1988-1991

درجة البكالوريوس - تقنية المختبرات الطبية

جامعة الملك عبدالعزيز، جدة، المملكة العربية السعودية

1993-1994

درجة الماجستير - الكيمياء الإكلينيكية السريرية

جامعة شيفيلد وجامعة شيفيلد هالام، شيفيلد، المملكة المتحدة

 1995-2000

درجة الدكتوراه - البيولوجيا الجزيئية والوراثة البشرية

جامعة شيفيلد ، شيفيلد ، المملكة المتحدة

Noriko Homma, Ruyun Zhou, Muhammad Imran Naseer, Adeel G. Chaudhary, Mohammed H.Al-Qahtani, and Nobutaka Hirokawa. KIF2A regulates the development of dentate granule cells and postnatal hippocampal wiring.. eLife Journal 2018 Jan 9;7. pii: e30935. (IF. 7.8).

Muhammad Imran Naseer*, Mohammad Khalid Alwasiyah1, Angham Abdulrahman Abdulkareem, Mahmood Rasool, Rayan Abdullah Bajammal, Adeel G. Chaudhary, Mohammed M. Jan, Mohammad H. Al-Qahtani. A novel homozygous mutation in SZT2 gene in Saudi family with developmental delay and epilepsy. (Genes and Genomics). (IF. 0.53).

Sajjad Karim, Hasan Salleh Jamal, Muhammad Imran Naseer, Rola Turki, Adeel Gulzar Chaudhary, Mamdooh Gari, Adel Mohammed Abuzenadah, Mohammed Husseain Al-Qahtani. Genomic answers for recurrent spontaneous abortion in Saudi Arabia: an array comparative genomic hybridization approach. (Reprod Biol. 2017 Jun;17(2):133-143). (IF 1.51).

Muhammad Imran Naseer*, Angham Abdulrahman Abdulkareem, Mahmood Rasool, Adeel G. Chaudhary, Mohammed M. Jan, Mohammad H. Al-Qahtani. A novel homozygous frameshift variant in the MCPH1 gene causes primary microcephaly in a consanguineous Saudi family. (Genes and Genomics 2017 Volume 39, Issue 12, pp 1317–1323) (IF 0.51).

Muhammad Imran Naseer*, Mahmood Rasool, Sameera Sogaty, Rukhaa Adeel Chaudhary, Haifa Mansour Mansour, Adeel G. Chaudhary, Adel M. Abuzenadah, Mohammad H. Al-Qahtani. A novel WDR62 mutation causes primary microcephaly in a consanguineous Saudi family. (Ann Saudi Med. 2017 Mar-Apr;37(2):148-153) (IF 0.55).

Muhammad Imran Naseer *, Adeel G. Chaudhary, Sameera Sogaty, Mahmood Rasool, Sajjad Karim, Hans-Juergen Schulten, Fehmida Bibi, Peter Natesan Pushparaj, Hussein A. Algahtani, Mohammad H. Al-Qahtani. Chromosomal micro-aberration in a Saudi family with Juvenile myoclonic epilepsy. (CNS Neurol Disord Drug Targets. 2017;16(9):1010-1017) (IF 2.50).

Naseer MI, Sogaty S, Rasool M, Chaudhary AG, Abutalib YA, Walker S, Marshall CR, Merico D, Carter MT, Scherer SW, Al-Qahtani MH, Zarrei M. Microcephaly-capillary malformation syndrome: Brothers with a homozygous STAMBP mutation, uncovered by exome sequencing. Am J Med Genet A. 2016 Aug 17. doi: 10.1002/ajmg.a.37845. (IF 2.25).