Muhammad Naeem

21PUBLICATIONS
22CO-AUTHORS
Neurology and neuromuscular diseasesMedical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)Autonomic nervous systemHaematological tumours
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Publications (21)

|Sep 01, 2026
Whole-exome sequencing reveals a novel frameshift and a recurrent nonsense SPG11 variant causing rare familial amyotrophic lateral sclerosis type 5 in two consanguineous Pakistani families.

|Aug 31, 2026
Hereditary neurodegenerative disorders with spastic-ataxic manifestations: genetic and clinical insights into previously reported variants.

|Aug 19, 2026
Report of Mucopolysaccharidosis Type VI Disorder in Pakistani Patients Presenting Two Novel ARSB Variants.

|May 27, 2026
Identification of Pathogenic Variants in CYP4F22, FLG, ALOX12B, and NIPAL4 in a Case Series of Inherited Ichthyosis.

|Sep 12, 2025
Rare autosomal recessive hereditary sensory and autonomic neuropathy type VI in a Pakistani family caused by a novel DST variant.

Riaz Ahmad, Mina Zamani, Muhammad Naeem

|Jul 09, 2025
Identification and Computational Analysis of a Novel Pathogenic DKC1 Variant Underlying X-Linked Dyskeratosis Congenita.

Namra Asghar, Wardah Sajjad, Muhammad Naeem

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Frequent Collaborators

3 joint publications

Noreen Karim

3 joint publications

Zubair M Ahmed

2 joint publications

Abdulraheem S A Almalki

2 joint publications

Junaid Asghar