Concepedia

Noriko Sangu

NS

Statistics

Publications

14

Citations

383

H-Index

13

Active since

2013

Affiliations

Tokyo Women's Medical University(Current)

Osaka International Cancer Institute

Tottori University

University of Tsukuba

National Epilepsy Center

Noriko Sangu is an author at Tokyo Women's Medical University specializing in molecular genetics, genetics, and life sciences.

ORCID

Publications per year

2013–2017

14

Publications

14

An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities

Toshiyuki Yamamoto, Anna Wilsdon, Shelagh Joss et al. · Journal of Human Genetics · 2014 · 75 citations · Full text

, , +13

Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications

Shino Shimada, Keiko Shimojima, Nobuhiko Okamoto et al. · Brain and Development · 2014 · 65 citations

, , +16

An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation

Keiko Shimojima, Nobuhiko Okamoto, Akiko Tamasaki et al. · American Journal of Medical Genetics Part A · 2015 · 52 citations

, , +15

Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including <i>PAX6</i>, <i>WT1</i>, and <i>PRRG4</i>

Toshiyuki Yamamoto, Masami Togawa, Shino Shimada et al. · American Journal of Medical Genetics Part A · 2013 · 41 citations

, , +17

A 7q31.33q32.1 microdeletion including LRRC4 and GRM8 is associated with severe intellectual disability and characteristics of autism

Noriko Sangu, Keiko Shimojima, Y Takahashi et al. · Human Genome Variation · 2017 · 28 citations · Full text

, , +17

1–5 of 14