| scholarly article | Q13442814 |
| P2093 | author name string | Debra Skinner | |
| Martha King | |||
| Kelly A Raspberry | |||
| P2860 | cites work | Evolving approaches to the ethical management of genomic data | Q24618993 |
| Recommendations for returning genomic incidental findings? We need to talk! | Q26995124 | ||
| ClinGen--the Clinical Genome Resource | Q28648173 | ||
| Guidelines for investigating causality of sequence variants in human disease | Q28655218 | ||
| Characterizing genetic variants for clinical action | Q28655937 | ||
| ACMG clinical laboratory standards for next-generation sequencing | Q33903280 | ||
| Translating personalized medicine using new genetic technologies in clinical practice: the ethical issues | Q34159801 | ||
| Negotiating desires and options: how mothers who carry the fragile X gene experience reproductive decisions | Q34762304 | ||
| Clinical exome sequencing for genetic identification of rare Mendelian disorders | Q34782655 | ||
| Molecular findings among patients referred for clinical whole-exome sequencing | Q35078373 | ||
| Flexible positions, managed hopes: the promissory bioeconomy of a whole genome sequencing cancer study | Q35187045 | ||
| Point-counterpoint. Patient autonomy and incidental findings in clinical genomics | Q37040336 | ||
| ClinVar: public archive of relationships among sequence variation and human phenotype | Q37661886 | ||
| Clinical exome sequencing in daily practice: 1,000 patients and beyond | Q37689764 | ||
| Parental beliefs about cause and course of their child's autism and outcomes of their beliefs: a review of the literature | Q37774654 | ||
| The sociology of medical screening: past, present and future | Q37988596 | ||
| The chromosome 22q11.2 deletion: from the unification of biomedical fields to a new kind of genetic condition | Q38032624 | ||
| Opportunities and challenges associated with clinical diagnostic genome sequencing: a report of the Association for Molecular Pathology. | Q38037294 | ||
| Informatics and clinical genome sequencing: opening the black box. | Q38043287 | ||
| Diagnostic clinical genome and exome sequencing | Q38221192 | ||
| Managing the ethical challenges of next-generation sequencing in genomic medicine | Q38239811 | ||
| Expanded newborn screening: articulating the ontology of diseases with bridging work in the clinic | Q38500677 | ||
| Who's to blame? Accounts of genetic responsibility and blame among Ashkenazi Jewish women at risk of BRCA breast cancer. | Q39662596 | ||
| Experiencing the genetic body: parents' encounters with pediatric clinical genetics | Q40162824 | ||
| Accommodating risk: responses to BRCA1/2 genetic testing of women who have had cancer. | Q40510267 | ||
| Kinscapes, timescapes and genescapes: families living with genetic risk | Q45788612 | ||
| Towards a sociology of diagnosis: reflections and opportunities | Q48605146 | ||
| Trust in standards: transitioning clinical exome sequencing from bench to bedside. | Q53567206 | ||
| Eclipse of the Gene and the Return of Divination | Q57632742 | ||
| Genome-scale sequencing in clinical care: establishing molecular diagnoses and measuring value | Q64049894 | ||
| Regulating diagnosis in post-genomic medicine: re-aligning clinical judgment? | Q64953912 | ||
| Diagnosis, dysmorphology, and the family: knowledge, motility, choice | Q80238114 | ||
| Making genetics not so important: family work in dealing with familial hypertrophic cardiomyopathy | Q84568300 | ||
| Constructing Grounded Theory: A practical guide through qualitative analysis | Q88480597 | ||
| P433 | issue | 8 | |
| P304 | page(s) | 1303-1317 | |
| P577 | publication date | 2016-08-19 | |
| P1433 | published in | Sociology of Health and Illness | Q7552840 |
| P1476 | title | The nuanced negative: Meanings of a negative diagnostic result in clinical exome sequencing | |
| P478 | volume | 38 |
| Q55089341 | "Possibly positive or certainly uncertain?": participants' responses to uncertain diagnostic results from exome sequencing. |
| Q38754326 | "Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD. |
| Q55074639 | Clinical providers' experiences with returning results from genomic sequencing: an interview study. |
| Q92380881 | Development and mixed-methods evaluation of an online animation for young people about genome sequencing |
| Q47278375 | Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact |
| Q90679190 | Diagnostic utility of transcriptome sequencing for rare Mendelian diseases |
| Q38993360 | Expert Knowledge Influences Decision-Making for Couples Receiving Positive Prenatal Chromosomal Microarray Testing Results. |
| Q91937762 | Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes |
| Q41686977 | How do providers discuss the results of pediatric exome sequencing with families? |
| Q92133078 | Parents' perceptions of personal utility of exome sequencing results |
| Q97569110 | Patient reactions to receiving negative genomic screening results by mail |
| Q47664781 | Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? |
| Q57163463 | Return of individual results in epilepsy genomic research: A view from the field |
| Q57178162 | Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies |
| Q49933290 | The Actionability of Exome sequencing testing results |
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