Shahnaz Ibrahim
5PUBLICATIONS
49CO-AUTHORS
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Publications (5)
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|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
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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
1 joint publications
Nida Sajjad
1 joint publications
Raima Kaleemi
1 joint publications
Amyn A Malik
1 joint publications
Shazia Mohsin
1 joint publications
Grant S Stewart
1 joint publications
Qian Yang
