جامعة الملك عبدالعزيز

KING ABDULAZIZ UNIVERSITY

Adeel Gulzar Ahmed Chaudhary


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Prof. Adeel Gulzar Chaudhary

chaudhary@kau.edu.sa

(966) 12-695-2000, Ext: 72140

Jeddah, KSA


Current Profile

Professor of Human Molecular Biology at Medical Laboratory Technology Department, Faculty of Applied Medical Sciences [FAMS], KAU
2016 - Current
Director for the Center of Innovation in Personalized Medicine [CIPM], KAU
2017 -Current
Consultant at GenaTi diagnostic services, KAU
2019 -Current
Head of the research center bioethics committee registered with national Bioethics board at King Abdulaziz City for Science & Technology [KACST], Riyadh
2016 -Current
Member of King Abdulaziz University academic promotion committee
2019 -Current
Vice Dean of the Faculty of Applied Medical Sciences for Development
2014 - 2018
Vice Director of the Center of Excellence In Genomic Medicine Research for Technical Affairs
2014 - 2018
Vice Director of King Fahd Center for Medical Research
2014 - 2015
Head of Diagnostic Radiology Department, Faculty of Applied Medical Sciences
2010 - 2012
Member of the Grants Program for Universities and Research Centers, Riyadh
2013 - 2015

Education

1988-1991
Bachelor Degree - Medical Laboratory Technology
King Abdulaziz University, Jeddah, KSA

1993-1994
Master Degree - Pathological Sciences
University of Sheffield & Sheffield Hallam University, Sheffield, UK

1995-2000
University of Sheffield, Sheffield, UK
PhD Degree - Molecular Biology & Human Genetics

Latest Publications

  • 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).