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Behavioral changes after psychiatric genetic counseling: an exploratory study
Behavioral changes after psychiatric genetic counseling: an exploratory study
Introduction: Though it is well established that genetic information does not produce behavior changes, there are limited ...
Human-centered design study to inform traceback cascade genetic testing programs at three integrated health systems
Human-centered design study to inform traceback cascade genetic testing programs at three integrated health systems
Introduction: A traceback genetic testing program for ovarian cancer has the potential to identify individuals with heredi...
Predictors of Women’s Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members
Predictors of Women’s Intentions to Communicate Updated Genetic Test Results to Immediate and Extended Family Members
<b><i>Introduction:</i></b> Many individuals who previously received negative genetic test results...
Is Habitual Dietary Intake of Fats Associated with Apelin Gene Expression in Visceral and Subcutaneous Adipose Tissues and Its Serum Levels in Obese Adults?
Is Habitual Dietary Intake of Fats Associated with Apelin Gene Expression in Visceral and Subcutaneous Adipose Tissues and Its Serum Levels in Obese Adults?
<b><i>Introduction:</i></b> Apelin could be one of the last protective defenses before developing ...
Integrating genomics into the care of people with palliative needs: A global scoping review of policy recommendations
Integrating genomics into the care of people with palliative needs: A global scoping review of policy recommendations
BACKGROUND: Genomics has growing relevance to palliative care, where testing largely benefits relatives. Integration of ge...
Genetic Variants in MIR3142HG Contribute to the Predisposition of IgA Nephropathy in a Chinese Han Population
Genetic Variants in MIR3142HG Contribute to the Predisposition of IgA Nephropathy in a Chinese Han Population
<b><i>Background:</i></b> The study aimed to evaluate the association of genetic variants in <i...
The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study
The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study
<b><i>Introduction:</i></b> Family history is an established risk factor for both cardiovascular d...
Which Test Is Best? A Cluster-Randomized Controlled Trial of a Risk Calculator and Recommendations on Colorectal Cancer Screening Behaviour in General Practice
Which Test Is Best? A Cluster-Randomized Controlled Trial of a Risk Calculator and Recommendations on Colorectal Cancer Screening Behaviour in General Practice
<b><i>Introduction:</i></b> This cluster-randomized controlled trial aimed to assess the effect of...
Knowledge and Attitudes about Privacy and Secondary Data Use among African-Americans Using Direct-to-Consumer Genetic Testing
Knowledge and Attitudes about Privacy and Secondary Data Use among African-Americans Using Direct-to-Consumer Genetic Testing
<b><i>Introduction:</i></b> The rapidly expanding direct-to-consumer genetic testing (DTC GT) mark...
Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing
Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing
<b><i>Objective:</i></b> The aim of this study was to explore the parental views, attitudes, and p...
Associations between TNFAIP3 Polymorphisms and Rheumatoid Arthritis: A Systematic Review and Meta-Analysis Update with Trial Sequential Analysis
Associations between TNFAIP3 Polymorphisms and Rheumatoid Arthritis: A Systematic Review and Meta-Analysis Update with Trial Sequential Analysis
<b><i>Introduction:</i></b> The tumor necrosis factor alpha inducible protein 3 (<i>TNFAIP3&...
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities
<b><i>Introduction:</i></b> Precision medicine research investigates the differences in individual...
Evaluating the Effectiveness of a Telehealth Cancer Genetics Program: A BRCA Pilot Study
Evaluating the Effectiveness of a Telehealth Cancer Genetics Program: A BRCA Pilot Study
<b><i>Introduction:</i></b> Ashkenazi Jewish (AJ) individuals face a 1 in 40 (2.5%) risk of having...
Screening of Serum miRNAs as Diagnostic Biomarkers for Lung Cancer Using the Minimal-Redundancy-Maximal-Relevance Algorithm and Random Forest Classifier Based on a Public Database
Screening of Serum miRNAs as Diagnostic Biomarkers for Lung Cancer Using the Minimal-Redundancy-Maximal-Relevance Algorithm and Random Forest Classifier Based on a Public Database
<b><i>Background:</i></b> Lung cancer is one of the deadliest cancers, early diagnosis of which ca...
An Electronic Health Record Tool Increases Genetic Counseling Referral of Individuals at Hereditary Cancer Risk: An Intervention Study
An Electronic Health Record Tool Increases Genetic Counseling Referral of Individuals at Hereditary Cancer Risk: An Intervention Study
<b><i>Introduction:</i></b> There is widespread under-identification of individuals at hereditary ...
“A Gift to My Family for Their Future”: Attitudes about Genetic Research Participation
“A Gift to My Family for Their Future”: Attitudes about Genetic Research Participation
<b><i>Background:</i></b> Broad participation in genetic research is needed to promote equitable a...
