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Is your paper here?
2,657 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.
14 matches for
Shi H.
A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity
Zhu Z,
Li J,
Si J,
Ma B,
Shi H,
Lv J,
Cao W,
Guo Y,
Millwood IY,
Walters RG,
Lin K,
Yang L
and 12 more — show all
Chen Y,
Du H,
Yu B,
Hasegawa K,
Camargo CA Jr,
Moffatt MF,
Cookson WOC,
Chen J,
Chen Z,
Li L,
Yu C,
Liang L
The European respiratory journal · 2021 · PMID 33766948
11 pages
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
Ishikawa Y,
Tanaka N,
Asano Y,
Kodera M,
Shirai Y,
Akahoshi M,
Hasegawa M,
Matsushita T,
Saito K,
Motegi SI,
Yoshifuji H,
Yoshizaki A
and 60 more — show all
Kohmoto T,
Takagi K,
Oka A,
Kanda M,
Tanaka Y,
Ito Y,
Nakano K,
Kasamatsu H,
Utsunomiya A,
Sekiguchi A,
Niiro H,
Jinnin M,
Makino K,
Makino T,
Ihn H,
Yamamoto M,
Suzuki C,
Takahashi H,
Nishida E,
Morita A,
Yamamoto T,
Fujimoto M,
Kondo Y,
Goto D,
Sumida T,
Ayuzawa N,
Yanagida H,
Horita T,
Atsumi T,
Endo H,
Shima Y,
Kumanogoh A,
Hirata J,
Otomo N,
Suetsugu H,
Koike Y,
Tomizuka K,
Yoshino S,
Liu X,
Ito S,
Hikino K,
Suzuki A,
Momozawa Y,
Ikegawa S,
Tanaka Y,
Ishikawa O,
Takehara K,
Torii T,
Sato S,
Okada Y,
Mimori T,
Matsuda F,
Matsuda K,
Amariuta T,
Imoto I,
Matsuo K,
Kuwana M,
Kawaguchi Y,
Ohmura K,
Terao C
Nature communications · 2024 · PMID 38296975 · open access
7 pages
Shared genetic and experimental links between obesity-related traits and asthma subtypes in UK Biobank
Zhu Z,
Guo Y,
Shi H,
Liu CL,
Panganiban RA,
Chung W,
O'Connor LJ,
Himes BE,
Gazal S,
Hasegawa K,
Camargo CA Jr,
Qi L
and 5 more — show all
The Journal of allergy and clinical immunology · 2020 · PMID 31669095
6 pages
Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population
Nakamura M,
Nishida N,
Kawashima M,
Aiba Y,
Tanaka A,
Yasunami M,
Nakamura H,
Komori A,
Nakamuta M,
Zeniya M,
Hashimoto E,
Ohira H
and 68 more — show all
Yamamoto K,
Onji M,
Kaneko S,
Honda M,
Yamagiwa S,
Nakao K,
Ichida T,
Takikawa H,
Seike M,
Umemura T,
Ueno Y,
Sakisaka S,
Kikuchi K,
Ebinuma H,
Yamashiki N,
Tamura S,
Sugawara Y,
Mori A,
Yagi S,
Shirabe K,
Taketomi A,
Arai K,
Monoe K,
Ichikawa T,
Taniai M,
Miyake Y,
Kumagi T,
Abe M,
Yoshizawa K,
Joshita S,
Shimoda S,
Honda K,
Takahashi H,
Hirano K,
Takeyama Y,
Harada K,
Migita K,
Ito M,
Yatsuhashi H,
Fukushima N,
Ota H,
Komatsu T,
Saoshiro T,
Ishida J,
Kouno H,
Kouno H,
Yagura M,
Kobayashi M,
Muro T,
Masaki N,
Hirata K,
Watanabe Y,
Nakamura Y,
Shimada M,
Hirashima N,
Komeda T,
Sugi K,
Koga M,
Ario K,
Takesaki E,
Maehara Y,
Uemoto S,
Kokudo N,
Tsubouchi H,
Mizokami M,
Nakanuma Y,
Tokunaga K,
Ishibashi H
American journal of human genetics · 2012 · PMID 23000144
3 pages
Genetic determinants and an epistasis of <i>LILRA3</i> and HLA-B*52 in Takayasu arteritis
Terao C,
Yoshifuji H,
Matsumura T,
Naruse TK,
Ishii T,
Nakaoka Y,
Kirino Y,
Matsuo K,
Origuchi T,
Shimizu M,
Maejima Y,
Amiya E
and 29 more — show all
Tamura N,
Kawaguchi T,
Takahashi M,
Setoh K,
Ohmura K,
Watanabe R,
Horita T,
Atsumi T,
Matsukura M,
Miyata T,
Kochi Y,
Suda T,
Tanemoto K,
Meguro A,
Okada Y,
Ogimoto A,
Yamamoto M,
Takahashi H,
Nakayamada S,
Saito K,
Kuwana M,
Mizuki N,
Tabara Y,
Ueda A,
Komuro I,
Kimura A,
Isobe M,
Mimori T,
Matsuda F
Proceedings of the National Academy of Sciences of the United States of America · 2018 · PMID 30498034
3 pages
Genome-wide association analyses using machine learning-based phenotyping reveal genetic architecture of occupational creativity and overlap with psychiatric disorders
Kim H,
Ahn Y,
Yoon J,
Jung K,
Kim S,
Shim I,
Park TH,
Ko H,
Jung SH,
Kim J,
Park S,
Lee DJ
and 15 more — show all
Choi S,
Cha S,
Kim B,
Cho MY,
Cho H,
Kim DS,
Jang Y,
