Search Results - "Genetic Counseling/ethics"

The Oxford Handbook of Genetic Counseling

Contributors: Deem, Michael J., editor Grubs, Robin E., editor Farrow, Emily G., editor

Availability: https://doi.org/10.1093/oxfordhb/9780190069964.001.0001

Attitudes Towards Non-directiveness Among Medical Geneticists in Germany and Switzerland

Authors: J. Eichinger B. S. Elger S. McLennan et al.

Source: J Bioeth Inq
Journal of bioethical inquiry, vol. 21, no. 4, pp. 711-722

Subject Terms: Male, Adult, 0301 basic medicine, Attitude of Health Personnel, Genetics, Medical, Beneficence, Genetic Counseling, Middle Aged, ddc, 3. Good health, Original Research, Medical ethics, Clinical decision-making, Genetic counseling, Personal autonomy, Directive counseling, Decision making, Shared, Physician-patient relations, Patient-centered care, 03 medical and health sciences, 0302 clinical medicine, Germany, Personal Autonomy, Humans, Switzerland, Genetic Counseling/ethics, Qualitative Research, Genetics, Medical/ethics, Genetic Testing/ethics, Female, Physician–patient relations, Genetic Testing

File Description: application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/39037641
https://serval.unil.ch/resource/serval:BIB_20EFA8E4A438.P001/REF.pdf
https://serval.unil.ch/notice/serval:BIB_20EFA8E4A438
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_20EFA8E4A4382
https://mediatum.ub.tum.de/1792072

Clinical Ethics and the Observant Jewish and Muslim Patient: Shared Theocentric Perspectives in Practice.

Authors: Hossain, F. Gabbay, E. Fins, J.J.

Subject Terms: WCM Library Coordinated Deposit, Islam, Humans, Jews, Religion and Medicine, Judaism, Ethics, Clinical, Genetic Counseling/ethics, Medical, Clinical Ethics, Orthodox Judaism, Religion, Religious Minorities, Religious Pluralism

File Description: application/pdf

Relation: Cambridge quarterly of healthcare ethics : CQ : the international journal of healthcare ethics committees; https://doi.org/10.1017/S0963180124000379; https://hdl.handle.net/1813/118135

Availability: https://hdl.handle.net/1813/118135

Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom

Authors: Daniele Carrieri Sandi Dheensa Shane Doheny et al.

Source: Eur J Hum Genet

Subject Terms: next generation sequencing, Duty to Recontact, 0301 basic medicine, Practice, Health Knowledge, Attitudes, Practice, 0303 health sciences, Attitude of Health Personnel, Health Knowledge, Genetic Counseling, ethics, R1, Article, United Kingdom, 3. Good health, 03 medical and health sciences, Genetic Testing/ethics, Attitudes, Humans, Genetic Testing, Genetic Counseling/ethics, recontact, clinical genetics

File Description: application/pdf; text

Access URL: https://europepmc.org/articles/pmc5315519?pdf=render
https://pubmed.ncbi.nlm.nih.gov/28051074
https://orca.cardiff.ac.uk/id/eprint/100620/1/ejhg2016188a.pdf
https://core.ac.uk/display/82959238
https://www.nature.com/articles/ejhg2016188
https://www.nature.com/articles/ejhg2016188.pdf
https://pubmed.ncbi.nlm.nih.gov/28051074/
https://ore.exeter.ac.uk/repository/handle/10871/24800
http://orca.cf.ac.uk/id/eprint/100620
https://eprints.soton.ac.uk/404354/

Ethical considerations for modern molecular pathology

Authors: Shoko Vos Paul J van Diest Margreet GEM Ausems et al.

Contributors: Shoko Vos Paul J van Diest Margreet GEM Ausems et al.

Source: The Journal of Pathology. 246:405-414

Subject Terms: 0301 basic medicine, Genetic Privacy/ethics, Genetic Counseling, Sequence Analysis, DNA/ethics, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, molecular pathology, Predictive Value of Tests, Neoplasms, Journal Article, Biomarkers, Tumor, cancer, Humans, genetics, Genetic Predisposition to Disease, Pathology, Molecular, Practice Patterns, Physicians', Genetic Privacy, DNA, Neoplasm/genetics, Genetic Counseling/ethics, Pathologists/ethics, 0303 health sciences, Informed Consent, Reproducibility of Results, personalized medicine, DNA, Neoplasm, Sequence Analysis, DNA, Informed Consent/ethics, Pathology, Molecular/ethics, ethics, Neoplasms/genetics, 3. Good health, Pathologists, Guideline Adherence/ethics, Phenotype, Practice Guidelines as Topic, Practice Patterns, Physicians'/ethics, pathology, next-generation sequencing, Guideline Adherence, Biomarkers, Tumor/genetics

