| Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial cases I Ullah, F Kabir, M Iqbal, CBS Gottsch, MA Naeem, MZ Assir, SN Khan, ... Molecular vision 22, 797, 2016 | 22 | 2016 |
| Loss of function mutations in RP1 are responsible for retinitis pigmentosa in consanguineous familial cases F Kabir, I Ullah, S Ali, ADH Gottsch, MA Naeem, MZ Assir, SN Khan, ... Molecular vision 22, 610, 2016 | 18 | 2016 |
| Mutations in phosphodiesterase 6 identified in familial cases of retinitis pigmentosa I Ullah, F Kabir, CBS Gottsch, MA Naeem, AA Guru, R Ayyagari, SN Khan, ... Human genome variation 3 (1), 1-4, 2016 | 12 | 2016 |
| Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness MA Naeem, ADH Gottsch, I Ullah, SN Khan, T Husnain, NH Butt, ZA Qazi, ... Molecular vision 21, 1261, 2015 | 9 | 2015 |
| Assessing the fate of recombinant plant DNA in rabbit’s tissues fed genetically modified cotton AA Shahid, IB Salisu, A Yaqoob, AQ Rao, I Ullah, T Husnain Journal of animal physiology and animal nutrition 104 (1), 343-351, 2020 | 1 | 2020 |
