Shahnaz Ibrahim

5PUBLICATIONS
49CO-AUTHORS
Cell and nuclear divisionNeurology and neuromuscular diseasesNeurogeneticsPaediatrics not elsewhere classifiedPacific Peoples and disability
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Publications (5)

|May 14, 2025
Inherited deficiency of DIAPH1 identifies a DNA double strand break repair pathway regulated by γ-actin.

Beth L Woodward, Sudipta Lahiri, Anoop S Chauhan

|Feb 20, 2025
Analysis of spinal muscular atrophy patients from the spinal muscular atrophy and muscular dystrophy registry of Pakistan.

Bisma Aziz, Ahmed A Arif, Kulsum Kazi

|Jul 11, 2023
Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders.

Carolina Gracia-Diaz, Yijing Zhou, Qian Yang

|Jun 20, 2022
Paediatric posterior reversible encephalopathy syndrome: is there an association of blood pressure with imaging severity and atypical magnetic resonance characteristics?

Kiran Hilal, Kumail Khandwala, Nida Sajjad

|Sep 22, 2021
Association of Risk Factors for Early Childhood Disability in Rural Pakistan.

Shahnaz H Ibrahim, Arjumand Rizvi, Anjum M Ahmed

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Frequent Collaborators

2 joint publications

Henry Houlden

2 joint publications

Stephanie Efthymiou

1 joint publications

Kiran Hilal

1 joint publications

Kumail Khandwala