研究業績 Publications


2018年

欧文原著

Romero V, Nakaoka H, Hosomichi K, Inoue I.
High order formation and evolution of hornerin in primates.
Genome Biol Evol 10(12):3167-3175, 2018.

Tada H, Kawashiri MA, Nomura A, Teramoto R, Hosomichi K, Nohara A, Inazu A, Mabuchi H, Tajima A, Yamagishi M.
Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease.
J Clin Lipidol 12(6):1436-1444, 2018.

Miki A, Sakurada Y, Tanaka K, Semba K, Mitamura Y, Yuzawa M, Tajima A, Nakatochi M, Yamamoto K, Matsuo K, Imoto I, Honda S.
Genome-wide association study to identify a new susceptibility locus for central serous chorioretinopathy in the Japanese population.
Invest Ophthalmol Vis Sci 59(13):5542-5547, 2018.

Morimoto J, Nishikawa Y, Kakimoto T, Furutani K, Kihara N, Matsumoto M, Tsuneyama K, Kozono Y, Kozono H, Hozumi K, Hosomichi K, Nishijima H, Matsumoto M.
Aire controls in trans the production of medullary thymic epithelial cells expressing Ly-6C/Ly-6G.
J Immunol 201(11):3244-3257, 2018.

Takahashi M, Hosomichi K, Yamaguchi T, Nagahama R, Yoshida H, Maki K, Marazita ML, Weinberg SM, Tajima A.
Whole‐genome sequencing in a pair of monozygotic twins with discordant cleft lip and palate subtypes.
Oral Dis 24(7):1303-1309, 2018.

Takahashi M, Hosomichi K, Yamaguchi T, Nagahama R, Yoshida H, Marazita ML, Weinberg SM, Maki K, Tajima A.
Exploration of genetic factors determining cleft side in a pair of monozygotic twins with mirror-image cleft lip and palate using whole-genome sequencing and comparison of craniofacial morphology.
Arch Oral Biol 96:33-38, 2018.

Koganebuchi K, Gakuhari T, Takeshima H, Sato K, Fujii K, Kumabe T, Kasagi S, Sato T, Tajima A, Shibata H, Ogawa M, Oota H.
A new targeted capture method using bacterial artificial chromosome (BAC) libraries as baits for sequencing relatively large genes.
PLoS One 13(7):e0200170, 2018.

McColl H, Racimo F, Vinner L, Demeter F, Gakuhari T, Moreno-Mayar JV, van Driem G, Gram Wilken U, Seguin-Orlando A, de la Fuente Castro C, Wasef S, Shoocongdej R, Souksavatdy V, Sayavongkhamdy T, Saidin MM, Allentoft ME, Sato T, Malaspinas AS, Aghakhanian FA, Korneliussen T, Prohaska A, Margaryan A, de Barros Damgaard P, Kaewsutthi S, Lertrit P, Nguyen TMH, Hung HC, Minh Tran T, Nghia Truong H, Nguyen GH, Shahidan S, Wiradnyana K, Matsumae H, Shigehara N, Yoneda M, Ishida H, Masuyama T, Yamada Y, Tajima A, Shibata H, Toyoda A, Hanihara T, Nakagome S, Deviese T, Bacon AM, Duringer P, Ponche JL, Shackelford L, Patole-Edoumba E, Nguyen AT, Bellina-Pryce B, Galipaud JC, Kinaston R, Buckley H, Pottier C, Rasmussen S, Higham T, Foley RA, Lahr MM, Orlando L, Sikora M, Phipps ME, Oota H, Higham C, Lambert DM, Willerslev E.
The prehistoric peopling of Southeast Asia.
Science 361(6397):88-92, 2018.
[PERSPECTIVES] Science 361(6397):31-32, 2018.

Wakae K, Nishiyama T, Kondo S, Izuka T, Que L, Chen C, Kase K, Kitamura K, Mohiuddin M, Wang Z, Ahasan MM, Nakamura M, Fujiwara H, Yoshizaki T, Hosomochi K, Tajima A, Nakahara T, Kiyono T, Muramatsu M.
Keratinocyte differentiation induces APOBEC3A, 3B, and mitochondrial DNA hypermutation.
Sci Rep 8(1):9745, 2018.

