Associate Professor, Molecular and Human Genetics, Baylor College of Medicine

Medical Genetics

Vernon Sutton practices Medical Genetics. He went to medical school at University of Kentucky College of Medicine. University of Kentucky College of Medicine has a rank of 63 in research and a 72 in primary care Vernon Sutton, MD is also a published doctor. He has 59 publication published. The most recent publication is: Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.

Publications

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• Elevations of C14:1 and C14:2 Plasma Acylcarnitines in Fasted Children: A Diagnostic Dilemma.
• DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome.
• Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism.
• Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.
• DVL1 Frameshift Mutations Clustering in the Penultimate Exon Cause Autosomal-Dominant Robinow Syndrome.
• 0041 Cross-sectional Multicenter Study of Osteogenesis Imperfecta in North America - Results from the Linked Clinical Research Centers.
• TBX6 null variants and a common hypomorphic allele in congenital scoliosis.
• Nonclassical congenital adrenal hyperplasia: targets of treatment and transition.
• A Rare Human Syndrome Provides Genetic Evidence that WNT Signaling Is Required for Reprogramming of Fibroblasts to Induced Pluripotent Stem Cells.
• Prenatal diagnosis of CLOVES syndrome confirmed by detection of a mosaic PIK3CA mutation in cultured amniocytes.
• Improved standards for prenatal diagnosis of citrullinemia.
• De Novo Truncating Mutations in AHDC1 in Individuals with Syndromic Expressive Language Delay, Hypotonia, and Sleep Apnea.
• Clinical utility of whole-exome sequencing in rare diseases: Galactosialidosis.
• Next-generation sequencing for disorders of low and high bone mineral density.
• Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate Syndrome
• An altered splice site is found in the DRB4 gene that is not expressed in HLA-DR7,Dw11 individuals.
• An aberrant DRB4 null gene transcript is found that could encode a novel HLA-DR beta chain.
• Coffin-Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive pattern.
• Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion.
• Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12).
• Chronic management and health supervision of individuals with propionic acidemia.
• CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency.
• 3-Hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency.
• Regional localization of the mouse argininosuccinate lyase gene to chromosome 5.
• Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria.
• Phenotype and management of Aicardi syndrome: new findings from a survey of 69 children.
• Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy.
• Low or absent unconjugated estriol in pregnancy: an indicator for steroid sulfatase deficiency detectable by fluorescence in situ hybridization and biochemical analysis.
• The gender medicine team: "it takes a village".
• Management of ornithine transcarbamylase deficiency in pregnancy.
• Tay-Sachs disease screening and counseling families at risk for metabolic disease.
• The right to ignore genetic status of late onset genetic disease in the genomic era; Prenatal testing for Huntington disease as a paradigm.
• Copy number gain at Xp22.31 includes complex duplication rearrangements and recurrent triplications.
• Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome.
• Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short arms.
• 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
• A dominantly inherited spondylometaphyseal dysplasia with "corner fractures" and congenital scoliosis.
• Consensus in Guidelines for Evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine Team.
• A genome-wide screen for copy number alterations in Aicardi syndrome.
• Suspected trisomy 22: Modification, clarification, or confirmation of the diagnosis by aCGH.
• Non-random X chromosome inactivation in Aicardi syndrome.
• Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin.
• Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.
• Facial and physical features of Aicardi syndrome: infants to teenagers.
• Neuroimaging aspects of Aicardi syndrome.
• Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome.
• Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.
• Craniofacial and anthropometric phenotype in ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (Hay-Wells syndrome) in a cohort of 17 patients.
• Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
• Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.
• Sleepiness and sleep disordered breathing in Prader-Willi syndrome: relationship to genotype, growth hormone therapy, and body composition.
• Mental retardation linked to mutations in the HSD17B10 gene interfering with neurosteroid and isoleucine metabolism.
• Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
• Low-level mosaicism of trisomy 14: phenotypic and molecular characterization.
• Ethical and legal implications of genetic testing in androgen insensitivity syndrome.
• Oral rapamycin in the treatment of patients with hamartoma syndromes and PTEN mutation.
• Cranio-meta-diaphyseal dysplasia: 25 year follow-up and review of literature.
• PORCN mutations and variants identified in patients with focal dermal hypoplasia through diagnostic gene sequencing.

Schools

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• University of Kentucky College of Medicine

• Baylor College Of Med

Doctors Specialties

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• Clinical Biochemical Genetics
• Clinical Genetics
• Pediatrics
• Medical Genetics

Accepted Insurances

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Education

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• Baylor College of Medicine
• University of Kentucky College of Medicine

Hospital

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• Texas Children's Hospital
• Baylor St. Luke's Medical Center

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