List of works - Julianne M O'Daniel

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

scientific article published on 13 August 2015

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.

scientific article published on 28 April 2016

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.

scientific article

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

scientific article (publication date: July 2013)

Approaching Complex Cases With a Crisis Intervention Model and Teamwork

scientific article published on 01 October 2002

Correction: Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

scientific article published on 01 December 2019

Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design

scientific article

Engaging community stakeholders in research on best practices for clinical genomic sequencing

scientific article published on 07 October 2020

Enhancing geneticists' perspectives of the public through community engagement.

scientific article

Genetic library: genetics and public health

scientific article published on 01 June 2004

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

scientific article published on 15 March 2021

Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

scientific article published on 17 July 2019

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.

scientific article

Is "incidental finding" the best term?: a study of patients' preferences

scientific article published on 04 August 2016

Professional perspectives about pharmacogenetic testing and managing ancillary findings

scientific article published on 19 July 2011

Promoting public awareness and engagement in genome sciences.

scientific article

Public perspectives about pharmacogenetic testing and managing ancillary findings

scientific article published on 2 November 2011

Secondary findings: How did we get here, and where are we going?

scientific article published on 01 March 2019

TRIG on TRACK: educating pathology residents in genomic medicine

scientific article published on 01 May 2012

The prospect of genome-guided preventive medicine: a need and opportunity for genetic counselors

scientific article published on 04 May 2010

Whole-genome and whole-exome sequencing in hereditary cancer: impact on genetic testing and counseling

scientific article published on July 1, 2012

List of works by Julianne M O'Daniel

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.

A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories.

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Approaching Complex Cases With a Crisis Intervention Model and Teamwork

Correction: Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design

Engaging community stakeholders in research on best practices for clinical genomic sequencing

Enhancing geneticists' perspectives of the public through community engagement.

Genetic library: genetics and public health

Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium

Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.

Is "incidental finding" the best term?: a study of patients' preferences

Professional perspectives about pharmacogenetic testing and managing ancillary findings

Promoting public awareness and engagement in genome sciences.

Public perspectives about pharmacogenetic testing and managing ancillary findings

Secondary findings: How did we get here, and where are we going?

TRIG on TRACK: educating pathology residents in genomic medicine

The prospect of genome-guided preventive medicine: a need and opportunity for genetic counselors

Whole-genome and whole-exome sequencing in hereditary cancer: impact on genetic testing and counseling