A. Patowary

发表

Detection of altered global DNA methylation in coronary artery disease patients.

J. Kumar, G. Garg, G. Karthikeyan, 2008, DNA and cell biology.

Dynamic Expression of Long Non-Coding RNAs (lncRNAs) in Adult Zebrafish

V. Scaria, Saakshi Jalali, S. Sivasubbu, 2013, PloS one.

Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder

R. Bernier, A. Patowary, Z. Brkanac, 2017, Autism research : official journal of the International Society for Autism Research.

The Sri Lankan Personal Genome Project

V. Scaria, S. Sivasubbu, A. Patowary, 2011 .

Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene

R. Bernier, A. Patowary, Ji Eun Lee, 2019, Translational Psychiatry.

Systematic Pharmacogenomics Analysis of a Malay Whole Genome: Proof of Concept for Personalized Medicine

Roziah Mohd Janor, Khalid Yusoff, Ashok Patowary, 2013, PloS one.

Draft Genome Sequence of a Clinical Isolate of Multidrug-Resistant Mycobacterium tuberculosis East African Indian Strain OSDD271

V. Scaria, S. Sivasubbu, A. Patowary, 2013, Genome Announcements.

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes

J. Munson, H. Coon, E. Wijsman, 2015, Human Genetics.

FishMap: a community resource for zebrafish genomics.

V. Scaria, S. Sivasubbu, Vaibhav Jadhav, 2008, Zebrafish.

Multivariate variance components analysis uncovers genetic architecture of brain isoform expression and novel psychiatric disease mechanisms

M. Gandal, A. Patowary, A. Bhattacharya, 2022, medRxiv.

in vivo protein trapping produces a functional expression codex of the vertebrate proteome

Stephen C. Ekker, Ashok Patowary, Vinod Scaria, 2011, Nature Methods.

Synthesis, characterization, reactivity and antibacterial activity of new peroxovanadium(V) complexes anchored to soluble polymers

A. Patowary, S. Sarmah, Siva Prasad Das, 2008 .

Comparative Whole-Genome Analysis of Clinical Isolates Reveals Characteristic Architecture of Mycobacterium tuberculosis Pangenome

Shamsudheen Karuthedath Vellarikkal, Ashok Patowary, Vinod Scaria, 2015, PloS one.

Human 45,X Fibroblast Transcriptome Reveals Distinct Differentially Expressed Genes Including Long Noncoding RNAs Potentially Associated with the Pathophysiology of Turner Syndrome

V. Scaria, S. Sivasubbu, A. Patowary, 2014, PloS one.

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes

J. Munson, H. Coon, E. Wijsman, 2015, Human Genetics.

Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism

E. Wijsman, W. Catterall, R. Bernier, 2016, Molecular Psychiatry.

miR-34 is maternally inherited in Drosophila melanogaster and Danio rerio

S. Sivasubbu, A. Patowary, B. Pillai, 2013, Nucleic acids research.

High Resolution Methylome Map of Rat Indicates Role of Intragenic DNA Methylation in Identification of Coding Region

M. Raghunath, M. Pellegrini, V. S. Tanwar, 2012, PloS one.

Systematic analysis and functional annotation of variations in the genome of an Indian individual

Deeksha Bhartiya, Ashok Patowary, Vinod Scaria, 2012, Human mutation.

Proximity of H2A.Z containing nucleosome to the transcription start site influences gene expression levels in the mammalian liver and brain

Ashok Patowary, Vinod Scaria, Beena Pillai, 2012, Nucleic acids research.

Silencing c-MYC expression by targeting quadruplex in P1 promoter using locked nucleic acid trap.

S. Sivasubbu, A. Patowary, S. Maiti, 2008, Biochemistry.

De novo identification of viral pathogens from cell culture hologenomes

Ashok Patowary, Vinod Scaria, Vinita Periwal, 2012, BMC Research Notes.

The Zebrafish GenomeWiki: a crowdsourcing approach to connect the long tail for zebrafish gene annotation

Meenakshi Sharma, Eric W. Klee, Ashish Mittal, 2014, Database J. Biol. Databases Curation.

Maternal vitamin B12 deficiency in rats alters DNA methylation in metabolically important genes in their offspring

M. Raghunath, V. S. Tanwar, S. Sengupta, 2020, Molecular and Cellular Biochemistry.

Reverse Genetics Screen in Zebrafish Identifies a Role of miR-142a-3p in Vascular Development and Integrity

V. Scaria, S. Sivasubbu, A. Patowary, 2012, PloS one.

Cell-type-specificity of isoform diversity in the developing human neocortex informs mechanisms of neurodevelopmental disorders

J. Li, B. Pasaniuc, Kangcheng Hou, 2023, bioRxiv.

A sequence-based variation map of zebrafish.

J. Kocher, D. Stemple, V. Scaria, 2013, Zebrafish.

Exome sequencing reveals a novel mutation, p.L325H, in the KRT5 gene associated with autosomal dominant Epidermolysis Bullosa Simplex Koebner type in a large family from western India

V. Scaria, S. Sivasubbu, A. Patowary, 2014, Human Genome Variation.

The Sri Lankan Personal Genome Project: an overview

V. Scaria, V. Dissanayake, A. Patowary, 2011 .

Micro RNA and non-coding DNA and repeats

V. Scaria, M. Hariharan, S. Sivasubbu, 2009, Genomic Medicine.

FishMap Zv8 update--a genomic regulatory map of zebrafish.

V. Scaria, Anshu Bhardwaj, Deeksha Bhartiya, 2010, Zebrafish.

Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanisms

J. Li, B. Pasaniuc, Kangcheng Hou, 2023, bioRxiv.

Systematic analysis and functional annotation of variations in the genome of an Indian individual

V. Scaria, D. Bharadwaj, Deeksha Bhartiya, 2012, Human mutation.

Forward genetic screen using a gene-breaking trap approach identifies a novel role of grin2bb-associated RNA transcript (grin2bbART) in zebrafish heart function

V. Scaria, S. Sivasubbu, A. Patowary, 2024, Frontiers in cell and developmental biology.