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1. Genetic testing and molecular biomarkers
Genetic testing and molecular biomarkers, ISSN 1945-0265, 2009
Human chromosome abnormalities | Cytogenetics | Diagnosis | Molecular genetics | Biochemical markers
Journal
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2. Direct-to-consumer genetic testing the implications of the US FDA's first marketing authorization for BRCA mutation testing
by Gill, Jennifer and Obley, Adam J and Prasad, Vinay
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 06/2018, Volume 319, Issue 23, pp. 2377 - 2378
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Predictive Value of Tests | Medical Overuse | United States | Genetic Testing - legislation & jurisprudence | Humans | Genetic Counseling - utilization | Breast Neoplasms - genetics | Direct-To-Consumer Screening and Testing - legislation & jurisprudence | Genes, BRCA2 | Government Regulation | Female | Genes, BRCA1 | Mutation | Breast Neoplasms - ethnology | Marketing - legislation & jurisprudence | United States Food and Drug Administration | BRCA2 protein | Biotechnology | Regulatory agencies | BRCA1 protein | Genomics | Innovations | Health risks | Breast cancer | Genetic screening | Marketing | Womens health | Risk assessment | Genetic testing
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3. Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel
by Sturm, Amy C and Knowles, Joshua W and Gidding, Samuel S and Ahmad, Zahid S and Ahmed, Catherine D and Ballantyne, Christie M and Baum, Seth J and Bourbon, Mafalda and Carrié, Alain and Cuchel, Marina and de Ferranti, Sarah D and Defesche, Joep C and Freiberger, Tomas and Hershberger, Ray E and Hovingh, G. Kees and Karayan, Lala and Kastelein, Johannes Jacob Pieter and Kindt, Iris and Lane, Stacey R and Leigh, Sarah E and Linton, MacRae F and Mata, Pedro and Neal, William A and Nordestgaard, Børge G and Santos, Raul D and Harada-Shiba, Mariko and Sijbrands, Eric J and Stitziel, Nathan O and Yamashita, Shizuya and Wilemon, Katherine A and Ledbetter, David H and Rader, Daniel J and Convened by the Familial Hypercholesterolemia Foundation
Journal of the American College of Cardiology, ISSN 0735-1097, 08/2018, Volume 72, Issue 6, pp. 662 - 680
genetic counseling | cascade testing | consensus statement | genetic testing | familial hypercholesterolemia | Receptors, LDL - genetics | Hyperlipoproteinemia Type II - blood | Genetic Testing - standards | Humans | Genetic Counseling - methods | Hyperlipoproteinemia Type II - diagnosis | Apolipoproteins B - blood | Apolipoproteins B - genetics | Proprotein Convertase 9 - genetics | Expert Testimony - methods | Genetic Testing - methods | Receptors, LDL - blood | Genetic Counseling - standards | Proprotein Convertase 9 - blood | Expert Testimony - standards | Hyperlipoproteinemia Type II - genetics | Phenotypes | Heart attacks | Genes | Health risks | Cardiovascular disease | Subtilisin | Family medical history | Angina pectoris | Genetic screening | Apolipoprotein B | Genetic counseling | Hypercholesterolemia | Kexin | Risk assessment | Receptor density | Lipoprotein (low density) receptors | Genetic testing | Cardiovascular diseases | Age | Deoxyribonucleic acid--DNA
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4. Full Text Genetic Testing and the Governance of Risk in the Contemporary Economy
: Comparative Reflections in the Insurance and Employment Law Contexts
by Khoury, Lara and Blackett, Adelle and Vanhonnaeker, Lukas
2020, Ius Comparatum - Global Studies in Comparative Law, ISBN 3030436985, 356
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5. Testing fate
: Tay-Sachs disease and the right to be responsible
by Reuter, Shelley Z. 1968- author. (Shelley Zipora)
2016, ISBN 081669995X, 264 pages
Human chromosome abnormalities | Tay-Sachs disease | Diagnosis | History | Racism | Great Britain | Genetic Testing | Jews | United States | Sociology | Tay-Sachs Disease | history | ethnology | Health Sciences | SOCIAL SCIENCE | Disease & Health Issues | MEDICAL
Book
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6. The age of genomes
: tales from the front lines of genetic medicine
by Lipkin, Steven Monroe and Luoma, Jon R., contributor
2016, ISBN 9780807074589, 234
Genetic Diseases, Inborn | Genetic Engineering | Genetic Testing | Genetic disorders | Genetic screening
Book
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7. Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer US Preventive Services Task Force Recommendation Statement
by Owens, Douglas K and Davidson, Karina W and Krist, Alex H and Barry, Michael J and Cabana, Michael and Caughey, Aaron B and Doubeni, Chyke A and Epling, John W and Kubik, Martha and Landefeld, C. Seth and Mangione, Carol M and Pbert, Lori and Silverstein, Michael and Simon, Melissa A and Tseng, Chien-Wen and Wong, John B and US Preventive Services Task Force
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 08/2019, Volume 322, Issue 7, pp. 652 - 665
