Publications by authors named "Muhammad Hashim Raza"

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Whole Genome Analysis in Consanguineous Families Reveals New Loci for Speech Sound Disorder (SSD).
Tahira Yasmin, Aatika Sadia, Laraib Nadeem, Muhammad Asim Raza Basra, Mabel L Rice, Muhammad Hashim Raza

Genes (Basel)· August 2024

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Genome-Wide Mapping of Consanguineous Families Confirms Previously Implicated Gene Loci and Suggests New Loci in Specific Language Impairment (SLI).
Adnan Yousaf, Huma Hafeez, Muhammad Asim Raza Basra, Mabel L Rice, Muhammad Hashim Raza

Children (Basel)· August 2024

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Innovative Family-Based Genetically Informed Series of Analyses of Whole-Exome Data Supports Likely Inheritance for Grammar in Children with Specific Language Impairment.
Erin M Andres, Kathleen Kelsey Earnest, Hao Xuan, Cuncong Zhong, Mabel L Rice, Muhammad Hashim Raza

Children (Basel)· June 2023

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Receptive vocabulary, memory span, and speech articulation in Pakistani children with developmental language disorders.
Huma Hafeez, Tahira Yasmin, Muhammad Hashim Raza, Lubna Mubarak, Komal Ashraf, Muhammad Asim Raza Basra

Child Neuropsychol· April 2023

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Genome-wide analysis of runs of homozygosity in Pakistani controls with no history of speech or language-related developmental phenotypes.
Tahira Yasmin, Erin M Andres, Komal Ashraf, Muhammad Asim Raza Basra, Muhammad Hashim Raza

Ann Hum Biol· February 2023

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Working memory span and receptive vocabulary assessment in Urdu speaking children with speech sound disorder.
Tahira Yasmin, Huma Hafeez, Aatika Sadia, Mubarak Lubna, Sharmeen Aslam Tarar, Muhammad Hashim Raza, Muhammad Asim Raza Basra

Acta Psychol (Amst)· November 2022

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Study of rare genetic variants in and in Pakistani probands and families with language impairment.
Erin M Andres, Heather L Neely, Huma Hafeez, Tahira Yasmin, Farzana Kausar, M Asim Raza Basra, Muhammad Hashim Raza

Meta Gene· December 2021

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Family-Based Whole-Exome Analysis of Specific Language Impairment (SLI) Identifies Rare Variants in , a Component of the Retention and Splicing (RES) Complex.
Erin M Andres, Kathleen Kelsey Earnest, Cuncong Zhong, Mabel L Rice, Muhammad Hashim Raza

Brain Sci· December 2021

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A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.
Angela Martinelli, Mabel L Rice, Joel B Talcott, Rebeca Diaz, Shelley Smith, Muhammad Hashim Raza

Hum Mol Genet· June 2021

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Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment.
Erin M Andres, Kathleen Kelsey Earnest, Shelley D Smith, Mabel L Rice, Muhammad Hashim Raza

J Speech Lang Hear Res· December 2020

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A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI).
Erin M Andres, Huma Hafeez, Adnan Yousaf, Sheikh Riazuddin, Mabel L Rice, Muhammad Asim Raza Basra, Muhammad Hashim Raza

Eur J Hum Genet· August 2019

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Breast Cancer in Pakistan a Critical Appraisal of the Situation Regarding Female Health and Where the Nation Stands?
Muhammad Asim R Basra, Manzoor Saher, Muhammad Makshoof Athar, Muhammad Hashim Raza

Asian Pac J Cancer Prev· January 2017

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A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.
Se-Kyung Oh, Jeong-In Baek, Karl M Weigand, Hanka Venselaar, Herman G P Swarts, Muhammad Hashim Raza

Eur J Hum Genet· May 2015

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Studies in a consanguineous family reveal a novel locus for stuttering on chromosome 16q.
Muhammad Hashim Raza, Rana Amjad, Sheikh Riazuddin, Dennis Drayna

Hum Genet· February 2012

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Identification of an autosomal recessive stuttering locus on chromosome 3q13.2-3q13.33.
Muhammad Hashim Raza, Sheikh Riazuddin, Dennis Drayna

Hum Genet· October 2010

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