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2,677 papers hold this site up. Every variant and condition page names
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145 matches for
He J,
showing the first 20.
Genome-wide association study of tanning phenotype in a population of European ancestry
Nan H,
Kraft P,
Qureshi AA,
Guo Q,
Chen C,
Hankinson SE,
Hu FB,
Thomas G,
Hoover RN,
Chanock S,
Hunter DJ,
Han J
The Journal of investigative dermatology · 2009 · PMID 19340012
2 pages
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population
Takata R,
Akamatsu S,
Kubo M,
Takahashi A,
Hosono N,
Kawaguchi T,
Tsunoda T,
Inazawa J,
Kamatani N,
Ogawa O,
Fujioka T,
Nakamura Y
and 1 more — show all
Nature genetics · 2010 · PMID 20676098
2 pages
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies
Reilly MP,
Li M,
He J,
Ferguson JF,
Stylianou IM,
Mehta NN,
Burnett MS,
Devaney JM,
Knouff CW,
Thompson JR,
Horne BD,
Stewart AF
and 20 more — show all
Assimes TL,
Wild PS,
Allayee H,
Nitschke PL,
Patel RS,
Martinelli N,
Girelli D,
Quyyumi AA,
Anderson JL,
Erdmann J,
Hall AS,
Schunkert H,
Quertermous T,
Blankenberg S,
Hazen SL,
Roberts R,
Kathiresan S,
Samani NJ,
Epstein SE,
Rader DJ
Myocardial Infarction Genetics Consortium · Wellcome Trust Case Control Consortium
Lancet (London, England) · 2011 · PMID 21239051
2 pages
Meta-analysis identifies common variants associated with body mass index in east Asians
Wen W,
Cho YS,
Zheng W,
Zheng W,
Dorajoo R,
Kato N,
Qi L,
Chen CH,
Delahanty RJ,
Okada Y,
Tabara Y,
Gu D
and 52 more — show all
Zhu D,
Haiman CA,
Mo Z,
Gao YT,
Saw SM,
Go MJ,
Takeuchi F,
Chang LC,
Kokubo Y,
Liang J,
Hao M,
Le Marchand L,
Zhang Y,
Hu Y,
Wong TY,
Long J,
Han BG,
Kubo M,
Yamamoto K,
Su MH,
Miki T,
Henderson BE,
Song H,
Tan A,
He J,
Ng DP,
Cai Q,
Tsunoda T,
Tsai FJ,
Iwai N,
Chen GK,
Shi J,
Xu J,
Sim X,
Xiang YB,
Maeda S,
Ong RT,
Li C,
Nakamura Y,
Aung T,
Kamatani N,
Liu JJ,
Lu W,
Yokota M,
Seielstad M,
Fann CS,
Wu JY,
Lee JY,
Hu FB,
Tanaka T,
Tai ES,
Shu XO
Genetic Investigation of ANthropometric Traits (GIANT) Consortium
Nature genetics · 2012 · PMID 22344219 · open access
2 pages
Evaluating genetic risk for prostate cancer among Japanese and Latinos
Cheng I,
Chen GK,
Nakagawa H,
He J,
Wan P,
Laurie CC,
Shen J,
Sheng X,
Pooler LC,
Crenshaw AT,
Mirel DB,
Takahashi A
and 19 more — show all
Kubo M,
Nakamura Y,
Al Olama AA,
Benlloch S,
Donovan JL,
Guy M,
Hamdy FC,
Kote-Jarai Z,
Neal DE,
Wilkens LR,
Monroe KR,
Stram DO,
Muir K,
Eeles RA,
Easton DF,
