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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 25, 2024
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Genetic counseling[original query]>>Original Studies[Product Type]
Associations between genomic aberrations, increased nuchal translucency, and pregnancy outcomes: a comprehensive analysis of 2,272 singleton pregnancies in women under 35.
Jia Huang et al. Front Med (Lausanne) 2024 111376319
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Postpartum Breast Cancer and Survival in Women With Germline BRCA Pathogenic Variants.
Zhenzhen Zhang et al. JAMA Netw Open 2024 7(4) e247421
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Practice Patterns and Barriers to Vascular Genetic Testing among Vascular Surgeons.
James M Dittman et al. Ann Vasc Surg 2024
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Clinical features of prostate cancer by polygenic risk score.
Christina Spears et al. Fam Cancer 2024
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Parental questions about sex chromosome aneuploidies regarding sex, gender, and sexual orientation as reported by genetic counselors in a prenatal setting.
Sarah Burzynski et al. J Genet Couns 2024
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Factors Influencing Patient Disclosure of Parkinson's Disease Genetic Testing Results to Relatives.
Jeanine Schulze et al. Mov Disord Clin Pract 2024
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The Health History of First-Degree Relatives' Dyslipidemia Can Affect Preferences and Intentions following the Return of Genomic Results for Monogenic Familial Hypercholesterolemia.
Tomoharu Tokutomi et al. Genes (Basel) 2024 15(3)
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A rapid PCR-free next-generation sequencing method for comprehensive diagnosis of chromosome disease syndromes in prenatal samples.
Hong Su et al. Medicine (Baltimore) 2024 103(13) e37610
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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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Parent perspectives following newborn screening resulting in diagnoses of fragile X syndrome or fragile X premutation.
Allyson Corbo et al. Res Dev Disabil 2024 148104719
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The effectiveness of psychiatric genetic counseling training: An analysis of 13 international workshops.
Tiera Mack et al. Am J Med Genet B Neuropsychiatr Genet 2024 e32978
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The dynamic buffering of social support on depressive symptoms and cancer worries in patients seeking cancer genetic counseling.
Sally Ho et al. J Cancer Surviv 2024
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Individuals' experiences in genetic counseling and predictive testing for familial amyotrophic lateral sclerosis.
Connolly G Steigerwald et al. J Genet Couns 2024
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Genetic counselors' and community clinicians' implementation and perceived barriers to informed consent during pre-test counseling for hereditary cancer risk.
Alexandra Capasso et al. J Genet Couns 2024
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Family Recall of and Response to Germline Pathologic Variants Found on Paired Tumor-Germline Sequencing in Pediatric Oncology.
Michelle F Jacobs et al. JCO Precis Oncol 2024 8e2300539
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Delivering Genetic Test Results for Parkinson Disease: A Qualitative Approach to Provider Experiences in the PD GENEration Study.
Mandy Miller et al. Neurol Clin Pract 2024 14(2) e200282
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Retrospective genetic testing (Traceback) in women with early-onset breast cancer after revised national guidelines: a clinical implementation study.
Annelie Augustinsson et al. Breast Cancer Res Treat 2024
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Association of sociodemographic and clinical factors with the quality of life of Brazilian individuals with Neurofibromatosis type 1: a cross-sectional study.
Natália Parenti Bicudo et al. An Bras Dermatol 2024
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TARGET: A Randomized, Noninferiority Trial of a Pretest, Patient-Driven Genetic Education Webtool Versus Genetic Counseling for Prostate Cancer Germline Testing.
Stacy Loeb et al. JCO Precis Oncol 2024 8e2300552
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The Role of Demographic and Clinical Factors in Germline Mutation Testing for Patients with Primary Hyperparathyroidism.
Patrick T Hangge et al. Ann Surg Oncol 2024
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Young Women's Perspectives on Being Screened for Hereditary Breast and Ovarian Cancer Risk During Routine Primary Care.
Mady Head et al. Womens Health Issues 2024
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The majority of parents of children undergoing genetic testing report preference for earlier genetic counseling appointments.
Cami Cochrane et al. J Genet Couns 2024
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Direct-to-Consumer Genetic Tests and Canadian Genetic Counselors: A Pilot Exploration of Professional Roles in Response to Novel Biotechnologies.
Cassandra E Haley et al. Genes (Basel) 2024 15(2)
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Implementing mainstream genetic counseling within the area-wide network of the German Consortium Hereditary Breast and Ovarian Cancer (GD-HBOC): Satisfaction of primary care providers with the provided state-of-the-art training by the Cologne Center.
Natalie Herold et al. J Genet Couns 2024
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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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Real-World Data on Institutional Implementation of Screening for Mismatch Repair Deficiency and Lynch Syndrome in Endometrial Cancer Patients.
Carmen Joder et al. Cancers (Basel) 2024 16(3)
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Experiences of hereditary cancer care among transgender and gender diverse people: "It's gender. It's cancer risk…it's everything".
Sarah Roth et al. J Genet Couns 2024
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Colorectal cancer genetic referral: Are we doing enough?
Whitnee C Broyles et al. Proc (Bayl Univ Med Cent) 2024 37(2) 250-254
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Thirty-year of genetic counselling education in Europe: a growing professional area
M Paneque et al, EJHG, February 15, 2024
The detection efficacy of noninvasive prenatal genetic testing (NIPT) for sex chromosome abnormalities and copy number variation and its differentiation in pregnant women of different ages.
Yimei Li et al. Heliyon 2024 10(2) e24155
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 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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