| Role of leptin deficiency, inefficiency, and leptin receptors in obesity M Wasim, FR Awan, SS Najam, AR Khan, HN Khan Biochemical genetics 54 (5), 565-572, 2016 | 205 | 2016 |
| Aminoacidopathies: Prevalence, etiology, screening, and treatment options M Wasim, FR Awan, HN Khan, A Tawab, M Iqbal, H Ayesha Biochemical genetics 56 (1-2), 7-21, 2018 | 77 | 2018 |
| Biochemical screening of intellectually disabled patients: a stepping stone to initiate a newborn screening program in Pakistan M Wasim, HN Khan, H Ayesha, SMI Goorden, FM Vaz, ... Frontiers in neurology 10, 762, 2019 | 15 | 2019 |
| Development and application of low-cost T-ARMS-PCR assay for AGT and CYP11B1 gene polymorphisms M Hussain, HN Khan, FR Awan Molecular biology reports 46 (1), 443-449, 2019 | 12 | 2019 |
| Adult GAMT deficiency: A literature review and report of two siblings BP Modi, HN Khan, R van der Lee, M Wasim, CA Haaxma, PA Richmond, ... Molecular Genetics and Metabolism Reports 27, 100761, 2021 | 11 | 2021 |
| An overview of traditional and novel therapeutic options for the management of Phenylketonuria M Wasim, FR Awan, HN Khan, H Ayesha Critical Reviews™ in Eukaryotic Gene Expression 28 (2), 2018 | 11 | 2018 |
| Genetic Association of Beta-Myosin Heavy-Chain Gene (MYH7) with Cardiac Dysfunction M Yousaf, WA Khan, K Shahzad, HN Khan, B Ali, M Hussain, FR Awan, ... Genes 13 (9), 1554, 2022 | 10 | 2022 |
| Molecular genetic diagnosis of Wilson disease by ARMS-PCR in a Pakistani family HN Khan, M Wasim, H Ayesha, FR Awan Molecular biology reports 45 (6), 2585-2591, 2018 | 8 | 2018 |
| Identification of three novel pathogenic mutations in cystathionine beta-synthase gene of Pakistani intellectually disabled patients M Wasim, HN Khan, H Ayesha, M Iqbal, A Tawab, M Irfan, W Kanhai, ... Journal of Pediatric Endocrinology and Metabolism 35 (3), 325-332, 2022 | 7 | 2022 |
| Need and Challenges in Establishing Newborn Screening Programs for Inherited Metabolic Disorders in Developing Countries M Wasim, HN Khan, H Ayesha, FR Awan Advanced Biology, 2200318, 2023 | 6 | 2023 |
| Genetic association of vitamin D receptor gene with female infertility M Ashraf, HN Khan, R Ibrahim, M Shahid, S Khan, A Fatima, S Ullah, ... Nucleosides, Nucleotides & Nucleic Acids, 1-18, 2023 | 4 | 2023 |
| Tetra-ARMS-PCR assay development for genotyping of AGT rs699 T/C polymorphism, its comparison with PCR-RFLP and application in a case-control association … M Hussain, HN Khan, S Abbas, A Ali, MN Aslam, FR Awan Nucleosides, nucleotides & nucleic acids, 1-16, 2023 | 4 | 2023 |
| Biochemical screening of intellectually disabled and healthy children in Punjab, Pakistan: Differences in liver function test and lipid profiles M Wasim, HN Khan, H Ayesha, FR Awan International Journal of Developmental Disabilities 66 (3), 190-195, 2020 | 4 | 2020 |
| High‐performance liquid chromatography‐based assay optimization for the detection of plasma amino acids for applications in metabolic disorders in developing countries M Wasim, HN Khan, A Tawab, F Habib, M Iqbal, FR Awan Separation Science Plus, 2300119, 2023 | 3 | 2023 |
| Association of vitamin D receptor polymorphisms with cardiometabolic conditions in Pakistani population H Fiaz, AR Khan, S Abbas, A Bilal, HN Khan, M Hussain, FR Awan International Journal for Vitamin and Nutrition Research, 2022 | 3 | 2022 |
| High levels of blood glutamic acid and ornithine in children with intellectual disability M Wasim, HN Khan, H Ayesha, A Tawab, F Habib, MR Asi, M Iqbal, ... International Journal of Developmental Disabilities 68 (5), 609-614, 2022 | 3 | 2022 |
| Molecular Analyses of Phenylketonuria in The Intellectually Disabled Children from Faisalabad, Punjab, Pakistan FRA Habiba Hussain, Muhammad Wasim, Haq Nawaz Khan, Hina Ayesha Pakistan Journal of Neurological Sciences 17 (2), 21-23, 2022 | 3* | 2022 |
| Development of low-cost in-house tetra-ARMS-PCR assay for the screening of five CBS mutations found in Pakistani homocystinuria patients A Khalil, HN Khan, M Wasim, H Ayesha, FR Awan Nucleosides, Nucleotides & Nucleic Acids, 1-13, 2023 | 1 | 2023 |
| Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders SM Saadi, E Cali, LB Khalid, H Yousaf, G Zafar, HN Khan, M Sher, B Vona, ... Genes 14 (7), 1404, 2023 | 1 | 2023 |
| Label free quantitative proteomic profiling of serum samples of intellectually disabled young patients revealed dysregulation of complement coagulation and cholesterol cascade … S Vankwani, MR Mirza, FR Awan, M Zafar, A Nawrocki, M Wasim, ... Metabolic Brain Disease, 1-15, 2024 | | 2024 |
