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International Journal of Cancer|August 23, 2018
Fine mapping of 2q35 high-risk neuroblastoma locus reveals independent functional risk variants and suggests full-length BARD1 as tumor-suppressorFlora Cimmino, Marianna Avitabile, Sharon J Diskin, et al.
Gastroenterology|June 8, 2020
Impaired Redox and Protein Homeostasis as Risk Factors and Therapeutic Targets in Toxin-Induced Biliary AtresiaXiao Zhao, Kristin Lorent, Diana Escobar-Zarate, et al.
European Journal of Human Genetics : EJHG|May 10, 2007
A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23-q24Alessia Deglincerti, Roberto De Giorgio, Kivanc Cefle, et al.
Addiction Biology|June 15, 2007
Prodynorphin gene promoter repeat associated with cocaine/alcohol codependenceTanya J Williams, K Steven LaForge, Derek Gordon, et al.
Statistical Applications in Genetics and Molecular Biology|May 2, 2006
Increasing power for tests of genetic association in the presence of phenotype and/or genotype error by use of double-samplingDerek Gordon, Yaning Yang, Chad Haynes, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 16, 2011
Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosisPaula C Goldenberg, Monica E Calkins, Jan Richard, et al.
Genes|September 5, 2019
Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart DiseaseAlessandro Testori, Vito A Lasorsa, Flora Cimmino, et al.
International Journal of Pediatric Otorhinolaryngology|November 6, 2012
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patientsJosine C C Widdershoven, Mark Bowser, Molly B Sheridan, et al.
Plos Genetics|May 26, 2017
Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastomaLee D McDaniel, Karina L Conkrite, Xiao Chang, et al.
Pharmacogenetics and Genomics|December 14, 2005
Association analysis of polymorphisms in serotonin 1B receptor (HTR1B) gene with heroin addiction: a comparison of molecular and statistically estimated haplotypesDmitri Proudnikov, K Steven LaForge, Heather Hofflich, et al.
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