Horikawa Y, Hosomichi K, Enya M, Ishiura H, Suzuki Y, Tsuji S, Sugano S, Inoue I, Takeda J.
No novel, high penetrant gene might remain to be found in Japanese patients with unknown MODY.
J Hum Genet 63(7):821-829, 2018.

Sato Y, Tajima A, Sato T, Nozawa S, Yoshiike M, Imoto I, Yamauchi A, Iwamoto T.
Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men.
J Med Genet 55(6):415-421, 2018.

Nishiyama A, Yamada T, Kita K, Wang R, Arai S, Fukuda K, Tanimoto A, Takeuchi S, Tange S, Tajima A, Furuya N, Kinoshita T, Yano S.
Foretinib overcomes entrectinib resistance associated with the NTRK1 G667C mutation in NTRK1 fusion-positive tumor cells in a brain metastasis model.
Clin Cancer Res 24(10):2357-2369, 2018.
[Highlights of This Issue] Clin Cancer Res 24(10):2235-2235, 2018.

Imi T, Katagiri T, Hosomichi K, Zaimoku Y, Hoang Nguyen V, Nakagawa N, Tajima A, Yoshizato T, Ogawa S, Nakao S.
Sustained clonal hematopoiesis by HLA-lacking hematopoietic stem cells without driver mutations in aplastic anemia.
Blood Adv 2(9):1000-1012, 2018.

Tomioka Y, Numata S, Kinoshita M, Umehara H, Watanabe SY, Nakataki M, Iwayama Y, Toyota T, Ikeda M, Yamamori H, Shimodera S, Tajima A, Hashimoto R, Iwata N, Yoshikawa T, Ohmori T.
Decreased serum pyridoxal levels in schizophrenia: meta-analysis and Mendelian randomization analysis.
J Psychiatry Neurosci 43(3):194-200, 2018.

Inoshita M, Umehara H, Watanabe SY, Nakataki M, Kinoshita M, Tomioka Y, Tajima A, Numata S, Ohmori T.
Elevated peripheral blood glutamate levels in major depressive disorder.
Neuropsychiatr Dis Treat 4:945-953, 2018.

Sato Y, Hasegawa C, Tajima A, Nozawa S, Yoshiike M, Koh E, Kanaya J, Namiki M, Matsumiya K, Tsujimura A, Komatsu K, Itoh N, Eguchi J, Yamauchi A, Iwamoto T.
Association of TUSC1 and DPF3 gene polymorphisms with male infertility.
J Assist Reprod Genet 35(2):257-263, 2018.

Nishijima H, Kajimoto T, Matsuoka Y, Mouri Y, Morimoto J, Matsumoto M, Kawano H, Nishioka Y, Uehara H, Izumi K, Tsuneyama K, Okazaki IM, Okazaki T, Hosomichi K, Shiraki A, Shibutani M, Mitsumori K, Matsumoto M.
Paradoxical development of polymyositis-like autoimmunity through augmented expression of autoimmune regulator (AIRE).
J Autoimmun 86:75-92, 2018.

Maruyama K, Aotsuka N, Kumano Y, Sato N, Kawashima N, Onda Y, Maruyama H, Katagiri T, Zaimoku Y, Nakagawa N, Hosomichi K, Ogawa S, Nakao S.
Immune-mediated hematopoietic failure after allogeneic hematopoietic stem cell transplantation: a common cause of late graft failure in patients with complete donor chimerism.
Biol Blood Marrow Transplant 24(1):43-49, 2018.

欧文報告

Kayahashi K, Mizumoto Y, Myojo S, Mitani Y, Tajima A, Fujiwara H.
A successful case of neoadjuvant chemotherapy and radical hysterectomy during pregnancy for advanced uterine cervical cancer accompanied by neonatal erythroderma.
J Obstet Gynaecol Res 44(10):2003-2007, 2018.

Koba H, Kimura H, Nishikawa S, Sone T, Abo M, Hara J, Hosomichi K, Tajima A, Kasahara K.
Next-generation sequencing analysis identifies genomic alterations in pathological morphologies: A case of pulmonary carcinosarcoma harboring EGFR mutations.
Lung Cancer 122:146-150, 2018.

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