,
Tucker KL,
Ziegler JT,
Arking DE,
Bis JC,
Boerwinkle E,
Bottinger EP,
Bowden DW,
Gilsanz V,
Houston DK,
Kalkwarf HJ,
Kelly A,
Lappe JM,
Liu Y,
Michos ED,
Oberfield SE,
Palmer ND,
Rotter JI,
Sapkota B,
Shepherd JA,
Wilson JG,
Basu S,
de Boer IH,
Divers J,
Freedman BI,
Grant SFA,
Hakanarson H,
Harris TB,
Kestenbaum BR,
Kritchevsky SB,
Loos RJF,
Norris JM,
Norwood AF,
Ordovas JM,
Pankow JS,
Psaty BM,
Sanghera DK,
Wagenknecht LE,
Zemel BS,
Meigs J,
Dupuis J,
Florez JC,
Wang T,
Liu CT,
Engelman CD,
Billings LK
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
6 pages
Cardiac Troponin T and Troponin I in the General Population
Welsh P,
Preiss D,
Hayward C,
Shah ASV,
McAllister D,
Briggs A,
Boachie C,
McConnachie A,
Padmanabhan S,
Welsh C,
Woodward M,
Campbell A
and 3 more — show all
Circulation · 2019 · PMID 31014085 · open access
5 pages
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study
Greenwood TA,
Lazzeroni LC,
Maihofer AX,
Swerdlow NR,
Calkins ME,
Freedman R,
Green MF,
Light GA,
Nievergelt CM,
Nuechterlein KH,
Radant AD,
Siever LJ
and 9 more — show all
JAMA psychiatry · 2019 · PMID 31596458
5 pages
Characterization of the genetic architecture of infant and early childhood body mass index
Helgeland Ø,
Vaudel M,
Sole-Navais P,
Flatley C,
Juodakis J,
Bacelis J,
Koløen IL,
Knudsen GP,
Johansson BB,
Magnus P,
Kjennerud TR,
Juliusson PB
and 6 more — show all
Nature metabolism · 2022 · PMID 35315439
5 pages
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
Shi Y,
Zhao H,
Shi Y,
Cao Y,
Yang D,
Li Z,
Zhang B,
Liang X,
Li T,
Chen J,
Shen J,
Zhao J
and 41 more — show all
You L,
Gao X,
Zhu D,
Zhao X,
Yan Y,
Qin Y,
Li W,
Yan J,
Wang Q,
Zhao J,
Geng L,
Ma J,
Zhao Y,
He G,
Zhang A,
Zou S,
Yang A,
Liu J,
Li W,
Li B,
Wan C,
Qin Y,
Shi J,
Yang J,
Jiang H,
Xu JE,
Qi X,
Sun Y,
Zhang Y,
Hao C,
Ju X,
Zhao D,
Ren CE,
Li X,
Zhang W,
Zhang Y,
Zhang J,
Wu D,
Zhang C,
He L,
Chen ZJ
Nature genetics · 2012 · PMID 22885925
4 pages
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Moayyeri A,
Hsu YH,
Karasik D,
Estrada K,
Xiao SM,
Nielson C,
Srikanth P,
Giroux S,
Wilson SG,
Zheng HF,
Smith AV,
Pye SR
and 118 more — show all
Leo PJ,
Teumer A,
Hwang JY,
Ohlsson C,
McGuigan F,
Minster RL,
Hayward C,
Olmos JM,
Lyytikäinen LP,
Lewis JR,
Swart KM,
Masi L,
Oldmeadow C,
Holliday EG,
Cheng S,
van Schoor NM,
Harvey NC,
Kruk M,
del Greco M F,
Igl W,
Trummer O,
Grigoriou E,
Luben R,
Liu CT,
Zhou Y,
Oei L,
Medina-Gomez C,
Zmuda J,
Tranah G,
Brown SJ,
Williams FM,
Soranzo N,
Jakobsdottir J,
Siggeirsdottir K,
Holliday KL,
Hannemann A,
Go MJ,
Garcia M,
Polasek O,
Laaksonen M,
Zhu K,
Enneman AW,
McEvoy M,
Peel R,
Sham PC,
Jaworski M,
Johansson Å,
Hicks AA,
Pludowski P,
Scott R,
Dhonukshe-Rutten RA,
van der Velde N,
Kähönen M,
Viikari JS,
Sievänen H,
Raitakari OT,
González-Macías J,
Hernández JL,
Mellström D,
Ljunggren O,
Cho YS,
Völker U,
Nauck M,
Homuth G,
Völzke H,
Haring R,
Brown MA,
McCloskey E,
Nicholson GC,
Eastell R,
Eisman JA,
Jones G,
Reid IR,
Dennison EM,
Wark J,
Boonen S,
Vanderschueren D,
Wu FC,
Aspelund T,
Richards JB,
Bauer D,
Hofman A,
Khaw KT,
Dedoussis G,
Obermayer-Pietsch B,
Gyllensten U,
Pramstaller PP,
Lorenc RS,
Cooper C,
Kung AW,
Lips P,
Alen M,
Attia J,
Brandi ML,
de Groot LC,
Lehtimäki T,
Riancho JA,
Campbell H,
Liu Y,
Harris TB,
Akesson K,
Karlsson M,
Lee JY,
Wallaschofski H,
Duncan EL,
O'Neill TW,
Gudnason V,
Spector TD,
Rousseau F,
Orwoll E,
Cummings SR,
Wareham NJ,
Rivadeneira F,
Uitterlinden AG,
Prince RL,
Kiel DP,
Reeve J,
Kaptoge SK
Human molecular genetics · 2014 · PMID 24430505