A Case-Control Study of the Luteinizing Hormone Level in Luteinizing Hormone Receptor Gene (rs2293275) Polymorphism in Polycystic Ovarian Syndrome Females
A Case-Control Study of the Luteinizing Hormone Level in Luteinizing Hormone Receptor Gene (rs2293275) Polymorphism in Polycystic Ovarian Syndrome Females
<b><i>Background:</i></b> Polycystic ovary syndrome (PCOS) is a common heterogeneous disorder char...
Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects
Translational Science, DNA Commercialization, and Informed Consent: The Need for Specific Terminology, Insights from a Review of H3Africa Projects
In the past decade, there has been an acceleration in genomic research, its applications, and its translation into healthc...
Temporal Patterns in the Evolutionary Genetic Distance of SARS-CoV-2 during the COVID-19 Pandemic
Temporal Patterns in the Evolutionary Genetic Distance of SARS-CoV-2 during the COVID-19 Pandemic
During coronavirus disease 2019 (COVID-19) pandemic, the genetic mutations of severe acute respiratory syndrome coronaviru...
Unlocking Access to Broad Molecular Profiling: Benefits, Barriers, and Policy Solutions
Unlocking Access to Broad Molecular Profiling: Benefits, Barriers, and Policy Solutions
<b><i>Objectives:</i></b> “Personalized healthcare” is generating new approaches to disease manage...
Comparison of a Cancer Family History Collection and Risk Assessment Tool – ItRunsInMyFamily – with Risk Assessment by Health-Care Professionals
Comparison of a Cancer Family History Collection and Risk Assessment Tool – ItRunsInMyFamily – with Risk Assessment by Health-Care Professionals
<b><i>Introduction:</i></b> Primary care providers (PCPs) and oncologists lack time and training t...
“We-Diseases” and Dyadic Decision-Making Processes: A Critical Perspective
“We-Diseases” and Dyadic Decision-Making Processes: A Critical Perspective
This is a critical perspective paper discussing the theoretical bases and methodological issues regarding dyadic decision-...
Association between Genetic Polymorphisms of MIR3142HG and the Risk of Steroid-Induced Osteonecrosis of the Femoral Head in the Population of Northern China
Association between Genetic Polymorphisms of MIR3142HG and the Risk of Steroid-Induced Osteonecrosis of the Femoral Head in the Population of Northern China
<b><i>Background:</i></b> Steroid-induced osteonecrosis of the femoral head (ONFH) is aseptic necr...
Genetic and Nongenetic Determinants of Variable Warfarin Dose Requirements: A Report from North India
Genetic and Nongenetic Determinants of Variable Warfarin Dose Requirements: A Report from North India
<b><i>Introduction:</i></b> Warfarin is widely used and will continue to be prescribed especially ...
Identification of Candidate Genes in Early-Stage Invasive Ductal Carcinoma Patients with High-Risk Mortality Using Genes Commonly Involved in Breast Cancer: A Retrospective Study
Identification of Candidate Genes in Early-Stage Invasive Ductal Carcinoma Patients with High-Risk Mortality Using Genes Commonly Involved in Breast Cancer: A Retrospective Study
<b><i>Introduction:</i></b> Invasive ductal carcinoma (IDC) of the breast is a heterogeneous disea...
Altruism as an Explanation for Human Consanguinity
Altruism as an Explanation for Human Consanguinity
<b><i>Background:</i></b> Human inbreeding is a sociobiological puzzle. Despite widespread knowled...
People with Cerebral Palsy and Their Family’s Preferences about Genomics Research
People with Cerebral Palsy and Their Family’s Preferences about Genomics Research
<b><i>Introduction:</i></b> The goal of this study was to understand individuals with cerebral pal...
Psychological Distress and Quality of Life in Participants Undergoing Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy Caused by TMEM43 p.S358L: Is It Time to Offer Population-Based Genetic Screening?
Psychological Distress and Quality of Life in Participants Undergoing Genetic Testing for Arrhythmogenic Right Ventricular Cardiomyopathy Caused by TMEM43 p.S358L: Is It Time to Offer Population-Based Genetic Screening?
<b><i>Purpose:</i></b> We have identified 27 families in Newfoundland and Labrador (NL) with the f...
Evaluating Primary Care Providers’ Readiness for Delivering Genetic and Genomic Services to Underserved Populations
Evaluating Primary Care Providers’ Readiness for Delivering Genetic and Genomic Services to Underserved Populations
<b><i>Introduction:</i></b> Increased genomics knowledge and access are advancing precision medici...
Mapping Users’ Experience of a Family History and Genetic Risk Algorithm Tool in Primary Care
Mapping Users’ Experience of a Family History and Genetic Risk Algorithm Tool in Primary Care
<b><i>Introduction:</i></b> The development of a family history (FH) questionnaire (FHQ) provides ...
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