Regan Veith
Children's Minnesota(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Ethics in Clinical Research, BRCA gene mutations in cancer, Immunodeficiency and Autoimmune Disorders, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease(2010)708 cited
- → Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency(2010)150 cited
- → Genomics in Clinical Practice: Lessons from the Front Lines(2013)121 cited
- → Successful Application of Whole Genome Sequencing in a Medical Genetics Clinic(2016)83 cited
- → Perspectives of clinical genetics professionals toward genome sequencing and incidental findings: a survey study(2012)80 cited
- → Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome(2015)50 cited
- → Views of primary care providers regarding the return of genome sequencing incidental findings(2014)30 cited
- Views of nonmedical, health system professionals regarding the return of whole genome sequencing incidental findings.(2014)
- → Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting(2024)8 cited
- → In the Absence of Evidentiary Harm, Existing Societal Norms Regarding Parental Authority Should Prevail(2014)6 cited