CYP3A5 gene polymorphisms and their impact on dosage and trough concentration of tacrolimus among kidney transplant patients: a systematic review and meta-analysis
Khan, Abdul Rafay, Raza, Ali, Firasat, Sadaf, Abid, Aiysha
Published in The pharmacogenomics journal (01.08.2020)
Published in The pharmacogenomics journal (01.08.2020)
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Journal Article
Association of vitamin D receptor gene polymorphisms and risk of urolithiasis: results of a genetic epidemiology study and comprehensive meta-analysis
Amar, Ali, Afzal, Ayesha, Hussain, Syed Atif, Hameed, Athar, Khan, Abdul Rafay, Shakoor, Madiha, Abid, Aiysha, Khaliq, Shagufta
Published in Urolithiasis (01.10.2020)
Published in Urolithiasis (01.10.2020)
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Journal Article
Rare and heterogeneous manifestations of leucocyte adhesion deficiency type 1: report of two cases with diagnostic dilemmas and novel ITGB2 mutation
Anis, Sabiha, Abid, Aiysha, Kodwavwala, Sadaf Aba Umer, Sarfaraz, Sabahat, Junejo, Samina, Shahid, Saba, Sultan, Sajid, Rizvi, Adibul Hasan
Published in Allergy, asthma, and clinical immunology (02.05.2023)
Published in Allergy, asthma, and clinical immunology (02.05.2023)
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Journal Article
A Novel Nonsense Mutation in FERMT3 Causes LAD-III in a Pakistani Family
Shahid, Saba, Zaidi, Samreen, Ahmed, Shariq, Siddiqui, Saima, Abid, Aiysha, Malik, Shabbir, Shamsi, Tahir
Published in Frontiers in genetics (24.04.2019)
Published in Frontiers in genetics (24.04.2019)
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Journal Article
Osteopontin promoter polymorphisms and risk of urolithiasis: a candidate gene association and meta-analysis study
Amar, Ali, Afzal, Ayesha, Hameed, Athar, Ahmad, Mumtaz, Khan, Abdul Rafay, Najma, Humaira, Abid, Aiysha, Khaliq, Shagufta
Published in BMC medical genetics (25.08.2020)
Published in BMC medical genetics (25.08.2020)
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Journal Article
Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani Population
Shahid, Saba, Shakeel, Muhammad, Siddiqui, Saima, Ahmed, Shariq, Sohail, Misha, Khan, Ishtiaq Ahmad, Abid, Aiysha, Shamsi, Tahir
Published in Frontiers in genetics (23.06.2020)
Published in Frontiers in genetics (23.06.2020)
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Journal Article
ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous
PRASOV, Lev, MASUD, Tehmina, KELBERMAN, Daniel, SOWDEN, Jane C, DATTANI, Mehul T, GLASER, Tom, KHALIQ, Shagufta, QASIM MEHDI, S, ABID, Aiysha, OLIVER, Edward R, SILVA, Eduardo D, LEWANDA, Amy, BRODSKY, Michael C, BORCHERT, Mark
Published in Human molecular genetics (15.08.2012)
Published in Human molecular genetics (15.08.2012)
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Journal Article
Absence of Glutathione S-Transferase Theta 1 Gene Is Significantly Associated With Breast Cancer Susceptibility in Pakistani Population and Poor Overall Survival in Breast Cancer Patients: A Case-Control and Case Series Analysis
Ajaz, Sadia, Zaidi, Sani-E-Zehra, Ali, Saleema Mehboob, Siddiqa, Aisha, Memon, Muhammad Ali, Firasat, Sadaf, Abid, Aiysha, Khaliq, Shagufta
Published in Frontiers in oncology (06.12.2021)
Published in Frontiers in oncology (06.12.2021)
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Journal Article
Screening of the LAMB2, WT1, NPHS1 , and NPHS2 Genes in Pediatric Nephrotic Syndrome
Abid, Aiysha, Shahid, Saba, Shakoor, Madiha, Lanewala, Ali A, Hashmi, Seema, Khaliq, Shagufta
Published in Frontiers in genetics (22.06.2018)
Published in Frontiers in genetics (22.06.2018)
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Journal Article
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan
Abid, Aiysha, Khaliq, Shagufta, Shahid, Saba, Lanewala, Ali, Mubarak, Mohammad, Hashmi, Seema, Kazi, Javed, Masood, Tahir, Hafeez, Farkhanda, Naqvi, Syed Ali Anwar, Rizvi, Syed Adeebul Hasan, Mehdi, Syed Qasim
Published in Gene (10.07.2012)
Published in Gene (10.07.2012)
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Journal Article
Analysis of the glutathione S-transferase genes polymorphisms in the risk and prognosis of renal cell carcinomas. Case-control and meta-analysis
Abid, Aiysha, Ph.D, Ajaz, Sadia, Ph.D, Khan, Abdul Rafay, B.S, Zehra, Fatima, M.Sc, Hasan, Asad Shahzad, M.D, Sultan, Gauhar, M.D, Mohsin, Rehan, M.D, Hashmi, Altaf, M.D, Niamatullah, Najeeb, M.D, Rizvi, Syed Adib-ul-Hasan, M.D, Mehdi, Syed Qasim, Ph.D, Khaliq, Shagufta, Ph.D
Published in Urologic oncology (01.09.2016)
Published in Urologic oncology (01.09.2016)
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Journal Article
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
Ismail, Muhammad, Abid, Aiysha, Anwar, Khalid, Qasim Mehdi, S, Khaliq, Shagufta
Published in Journal of human genetics (01.09.2006)
Published in Journal of human genetics (01.09.2006)
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Journal Article
The prevalence of pharmacogenetic variants of vitamin K epoxide reductase complex subunit 1 gene (rs9923231), cytochrome P450 family 2 subfamily C member 9 gene (rs1799853) and cytochrome P450 family 3 subfamily-A member-5 gene (rs776746) among 13 ethnic groups of Pakistan
Firasat, Sadaf, Raza, Ali, Khan, Abdul Rafay, Abid, Aiysha
Published in Molecular biology reports (01.05.2023)
Published in Molecular biology reports (01.05.2023)
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Journal Article
Primary hyperoxaluria and genetic linkages: an insight into the disease burden from Pakistan
Hashmi, Seema, Abid, Aiysha, Sultan, Sajid, Shekhani, Sualeha Siddiq, Lanewala, Ali Asghar, Zafar, Mirza Naqi
Published in Urolithiasis (01.08.2022)
Published in Urolithiasis (01.08.2022)
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Journal Article
Association of specific single nucleotide variants (SNVs) in the promoter and 3′-Untranslated region of Vascular Endothelial growth factor (VEGF) gene with risk and higher tumour grade of head and neck cancers
Ajaz, Sadia, Muneer, Rabbia, Siddiqa, Aisha, Ali Memon, Muhammad, Firasat, Sadaf, Abid, Aiysha, Khaliq, Shagufta
Published in Oral oncology (01.11.2021)
Published in Oral oncology (01.11.2021)
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