Muhammad Imran Naseer

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 9

Top Venues

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Gyeongsang National University (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Gyeongsang National University Sep 01 2006 - Feb 15 2010

South Korea

PHD :: Applied Life Science

Publications

Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics 46 (4) (2024)
Osama Yousef Muthaffar, Asma Alqarni, Jumana A Shafei, Sarah Y Bahowarth, Anas S Alyazidi, Muhammad Imran Naseer
Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis. Genes & genomics (2024)
Yuansong Wan, Momo Morikawa, Manatsu Morikawa, Suguru Iwata, Muhammad Imran Naseer, Adeel Gulzar Ahmed Chaudhary, Yosuke Tanaka, Nobutaka Hirokawa
KIF4 regulates neuronal morphology and seizure susceptibility via the PARP1 signaling pathway. The Journal of cell biology 222 (2) (2022)
Muhammad Ismail Khan, Muhammad Latif, Maria Saif, Hilal Ahmad, Atta Ullah Khan, Muhammad Imran Naseer, Hafiz Muhammad Jafar Hussain, Musharraf Jelani
Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. The journal of gene medicine 23 (1) (2020)
Muhammad Imran Naseer, Mohammad Khalid Alwasiyah, Angham Abdulrahman Abdulkareem, Rayan Abdullah Bajammal, Carlos Trujillo, Muhammad Abu-Elmagd, Mohammad Alam Jafri, Adeel G Chaudhary, Mohammad H Al-Qahtani
A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay, macrocephaly and epilepsy. Genes & genomics 40 (11) (2018)
Angham Abdulrahman Abdulkareem, Khalid Omar Abulnaja, Mohammad M Jan, Sajjad Karim, Mahmood Rasool, Shakeel Ahmed Ansari, Adeel G Chaudhary, Mohammad H Al-Qahtani, Muhammad Imran Naseer
A novel homozygous nonsense mutation in CCDC88A gene cause PEHO-like syndrome in consanguineous Saudi family. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 40 (2) (2018)

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Publication Activity (10 Years)

Top Topics

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Muhammad Imran Naseer