| CLRN1 mutations cause nonsyndromic retinitis pigmentosa MI Khan, FFJ Kersten, M Azam, RWJ Collin, A Hussain, STA Shah, ... Ophthalmology, 2011 | 70 | 2011 |
| Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families S Shafique, S Siddiqi, M Schraders, J Oostrik, H Ayub, A Bilal, M Ajmal, ... PloS one 9 (6), e100146, 2014 | 67 | 2014 |
| Toxic metals signature in the human seminal plasma of Pakistani population and their potential role in male infertility A Zafar, SAMAS Eqani, N Bostan, A Cincinelli, F Tahir, STA Shah, ... Environmental geochemistry and health 37, 515-527, 2015 | 65 | 2015 |
| TEC‐family kinases in health and disease: Loss‐of‐function of BTK and ITK and the gain‐of‐function fusions ITK‐SYK and BTK‐SYK A Hussain, L Yu, R Faryal, DK Mohammad, AJ Mohamed, ... FEBS Journal, 2011 | 55 | 2011 |
| Role of receptor tyrosine kinases mediated signal transduction pathways in tumor growth and angiogenesis—New insight and futuristic vision XL Huang, MI Khan, J Wang, R Ali, SW Ali, A Kazmi, A Lolai, YL Huang, ... International Journal of Biological Macromolecules 180, 739-752, 2021 | 45 | 2021 |
| Dual phosphorylation of Btk by Akt/protein kinase b provides docking for 14-3-3ζ, regulates shuttling, and attenuates both tonic and induced signaling in B cells DK Mohammad, BF Nore, A Hussain, MO Gustafsson, AJ Mohamed, ... Molecular and cellular biology 33 (16), 3214-3226, 2013 | 45 | 2013 |
| Regulation of nucleocytoplasmic shuttling of Bruton's tyrosine kinase (Btk) through a novel SH3-dependent interaction with ankyrin repeat domain 54 (ANKRD54) MO Gustafsson, A Hussain, DK Mohammad, AJ Mohamed, V Nguyen, ... Molecular and cellular biology, 2012 | 36 | 2012 |
| Ischemia-reperfusion injury and pregnancy initiate time-dependent and robust signs of up-regulation of cardiac progenitor cells R Genead, H Fischer, A Hussain, M Jaksch, AB Andersson, K Ljung, ... PloS one 7 (5), e36804, 2012 | 35 | 2012 |
| Environmental exposure pathway analysis of trace elements and autism risk in Pakistani children population SAMAS Eqani, F Khuram, A Alamdar, A Tahir, STA Shah, A Nasir, ... Science of the total environment 712, 136471, 2020 | 33 | 2020 |
| Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan M Maria, M Ajmal, M Azam, NK Waheed, SN Siddiqui, B Mustafa, H Ayub, ... PLoS One 10 (3), e0119806, 2015 | 33 | 2015 |
| TNF-α genetic predisposition and higher expression of inflammatory pathway components in keratoconus M Arbab, S Tahir, MK Niazi, M Ishaq, A Hussain, PM Siddique, S Saeed, ... Investigative Ophthalmology & Visual Science 58 (9), 3481-3487, 2017 | 31 | 2017 |
| 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 | 29 | 2010 |
| Caveolin‑1 and dynamin‑2 overexpression is associated with the progression of bladder cancer SA Raja, STA Shah, A Tariq, N Bibi, K Sughra, A Yousuf, A Khawaja, ... Oncology Letters 18 (1), 219-226, 2019 | 28 | 2019 |
| 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, 2011 | 26 | 2011 |
| 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 | 24 | 2009 |
| Cattle egrets as a biosentinels of persistent organic pollutants exposure M Khan, A Mohammad, K Ahad, A Katsoyiannis, SA Malik, M Abdullaha, ... Environmental geochemistry and health 36, 375-384, 2014 | 19 | 2014 |
| Signaling of the ITK (IL2-inducible T-cell kinase)-SYK fusion kinase is dependent on adapter SLP-76 (SH2 domain-containing leukocyte protein of 76 kD) and on the adapter … A Hussain, DK Mohammad, MO Gustafsson, M Uslu, A Hamasy, BF Nore, ... Journal of Biological Chemistry, 2013 | 19* | 2013 |
| Homozygosity mapping identifies genetic defects in four consanguineous families with retinal dystrophy from Pakistan A Hussain, A Shahzad, H Venselaar, H Bokhari, IJ de Wijs, LH Hoefsloot, ... GENETIC BASIS OF INHERITED EYE DISEASES, 107, 2013 | 16 | 2013 |
| Phosphatidylinositol-3-kinase-dependent phosphorylation of SLP-76 by the lymphoma-associated ITK-SYK fusion-protein A Hussain, R Faryal, BF Nore, AJ Mohamed, CIE Smith Biochemical and biophysical research communications 390 (3), 892-896, 2009 | 16 | 2009 |
| Impact of performance status on overall survival in patients with relapsed and/or refractory multiple myeloma: Real‐life outcomes of daratumumab treatment G Afram, C Gran, J Borg Bruchfeld, AK Wagner, A Hussain, E Alici, H Nahi European Journal of Haematology 105 (2), 196-202, 2020 | 14 | 2020 |