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Access URL: https://pubmed.ncbi.nlm.nih.gov/30125358
https://dspace.library.uu.nl/handle/1874/388470
https://europepmc.org/article/MED/30125358
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=201802258422339550
https://www.ncbi.nlm.nih.gov/pubmed/30125358
https://www.narcis.nl/publication/RecordID/oai%3Adspace.library.uu.nl%3A1874%2F388470
https://onlinelibrary.wiley.com/doi/abs/10.1002/path.5157
https://dspace.library.uu.nl/handle/1874/388470

Childhood cancer predisposition syndromes—A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology

Authors: Thorsten Simon Stefan Rutkowski Kornelius Kerl et al.

Contributors: Thorsten Simon Stefan Rutkowski Kornelius Kerl et al.

Source: American Journal of Medical Genetics. A, Vol. 173, No 4 (2017) pp. 1017-1037

Subject Terms: 0301 basic medicine, History, Adolescent, Genetics, Medical, Medizin, Gene Expression, Genetic Counseling, History, 21st Century, Medical/history/instrumentation/methods, 03 medical and health sciences, 0302 clinical medicine, Neoplasm Proteins/genetics, Neoplasms, Genetics, Humans, Focus Groups/methods, Genetic Predisposition to Disease, genetic cancer predisposition, Genetic Testing, Child, Genetic Counseling/ethics, Societies, Medical, hereditary cancer syndrome, ddc:618, Hematologic Neoplasms/diagnosis/genetics/pathology, Syndrome, genetic screening, Focus Groups, 21st Century, Neoplasm Proteins, 3. Good health, germline mutation, Neoplasms/diagnosis/genetics/pathology, Hematologic Neoplasms, Mutation, Medical/history, Societies, Genetic Testing/methods, genetic predisposition testing

File Description: application/pdf

Access URL: https://pubmed.ncbi.nlm.nih.gov/28168833
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.38142
https://edoc.mdc-berlin.de/17114/
https://publications.rwth-aachen.de/record/706918
https://pubmed.ncbi.nlm.nih.gov/28168833/
https://www.ncbi.nlm.nih.gov/pubmed/28168833
https://mdanderson.influuent.utsystem.edu/en/publications/childhood-cancer-predisposition-syndromesa-concise-review-and-rec
https://archive-ouverte.unige.ch/unige:107412
https://resolver.sub.uni-goettingen.de/purl?gro-2/86205
https://www.ncbi.nlm.nih.gov/pubmed/28168833
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85012005135
https://doi.org/10.1002/ajmg.a.38142

Responsible implementation of expanded carrier screening

Authors: Henneman, L. Borry, P. Chokoshvili, D. et al.

Source: Eur J Hum Genet. 24(6):e1-e12

Subject Terms: Decision Making, Europe, Genetic Counseling/ethics/*psychology, Genetic Testing/ethics/*standards, Genetics, Medical/ethics/organization & administration, *Heterozygote, Humans, *Practice Guidelines as Topic, Societies, Medical, Bioetik, Bioethics

File Description: print

Access URL: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-342721

Sojourner in a foreign land.

Authors: Unger, S.

Subject Terms: Communication Barriers, Female, Genetic Counseling/ethics, Genetics, Medical/ethics, Humans, Language, Male, Pregnancy

Relation: The American Journal of Medical Genetics - Part A; https://iris.unil.ch/handle/iris/129969; serval:BIB_537E273F272E; 000383612200015

Availability: https://iris.unil.ch/handle/iris/129969
https://doi.org/10.1002/ajmg.a.37738

Familial glioma

Authors: Bazzoni, Riccardo Bentivegna, Angela School of Medicine and Surgery, University of Milan-Bicocca, via Cadore, Monza, Italy (RB,AB) et al.

Contributors: Bazzoni, Riccardo Bentivegna, Angela School of Medicine and Surgery, University of Milan-Bicocca, via Cadore, Monza, Italy (RB,AB) et al.

