| Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability RLP Santos-Cortez, V Khan, FS Khan, ZN Mughal, I Chakchouk, K Lee, ... Human genetics 137, 735-752, 2018 | 59 | 2018 |
| Biallelic missense variants in ZBTB11 can cause intellectual disability in humans Z Fattahi, TI Sheikh, L Musante, M Rasheed, II Taskiran, R Harripaul, ... Human molecular genetics 27 (18), 3177-3188, 2018 | 20 | 2018 |
| Factors associated with uncontrolled type 2 diabetes mellitus M Rasheed, N Islam, W Mahjabeen Journal of Islamabad Medical & Dental College (JIMDC) 4 (2), 68-71, 2015 | 15 | 2015 |
| Homozygous missense variant in POPDC3 causes recessive limb‐girdle muscular dystrophy type 26 A Ullah, Z Lin, M Younus, S Shafiq, S Khan, M Rasheed, A Mahmood, ... The Journal of Gene Medicine 24 (4), e3412, 2022 | 11 | 2022 |
| Exome sequencing identifies novel and known mutations in families with intellectual disability M Rasheed, V Khan, R Harripaul, M Siddiqui, MA Malik, Z Ullah, M Zahid, ... BMC Medical Genomics 14, 1-12, 2021 | 8 | 2021 |
| Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias K Kaivola, R Chia, J Ding, M Rasheed, M Fujita, V Menon, RL Walton, ... Cell genomics 3 (6), 2023 | 7 | 2023 |
| Expanded Programme of Immunization (EPI) status among children of factory workers M Rasheed, U Akram, N Asif, K Ahmed, S Zafar, S Mumtaz J Islam Med Dent Coll 3 (2), 62-6, 2014 | 5 | 2014 |
| Next generation sequencing as an emerging technology in rare disease genetics M Rasheed Journal of Islamabad Medical & Dental College 9 (1), 1-3, 2020 | 3 | 2020 |
| Homozygous missense variant in the N-terminal region of ANK3 gene is associated with developmental delay, seizures, speech abnormality, and aggressive behavior M Younus, M Rasheed, Z Lin, SA Asiri, IA Almazni, MA Alshehri, S Shafiq, ... Molecular syndromology 14 (1), 11-20, 2023 | 2 | 2023 |
| Indirect Genetic Analysis of Pakistani Hemophilia a Pedigrees by using BclI and HindIII Polymorphic Markers M Rasheed, N Asif, A Zawar, K Hassan, T Anwar Journal of Haematology and Stem Cell Research 2 (1), 8-12, 2022 | 1 | 2022 |
| Knowledge and Awareness about Genetic Problems Associated with Consanguineous Marriages among Non-Medical Students of Islamabad M Rasheed, N Asif, K Hassan Journal of Islamabad Medical & Dental College 6 (4), 263-267, 2017 | 1 | 2017 |
| Spectrum of mutations of beta thalassemia K Hassan, M Rasheed, N Asif, T Anwar, M Tahir Journal of Islamabad Medical & Dental College 6 (4), 196-202, 2017 | 1 | 2017 |
