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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 21, 2024
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Communication[original query]>>Original Studies[Product Type]
AI-Generated Draft Replies Integrated Into Health Records and Physicians' Electronic Communication.
Ming Tai-Seale et al. JAMA Netw Open 2024 7(4) e246565
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Oncologists' perceptions of tumor genomic profiling and barriers to communicating secondary hereditary risks to African American cancer patients.
Michael J Hall et al. BMC Cancer 2024 24(1) 412
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Clinician perspectives on policy approaches to genetic risk disclosure in families.
Amicia Phillips et al. Fam Cancer 2024
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Men's sociotechnical imaginaries of artificial intelligence for prostate cancer diagnostics - A focus group study.
Emilie Hybertsen Lysø et al. Soc Sci Med 2024 347116771
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The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?
Natalia Campacci et al. Front Psychol 2024 151306388
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Family health beliefs and cascade genetic testing in Asian families with hereditary cancer risk: "Okay, now what?".
Leena Tran et al. J Genet Couns 2024
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De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam.
Hoa Thi Phuong Bui et al. PLoS One 2024 19(3) e0290936
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Parental Engagement in Identifying Information Needs After Newborn Screening for Families of Infants with Suspected Athymia.
Evey Howley et al. J Clin Immunol 2024 44(3) 79
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A novel machine learning prediction model for metastasis in breast cancer.
Huan Li et al. Cancer Rep (Hoboken) 2024 7(3) e2006
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Efficacy of Community Health Worker-Delivered Family Health History-Based Breast Cancer Education and Services Among Chinese Americans.
Bertille Assoumou et al. J Cancer Educ 2024
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Parental Perspectives on Early Life Screening and Genetic Testing for ASD: A Systematic Review.
Katerina Dounavi et al. J Autism Dev Disord 2024
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Lived experiences of genetic diagnosis for rare disease patients: a qualitative interview study.
Antonia Modelhart et al. Orphanet J Rare Dis 2024 19(1) 68
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Understanding what drives genetic study participation: Perspectives of patients, carers, and relatives.
Emilia M Swietlik et al. Pulm Circ 2024 14(1) e12346
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A qualitative focus group analysis: Increasing fieldwork capacity in genetic counseling training programs.
Rebecca Jirik et al. J Genet Couns 2024
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Understanding perceptions of tumor genomic profile testing in Black/African American cancer patients in a qualitative study: the role of medical mistrust, provider communication, and family support
CC Luck et al, J Comm Genetics, Feb 16, 2024
Primary care providers' preferences for the communication and management of actionable genomic findings from a research biobank.
Elizabeth L Kudron et al. Genet Med Open 2024 1(1)
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Patients' perceptions and practices of informing relatives: a qualitative study within a randomised trial on healthcare-assisted risk disclosure.
Charlotta Nääs et al. Eur J Hum Genet 2024
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Talking about Familial Breast and Ovarian Cancer Risk-Evaluation of a Psychosocial Training Module for Gynecologists in Germany.
Friederike Kendel et al. Cancers (Basel) 2024 16(2)
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Patient experiences with tissue-based genomic testing during active surveillance for prostate cancer.
Michael S Leapman et al. BJUI Compass 2024 5(1) 142-149
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Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population.
Marian J Gilmore et al. Transl Behav Med 2024
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"We are just not sure what that means or if it's relevant": Uncertainty when gathering family history information in South African prenatal genetic counseling consultations.
Megan Scott et al. Soc Sci Med 2024 342116555
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The psychosocial impact of haemophilia from patients' and caregivers' point of view: The results of an Italian survey.
Arianna Fornari et al. Haemophilia 2023
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Returning Genetic Information About Risk for Alcohol Use Disorder to Adolescents: Findings of a Preliminary Qualitative Study of Precision Prevention.
Elissa R Weitzman et al. AJPM Focus 2023 3(1) 100153
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Development of a web-based care networking system to support visiting healthcare professionals in the community.
Jakyung Lee et al. BMC Health Serv Res 2023 23(1) 1427
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Time to diagnosis in rapid exome/genome sequencing in the clinical inpatient setting.
Alison Schildt et al. Am J Med Genet A 2023
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Exploring the Potential of AI Language Models in Obstetrics with a Focus on Fetal Medicine: An Evaluation of the Perplexity AI Model.
Angel Chimenea et al. Fetal Diagn Ther 2023
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Validation and cross-cultural adaptation of the Italian version of the paediatric eating assessment tool (I-PEDI-EAT-10) in genetic syndromes.
Roberta Onesimo et al. Int J Lang Commun Disord 2023
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Only 32.3% of Breast Cancer Families with Pathogenic Variants in Cancer Genes Utilized Cascade Genetic Testing.
Konstantinos Agiannitopoulos et al. Cancers (Basel) 2023 15(21)
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Availability of psychological resources for parents receiving communication of positivity at newborn screening for metabolic diseases in Italy.
Marco Bani et al. Eur J Pediatr 2023
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Experiences of Family Communication and Cascade Genetic Testing for Hereditary Cancer in Medically Underserved Populations-A Qualitative Study.
Erica M Bednar et al. Cancer Prev Res (Phila) 2023
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 21, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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