Newman, William G.

Top Publications

Top Publications Authored or Co-Authored by "Newman, William G."

• Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease

  Nature Genetics, Volume 49, No. 2, Year 2017, Citations 874
• Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

  Nature Genetics, Volume 49, No. 2, Year 2017, Citations 147
• Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6

  American Journal of Human Genetics, Volume 97, No. 4, Year 2015, Citations 101
• Identification of a mutation in the ubiquitin-fold modifier 1-specific peptidase 2 gene, UFSP2, in an extended South African family with Beukes hip dysplasia

  South African Medical Journal, Volume 105, No. 7, Year 2015, Citations 50
• Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome

  Clinical Genetics, Volume 91, No. 2, Year 2017, Citations 38