Attending physician, Nationwide Children's Hospital

Medical Genetics

Doctor Kim L. McBride, MD practices Medical Genetics. He researched medicine at Baylor College of Medicine. He has 3 awards "Regional Top Doctor", "Best doctor" and "Fellow (FAAP)". McBride is a published doctor and has 50 publications published. The lastest was: 'Validation of the Ottawa ankle rules. Experience at a community hospital.'

Publications

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• Lifetime prevalence of sexual intercourse and contraception use at last sex among adolescents and young adults with congenital heart disease.
• Sanfilippo syndrome registry project and natural history studies: an example of patients, parents and researchers collaborating for a cure.
• Genetic knowledge and attitudes of parents of children with congenital heart defects.
• GATA5 Sequence Variants Identified in Individuals with Bicuspid Aortic Valve.
• Feasibility and Safety of Systemic rAAV9-hNAGLU Delivery for Treating Mucopolysaccharidosis IIIB: Toxicology, Biodistribution, and Immunological Assessments in Primates.
• Feasibility and Safety of Systemic rAAV9-hNAGLU Delivery for Treating MPS IIIB: Toxicology, Bio-distribution and Immunological Assessments in Primates.
• Genetic Abnormalities in FOXP1 Are Associated with Congenital Heart Defects.
• Understanding of informed consent by parents of children enrolled in a genetic biobank.
• Neurodevelopmental disorders among individuals with duplication of 4p13 to 4p12 containing a GABAA receptor subunit gene cluster.
• Severe hypertrophic cardiomyopathy in Noonan syndrome-consider sequencing genes encoding sarcomeric proteins.
• Modifying mendel: approaches for identification of susceptibility alleles for human cardiovascular malformations.
• Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.
• Rebuttal to the invited comment of Opitz and Carey.
• Pediatric Sub-specialist Controversies in the Treatment of Congenital Heart Disease in Trisomy 13 or 18.
• Heredity of bicuspid aortic valve: is family screening indicated?
• Association of common variants in ERBB4 with congenital left ventricular outflow tract obstruction defects.
• Contactin 4 as an autism susceptibility locus.
• Novel X-linked glomerulopathy is associated with a COL4A5 missense mutation in a non-collagenous interruption.
• Impact of Mendelian inheritance in cardiovascular disease.
• Confirmation study of PTEN mutations among individuals with autism or developmental delays/mental retardation and macrocephaly.
• Identification of a recurrent microdeletion at 17q23.1q23.2 flanked by segmental duplications associated with heart defects and limb abnormalities.
• Parental knowledge and attitudes toward hypertrophic cardiomyopathy genetic testing.
• Acute dilated cardiomyopathy in a patient with deficiency of long-chain 3-hydroxyacyl-CoA dehydrogenase.
• The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.
• Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for an...
• Genetic testing in autism: how much is enough?
• Heritability of plasma amino acid levels in different nutritional states.
• Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) ...
• Cardiovascular genetics clinics.
• Inheritance analysis of congenital left ventricular outflow tract obstruction malformations: Segregation, multiplex relative risk, and heritability.
• A family-based association study of congenital left-sided heart malformations and 5,10 methylenetetrahydrofolate reductase.
• Developmental outcomes with early orthotopic liver transplantation for infants with neonatal-onset urea cycle defects and a female patient with late-onset ornithine tr...
• Echocardiographic evaluation of asymptomatic parental and sibling cardiovascular anomalies associated with congenital left ventricular outflow tract lesions.
• Case 27-2002: late-onset infantile neuronal ceroid lipofuscinosis.
• Toward a genetic etiology of CHARGE syndrome: I. A systematic scan for submicroscopic deletions.
• Aortoesophageal fistula in a 13-yr-old girl: complication after nasogastric tube placement in the setting of right-sided aortic arch.
• Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve.
• Successful Medical Therapy for Hypophosphatemic Rickets due to Mitochondrial Complex I Deficiency Induced de Toni-Debré-Fanconi Syndrome.
• Validation of the Ottawa ankle rules. Experience at a community hospital.
• 14-year-old boy with blurred vision and diplopia.
• Severe 6-thioguanine-induced marrow aplasia in a child with acute lymphoblastic leukemia and inherited thiopurine methyltransferase deficiency.
• Hb Dartmouth [alpha66(E15)Leu-->Pro (alpha2) (CTG-->CCG)]: a novel alpha2-globin gene mutation associated with severe neonatal anemia when inherited in trans with Sout...
• Renal anomalies in family members of infants with bilateral renal agenesis/adysplasia.
• Genome-wide linkage scan for spontaneous DZ twinning.
• NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.
• Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).
• Significant contributions of the extraembryonic membranes and maternal genotype to the placental pathology in heterozygous Nsdhl deficient female embryos.
• NOTCH1 missense alleles associated with left ventricular outflow tract defects exhibit impaired receptor processing and defective EMT.
• A Genome Wide Association Study of Congenital Cardiovascular Left-Sided Lesions Shows Association with a Locus on Chromosome 20.

Schools

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• University Of Saskatchewan College Of Medicine

• Regina Gen Hospital

• Mayo Clinic

• Baylor College Med

Doctors Specialties

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

Accepted Insurances

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Awards

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• Regional Top Doctor
• Best doctor
• Fellow (FAAP)

Education

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• Baylor College of Medicine
• Mayo School of Graduate Medical Education
• University of Saskatchewan College of Medicine

Hospital

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• Nationwide Children's Hospital
• Ohio State University Wexner Medical Center

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