Muhammad Touseef
Lecturer (PhD (Continue))
Research Area: Human GeneticsAbout Me
I did my M. Phil. in Human Genetics (Animal Sciences) from QA University, Islamabad in 2012. I joined the Department of Zoology in March, 2017. Dedicated, resourceful and goal-driven professional educator with a solid commitment to the social and academic growth and development of students. My research interests are in the area of Human Genetics.
| Degree | Major | University | Start Date | End Date |
|---|---|---|---|---|
| PhD (Continue) | Zoology | University of Poonch Rawalakot | December 2020 | November 2024 |
| M. Phil. | Human Genetics | Quaid-e-Azam University Islamabad | January 2010 | January 2012 |
| Designation | Organization | Duration |
|---|---|---|
| Lecturer (BPS-18) | University of Poonch Rawalakot | March 2017 - November 2024 |
| Lecturer (BPS-17) | Kashmir Model College, Mirpur AJ&K | May 2013 - March 2017 |
| Title | Description | Sponsoring Agency | Amount | Year |
|---|
| Designation | Department | Organization | From Date | To Date |
|---|---|---|---|---|
| Associate Professor | Animal Sciences | Qauid e Azam University, Islamabad | March, 2012 |
| Description | Year | Journal Name | Impact Factor |
|---|---|---|---|
|
Sara Mumtaz, Hafiza Fizzah Riaz, Mohammad Touseef, Sulman Basit, Muhammad Faiyaz Ul Haque, Sajid Malik
Recurrent mutation in CDMP1 in a family with Grebe chondrodysplasia: broadening the phenotypic manifestation of syndrome in Pakistani population
Pak J Med Sci 2015;31(6):1542-1544.
DOI : http://dx.doi.org/10.12669/pjms.316.8115 |
2015 | ||
|
Hina Mir, Syed Irfan Raza, Muhammad Touseef, Mazhar Mustafa Memon, Muhammad Nasim Khan, Sulman Jaffar, Wasim Ahmad
A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivity
BMC Med Genet. 2014 Feb 26;15:25.
DOI : 10.1186/1471-2350-15-25. |
2014 | ||
|
Saadullah Khan, Imran Ullah, Irfanullah, Muhammad Touseef, Sulman Basit, Muhammad Nasim Khan, Wasim Ahmad
Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome
Gene. 2013 Feb 15;515(1):84-8.
DOI : 10.1016/j.gene.2012.11.023 |
2013 | ||
|
Bushra Khan, Sulman Basit, Muhammad Touseef, Muhammad Tariq, Muhammad Nasim Khan, Wasim Ahmad
A novel chondroectodermal dysplasia mapped to chromosome 2q24.1-q31.1
Eur J Med Genet. 2012 Aug-Sep;55(8-9):455-60
DOI : 10.1016/j.ejmg.2012.04.004 |
2012 |
