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| Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy CA Martin, I Ahmad, A Klingseisen, MS Hussain, LS Bicknell, A Leitch, ... Nature genetics 46 (12), 1283-1292, 2014 | 190 | 2014 |
| CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly MS Hussain, SM Baig, S Neumann, VS Peche, S Szczepanski, ... Human molecular genetics 22 (25), 5199-5214, 2013 | 148 | 2013 |
| Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome DA Braun, S Lovric, D Schapiro, R Schneider, J Marquez, M Asif, ... The Journal of clinical investigation 128 (10), 4313-4328, 2018 | 111 | 2018 |
| Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies SU Iseri, RJ Osborne, M Farrall, AW Wyatt, G Mirza, G Nürnberg, C Kluck, ... Human mutation 30 (10), 1378-1386, 2009 | 98 | 2009 |
| A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family MA Khan, VM Rupp, M Orpinell, MS Hussain, J Altmüller, MO Steinmetz, ... Human molecular genetics 23 (22), 5940-5949, 2014 | 79 | 2014 |
| Mutations of KIF14 cause primary microcephaly by impairing cytokinesis A Moawia, R Shaheen, S Rasool, SS Waseem, N Ewida, B Budde, ... Annals of neurology 82 (4), 562-577, 2017 | 77 | 2017 |
| Genetic heterogeneity in Pakistani microcephaly families M Sajid Hussain, S Marriam Bakhtiar, M Farooq, I Anjum, E Janzen, ... Clinical genetics 83 (5), 446-451, 2013 | 73 | 2013 |
| Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis … M Farooq, JT Troelsen, M Boyd, H Eiberg, L Hansen, MS Hussain, ... European Journal of Human Genetics 18 (6), 733-736, 2010 | 58 | 2010 |
| Compound heterozygous ASPM mutations in Pakistani MCPH families F Muhammad, S Mahmood Baig, L Hansen, M Sajid Hussain, ... American journal of medical genetics Part A 149 (5), 926-930, 2009 | 54 | 2009 |
| Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome MS Hussain, A Battaglia, S Szczepanski, E Kaygusuz, MR Toliat, ... The American Journal of Human Genetics 95 (5), 622-632, 2014 | 47 | 2014 |
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| A novel homozygous splicing mutation of CASC5 causes primary microcephaly in a large Pakistani family S Szczepanski, MS Hussain, I Sur, J Altmüller, H Thiele, U Abdullah, ... Human genetics 135, 157-170, 2016 | 42 | 2016 |
| Genetic heterogeneity in Pakistani microcephaly families revisited I Ahmad, SM Baig, AR Abdulkareem, MS Hussain, I Sur, MR Toliat, ... Clinical genetics 92 (1), 62-68, 2017 | 39 | 2017 |
| Prevention of β-thalassemia in a large Pakistani family through cascade testing SM Baig, MA Din, H Hassan, A Azhar, JM Baig, M Aslam, I Anjum, ... Community Genetics 11 (1), 68-70, 2008 | 31 | 2008 |
| An update of pathogenic variants in ASPM, WDR62, CDK5RAP2, STIL, CENPJ, and CEP135 underlying autosomal recessive primary microcephaly in 32 … S Rasool, JM Baig, A Moawia, I Ahmad, M Iqbal, SS Waseem, M Asif, ... Molecular genetics & genomic medicine 8 (9), e1408, 2020 | 30 | 2020 |
| Unilateral L4-dorsal root ganglion stimulation evokes pain relief in chronic neuropathic postsurgical knee pain and changes of inflammatory markers: part II whole transcriptome … TM Kinfe, M Asif, KV Chakravarthy, TR Deer, JM Kramer, TL Yearwood, ... Journal of translational medicine 17, 1-13, 2019 | 27 | 2019 |
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| β-Thalassemia in Pakistan: a pilot program on prenatal diagnosis in Multan SM Baig, D Sabih, MK Rahim, A Azhar, M Tariq, MS Hussain, SMS Naqvi, ... Journal of pediatric hematology/oncology 34 (2), 90-92, 2012 | 20 | 2012 |
