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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.
12 matches for
Ikari K.
Genetics of rheumatoid arthritis contributes to biology and drug discovery
Okada Y,
Wu D,
Trynka G,
Raj T,
Terao C,
Ikari K,
Kochi Y,
Ohmura K,
Suzuki A,
Yoshida S,
Graham RR,
Manoharan A
and 83 more — show all
Ortmann W,
Bhangale T,
Denny JC,
Carroll RJ,
Eyler AE,
Greenberg JD,
Kremer JM,
Pappas DA,
Jiang L,
Yin J,
Ye L,
Su DF,
Yang J,
Xie G,
Keystone E,
Westra HJ,
Esko T,
Metspalu A,
Zhou X,
Gupta N,
Mirel D,
Stahl EA,
Diogo D,
Cui J,
Liao K,
Guo MH,
Myouzen K,
Kawaguchi T,
Coenen MJ,
van Riel PL,
van de Laar MA,
Guchelaar HJ,
Huizinga TW,
Dieudé P,
Mariette X,
Bridges SL Jr,
Zhernakova A,
Toes RE,
Tak PP,
Miceli-Richard C,
Bang SY,
Lee HS,
Martin J,
Gonzalez-Gay MA,
Rodriguez-Rodriguez L,
Rantapää-Dahlqvist S,
Arlestig L,
Choi HK,
Kamatani Y,
Galan P,
Lathrop M,
Eyre S,
Bowes J,
Barton A,
de Vries N,
Moreland LW,
Criswell LA,
Karlson EW,
Taniguchi A,
Yamada R,
Kubo M,
Liu JS,
Bae SC,
Worthington J,
Padyukov L,
Klareskog L,
Gregersen PK,
Raychaudhuri S,
Stranger BE,
De Jager PL,
Franke L,
Visscher PM,
Brown MA,
Yamanaka H,
Mimori T,
Takahashi A,
Xu H,
Behrens TW,
Siminovitch KA,
Momohara S,
Matsuda F,
Yamamoto K,
Plenge RM
RACI consortium · GARNET consortium
Nature · 2014 · PMID 24390342 · open access
12 pages+
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
Ishigaki K,
Sakaue S,
Terao C,
Luo Y,
Sonehara K,
Yamaguchi K,
Amariuta T,
Too CL,
Laufer VA,
Scott IC,
Viatte S,
Takahashi M
and 78 more — show all
Ohmura K,
Murasawa A,
Hashimoto M,
Ito H,
Hammoudeh M,
Emadi SA,
Masri BK,
Halabi H,
Badsha H,
Uthman IW,
Wu X,
Lin L,
Li T,
Plant D,
Barton A,
Orozco G,
Verstappen SMM,
Bowes J,
MacGregor AJ,
Honda S,
Koido M,
Tomizuka K,
Kamatani Y,
Tanaka H,
Tanaka E,
Suzuki A,
Maeda Y,
Yamamoto K,
Miyawaki S,
Xie G,
Zhang J,
Amos CI,
Keystone E,
Wolbink G,
van der Horst-Bruinsma I,
Cui J,
Liao KP,
Carroll RJ,
Lee HS,
Bang SY,
Siminovitch KA,
de Vries N,
Alfredsson L,
Rantapää-Dahlqvist S,
Karlson EW,
Bae SC,
Kimberly RP,
Edberg JC,
Mariette X,
Huizinga T,
Dieudé P,
Schneider M,
Kerick M,
Denny JC,
Matsuda K,
Matsuo K,
Mimori T,
Matsuda F,
Fujio K,
Tanaka Y,
Kumanogoh A,
Traylor M,
Lewis CM,
Eyre S,
Xu H,
Saxena R,
Arayssi T,
Kochi Y,
Ikari K,
Harigai M,
Gregersen PK,
Yamamoto K,
Louis Bridges S Jr,
Padyukov L,
Martin J,
Klareskog L,
Okada Y,
Raychaudhuri S
BioBank Japan Project
Nature genetics · 2022 · PMID 36333501
12 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 genetic loci affecting facial shape variation in humans
