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science & technology (28) 28
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1. Full Text Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
by Hart, M. Ragan and Biesecker, Barbara B and Blout, Carrie L and Christensen, Kurt D and Amendola, Laura M and Bergstrom, Katie L and Biswas, Sawona and Bowling, Kevin M and Brothers, Kyle B and Conlin, Laura K and Cooper, Greg M and Dulik, Matthew C and East, Kelly M and Everett, Jessica N and Finnila, Candice R and Ghazani, Arezou A and Gilmore, Marian J and Goddard, Katrina A. B and Jarvik, Gail P and Johnston, Jennifer J and Kauffman, Tia L and Kelley, Whitley V and Krier, Joel B and Lewis, Katie L and McGuire, Amy L and McMullen, Carmit and Ou, Jeffrey and Plon, Sharon E and Rehm, Heidi L and Richards, C. Sue and Romasko, Edward J and Miren Sagardia, Ane and Spinner, Nancy B and Thompson, Michelle L and Turbitt, Erin and Vassy, Jason L and Wilfond, Benjamin S and Veenstra, David L and Berg, Jonathan S and Green, Robert C and Biesecker, Leslie G and Hindorff, Lucia A
Genetics in medicine, ISSN 1098-3600, 05/2019, Volume 21, Issue 5, pp. 1100 - 1110
genomic sequencing | health-care resource utilization | secondary findings | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Prevalence | Genetic Testing - standards | Humans | Incidental Findings | Male | Genetic Testing - ethics | Disclosure | Health Knowledge, Attitudes, Practice | Patients | High-Throughput Nucleotide Sequencing - ethics | Exome | Health Care Costs | Decision Making - ethics | Health Personnel | Adult | Female | Intention | Whole Genome Sequencing - economics | Genetic Testing - economics | Genomics - methods | Whole Genome Sequencing - ethics | Consortia | Index Medicus
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2. Full Text Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
by Hart, M Ragan and Biesecker, Barbara B and Blout, Carrie L and Christensen, Kurt D and Amendola, Laura M and Bergstrom, Katie L and Biswas, Sawona and Bowling, Kevin M and Brothers, Kyle B and Conlin, Laura K and Cooper, Greg M and Dulik, Matthew C and East, Kelly M and Everett, Jessica N and Finnila, Candice R and Ghazani, Arezou A and Gilmore, Marian J and Goddard, Katrina A B and Jarvik, Gail P and Johnston, Jennifer J and Kauffman, Tia L and Kelley, Whitley V and Krier, Joel B and Lewis, Katie L and McGuire, Amy L and McMullen, Carmit and Ou, Jeffrey and Plon, Sharon E and Rehm, Heidi L and Richards, C Sue and Romasko, Edward J and Sagardia, Ane Miren and Spinner, Nancy B and Thompson, Michelle L and Turbitt, Erin and Vassy, Jason L and Wilfond, Benjamin S and Veenstra, David L and Berg, Jonathan S and Green, Robert C and Biesecker, Leslie G and Hindorff, Lucia A
Genetics in medicine, ISSN 1098-3600, 05/2019, Volume 21, Issue 5, pp. 1261 - 1262
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3. Full Text Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium
by Amendola, Laura M and Robinson, Jill O and Hart, Ragan and Biswas, Sawona and Lee, Kaitlyn and Bernhardt, Barbara A and East, Kelly and Gilmore, Marian J and Kauffman, Tia L and Lewis, Katie L and Roche, Myra and Scollon, Sarah and Wynn, Julia and Blout, Carrie
Journal of genetic counseling, ISSN 1059-7700, 10/2018, Volume 27, Issue 5, pp. 1220 - 1227
Human Genetics | Rate of decline | Ethics | Public Health | Biomedicine | Genome sequencing | Gynecology | Reason for decline | Exome sequencing | Clinical Psychology | Clinical Sequencing Exploratory Research (CSER) consortium | Social Sciences | Life Sciences & Biomedicine | Social Sciences, Biomedical | Health Care Sciences & Services | Health Policy & Services | Genetics & Heredity | Biomedical Social Sciences | Science & Technology | Genetic research | Medicine, Experimental | Medical research | Analysis | Genomics | Health care | Participation | Decision making | Enrollments | Data processing | Clinical research | Research | Genetic screening | Recruitment | Studies | Consortia | Privacy | Discrimination | Barriers | Informed consent | Aggregate level data | Genetic factors | Index Medicus
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4. Full Text Recommended care and care adherence following a diagnosis of Lynch syndrome: a mixed-methods study
by Mittendorf, Kathleen F and Hunter, Jessica Ezzell and Schneider, Jennifer L and Shuster, Elizabeth and Rope, Alan F and Zepp, Jamilyn and Gilmore, Marian J and Muessig, Kristin R and Davis, James V and Kauffman, Tia L and Bergen, Kellene M and Wiesner, Georgia L and Acheson, Louise S and Peterson, Susan K and Syngal, Sapna and Reiss, Jacob A and Goddard, Katrina A. B
