Search filters

List of works by Bradley P. Coe

A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

scientific article

A high-quality human reference panel reveals the complexity and distribution of genomic structural variants

scientific article published on 06 October 2016

Characteristics of de novo structural changes in the human genome

scientific article

Copy-number variation and false positive prenatal aneuploidy screening results

scientific article

Disruptive CHD8 mutations define a subtype of autism early in development

scientific article

Genomic Patterns of De Novo Mutation in Simplex Autism.

scientific article published on 27 September 2017

Global diversity, population stratification, and selection of human copy-number variation

scientific article

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

scientific article

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity

scientific article published on 17 December 2018

Refining analyses of copy number variation identifies specific genes associated with developmental delay

scientific article

Relative burden of large CNVs on a range of neurodevelopmental phenotypes

scientific article

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

scientific article (publication date: 4 April 2012)

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

scientific article published on 13 February 2017

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.

scientific article published on 26 August 2015

Paulina is supported by:

About Paulina

Help