| Automated multi-class classification of skin lesions through deep convolutional neural network with dermoscopic images I Iqbal, M Younus, K Walayat, MU Kakar, J Ma Computerized medical imaging and graphics 88, 101843, 2021 | 112 | 2021 |
| SGCD Homozygous Nonsense Mutation (p.Arg97∗) Causing Limb-Girdle Muscular Dystrophy Type 2F (LGMD2F) in a Consanguineous Family, a Case Report M Younus, F Ahmad, E Malik, M Bilal, M Kausar, S Abbas, S Shaheen, ... Frontiers in Genetics 9, 727, 2019 | 22 | 2019 |
| Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type A M Umair, O Palander, M Bilal, B Almuzzaini, Q Alam, F Ahmad, M Younus, ... Genomics 113 (4), 2495-2502, 2021 | 20 | 2021 |
| Impaired D2 receptor-dependent dopaminergic transmission in prefrontal cortex of awake mouse model of Parkinson’s disease M Li, H Xu, G Chen, S Sun, Q Wang, B Liu, X Wu, L Zhou, Z Chai, X Sun, ... Brain 142 (10), 3099-3115, 2019 | 18 | 2019 |
| A comprehensive review of genetic skeletal disorders reported from Pakistan: a brief commentary M Umair, F Ahamd, M Bilal, A Asiri, M Younus, A Khan Meta Gene 20, 100559, 2019 | 18 | 2019 |
| Biallelic Missense Mutation in the ECEL1 Underlies Distal Arthrogryposis Type 5 (DA5D) M Umair, A Khan, A Hayat, S Abbas, A Asiri, M Younus, W Amin, S Nawaz, ... Frontiers in Pediatrics 7, 343, 2019 | 17 | 2019 |
| Regulating quantal size of neurotransmitter release through a GPCR voltage sensor Q Zhang, B Liu, Y Li, L Yin, M Younus, X Jiang, Z Lin, X Sun, R Huang, ... Proceedings of the National Academy of Sciences 117 (43), 26985-26995, 2020 | 15 | 2020 |
| Mutations in the lipase‐H gene causing autosomal recessive hypotrichosis and woolly hair S Mehmood, A Jan, D Muhammad, F Ahmad, H Mir, M Younus, G Ali, ... Australasian Journal of Dermatology 56 (3), e66-e70, 2015 | 13 | 2015 |
| Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy J Alonso-Pérez, L González-Quereda, C Bruno, C Panicucci, A Alavi, ... Brain 145 (2), 596-606, 2022 | 12 | 2022 |
| 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 |
| Identification and Characterization of Malate Dehydrogenases in Tomato (Solanum lycopersicum L.) M Imran, MZ Munir, S Ialhi, F Abbas, M Younus, S Ahmad, MK Naeem, ... International Journal of Molecular Sciences 23 (17), 10028, 2022 | 10 | 2022 |
| Disease causing homozygous variants in the human hairless gene S Mehmood, A Jan, SI Raza, F Ahmad, M Younus, Irfanullah, S Shahi, ... International Journal of Dermatology 55 (9), 977-981, 2016 | 10 | 2016 |
| Cocaine increases quantal norepinephrine secretion through NET-dependent PKC activation in locus coeruleus neurons F Zhu, L Liu, J Li, B Liu, Q Wang, R Jiao, Y Xu, L Wang, S Sun, X Sun, ... Cell Reports 40 (7), 2022 | 8 | 2022 |
| Clinical genetics of spondylocostal dysostosis: A mini review M Umair, M Younus, S Shafiq, A Nayab, M Alfadhel Frontiers in Genetics 13, 996364, 2022 | 7 | 2022 |
| A single dose of cocaine potentiates glutamatergic synaptic transmission onto locus coeruleus neurons F Zhu, Q Wu, J Li, K Grycel, B Liu, X Sun, L Zhou, R Jiao, R Song, ... Cell calcium 67, 11-20, 2017 | 6 | 2017 |
| Frameshift sequence variants in the human lipase‐H gene causing hypotrichosis S Mehmood, SH Shah, A Jan, M Younus, F Ahmad, M Ayub, W Ahmad Pediatric Dermatology 33 (1), e40-e42, 2016 | 4 | 2016 |
| Cocaine induces locomotor sensitization through a dopamine-dependent VTA-mPFC-FrA cortico-cortical pathway in male mice L Wang, M Gao, Q Wang, L Sun, M Younus, S Ma, C Liu, L Shi, Y Lu, ... Nature Communications 14 (1), 1568, 2023 | 2 | 2023 |
| 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 |
| Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment MU Kakar, M Akram, M Zubair Mehboob, M Younus, M Bilal, A Waqas, ... Plos one 17 (6), e0268078, 2022 | 2 | 2022 |
| Reply to “TRPA1-dependent calcium transients and CGRP release in DRG neurons require extracellular calcium” B Liu, M Younus, S Sun, Y Li, Y Wang, X Wu, X Sun, S Shang, C Wang, ... Journal of Cell Biology 219 (6), 2020 | 1 | 2020 |
Muhammad UmairPI-Team Leader-Scientist at King Abdullah International Medical Research Center (KAIMRC)Verified email at ngha.med.sa
