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Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse

Egyptian Journal of Medical Human Genetics, 2021-03, Vol.22 (1), p.22, Article 22

2021

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Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn's disease in monozygotic twins

Autoimmunity (Chur, Switzerland), 2017-07, Vol.50 (5), p.275-276

2017

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Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders

Genomics (San Diego, Calif.), 2021-01, Vol.113 (1), p.999-1017

2021

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Integrated Network and Gene Ontology Analysis Identifies Key Genes and Pathways for Coronary Artery Diseases

Avicenna journal of medical biotechnology, 2021-01, Vol.13 (1), p.15-23

2021

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Mucosa-associated specific bacterial species disrupt the intestinal epithelial barrier in the autism phenome

Brain, behavior, & immunity. Health, 2021-08, Vol.15, p.100269-100269, Article 100269

2021

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Risk homozygous haplotype regions for autism identifies population-specific ten genes for numerous pathways

The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 2021-06, Vol.57 (1), Article 69

2021

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Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2013-12, Vol.162B (8), p.889-897

2013

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Integrated in silico functional analysis predicts autism spectrum disorders to be burdened by deleterious variations within CHD8 core domains and its CHD7-binding motif

Network modeling and analysis in health informatics and bioinformatics (Wien), 2022-12, Vol.11 (1), p.33, Article 33

2022

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Simultaneous Detection of Drug-resistant Mutations in Mycobacterium tuberculosis and Determining their Role through In Silico Docking

Infectious disorders drug targets, 2021, Vol.21 (1), p.134-141

2021

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Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism

Egyptian Journal of Medical Human Genetics, 2020-12, Vol.21 (1), p.55, Article 55

2020

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Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes

PloS one, 2015-04, Vol.10 (4), p.e0121846-e0121846

2015

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Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population

Journal of human genetics, 2013-08, Vol.58 (8), p.531-538

2013

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IL-10 and IL-17F Promoter Single Nucleotide Polymorphism and Asthma: A Case-Control Study in South India

Lung, 2015-10, Vol.193 (5), p.739-747

2015

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Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

Egyptian Journal of Medical Human Genetics, 2020-10, Vol.21 (1), p.58, Article 58

2020

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Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays

PloS one, 2013-07, Vol.8 (7), p.e66843-e66843

2013

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Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression

PloS one, 2014-02, Vol.9 (2), p.e90391-e90391

2014

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Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders

Neuroscience, 2020-07, Vol.438, p.25-40

2020

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Differential expression of the Mycobacterium tuberculosis heat shock protein genes in response to drug-induced stress

Tuberculosis (Edinburgh, Scotland), 2022-05, Vol.134, p.102201-102201, Article 102201

2022

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Development of Rapid Automatized Naming (RAN) in Simultaneous Kannada-English Biliterate Children

Journal of psycholinguistic research, 2016-02, Vol.45 (1), p.177-187

2016

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Allopatric sibling species pair Drosophila nasuta nasuta and Drosophila nasuta albomicans exhibit expression divergence in ovarian transcriptomes

Gene, 2021-04, Vol.777, p.145189-145189, Article 145189

2021

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Egg-derived tyrosine phosphatase as a Potential Biomarker for Muscle Ageing and Degeneration in Drosophila melanogaster

Journal of genetics and genomics, 2014-04, Vol.41 (4), p.221-224

2014

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Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers

Allergy, 2015, Asthma & Immunology Research, 7(3), , pp.265-275

2015

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Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans

Journal of Nucleic Acids, 2016-01, Vol.2016 (2016), p.1-7

2016

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Damaging stop gain/loss and frameshift mutations in autism subjects outline impairment in neuronal migration and adhesion pathways

Canadian Journal of Biotechnology, 2017-10, Vol.1 (Special Issue), p.94-94

2017

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An understanding of the genetic basis of asthma

Indian journal of medical research (New Delhi, India : 1994), 2011-08, Vol.134, p.149

2011

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Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse

Complex interaction between HNRNPD mutations and risk polymorphisms is associated with discordant Crohn's disease in monozygotic twins

Comprehensive in silico mutational-sensitivity analysis of PTEN establishes signature regions implicated in pathogenesis of Autism Spectrum Disorders

Integrated Network and Gene Ontology Analysis Identifies Key Genes and Pathways for Coronary Artery Diseases

Mucosa-associated specific bacterial species disrupt the intestinal epithelial barrier in the autism phenome

Risk homozygous haplotype regions for autism identifies population-specific ten genes for numerous pathways

Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia

Integrated in silico functional analysis predicts autism spectrum disorders to be burdened by deleterious variations within CHD8 core domains and its CHD7-binding motif

Simultaneous Detection of Drug-resistant Mutations in Mycobacterium tuberculosis and Determining their Role through In Silico Docking

Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism

Global spectrum of copy number variations reveals genome organizational plasticity and proposes new migration routes

Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population

IL-10 and IL-17F Promoter Single Nucleotide Polymorphism and Asthma: A Case-Control Study in South India

Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

Unravelling the complexity of human olfactory receptor repertoire by copy number analysis across population using high resolution arrays

Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression

Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders

Differential expression of the Mycobacterium tuberculosis heat shock protein genes in response to drug-induced stress

Development of Rapid Automatized Naming (RAN) in Simultaneous Kannada-English Biliterate Children

Allopatric sibling species pair Drosophila nasuta nasuta and Drosophila nasuta albomicans exhibit expression divergence in ovarian transcriptomes

Egg-derived tyrosine phosphatase as a Potential Biomarker for Muscle Ageing and Degeneration in Drosophila melanogaster

Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers

Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans

Damaging stop gain/loss and frameshift mutations in autism subjects outline impairment in neuronal migration and adhesion pathways

An understanding of the genetic basis of asthma

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