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35 matches for
Terao C,
showing the first 15.
Genetic study identifies novel genes in developmental dysplasia of the hip
Yoshino S,
Chen S,
Yamaguchi R,
Kurakazu T,
Hatzikotoulas K,
Koike Y,
Inoue D,
Kohno Y,
Sasaki K,
Choe H,
Baba S,
Hara T
and 31 more — show all
Ito J,
Okuzu Y,
Shiomoto K,
Nakamura T,
Koyano G,
Shimizu T,
Kinoshita K,
Takahashi E,
Utsunomiya T,
Hara D,
Sato T,
Kawahara S,
Kaneuji A,
Yamamoto T,
Takahashi D,
Jinno T,
Kawano T,
Goto K,
Takagi M,
Mawatari T,
Inaba Y,
Nakamura T,
Kabata T,
Hamai S,
Motomura G,
Southam L,
Wilkinson JM,
Zeggini E,
Ikegawa S,
Nakashima Y,
Terao C
Bone research · 2026 · PMID 41912496 · open access
9 pages
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Kanoni S,
Graham SE,
Wang Y,
Surakka I,
Ramdas S,
Zhu X,
Clarke SL,
Bhatti KF,
Vedantam S,
Winkler TW,
Locke AE,
Marouli E
and 527 more — show all
Zajac GJM,
Wu KH,
Ntalla I,
Hui Q,
Klarin D,
Hilliard AT,
Wang Z,
Xue C,
Thorleifsson G,
Helgadottir A,
Gudbjartsson DF,
Holm H,
Olafsson I,
Hwang MY,
Han S,
Akiyama M,
Sakaue S,
Terao C,
Kanai M,
Zhou W,
Brumpton BM,
Rasheed H,
Havulinna AS,
Veturi Y,
Pacheco JA,
Rosenthal EA,
Lingren T,
Feng Q,
Kullo IJ,
Narita A,
Takayama J,
Martin HC,
Hunt KA,
Trivedi B,
Haessler J,
Giulianini F,
Bradford Y,
Miller JE,
Campbell A,
Lin K,
Millwood IY,
Rasheed A,
Hindy G,
Faul JD,
Zhao W,
Weir DR,
Turman C,
Huang H,
Graff M,
Choudhury A,
Sengupta D,
Mahajan A,
Brown MR,
Zhang W,
Yu K,
Schmidt EM,
Pandit A,
Gustafsson S,
Yin X,
Luan J,
Zhao JH,
Matsuda F,
Jang HM,
Yoon K,
Medina-Gomez C,
Pitsillides A,
Hottenga JJ,
Wood AR,
Ji Y,
Gao Z,
Haworth S,
Yousri NA,
Mitchell RE,
Chai JF,
Aadahl M,
Bjerregaard AA,
Yao J,
Manichaikul A,
Hwu CM,
Hung YJ,
Warren HR,
Ramirez J,
Bork-Jensen J,
Kårhus LL,
Goel A,
Sabater-Lleal M,
Noordam R,
Mauro P,
Matteo F,
McDaid AF,
Marques-Vidal P,
Wielscher M,
Trompet S,
Sattar N,
Møllehave LT,
Munz M,
Zeng L,
Huang J,
Yang B,
Poveda A,
Kurbasic A,
Lamina C,
Forer L,
Scholz M,
Galesloot TE,
Bradfield JP,
Ruotsalainen SE,
Daw E,
Zmuda JM,
Mitchell JS,
Fuchsberger C,
Christensen H,
Brody JA,
Vazquez-Moreno M,
Feitosa MF,
Wojczynski MK,
Wang Z,
Preuss MH,
Mangino M,
Christofidou P,
Verweij N,
Benjamins JW,
Engmann J,
Tsao NL,
Verma A,
Slieker RC,
Lo KS,
Zilhao NR,
Le P,
Kleber ME,
Delgado GE,
Huo S,
Ikeda DD,
Iha H,
Yang J,
Liu J,
Demirkan A,
Leonard HL,
Marten J,
Frank M,
Schmidt B,
Smyth LJ,
Cañadas-Garre M,
Wang C,
Nakatochi M,
Wong A,
Hutri-Kähönen N,
Sim X,
Xia R,
Huerta-Chagoya A,
Fernandez-Lopez JC,
Lyssenko V,
Nongmaithem SS,
Bayyana S,
Stringham HM,
Irvin MR,
Oldmeadow C,
Kim HN,
Ryu S,
Timmers PRHJ,
Arbeeva L,
Dorajoo R,
Lange LA,
Prasad G,
Lorés-Motta L,
Pauper M,
Long J,
Li X,
Theusch E,
Takeuchi F,
Spracklen CN,
Loukola A,
