List of works by Aparna Prasad

A 2cM genome-wide scan of European Holstein cattle affected by classical BSE.

scientific article

A Whole-Genome Scan to Map Quantitative Trait Loci for Conformation and Functional Traits in Canadian Holstein Bulls

article

A discovery resource of rare copy number variations in individuals with autism spectrum disorder

scientific article

A first generation whole genome RH map of the river buffalo with comparison to domestic cattle

scientific article

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

A second generation radiation hybrid map to aid the assembly of the bovine genome sequence

scientific article published on 6 November 2006

A whole genome scan to map QTL for milk production traits and somatic cell score in Canadian Holstein bulls

article

Clinical utility of exome sequencing in individuals with large homozygous regions detected by chromosomal microarray analysis.

scientific article published on 20 March 2018

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants

scientific article (publication date: 8 May 2011)

Fate of SRY, PABY, DYS1, DYZ3 and DYZ1 loci in Indian patients harbouring sex chromosomal anomalies

scientific article published on 03 December 2004

Functional impact of global rare copy number variation in autism spectrum disorders

scientific article published on 15 July 2010

Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder

scientific article published on 29 November 2010

High resolution radiation hybrid maps of bovine chromosomes 19 and 29: comparison with the bovine genome sequence assembly

scientific article

Identification of Gene Mutations and Fusion Genes in Patients with Sézary Syndrome

scientific article published on 30 March 2016

Linkage disequilibrium and signatures of selection on chromosomes 19 and 29 in beef and dairy cattle

scientific article published on 18 August 2008

Organizational variation of DYZ1 repeat sequences on the human Y chromosome and its diagnostic potentials.

scientific article

Rare deletions at the neurexin 3 locus in autism spectrum disorder

scientific article

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures

scientific article published on 7 February 2013

SHANK1 Deletions in Males with Autism Spectrum Disorder

scientific article

The Temple Grandin Genome: Comprehensive Analysis in a Scientist with High-Functioning Autism

scientific article published on 29 December 2020

Variant detection and the Autism sequencing project

scientific article published on 21 November 2011

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