Factors impacting experience of genetic testing among adults with inherited retinal diseases [0.03%]
遗传性视网膜疾病成人患者的基因检测体验影响因素分析
Emma Melhuish,Joshua Schultz,Alexis Ceecee Britten-Jones
Emma Melhuish
Genetic testing for inherited retinal diseases (IRDs) has become more accessible in Australia in recent years; however, it is not clear how different factors influence the experiences of genetic counseling and support needs. This study used...
Power of the pedigree: Specialty referrals from a pharmacogenomics clinic [0.03%]
家谱的力量：药物基因组学诊所的专科转诊
Elizabeth Fieg,Benjamin Kerman,Samantha Frear et al.
Elizabeth Fieg et al.
Pharmacogenomic testing, or genetic testing to inform medication selection and dosing, is now available to patients through various practice models including dedicated pharmacogenomics clinics that may include a genetic counselor as part of...
Narratives before numbers: Reimagining conversations about race, ethnicity, and ancestry information in genetic counseling practice [0.03%]
叙事先于数字：遗传咨询实践中种族、族裔和祖先信息对话的重构
Emily Peugh,Sara Chandros Hull,Leila Jamal
Emily Peugh
As genomic testing becomes more common, it is essential to re-examine practical and ethical arguments for and against eliciting race, ethnicity, and ancestry (REA) information from patients as a default practice in genetic counseling. In th...
Views of genetic health professionals, patients, and next of kin on retesting and recontact with results from updated genetic testing [0.03%]
遗传保健专业人员、患者和近亲对更新的基因检测结果的重新检测和重新联系的看法
Alison Luk Young,Catherine Speechly,April Morrow et al.
Alison Luk Young et al.
Retesting individuals who previously had uninformative BRCA1/2 genetic testing can identify new clinically actionable information. However, this practice is limited due to concerns regarding how to retest and recontact ethically with limite...
Patients' experiences using an educational virtual assistant for review of reproductive genetic screening results [0.03%]
患者使用教育型虚拟助理复查生殖遗传筛查结果的体验
Sarah Yarnall,Jessica L Saben,Nicholas Sun et al.
Sarah Yarnall et al.
This observational study aimed to capture patients' experiences after reviewing carrier screening (CS) and/or noninvasive prenatal cell-free DNA testing (NIPT) results with Natera's Educational Virtual Assistant (NEVA). Patients, partners o...
Patients' and healthcare professionals' experiences with implementing the Rosa chatbot in mainstream genetic testing for hereditary breast and ovarian cancer [0.03%]
_rosa聊天机器人在主流遗传性乳腺癌和卵巢癌基因检测中实施的经验研究：患者和医疗专业人员的视角
Elen Siglen,Hildegunn Høberg Vetti,Anita Lyssand et al.
Elen Siglen et al.
Mainstream genetic testing (MGT) refers to genetic testing conducted at the time of a cancer diagnosis without undergoing comprehensive genetic counseling. MGT has been the standard of care for patients with breast or ovarian cancer in Norw...
Bringing Genetics to Mental Health: Integrating Genetic Counseling into a Mental Health Program at Monash Health, Australia [0.03%]
遗传学在心理健康中的应用：将基因咨询整合到澳大利亚莫纳什卫生局的心理健康计划中
Joanne Isbister,Anita Gorrie,Lia Laios et al.
Joanne Isbister et al.
Psychiatric disorders such as anxiety, bipolar disorder, depression, substance use disorder, and schizophrenia are highly heritable, yet access to genetic counseling for psychiatric disorders remains limited. Despite evidence supporting its...
Psychosocial predictors of hereditary cancer genetic testing motivation in untested individuals [0.03%]
未经基因检测者进行遗传性癌症基因检测的心理社会预测因素
Sarah Austin,Emerson Delacroix,John D Rice et al.
Sarah Austin et al.
Genetic testing for hereditary cancer syndromes can provide lifesaving information allowing for individualized cancer screening, prevention, and treatment. A broader understanding of how psychosocial factors impact motivation to undergo gen...
Patient-initiated lifestyle changes following receipt of genetic test results in a predominantly marginalized population [0.03%]
边缘化群体接受基因检测结果后由患者发起的生活方式改变
Marian J Gilmore,Hannah E Frawley,Elizabeth Shuster et al.
Marian J Gilmore et al.
Genetic testing for cancer predisposition and other actionable findings aims to improve health outcomes by informing patients and practitioners about genetic disease risks and guiding decisions on risk-reducing actions. This study explored ...
Early-career genetic counselors' professional identity formation through experiences with continuing education at a professional conference [0.03%]
早期职业遗传咨询师通过专业会议继续教育经历形成职业身份感
Rachel Mills,Susan J Barcinas
Rachel Mills
This research aimed to describe professional identity (PI) and professional identity formation (PIF) of early-career genetic counselors (GCs) attending a professional conference. PI is a sense of self within a professional community and inc...