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Hospital Pediatrics|January 28, 2017
Putting the Pieces Together: Clinically Relevant Genetic and Genomic Resources for Hospitalists and NeonatologistsRebecca Miller, Alina Khromykh, Holly Babcock, et al.Molecular Genetics & Genomic Medicine|September 22, 2016
ADGRL3 (LPHN3) variants are associated with a refined phenotype of ADHD in the MTA studyMaria T Acosta, James Swanson, Annamarie Stehli, et al.American Journal of Medical Genetics. Part A|December 28, 2002
Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmiaLisa A Schimmenti, June de la Cruz, Richard Alan Lewis, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 25, 2010
Screening of human LPHN3 for variants with a potential impact on ADHD susceptibilitySabina Domené, Horia Stanescu, Deeann Wallis, et al.Proceedings of the National Academy of Sciences of the United States of America|May 23, 2013
Clinical genomic databaseBenjamin D Solomon, Anh-Dao Nguyen, Kelly A Bear, et al.Birth Defects Research. Part A, Clinical and Molecular Teratology|February 11, 2011
VACTERL association and mitochondrial dysfunctionBenjamin D Solomon, Ankita Patel, Sau Wai Cheung, et al.Journal of Medical Genetics|April 19, 2014
Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephalyKelly A Bear, Benjamin D Solomon, Sonir Antonini, et al.European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|December 19, 2012
Influence of a latrophilin 3 (LPHN3) risk haplotype on event-related potential measures of cognitive response control in attention-deficit hyperactivity disorder (ADHD)Andreas J Fallgatter, Ann-Christine Ehlis, Thomas Dresler, et al.Journal of Pediatric Psychology|March 10, 2006
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effectsHeather F Russell, Deeann Wallis, Michèle M M Mazzocco, et al.Human Mutation|July 6, 2017
BOC is a modifier gene in holoprosencephalyMingi Hong, Kshitij Srivastava, Sungjin Kim, et al.Pageof 29