Publications by authors named "Julia Wynn"

55Publications

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

Genet Med 2020 Oct 18;22(10):1667-1672. Epub 2020 Jun 18.

Center for Biomedical Ethics and Society, Vanderbilt University Medical Center, Nashville, TN, USA.

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http://dx.doi.org/10.1038/s41436-020-0863-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521988PMC
October 2020

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

J Community Genet 2020 Oct 7;11(4):391-403. Epub 2020 May 7.

Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.

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http://dx.doi.org/10.1007/s12687-020-00464-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475159PMC
October 2020

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

AMIA Annu Symp Proc 2019 4;2019:923-932. Epub 2020 Mar 4.

Department of Pediatrics, Columbia University Irving Medical Center, New York, NY.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153116PMC
August 2020

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

J Genet Couns 2020 Aug 16;29(4):574-586. Epub 2020 Apr 16.

Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.

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http://dx.doi.org/10.1002/jgc4.1276DOI Listing
August 2020

Developing effective and efficient genomic educational tools for our diverse population.

Ann Transl Med 2019 Dec;7(Suppl 8):S304

Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.

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http://dx.doi.org/10.21037/atm.2019.10.98DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6976475PMC
December 2019

The influence of genetics in congenital diaphragmatic hernia.

Semin Perinatol 2020 02 1;44(1):151169. Epub 2019 Aug 1.

Department of Pediatrics, Columbia University, New York, NY 10032, USA; Department of Medicine, Columbia University, New York, NY 10032, USA. Electronic address:

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http://dx.doi.org/10.1053/j.semperi.2019.07.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994346PMC
February 2020

Parental perceptions of prenatal whole exome sequencing (PPPWES) study.

Prenat Diagn 2018 10 5;38(11):801-811. Epub 2018 Aug 5.

Department of Pediatrics, Division of Clinical Genetics, Columbia University, New York, NY, USA.

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http://dx.doi.org/10.1002/pd.5332DOI Listing
October 2018

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

BMC Med Genomics 2018 05 8;11(1):45. Epub 2018 May 8.

Department of Pediatrics, Baylor College of Medicine, 1102 Bates St. FC 1200, Houston, TX, 77030, USA.

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http://dx.doi.org/10.1186/s12920-018-0360-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5941324PMC
May 2018

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

Diabetes Self Manag 2017 May;34(3):70-71

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May 2017

Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies.

J Genet Couns 2018 08 15;27(4):927-934. Epub 2017 Dec 15.

Department of Pediatrics, Division of Molecular Genetics, Columbia University Medical Center, New York, NY, USA.

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http://dx.doi.org/10.1007/s10897-017-0186-4DOI Listing
August 2018

Congenital diaphragmatic hernias: from genes to mechanisms to therapies.

Dis Model Mech 2017 08;10(8):955-970

Department of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA

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http://dx.doi.org/10.1242/dmm.028365DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560060PMC
August 2017

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

Ann Intern Med 2017 Jul 30;167(2):125-126. Epub 2017 May 30.

From Columbia University, New York, New York.

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http://dx.doi.org/10.7326/M17-1045DOI Listing
July 2017

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

J Genet Couns 2017 Oct 29;26(5):1116-1129. Epub 2017 Mar 29.

Departments of Pediatrics and Medicine, Columbia University, New York, NY, USA.

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http://dx.doi.org/10.1007/s10897-017-0090-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250529PMC
October 2017

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

J Pediatr Surg 2017 Nov 26;52(11):1747-1750. Epub 2017 Jan 26.

Department of Pediatrics, Division of Molecular Genetics, Columbia University Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY 10032, USA.

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http://dx.doi.org/10.1016/j.jpedsurg.2017.01.007DOI Listing
November 2017

Research Participants' Preferences for Hypothetical Secondary Results from Genomic Research.

J Genet Couns 2017 Aug 29;26(4):841-851. Epub 2016 Dec 29.

Department of Pediatrics, Columbia University Medical Center, 1150 St. Nicholas Ave., Russ Berrie Pavilion, 6th Fl, Rm 620, New York, NY, 10032, USA.

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http://dx.doi.org/10.1007/s10897-016-0059-2DOI Listing
August 2017

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

Authors:
Julia Wynn

J Genet Couns 2016 08 5;25(4):691-7. Epub 2015 Aug 5.

Department of Pediatrics, Division of Genetics, Columbia University Medical Center, New York, NY, USA.

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http://dx.doi.org/10.1007/s10897-015-9868-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744148PMC
August 2016

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

J Autism Dev Disord 2015 Nov;45(11):3764-70

Department of Pediatrics and Medicine, Columbia University, 1150 St. Nicholas Avenue, Room 620, New York, NY, 10032, USA.

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http://link.springer.com/10.1007/s10803-015-2484-8
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http://dx.doi.org/10.1007/s10803-015-2484-8DOI Listing
November 2015

Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing.

Clin Case Rep 2015 Apr 2;3(4):237-9. Epub 2015 Feb 2.

Columbia University Medical Center New York, New York.

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http://dx.doi.org/10.1002/ccr3.205DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4405308PMC
April 2015

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

J Genet Couns 2015 Oct 17;24(5):833-41. Epub 2015 Jan 17.

Department of Pediatrics, Columbia University Medical Center, 1150 St. Nicholas Ave., Russ Berrie Pavilion, 6th Fl, Rm 620, New York, NY, 10032, USA.

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http://dx.doi.org/10.1007/s10897-014-9817-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506262PMC
October 2015

Genetic causes of congenital diaphragmatic hernia.

Semin Fetal Neonatal Med 2014 Dec 28;19(6):324-30. Epub 2014 Oct 28.

Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, NY 10032, USA. Electronic address:

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http://dx.doi.org/10.1016/j.siny.2014.09.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259843PMC
December 2014

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

J Pediatr Gastroenterol Nutr 2014 Oct;59(4):527-30

*Division of Pediatric Gastroenterology, Hepatology, and Nutrition †Division of Pediatric Surgery ‡Division of Neonatology §Mailman School of Public Health ||Division of Clinical Genetics ¶Division of Pediatric Cardiology, Columbia University, New York, NY.

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http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:land
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http://dx.doi.org/10.1097/MPG.0000000000000454DOI Listing
October 2014

The usefulness of whole-exome sequencing in routine clinical practice.

Genet Med 2014 Dec 5;16(12):922-31. Epub 2014 Jun 5.

1] Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, New York, New York, USA [2] Department of Medicine, Columbia University Medical Center, New York, New York, USA.

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http://dx.doi.org/10.1038/gim.2014.58DOI Listing
December 2014

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

Genet Med 2013 Nov 27;15(11):888-95. Epub 2013 Jun 27.

Department of Psychiatry, Columbia University Medical Center and NY State Psychiatric Institute New York, New York, USA.

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http://dx.doi.org/10.1038/gim.2013.87DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823712PMC
November 2013

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

Hum Genet 2013 Mar 9;132(3):285-92. Epub 2012 Nov 9.

Division of Molecular Genetics, Department of Pediatrics, Columbia University Medical Center, 1150 St. Nicholas Avenue, Room 620, New York, NY 10032, USA.

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http://dx.doi.org/10.1007/s00439-012-1249-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570587PMC
March 2013

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

Am J Med Genet A 2007 Nov;143A(21):2502-11

Department of Pediatrics, University of Texas Health Science Center at Houston, Texas 77030, USA.

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http://dx.doi.org/10.1002/ajmg.a.31919DOI Listing
November 2007