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Publications by Neil A. Hanchard
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay
American Journal of Human Genetics
Genetics
IRF2BPL Is Associated With Neurological Phenotypes
American Journal of Human Genetics
Genetics
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
American Journal of Human Genetics
Genetics
A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci Among Red Blood Cell Transfusion Recipients With Sickle Cell Disease
Transfusion Medicine and Hemotherapy
Allergy
Immunology
Hematology
Screening for Recently Selected Alleles by Analysis of Human Haplotype Similarity
American Journal of Human Genetics
Genetics
Genetic Variation on Chromosome 6 Influences F Cell Levels in Healthy Individuals of African Descent and HbF Levels in Sickle Cell Patients
PLoS ONE
Multidisciplinary