Bollepalli S,
Warner SC,
Wang YX,
Wei WB,
Nutile T,
Ruggiero D,
Sung YJ,
Chen S,
Liu F,
Yang J,
Kentistou KA,
Banas B,
Nardone GG,
Meidtner K,
Bielak LF,
Smith JA,
Hebbar P,
Farmaki AE,
Hofer E,
Lin M,
Concas MP,
Vaccargiu S,
van der Most PJ,
Pitkänen N,
Cade BE,
van der Laan SW,
Chitrala KN,
Weiss S,
Bentley AR,
Doumatey AP,
Adeyemo AA,
Lee JY,
Petersen ERB,
Nielsen AA,
Choi HS,
Nethander M,
Freitag-Wolf S,
Southam L,
Rayner NW,
Wang CA,
Lin SY,
Wang JS,
Couture C,
Lyytikäinen LP,
Nikus K,
Cuellar-Partida G,
Vestergaard H,
Hidalgo B,
Giannakopoulou O,
Cai Q,
Obura MO,
van Setten J,
Li X,
Liang J,
Tang H,
Terzikhan N,
Shin JH,
Jackson RD,
Reiner AP,
Martin LW,
Chen Z,
Li L,
Kawaguchi T,
Thiery J,
Bis JC,
Launer LJ,
Li H,
Nalls MA,
Raitakari OT,
Ichihara S,
Wild SH,
Nelson CP,
Campbell H,
Jäger S,
Nabika T,
Al-Mulla F,
Niinikoski H,
Braund PS,
Kolcic I,
Kovacs P,
Giardoglou T,
Katsuya T,
de Kleijn D,
de Borst GJ,
Kim EK,
Adams HHH,
Ikram MA,
Zhu X,
Asselbergs FW,
Kraaijeveld AO,
Beulens JWJ,
Shu XO,
Rallidis LS,
Pedersen O,
Hansen T,
Mitchell P,
Hewitt AW,
Kähönen M,
Pérusse L,
Bouchard C,
Tönjes A,
Chen YI,
Pennell CE,
Mori TA,
Lieb W,
Franke A,
Ohlsson C,
Mellström D,
Cho YS,
Lee H,
Yuan JM,
Koh WP,
Rhee SY,
Woo JT,
Heid IM,
Stark KJ,
Zimmermann ME,
Völzke H,
Homuth G,
Evans MK,
Zonderman AB,
Polasek O,
Pasterkamp G,
Hoefer IE,
Redline S,
Pahkala K,
Oldehinkel AJ,
Snieder H,
Biino G,
Schmidt R,
Schmidt H,
Bandinelli S,
Dedoussis G,
Thanaraj TA,
Kardia SLR,
Peyser PA,
Kato N,
Schulze MB,
Girotto G,
Böger CA,
Jung B,
Joshi PK,
Bennett DA,
De Jager PL,
Lu X,
Mamakou V,
Brown M,
Caulfield MJ,
Munroe PB,
Guo X,
Ciullo M,
Jonas JB,
Samani NJ,
Kaprio J,
Pajukanta P,
Tusié-Luna T,
Aguilar-Salinas CA,
Adair LS,
Bechayda SA,
de Silva HJ,
Wickremasinghe AR,
Krauss RM,
Wu JY,
Zheng W,
Hollander AI,
Bharadwaj D,
Correa A,
Wilson JG,
Lind L,
Heng CK,
Nelson AE,
Golightly YM,
Wilson JF,
Penninx B,
Kim HL,
Attia J,
Scott RJ,
Rao DC,
Arnett DK,
Hunt SC,
Walker M,
Koistinen HA,
Chandak GR,
Mercader JM,
Costanzo MC,
Jang D,
Burtt NP,
Villalpando CG,
Orozco L,
Fornage M,
Tai E,
van Dam RM,
Lehtimäki T,
Chaturvedi N,
Yokota M,
Liu J,
Reilly DF,
McKnight AJ,
Kee F,
Jöckel KH,
McCarthy MI,
Palmer CNA,
Vitart V,
Hayward C,
Simonsick E,
van Duijn CM,
Jin ZB,
Qu J,
Hishigaki H,
Lin X,
März W,
Gudnason V,
Tardif JC,
Lettre G,
Hart LM',
Elders PJM,
Damrauer SM,
Kumari M,
Kivimaki M,
van der Harst P,
Spector TD,
Loos RJF,
Province MA,
Parra EJ,
Cruz M,
Psaty BM,
Brandslund I,
Pramstaller PP,
Rotimi CN,
Christensen K,
Ripatti S,
Widén E,
Hakonarson H,
Grant SFA,
Kiemeney LALM,
de Graaf J,
Loeffler M,
Kronenberg F,
Gu D,
Erdmann J,
Schunkert H,
Franks PW,
Linneberg A,
Jukema JW,
Khera AV,
Männikkö M,
Jarvelin MR,
Kutalik Z,
Francesco C,
Mook-Kanamori DO,
van Dijk KW,
Watkins H,
