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List of works by Gregory M. Cooper

A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease

scientific article published on 08 June 2009

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

scientific article published on 17 February 2008

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

scientific article

Accelerated exon evolution within primate segmental duplications.

scientific article published on 29 January 2013

BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder

scientific article published on 30 January 2020

Closing gaps in the human genome with fosmid resources generated from multiple individuals

scientific article

Genome sequence of the Brown Norway rat yields insights into mammalian evolution

scientific article

Mapping and sequencing of structural variation from eight human genomes

scientific article

Mutational and selective effects on copy-number variants in the human genome

scientific article published on July 2007

Population analysis of large copy number variants and hotspots of human genetic disease

scientific article published on 22 January 2009

Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy

scientific article

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

scientific article published on 07 September 2008

Targeted interrogation of copy number variation using SCIMMkit

scientific article published on 21 October 2009

Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies.

scientific article published on 9 April 2018

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