Naureen Aslam

1. Vincent JB, Jamil T, Rafiq MA, Anwar Z, Ayaz M, Hameed A, Nasr T, Naeem F, Khattak NA et al., “Phosphoserine Phosphatase (PSPH)gene mutation in an intellectual disability family from Pakistan”, Clin. Genet, 87(3): pp 296-298. 2015.
2. Khattak NA and Mir A, “Computational analysis of TRAPPC9: Candidate Gene for Autosomal Recessive Non-Syndromic Mental Retardation”, CNS Neurol Disord Drug Targets, 13(4): pp 699-711, 2014.
3. Tahir RA, Sehgal SA, Khattak NA, Khattak JZK and Mir A, “Tumor Necrosis Factor Receptor Superfamily 10B(TNFRSF10B), An insight from structure modeling to virtual screening for candidate gene interaction studies”, Theoretical Biology and Medical Modelling , 10:38, 2013.
4. Sehgal SA, Khattak NA and Mir A, “Structural, Phylogenetic and docking studies of D- amino acid oxidase activator(DAOA), a candidate gene of Schizophrenia”, Theoretical Biology and Medical Modelling, 10:3, 2013.
5. E-Zahra SN, Khattak NA and Mir A, “Comparative modeling and docking studies of p16INK4/cyclinD1/Rb pathway gene in lung cancer revealed functionally active residue of RB1and its functional partner E2F1”, Theoretical Biologyand Medical Modelling, 10:1, 2013
6. Khattak NA, Rauf S, Sehgal SA, Shahwar D and Ismail M, “Insilico gene prediction for autosomal recessive cone-rod dystrophy (CORD8)”, OJB, 14 (2): pp 104-117, 2013.
7. Khattak NA, E-Zahra SN and Awan WA, “Molecular Modeling of Discoidin Domain Receptor Tyrosine Kinase 2(DDR2) and ATPase, Na+/K+ Transporting, Alpha 4 polypeptide (ATP1A4): Candidate genes for autosomal recessive cone-rod dystrophy (CORD8)”, Int. J. Rehab. Sci., 1.2, pp 53-57. 2012.
8. Raza A, Khattak NA, “Applications of Real Time PCR in diagnostics and research”, Professional Med J, 19(6), pp 751-759, 2012.
9. Khattak N, Khan MA and Raza A, “Mental Retardation; Molecular cytogenetic techniques used for Diagnosis, A literature survey”, Professional Med J., 18(4), pp 547-551. 2011