Hereditary cancer in clinical practice, ISSN 1731-2302, 12/2019, Volume 17, Issue 1, pp. 31 - 31
Life Sciences & Biomedicine | Oncology | Science & Technology | Codes | Colorectal carcinoma | Malignancy | Family medical history | Medical diagnosis | Patients | Electronic medical records | Studies | Genetic counseling | Surveillance | Colonoscopy | Data collection | Genetics | Diagnosis | Interviews | Cancer | Adherence | Hereditary Cancer | Risk reduction | Lynch syndrome
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5. Full Text Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing
by Gilmore, Marian J and Schneider, Jennifer and Davis, James V and Kauffman, Tia L and Leo, Michael C and Bergen, Kellene and Reiss, Jacob A and Himes, Patricia and Morris, Elissa and Young, Carol and McMullen, Carmit and Wilfond, Benjamin S and Goddard, Katrina A.B
Journal of genetic counseling, ISSN 1059-7700, 10/2017, Volume 26, Issue 5, pp. 971 - 979
Human Genetics | Qualitative research | Public Health | Reproductive decisions | Genome sequencing | Genomic medicine | Gynecology | Preconception expanded carrier screening | Clinical Psychology | Declining genetic testing | Ethics | Patient testing decisions | Biomedicine | Social Sciences | Life Sciences & Biomedicine | Social Sciences, Biomedical | Health Care Sciences & Services | Health Policy & Services | Genetics & Heredity | Biomedical Social Sciences | Science & Technology | Decision Making | Family Planning Services - methods | Genetic Counseling - psychology | Humans | Genetic Counseling - methods | Adult | Female | Male | Preconception Care - methods | Surveys and Questionnaires | Genetic Testing - methods | Genetic Carrier Screening - methods | Health maintenance organizations | Genes | Genomics | Medical genetics | Bioethics | Genomes | Nucleotide sequencing | Medical screening | Genetic screening | DNA sequencing | Women | Uptake | Randomized controlled trials | Carriers | Screening | Variants | Risk assessment | Anxiety | Opting out | Index Medicus
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6. Full Text A review and definition of ‘usual care’ in genetic counseling trials to standardize use in research
by Biesecker, Barbara B and Lillie, Sarah E and Amendola, Laura M and Donohue, Katherine E and East, Kelly M and Foreman, Ann Katherine M and Gilmore, Marian J and Greve, Veronica and Liangolou, Billie and O'Daniel, Julianne M and Odgis, Jacqueline A and Rego, Shannon and Rolf, Bradley and Scollon, Sarah and Suckiel, Sabrina A and Zepp, Jamilyn and Joseph, Galen
Journal of genetic counseling, ISSN 1059-7700, 02/2021, Volume 30, Issue 1, pp. 42 - 50
genetic counseling interventions | genetic counseling research | randomized controlled trials | usual care | Social Sciences | Life Sciences & Biomedicine | Social Sciences, Biomedical | Health Care Sciences & Services | Health Policy & Services | Genetics & Heredity | Biomedical Social Sciences | Science & Technology | Genetic susceptibility | Generalizability | Standardization | Clinical trials | Clinical research | Research | Clinical outcomes | Risk factors | Randomized controlled trials | Genetic counseling | Risk assessment | Counseling | Genetic counselling | Clinical standards | Index Medicus
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7. Full Text Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing
by Lynch, Frances L and Himes, Patricia and Gilmore, Marian J and Morris, Elissa M and Schneider, Jennifer L and Kauffman, Tia L and Shuster, Elizabeth and Reiss, Jacob A and Dickerson, John F and Leo, Michael C and Davis, James V and McMullen, Carmit K and Wilfond, Benjamin S and Goddard, Katrina A.B
Journal of genetic counseling, ISSN 1059-7700, 8/2018, Volume 27, Issue 4, pp. 823 - 833
Human Genetics | Time study | Ethics | Public Health | Biomedicine | Genetic counseling | Whole genome sequencing | Mixed methods | Gynecology | Clinical Psychology | Preconception | Carrier testing | Social Sciences | Life Sciences & Biomedicine | Social Sciences, Biomedical | Health Care Sciences & Services | Health Policy & Services | Genetics & Heredity | Biomedical Social Sciences | Science & Technology | Health maintenance organizations | Analysis | Genomics | Medical genetics | Genomes | Nucleotide sequencing | DNA sequencing | Time use | Case conferences | Individualized | Disclosure | Medical screening | Genetic screening | Carriers | Screening | Health care expenditures | Technology | Counseling | Workloads | Cost analysis | Genetic counselling | Index Medicus | Original Research
