A. Narita

发表

A global atlas of genetic associations of 220 deep phenotypes

M. Rivas, M. Daly, M. Kanai, 2020, medRxiv.

Using endothelial nitric oxide synthase gene polymorphisms to identify intracranial aneurysms more prone to rupture in Japanese patients.

T. Hori, I. Inoue, A. Tajima, 2006, Journal of neurosurgery.

Genome-wide linkage and exome analyses identify variants of HMCN1 for splenic epidermoid cyst

I. Inoue, A. Narita, Y. Hayashi, 2014, BMC Medical Genetics.

Genome-wide linkage and exome analyses identify var iants of HMCN 1 1 for splenic epidermoid cyst 2 3

A. Narita, K. Hosomichi, S. Mitsunaga, 2014 .

Particular human leukocyte antigen alleles are associated with biochemical traits in the Japanese population.

H. Inoko, I. Inoue, A. Narita, 2011, Human immunology.

Genome-wide Linkage Analysis of Mandibular Prognathism in Korean and Japanese Patients

A. Narita, T. Yamaguchi, I. Inoue, 2005, Journal of dental research.

Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

Anurag, Cassandra N. Spracklen, I. Ntalla, 2021, medRxiv.

Identification of epistatic interactions involved in non-insulin-dependent diabetes mellitus in the Otsuka Long-Evans Tokushima Fatty rat.

A. Narita, Y. Sasaki, D. Moralejo, 2001, Experimental animals.

Systematic screening of lysyl oxidase-like (LOXL) family genes demonstrates that LOXL2 is a susceptibility gene to intracranial aneurysms

T. Hori, A. Hata, I. Inoue, 2007, Human Genetics.

Associations between six classical HLA loci and rheumatoid arthritis: a comprehensive analysis.

H. Inoko, I. Inoue, A. Narita, 2012, Tissue antigens.

Genome-wide linkage disequilibrium in two Japanese beef cattle breeds.

A. Narita, Y. Sasaki, Y. Sugimoto, 2006, Animal genetics.

Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohort

I. Inoue, Y. Ruigrok, A. Tajima, 2010, Neuroscience.

Effectiveness of adjusting for heterogeneity of variance in genetic evaluation of Japanese Black cattle.

A. Narita, Y. Sasaki, T. Ibi, 2007, Journal of animal science.

The Alanine/Threonine Polymorphism of the Alpha-1-Antichymotrypsin (SERPINA3) Gene and Ruptured Intracranial Aneurysms in the Japanese Population

Ituro Inoue, Tomokatsu Hori, Hiroyuki Akagawa, 2006, Cerebrovascular Diseases.

Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice

M. Kimura, T. Jakob, I. Rubio-Aliaga, 2009, Mammalian Genome.

Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese

Ituro Inoue, Tatsuo Shirota, Koutaro Maki, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms

Katsuhito Yasuno, A. Hata, I. Inoue, 2010, Journal of Human Genetics.

Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?

T. Hori, I. Inoue, A. Tajima, 2006, Journal of Human Genetics.

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

I. Ntalla, M. Kanai, I. Olafsson, 2022, Genome Biology.