研究業績 Publications


2016年

欧文原著

Kinoshita M, Numata S, Tajima A, Nishi A, Muraki S, Tsuchiya A, Umehara H, Watanabe SY, Imoto I, Ohmori T.
Cumulative effect of the plasma total homocysteine-related genetic variants on schizophrenia risk.
Psychiatry Res 246:833-837, 2016.

Sato Y, Tajima A, Katsurayama M, Nozawa S, Miki Y, Koh E, Kanaya J, Namiki M, Matsumiya K, Tsujimura A, Komatsu K, Itoh N, Eguchi J, Imoto I, Yamauchi A, Iwamoto T.
A replication study of a candidate locus for follicle-stimulating hormone levels and association analysis for semen quality traits in Japanese men.
J Hum Genet 61(11):911-915, 2016.

Hayano T, Matsui H, Nakaoka H, Ohtake N, Hosomichi K, Suzuki K, Inoue I.
Germline variants of prostate cancer in Japanese families.
PLoS One 11(10):e0164233, 2016.

Okamoto Y, Ishida H, Kimura R, Sato T, Tsuchiya N, Murayama S, Fukase H, Nagaoka T, Adachi N, Yoneda M, Weber A, Kato H.
An Okhotsk adult female human skeleton (11th/12th century AD) with possible SAPHO syndrome from Hamanaka 2 site, Rebun Island, northern Japan.
Anthropol Sci 124(2):107-115, 2016.

Umehara H, Numata S, Tajima A, Nishi A, Nakataki M, Imoto I, Sumitani S, Ohmori T.
Calcium signaling pathway is associated with the long-term clinical response to selective serotonin reuptake inhibitors (SSRI) and SSRI with antipsychotics in patients with obsessive-compulsive disorder.
PLoS One 11(6):e0157232, 2016.

Kawarai T, Tajima A, Kuroda Y, Saji N, Orlacchio A, Terasawa H, Shimizu H, Kita Y, Izumi Y, Mitsui T, Imoto I, Kaji R.
A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability.
J Neurol Neurosurg Psychiatry 87(6):656-662, 2016.

Inoshita M, Numata S, Tajima A, Kinoshita M, Umehara H, Nakataki M, Ikeda M, Maruyama S, Yamamori H, Kanazawa T, Shimodera S, Hashimoto R, Imoto I, Yoneda H, Iwata N, Ohmori T.
A significant causal association between C-reactive protein levels and schizophrenia.
Sci Rep 6:26105, 2016.
[Retraction] Sci Rep 8:46947, 2018.

Nakaoka H, Gurumurthy A, Hayano T, Ahmadloo S, Omer WH, Yoshihara K, Yamamoto A, Kurose K, Enomoto T, Akira S, Hosomichi K, Inoue I.
Allelic imbalance in regulation of ANRIL through chromatin interaction at 9p21 endometriosis risk locus.
PLoS Genet 12(4):e1005893, 2016.

Yamauchi T, Kimura R, Kawaguchi A, Sato T, Yamaguchi K, Toma T, Miyamoto K, Fukase H, Yamaguchi T, Ishida H.
A comparative study of craniofacial measurements between Ryukyuan and mainland Japanese females using lateral cephalometric images.
Anthropol Sci 124(1):45?62, 2016.

Shinmyo Y, Tanaka S, Tsunoda S, Hosomichi K, Tajima A, Kawasaki H.
CRISPR/Cas9-mediated gene knockout in the mouse brain using in utero electroporation.
Sci Rep 6:20611, 2016.

Polat M, Takeshima SN, Hosomichi K, Kim J, Miyasaka T, Yamada K, Arainga M, Murakami T, Matsumoto Y, de la Barra Diaz V, Panei CJ, Gonzalez ET, Kanemaki M, Onuma M, Giovambattista G.
A new genotype of bovine leukemia virus in South America identified by NGS-based whole genome sequencing and molecular evolutionary genetic analysis.
Retrovirology 13(1):4, 2016.

欧文報告

Tada H, Hosomichi K, Okada H, Kawashiri M, Nohara A, Inazu A, Tomizawa S, Tajima A, Mabuchi H, Hayashi K.
A de novo mutation of the LDL receptor gene as the cause of familial hypercholesterolemia identified using whole exome sequencing.
Clin Chim Acta 453:194?196, 2016.

Okudaira Y, Hosomichi K, Ozaki Y, Shiina T, Mitsunaga S.
Correction of the HLA-DQB1*04:01:01 sequence at position 79 in exon 1.
HLA 87(1):57?58, 2016.

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