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Human Genetics|November 23, 2021
Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findingsWafaa Abbasi, Courtney E French, Shira Rockowitz, et al.
Scientific Reports|January 29, 2021
Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological diseaseDale J Annear, Geert Vandeweyer, Ellen Elinck, et al.
Plos One|October 7, 2009
Two alleles of NF-kappaB in the sea anemone Nematostella vectensis are widely dispersed in nature and encode proteins with distinct activitiesJames C Sullivan, Francis S Wolenski, Adam M Reitzel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 12, 2025
Common and rare genetic variants explain distinct diagnostic variance in pediatric attention deficit hyperactivity disorderAnne B Arnett, Ryan Koesterer, Paulina Gonzalez Tovar, et al.
Frontiers in Genetics|July 19, 2019
Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual DisabilityAlba Sanchis-Juan, Christina Bitsara, Kay Yi Low, et al.
Intensive Care Medicine|March 9, 2019
Whole genome sequencing reveals that genetic conditions are frequent in intensively ill childrenCourtney E French, Isabelle Delon, Helen Dolling, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 19, 2020
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing dataXiao Chen, Alba Sanchis-Juan, Courtney E French, et al.
HGG Advances|May 19, 2022
Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhoodCourtney E French, Helen Dolling, Karyn Mégy, et al.
JAMA Neurology|March 7, 2022
Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A ReviewSarah U Morton, John Christodoulou, Gregory Costain, et al.
Neurology|December 19, 2024
Exome and Genome Sequencing to Diagnose the Genetic Basis of Neonatal Hypotonia: An International Consortium StudySarah U Morton, Gregory Costain, Courtney E French, et al.
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