|
| 37098602 | A picture is worth a thousand words: advancing the use of visualization tools in implementation science through process mapping and matrix heat mapping. | Implement Sci Commun | 2023 |
| 37978552 | "Go ahead and screen" - advice to healthcare systems for routine lynch syndrome screening from interviews with newly diagnosed colorectal cancer patients. | Hered Cancer Clin Pract | 2023 |
| 37421176 | Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population. | Genet Med | 2023 |
| 35144679 | Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system. | Hered Cancer Clin Pract | 2022 |
| 35436948 | Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system. | Hered Cancer Clin Pract | 2022 |
| 35341655 | ClinGen's Pediatric Actionability Working Group: Clinical actionability of secondary findings from genome-scale sequencing in children and adolescents. | Genet Med | 2022 |
| 35363504 | Establishing the Medical Actionability of Genomic Variants. | Annu Rev Genomics Hum Genet | 2022 |
| 36883408 | An Examination of the Ethical and Legal Limits in Implementing "Traceback Testing" for Deceased Patients. | J Law Med Ethics | 2022 |
| 36340570 | Should Health Systems Share Genetic Findings With At-Risk Relatives When the Proband Is Deceased? Interviews With Individuals Diagnosed With Lynch Syndrome. | J Patient Cent Res Rev | 2022 |
| 36053287 | An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial. | Genet Med | 2022 |
| 33754278 | Adaptation and early implementation of the PREdiction model for gene mutations (PREMM<sub>5</sub>â¿¢) for lynch syndrome risk assessment in a diverse population. | Fam Cancer | 2022 |
| 35123916 | Corrigendum to "Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations" [Contemporary Clinical Trials 106 (2021) 106432]. | Contemp Clin Trials | 2022 |
| 34906471 | Motivations and concerns of patients considering participation in an implementation study of a hereditary cancer risk assessment program in diverse primary care settings. | Genet Med | 2022 |
| 33984519 | Cancer Health Assessments Reaching Many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations. | Contemp Clin Trials | 2021 |
| 34976894 | Congenital Cytomegalovirus and Human Immunodeficiency Virus: Effects on Hearing, Speech and Language Development, and Clinical Outcomes in Children. | Front Pediatr | 2021 |
| 34778694 | Systemic Barriers to Risk-Reducing Interventions for Hereditary Cancer Syndromes: Implications for Health Care Inequities. | JCO Precis Oncol | 2021 |
| 34658954 | Predictors of Comorbid Conditions in Women Who Carry an <i>FMR1</i> Premutation. | Front Psychiatry | 2021 |
| 34834546 | Feasibility of a Traceback Approach for Using Pathology Specimens to Facilitate Genetic Testing in the Genetic Risk Analysis in Ovarian Cancer (GRACE) Study Protocol. | J Pers Med | 2021 |
| 31519426 | The association between maternal occupation and down syndrome: A report from the national Down syndrome project. | Int J Hyg Environ Health | 2020 |
| 33948230 | Lessons learned about harmonizing survey measures for the CSER consortium. | J Clin Transl Sci | 2020 |
| 31896764 | Clustering of comorbid conditions among women who carry an FMR1 premutation. | Genet Med | 2020 |
| 30959430 | Feasibility of an app-based mindfulness intervention among women with an FMR1 premutation experiencing maternal stress. | Res Dev Disabil | 2019 |
| 31890059 | Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study. | Hered Cancer Clin Pract | 2019 |
| 31487201 | Clinical Molecular Marker Testing Data Capture to Promote Precision Medicine Research Within the Cancer Research Network. | JCO Clin Cancer Inform | 2019 |
| 30984796 | The Healthcare Systems Research Network (HCSRN) as an Environment for Dissemination and Implementation Research: A Case Study of Developing a Multi-Site Research Study in Precision Medicine. | EGEMS (Wash DC) | 2019 |
| 30729418 | Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting. | Fam Cancer | 2019 |
| 31028355 | Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders. | Genet Med | 2019 |
| 29760830 | Patient and provider perspectives on adherence to and care coordination of lynch syndrome surveillance recommendations: findings from qualitative interviews. | Hered Cancer Clin Pract | 2018 |
| 30376847 | Implementing universal Lynch syndrome screening (IMPULSS): protocol for a multi-site study to identify strategies to implement, adapt, and sustain genomic medicine programs in different organizational contexts. | BMC Health Serv Res | 2018 |
| 30311382 | Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group. | Hum Mutat | 2018 |
| 28176204 | Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives. | Fam Cancer | 2017 |
| 25683160 | Influence of CHDs on psycho-social and neurodevelopmental outcomes in children with Down syndrome. | Cardiol Young | 2016 |
| 27124788 | A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation. | Genet Med | 2016 |
| 26948972 | Genetic effects on sleep/wake variation of seizures. | Epilepsia | 2016 |
| 26036338 | Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers. | Cancer | 2015 |
| 24700618 | Epidemiology of fragile X syndrome: a systematic review and meta-analysis. | Am J Med Genet A | 2014 |
| 23558253 | The association of low socioeconomic status and the risk of having a child with Down syndrome: a report from the National Down Syndrome Project. | Genet Med | 2013 |
| 22101959 | The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritance. | Behav Genet | 2012 |
| 22998353 | Genetic load is associated with hypothalamic-pituitary-adrenal axis dysregulation in macaques. | Genes Brain Behav | 2012 |
| 22573456 | Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms. | Am J Med Genet B Neuropsychiatr Genet | 2012 |
| 22251309 | Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts. | Neuropsychology | 2012 |
| 21455293 | Evaluating gene expression in C57BL/6J and DBA/2J mouse striatum using RNA-Seq and microarrays. | PLoS One | 2011 |
| 21443343 | Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome. | Neuropsychology | 2011 |
| 20059484 | Co-occurring diagnoses among FMR1 premutation allele carriers. | Clin Genet | 2010 |
| 19265746 | Is there evidence for neuropsychological and neurobehavioral phenotypes among adults without FXTAS who carry the FMR1 premutation? A review of current literature. | Genet Med | 2009 |
| 20436936 | A Variance-Component Framework for Pedigree Analysis of Continuous and Categorical Outcomes. | Stat Biosci | 2009 |
| 19409490 | A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation. | Neurobiol Dis | 2009 |
| 18357616 | Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. | Genet Epidemiol | 2008 |
| 19026394 | No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50. | Am J Hum Genet | 2008 |
| 18535897 | Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers. | Behav Genet | 2008 |