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Muhammad Imran Naseer

5PUBLICATIONS

13CO-AUTHORS

Autonomic nervous systemNeurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Gene mapping

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Publications (5)

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|Jan 19, 2024

Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis.

Osama Y Muthaffar, Asma Alqarni, Jumana A Shafei

|Dec 09, 2022

KIF4 regulates neuronal morphology and seizure susceptibility via the PARP1 signaling pathway.

Yuansong Wan, Momo Morikawa, Manatsu Morikawa

|Sep 29, 2020

Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family.

Muhammad Ismail Khan, Muhammad Latif, Maria Saif

|Nov 05, 2018

A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family.

Angham Abdulrahman Abdulkareem, Khalid Omar Abulnaja, Mohammad M Jan

|Oct 14, 2018

A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy.

Muhammad Imran Naseer, Mohammad Khalid Alwasiyah, Angham Abdulrahman Abdulkareem

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Frequent Collaborators

1 joint publications

Muhammad Latif

1 joint publications

Hafiz Muhammad Jafar Hussain

1 joint publications

Musharraf Jelani

1 joint publications

Yuansong Wan

1 joint publications

Momo Morikawa

1 joint publications

Manatsu Morikawa

1 joint publications

Suguru Iwata

1 joint publications

Yosuke Tanaka

1 joint publications

Nobutaka Hirokawa

1 joint publications

Osama Y Muthaffar

Frequent Collaborators

1 joint publications

Muhammad Latif

1 joint publications

Hafiz Muhammad Jafar Hussain

1 joint publications

Musharraf Jelani

1 joint publications

Yuansong Wan

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