Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature

Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome

Timothy D. Howard, William A. Paznekas, Eric D. Green et al. · Nature Genetics · 1997 · 654 citations

Mendelian Disorder, Genetic Disorder, Genetics +4

Mutations of the TWIST gene in the Saethre-Chotzene syndrome

Vincent El Ghouzzi, M Le Merrer, Fabienne Perrin‐Schmitt et al. · Nature Genetics · 1997 · 642 citations

Mendelian Disorder, Genetic Disorder, Genetics +4

A Comprehensive Screen for TWIST Mutations in Patients with Craniosynostosis Identifies a New Microdeletion Syndrome of Chromosome Band 7p21.1

David Johnson, Sharon W. Horsley, Dominique M. Moloney et al. · The American Journal of Human Genetics · 1998 · 230 citations · Full text

Chromatin, Developmental Biology, Twist Mutations +10

Identification of a genetic cluster influencing memory performance and hippocampal activity in humans

Dominique J.‐F. de Quervain, Andreas Papassotiropoulos · Proceedings of the National Academy of Sciences · 2006 · 167 citations · Full text

Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays

Juliane Hoyer, Alexander Dreweke, C. Becker et al. · Journal of Medical Genetics · 2007 · 118 citations · Full text