Shahid Mahmood Baig

6PUBLICATIONS
37CO-AUTHORS
Pacific Peoples and disabilityNeurology and neuromuscular diseasesGene mappingMedical infection agents (incl. prions)Developmental genetics (incl. sex determination)
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Publications (6)

|Sep 28, 2024
A Novel MAG Variant Causes Hereditary Spastic Paraplegia in a Consanguineous Pakistani Family.

Rabia Akram, Haseeb Anwar, Humaira Muzaffar

|Jul 29, 2023
Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders.

Saadia Maryam Saadi, Elisa Cali, Lubaba Bintee Khalid

|Jan 21, 2023
Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability.

Maria Asif, Maryam Anayat, Faiza Tariq

|Mar 14, 2022
Identification of Pathogenic Mutations in Primary Microcephaly- (MCPH-) Related Three Genes CENPJ, CASK, and MCPH1 in Consanguineous Pakistani Families.

Niaz Muhammad Khan, Muhammad Shareef Masoud, Shahid Mahmood Baig

|May 01, 2019
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystonia.

Kamal Khan, Michael Zech, Angela T Morgan

|Sep 19, 2017
Homozygous mutation in the NPHP3 gene causing foetal nephronophthisis.

Uzma Abdullah, Muhammad Farooq, Ambrin Fatima

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Frequent Collaborators

2 joint publications

Stephanie Efthymiou

2 joint publications

Barbara Vona

2 joint publications

Uzma Abdullah

1 joint publications

Ghulam Hussain