Physician

Medical Genetics

Neil A. Hanchard, MB

Neil Hanchard practices Medical Genetics. He went to medical school at Baylor College of Medicine. Neil Hanchard is also a published MD. He has 28 paper published. The most recent paper is: Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiency.

Publications

Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.
A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease.
TM4SF20 Ancestral Deletion and Susceptibility to a Pediatric Disorder of Early Language Delay and Cerebral White Matter Hyperintensities.
Exploring the utility of whole-exome sequencing as a diagnostic tool in a child with atypical episodic muscle weakness.
Where are we now?
Tumor necrosis factor SNP haplotypes are associated with iron deficiency anemia in West African children.
Population-specific patterns of linkage disequilibrium in the human 5q31 region.
An assessment of the association between childhood asthma and HLA DRB1*03 using extended haplotype analysis.
Haplotype mapping of the bronchiolitis susceptibility locus near IL8.
Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.
Implications of inter-population linkage disequilibrium patterns on the approach to a disease association study in the human MHC class III.
An investigation of transmission ratio distortion in the central region of the human MHC.
Predicted declines in sickle allele frequency in Jamaica using empirical data.
Genetic association study for RSV bronchiolitis in infancy at the 5q31 cytokine cluster.
Genetic variation at the TNF locus and the risk of severe sequelae of ocular Chlamydia trachomatis infection in Gambians.
Classical sickle beta-globin haplotypes exhibit a high degree of long-range haplotype similarity in African and Afro-Caribbean populations.
The frequency of the sickle allele in Jamaica has not declined over the last 22 years.
UGT1A1 sequence variants and bilirubin levels in early postnatal life: a quantitative approach.
Deoxyguanosine kinase deficiency presenting as neonatal hemochromatosis.
Rate of change of sickle allele frequency may be influenced by total fertility rate: a sesquicentenary reflection on human micro-evolution.
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.
Ethnic differences in F cell levels in Jamaica: a potential tool for identifying new genetic loci controlling fetal haemoglobin.
Childhood malnutrition is associated with a reduction in the total melanin content of scalp hair.
Screening for recently selected alleles by analysis of human haplotype similarity.
Genetic susceptibility and single-nucleotide polymorphisms.
Evidence for extensive transmission distortion in the human genome.
Functional cellular analyses reveal energy metabolism defect and mitochondrial DNA depletion in a case of mitochondrial aconitase deficiency.

Doctors Specialties

Clinical Genetics
Pediatrics
Medical Genetics

Accepted Insurances

Education

Baylor College of Medicine
Mayo School of Graduate Medical Education
University of the West Indies Faculty of Medical Sciences

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