For researchers
Is your paper here?
2,661 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.
9 matches for
Lu T.
Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases
Chen Y,
Lu T,
Pettersson-Kymmer U,
Stewart ID,
Butler-Laporte G,
Nakanishi T,
Cerani A,
Liang KYH,
Yoshiji S,
Willett JDS,
Su CY,
Raina P
and 7 more — show all
Nature genetics · 2023 · PMID 36635386
12 pages+
An atlas of genetic determinants of forearm fracture
Nethander M,
Movérare-Skrtic S,
Kämpe A,
Coward E,
Reimann E,
Grahnemo L,
Borbély É,
Helyes Z,
Funck-Brentano T,
Cohen-Solal M,
Tuukkanen J,
Koskela A
and 23 more — show all
Wu J,
Li L,
Lu T,
Gabrielsen ME,
Mägi R,
Hoff M,
Lerner UH,
Henning P,
Ullum H,
Erikstrup C,
Brunak S,
Langhammer A,
Tuomi T,
Oddsson A,
Stefansson K,
Pettersson-Kymmer U,
Ostrowski SR,
Pedersen OBV,
Styrkarsdottir U,
Mäkitie O,
Hveem K,
Richards JB,
Ohlsson C
Estonian Biobank Research Team · DBDS Genomic Consortium
Nature genetics · 2023 · PMID 37919453 · open access
10 pages
Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study
Ortiz-Fernández L,
Saruhan-Direskeneli G,
Alibaz-Oner F,
Kaymaz-Tahra S,
Coit P,
Kong X,
Kiprianos AP,
Maughan RT,
Aydin SZ,
Aksu K,
Keser G,
Kamali S
and 59 more — show all
Inanc M,
Springer J,
Akar S,
Onen F,
Akkoc N,
Khalidi NA,
Koening C,
Karadag O,
Kiraz S,
Forbess L,
Langford CA,
McAlear CA,
Ozbalkan Z,
Yavuz S,
Çetin GY,
Alpay-Kanitez N,
Chung S,
Ates A,
Karaaslan Y,
McKinnon-Maksimowicz K,
Monach PA,
Ozer HTE,
Seyahi E,
Fresko I,
Cefle A,
Seo P,
Warrington KJ,
Ozturk MA,
Ytterberg SR,
Cobankara V,
Onat AM,
Duzgun N,
Bıcakcıgil M,
Yentür SP,
Lally L,
Manfredi AA,
Baldissera E,
Erken E,
Yazici A,
Kısacık B,
Kaşifoğlu T,
Dalkilic E,
Cuthbertson D,
Pagnoux C,
Sreih A,
Reales G,
Wallace C,
Wren JD,
Cunninghame-Graham DS,
Vyse TJ,
Sun Y,
Chen H,
Grayson PC,
Tombetti E,
Jiang L,
Mason JC,
Merkel PA,
Direskeneli H,
Sawalha AH
American journal of human genetics · 2021 · PMID 33308445
6 pages
Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study
Yu H,
Yan H,
Wang L,
Li J,
Tan L,
Deng W,
Chen Q,
Yang G,
Zhang F,
Lu T,
Yang J,
Li K
and 12 more — show all
Lv L,
Tan Q,
Zhang H,
Xiao X,
Li M,
Ma X,
Yang F,
Li L,
Wang C,
Li T,
Zhang D,
Yue W
Chinese Antipsychotics Pharmacogenomics Consortium
The lancet. Psychiatry · 2018 · PMID 29503163
4 pages
The largest genome-wide association study for breast cancer in Taiwanese Han population
Hsu YC,
Chen HL,
Cheng CF,
Chattopadhyay A,
Chen PS,
Lin CC,
Chiang HY,
Liu TY,
Huang CH,
Kuo CC,
Chuang EY,
Lu TP
and 1 more — show all
Breast cancer research and treatment · 2024 · PMID 37851288
4 pages
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk loci
Ishikawa T,
Masuda T,
Hachiya T,
Dina C,
Simonet F,
Nagata Y,
Tanck MWT,
Sonehara K,
Glinge C,
Tadros R,
Khongphatthanayothin A,
Lu TP
and 26 more — show all
Higuchi C,
Nakajima T,
Hayashi K,
Aizawa Y,
Nakano Y,
Nogami A,
Morita H,
Ohno S,
Aiba T,
Krijger Juárez C,
Mauleekoonphairoj J,
Poovorawan Y,
Gourraud JB,
Shimizu W,
Probst V,
Horie M,
Wilde AAM,
Redon R,
Juang JJ,
Nademanee K,
Bezzina CR,
Barc J,
Tanaka T,
Okada Y,
Schott JJ,
Makita N
European heart journal · 2024 · PMID 38747976
3 pages
Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study
Renauer PA,
Saruhan-Direskeneli G,
Coit P,
Adler A,
Aksu K,
Keser G,
Alibaz-Oner F,
Aydin SZ,
Kamali S,
Inanc M,
Carette S,
Cuthbertson D
and 43 more — show all
Hoffman GS,
Akar S,
Onen F,
Akkoc N,
Khalidi NA,
Koening C,
Karadag O,
Kiraz S,
Langford CA,
Maksimowicz-McKinnon K,
McAlear CA,
Ozbalkan Z,
Ates A,
Karaaslan Y,
Duzgun N,
Monach PA,
Ozer HT,
Erken E,
Ozturk MA,
Yazici A,
Cefle A,
Onat AM,
Kisacik B,
Pagnoux C,
Kasifoglu T,
Seyahi E,
Fresko I,
Seo P,
Sreih AG,
Warrington KJ,
Ytterberg SR,
Cobankara V,
Cunninghame-Graham DS,
Vyse TJ,
Pamuk ON,
Tunc SE,
Dalkilic E,
Bicakcigil M,
Yentur SP,
Wren JD,
Merkel PA,
Direskeneli H,
Sawalha AH
Arthritis & rheumatology (Hoboken, N.J.) · 2015 · PMID 25604533
1 page
ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response
Adeyemo AA,
Zaghloul NA,
Chen G,
Doumatey AP,
Leitch CC,
Hostelley TL,
Nesmith JE,
Zhou J,
Bentley AR,
Shriner D,
Fasanmade O,
Okafor G
and 14 more — show all
Eghan B Jr,
Agyenim-Boateng K,
Chandrasekharappa S,
Adeleye J,
Balogun W,
Owusu S,
Amoah A,
Acheampong J,
Johnson T,
Oli J,
Adebamowo C,
Collins F,
Dunston G,
Rotimi CN
South Africa Zulu Type 2 Diabetes Case-Control Study
Nature communications · 2019 · PMID 31324766 · open access
1 page
Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease
Ortiz Fernández L,
Coit P,
Yilmaz V,
Yentür SP,
Alibaz-Oner F,
Aksu K,
Erken E,
Düzgün N,
Keser G,
Cefle A,
Yazici A,
Ergen A
and 25 more — show all
Alpsoy E,
Salvarani C,
Casali B,
Kısacık B,
Kötter I,
Henes J,
Çınar M,
Schaefer A,
Nohutcu RM,
Zhernakova A,
Wijmenga C,
Takeuchi F,
Harihara S,
Kaburaki T,
Messedi M,
Song YW,
Kaşifoğlu T,
Carmona FD,
Guthridge JM,
James JA,
Martin J,
González Escribano MF,
Saruhan-Direskeneli G,
Direskeneli H,
Sawalha AH
Arthritis & rheumatology (Hoboken, N.J.) · 2021 · PMID 33393726
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.