Strachan DP,
Grarup N,
Sever P,
Poulter N,
Chuang LM,
Rotter JI,
Dantoft TM,
Karpe F,
Neville MJ,
Timpson NJ,
Cheng CY,
Wong TY,
Khor CC,
Li H,
Sabanayagam C,
Peters A,
Gieger C,
Hattersley AT,
Pedersen NL,
Magnusson PKE,
Boomsma DI,
Willemsen AHM,
Cupples L,
van Meurs JBJ,
Ghanbari M,
Gordon-Larsen P,
Huang W,
Kim YJ,
Tabara Y,
Wareham NJ,
Langenberg C,
Zeggini E,
Kuusisto J,
Laakso M,
Ingelsson E,
Abecasis G,
Chambers JC,
Kooner JS,
de Vries PS,
Morrison AC,
Hazelhurst S,
Ramsay M,
North KE,
Daviglus M,
Kraft P,
Martin NG,
Whitfield JB,
Abbas S,
Saleheen D,
Walters RG,
Holmes MV,
Black C,
Smith BH,
Baras A,
Justice AE,
Buring JE,
Ridker PM,
Chasman DI,
Kooperberg C,
Tamiya G,
Yamamoto M,
van Heel DA,
Trembath RC,
Wei WQ,
Jarvik GP,
Namjou B,
Hayes MG,
Ritchie MD,
Jousilahti P,
Salomaa V,
Hveem K,
Åsvold BO,
Kubo M,
Kamatani Y,
Okada Y,
Murakami Y,
Kim BJ,
Thorsteinsdottir U,
Stefansson K,
Zhang J,
Chen Y,
Ho YL,
Lynch JA,
Rader DJ,
Tsao PS,
Chang KM,
Cho K,
O'Donnell CJ,
Gaziano JM,
Wilson PWF,
Frayling TM,
Hirschhorn JN,
Kathiresan S,
Mohlke KL,
Sun YV,
Morris AP,
Boehnke M,
Brown CD,
Natarajan P,
Deloukas P,
Willer CJ,
Assimes TL,
Peloso GM
Genome biology · 2022 · PMID 36575460 · open access
8 pages
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
Okada Y,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Kawaguchi T,
Stahl EA,
Kurreeman FA,
Nishida N,
Ohmiya H,
Myouzen K
and 39 more — show all
Takahashi M,
Sawada T,
Nishioka Y,
Yukioka M,
Matsubara T,
Wakitani S,
Teshima R,
Tohma S,
Takasugi K,
Shimada K,
Murasawa A,
Honjo S,
Matsuo K,
Tanaka H,
Tajima K,
Suzuki T,
Iwamoto T,
Kawamura Y,
Tanii H,
Okazaki Y,
Sasaki T,
Gregersen PK,
Padyukov L,
Worthington J,
Siminovitch KA,
Lathrop M,
Taniguchi A,
Takahashi A,
Tokunaga K,
Kubo M,
Nakamura Y,
Kamatani N,
Mimori T,
Plenge RM,
Yamanaka H,
Momohara S,
Yamada R,
Matsuda F,
Yamamoto K
Nature genetics · 2012 · PMID 22446963
7 pages
Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population
Tanikawa C,
Kamatani Y,
Terao C,
Usami M,
Takahashi A,
Momozawa Y,
Suzuki K,
Ogishima S,
Shimizu A,
Satoh M,
Matsuo K,
Mikami H
and 12 more — show all
Naito M,
Wakai K,
Yamaji T,
Sawada N,
Iwasaki M,
Tsugane S,
Kohri K,
Yu ASL,
Yasui T,
Murakami Y,
Kubo M,
Matsuda K
Journal of the American Society of Nephrology : JASN · 2019 · PMID 30975718
7 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
Genome-wide association studies for pelvic organ prolapse in the Japanese population
Matsunami M,
Imamura M,
Ashikari A,
Liu X,
Tomizuka K,
Hikino K,
Miwa K,
Kadekawa K,
Suda T,
Matsuda K,
Miyazato M,
Terao C
and 1 more — show all
Biobank Japan project
Communications biology · 2024 · PMID 39349682 · open access
7 pages
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Bakker MK,
van der Spek RAA,