Ihm HK,
Park WY,
Bakhshi H,
O Connell KS,
Andreassen OA,
Kendler KS,
Myung W,
Won HH
Psychiatry research · 2024 · PMID 38335777
3 pages
A genome-wide association study identified PTPN2 as a population-specific susceptibility gene locus for primary biliary cholangitis
Hitomi Y,
Ueno K,
Aiba Y,
Nishida N,
Kono M,
Sugihara M,
Kawai Y,
Kawashima M,
Khor SS,
Sugi K,
Kouno H,
Kohno H
and 52 more — show all
Naganuma A,
Iwamoto S,
Katsushima S,
Furuta K,
Nikami T,
Mannami T,
Yamashita T,
Ario K,
Komatsu T,
Makita F,
Shimada M,
Hirashima N,
Yokohama S,
Nishimura H,
Sugimoto R,
Komura T,
Ota H,
Kojima M,
Nakamuta M,
Fujimori N,
Yoshizawa K,
Mano Y,
Takahashi H,
Hirooka K,
Tsuruta S,
Sato T,
Yamasaki K,
Kugiyama Y,
Motoyoshi Y,
Suehiro T,
Saeki A,
Matsumoto K,
Nagaoka S,
Abiru S,
Yatsuhashi H,
Ito M,
Kawata K,
Takaki A,
Arai K,
Arinaga-Hino T,
Abe M,
Harada M,
Taniai M,
Zeniya M,
Ohira H,
Shimoda S,
Komori A,
Tanaka A,
Ishigaki K,
Nagasaki M,
Tokunaga K,
Nakamura M
Hepatology (Baltimore, Md.) · 2024 · PMID 38652555
3 pages
IgG4-related disease in the Japanese population: a whole-genome sequencing study
Zhang YO,
Iwasaki T,
Kawaguchi T,
Takahashi H,
Kawaguchi S,
Kanno A,
Yamaguchi I,
Kubota K,
Dobashi H,
Nagasaki M,
Yamamoto M,
Takahashi M
and 39 more — show all
Shimizu M,
Ikeura T,
Matsui S,
Kanda M,
Nakamura K,
Yokoyama K,
Azumi A,
Masaki Y,
Mizushima I,
Kurita Y,
Seno H,
Origuchi T,
Yazumi S,
Hirano K,
Masamune A,
Mizuno N,
Shimada H,
Moriyama M,
Hori Y,
Kodama Y,
Saeki T,
Kin T,
Kawanami C,
Asada M,
Akamizu T,
Nakamura A,
Oshima K,
Tanaka Y,
Yoshifuji H,
Kamisawa T,
Kimura T,
Umehara H,
Ishikawa H,
Chiba T,
Okazaki K,
Mimori T,
Nakamura S,
Kawano M,
Matsuda F
Japanese IgG4-Related Disease Working Consortium
The Lancet. Rheumatology · 2026 · PMID 41197642
3 pages
A SNP in the ABCC11 gene is the determinant of human earwax type
Yoshiura K,
Kinoshita A,
Ishida T,
Ninokata A,
Ishikawa T,
Kaname T,
Bannai M,
Tokunaga K,
Sonoda S,
Komaki R,
Ihara M,
Saenko VA
and 27 more — show all
Alipov GK,
Sekine I,
Komatsu K,
Takahashi H,
Nakashima M,
Sosonkina N,
Mapendano CK,
Ghadami M,
Nomura M,
Liang DS,
Miwa N,
Kim DK,
Garidkhuu A,
Natsume N,
Ohta T,
Tomita H,
Kaneko A,
Kikuchi M,
Russomando G,
Hirayama K,
Ishibashi M,
Takahashi A,
Saitou N,
Murray JC,
Saito S,
Nakamura Y,
Niikawa N
Nature genetics · 2006 · PMID 16444273
1 page
Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C
Tanaka Y,
Kurosaki M,
Nishida N,
Sugiyama M,
Matsuura K,
Sakamoto N,
Enomoto N,
Yatsuhashi H,
Nishiguchi S,
Hino K,
Hige S,
Itoh Y
and 10 more — show all
Human molecular genetics · 2011 · PMID 21659334
1 page
Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies
Ng SC,
Shi HY,
Hamidi N,
Underwood FE,
Tang W,
Benchimol EI,
Panaccione R,
Ghosh S,
Wu JCY,
Chan FKL,
Sung JJY,
Kaplan GG
Lancet (London, England) · 2017 · PMID 29050646
1 page
CCDC102B confers risk of low vision and blindness in high myopia
Hosoda Y,
Yoshikawa M,
Miyake M,
Tabara Y,
Shimada N,
Zhao W,
Oishi A,
Nakanishi H,
Hata M,
Akagi T,
Ooto S,
Nagaoka N
and 8 more — show all
Nagahama Study group
Nature communications · 2018 · PMID 29725004 · open access
1 page
Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy
Hosoda Y,
Miyake M,
Schellevis RL,
Boon CJF,
Hoyng CB,
Miki A,
Meguro A,
Sakurada Y,
Yoneyama S,
Takasago Y,
Hata M,
Muraoka Y
and 22 more — show all
Nakanishi H,
Oishi A,
Ooto S,
Tamura H,
Uji A,
Miyata M,
Takahashi A,
Ueda-Arakawa N,
Tajima A,
Sato T,
Mizuki N,
Shiragami C,
Iida T,
Khor CC,
Wong TY,
Yamada R,
Honda S,
de Jong EK,
Hollander AID,
Matsuda F,
Yamashiro K,
Tsujikawa A
Communications biology · 2019 · PMID 31872073 · open access
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.