| Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndrome M Ajmal, MI Khan, K Neveling, A Tayyab, S Jaffar, A Sadeque, H Ayub, ... Molecular Vision, 2013 | 35 | 2013 |
| Identification and characterization of alternative exon usage linked glioblastoma multiforme survival A Sadeque, NVL Serão, BR Southey, KR Delfino, SL Rodriguez-Zas BMC medical genomics 5 (1), 59, 2012 | 35 | 2012 |
| Association of ANRIL polymorphism (rs1333049: C> G) with myocardial infarction and its pharmacogenomic role in hypercholesterolemia W Ahmed, IS Ali, M Riaz, A Younas, A Sadeque, AK Niazi, SH Niazi, ... Gene 515 (2), 416-420, 2013 | 27 | 2013 |
| Role of tissue plasminogen activator and plasminogen activator inhibitor polymorphism in myocardial infarction W Ahmed, M Malik, I Saeed, AA Khan, A Sadeque, U Kaleem, N Ahmed, ... Molecular biology reports 38 (4), 2541-2548, 2011 | 25 | 2011 |
| Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia M Azam, RWJ Collin, STA Shah, AA Shah, MI Khan, A Hussain, ... Molecular vision 16, 774, 2010 | 23 | 2010 |
| A homozygous p. Glu150Lys mutation in the opsin gene of two Pakistani families with autosomal recessive retinitis pigmentosa M Azam, MI Khan, A Gal, A Hussain, STA Shah, MS Khan, A Sadeque, ... Molecular vision 15, 2526, 2009 | 22 | 2009 |
| Identification of novel mutations in Pakistani families with autosomal recessive retinitis pigmentosa M Azam, RWJ Collin, A Malik, MI Khan, STA Shah, AA Shah, A Hussain, ... Archives of Ophthalmology 129 (10), 1377-1378, 2011 | 20 | 2011 |
| The genetic spectrum of familial hypercholesterolemia in Pakistan W Ahmed, R Whittall, M Riaz, M Ajmal, A Sadeque, H Ayub, R Qamar, ... Clinica Chimica Acta 421, 219-225, 2013 | 13 | 2013 |
| Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia M Ajmal, W Ahmed, A Sadeque, SHB Ali, SH Bokhari, N Ahmed, R Qamar Molecular biology reports 37 (8), 3869-3875, 2010 | 13 | 2010 |
| Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients W Ahmed, M Ajmal, A Sadeque, RA Whittall, S Rafiq, W Putt, A Khawaja, ... Molecular biology reports 39 (7), 7365-7372, 2012 | 7 | 2012 |
| Target-Site Resistances to ALS and PPO Inhibitors Are Linked in Waterhemp (Amaranthus tuberculatus) PJ Tranel, C Wu, A Sadeque Weed Science 65 (1), 4-8, 2017 | 6 | 2017 |
| A novel pathogenic nonsense triple-nucleotide mutation in the low-density lipoprotein receptor gene and its clinical correlation with familial hypercholesterolemia M Ajmal, W Ahmed, N Akhtar, A Sadeque, A Khalid, SH Benish Ali, ... Genetic testing and molecular biomarkers 15 (9), 601-606, 2011 | 6 | 2011 |
| Sex-specific markers for waterhemp (Amaranthus tuberculatus) and Palmer amaranth (Amaranthus palmeri) JS Montgomery, A Sadeque, DA Giacomini, PJ Brown, PJ Tranel Weed Science 67 (4), 412-418, 2019 | 1 | 2019 |
| Model of ion intensity from tandem mass spectra for improved peptide identification and simulation Z Fazal, BR Southey, A Sadeque, JV Sweedler, SL Rodriguez-Zas 2011 IEEE International Conference on Bioinformatics and Biomedicine …, 2011 | 1 | 2011 |
| Genome-wide expression of low temperature response genes in Rosa hybrida L. MV dos Reis, LV Rouhana, A Sadeque, L Koga, SJ Clough, B Calla, ... Plant Physiology and Biochemistry 146, 238-248, 2020 | | 2020 |
| Identification of alternative exon usage in cancer survival using hierarchical modeling A Sadeque | | 2012 |
| Hierarchical modeling of alternative exon usage associations with survival A Sadeque, NVL Serão, BR Southey, Z Fazal, SL Rodriguez-Zas 2011 IEEE International Conference on Bioinformatics and Biomedicine …, 2011 | | 2011 |
| Retinitis pigmentosa (RP) is M Azam, RWJ Collin, A Malik, MI Khan, STA Shah, AA Shah, A Hussain, ... ARCH OPHTHALMOL 129 (10), 2011 | | 2011 |
| Novel CNGA3and CNGB3mutations in two Pakistani families with achromatopsia M Azam, RWJ Collin, STA Shah, AA Shah, MI Khan, A Hussain, ... | | 2010 |
| Exome sequencing identifies a novel and a known BBS1 mutation in Pakistani families with Bardet-Biedl syndrome M Ajmal, MI Khan, K Neveling, A Tayyab, S Jaffar, A Sadeque, H Ayub, ... GENETIC BASIS OF INHERITED EYE DISEASES, 87, 0 | | |
