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2,662 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.
16 matches for
He K.
Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney
Wain LV,
Vaez A,
Jansen R,
Joehanes R,
van der Most PJ,
Erzurumluoglu AM,
O'Reilly PF,
Cabrera CP,
Warren HR,
Rose LM,
Verwoert GC,
Hottenga JJ
and 239 more — show all
Strawbridge RJ,
Esko T,
Arking DE,
Hwang SJ,
Guo X,
Kutalik Z,
Trompet S,
Shrine N,
Teumer A,
Ried JS,
Bis JC,
Smith AV,
Amin N,
Nolte IM,
Lyytikäinen LP,
Mahajan A,
Wareham NJ,
Hofer E,
Joshi PK,
Kristiansson K,
Traglia M,
Havulinna AS,
Goel A,
Nalls MA,
Sõber S,
Vuckovic D,
Luan J,
Del Greco M F,
Ayers KL,
Marrugat J,
Ruggiero D,
Lopez LM,
Niiranen T,
Enroth S,
Jackson AU,
Nelson CP,
Huffman JE,
Zhang W,
Marten J,
Gandin I,
Harris SE,
Zemunik T,
Lu Y,
Evangelou E,
Shah N,
de Borst MH,
Mangino M,
Prins BP,
Campbell A,
Li-Gao R,
Chauhan G,
Oldmeadow C,
Abecasis G,
Abedi M,
Barbieri CM,
Barnes MR,
Batini C,
Beilby J,
Blake T,
Boehnke M,
Bottinger EP,
Braund PS,
Brown M,
Brumat M,
Campbell H,
Chambers JC,
Cocca M,
Collins F,
Connell J,
Cordell HJ,
Damman JJ,
Davies G,
de Geus EJ,
de Mutsert R,
Deelen J,
Demirkale Y,
Doney ASF,
Doney ASF,
Dörr M,
Farrall M,
Ferreira T,
Frånberg M,
Gao H,
Giedraitis V,
Gieger C,
Giulianini F,
Gow AJ,
Hamsten A,
Harris TB,
Hofman A,
Holliday EG,
Hui J,
Jarvelin MR,
Johansson Å,
Johnson AD,
Jousilahti P,
Jula A,
Kähönen M,
Kathiresan S,
Khaw KT,
Kolcic I,
Koskinen S,
Langenberg C,
Larson M,
Launer LJ,
Lehne B,
Liewald DCM,
Lin L,
Lind L,
Mach F,
Mamasoula C,
Menni C,
Menni C,
Mifsud B,
Milaneschi Y,
Morgan A,
Morris AD,
Morrison AC,
Munson PJ,
Nandakumar P,
Nguyen QT,
Nutile T,
Oldehinkel AJ,
Oostra BA,
Org E,
Org E,
Padmanabhan S,
Palotie A,
Paré G,
Pattie A,
Penninx BWJH,
Poulter N,
Pramstaller PP,
Raitakari OT,
Ren M,
Rice K,
Ridker PM,
Riese H,
Ripatti S,
Robino A,
Rotter JI,
Rudan I,
Saba Y,
Saint Pierre A,
Sala CF,
Sarin AP,
Schmidt R,
Scott R,
Seelen MA,
Shields DC,
Siscovick D,
Sorice R,
Stanton A,
Stott DJ,
Sundström J,
Swertz M,
Taylor KD,
Thom S,
Tzoulaki I,
Tzourio C,
Uitterlinden AG,
Uitterlinden AG,
Völker U,
Vollenweider P,
Wild S,
Willemsen G,
Wright AF,
Yao J,
Thériault S,
Conen D,
Attia J,
Sever P,
Debette S,
Mook-Kanamori DO,
Zeggini E,
Spector TD,
van der Harst P,
Palmer CNA,
Vergnaud AC,
Loos RJF,
Polasek O,
Polasek O,
Starr JM,
Girotto G,
Hayward C,
Kooner JS,
Lindgren CM,
Vitart V,
Samani NJ,
Tuomilehto J,
Gyllensten U,
Knekt P,
Deary IJ,
Ciullo M,
Elosua R,
Elosua R,
Keavney BD,
Hicks AA,
Scott RA,
Gasparini P,
Laan M,
Liu Y,
Watkins H,
Hartman CA,
Salomaa V,
Toniolo D,
Perola M,
Wilson JF,
Schmidt H,
Zhao JH,
Lehtimäki T,
Lehtimäki T,
van Duijn CM,
Gudnason V,
Psaty BM,
Peters A,
Rettig R,
James A,
Jukema JW,
Strachan DP,
Palmas W,
Metspalu A,
Ingelsson E,
Boomsma DI,
Franco OH,
Bochud M,
Newton-Cheh C,
Munroe PB,
Elliott P,
Chasman DI,
Chakravarti A,
Knight J,
Knight J,
Morris AP,
Levy D,
Tobin MD,
Snieder H,
Caulfield MJ,
Ehret GB
BIOS Consortium · Understanding Society Scientific Group
Hypertension (Dallas, Tex. : 1979) · 2017 · PMID 28739976
12 pages+
Causal Relationship and Shared Genetic Loci between Psoriasis and Type 2 Diabetes through Trans-Disease Meta-Analysis
Patrick MT,
Stuart PE,
Zhang H,
Zhao Q,
Yin X,
He K,
Zhou XJ,
Mehta NN,
Voorhees JJ,
Boehnke M,
Gudjonsson JE,
Nair RP
and 4 more — show all
The Journal of investigative dermatology · 2021 · PMID 33385400
12 pages+
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors
Melin BS,
Barnholtz-Sloan JS,
Wrensch MR,
Johansen C,
Il'yasova D,
