| WNT10A mutations account for ¼ of population‐based isolated oligodontia and show phenotypic correlations PS Arzoo, J Klar, B Bergendal, J Norderyd, N Dahl American Journal of Medical Genetics Part A 164 (2), 353-359, 2014 | 104 | 2014 |
| Recurrent GATA1 mutations in Diamond-Blackfan anaemia. J Klar, A Khalfallah, PS Arzoo, HT Gazda, N Dahl British journal of haematology 166 (6), 949-951, 2014 | 60 | 2014 |
| Genetic associations of psoriasis in a Pakistani population PA Shaiq, PE Stuart, A Latif, C Schmotzer, AH Kazmi, MS Khan, M Azam, ... British Journal of Dermatology 169 (2), 406-411, 2013 | 31 | 2013 |
| Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy J Schuster, TN Khan, M Tariq, PA Shaiq, K Mäbert, SM Baig, J Klar BMC medical genetics 15, 1-6, 2014 | 23 | 2014 |
| Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine mapping in the MHC and genome wide PE Stuart, LC Tsoi, RP Nair, M Ghosh, M Kabra, PA Shaiq, GK Raja, ... Human Genetics and Genomics Advances 3 (1), 2022 | 19 | 2022 |
| A single SNP surrogate for genotyping HLA-C* 06: 02 in diverse populations PE Stuart, T Tejasvi, PA Shaiq, P Kullavanijaya, R Qamar, GK Raja, Y Li, ... The Journal of investigative dermatology 135 (4), 1177, 2015 | 11 | 2015 |
| Association study of Apolipoprotein A5 gene (APOA5 gene) variant with the metabolic syndrome in local Pakistani population M Fiaz, PA Shaiq, GK Raj, M Saqlain, A Mehmood, SMS Naqvi, ... J Pak Med Assoc 69 (3), 301-305, 2019 | 10 | 2019 |
| Identification of population specific risk phenotypes contributing towards development of metabolic syndrome. M Fiaz, F Rani, M Saqlain, A Mahmood, PA Shaiq, SM Naqvi, RA Qazi, ... Pakistan Journal of Zoology 48 (4), 2016 | 9 | 2016 |
| Whole-exome sequencing of Pakistani consanguineous families identified pathogenic variants in genes of intellectual disability M Asif, M Anayat, F Tariq, T Noureen, GNU Din, C Becker, K Becker, ... Genes 14 (1), 48, 2022 | 5 | 2022 |
| Association of Intestinal Fatty Acid Binding Protein (FABP2) Polymorphism with Metabolic Syndrome Risk. M Saqlain, H Kalsoom, M Fiaz, A Mahmood, RA Qazi, W Safdar, PA Shaiq, ... Pakistan Journal of Zoology 50 (1), 2018 | 5 | 2018 |
| A study of ACE, eNOS and MTHFR association with psoriasis in Pakistani population Z Agha, PA Shaiq, S Ahmed, L Ali, M Azam, SHB Ali, G Kaukab, R Qamar Meta Gene 15, 65-69, 2018 | 5 | 2018 |
| Founder mutation c. 676insC in three unrelated Kindler syndrome families belonging to a particular clan from Pakistan PA Shaiq, A Klausegger, F Muzaffar, JW Bauer, MI Khan, A Khanum, ... The Journal of Dermatology 39 (7), 640-641, 2012 | 5 | 2012 |
| Association of β-lactoglobulin protein isoforms with milk constituents in goat breeds. A Mahmood, M Jamy, M Saqlain, PA Shaiq, SMS Naqvi, GK Raja | 4 | 2016 |
| Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy M Ilyas, D Holzwarth, R Ishaq, Y Ali, U Habiba, AM Raja, S Saeed, ... Seizure: European Journal of Epilepsy, 2023 | 2 | 2023 |
| Demographic and Clinical Determinants of Tuberculosis and TB Recurrence: A Double-Edged Retrospective Study from Pakistan MA Mujtaba, M Richardson, H Shahzad, MI Javed, GK Raja, PA Shaiq, ... Journal of Tropical Medicine 2022, 2022 | 2 | 2022 |
| Future trends in the treatment of MRSA in Pakistan MN Noorulamin, ZB Zarafsah, A Janjua, A Iqbal, S Humerah, PA Shaiq Journal of Islamabad Medical & Dental College 11 (2), 96-102, 2022 | 2 | 2022 |
| B allele of β-lactoglobulin as a marker of dairy traits in Pakistani goat breeds. GK Raja, A Mahmood, RM Saqlain, MM Zafar, AM Raja, PA Shaiq, ... | 2 | 2020 |
| Missense mutation in LAMA3 associated with herlitz junctional epidermolysis bullosa in a Pakistani family PA Shaiq, A Klausegger, A Latif, J Bauer, R Qamar, GK Raja Pakistan Journal of Zoology 44 (6), 2012 | 2 | 2012 |
| Compound heterozygous mutations p. Q1530X and 6103delG in COL7A1 causing recessive dystrophic epidermolysis bullosa in a Pakistani family PA Shaiq, A Klausegger, JW Bauer, M Azam, GK Raja, R Qamar The Journal of Dermatology 39 (5), 472-474, 2012 | 2 | 2012 |
| 9p21 locus polymorphism is a strong predictor of metabolic syndrome and cardiometabolic risk phenotypes regardless of coronary heart disease M Mobeen Zafar, M Saqlain, A Mehmood Raja, P Arzoo Shaiq, ... Genes 13 (12), 2226, 2022 | 1 | 2022 |
