Deanna Alexis Carere

发表

Design, methods, and participant characteristics of the Impact of Personal Genomics (PGen) Study, a prospective cohort study of direct-to-consumer personal genomic testing customers

Mick P Couper, Robert C Green, R. Green, 2014, Genome Medicine.

Prescription medication changes following direct-to-consumer personal genomic testing: Findings from the Impact of Personal Genomics (PGen) Study

Peter Kraft, Tyler J VanderWeele, Robert C Green, 2016, Genetics in Medicine.

Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results

Robert C. Green, Mack T. Ruffin, R. Green, 2017, Public Health Genomics.

Adopting Genetics: Motivations and Outcomes of Personal Genomic Testing in Adult Adoptees

R. Green, S. Broadley, J. Roberts, 2015, Genetics in Medicine.

Predictive Genetic Testing Using Common Variants: Evidence and Translation

Deanna Alexis Carere, D. A. Carere, 2015 .

Diet and exercise changes following direct-to-consumer personal genomic testing

M. Couper, A. Kiefer, P. Kraft, 2017, BMC Medical Genomics.

Consumers report lower confidence in their genetics knowledge following direct-to-consumer personal genomic testing

R. Green, P. Kraft, J. Roberts, 2015, Genetics in Medicine.

Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.

B. Burton, Katherine H Kim, W. Dobyns, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

P. Grant, N. Brunetti‐Pierri, D. Calame, 2022, American journal of human genetics.

Expanding the phenotype of ASXL3‐related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3

J. Graham, F. Alkuraya, N. Hauser, 2021, American journal of medical genetics. Part A.

Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach

P. Ainsworth, B. Sadikovic, M. Volodarsky, 2021, Frontiers in Genetics.

Genome‐wide DNA methylation and RNA analyses enable reclassification of two variants of uncertain significance in a patient with clinical Kabuki syndrome

P. Ainsworth, B. Sadikovic, E. Aref-Eshghi, 2019, Human mutation.

Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions.

I. Krantz, A. Beaudet, C. Schwartz, 2019, American journal of human genetics.

BAFopathies’ DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes

S. Cheung, R. Hennekam, C. Schwartz, 2018, Nature Communications.