| Biomedical applications of green synthesized Nobel metal nanoparticles ZUH Khan, A Khan, Y Chen, NS Shah, N Muhammad, AU Khan, K Tahir, ... Journal of Photochemistry and Photobiology B: Biology 173, 150-164, 2017 | 127 | 2017 |
| Photo catalytic applications of gold nanoparticles synthesized by green route and electrochemical degradation of phenolic Azo dyes using AuNPs/GC as modified paste electrode ZUH Khan, A Khan, Y Chen, A ullah Khan, NS Shah, N Muhammad, ... Journal of Alloys and Compounds 725, 869-876, 2017 | 97 | 2017 |
| Enhanced photocatalytic and electrocatalytic applications of green synthesized silver nanoparticles ZUH Khan, A Khan, A Shah, P Wan, Y Chen, GM Khan, AU Khan, K Tahir, ... Journal of Molecular liquids 220, 248-257, 2016 | 80 | 2016 |
| NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation CN Castro, M Rosenzwajg, R Carapito, M Shahrooei, M Konantz, A Khan, ... Journal of Experimental Medicine 217 (12), e20192275, 2020 | 63 | 2020 |
| Enhanced antimicrobial, anti-oxidant applications of green synthesized AgNPs-an acute chronic toxicity study of phenolic azo dyes & study of materials surface using X-ray … ZUH Khan, A Khan, YM Chen, NS Shah, AU Khan, N Muhammad, K Tahir, ... Journal of Photochemistry and Photobiology B: Biology 180, 208-217, 2018 | 51 | 2018 |
| Photocatalytic, antimicrobial activities of biogenic silver nanoparticles and electrochemical degradation of water soluble dyes at glassy carbon/silver modified past electrode … ZUH Khan, A Khan, A Shah, Y Chen, P Wan, A ullah Khan, K Tahir, ... Journal of Photochemistry and Photobiology B: Biology 156, 100-107, 2016 | 50 | 2016 |
| Biallelic variants in four genes underlying recessive osteogenesis imperfecta A Hayat, S Hussain, M Bilal, M Kausar, B Almuzzaini, S Abbas, A Tanveer, ... European journal of medical genetics 63 (8), 103954, 2020 | 34 | 2020 |
| Use of pharmacogenetic drugs by the Dutch population MA Alshabeeb, VHM Deneer, A Khan, FW Asselbergs Frontiers in genetics 10, 567, 2019 | 32 | 2019 |
| Forensic characterization of 15 autosomal STRs in four populations from Xinjiang, China, and genetic relationships with neighboring populations X Zhan, A Adnan, Y Zhou, A Khan, K Kasim, D McNevin Scientific Reports 8 (1), 4673, 2018 | 31 | 2018 |
| Molecular analysis of 23 Pakistani families with autosomal recessive primary microcephaly using targeted next-generation sequencing R Wang, A Khan, S Han, X Zhang Journal of human genetics 62 (2), 299-304, 2017 | 26 | 2017 |
| 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 | 24 | 2021 |
| 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 | 23 | 2019 |
| Molecular analysis of twelve Pakistani families with nonsyndromic or syndromic hearing loss R Wang, S Han, A Khan, X Zhang Genetic testing and molecular biomarkers 21 (5), 316-321, 2017 | 23 | 2017 |
| Sequence variants in genes causing nonsyndromic hearing loss in a Pakistani cohort A Khan, S Han, R Wang, M Ansar, W Ahmad, X Zhang Molecular Genetics & Genomic Medicine 7 (9), e917, 2019 | 22 | 2019 |
| A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic features DD Shao, R Straussberg, H Ahmed, A Khan, S Tian, RS Hill, RS Smith, ... Genetics in Medicine 23 (6), 1158-1162, 2021 | 19 | 2021 |
| 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 | 18 | 2019 |
| Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report F Al Mutairi, R Alkhalaf, A Alkhorayyef, F Alroqi, A Yusra, M Umair, F Nouf, ... BMC Pulmonary Medicine 20, 1-5, 2020 | 17 | 2020 |
| Homozygous missense variant in the TTN gene causing autosomal recessive limb-girdle muscular dystrophy type 10 A Khan, R Wang, S Han, M Umair, S Abbas, MI Khan, MA Alshabeeb, ... BMC medical genetics 20, 1-8, 2019 | 16 | 2019 |
| SPTBN5, Encoding the βV-Spectrin Protein, Leads to a Syndrome of Intellectual Disability, Developmental Delay, and Seizures A Khan, LP Bruno, F Alomar, M Umair, AM Pinto, AA Khan, A Khan, Saima, ... Frontiers in Molecular Neuroscience 15, 877258, 2022 | 14 | 2022 |
| Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants A Khan, Z Miao, M Umair, A Ullah, MA Alshabeeb, M Bilal, F Ahmad, ... Genes 11 (9), 1021, 2020 | 14 | 2020 |
