| Evidence of RPGRIP1 gene mutations associated with recessive cone-rod dystrophy A Hameed, A Abid, A Aziz, M Ismail, SQ Mehdi, S Khaliq Journal of medical genetics 40 (8), 616-619, 2003 | 140 | 2003 |
| Identification of novel mutations in the SEMA4A gene associated with retinal degenerative diseases A Abid, M Ismail, SQ Mehdi, S Khaliq Journal of medical genetics 43 (4), 378-381, 2006 | 105 | 2006 |
| Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa S Khaliq, A Abid, M Ismail, A Hameed, A Mohyuddin, P Lall, A Aziz, ... Journal of medical genetics 42 (5), 436-438, 2005 | 88 | 2005 |
| ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous L Prasov, T Masud, S Khaliq, SQ Mehdi, A Abid, ER Oliver, ED Silva, ... Human molecular genetics 21 (16), 3681-3694, 2012 | 80 | 2012 |
| A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan A Abid, S Khaliq, S Shahid, A Lanewala, M Mubarak, S Hashmi, J Kazi, ... Gene 502 (2), 133-137, 2012 | 59 | 2012 |
| CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysis AR Khan, A Raza, S Firasat, A Abid The Pharmacogenomics Journal 20 (4), 553-562, 2020 | 55 | 2020 |
| Association of a single-nucleotide polymorphism in the promoter region of the VEGF gene with the risk of renal cell carcinoma S Ajaz, S Khaliq, A Abid, AS Hassan, A Hashmi, G Sultan, R Mohsin, ... Genetic testing and molecular biomarkers 15 (9), 653-657, 2011 | 40 | 2011 |
| Mutation screening of Pakistani families with congenital eye disorders S Khaliq, A Abid, A Hameed, K Anwar, A Mohyuddin, Z Azmat, SA Shami, ... Experimental eye research 76 (3), 343-348, 2003 | 30 | 2003 |
| The association of urinary interferon-gamma inducible protein-10 (IP10/CXCL10) levels with kidney allograft rejection A Raza, S Firasat, S Khaliq, T Aziz, M Mubarak, SAA Naqvi, SQ Mehdi, ... Inflammation Research 66, 425-432, 2017 | 28 | 2017 |
| Locus heterogeneity and Knobloch syndrome S Joyce, L Tee, A Abid, S Khaliq, SQ Mehdi, ER Maher American journal of medical genetics. Part A 152 (11), 2880-2881, 2010 | 23 | 2010 |
| Mapping of a novel type III variant of Knobloch syndrome (KNO3) to chromosome 17q11. 2 S Khaliq, A Abid, DRA White, CA Johnson, M Ismail, A Khan, Q Ayub, ... American Journal of Medical Genetics Part A 143 (23), 2768-2774, 2007 | 22 | 2007 |
| Monocyte chemoattractant protein-1 (MCP-1/CCL2) levels and its association with renal allograft rejection A Raza, S Firasat, S Khaliq, AR Khan, S Mahmood, T Aziz, M Mubarak, ... Immunological investigations 46 (3), 251-262, 2017 | 19 | 2017 |
| Association of vitamin D receptor gene polymorphisms and risk of urolithiasis: results of a genetic epidemiology study and comprehensive meta-analysis A Amar, A Afzal, SA Hussain, A Hameed, AR Khan, M Shakoor, A Abid, ... Urolithiasis 48 (5), 385-401, 2020 | 18 | 2020 |
| Analysis of the glutathione S-transferase genes polymorphisms in the risk and prognosis of renal cell carcinomas. Case-control and meta-analysis A Abid, S Ajaz, AR Khan, F Zehra, AS Hasan, G Sultan, R Mohsin, ... Urologic Oncology: Seminars and Original Investigations 34 (9), 419. e1-419. e12, 2016 | 18 | 2016 |
| Refinement of the locus for autosomal recessive cone–rod dystrophy (CORD8) linked to chromosome 1q23–q24 in a Pakistani family and exclusion of candidate genes M Ismail, A Abid, K Anwar, S Qasim Mehdi, S Khaliq Journal of human genetics 51 (9), 827-831, 2006 | 16 | 2006 |
| A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family S Shahid, S Zaidi, S Ahmed, S Siddiqui, A Abid, S Malik, T Shamsi Frontiers in Genetics 10, 360, 2019 | 12 | 2019 |
| HLA class I and II polymorphisms in the Gujjar population from Pakistan A Raza, S Firasat, S Khaliq, A Abid, SS Shah, SQ Mehdi, A Mohyuddin Immunological investigations 42 (8), 691-700, 2013 | 12 | 2013 |
| Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children S Shahid, A Abid, QS Mehdi, S Firasat, A Lanewala, AAS Naqvi, S Khaliq Gene 493 (1), 165-168, 2012 | 11 | 2012 |
| Screening of the LAMB2, WT1, NPHS1, and NPHS2 Genes in Pediatric Nephrotic Syndrome A Abid, S Shahid, M Shakoor, AA Lanewala, S Hashmi, S Khaliq Frontiers in Genetics 9, 214, 2018 | 10 | 2018 |
| Primary hyperoxaluria: Comprehensive mutation screening of the disease causing genes and spectrum of disease‐associated pathogenic variants A Abid, A Raza, AR Khan, S Firasat, S Shahid, S Hashmi, MN Zafar, ... Clinical Genetics 103 (1), 53-66, 2023 | 8 | 2023 |
Dr. Shagufta Khaliq, Dir. Research, U...University College of Medicine & Dentistry-The University of Lahore在 ucm.uol.edu.pk 的电子邮件经过验证