Kolonel LN,
Henderson BE,
Le Marchand L,
Haiman CA
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2012 · PMID 22923026
2 pages
T2R38 taste receptor polymorphisms underlie susceptibility to upper respiratory infection
Lee RJ,
Xiong G,
Kofonow JM,
Chen B,
Lysenko A,
Jiang P,
Abraham V,
Doghramji L,
Adappa ND,
Palmer JN,
Kennedy DW,
Beauchamp GK
and 5 more — show all
The Journal of clinical investigation · 2012 · PMID 23041624
2 pages
Genome-wide association study in Han Chinese identifies three novel loci for human height
Hao Y,
Liu X,
Lu X,
Yang X,
Wang L,
Chen S,
Li H,
Li J,
Cao J,
Chen J,
Li Y,
Zhao L
and 6 more — show all
Human genetics · 2013 · PMID 23456168
2 pages
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome
Dai Y,
Chen Y,
Huang H,
Zhou W,
Niu Y,
Zhang M,
Bin P,
Dong H,
Jia Q,
Huang J,
Yi J,
Liao Q
and 26 more — show all
Li H,
Teng Y,
Zang D,
Zhai Q,
Duan H,
Shen J,
He J,
Meng T,
Sha Y,
Shen M,
Ye M,
Jia X,
Xiang Y,
Huang H,
Wu Q,
Shi M,
Huang X,
Yang H,
Luo L,
Li S,
Li L,
Zhao J,
Li L,
Wang J,
Wang J,
Zheng Y
Scientific reports · 2015 · PMID 26190474 · open access
2 pages
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Kato N,
Loh M,
Takeuchi F,
Verweij N,
Wang X,
Zhang W,
Kelly TN,
Saleheen D,
Lehne B,
Leach IM,
Drong AW,
Abbott J
and 233 more — show all
Wahl S,
Tan ST,
Scott WR,
Campanella G,
Chadeau-Hyam M,
Afzal U,
Ahluwalia TS,
Bonder MJ,
Chen P,
Dehghan A,
Edwards TL,
Esko T,
Go MJ,
Harris SE,
Hartiala J,
Kasela S,
Kasturiratne A,
Khor CC,
Kleber ME,
Li H,
Yu Mok Z,
Nakatochi M,
Sapari NS,
Saxena R,
Stewart AFR,
Stolk L,
Tabara Y,
Teh AL,
Wu Y,
Wu JY,
Zhang Y,
Aits I,
Da Silva Couto Alves A,
Das S,
Dorajoo R,
Hopewell JC,
Kim YK,
Koivula RW,
Luan J,
Lyytikäinen LP,
Nguyen QN,
Pereira MA,
Postmus I,
Raitakari OT,
Scannell Bryan M,
Scott RA,
Sorice R,
Tragante V,
Traglia M,
White J,
Yamamoto K,
Zhang Y,
Adair LS,
Ahmed A,
Akiyama K,
Asif R,
Aung T,
Barroso I,
Bjonnes A,
Braun TR,
Cai H,
Chang LC,
Chen CH,
Cheng CY,
Chong YS,
Collins R,
Courtney R,
Davies G,
Delgado G,
Do LD,
Doevendans PA,
Gansevoort RT,
Gao YT,
Grammer TB,
Grarup N,
Grewal J,
Gu D,
Wander GS,
Hartikainen AL,
Hazen SL,
He J,
Heng CK,
Hixson JE,
Hofman A,
Hsu C,
Huang W,
Husemoen LLN,
Hwang JY,
Ichihara S,
Igase M,
Isono M,
Justesen JM,
Katsuya T,
Kibriya MG,
Kim YJ,
Kishimoto M,
Koh WP,
Kohara K,
Kumari M,
Kwek K,
Lee NR,
Lee J,
Liao J,
Lieb W,
Liewald DCM,
Matsubara T,
Matsushita Y,
Meitinger T,
Mihailov E,
Milani L,
Mills R,
Mononen N,
Müller-Nurasyid M,
Nabika T,