Xiong Z,
Dankova G,
Howe LJ,
Lee MK,
Hysi PG,
de Jong MA,
Zhu G,
Adhikari K,
Li D,
Li Y,
Pan B,
Feingold E
and 37 more — show all
Marazita ML,
Shaffer JR,
McAloney K,
Xu SH,
Jin L,
Wang S,
de Vrij FM,
Lendemeijer B,
Richmond S,
Zhurov A,
Lewis S,
Sharp GC,
Paternoster L,
Thompson H,
Gonzalez-Jose R,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
Poletti G,
Bedoya G,
Rothhammer F,
Uitterlinden AG,
Ikram MA,
Wolvius E,
Kushner SA,
Nijsten TE,
Palstra RT,
Boehringer S,
Medland SE,
Tang K,
Ruiz-Linares A,
Martin NG,
Spector TD,
Stergiakouli E,
Weinberg SM,
Liu F,
Kayser M
International Visible Trait Genetics (VisiGen) Consortium
eLife · 2019 · PMID 31763980 · open access
5 pages
Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair
Liu F,
Chen Y,
Zhu G,
Hysi PG,
Wu S,
Adhikari K,
Breslin K,
Pospiech E,
Hamer MA,
Peng F,
Muralidharan C,
Acuna-Alonzo V
and 22 more — show all
Canizales-Quinteros S,
Bedoya G,
Gallo C,
Poletti G,
Rothhammer F,
Bortolini MC,
Gonzalez-Jose R,
Zeng C,
Xu S,
Jin L,
Uitterlinden AG,
Ikram MA,
van Duijn CM,
Nijsten T,
Walsh S,
Branicki W,
Wang S,
Ruiz-Linares A,
Spector TD,
Martin NG,
Medland SE,
Kayser M
Human molecular genetics · 2018 · PMID 29220522 · open access
4 pages
A genome-wide association study identifies multiple loci for variation in human ear morphology
Adhikari K,
Reales G,
Smith AJ,
Konka E,
Palmen J,
Quinto-Sanchez M,
Acuña-Alonzo V,
Jaramillo C,
Arias W,
Fuentes M,
Pizarro M,
Barquera Lozano R
and 26 more — show all
Macín Pérez G,
Gómez-Valdés J,
Villamil-Ramírez H,
Hunemeier T,
Ramallo V,
Silva de Cerqueira CC,
Hurtado M,
Villegas V,
Granja V,
Gallo C,
Poletti G,
Schuler-Faccini L,
Salzano FM,
Bortolini MC,
Canizales-Quinteros S,
Rothhammer F,
Bedoya G,
Calderón R,
Rosique J,
Cheeseman M,
Bhutta MF,
Humphries SE,
Gonzalez-José R,
Headon D,
Balding D,
Ruiz-Linares A
Nature communications · 2015 · PMID 26105758 · open access
3 pages
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
Fernández-Rhodes L,
Graff M,
Buchanan VL,
Justice AE,
Highland HM,
Guo X,
Zhu W,
Chen HH,
Young KL,
Adhikari K,
Palmer ND,
Below JE
and 104 more — show all
Bradfield J,
Pereira AC,
Glover L,
Kim D,
Lilly AG,
Shrestha P,
Thomas AG,
Zhang X,
Chen M,
Chiang CWK,
Pulit S,
Horimoto A,
Krieger JE,
Guindo-Martínez M,
Preuss M,
Schumann C,
Smit RAJ,
Torres-Mejía G,
Acuña-Alonzo V,
Bedoya G,
Bortolini MC,
Canizales-Quinteros S,
Gallo C,
González-José R,
Poletti G,
Rothhammer F,
Hakonarson H,
Igo R,
Adler SG,
Iyengar SK,
Nicholas SB,
Gogarten SM,
