Pakeeza Arzoo Shaiq
Pakeeza Arzoo Shaiq
Assistant Professor, University Institute of Biochemistry and Biotechnology, PMAS-AAUR
Verified email at - Homepage
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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
Recurrent GATA1 mutations in Diamond-Blackfan anaemia.
J Klar, A Khalfallah, PS Arzoo, HT Gazda, N Dahl
British journal of haematology 166 (6), 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
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
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
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
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
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
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
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
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
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
Association of β-lactoglobulin protein isoforms with milk constituents in goat breeds.
A Mahmood, M Jamy, M Saqlain, PA Shaiq, SMS Naqvi, GK Raja
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 116, 74-80, 2024
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
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
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 (1), 4408306, 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, ...
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
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
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