Nakashima E,
Ng HK,
Nikus K,
Nutile T,
Ohkubo T,
Ohnaka K,
Parish S,
Paternoster L,
Peng H,
Peters A,
Pham ST,
Pinidiyapathirage MJ,
Rahman M,
Rakugi H,
Rolandsson O,
Ann Rozario M,
Ruggiero D,
Sala CF,
Sarju R,
Shimokawa K,
Snieder H,
Sparsø T,
Spiering W,
Starr JM,
Stott DJ,
Stram DO,
Sugiyama T,
Szymczak S,
Tang WHW,
Tong L,
Trompet S,
Turjanmaa V,
Ueshima H,
Uitterlinden AG,
Umemura S,
Vaarasmaki M,
van Dam RM,
van Gilst WH,
van Veldhuisen DJ,
Viikari JS,
Waldenberger M,
Wang Y,
Wang A,
Wilson R,
Wong TY,
Xiang YB,
Yamaguchi S,
Ye X,
Young RD,
Young TL,
Yuan JM,
Zhou X,
Asselbergs FW,
Ciullo M,
Clarke R,
Deloukas P,
Franke A,
Franks PW,
Franks S,
Friedlander Y,
Gross MD,
Guo Z,
Hansen T,
Jarvelin MR,
Jørgensen T,
Jukema JW,
Kähönen M,
Kajio H,
Kivimaki M,
Lee JY,
Lehtimäki T,
Linneberg A,
Miki T,
Pedersen O,
Samani NJ,
Sørensen TIA,
Takayanagi R,
Toniolo D,
Ahsan H,
Allayee H,
Chen YT,
Danesh J,
Deary IJ,
Franco OH,
Franke L,
Heijman BT,
Holbrook JD,
Isaacs A,
Kim BJ,
Lin X,
Liu J,
März W,
Metspalu A,
Mohlke KL,
Sanghera DK,
Shu XO,
van Meurs JBJ,
Vithana E,
Wickremasinghe AR,
Wijmenga C,
Wolffenbuttel BHW,
Yokota M,
Zheng W,
Zheng W,
Zhu D,
Vineis P,
Kyrtopoulos SA,
Kleinjans JCS,
McCarthy MI,
Soong R,
Gieger C,
Scott J,
Teo YY,
He J,
Elliott P,
Tai ES,
van der Harst P,
Kooner JS,
Chambers JC
BIOS-consortium · CARDIo GRAMplusCD and 2 more consortia
Nature genetics · 2015 · PMID 26390057
2 pages
Association Study and Fine-Mapping Major Histocompatibility Complex Analysis of Pemphigus Vulgaris in a Han Chinese Population
Gao J,
Zhu C,
Zhang Y,
Sheng Y,
Yang F,
Wang W,
Qian W,
Chen S,
Zhu Q,
Zuo X,
Tang H,
Tang X
and 13 more — show all
Li Y,
Cheng H,
Zhou F,
Liu S,
Chen G,
Zheng X,
Zhu Z,
Wang Z,
Yang S,
Luo X,
Ye D,
Zhang X,
Sun L
The Journal of investigative dermatology · 2018 · PMID 29857070
2 pages
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Jones E,
Hummerich H,
Viré E,
Uphill J,
Dimitriadis A,
Speedy H,
Campbell T,
Norsworthy P,
Quinn L,
Whitfield J,
Linehan J,
Jaunmuktane Z
and 53 more — show all
Brandner S,
Jat P,
Nihat A,
How Mok T,
Ahmed P,
Collins S,
Stehmann C,
Sarros S,
Kovacs GG,
Geschwind MD,
Golubjatnikov A,
Frontzek K,
Budka H,
Aguzzi A,
Karamujić-Čomić H,
van der Lee SJ,
Ibrahim-Verbaas CA,
van Duijn CM,
Sikorska B,
Golanska E,
Liberski PP,
Calero M,
Calero O,
Sanchez-Juan P,
Salas A,
Martinón-Torres F,
Bouaziz-Amar E,
Haïk S,
Laplanche JL,
Brandel JP,
Amouyel P,
Lambert JC,
Parchi P,
Bartoletti-Stella A,
Capellari S,
Poleggi A,
Ladogana A,
