|
| 37698424 | The Alzheimer's Disease Neuroimaging Initiative in the era of Alzheimer's disease treatment: A review of ADNI studies from 2021 to 2022. | Alzheimers Dement | 2024 |
| 36209495 | Increasing participant diversity in AD research: Plans for digital screening, blood testing, and a community-engaged approach in the Alzheimer's Disease Neuroimaging Initiative 4. | Alzheimers Dement | 2023 |
| 37755714 | An Ethical Framework for Research Using Genetic Ancestry. | Perspect Biol Med | 2023 |
| 37593415 | Phenotypes of undiagnosed adults with actionable <i>OTC</i> and <i>GLA</i> variants. | HGG Adv | 2023 |
| 37961173 | Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. | medRxiv | 2023 |
| 37922883 | The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care. | Am J Hum Genet | 2023 |
| 37458095 | Attitudes about pharmacogenomic testing vary by healthcare specialty. | Pharmacogenomics | 2023 |
| 37155167 | Perspectives of Rare Disease Experts on Newborn Genome Sequencing. | JAMA Netw Open | 2023 |
| 37279760 | Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project. | Am J Hum Genet | 2023 |
| 37245089 | Response to Beretich and Beretich. | Genet Med | 2023 |
| 37232094 | <i>SLCO1B1</i> gene-based clinical decision support reduces statin-associated muscle symptoms risk with simvastatin. | Pharmacogenomics | 2023 |
| 37267897 | Response to Grosse et al. | Am J Hum Genet | 2023 |
| 37461624 | Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies <i>LRRC4C, LHX5-AS1</i> and nominates ancestry-specific loci <i>PTPRK</i> , <i>GRB14</i> , and <i>KIAA0825</i> as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. | medRxiv | 2023 |
| 36691939 | Are we prepared to deliver gene-targeted therapies for rare diseases? | Am J Med Genet C Semin Med Genet | 2023 |
| 36913714 | Return of Results in Genomic Research Using Large-Scale or Whole Genome Sequencing: Toward a New Normal. | Annu Rev Genomics Hum Genet | 2023 |
| 36738469 | Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies. | Am J Med Genet C Semin Med Genet | 2023 |
| 36681872 | The evolving role of medical geneticists in the era of gene therapy: An urgency to prepare. | Genet Med | 2023 |
| 36639513 | Prioritizing the detection of rare pathogenic variants in population screening. | Nat Rev Genet | 2023 |
| 36450406 | Public willingness to participate in population DNA screening in Australia. | J Med Genet | 2023 |
| 34309124 | Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. | J Genet Couns | 2022 |
| 35437332 | Development of a clinical polygenic risk score assay and reporting workflow. | Nat Med | 2022 |
| 35401566 | Improving Access to HLA-Matched Kidney Transplants for African American Patients. | Front Immunol | 2022 |
| 35571041 | Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study. | Front Genet | 2022 |
| 35446370 | Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases. | JAMA Oncol | 2022 |
| 36422106 | Workforce Considerations When Building a Precision Medicine Program. | J Pers Med | 2022 |
| 36483158 | Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos. | HGG Adv | 2022 |
| 36207733 | Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization. | Genome Med | 2022 |
| 36007526 | A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases. | Am J Hum Genet | 2022 |
| 35216901 | The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network. | Genet Med | 2022 |
| 34906468 | Reevaluating the "right not to know" in genomics research. | Genet Med | 2022 |
| 34906462 | Improved provider preparedness through an 8-part genetics and genomic education program. | Genet Med | 2022 |
| 34665896 | Do research participants share genomic screening results with family members? | J Genet Couns | 2022 |
| 34581485 | Using the Alzheimer's Disease Neuroimaging Initiative to improve early detection, diagnosis, and treatment of Alzheimer's disease. | Alzheimers Dement | 2022 |
| 32648332 | Genetic counseling following direct-to consumer genetic testing: Consumer perspectives. | J Genet Couns | 2021 |
| 33767345 | Universal newborn genetic screening for pediatric cancer predisposition syndromes: model-based insights. | Genet Med | 2021 |
| 33790423 | DNA-based screening and personal health: a points to consider statement for individuals and health-care providers from the American College of Medical Genetics and Genomics (ACMG). | Genet Med | 2021 |
| 33509269 | Polygenic risk scores in the clinic: new perspectives needed on familiar ethical issues. | Genome Med | 2021 |
| 35072136 | GA4GH: International policies and standards for data sharing across genomic research and healthcare. | Cell Genom | 2021 |
| 35047849 | Low frequency of treatable pediatric disease alleles in gnomAD: An opportunity for future genomic screening of newborns. | HGG Adv | 2021 |
| 35047839 | Polygenic risk scores in the clinic: Translating risk into action. | HGG Adv | 2021 |
| 34585209 | Editorial: How Will Aducanumab Approval Impact AD Research? | J Prev Alzheimers Dis | 2021 |
| 34404389 | Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study. | BMC Med | 2021 |
| 34429410 | Behavioral and psychological impact of genome sequencing: a pilot randomized trial of primary care and cardiology patients. | NPJ Genom Med | 2021 |
| 34752750 | Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization. | Am J Hum Genet | 2021 |
| 34424265 | Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial. | JAMA Pediatr | 2021 |
| 33963077 | Purifying selection on noncoding deletions of human regulatory loci detected using their cellular pleiotropy. | Genome Res | 2021 |
| 34211183 | Molecular cancer screening: in search of evidence. | Nat Med | 2021 |
| 34266500 | An international policy on returning genomic research results. | Genome Med | 2021 |
| 34058740 | Development and Validation of a Comprehensive Genomics Knowledge Scale. | Public Health Genomics | 2021 |
| 34113000 | Primary care providers' responses to unsolicited Lynch syndrome secondary findings of varying clinical significance. | Genet Med | 2021 |