Isasi CR,
Papnicolaou G,
Stilp AM,
Qi Q,
Kho M,
Smith JA,
Langefeld CD,
Wagenknecht L,
Mckean-Cowdin R,
Gao XR,
Nousome D,
Conti DV,
Feng Y,
Allison MA,
Arzumanyan Z,
Buchanan TA,
Ida Chen YD,
Genter PM,
Goodarzi MO,
Hai Y,
Hsueh W,
Ipp E,
Kandeel FR,
Lam K,
Li X,
Nadler JL,
Raffel LJ,
Roll K,
Sandow K,
Tan J,
Taylor KD,
Xiang AH,
Yao J,
Audirac-Chalifour A,
de Jesus Peralta Romero J,
Hartwig F,
Horta B,
Blangero J,
Curran JE,
Duggirala R,
Lehman DE,
Puppala S,
Fejerman L,
John EM,
Aguilar-Salinas C,
Burtt NP,
Florez JC,
García-Ortíz H,
González-Villalpando C,
Mercader J,
Orozco L,
Tusié-Luna T,
Blanco E,
Gahagan S,
Cox NJ,
Hanis C,
Butte NF,
Cole SA,
Comuzzie AG,
Voruganti VS,
Rohde R,
Wang Y,
Sofer T,
Ziv E,
Grant SFA,
Ruiz-Linares A,
Rotter JI,
Haiman CA,
Parra EJ,
Cruz M,
Loos RJF,
North KE
HGG advances · 2022 · PMID 35399580 · open access
3 pages
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation
Adhikari K,
Fuentes-Guajardo M,
Quinto-Sánchez M,
Mendoza-Revilla J,
Camilo Chacón-Duque J,
Acuña-Alonzo V,
Jaramillo C,
Arias W,
Lozano RB,
Pérez GM,
Gómez-Valdés J,
Villamil-Ramírez H
and 20 more — show all
Hunemeier T,
Ramallo V,
Silva de Cerqueira CC,
Hurtado M,
Villegas V,
Granja V,
Gallo C,
Poletti G,
Schuler-Faccini L,
Salzano FM,
Bortolini MC,
Canizales-Quinteros S,
Cheeseman M,
Rosique J,
Bedoya G,
Rothhammer F,
Headon D,
González-José R,
Balding D,
Ruiz-Linares A
Nature communications · 2016 · PMID 27193062 · open access
2 pages
Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans
Wu S,
Zhang M,
Yang X,
Peng F,
Zhang J,
Tan J,
Yang Y,
Wang L,
Hu Y,
Peng Q,
Li J,
Liu Y
and 24 more — show all
Guan Y,
Chen C,
Hamer MA,
Nijsten T,
Zeng C,
Adhikari K,
Gallo C,
Poletti G,
Schuler-Faccini L,
Bortolini MC,
Canizales-Quinteros S,
Rothhammer F,
Bedoya G,
González-José R,
Li H,
Krutmann J,
Liu F,
Kayser M,
Ruiz-Linares A,
Tang K,
Xu S,
Zhang L,
Jin L,
Wang S
PLoS genetics · 2018 · PMID 30248107 · open access
2 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
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese
Okada Y,
Shimane K,
Kochi Y,
Tahira T,
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,
Kondo Y,
Ito S,
Takada K,
Mimori A,
Saito K,
Kamachi M,
Kawaguchi Y,
Ikari K,
Mohammed OW,
Matsuda K,
Terao C,
Ohmura K,
Myouzen K,
Hosono N,
Tsunoda T,
Nishimoto N,
Mimori T,
Matsuda F,
Tanaka Y,
Sumida T,
Yamanaka H,
Takasaki Y,
Koike T,
Horiuchi T,
Hayashi K,
Kubo M,
Kamatani N,
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
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.