Ahmed N. Alkanaq

Comparison of mitochondrial DNA variants detection using short- and long-read sequencing

A. Takata, N. Matsumoto, M. Taguri, 2019, Journal of Human Genetics.

Genetic Insights into Cerebrovascular Disorders: A Comprehensive Review.

C. Hayes-Rosen, C. Prestigiacomo, C. Gandhi, 2017, Journal of vascular and interventional neurology.

Updates in the Management of Cerebral Infarctions and Subarachnoid Hemorrhage Secondary to Intracranial Arterial Dissection: A Systematic Review.

S. Schonfeld, F. Al‐Mufti, R. Nuoman, 2019, World neurosurgery.

RNA sequencing solved the most common but unrecognized NEB pathogenic variant in Japanese nemaline myopathy

A. Takata, I. Nishino, N. Matsumoto, 2018, Genetics in Medicine.

RNA sequencing solved the most common but unrecognized NEB pathogenic variant in Japanese nemaline myopathy

A. Takata, I. Nishino, N. Matsumoto, 2018, Genetics in Medicine.

Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder

N. Matoba, A. Takata, M. Ikeda, 2021, Nature Communications.

De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies

K. Yamakawa, A. Takata, N. Matsumoto, 2018, European Journal of Human Genetics.

MYRF haploinsufficiency causes 46,XY and 46,XX disorders of sex development: bioinformatics consideration.

A. Takata, T. Ogata, N. Matsumoto, 2019, Human molecular genetics.

De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies

K. Yamakawa, A. Takata, N. Matsumoto, 2018, European Journal of Human Genetics.