Subject Terms: familial glioma, glioma, Kprones Section, Alleles, Brain Neoplasms/classification/*genetics, Gene Expression Regulation, Neoplastic, Genetic Predisposition to Disease/*genetics, Genome-Wide Association Study/*methods, Genotype, Glioblastoma/classification/*genetics, Glioma/classification/*genetics, Humans, Meta-Analysis as Topic, Polymorphism, Single Nucleotide, Quantitative Trait Loci/genetics, Adolescent, Child, Focus Groups/methods, Gene Expression, Genetic Counseling/ethics, Genetic Predisposition to Disease

Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Kprones/FamilialGliomaID10123.html; Riccardo, Bazzoni; Angela, Bentivegna. Familial glioma. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 6, p. 159-167; http://hdl.handle.net/2042/70461; https://doi.org/10.4267/2042/70461

Availability: http://hdl.handle.net/2042/70461
https://doi.org/10.4267/2042/70461

Reprogenetics, reproductive risks and cultural awareness: what may we learn from Israeli and Croatian medical students?

Authors: Miriam Ethel Bentwich Michal Mashiach-Eizenberg Ana Borovečki et al.

Source: BMC Med Ethics
BMC Medical Ethics, Vol 20, Iss 1, Pp 1-11 (2019)

Subject Terms: Adult, Male, 0301 basic medicine, Genetic Counseling / ethics, Genetic Research, Health Knowledge, Attitudes, Practice, Students, Medical, Reproductive Techniques, Assisted, Medical philosophy. Medical ethics, Croatia, Genetic Counseling, Preimplantation Diagnosis / ethics, Young Adult, 03 medical and health sciences, Cultural awareness, Genetic Testing / ethics, Humans, Reproductive Techniques, Assisted / ethics, Genetic Testing, Prospective Studies, Cultural Competency, Israel, Preimplantation Diagnosis, 0303 health sciences, R723-726, 4. Education, Students, Medical / psychology, 1. No poverty, Cultural Diversity, Awareness, Medical students, Reprogenetics, 3. Good health, Socioeconomic Factors, Attitudes, Genetic Research / ethics, Female, Research Article

File Description: application/pdf

Access URL: https://bmcmedethics.biomedcentral.com/track/pdf/10.1186/s12910-019-0427-1
https://pubmed.ncbi.nlm.nih.gov/31771574
https://doaj.org/article/e8f136cac5434a178c5a191679b9a6fb
https://pubmed.ncbi.nlm.nih.gov/31771574/
https://link.springer.com/content/pdf/10.1186/s12910-019-0427-1.pdf
https://repozitorij.mef.unizg.hr/islandora/object/mef%3A2713
https://repozitorij.unizg.hr/islandora/object/mef:2713/datastream/FILE0/download
https://www.bib.irb.hr/1035201
https://link.springer.com/article/10.1186/s12910-019-0427-1
https://urn.nsk.hr/urn:nbn:hr:105:084459
https://doi.org/10.1186/s12910-019-0427-1

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics

Authors: Carrieri, Daniele Howard, Heidi, C Benjamin, Caroline et al.

Contributors: Carrieri, Daniele Howard, Heidi, C Benjamin, Caroline et al.

Source: ISSN: 1018-4813.

Subject Terms: MESH: Duty to Recontact, MESH: European Union, MESH: Societies, Medical / standards, MESH: Genetic Counseling / ethics, MESH: Genetic Counseling / legislation & jurisprudence, MESH: Genetic Counseling / standards, MESH: Genetic Testing / ethics, MESH: Genetic Testing / legislation & jurisprudence, MESH: Genetic Testing / standards, MESH: Humans, MESH: Practice Guidelines as Topic, [SDV]Life Sciences [q-bio]

Relation: info:eu-repo/semantics/altIdentifier/pmid/30310124; PUBMED: 30310124; PUBMEDCENTRAL: PMC6336881

Availability: https://ut3-toulouseinp.hal.science/hal-04675046
https://ut3-toulouseinp.hal.science/hal-04675046v1/document
https://ut3-toulouseinp.hal.science/hal-04675046v1/file/CARRERI_2019.pdf
https://doi.org/10.1038/s41431-018-0285-1

Caracterización de los Servicios de Asesoramiento Genético en San Juan y Martínez ; Characterization of Genetic Counseling in San Juan y Martínez

Authors: Hernández Fernández, Anabel Chagimes Batista, Yadira Licourt Otero, Deysi et al.

