Vickie Hannig
Vanderbilt University Medical Center(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Ubiquitin and proteasome pathways, Congenital heart defects research
Most-Cited Works
- → A copy number variation morbidity map of developmental delay(2011)1,390 cited
- → Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region(2007)191 cited
- → Developmental change in human intestinal alkaline phosphatase.(1978)103 cited
- → Limitations of exome sequencing in detecting rare and undiagnosed diseases(2020)102 cited
- Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening.(1996)
- → The Cognitive and Behavioral Phenotypes of Individuals with CHRNA7 Duplications(2016)82 cited
- → Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features(2017)62 cited
- Teaching about cystic fibrosis carrier screening by using written and video information.(1995)
- → A Recurrent RNA-Splicing Mutation in the SEDL Gene Causes X-Linked Spondyloepiphyseal Dysplasia Tarda(2001)49 cited
- → The broad phenotypic spectrum of PPP2R1A-related neurodevelopmental disorders correlates with the degree of biochemical dysfunction(2020)48 cited