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2,663 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.
28 matches for
Ma T,
showing the first 8.
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
A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder
Ikeda M,
Takahashi A,
Kamatani Y,
Okahisa Y,
Kunugi H,
Mori N,
Sasaki T,
Ohmori T,
Okamoto Y,
Kawasaki H,
Shimodera S,
Kato T
and 28 more — show all
Yoneda H,
Yoshimura R,
Iyo M,
Matsuda K,
Akiyama M,
Ashikawa K,
Kashiwase K,
Tokunaga K,
Kondo K,
Saito T,
Shimasaki A,
Kawase K,
Kitajima T,
Matsuo K,
Itokawa M,
Someya T,
Inada T,
Hashimoto R,
Inoue T,
Akiyama K,
Tanii H,
Arai H,
Kanba S,
Ozaki N,
Kusumi I,
Yoshikawa T,
Kubo M,
Iwata N
Molecular psychiatry · 2018 · PMID 28115744 · open access
2 pages
A cross-population compendium of gene-environment interactions
Namba S,
Sonehara K,
Koyanagi YN,
Kikuchi T,
Ojima T,
Edahiro R,
Sato G,
Yamaji T,
Tomofuji Y,
Ueda H,
Yamamoto K,
Ogawa Y
and 26 more — show all
Suzuki K,
Kanai A,
Higashiue S,
Kobayashi S,
Yamaguchi H,
Nagata Y,
Okazaki Y,
Matsumoto N,
Motomura K,
Koga H,
Hishida A,
Ikezaki H,
Hara M,
Nagayoshi M,
Oze I,
Nakano S,
Oda Y,
Suzuki Y,
Iwasaki M,
Sawada N,
Matsuo K,
Morisaki T,
Yamauchi T,
Kadowaki T,
Matsuda K,
Okada Y
BioBank Japan Project
Nature · 2026 · PMID 41606330 · open access
2 pages
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population
Takeuchi F,
Serizawa M,
Yamamoto K,
Fujisawa T,
Nakashima E,
Ohnaka K,
Ikegami H,
Sugiyama T,
Katsuya T,
Miyagishi M,
Nakashima N,
Nawata H
and 4 more — show all
Diabetes · 2009 · PMID 19401414 · open access
1 page
A Loss-of-Function Splice Acceptor Variant in <i>IGF2</i> Is Protective for Type 2 Diabetes
Mercader JM,
Liao RG,
Bell AD,
Dymek Z,
Estrada K,
Tukiainen T,
Huerta-Chagoya A,
Moreno-Macías H,
Jablonski KA,
Hanson RL,
Walford GA,
Moran I
and 66 more — show all
Chen L,
Agarwala V,
Ordoñez-Sánchez ML,
Rodríguez-Guillen R,
Rodríguez-Torres M,
Segura-Kato Y,
García-Ortiz H,
Centeno-Cruz F,
Barajas-Olmos F,
Caulkins L,
Puppala S,
Fontanillas P,
Williams AL,
Bonàs-Guarch S,
Hartl C,
Ripke S,
Tooley K,
Lane J,
Zerrweck C,
Martínez-Hernández A,
Córdova EJ,
Mendoza-Caamal E,
Contreras-Cubas C,
González-Villalpando ME,
Cruz-Bautista I,
Muñoz-Hernández L,
Gómez-Velasco D,
Alvirde U,
Henderson BE,
Wilkens LR,
Le Marchand L,
Arellano-Campos O,
Riba L,
Harden M,
Gabriel S,
Abboud HE,
Cortes ML,
Revilla-Monsalve C,
Islas-Andrade S,
Soberon X,
Curran JE,
Jenkinson CP,
DeFronzo RA,
Lehman DM,
Hanis CL,
Bell GI,
Boehnke M,
Blangero J,
Duggirala R,
Saxena R,
MacArthur D,
Ferrer J,
McCarroll SA,
Torrents D,
Knowler WC,
Baier LJ,
Burtt N,
González-Villalpando C,
Haiman CA,
Aguilar-Salinas CA,
Tusié-Luna T,
Flannick J,
Jacobs SBR,
Orozco L,
Altshuler D,
Florez JC
Diabetes Prevention Program Research Group · Broad Genomics Platform and 2 more consortia
Diabetes · 2017 · PMID 28838971 · open access
1 page
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
Gharahkhani P,
Burdon KP,
Cooke Bailey JN,
Hewitt AW,
Law MH,
Pasquale LR,
Kang JH,
Haines JL,
Souzeau E,
Zhou T,
Siggs OM,
Landers J
and 27 more — show all
Awadalla M,
Sharma S,
Mills RA,
Ridge B,
Lynn D,
Casson R,
Graham SL,
Goldberg I,
White A,
Healey PR,
Grigg J,
Lawlor M,
Mitchell P,
Ruddle J,
Coote M,
Walland M,
Best S,
Vincent A,
Gale J,
RadfordSmith G,
Whiteman DC,
Montgomery GW,
Martin NG,
Mackey DA,
Wiggs JL,
MacGregor S,
Craig JE
NEIGHBORHOOD consortium
Scientific reports · 2018 · PMID 29449654 · open access
1 page
GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy
Hishida A,
Ugai T,
Fujii R,
Nakatochi M,
Wu MC,
Ito H,
Oze I,
Tajika M,
Niwa Y,
Nishiyama T,
Nakagawa-Senda H,
Suzuki S
and 10 more — show all
Carcinogenesis · 2019 · PMID 30753327
1 page
Comparison of the loci associated with HbA1c and blood glucose levels identified by a genome-wide association study in the Japanese population
Sakashita T,
Nakamura Y,
Sutoh Y,
Shimizu A,
Hachiya T,
Otsuka-Yamasaki Y,
Takashima N,
Kadota A,
Miura K,
Kita Y,
Ikezaki H,
Otonari J
and 23 more — show all
Tanaka K,
Shimanoe C,
Koyama T,
Watanabe I,
Suzuki S,
Nakagawa-Senda H,
Hishida A,
Tamura T,
Kato Y,
Okada R,
Kuriki K,
Katsuura-Kamano S,
Watanabe T,
Tanoue S,
Koriyama C,
Oze I,
Koyanagi YN,
Nakamura Y,
Kusakabe M,
Nakatochi M,
Momozawa Y,
Wakai K,
Matsuo K
Diabetology international · 2023 · PMID 37090135
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.