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Nadia Farooqi
Nadia Farooqi
Visiting faculty
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标题
引用次数
引用次数
年份
Male infertility: etiological factors [a review]
H Muhammad, AA Shah, G Nabi, N Farooqi
Am Eurasian J Toxicol Sci 7, 95-103, 2015
152015
Association of AFF3 gene polymorphism rs10865035 with rheumatoid arthritis: a population-based case-control study on a Pakistani cohort
Y Ali, S Khan, Y Chen, N Farooqi, ZU Islam, M Akhtar, A Aman, AA Shah, ...
Genetics Research 2021, e15, 2021
62021
Association of TORCH Agents with Spontaneous Abortion in Patients with Bad Obstetric History
AA Shah, H Muhammad, N Farooqi, N Gul, AA Khan, G Nabi, SN Khan
World J. Zool 10, 291-294, 2015
52015
Association of IL-17F rs2397084 (E126G), rs11465553 (V155I) and rs763780 (H161R) variants with rheumatoid arthritis and their effects on the stability of protein
Y Ali, M Kausar, M Farooq, N Farooqi, Z Ul Islam, S Khan, A Aman, ...
Plos one 18 (9), e0285874, 2023
12023
Exome sequencing identifies a novel FBN1 variant in a Pakistani family with Marfan syndrome that includes left ventricle diastolic dysfunction
N Farooqi, LA Metherell, I Schrauwen, A Acharya, Q Khan, ...
Genes 12 (12), 1915, 2021
12021
Phylogenetic analysis of promoter regions of human Dolichol kinase (DOLK) and orthologous genes using bioinformatics tools
N Farooqi, A Rahman, Y Ali, K Ali, MEH Khan, DA Jones, M Abdelkarim, ...
Open Life Sciences 18 (1), 20220591, 2023
2023
Exploring the Associations and Molecular Impacts of miR-146a/rs2910164 and miR-196a2/rs185070757 with Rheumatoid Arthritis in a Pakistani Population
Y Ali, A Khan, M Akhtar, S Khan, ZU Islam, N Farooqi, AA Shah, Y Chen, ...
Lifestyle Genomics 16 (1), 139-150, 2023
2023
Screening for Deleterious non-synonymous SNPs in Human CCL21 Gene using in-silico analysis
Y Ali, M Akhtar, K Khan, N Farooqi, S Gohar, SI Ahmad, M Ayaz, ZU Islam, ...
NUST Journal of Natural Sciences 6 (2), 2021
2021
Review Studies of GJB2 Gene in Patients with Hearing Impairment in Pakistan
N Farooqi, O Khan, S Ellaham, SF Jalil
J Mol Genet Med 11 (316), 1747-0862.1000316, 2017
2017
Whole exome sequencing identified a novel genetic variant in an infertile family with azoospermia and severe oligozoospermia
H MUHAMMAD, Y ALI, N FAROOQI, N ALI, F JALIL, S ALI
AN OVERVIEW ON BRUCELLOSIS
H Muhammad, N Farooqi, AA Shah, G Nabi2i
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