| Syndactyly: phenotypes, genetics and current classification S Malik European Journal of Human Genetics 20 (8), 817-824, 2012 | 196 | 2012 |
| Polydactyly: phenotypes, genetics and classification S Malik Clinical genetics 85 (3), 203-212, 2014 | 152 | 2014 |
| Prevalence of multi-drug resistant uropathogenic Escherichia coli in Potohar region of Pakistan I Ali, Z Rafaque, S Ahmed, S Malik, JI Dasti Asian Pacific Journal of Tropical Biomedicine 6 (1), 60-66, 2016 | 100 | 2016 |
| Multiple familial trichoepithelioma caused by mutations in the cylindromatosis tumor suppressor gene A Salhi, D Bornholdt, F Oeffner, S Malik, E Heid, R Happle, KH Grzeschik Cancer research 64 (15), 5113-5117, 2004 | 90 | 2004 |
| Synpolydactyly: clinical and molecular advances S Malik, KH Grzeschik Clinical genetics 73 (2), 113-120, 2008 | 80 | 2008 |
| Human GLI3 Intragenic Conserved Non-Coding Sequences Are Tissue-Specific Enhancers AA Abbasi, Z Paparidis, S Malik, DK Goode, H Callaway, G Elgar, ... PloS ONE 2 (4), e366, 2007 | 61 | 2007 |
| Prevalence of hepatitis C virus infection among thalassemia patients: a perspective from a multi-ethnic population of Pakistan G Din, S Malik, I Ali, S Ahmed, JI Dasti Asian Pacific journal of tropical medicine 7, S127-S133, 2014 | 53 | 2014 |
| Consanguinity and its sociodemographic differentials in Bhimber district, Azad Jammu and Kashmir, Pakistan N Jabeen, S Malik Journal of health, population, and nutrition 32 (2), 301, 2014 | 52 | 2014 |
| Human intronic enhancers control distinct sub-domains of Gli3 expression during mouse CNS and limb development AA Abbasi, Z Paparidis, S Malik, F Bangs, A Schmidt, S Koch, ... BMC developmental biology 10 (1), 1-13, 2010 | 47 | 2010 |
| Ultraconserved non‐coding sequence element controls a subset of spatiotemporal GLI3 expression Z Paparidis, AA Abbasi, S Malik, DK Goode, H Callaway, G Elgar, ... Development, growth & differentiation 49 (6), 543-553, 2007 | 45 | 2007 |
| Epidemiological and clinical correlates of oral squamous cell carcinoma in patients from north-west Pakistan R Ahmed, S Malik, MF Khan, MR Khattak J Pak Med Assoc. kolovoz 69 (8), 1074-8, 2019 | 43 | 2019 |
| A locus for hereditary hypotrichosis localized to human chromosome 18q21. 1 MA Rafique, M Ansar, SM Jamal, S Malik, M Sohail, M Faiyaz-Ul-Haque, ... European journal of human genetics 11 (8), 623-628, 2003 | 39 | 2003 |
| Exome sequencing and rare variant analysis reveals multiple filaggrin mutations in Bangladeshi families with atopic eczema and additional risk genes M Pigors, JEA Common, XFCC Wong, S Malik, CA Scott, N Tabarra, ... Journal of Investigative Dermatology 138 (12), 2674-2677, 2018 | 38 | 2018 |
| Consanguinity and its socio-biological parameters in Rahim yar Khan district, Southern Punjab, Pakistan HF Riaz, S Mannan, S Malik Journal of Health, Population and Nutrition 35 (1), 1-11, 2016 | 37 | 2016 |
| Clinical and descriptive genetic study of polydactyly: a Pakistani experience of 313 cases S Malik, S Ullah, M Afzal, K Lal, S Haque Clinical genetics 85 (5), 482-486, 2014 | 37 | 2014 |
| Pattern of consanguinity and inbreeding coefficient in Sargodha district, Punjab, Pakistan S Hina, S Malik Journal of biosocial science 47 (6), 803-811, 2015 | 32 | 2015 |
| Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type S Malik, FE Percin, D Bornholdt, B Albrecht, A Percesepe, MC Koch, ... The American Journal of Human Genetics 95 (6), 649-659, 2014 | 31 | 2014 |
| Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11. 2‐q12 S Malik, AA Abbasi, M Ansar, W Ahmad, MC Koch, KH Grzeschik Clinical genetics 69 (6), 518-524, 2006 | 30 | 2006 |
| Evidence for clinical and genetic heterogeneity of syndactyly type I: the phenotype of second and third toe syndactyly maps to chromosome 3p21. 31 S Malik, J Schott, SW Ali, F Oeffner, M Amin-ud-Din, W Ahmad, ... European journal of human genetics 13 (12), 1268-1274, 2005 | 30 | 2005 |
| Homozygous mutation in CEP19, a gene mutated in morbid obesity E Yıldız Bölükbaşı, S Mumtaz, M Afzal, U Woehlbier, S Malik, A Tolun Bardet-Biedl syndrome with predominant postaxial polydactyly. J Med Genet 55 …, 2018 | 29 | 2018 |
Sara MumtazNUMS, PakistanVerified email at numspak.edu.pk
