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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2011
Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problemsTrilochan Sahoo, Aaron Theisen, Jill A Rosenfeld, et al.
The Journal of Pediatrics|August 5, 2006
Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesityJennifer Miller, John Kranzler, Yijun Liu, et al.
Human Mutation|August 30, 2008
Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridizationDaniela del Gaudio, Yaping Yang, Barbara A Boggs, et al.
Journal of Autism and Developmental Disorders|November 21, 2007
Brief report: autistic symptoms, developmental regression, mental retardation, epilepsy, and dyskinesias in CNS folate deficiencyPaolo Moretti, Sarika U Peters, Daniela Del Gaudio, et al.
Optics Express|February 15, 2012
Localized surface plasmon enhanced quantum efficiency of InGaN/GaN quantum wells by Ag/SiO2 nanoparticlesLee-Woon Jang, Dae-Woo Jeon, Trilochan Sahoo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 24, 2016
Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challengesTrilochan Sahoo, Natasa Dzidic, Michelle N Strecker, et al.
Biomedicines|December 23, 2023
Analytic Validation of Optical Genome Mapping in Hematological MalignanciesAndy W C Pang, Karena Kosco, Nikhil S Sahajpal, et al.
European Journal of Human Genetics : EJHG|July 1, 2010
Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndromeAngela L Duker, Blake C Ballif, Erawati V Bawle, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocationPaweł Stankiewicz, Alma Kuechler, C Daniel Eller, et al.
European Journal of Human Genetics : EJHG|April 10, 2014
Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangementsTrilochan Sahoo, Jia-Chi Wang, Mohamed M Elnaggar, et al.
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