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List of works by Julia Wynn

23andMe Paves the Way for Direct-to-Consumer Genetic Health Risk Tests of Limited Clinical Utility

scientific article published on 30 May 2017

A definition of gentle ventilation in congenital diaphragmatic hernia: a survey of neonatologists and pediatric surgeons

scientific article published on 28 January 2017

A qualitative study of Latinx parents' experiences of clinical exome sequencing

scientific article published on 16 April 2020

Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force

scientific article published on 23 September 2020

Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research

scientific article published on 17 January 2015

Brief Report: SETD2 Mutation in a Child with Autism, Intellectual Disabilities and Epilepsy

scientific article

Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals

scientific article published on 07 May 2020

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

scientific article

Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine

article

Clinical providers' experiences with returning results from genomic sequencing: an interview study.

scientific article

Comparative outcomes of right versus left congenital diaphragmatic hernia: A multicenter analysis

scientific article published on 26 October 2019

Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

scientific article published on August 2017

Correction: Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study

scientific article published on 01 October 2019

De novo copy number variants are associated with congenital diaphragmatic hernia

scientific article published on October 2012

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

scientific article published on 10 December 2018

Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias

scientific article published on 25 August 2020

Developing effective and efficient genomic educational tools for our diverse population

scientific article published on 01 December 2019

Developmental outcomes of children with congenital diaphragmatic hernia: a multicenter prospective study.

scientific article published on October 2013

Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact

scientific article published on 20 December 2017

Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience

scientific article

Ethical conflicts in translational genetic research: lessons learned from the eMERGE-III experience

scientific article published on 18 June 2020

Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study

scientific article published on 01 April 2019

Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies.

scientific article

GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing

scientific article published on 26 December 2020

Genetic causes of congenital diaphragmatic hernia

scientific article

Genome-wide enrichment of damaging de novo variants in patients with isolated and complex congenital diaphragmatic hernia.

scientific article published on 16 March 2017

Genomic Testing: a Genetic Counselor's Personal Reflection on Three Years of Consenting and Testing.

scientific article

Illustrative case studies in the return of exome and genome sequencing results

scientific article

Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients

scientific article

Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study

scientific article

Impact of patient education videos on genetic counseling outcomes after exome sequencing

scientific article published on 24 August 2019

Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia

scientific article published in June 2015

Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes

scientific article published on 28 July 2020

Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defects

scientific article published on 7 June 2017

Mortality in achondroplasia study: a 42-year follow-up

scientific article

Mutations in BMPR2 are not present in patients with pulmonary hypertension associated with congenital diaphragmatic hernia.

scientific article published on 26 January 2017

Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

scientific article published on 4 September 2012

Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects

scientific article published on June 2016

Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing

scientific article published on 2 February 2015

Outcomes of congenital diaphragmatic hernia in the modern era of management.

scientific article published on 30 January 2013

Parental perceptions of prenatal whole exome sequencing (PPPWES) study

scientific article published on 05 August 2018

Participant choices for return of genomic results in the eMERGE Network

scientific article published on 16 July 2020

Predictors of low weight and tube feedings in children with congenital diaphragmatic hernia at 1 year of age.

scientific article

Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies

scientific article published on 13 June 2019

Research Participants' Preferences for Hypothetical Secondary Results from Genomic Research

scientific article published on 29 December 2016

Researchers' views on return of incidental genomic research results: qualitative and quantitative findings

scientific article published on 27 June 2013

Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network

scientific article published on 27 April 2020

Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathy

scientific article published on 8 April 2010

Smairt Snacking BYPASS JUNK FOOD AND PICK HEALTHY GO-TO SNACKS

Technetium pyrophosphate myocardial uptake and peripheral neuropathy in a rare variant of familial transthyretin (TTR) amyloidosis (Ser23Asn): a case report and literature review ⬇️

scientific article published on 08 December 2011

The association between congenital diaphragmatic hernia and undescended testes

scientific article published on 19 February 2015

The influence of genetics in congenital diaphragmatic hernia

scientific article published on 01 August 2019

The usefulness of whole-exome sequencing in routine clinical practice

scientific article published on 5 June 2014

Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network

scientific article published on 13 May 2020

User engagement with web-based genomics education videos and implications for designing scalable patient education materials

scientific article published on 01 January 2019

Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia

scientific article

Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

scientific article (publication date: March 2014)

Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium

scientific article published in March 2018

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