List of works - Nafees Ahmad

A report of whole-genome sequencing in neurologic Wilson's disease

scientific article published in May 2017

Absence of SNCA polymorphisms in Pakistani Parkinsons disease patients

scientific article published in October 2017

Association of arg16gly and gln27glu, b2-adrenergic receptor gene polymorphism with asthma. A systematic review and meta-analysis of case control studies

scientific article published in January 2018

Association of vitamin D receptor gene polymorphisms with prostate cancer risk in the Pakistani population

scientific article published on 01 January 2014

Cost analysis of registered brands of oral antidepressant drugs in Pakistan: a descriptive analysis

scientific article published on 13 September 2019

Crybb2 associates with Tmsb4X and is crucial for dendrite morphogenesis

scientific article published on 06 June 2018

Epigenetic regulation of inflammatory cytokines and associated genes in human malignancies

scientific article

First mutation in the βA2-crystallin encoding gene is associated with small lenses and age-related cataracts

scientific journal article

Further evidence for the association of CYP2D6*4 gene polymorphism with Parkinson's disease: a case control study

scientific article

Genetic determinants of β-thalassemia intermedia in Pakistan.

scientific article published on 24 February 2015

Homozygous CHST11 mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactyly

scientific article published on 07 March 2018

Identification and association of recurrent ALOXE3 mutation with non-bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families

scientific article published on 18 July 2018

Identification of recurrent c.742G>T nonsense mutation in ECM1 in Pakistani families suffering from lipoid proteinosis.

scientific article

In silico characterization of a novel pathogenic deletion mutation identified in XPA gene in a Pakistani family with severe xeroderma pigmentosum.

scientific article

Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse.

scientific article

Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome.

scientific article

Patient HLA-DRB1* and -DQB1* allele and haplotype association with hepatitis C virus persistence and clearance.

scientific article published on 14 April 2010

Pitx3 directly regulates Foxe3 during early lens development

scientific article published in January 2013

Profiling trait anxiety: transcriptome analysis reveals cathepsin B (Ctsb) as a novel candidate gene for emotionality in mice

scientific article (publication date: 2011)

Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain.

scientific article

Segregation and potential functional impact of a rare stop-gain PABPC4L variant in familial atypical Parkinsonism

scientific article published on 19 September 2019

Study of PKRBD in HCV genotype 3a infected patients in response to interferon therapy in Pakistani population.

scientific article

TNF-alpha induced NFκB signaling and p65 (RelA) overexpression repress Cldn5 promoter in mouse brain endothelial cells

scientific article published on 03 December 2011

Targeting of JAK-STAT Signaling in Breast Cancer: Therapeutic Strategies to Overcome Drug Resistance

scientific article published on 01 January 2019

List of works by Nafees Ahmad

A report of whole-genome sequencing in neurologic Wilson's disease

Absence of SNCA polymorphisms in Pakistani Parkinsons disease patients

Association of arg16gly and gln27glu, b2-adrenergic receptor gene polymorphism with asthma. A systematic review and meta-analysis of case control studies

Association of vitamin D receptor gene polymorphisms with prostate cancer risk in the Pakistani population

Cost analysis of registered brands of oral antidepressant drugs in Pakistan: a descriptive analysis

Crybb2 associates with Tmsb4X and is crucial for dendrite morphogenesis

Epigenetic regulation of inflammatory cytokines and associated genes in human malignancies

First mutation in the βA2-crystallin encoding gene is associated with small lenses and age-related cataracts

Further evidence for the association of CYP2D6*4 gene polymorphism with Parkinson's disease: a case control study

Genetic determinants of β-thalassemia intermedia in Pakistan.

Homozygous CHST11 mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactyly

Identification and association of recurrent ALOXE3 mutation with non-bullous congenital ichthyosiform erythroderma in two ethnically distinct Pakistani families

Identification of recurrent c.742G>T nonsense mutation in ECM1 in Pakistani families suffering from lipoid proteinosis.

In silico characterization of a novel pathogenic deletion mutation identified in XPA gene in a Pakistani family with severe xeroderma pigmentosum.

Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse.

Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome.

Patient HLA-DRB1* and -DQB1* allele and haplotype association with hepatitis C virus persistence and clearance.

Pitx3 directly regulates Foxe3 during early lens development

Profiling trait anxiety: transcriptome analysis reveals cathepsin B (Ctsb) as a novel candidate gene for emotionality in mice

Progressive SCAR14 with unclear speech, developmental delay, tremor, and behavioral problems caused by a homozygous deletion of the SPTBN2 pleckstrin homology domain.

Segregation and potential functional impact of a rare stop-gain PABPC4L variant in familial atypical Parkinsonism

Study of PKRBD in HCV genotype 3a infected patients in response to interferon therapy in Pakistani population.

TNF-alpha induced NFκB signaling and p65 (RelA) overexpression repress Cldn5 promoter in mouse brain endothelial cells

Targeting of JAK-STAT Signaling in Breast Cancer: Therapeutic Strategies to Overcome Drug Resistance