Pei-Chieng Cha - Concepedia

Author

Pei-Chieng Cha

The University of Tokyo ORCID

Also Known As

P.-C. Cha, P.C. Cha, Pei-Chieng Cha, Pei-Chun Cha

Publications

818

Citations

H-Index

Concepts

All Affiliations

The University of Tokyo Kobe University Peking University National Center of Neurology and Psychiatry RIKEN Center for Integrative Medical Sciences

About

Pei-Chieng Cha is an author at The University of Tokyo specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	82
2	Health Sciences	1	1	12
3	Public Health	1	1	22
4	Epidemiology	1	1	22
5	Genetic Medicine	1	1	22

Pei-Chieng Cha

Publications

667

Citations

H-Index

Page 1

	Year	Citations
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases Philip Haycock, Stephen Burgess, Aayah Nounu, JAMA Oncology	2017	514
Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression Pei-Chieng Cha, Taisei Mushiroda, Hitoshi Zembutsu, Journal of Human Genetics Hematological MalignancyIrinotecan-induced Severe MyelosuppressionSingle Nucleotide PolymorphismGenetic DisorderGenetics	2009	48
In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson’s disease Takeshi Uenaka, Wataru Satake, Pei-Chieng Cha, Human Molecular Genetics	2018	46
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 Pei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, Journal of Human Genetics Genome-wide Association StudyGeneticsGenetic EpidemiologyHuman PolymorphismPharmacogenomics	2007	22
Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients Pei-Chieng Cha, Wataru Satake, Yuko Ando-Kanagawa, Journal of Human Genetics	2020	14
Bardet–Biedl syndrome and related disorders in Japan Makito Hirano, Wataru Satake, Nobuko Moriyama, Journal of Human Genetics Clinical DisordersGenetic DisorderInherited Metabolic DiseaseHematologyPathology	2020	12
A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy Tetsuya Oda, Hui Xiong, Kazuhiro Kobayashi, Human Genome Variation	2015	11

Page 1