P H Birch. Clin Genet 2015
Times Cited: 26
Times Cited: 26
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Patricia Birch, S Adam, N Bansback, R R Coe, J Hicklin, A Lehman, K C Li, J M Friedman. J Genet Couns 2016
47
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
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19
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
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15
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15
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Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.
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15
15
Communicating genetic risk information for common disorders in the era of genomic medicine.
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30
Choices for return of primary and secondary genomic research results of 790 members of families with Mendelian disease.
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21
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11
Molecular findings among patients referred for clinical whole-exome sequencing.
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11
Return of incidental findings in genomic medicine: measuring what patients value--development of an instrument to measure preferences for information from next-generation testing (IMPRINT).
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11
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11
Intentions to receive individual results from whole-genome sequencing among participants in the ClinSeq study.
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11
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Effects of informed consent for individual genome sequencing on relevant knowledge.
K A Kaphingst, F M Facio, M-R Cheng, S Brooks, H Eidem, A Linn, B B Biesecker, L G Biesecker. Clin Genet 2012
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13
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16
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12
Impact of delivery models on understanding genomic risk for type 2 diabetes.
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20
Models of service delivery for cancer genetic risk assessment and counseling.
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11
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11
Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance.
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Sampling in qualitative research. Purposeful and theoretical sampling; merging or clear boundaries?
I T Coyne. J Adv Nurs 1997
I T Coyne. J Adv Nurs 1997
11
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial.
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33
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7
Disclosure of APOE genotype for risk of Alzheimer's disease.
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7
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7
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7
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7
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15
An interactive computer program can effectively educate patients about genetic testing for breast cancer susceptibility.
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7
Models of consent to return of incidental findings in genomic research.
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7
Teaching genomic counseling: preparing the genetic counseling workforce for the genomic era.
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7
Informed consent for whole-genome sequencing studies in the clinical setting. Proposed recommendations on essential content and process.
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7
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7
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.