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2,651 papers hold this site up. Every variant and condition page names
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Search your name, your journal, or a PMID.
10 matches for
Lee JH.
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
Nalls MA,
Pankratz N,
Lill CM,
Do CB,
Hernandez DG,
Saad M,
DeStefano AL,
Kara E,
Bras J,
Sharma M,
Schulte C,
Keller MF
and 35 more — show all
Arepalli S,
Letson C,
Edsall C,
Stefansson H,
Liu X,
Pliner H,
Lee JH,
Cheng R,
Ikram MA,
Ioannidis JP,
Hadjigeorgiou GM,
Bis JC,
Martinez M,
Perlmutter JS,
Goate A,
Marder K,
Fiske B,
Sutherland M,
Xiromerisiou G,
Myers RH,
Clark LN,
Stefansson K,
Hardy JA,
Heutink P,
Chen H,
Wood NW,
Houlden H,
Payami H,
Brice A,
Scott WK,
Gasser T,
Bertram L,
Eriksson N,
Foroud T,
Singleton AB
International Parkinson's Disease Genomics Consortium (IPDGC) · Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI) and 10 more consortia
Nature genetics · 2014 · PMID 25064009 · open access
12 pages+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
and 136 more — show all
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
Genetic architecture of cerebrospinal fluid and brain metabolite levels and the genetic colocalization of metabolites with human traits
Wang C,
Yang C,
Western D,
Ali M,
Wang Y,
Phuah CL,
Budde J,
Wang L,
Gorijala P,
Timsina J,
Ruiz A,
Pastor P
and 14 more — show all
Fernandez MV,
Panyard DJ,
Engelman CD,
Deming Y,
Boada M,
Cano A,
Garcia-Gonzalez P,
Graff-Radford NR,
Mori H,
Lee JH,
Perrin RJ,
Ibanez L,
Sung YJ,
Cruchaga C
Dominantly Inherited Alzheimer Network (DIAN) · Alzheimer’s Disease Neuroimaging Initiative (ADNI)
Nature genetics · 2024 · PMID 39528826
12 pages+
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
de Vries PS,
Brown MR,
Bentley AR,
Sung YJ,
Winkler TW,
Ntalla I,
Schwander K,
Kraja AT,
Guo X,
Franceschini N,
Cheng CY,
Sim X
and 254 more — show all
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Aschard H,
Bartz TM,
Bielak LF,
Deng X,
Dorajoo R,
Lohman KK,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Evangelou E,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Laguzzi F,
Lee JH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Riaz M,
Said MA,
Scott RA,
Sofer T,
Stančáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang Y,
Ware EB,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Amin N,
Amini M,
Arking DE,
Aung T,
Ballantyne C,
Boerwinkle E,
Broeckel U,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Connell JM,
de Faire U,
de las Fuentes L,
de Mutsert R,
de Silva HJ,
Ding J,
Dominiczak AF,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Fisher V,
Forrester T,
Franco OH,
Friedlander Y,
Ghanbari M,
Giulianini F,
Grabe HJ,
Grove ML,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Howard BV,
Ikram MA,
Jacobs DR,
Johnson C,
Jonas JB,
Kammerer CM,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Koistinen HA,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lemaitre RN,
Li Y,
Liang J,
Liu J,
Liu K,
Loh M,
Louie T,
Mägi R,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Mosley TH,
Mukamal KJ,
Nalls MA,
Nauck M,
Nelson CP,
Sotoodehnia N,
O'Connell JR,
Palmer ND,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raffel LJ,
Raitakari OT,
Reiner AP,
Rice TK,
Rich SS,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith BH,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tan N,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
van Heemst D,
Vuckovic D,
Waldenberger M,
Wang L,
Wang Y,
Wang Z,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Kamatani Y,
Kato N,
Kooner JS,
Laakso M,
Leander K,
Lehtimäki T,
Magnusson PKE,
Penninx B,
Pereira AC,
Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Zheng W,
Elliott P,
North KE,
Bouchard C,
Evans MK,
Gudnason V,
Liu CT,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Kardia SLR,
Zhu X,
Rotimi CN,
Mook-Kanamori DO,
Fornage M,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Liu J,
Rotter JI,
Gauderman WJ,
Province MA,
Munroe PB,
Rice K,
Chasman DI,
Cupples LA,
Rao DC,
Morrison AC
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations
Yang SK,
Hong M,
Zhao W,
Jung Y,
Baek J,
Tayebi N,
Kim KM,
Ye BD,
Kim KJ,
Park SH,
Lee I,
Lee EJ
and 16 more — show all
Kim WH,
Cheon JH,
Kim YH,
Jang BI,
Kim HS,
Choi JH,
Koo JS,
Lee JH,
Jung SA,
Lee YJ,
Jang JY,
Shin HD,
Kang D,
Youn HS,
Liu J,
Song K
Gut · 2014 · PMID 23850713
3 pages
HLA-C*01 is a Risk Factor for Crohn's Disease
Jung ES,
Cheon JH,
Lee JH,
Park SJ,
Jang HW,
Chung SH,
Park MH,
Kim TG,
Oh HB,
Yang SK,
Park SH,
Han JY
and 4 more — show all
Inflammatory bowel diseases · 2016 · PMID 26891255
3 pages
Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions
Kim YK,
Kim Y,
Hwang MY,
Shimokawa K,
Won S,
Kato N,
Tabara Y,
Yokota M,
Han BG,
Lee JH,
Kim BJ
BMC medical genetics · 2014 · PMID 24903457 · open access
1 page
Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans
Yang SK,
Hong M,
Choi H,
Zhao W,
Jung Y,
Haritunians T,
Ye BD,
Kim KJ,
Park SH,
Lee I,
Kim WH,
Cheon JH
and 15 more — show all
Kim YH,
Jang BI,
Kim HS,
Choi JH,
Koo JS,
Lee JH,
Jung SA,
Shin HD,
Kang D,
Youn HS,
Taylor KD,
Rotter JI,
Liu J,
McGovern DP,
Song K
Inflammatory bowel diseases · 2015 · PMID 25489960
1 page
A coding variant in <i>FTO</i> confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD
Kim HS,
Cheon JH,
Jung ES,
Park J,
Aum S,
Park SJ,
Eun S,
Lee J,
Rüther U,
Yeo GSH,
Ma M,
Park KS
and 5 more — show all
Gut · 2017 · PMID 27558924
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.