Pocchiari M,
Aneli S,
Matullo G,
Knight R,
Zafar S,
Zerr I,
Booth S,
Coulthart MB,
Jansen GH,
Glisic K,
Blevins J,
Gambetti P,
Safar J,
Appleby B,
Collinge J,
Mead S
The Lancet. Neurology · 2020 · PMID 32949544
2 pages
Exome-Wide Association Analysis Suggests LRP2BP as a Susceptibility Gene for Endothelial Injury in Systemic Sclerosis in the Han Chinese Population
Pu W,
Wu W,
Liu Q,
Ma Y,
Tu W,
Zuo X,
Guo G,
Jiang S,
Zhao Y,
Zuo X,
Wang Q,
Yang L
and 32 more — show all
Xiao R,
Chu H,
Wang L,
Sun L,
Cui J,
Yu L,
Li H,
Li Y,
Shi Y,
Zhang J,
Zhang H,
Liang M,
Chen D,
Ding Y,
Chen X,
Chen Y,
Zhang R,
Zhao H,
Li Y,
Qi Q,
Bai P,
Zhao L,
Reveille JD,
Mayes MD,
Jin L,
Lee EB,
Zhang X,
Xu J,
Zhang Z,
Zhou X,
Zou H,
Wang J
The Journal of investigative dermatology · 2021 · PMID 33069728
2 pages
Identification of novel genes influencing eosinophil-specific protein levels in asthma families
Vernet R,
Matran R,
Zerimech F,
Madore AM,
Lavoie ME,
Gagnon PA,
Mohamdi H,
Margaritte-Jeannin P,
Siroux V,
Dizier MH,
Demenais F,
Laprise C
and 2 more — show all
The Journal of allergy and clinical immunology · 2022 · PMID 35671886
2 pages
Genome-Wide Association Study Identifies the First Germline Genetic Variant Associated With Erdheim-Chester Disease
Martínez-López J,
Márquez A,
Pegoraro F,
Ortiz-Fernández L,
Acosta-Herrera M,
Kerick M,
Gelain E,
Diamond EL,
Durham BH,
Abdel-Wahab O,
Go RS,
Koster MJ
and 12 more — show all
Dagna L,
Campochiaro C,
Collin M,
Milne P,
Estrada-Veras JI,
O'Brien K,
Papo M,
Cohen-Aubar F,
Amoura Z,
Haroche J,
Martín J,
Vaglio A
Arthritis & rheumatology (Hoboken, N.J.) · 2024 · PMID 37561109
2 pages
Meta-analysis of ACE inhibitor-induced angioedema identifies novel risk locus
Mathey CM,
Maj C,
Eriksson N,
Krebs K,
Westmeier J,
David FS,
Koromina M,
Scheer AB,
Szabo N,
Wedi B,
Wieczorek D,
Amann PM
and 39 more — show all
Löffler H,
Koch L,
Schöffl C,
Dickel H,
Ganjuur N,
Hornung T,
Buhl T,
Greve J,
Wurpts G,
Aygören-Pürsün E,
Steffens M,
Herms S,
Heilmann-Heimbach S,
Hoffmann P,
Schmidt B,
Mavarani L,
Andresen T,
Sørensen SB,
Andersen V,
Vogel U,
Landén M,
Bulik CM,
Bygum A,
Magnusson PKE,
von Buchwald C,
Hallberg P,
Rye Ostrowski S,
Sørensen E,
Pedersen OB,
Ullum H,
Erikstrup C,
Bundgaard H,
Milani L,
Rasmussen ER,
Wadelius M,
Ghouse J,
Sachs B,
Nöthen MM,
Forstner AJ
Estonian Biobank Research Team · DBDS Genomic Consortium
The Journal of allergy and clinical immunology · 2024 · PMID 38300190
2 pages
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.