Source: Revista de ciencias médicas de Pinar del Río; Vol. 17, No. 2 (2013); 58-68 ; 1561-3194

Subject Terms: Asesoramiento genético/ética, Genética, Genetic counseling/ethics, Genetics

File Description: text/html; application/pdf

Relation: https://revcmpinar.sld.cu/index.php/publicaciones/article/view/594/html; https://revcmpinar.sld.cu/index.php/publicaciones/article/view/594/pdf; Colectivo de autores. Por la vida. Estudio psicosocial de las personas con discapacidades y estudio psicopedagógico, social y clínico-genético de las personas con retraso mental en Cuba. La Habana: Casa Editora Abril; 2003. 2. Guido LL. Taller Internacional de Centros Colaboradores OMS e Instituciones de Excelencia Científica. Cuba: MINSAP; 2006. 3. Offiah A, Alman B, Cornie A, Giampietro P, Tassy O, Wade A. Pilot assessment of a radiologic classification system for segmentation defects of the vertebrae. American Journal of Medical Genetics. 2010; 152(6): 1357-1371. 4. Hunter A, Collins J, Deardorff M, Frantz I. Detailed assessment of the ear in Cornelia de Lange syndrome: Comparison with a control sample using the new dysmorphology guidelines. American Journal of Medical Genética. 2009; 149(10): 2181-2192. 5. Morales E. Comunicación personal. Conferencia sobre Asesoramiento Genético. Centro Nacional de Genética Médica, 2006. 6. Rojas Betancourt IA. Prevención de las enfermedades genéticas y asesoramiento genético. En: Lantigua Cruz A. Introducción a la genética médica. La Habana: Editorial Ciencias Médicas; 2004.p. 240-269. 7. Casagrandi Casanova D, Zaldívar Vaillant T, Nodarse Rodríguez A, Carballo Casas S. Algunos aspectos éticos del diagnóstico prenatal, la medicina y terapia fetales. Rev Cubana Obstet Ginecol [revista en la Internet]. 2005 Dic [citado 2009 Oct 24]; 31(3): Disponible en: http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0138-600X2005000300010&lng=es 8. Martín Ruiz MR, Lemus Valdés MT, Marcheco Teruel B. El programa cubano de prevención de Anemia Falciforme. Resultados del período 1990-2005. Rev. Cubana Genet Comunit. [Internet] 2008 [citado 2009 Abr 11]; 2(2): p. 59-66. Disponible en: http://www.bvs.sld.cu/revistas/rcgc/v2n2/PDFs%20Infomed/rcgc10208.pdf 9. Martín Ruiz MR, Duania Frómeta E, Domínguez Mena M, Alfonso Díaz K, Santana Hernández ME, Viñales Pedraza MI. Anemia Falciforme: Conocimiento y percepción actual del riesgo en jóvenes detectados al nacimiento como portadores sanos. Rev. Cubana Genet Comunit. [Internet] 2008 [citado 2009 Abr 11]; 2(3): 44-51. Disponible en: http://www.bvs.sld.cu/revistas/rcgc/v2n3/PDFs%20Infomed/rcgc09308.pdf 10. Lantigua Cruz A, Lemus Valdés MT, Marcheco Teruel. Medical genetics services in Cuba. Rev. Cubana Genet Comunit. [Internet] 2007 [citado 2009 Abr 11]; 1(1): 15-9. Disponible en: http://www.sld.cu/galerias/pdf/sitios/genetica/gco02107.pdf 11. Martín Ruiz MR, Casa Buchillón. Conocimientos sobre Sicklemia y riesgo genético en portadores sanos que habían recibido AG. Rev. Habanera Ciencias Médicas. [Internet] 2006 [citado 2009 Abr 11]; 5(4). Disponible en: http://bvs.sld.cu/revistas/rhab/vol5_num4/rhcm09406.htm 12. Corbella A, Saturno P. La garantía de la calidad en atención primaria de salud. Madrid: Instituto Nacional de Salud, Secretaría General; 1990. p. 397-399. 13. Li Y, Steinberg A, Bain L, Yaeger D, Bieler A, Ewing R, et al. Assessing parental attitudes toward genetic testing for childhood hearing loss: Before and after genetic consultation. American Journal of Medical Genetics. 2007; 143(14): 1546-1553. 14. Falcón Y. Estrategia para la excelencia en el asesoramiento genético en el municipio Pinar del Río. Tesis para optar por el título académico en máster en Asesoramiento Genérico. Ciudad de La Habana: CNGM; 2009. 15. Hernández MJ. Estrategia para la excelencia del asesoramiento genético en el municipio Cabaiguán. Tesis para optar por el título académico en máster en Asesoramiento Genético. Ciudad de La Habana: CNGM; 2008. 16. Ajete RM. Estrategia para la excelencia en el asesoramiento genético en el municipio Sandino. Tesis para optar por el título académico en máster en Asesoramiento Genético. Ciudad de la Habana: CNGM; 2007. 17. Capote N. Estrategia para la excelencia en el asesoramiento genético en el municipio Pinar del Río. Tesis para optar por el título académico en máster en Asesoramiento Genético. Ciudad de la Habana: CNGM; 2007. 18. Nissell A, Forbes R, Bankier A, Hughes E, Aitken MA. Consumer contribution to the delivery of genetic health services. American Journal of Medical Genetics. [Internet]. 2008 [Citado 20 de mayo de 2011]; 146(17): [Aprox.8p.]. Disponible en: http://www.ncbi.nlm.nih.gov/pubmed/18697195 19. McAllister M, Davies L, Payne K, Nicholls S, Donnai D, MacLeod R. The emotional effects of genetic diseases: Implications for clinical genetics. American Journal of Medical Genetics. 2007; 143(22): 2651-2661.; https://revcmpinar.sld.cu/index.php/publicaciones/article/view/594