van Rheenen W,
Morel S,
Bourcier R,
Hostettler IC,
Alg VS,
van Eijk KR,
Koido M,
Akiyama M,
Terao C,
Matsuda K
and 62 more — show all
Walters RG,
Lin K,
Li L,
Millwood IY,
Chen Z,
Rouleau GA,
Zhou S,
Rannikmäe K,
Sudlow CLM,
Houlden H,
van den Berg LH,
Dina C,
Naggara O,
Gentric JC,
Shotar E,
Eugène F,
Desal H,
Winsvold BS,
Børte S,
Johnsen MB,
Brumpton BM,
Sandvei MS,
Willer CJ,
Hveem K,
Zwart JA,
Verschuren WMM,
Friedrich CM,
Hirsch S,
Schilling S,
Dauvillier J,
Martin O,
Jones GT,
Bown MJ,
Ko NU,
Kim H,
Coleman JRI,
Breen G,
Zaroff JG,
Klijn CJM,
Malik R,
Dichgans M,
Sargurupremraj M,
Tatlisumak T,
Amouyel P,
Debette S,
Rinkel GJE,
Worrall BB,
Pera J,
Slowik A,
Gaál-Paavola EI,
Niemelä M,
Jääskeläinen JE,
von Und Zu Fraunberg M,
Lindgren A,
Broderick JP,
Werring DJ,
Woo D,
Redon R,
Bijlenga P,
Kamatani Y,
Veldink JH,
Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 pages
Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese
Kou I,
Otomo N,
Takeda K,
Momozawa Y,
Lu HF,
Kubo M,
Kamatani Y,
Ogura Y,
Takahashi Y,
Nakajima M,
Minami S,
Uno K
and 35 more — show all
Kawakami N,
Ito M,
Yonezawa I,
Watanabe K,
Kaito T,
Yanagida H,
Taneichi H,
Harimaya K,
Taniguchi Y,
Shigematsu H,
Iida T,
Demura S,
Sugawara R,
Fujita N,
Yagi M,
Okada E,
Hosogane N,
Kono K,
Nakamura M,
Chiba K,
Kotani T,
Sakuma T,
Akazawa T,
Suzuki T,
Nishida K,
Kakutani K,
Tsuji T,
Sudo H,
Iwata A,
Sato T,
Inami S,
Matsumoto M,
Terao C,
Watanabe K,
Ikegawa S
Nature communications · 2019 · PMID 31417091 · open access
4 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
Genetic variants of calcium and vitamin D metabolism in kidney stone disease
Howles SA,
Wiberg A,
Goldsworthy M,
Bayliss AL,
Gluck AK,
Ng M,
Grout E,
Tanikawa C,
Kamatani Y,
Terao C,
Takahashi A,
Kubo M
and 4 more — show all
Nature communications · 2019 · PMID 31729369 · open access
3 pages
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
Suetsugu H,
Kim K,
Yamamoto T,
Bang SY,
Sakamoto Y,
Shin JM,
Sugano N,
Kim JS,
Mukai M,
Lee YK,
Ohmura K,
Park DJ
and 43 more — show all
Takahashi D,
Ahn GY,
Karino K,
Kwon YC,
Miyamura T,
Kim J,
Nakamura J,
Motomura G,
Kuroda T,
Niiro H,
Miyamoto T,
Takeuchi T,
Ikari K,
Amano K,
Tada Y,
Yamaji K,
Shimizu M,
Atsumi T,
Seki T,
Tanaka Y,
Kubo T,
Hisada R,
Yoshioka T,
Yamazaki M,
Kabata T,
Kajino T,
Ohta Y,
Okawa T,
Naito Y,
Kaneuji A,
Yasunaga Y,
Ohzono K,
Tomizuka K,
Koido M,
Matsuda K,
Okada Y,
Suzuki A,
Kim BJ,
Kochi Y,
Lee HS,
Ikegawa S,
Bae SC,
Terao C
Human molecular genetics · 2022 · PMID 34850884
2 pages
Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Flanagan J,
Liu X,
Ortega-Reyes D,
Tomizuka K,
Matoba N,
Akiyama M,
Koido M,
Ishigaki K,
Ashikawa K,
Takata S,
Shi M,
Aoi T
and 8 more — show all
Biobank Japan Project
Communications biology · 2024 · PMID 39702642 · open access
