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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1975 3
1976 1
1978 1
1980 1
1982 1
1983 1
1985 7
1986 4
1987 1
1988 4
1989 7
1990 8
1991 4
1992 15
1993 12
1994 10
1995 14
1996 11
1997 4
1998 16
1999 11
2000 9
2001 12
2002 13
2003 13
2004 12
2005 14
2006 20
2007 26
2008 29
2009 20
2010 33
2011 41
2012 23
2013 28
2014 18
2015 21
2016 42
2017 23
2018 26
2019 26
2020 16
2021 31
2022 25
2023 19
2024 9

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Search Results

620 results

Results by year

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Page 1
Core planar cell polarity genes VANGL1 and VANGL2 in predisposition to congenital vertebral malformations.
Feng X, Ye Y, Zhang J, Zhang Y, Zhao S, Mak JCW, Otomo N, Zhao Z, Niu Y, Yonezawa Y, Li G, Lin M, Li X, Cheung PWH, Xu K, Takeda K, Wang S, Xie J, Kotani T, Choi VNT, Song YQ, Yang Y, Luk KDK, Lee KS, Li Z, Li PS, Leung CYH, Lin X, Wang X, Qiu G; DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) study group; Watanabe K; Japanese Early Onset Scoliosis Research Group; Wu Z, Posey JE, Ikegawa S, Lupski JR, Cheung JPY, Zhang TJ, Gao B, Wu N. Feng X, et al. Among authors: ikegawa s. Proc Natl Acad Sci U S A. 2024 Apr 30;121(18):e2310283121. doi: 10.1073/pnas.2310283121. Epub 2024 Apr 26. Proc Natl Acad Sci U S A. 2024. PMID: 38669183
Identification of a de novo PUF60 variant associated with craniofacial microsomia.
Ogawa T, Xue J, Guo L, Inoue-Arai MS, Vendramini-Pittoli S, Zechi-Ceide RM, Candido-Souza RM, Tonello C, Brandão MM, Ozawa TO, Peixoto AP, Ruiz DMCF, Nakashima T, Ikegawa S, Moriyama K, Kokitsu-Nakata NM. Ogawa T, et al. Among authors: ikegawa s. Am J Med Genet A. 2024 Apr 22:e63631. doi: 10.1002/ajmg.a.63631. Online ahead of print. Am J Med Genet A. 2024. PMID: 38647383
Decoding triancestral origins, archaic introgression, and natural selection in the Japanese population by whole-genome sequencing.
Liu X, Koyama S, Tomizuka K, Takata S, Ishikawa Y, Ito S, Kosugi S, Suzuki K, Hikino K, Koido M, Koike Y, Horikoshi M, Gakuhari T, Ikegawa S, Matsuda K, Momozawa Y, Ito K, Kamatani Y, Terao C. Liu X, et al. Among authors: ikegawa s. Sci Adv. 2024 Apr 19;10(16):eadi8419. doi: 10.1126/sciadv.adi8419. Epub 2024 Apr 17. Sci Adv. 2024. PMID: 38630824 Free PMC article.
Dyssegmental dysplasia Rolland-Desbuquois type is caused by pathogenic variants in HSPG2 - a founder haplotype shared in five patients.
Farshadyeganeh P, Yamada T, Ohashi H, Nishimura G, Fujita H, Oishi Y, Nunode M, Ishikawa S, Murotsuki J, Yamashita Y, Ikegawa S, Ogi T, Arikawa-Hirasawa E, Ohno K. Farshadyeganeh P, et al. Among authors: ikegawa s. J Hum Genet. 2024 Feb 29. doi: 10.1038/s10038-024-01229-6. Online ahead of print. J Hum Genet. 2024. PMID: 38424183
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, 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. Ishikawa Y, et al. Among authors: ikegawa s. Nat Commun. 2024 Jan 31;15(1):319. doi: 10.1038/s41467-023-44541-z. Nat Commun. 2024. PMID: 38296975 Free PMC article.
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H, Khanshour AM, Ushiki A, Otomo N, Koike Y, Einarsdottir E, Fan Y, Antunes L, Kidane YH, Cornelia R, Sheng RR, Zhang Y, Pei J, Grishin NV, Evers BM, Cheung JPY, Herring JA, Terao C, Song YQ, Gurnett CA, Gerdhem P, Ikegawa S, Rios JJ, Ahituv N, Wise CA. Yu H, et al. Among authors: ikegawa s. Elife. 2024 Jan 26;12:RP89762. doi: 10.7554/eLife.89762. Elife. 2024. PMID: 38277211 Free PMC article.
Impaired glycine neurotransmission causes adolescent idiopathic scoliosis.
Wang X, Yue M, Cheung JPY, Cheung PWH, Fan Y, Wu M, Wang X, Zhao S, Khanshour AM, Rios JJ, Chen Z, Wang X, Tu W, Chan D, Yuan Q, Qin D, Qiu G, Wu Z, Zhang TJ, Ikegawa S, Wu N, Wise CA, Hu Y, Luk KDK, Song YQ, Gao B. Wang X, et al. Among authors: ikegawa s. J Clin Invest. 2024 Jan 16;134(2):e168783. doi: 10.1172/JCI168783. J Clin Invest. 2024. PMID: 37962965 Free PMC article.
Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects.
Ito S, Liu X, Ishikawa Y, Conti DD, Otomo N, Kote-Jarai Z, Suetsugu H, Eeles RA, Koike Y, Hikino K, Yoshino S, Tomizuka K, Horikoshi M, Ito K, Uchio Y, Momozawa Y, Kubo M; BioBank Japan Project; Kamatani Y, Matsuda K, Haiman CA, Ikegawa S, Nakagawa H, Terao C. Ito S, et al. Among authors: ikegawa s. Nat Commun. 2023 Aug 23;14(1):4863. doi: 10.1038/s41467-023-39858-8. Nat Commun. 2023. PMID: 37612283 Free PMC article.
620 results