Availability: https://revcmpinar.sld.cu/index.php/publicaciones/article/view/594

More symptoms than earlier known caused by the disease gene. New discoveries about the fragile X syndrome complicate genetic counseling / Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt. Nya rön om fragil X-syndromet komplicerar genetisk vägledning

Authors: Kristoffersson, U Wahlström, J Lynöe, N

Source: Läkartidningen. 102(44):3232

Ethical considerations for modern molecular pathology

Authors: Vos, Shoko van Diest, Paul J Ausems, Margreet G E M et al.

Contributors: Vos, Shoko van Diest, Paul J Ausems, Margreet G E M et al.

Subject Terms: genetics, pathology, next-generation sequencing, cancer, ethics, molecular pathology, personalized medicine, Predictive Value of Tests, Genetic Privacy/ethics, Humans, Neoplasms/genetics, Biomarkers, Tumor/genetics, Genetic Predisposition to Disease, Reproducibility of Results, Informed Consent/ethics, Pathologists/ethics, Practice Patterns, Physicians'/ethics, DNA, Neoplasm/genetics, Phenotype, Guideline Adherence/ethics, Genetic Counseling/ethics, Molecular/ethics, Sequence Analysis, DNA/ethics, Practice Guidelines as Topic, Pathology and Forensic Medicine, Journal Article

File Description: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/388470

Availability: https://dspace.library.uu.nl/handle/1874/388470

Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology

Authors: Ripperger, Tim Bielack, Stefan S Borkhardt, Arndt et al.

Source: ISSN: 1552-4825 ; American Journal of Medical Genetics. A, vol. 173, no. 4 (2017) p. 1017-1037.

Subject Terms: info:eu-repo/classification/ddc/618, Adolescent, Child, Focus Groups/methods, Gene Expression, Genetic Counseling/ethics, Genetic Predisposition to Disease, Genetic Testing/methods, Genetics, Medical/history/instrumentation/methods, Hematologic Neoplasms/diagnosis/genetics/pathology, History, Humans, Mutation, Neoplasm Proteins/genetics, Neoplasms/diagnosis/genetics/pathology, Societies, Medical/history, Syndrome

Time: 21st Century

Relation: info:eu-repo/semantics/altIdentifier/pmid/28168833; unige:107412

Availability: https://archive-ouverte.unige.ch/unige:107412

Ethical, legal, and counseling challenges surrounding the return of genetic results in oncology

Authors: Lolkema, Martijn P Gadellaa-van Hooijdonk, Christa G Bredenoord, Annelien L et al.

Source: Journal of Clinical Oncology. 31(15):1842-1848

Subject Terms: Confidentiality/ethics, Genetic Testing/ethics, Medical Oncology/ethics, Genetic Predisposition to Disease/genetics, Mutation, Humans, Disclosure/ethics, Genetic Counseling/ethics, Neoplasms/genetics

Access URL: https://hdl.handle.net/11370/d641f49c-af25-4639-88fb-c05618372a11
https://research.rug.nl/en/publications/d641f49c-af25-4639-88fb-c05618372a11

Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt

Authors: Kristoffersson, Ulf Wahlstrom, Jan Lynoe, Niels

Source: Läkartidningen; 102(44), pp 3232-3236 (2005) ; ISSN: 0023-7205

Subject Terms: Medical Genetics and Genomics (including Gene Therapy), Adult, Child, Consensus, English Abstract, Female, Fragile X Mental Retardation Protein: genetics, Fragile X Syndrome: genetics, Genetic Counseling: ethics, Genetic Screening: ethics, Humans, Male, Middle Aged, Nerve Tissue Proteins: genetics, Risk Factors

Relation: https://lup.lub.lu.se/record/148904; scopus:27744471927

Availability: https://lup.lub.lu.se/record/148904