2 pages
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Lee S,
Miller CL,
Bentley AR,
Brown MR,
Nagarajan P,
Noordam R,
Morrison JL,
Schwander K,
Westerman K,
Kho M,
Kraja AT,
de Vries PS
and 137 more — show all
Ammous F,
Aschard H,
Bartz TM,
Do A,
Dupont CT,
Feitosa MF,
Gudmundsdottir V,
Guo X,
Harris SE,
Hikino K,
Huang Z,
Lefevre C,
Lyytikäinen LP,
Milaneschi Y,
Nardone GG,
Santin A,
Schmidt H,
Shen B,
Sofer T,
Sun Q,
Tan YA,
Tang J,
Thériault S,
van der Most PJ,
Ware EB,
Weiss S,
Xing WY,
Yu C,
Zhao W,
Ansari MAY,
Anugu P,
Attia JR,
Bazzano LA,
Bis JC,
Breyer M,
Cade B,
Chen G,
Collins S,
Corley J,
Davies G,
Dörr M,
Du J,
Edwards TL,
Faquih T,
Faul JD,
Fohner AE,
Fretts AM,
Gangireddy S,
Gepner A,
Graff M,
Hofer E,
Homuth G,
Hood MM,
Jie X,
Kähönen M,
Kardia SLR,
Karvonen-Gutierrez CA,
Launer LJ,
Levy D,
Maheshwari M,
Martin LW,
Matsuda K,
McNeil JJ,
Nolte IM,
Okochi T,
Raffield LM,
Raitakari OT,
Risch L,
Risch M,
Roux AD,
Ruiz-Narvaez EA,
Russ TC,
Saito T,
Schreiner PJ,
Scott RJ,
Shikany J,
Smith JA,
Snieder H,
Spedicati B,
Tai ES,
Taylor AM,
Taylor KD,
Tesolin P,
van Dam RM,
Wang R,
Wenbin W,
Xie T,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Concas MP,
Conen D,
Cox SR,
Evans MK,
Fox ER,
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Gu C,
Gudnason V,
Harlow SD,
Holliday E,
Jost JB,
Lacaze P,
Lee S,
Lehtimäki T,
Li C,
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Penninx BWJH,
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Wang H,
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Chen H,
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Fornage M
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
2 pages
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population
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and 1 more — show all
Human Disease Genomics Working Group · RA Clinical and Genetic Study Consortium
Human molecular genetics · 2011 · PMID 21505073
1 page
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese
Okada Y,
Shimane K,
Kochi Y,
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Suzuki A,
Higasa K,
Takahashi A,
Horita T,
Atsumi T,
Ishii T,
Okamoto A,
Fujio K
and 32 more — show all
Hirakata M,
Amano H,
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Mimori A,
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Terao C,
Ohmura K,
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Nishimoto N,
Mimori T,
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Kubo M,
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Yamada R,
Nakamura Y,
Yamamoto K
PLoS genetics · 2012 · PMID 22291604 · 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
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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.