4 pages
Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution
Boueiz A,
Lutz SM,
Cho MH,
Hersh CP,
Bowler RP,
Washko GR,
Halper-Stromberg E,
Bakke P,
Gulsvik A,
Laird NM,
Beaty TH,
Coxson HO
and 4 more — show all
COPDGene and ECLIPSE Investigators
American journal of respiratory and critical care medicine · 2017 · PMID 27669027
4 pages
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population
Salo PP,
Havulinna AS,
Tukiainen T,
Raitakari O,
Lehtimäki T,
Kähönen M,
Kettunen J,
Männikkö M,
Eriksson JG,
Jula A,
Blankenberg S,
Zeller T
and 3 more — show all
Circulation. Cardiovascular genetics · 2017 · PMID 29237677 · open access
4 pages
Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans
Bigdeli TB,
Fanous AH,
Li Y,
Rajeevan N,
Sayward F,
Genovese G,
Gupta R,
Radhakrishnan K,
Malhotra AK,
Sun N,
Lu Q,
Hu Y
and 33 more — show all
Li B,
Chen Q,
Mane S,
Miller P,
Cheung KH,
Gur RE,
Greenwood TA,
Braff DL,
Achtyes ED,
Buckley PF,
Escamilla MA,
Lehrer D,
Malaspina DP,
McCarroll SA,
Rapaport MH,
Vawter MP,
Pato MT,
Pato CN,
Zhao H,
Kosten TR,
Brophy M,
Pyarajan S,
Shi Y,
O'Leary TJ,
Gleason T,
Przygodzki R,
Muralidhar S,
Gaziano JM,
Huang GD,
Concato J,
Siever LJ,
Aslan M,
Harvey PD
Consortium on the Genetics of Schizophrenia (COGS) · Genomic Psychiatry Cohort (GPC) Investigators and 1 more consortia
Schizophrenia bulletin · 2021 · PMID 33169155
4 pages
The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study
Giannakopoulou O,
Lin K,
Meng X,
Su MH,
Kuo PH,
Peterson RE,
Awasthi S,
Moscati A,
Coleman JRI,
Bass N,
Millwood IY,
Chen Y
and 25 more — show all
Chen Z,
Chen HC,
Lu ML,
Huang MC,
Chen CH,
Stahl EA,
Loos RJF,
Mullins N,
Ursano RJ,
Kessler RC,
Stein MB,
Sen S,
Scott LJ,
Burmeister M,
Fang Y,
Tyrrell J,
Jiang Y,
Tian C,
McIntosh AM,
Ripke S,
Dunn EC,
Kendler KS,
Walters RG,
Lewis CM,
Kuchenbaecker K
23andMe Research Team, China Kadoorie Biobank Collaborative Group, and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
JAMA psychiatry · 2021 · PMID 34586374 · open access
4 pages
Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function
Aung N,
Vargas JD,
Yang C,
Fung K,
Sanghvi MM,
Piechnik SK,
Neubauer S,
Manichaikul A,
Rotter JI,
Taylor KD,
Lima JAC,
Bluemke DA
and 3 more — show all
Nature genetics · 2022 · PMID 35697868
4 pages
Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
Demontis D,
Walters GB,
Athanasiadis G,
Walters R,
Therrien K,
Nielsen TT,
Farajzadeh L,
Voloudakis G,
Bendl J,
Zeng B,
Zhang W,
Grove J
and 35 more — show all
Als TD,
Duan J,
Satterstrom FK,
Bybjerg-Grauholm J,
Bækved-Hansen M,
Gudmundsson OO,
Magnusson SH,
Baldursson G,
Davidsdottir K,
Haraldsdottir GS,
Agerbo E,
Hoffman GE,
Dalsgaard S,
Martin J,
Ribasés M,
Boomsma DI,
Soler Artigas M,
Roth Mota N,
Howrigan D,
Medland SE,
Zayats T,
Rajagopal VM,
Nordentoft M,
Mors O,
Hougaard DM,
Mortensen PB,
Daly MJ,
Faraone SV,
Stefansson H,
Roussos P,
Franke B,
Werge T,
Neale BM,
Stefansson K,
Børglum AD
ADHD Working Group of the Psychiatric Genomics Consortium · iPSYCH-Broad Consortium
Nature genetics · 2023 · PMID 36702997
4 pages
GWAS meta-analyses clarify the genetics of cervical phenotypes and inform risk stratification for cervical cancer
Koel M,
Võsa U,
Jõeloo M,
Läll K,
Gualdo NP,
Laivuori H,
Lemmelä S,
Daly M,
Palta P,
Mägi R,
Laisk T
Estonian Biobank Research Team; FinnGen
Human molecular genetics · 2023 · PMID 36929174 · open access
4 pages
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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.