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Genetic Transparency? tackles the question of who has, or should have access to personal genomic information. Genomic science is revolutionary in how it changes the way we live, individually and together, and how it changes the shape of society. If this is so, then – the authors of this volume claim – the rules that regulate genetic transparency should be debated carefully, openly and critically. It is important to see that the social and cultural meanings of DNA and genetic sequences are much richer than can be accounted for by purely biomedical knowledge. In this book, an international group of leading genomics experts and scholars from the humanities and social sciences discuss how the new accessibility of genomic information affects interpersonal relationships, our self-understandings, ethics, law, and healthcare systems. Contributors are: Kirsten Brukamp, Gabrielle Christenhusz, Lorraine Cowley, Malte Dreyer, Jeanette Erdmann, Andrei Famenka, Teresa Finlay, Caroline Fündling, Shannon Gibson, Cathy Herbrand, Angeliki Kerasidou, Lene Koch, Fruzsina Molnár-Gábor, Tim Ohnhäuser, Christoph Rehmann-Sutter, Benedikt Reiz, Vasilja Rolfes, Sara Tocchetti

Genomics --- Genetics --- Genetic Privacy --- #SBIB:316.334.3M11 --- #SBIB:316.334.3M13 --- Genome research --- Genomes --- Molecular genetics --- Moral and ethical aspects. --- ethics. --- Medische sociologie: concepten en theorieën --- Medische sociologie: aanverwante disciplines --- Research --- Human genetics. --- Heredity, Human --- Human biology --- Physical anthropology --- Moral and ethical aspects --- ethics --- Medical genetics

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DNA Fingerprinting. --- 614.1 --- DNA Fingerprints --- DNA Profiling --- DNA Typing --- Genetic Fingerprinting --- DNA Fingerprint --- DNA Fingerprintings --- DNA Profilings --- DNA Typings --- Fingerprint, DNA --- Fingerprinting, DNA --- Fingerprinting, Genetic --- Fingerprintings, DNA --- Fingerprintings, Genetic --- Fingerprints, DNA --- Genetic Fingerprintings --- Profiling, DNA --- Typing, DNA --- Typings, DNA --- Paternity --- Polymorphism, Restriction Fragment Length --- Minisatellite Repeats --- Random Amplified Polymorphic DNA Technique --- Databases, Nucleic Acid --- Genetic Privacy --- Genotyping Techniques --- Population. Depopulation --- 614.1 Population. Depopulation --- DNA Fingerprinting

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This Special Issue focuses on the current state of pharmacogenomics (PGx) and the extensive translational process, including the identification of functionally important PGx variation; the characterization of PGx haplotypes and metabolizer statuses, their clinical interpretation, clinical decision support, and the incorporation of PGx into clinical care.

pharmacogenomics --- return of results --- genetic counseling --- qualitative --- pharmacogenetics --- implementation --- pharmacogenetics service --- screening --- pre-emptive --- personalized medicine --- precision medicine --- community pharmacy --- pharmacogenomic testing --- genetic privacy --- pharmaco-economics --- polymorphisms --- pharmacogenes --- pharmacogenomic --- machine learning --- adaptation --- human evolution --- US Food and Drug Administration --- clinical actionability --- clinical translation --- chronic kidney disease --- CYP3A5 --- polymorphism --- progression --- pharmacogenomics (PGx) --- pediatrics --- best practice alerts (BPAs) --- electronic health records (EHR) --- genomic indicators --- clinical decision support (CDS) --- phenotype --- genotype --- polypharmacy --- chronic disease --- medication management --- electronic medical record --- artificial intelligence --- n/a

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DNA fingerprinting --- DNA Fingerprinting --- DNA Fingerprinting. --- DNA fingerprints --- DNA identification --- DNA profiles --- DNA profiling --- Genetic fingerprinting --- Genetic fingerprints --- Forensic genetics --- Identification --- DNA Fingerprints --- DNA Profiling --- DNA Typing --- Genetic Fingerprinting --- DNA Fingerprint --- DNA Fingerprintings --- DNA Profilings --- DNA Typings --- Fingerprint, DNA --- Fingerprinting, DNA --- Fingerprinting, Genetic --- Fingerprintings, DNA --- Fingerprintings, Genetic --- Fingerprints, DNA --- Genetic Fingerprintings --- Profiling, DNA --- Typing, DNA --- Typings, DNA --- Paternity --- Polymorphism, Restriction Fragment Length --- Minisatellite Repeats --- Random Amplified Polymorphic DNA Technique --- Databases, Nucleic Acid --- Genetic Privacy --- Genotyping Techniques --- Technique --- DNA fingerprinting. --- DNA --- Forensic Medicine. --- genetics. --- Dna fingerprinting. --- Dna --- Forensic medicine. --- Genetics.

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Connecting an abnormal physical exam to a possible genetic condition is a daunting and inexact task for any physician, be they a primary care provider, non-geneticist specialist, or fellowship-trained geneticist. Comprising 31 clinical protocols from the world's foremost clinical geneticists, Signs and Symptoms of Genetic Conditions provides a practical manual for the diagnosis and management of common human genetic conditions based on their presenting signs and/or symptoms. Each chapter examines a specific clinical finding and leads the user through a step-by-step approach to a differential d

Genetic disorders. --- Symptoms --- Child. --- Genetic Diseases, Inborn --- Diagnosis, Differential. --- Genetic Testing. --- Signs and Symptoms. --- Symptoms and Signs --- Genetic Screening --- Predictive Genetic Testing --- Predictive Testing, Genetic --- Testing, Genetic Predisposition --- Genetic Predisposition Testing --- Genetic Predictive Testing --- Genetic Screenings --- Genetic Testing, Predictive --- Predisposition Testing, Genetic --- Screening, Genetic --- Screenings, Genetic --- Testing, Genetic --- Testing, Genetic Predictive --- Testing, Predictive Genetic --- Genetic Predisposition to Disease --- Prenatal Diagnosis --- Preimplantation Diagnosis --- Cytogenetic Analysis --- Molecular Diagnostic Techniques --- Databases, Genetic --- Databases, Nucleic Acid --- Genetic Privacy --- Diagnoses, Differential --- Differential Diagnoses --- Differential Diagnosis --- Children --- Minors --- Congenital diseases --- Disorders, Genetic --- Disorders, Inherited --- Genetic diseases --- Hereditary diseases --- Inherited diseases --- Diseases --- Medical genetics --- diagnosis. --- diagnosis