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Saba Shahid
Saba Shahid
National Institute of Blood Diseases and Bone Marrow Transplantation
Verified email at nibd.edu.pk
Title
Cited by
Cited by
Year
A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan
A Abid, S Khaliq, S Shahid, A Lanewala, M Mubarak, S Hashmi, J Kazi, ...
Gene 502 (2), 133-137, 2012
672012
Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population.
TS Saba Shahid, Mohammad Nadeem, Danish Zahid, Jawwad Hassan, Saqib Ansari
Pak J. Med Sci. 2 (33), 411-416, 2017
17*2017
Genomic profile of a patient with triple negative essential thrombocythemia, unresponsive to therapy: A case report and literature review.
TS Uzma Zaidi, Saba Shahid, Naveen Fatima, Shariq Ahmed, Gull Sufaida ...
J Adv Res. 4 (8), 375-378, 2017
14*2017
Synthesis, immunomodulation and cytotoxic effects of vanadium (IV) complexes
U Ashiq, R Ara Jamal, M Ahmed Mesaik, M Mahroof-Tahir, S Shahid, ...
Medicinal Chemistry 10 (3), 287-299, 2014
132014
Association of the ACE-II genotype with the risk of nephrotic syndrome in Pakistani children
S Shahid, A Abid, QS Mehdi, S Firasat, A Lanewala, AAS Naqvi, ...
Gene 493 (1), 165-168, 2012
122012
Unique molecular alteration patterns in von Hippel-Lindau (VHL) gene in a cohort of sporadic renal cell carcinoma patients from Pakistan
S Khaliq, S Ajaz, S Firasat, S Shahid, AS Hasan, G Sultan, R Mohsin, ...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 763, 45-52, 2014
92014
Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotype
SH Shah, A Abid, S Shahid, S Khaliq
JPMA-Journal of the Pakistan Medical Association 61 (11), 1060, 2011
42011
Co-occurrence of oncogenic driver mutations (SF3B1, RUNX1 and CSF3R) with distinct prognostic Implication in a lower risk myelodysplastic syndrome patient.
TS Aisha Jamal , Nida Anwar , Saba Shahid , Shariq Ahmed
Merit Res J Med Sci. 4 (5), 192-196, 2017
2017
A spectrum of novel NPHS1 and NPHS2 gene mutations in Pediatric Nephrotic syndrome patients from Pakistan
A Abid, S Khalique, S Shahid, A Lanewala, M Mubarak, S Hashmi, ...
PEDIATRIC NEPHROLOGY 28 (8), 1461-1461, 2013
2013
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Articles 1–9