Concepedia

Author

Saima Anwar

Centre of Excellence in Molecular BiologyORCID

Also Known As

Saima Anwar

8

Publications

578

Citations

6

H-Index

13

Concepts

All Affiliations

Centre of Excellence in Molecular BiologyUniversity of the PunjabNational Institute on Deafness and Other Communication DisordersNational Institutes of HealthCincinnati Children's Hospital Medical Center
SA

About

Saima Anwar is an author at Centre of Excellence in Molecular Biology specializing in genetics, pathology, and medicine.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

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2

Pathology

4

4

526

3

Cell Biology

1

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247

4

Molecular Genetics

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95

5

Cell Signaling

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247

Saima Anwar

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6

Publications

578

Citations

6

H-Index

YearCitations

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

Saima Riazuddin, Inna A. Belyantseva, Arnaud P. J. Giese,

Nature Genetics

2012

247

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

Saima Anwar, Saima Riazuddin, Zubair M. Ahmed,

Journal of Human Genetics

2009

98

Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome

Zubair M. Ahmed, Saima Riazuddin, Sandar Aye,

Human Genetics

2008

95

Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome

Saima Riazuddin, Saima Anwar, Martin Fischer,

The American Journal of Human Genetics

2009

86

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3

Shahid Y. Khan, Saima Riazuddin, Muhammad Tariq,

Human Genetics

2006

30

MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin

Ivica Mašindová, Andrea Šoltýsová, Lukáš Varga,

PLoS ONE

2015

22

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