Kinnersley B,
Ostrom QT,
Labreche K,
Chen Y,
Armstrong G,
Liu Y,
Eckel-Passow JE
and 51 more — show all
Decker PA,
Labussière M,
Idbaih A,
Hoang-Xuan K,
Di Stefano AL,
Mokhtari K,
Delattre JY,
Broderick P,
Galan P,
Gousias K,
Schramm J,
Schoemaker MJ,
Fleming SJ,
Herms S,
Heilmann S,
Nöthen MM,
Wichmann HE,
Schreiber S,
Swerdlow A,
Lathrop M,
Simon M,
Sanson M,
Andersson U,
Rajaraman P,
Chanock S,
Linet M,
Wang Z,
Yeager M,
Wiencke JK,
Hansen H,
McCoy L,
Rice T,
Kosel ML,
Sicotte H,
Amos CI,
Bernstein JL,
Davis F,
Lachance D,
Lau C,
Merrell RT,
Shildkraut J,
Ali-Osman F,
Sadetzki S,
Scheurer M,
Shete S,
Lai RK,
Claus EB,
Olson SH,
Jenkins RB,
Houlston RS,
Bondy ML
GliomaScan Consortium
Nature genetics · 2017 · PMID 28346443
10 pages
Genome-wide association study of selenium concentrations
Cornelis MC,
Fornage M,
Foy M,
Xun P,
Gladyshev VN,
Morris S,
Chasman DI,
Hu FB,
Rimm EB,
Kraft P,
Jordan JM,
Mozaffarian D
and 1 more — show all
Human molecular genetics · 2015 · PMID 25343990
7 pages
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits
Moon S,
Kim YJ,
Han S,
Hwang MY,
Shin DM,
Park MY,
Lu Y,
Yoon K,
Jang HM,
Kim YK,
Park TJ,
Song DS
and 3 more — show all
Scientific reports · 2019 · PMID 30718733 · open access
6 pages
Five endometrial cancer risk loci identified through genome-wide association analysis
Cheng TH,
Thompson DJ,
O'Mara TA,
Painter JN,
Glubb DM,
Flach S,
Lewis A,
French JD,
Freeman-Mills L,
Church D,
Gorman M,
Martin L
and 76 more — show all
Hodgson S,
Webb PM,
Attia J,
Holliday EG,
McEvoy M,
Scott RJ,
Henders AK,
Martin NG,
Montgomery GW,
Nyholt DR,
Ahmed S,
Healey CS,
Shah M,
Dennis J,
Fasching PA,
Beckmann MW,
Hein A,
Ekici AB,
Hall P,
Czene K,
Darabi H,
Li J,
Dörk T,
Dürst M,
Hillemanns P,
Runnebaum I,
Amant F,
Schrauwen S,
Zhao H,
Lambrechts D,
Depreeuw J,
Dowdy SC,
Goode EL,
Fridley BL,
Winham SJ,
Njølstad TS,
Salvesen HB,
Trovik J,
Werner HM,
Ashton K,
Otton G,
Proietto T,
Liu T,
Mints M,
Tham E,
Consortium C,
Jun Li M,
Yip SH,
Wang J,
Bolla MK,
Michailidou K,
Wang Q,
Tyrer JP,
Dunlop M,
Houlston R,
Palles C,
Hopper JL,
Peto J,
Swerdlow AJ,
Burwinkel B,
Brenner H,
Meindl A,
Brauch H,
Lindblom A,
Chang-Claude J,
Couch FJ,
Giles GG,
Kristensen VN,
Cox A,
Cunningham JM,
Pharoah PDP,
Dunning AM,
Edwards SL,
Easton DF,
Tomlinson I,
Spurdle AB
National Study of Endometrial Cancer Genetics Group (NSECG) · Australian National Endometrial Cancer Study Group (ANECS) and 2 more consortia
Nature genetics · 2016 · PMID 27135401 · open access
3 pages
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population
Yoon KA,
Park JH,
Han J,
Park S,
Lee GK,
Han JY,
Zo JI,
Kim J,
Lee JE,
Takahashi A,
Kubo M,
Nakamura Y
and 1 more — show all
Human molecular genetics · 2010 · PMID 20876614
1 page
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval
Marjamaa A,
Oikarinen L,
Porthan K,
Ripatti S,
Peloso G,
Noseworthy PA,
Viitasalo M,
Nieminen MS,
Toivonen L,
Kontula K,
Peltonen L,
Havulinna AS
and 5 more — show all
Heart rhythm · 2012 · PMID 22342860
1 page
New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population
Go MJ,
Hwang JY,
Kim YJ,
Hee Oh J,
Kim YJ,
Heon Kwak S,
Soo Park K,
Lee J,
Kim BJ,
Han BG,
Cho MC,
Cho YS
and 1 more — show all
Journal of human genetics · 2013 · PMID 23575436
1 page
Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels
Zhang W,
Jernerén F,
Lehne BC,
Chen MH,
Luben RN,
Johnston C,
Elshorbagy A,
Eppinga RN,
Scott WR,
Adeyeye E,
Scott J,
Böger RH
and 7 more — show all
Thrombosis and haemostasis · 2016 · PMID 27656708
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.