| MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study FF Khidri, YM Waryah, FK Ali, H Shaikh, ID Ujjan, AM Waryah BMC medical genetics 20, 1-12, 2019 | 36 | 2019 |
| Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population M Shahzad, S Yousaf, YM Waryah, H Gul, T Kausar, N Tariq, U Mahmood, ... Scientific reports 7 (1), 44185, 2017 | 32 | 2017 |
| Visual impairment and progressive phthisis bulbi caused by recessive pathogenic variant in MARK3 M Ansar, H Chung, YM Waryah, P Makrythanasis, E Falconnet, AR Rao, ... Human molecular genetics 27 (15), 2703-2711, 2018 | 27 | 2018 |
| Homozygous variant in ARL3 causes autosomal recessive cone rod dystrophy SA Sheikh, RA Sisk, CR Schiavon, YM Waryah, MA Usmani, DH Steel, ... Investigative Ophthalmology & Visual Science 60 (14), 4811-4819, 2019 | 13 | 2019 |
| Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients YM Waryah, M Iqbal, SA Sheikh, MA Baig, AK Narsani, M Atif, MA Bhinder, ... International journal of ophthalmology 12 (1), 8, 2019 | 12 | 2019 |
| Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling H Shaikh, AM Waryah, AK Narsani, M Iqbal, M Shahzad, YM Waryah, ... Biochemical genetics 55, 410-420, 2017 | 10 | 2017 |
| Genetic causes of oculocutaneous albinism in Pakistani population Z Sajid, S Yousaf, YM Waryah, TA Mughal, T Kausar, M Shahzad, AR Rao, ... Genes 12 (4), 492, 2021 | 9 | 2021 |
| Delineating the spectrum of genetic variants associated with Bardet-Biedl syndrome in consanguineous Pakistani pedigrees AR Rao, A Nazir, S Imtiaz, SA Paracha, YM Waryah, ID Ujjan, I Anwar, ... Genes 14 (2), 404, 2023 | 8 | 2023 |
| Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract P Jarwar, SA Sheikh, YM Waryah, IU Ujjan, S Riazuddin, AM Waryah, ... International Journal of Molecular Sciences 22 (19), 10655, 2021 | 5 | 2021 |
| Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population M Shahzad, J Sires Campos, N Tariq, C Herraiz Serrano, R Yousaf, ... Pigment cell & melanoma research 28 (6), 730-735, 2015 | 5 | 2015 |
| P. arg102ser is a common Pde6a mutation causing autosomal recessive retinitis pigmentosa in Pakistani families. AA Khan, YM Waryah, M Iqbal, AB HM, M Rafique, AM Waryah JPMA. The Journal of the Pakistan Medical Association 71 (3), 816-821, 2021 | 3 | 2021 |
| Association of MSX1 Gene Variants with Nonsyndromic Cleft Lip and/or Palate in the Pakistani Population A Memon, FF Khidri, YM Waryah, R Nigar, MA Bhinder, AM Shaikh, ... The Cleft Palate Craniofacial Journal, 10556656231185218, 2023 | 2 | 2023 |
| Serum and salivary Cu/Zn ratio as a diagnostic biomarker for oral submucosal fibrosis: an analysis of trace metals and LOX gene variants R Shah, FF Khidri, YM Waryah, R Nigar, A Mahmood, H Shaikh, MQ Awan, ... BioMetals 37 (2), 447-459, 2024 | 1 | 2024 |
| Prevalence of Factor V Leiden Mutation in Healthy Females of Sindh, Pakistan and Comparison of Three Detection Methods in Resource-Limited Settings: Prevalence of Factor V … FF Khidri, H Riaz, YM Waryah, R Nigar, AM Waryah Pakistan Journal of Health Sciences, 49-55, 2023 | 1 | 2023 |
| Association of N and E genes with ORF1b gene for early detection of COVID-19 in Pakistani patients YM Waryah, S Ehsan, R Nigar Journal of Liaquat University of Medical & Health Sciences 22 (03), 197-200, 2023 | 1 | 2023 |
| Association of single nucleotide polymorphism variations in CRYAA and CRYAB genes with congenital cataract in Pakistani population P Jarwar, YM Waryah, M Rafiq, AM Waryah Saudi Journal of Biological Sciences 29 (4), 2727-2732, 2022 | 1 | 2022 |
| Delineating the Molecular and Phenotypic Spectrum of the CNGA3-Related Cone Photoreceptor Disorder in Pakistani Families S Yousaf, N Tariq, Z Sajid, SA Sheikh, T Kausar, YM Waryah, RS Shaikh, ... Genes 13 (4), 617, 2022 | 1 | 2022 |
| Proceedings of the 1st Liaquat University of Medical & Health Sciences (LUMHS) International Medical Research Conference M Iqbal, MV Clement-Pervaiz, MJ Ansari, S Pervaiz, S Sheikh, S Katpar, ... European Journal of Medical Research 22, 1-20, 2017 | 1 | 2017 |
| Association of the c. 75C> A Variant in CLCC1 with Autosomal Recessive Retinitis Pigmentosa in Pakistan YM Waryah, FF Khidri, A Ansari, S Mehmood, S Abbasi, S Memon Journal of Liaquat University of Medical & Health Sciences 23 (03), 249-253, 2024 | | 2024 |
| Mutation Screening of the CYP1B1 Gene Reveals Novel and Recurrent Pathogenic Variants in Pakistani Primary Congenital Glaucoma Patients WA Surhio, FF Khidri, MI Haroon, S Mehmood, YM Waryah Journal of Liaquat University of Medical & Health Sciences 23 (02), 140-145, 2024 | | 2024 |