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8. Full Text “Is It Worth Knowing?” Focus Group Participants’ Perceived Utility of Genomic Preconception Carrier Screening
by Schneider, Jennifer L and Goddard, Katrina A. B and Davis, James and Wilfond, Benjamin and Kauffman, Tia L and Reiss, Jacob A and Gilmore, Marian and Himes, Patricia and Lynch, Frances L and Leo, Michael C and McMullen, Carmit
Journal of genetic counseling, ISSN 1059-7700, 02/2016, Volume 25, Issue 1, pp. 135 - 145
Decision‐making | Qualitative research | Whole genome sequencing | Barriers and facilitators | Focus groups | Patient perspectives | Genomic preconception carrier screening | Decision-making | Social Sciences | Life Sciences & Biomedicine | Social Sciences, Biomedical | Health Care Sciences & Services | Health Policy & Services | Genetics & Heredity | Biomedical Social Sciences | Science & Technology | Decision Making | Genetic Counseling - psychology | Genetic Testing | Attitude to Health | Genomics | Humans | Focus Groups | Preimplantation Diagnosis - psychology | Male | Parents - psychology | Counseling | Adult | Female | Preconception Care | Health maintenance organizations | Analysis | Bioethics | Market research | Nucleotide sequencing | DNA sequencing | Decision making | Necessity | Perceptions | Genomes | Medical screening | Counselling | Genetic screening | Carriers | Fear | Screening | Genetic counseling | Consent | Technology | Genetic analysis | Anxiety | Genetic factors | Index Medicus | Original Research
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9. Full Text Stakeholder perspectives on implementing a universal Lynch syndrome screening program: A qualitative study of early barriers and facilitators
by Schneider, Jennifer L and Davis, James and Kauffman, Tia L and Reiss, Jacob A and Mcginley, Cheryl and Arnold, Kathleen and Zepp, Jamilyn and Gilmore, Marian and Muessig, Kristin R and Syngal, Sapna and Acheson, Louise and Wiesner, Georgia L and Peterson, Susan K and Goddard, Katrina A. B
Genetics in medicine, ISSN 1098-3600, 02/2016, Volume 18, Issue 2, pp. 152 - 161
implementation factors | stakeholder interviews | universal Lynch syndrome screening | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Mass Screening | Health Surveys | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Humans | Health Planning | Female | Interviews as Topic | Male | Index Medicus | universal lynch syndrome screening
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10. Full Text Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model
by Riddle, Leslie and Amendola, Laura M and Gilmore, Marian J and Guerra, Claudia and Biesecker, Barbara and Kauffman, Tia L and Anderson, Katherine and Rope, Alan F and Leo, Michael C and Caruncho, Mikaella and Jarvik, Gail P and Wilfond, Benjamin and Goddard, Katrina A B and Joseph, Galen
Patient education and counseling, ISSN 0738-3991, 12/2020
Nursing
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11. Full Text Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting
by Clarke, Elizabeth V and Muessig, Kristin R and Zepp, Jamilyn and Hunter, Jessica E and Syngal, Sapna and Acheson, Louise S and Wiesner, Georgia L and Peterson, Susan K and Bergen, Kellene M and Shuster, Elizabeth and Davis, James V and Schneider, Jennifer L and Kauffman, Tia L and Gilmore, Marian J and Reiss, Jacob A and Rope, Alan F and Cook, Jennifer E and Goddard, Katrina A. B
Familial cancer, ISSN 1389-9600, 07/2019, Volume 18, Issue 3, pp. 317 - 325
Genetics | Colorectal cancer (CRC) | DNA mismatch repair (MMR) genes | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Genetic Testing - statistics & numerical data | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Humans | Middle Aged | Mass Screening - organization & administration | Mass Screening - statistics & numerical data | Male | MutS Homolog 2 Protein - genetics | Referral and Consultation - statistics & numerical data | DNA-Binding Proteins - genetics | Program Development | Referral and Consultation - organization & administration | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | MutL Protein Homolog 1 - genetics | Female | Aged | Mismatch Repair Endonuclease PMS2 - genetics | Prevention | Health maintenance organizations | Medical records | Medical colleges | Colorectal cancer | Cancer | Statistical analysis | Medical diagnosis | Medical screening | Colorectal carcinoma | Tumors | Index Medicus | colorectal cancer (CRC)
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