Laura M Amendola

Laura M Amendola

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Laura M Amendola

Laura M Amendola

Publications by authors named "Laura M Amendola"

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Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting.

Am J Hum Genet 2019 Sep 15;105(3):526-533. Epub 2019 Aug 15.

Department of Medicine (Medical Genetics), University of Washington School of Medicine, Seattle, WA 98195, USA; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA 98195, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.07.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6731361PMC
September 2019

Insurance coverage does not predict outcomes of genetic testing: The search for meaning in payer decisions for germline cancer tests.

J Genet Couns 2019 Jul 17. Epub 2019 Jul 17.

Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.

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http://dx.doi.org/10.1002/jgc4.1155DOI Listing
July 2019

The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.

J Genet Couns 2019 Apr 14;28(2):477-490. Epub 2018 Dec 14.

Department of Health Services, School of Public Health, University of Washington, Box 357660, Seattle, WA, 98195-7660, USA.

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http://dx.doi.org/10.1007/s10897-018-0286-9DOI Listing
April 2019

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

Discordance in selected designee for return of genomic findings in the event of participant death and estate executor.

Mol Genet Genomic Med 2017 Mar 16;5(2):172-176. Epub 2017 Jan 16.

Division of Medical GeneticsUniversity of WashingtonSeattleWashington; Department of Genome SciencesUniversity of WashingtonSeattleWashington.

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http://doi.wiley.com/10.1002/mgg3.274
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http://dx.doi.org/10.1002/mgg3.274DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370224PMC
March 2017

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

Genet Med 2017 02 4;19(2):176-181. Epub 2016 Aug 4.

Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, Washington, USA.

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http://dx.doi.org/10.1038/gim.2016.96DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291803PMC
February 2017

Patients' Choices for Return of Exome Sequencing Results to Relatives in the Event of Their Death.

J Law Med Ethics 2015 ;43(3):476-85

Head of the Division of Medical Genetics and holds the Arno G. Motulsky Chair of Medicine at the University of Washington, Seattle, where she is a Professor of Medicine (Medical Genetics) and Genome Sciences. She received her Ph.D. in Human Genetics at the University of Michigan and her M.D. at the University of Iowa in the Medical Scientists Training Program. She completed her residency in Internal Medicine at the Hospital of the University of Pennsylvania and her fellowship in Medical Genetics at the University of Washington.

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http://dx.doi.org/10.1111/jlme.12290DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4617192PMC
January 2017

Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational Tool.

J Genet Couns 2016 12 16;25(6):1146-1156. Epub 2016 Jul 16.

Department of Laboratory Medicine, University of Washington, Rm NW120, Box 357110, 1959 NE Pacific Street, Seattle, WA, 98195, USA.

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http://dx.doi.org/10.1007/s10897-016-9993-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114323PMC
December 2016

Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome.

J Genet Couns 2016 06 5;25(3):515-9. Epub 2015 Dec 5.

Department of Medicine, Division of Medical Genetics, University of Washington, 1705 NE Pacific Street, K228, UW Box 357720, Seattle, WA, 98195, USA.

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http://dx.doi.org/10.1007/s10897-015-9902-0DOI Listing
June 2016

ADCY5-related dyskinesia: Broader spectrum and genotype-phenotype correlations.

Neurology 2015 Dec 4;85(23):2026-35. Epub 2015 Nov 4.

From the Departments of Neurology (D.-H.C., E.S.B., M.Y.D., P.D.S., M.W., T.D.B.), Psychiatry and Behavioral Sciences (O.K., W.H.R.), Genome Sciences (H.A.S., E.E.E.), Medicine (F.M.H., L.M.A., W.H.R.), and Pathology (M.O.D.), and Howard Hughes Medical Institute (E.E.E.), University of Washington, Seattle; Inserm (A.M., D. Grabli, M.V., O.T., E.R.), U 1127; CNRS (A.M., D. Grabli, M.V., O.T., E.R.), UMR 7225; Sorbonne Université (A.M., D. Grabli, M.V., O.T., E.R.), UPMC Univ Paris 06, UMR S 1127; Institut du Cerveau et de la Moelle Épinière (A.M., D. Grabli, M.V., O.T., E.R.), ICM; Départements de Neurologie (A.M., B.D., D. Grabli, M.V., O.T., E.R.) et de Génétique (C.M.), Hôpital de la Pitié Salpêtrière, AP-HP, Paris, France; the Departments of Neurosciences and Pediatrics (J.R.F.), University of California, San Diego; Rady Childrens Hospital (J.R.F.), San Diego, CA; Tel-Aviv Brill Community Mental Health Center (A.G.), Tel Aviv Medical School, Israel; Service de Neuropédiatrie (D.D.), Hôpital Trousseau, AP-HP; Centre de Référence Mouvements Anormaux de l'Enfant à l'Adulte (D.D.); Centre des Déficiences Intellectuelles de Causes Rares (C.M.), Paris; Département de Neurologie (M.A., C.T.), Hôpital Civil de Strasbourg; Fédération de Médecine Translationnelle de Strasbourg (FMTS) (M.A., C.T.), Université de Strasbourg; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC) (M.A., C.T.), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France; Phoenix Children's Hospital (S.B.), AZ; CHU de Bordeaux (N.D.-P.), Explorations Fonctionnelles du Système Nerveux; Service de Neuropédiatrie (D. Gras), Hôpital Robert Debré, AP-HP, Paris, France; Department of Child Neurology (K.M.M.), Lucile Packard Children's Hospital, Stanford University, Palo Alto, CA; Johns Hopkins All Children's Hospital (S.W.), St. Petersburg, FL; The Scripps Translational Science Institute (A.T.), Scripps Health and The Scripps Research Institute, S

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http://dx.doi.org/10.1212/WNL.0000000000002058DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676753PMC
December 2015

Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing.

Genet Med 2015 Nov 5;17(11):939-42. Epub 2015 Mar 5.

Department of Biomedical Informatics and Medical Education, University of Washington, Seattle, Washington, USA.

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http://dx.doi.org/10.1038/gim.2015.5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976082PMC
November 2015

Actionable exomic incidental findings in 6503 participants: challenges of variant classification.

Genome Res 2015 Mar 30;25(3):305-15. Epub 2015 Jan 30.

Department of Medicine, Division of Medical Genetics, University of Washington, Seattle, Washington 98195, USA; Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA;

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http://dx.doi.org/10.1101/gr.183483.114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352885PMC
March 2015

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.

Genet Med 2013 Nov 24;15(11):860-7. Epub 2013 Oct 24.

1] Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA [2] Carolina Center for Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA [3] Center for Genomics and Society, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA [4] Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

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http://dx.doi.org/10.1038/gim.2013.133DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3935342PMC
November 2013

Actionable, pathogenic incidental findings in 1,000 participants' exomes.

Am J Hum Genet 2013 Oct 19;93(4):631-40. Epub 2013 Sep 19.

Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA; Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA 98195, USA; Department of Laboratory Medicine, University of Washington, Seattle, WA 98195, USA.

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http://dx.doi.org/10.1016/j.ajhg.2013.08.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791261PMC
October 2013