P. Cha

发表

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study

Tom R. Gaunt, Manuel A. R. Ferreira, David M. Evans, 2017 .

Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population

Yusuke Nakamura, K. Matsuda, M. Kubo, 2011, Journal of Human Genetics.

Bardet–Biedl syndrome and related disorders in Japan

Yutaka Suzuki, S. Kusunoki, N. Okamoto, 2020, Journal of Human Genetics.

Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium–glucose cotransporter 2 inhibitor

Yasushi Nakagawa, W. Ogawa, Y. Hirota, 2018, Journal of diabetes investigation.

A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy

S. Sugano, Yutaka Suzuki, Y. Hayashi, 2015, Human Genome Variation.

Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels

Jun Sese, Tatsushi Toda, Kazuya Iwamoto, 2012, PloS one.

Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese.

Yusuke Nakamura, T. Mushiroda, M. Kubo, 2010, Human molecular genetics.

Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations

Yusuke Nakamura, A. Sekine, C. Koh, 2004, Journal of Human Genetics.

Comparative whole transcriptome analysis of Parkinson’s disease focusing on the efficacy of zonisamide

P. Cha, W. Satake, M. Murata, 2022, Journal of Neurology, Neurosurgery, and Psychiatry.

Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression

Yusuke Nakamura, T. Mushiroda, T. Nishidate, 2009, Journal of Human Genetics.

Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.

Yusuke Nakamura, M. Kubo, A. Takahashi, 2012, Human molecular genetics.

Bardet–Biedl syndrome and related disorders in Japan

Yutaka Suzuki, S. Kusunoki, N. Okamoto, 2020, Journal of Human Genetics.

A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids

Yusuke Nakamura, M. Kubo, A. Takahashi, 2011, Nature Genetics.

In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson’s disease

Y. Okada, T. Toda, H. Mochizuki, 2018, Human molecular genetics.

A genome-wide association study identiﬁes SNP in DCC is associated with gallbladder cancer in the Japanese population

Yusuke Nakamura, M. Kubo, A. Takahashi, 2022 .

TUBB3 E410K syndrome with childhood-onset non-alcoholic steatohepatitis.

K. Itoh, P. Cha, W. Satake, 2021, Journal of Clinical Endocrinology and Metabolism.

High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population

Yusuke Nakamura, T. Mushiroda, A. Takahashi, 2007, Journal of Human Genetics.

Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients

Ken Yamamoto, T. Toda, P. Cha, 2020, Journal of Human Genetics.