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Genetic Predisposition to Disease | Genetic Testing | Ovarian Neoplasms - prevention & control | Risk Assessment | Humans | Genetic Counseling | Breast Neoplasms - prevention & control | Ovarian Neoplasms - genetics | Breast Neoplasms - genetics | Peritoneal Neoplasms - genetics | Fallopian Tube Neoplasms - genetics | Genes, BRCA2 | Female | Genes, BRCA1 | Mutation | Task forces | Genealogy | Ovarian carcinoma | BRCA1 protein | Genes | Health risks | Risk reduction | Breast cancer | Family medical history | Fallopian tube | Medical screening | Genetic screening | Skin cancer | Ovarian cancer | Genetic counseling | Womens health | Risk assessment | Surgery | Genetics | Skin | Health risk assessment | Peritoneum
Journal Article
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8. Full Text Group Testing for Severe Acute Respiratory Syndrome– Coronavirus 2 to Enable Rapid Scale-up of Testing and Real-Time Surveillance of Incidence
by Pilcher, Christopher D and Westreich, Daniel and Hudgens, Michael G
The Journal of infectious diseases, ISSN 0022-1899, 08/2020, Volume 222, Issue 6, pp. 903 - 909
Infectious Diseases | Immunology | Life Sciences & Biomedicine | Microbiology | Science & Technology | Predictive Value of Tests | Pandemics | Betacoronavirus - isolation & purification | COVID-19 Testing | Coronavirus Infections - diagnosis | Humans | Specimen Handling - methods | Reverse Transcriptase Polymerase Chain Reaction | Incidence | COVID-19 | Clinical Laboratory Techniques - methods | SARS-CoV-2 | Algorithms | RNA, Viral - genetics | Coronavirus Infections - epidemiology | Pneumonia, Viral - epidemiology | Sensitivity and Specificity | Pneumonia, Viral - diagnosis | RNA, Viral - isolation & purification | Viral Load - methods | Betacoronavirus - genetics | Severe acute respiratory syndrome coronavirus 2 | Coronaviruses | Laboratories | Index Medicus | Abridged Index Medicus
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9. Genetics and public health in the 21st century
: using genetic information to improve health and prevent disease
by Burke, Wylie and Khoury, Muin J and Thomson, Elizabeth J. 1950- (Elizabeth Jean)
2000, Oxford monographs on medical genetics, ISBN 9780195128307, Volume no. 40, xx, 639
Genetic Predisposition to Disease | Public Health | Genetic Engineering | Preventive Medicine | Medical genetics | Genetics, Biochemical | Health Planning | Epidemiology, Molecular | prevention & control | Genetic Screening | Human Genome Project | Epidemiology | Disease prevention | Human genes | Health promotion | Public health research | Newborn screening | Communication issues | Genetics | Genetic screening
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10. Full Text Patients’ Views of Treatment-Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of BRCA1 and BRCA2 Testing
by Wright, Sarah and Porteous, Mary and Stirling, Diane and Lawton, Julia and Young, Oliver and Gourley, Charlie and Hallowell, Nina
Journal of genetic counseling, ISSN 1059-7700, 12/2018, Volume 27, Issue 6, pp. 1459 - 1472
Human Genetics | Ethics | Public Health | Breast/ovarian cancer | Biomedicine | BRCA1 and BRCA2 testing | Treatment-focused genetic testing (TFGT) | Gynecology | Patient experience | Clinical Psychology | Mainstreaming | Clinical implementation | Treatment‐focused genetic testing (TFGT) | Social Sciences | Life Sciences & Biomedicine | Social Sciences, Biomedical | Health Care Sciences & Services | Health Policy & Services | Genetics & Heredity | Biomedical Social Sciences | Science & Technology | Medical colleges | Medical research | Care and treatment | Medical genetics | Medicine, Experimental | Genetic screening | Ovarian cancer | BRCA2 protein | Integration | BRCA1 protein | Oncology | Relatives | Breast cancer | Patient satisfaction | Timing | Patients | Quality of care | Original Research | ovarian cancer | Breast
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11. Full Text MGMT testing - The challenges for biomarker-based glioma treatment
by Wick, Wolfgang and Weller, Michael and Van Den Bent, Martin and Sanson, Marc and Weiler, Markus and Von Deimling, Andreas and Plass, Christoph and Hegi, Monika and Platten, Michael and Reifenberger, Guido
Nature reviews. Neurology, ISSN 1759-4758, 2014, Volume 10, Issue 7, pp. 372 - 385
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Biomarkers - metabolism | Tumor Suppressor Proteins - metabolism | DNA Modification Methylases - metabolism | Glioma - diagnosis | Brain Neoplasms - diagnosis | Humans | DNA Repair Enzymes - genetics | Models, Molecular | Glioma - genetics | DNA Methylation | DNA Modification Methylases - genetics | Tumor Suppressor Proteins - genetics | Brain Neoplasms - therapy | DNA Repair Enzymes - metabolism | Glioma - therapy | Molecular targeted therapy | Medical research | Care and treatment | Methyltransferases | Gliomas | Medicine, Experimental | Genetic aspects | Research | Properties | Index Medicus
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