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European Journal of Human Genetics : EJHG|April 10, 2008
Fragile X syndromeKathryn B Garber, Jeannie Visootsak, Stephen T WarrenDevelopmental Disabilities Research Reviews|July 19, 2008
Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangementsBeverly S EmanuelNature Reviews. Genetics|October 19, 2007
From microscopes to microarrays: dissecting recurrent chromosomal rearrangementsBeverly S Emanuel, Sulagna C SaittaCurrent Opinion in Genetics & Development|March 10, 2012
Chromosomal translocations and palindromic AT-rich repeatsTakema Kato, Hiroki Kurahashi, Beverly S EmanuelJournal of Molecular Biology|December 5, 2006
Mammalian TIMELESS and Tipin are evolutionarily conserved replication fork-associated factorsAnthony L Gotter, Christine Suppa, Beverly S EmanuelTrends in Genetics : TIG|April 28, 2016
Participatory Genomic Testing as an Educational ExperienceKathryn B Garber, Katherine M Hyland, Shoumita DasguptaJournal of Genetic Counseling|September 22, 2023
Poor recall of genetics curriculum by medical students highlights barriers to use in clinical practiceSunaina Kapur, Lauren Lichten, Nadia Ali, et al.American Journal of Human Genetics|January 31, 2003
The constitutional t(17;22): another translocation mediated by palindromic AT-rich repeatsHiroki Kurahashi, Tamim Shaikh, Masayuki Takata, et al.Trends in Biochemical Sciences|March 14, 2003
New insights into fragile X syndrome: from molecules to neurobehaviorsPeng Jin, Stephen T WarrenHuman Molecular Genetics|September 4, 2003
A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22)Manjunath A Nimmakayalu, Anthony L Gotter, Tamim H Shaikh, et al.Pageof 24