Concepedia

Yalda Nilipour

YN

Statistics

Publications

20

Citations

749

H-Index

15

Active since

2007

Affiliations

Shahid Beheshti University of Medical Sciences(Current)

Tehran University of Medical Sciences

Shariati Hospital

University of Social Welfare and Rehabilitation Sciences

Newcastle University

Yalda Nilipour is an author at Shahid Beheshti University of Medical Sciences specializing in genetics, life sciences, and genetic disorders.

Publications per year

2007–2024

20

Publications

20

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect

Jan Senderek, Juliane Müller, Marina Dusl et al. · The American Journal of Human Genetics · 2011 · 173 citations · Full text

Medicine, Genetics, Neuroscience +10

Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations

Velina Guergueltcheva, Juliane Müller, Marina Dusl et al. · Journal of Neurology · 2011 · 98 citations

Medicine, Genetics, Molecular Genetics +7

Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24

Carola Hedberg‐Oldfors, Alexandra Abramsson, Daniel P. S. Osborn et al. · Human Molecular Genetics · 2019 · 59 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population

Zohreh Fattahi, Zahra Kalhor, M. Fadaee et al. · Clinical Genetics · 2016 · 57 citations

Life Sciences, Genetics, Molecular Genetics +17

Ryanodine receptor type 3 (<i><scp>RYR</scp>3</i>) as a novel gene associated with a myopathy with nemaline bodies

Yalda Nilipour, Shahriar Nafissi, Anton Tjust et al. · European Journal of Neurology · 2018 · 47 citations · Full text

Medicine, Genetics, Molecular Genetics +17

1–5 of 20