Susan Zeesman

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants

Lucilla Pizzo, Matthew Jensen, Andrew Polyak et al. · Genetics in Medicine · 2018 · 218 citations · Full text

Human Chromosome 7: DNA Sequence and Biology

Stephen W. Scherer, Joseph Cheung, Jeffrey R. MacDonald et al. · Science · 2003 · 214 citations · Full text

Dna, Cytogenetics, Genetics +24

Ovarian Failure Related to Eukaryotic Initiation Factor 2B Mutations

Anne Fogli, Diana Rodriguez, Éléonore Eymard-Pierre et al. · The American Journal of Human Genetics · 2003 · 193 citations · Full text

Genome Instability, Oogenesis, Genetic Disorder +6

Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia

Lars Feuk, Aino Kalervo, Marita Lipsanen‐Nyman et al. · The American Journal of Human Genetics · 2006 · 185 citations · Full text

Developmental Anomaly, Developmental Biology, Mendelian Disorder +8

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves <i>FOXP2</i>

Susan Zeesman, Małgorzata J.M. Nowaczyk, Ikuko Teshima et al. · American Journal of Medical Genetics Part A · 2006 · 121 citations

Genetics, Foxp2 Gene, Speech Disorders +28