Literature DB >> 27171546

Recommendations for the integration of genomics into clinical practice.

Sarah Bowdin1,2, Adel Gilbert1, Emma Bedoukian3,4, Christopher Carew1, Margaret P Adam5, John Belmont6, Barbara Bernhardt7, Leslie Biesecker8, Hans T Bjornsson9,10, Miriam Blitzer11, Lisa C A D'Alessandro12, Matthew A Deardorff3,4,13, Laurie Demmer14, Alison Elliott15, Gerald L Feldman16, Ian A Glass5, Gail Herman17, Lucia Hindorff18, Fuki Hisama19, Louanne Hudgins20, A Micheil Innes21, Laird Jackson22, Gail Jarvik18, Raymond Kim22, Bruce Korf23, David H Ledbetter24, Mindy Li25, Eriskay Liston22, Christian Marshall26, Livija Medne2,3, M Stephen Meyn1,22, Nasim Monfared22, Cynthia Morton27, John J Mulvihill28, Sharon E Plon29, Heidi Rehm27, Amy Roberts30, Cheryl Shuman1,22, Nancy B Spinner25, D James Stavropoulos26, Kathleen Valverde31, Darrel J Waggoner32, Alisha Wilkens3,4, Ronald D Cohn1,22, Ian D Krantz3,13.   

Abstract

The introduction of diagnostic clinical genome and exome sequencing (CGES) is changing the scope of practice for clinical geneticists. Many large institutions are making a significant investment in infrastructure and technology, allowing clinicians to access CGES, especially as health-care coverage begins to extend to clinically indicated genomic sequencing-based tests. Translating and realizing the comprehensive clinical benefits of genomic medicine remain a key challenge for the current and future care of patients. With the increasing application of CGES, it is necessary for geneticists and other health-care providers to understand its benefits and limitations in order to interpret the clinical relevance of genomic variants identified in the context of health and disease. New, collaborative working relationships with specialists across diverse disciplines (e.g., clinicians, laboratorians, bioinformaticians) will undoubtedly be key attributes of the future practice of clinical genetics and may serve as an example for other specialties in medicine. These new skills and relationships will also inform the development of the future model of clinical genetics training curricula. To address the evolving role of the clinical geneticist in the rapidly changing climate of genomic medicine, two Clinical Genetics Think Tank meetings were held that brought together physicians, laboratorians, scientists, genetic counselors, trainees, and patients with experience in clinical genetics, genetic diagnostics, and genetics education. This article provides recommendations that will guide the integration of genomics into clinical practice.Genet Med 18 11, 1075-1084.

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Year:  2016        PMID: 27171546      PMCID: PMC5557020          DOI: 10.1038/gim.2016.17

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


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10.  DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome.

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  51 in total

1.  A comparative study of patients' perceptions of genetic and genomic medicine services in California and Malaysia.

Authors:  Emily Qian; Meow-Keong Thong; Pamela Flodman; Jay Gargus
Journal:  J Community Genet       Date:  2018-12-03

2.  Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.

Authors:  Liza-Marie Johnson; Jessica M Valdez; Emily A Quinn; April D Sykes; Rose B McGee; Regina Nuccio; Stacy J Hines-Dowell; Justin N Baker; Chimene Kesserwan; Kim E Nichols; Belinda N Mandrell
Journal:  Cancer       Date:  2017-02-13       Impact factor: 6.860

Review 3.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

Review 4.  From Genetic Testing to Precision Medicine in Epilepsy.

Authors:  Pasquale Striano; Berge A Minassian
Journal:  Neurotherapeutics       Date:  2020-04       Impact factor: 7.620

5.  Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.

Authors:  Sneh Lata; Maddalena Marasa; Yifu Li; David A Fasel; Emily Groopman; Vaidehi Jobanputra; Hila Rasouly; Adele Mitrotti; Rik Westland; Miguel Verbitsky; Jordan Nestor; Lindsey M Slater; Vivette D'Agati; Marcin Zaniew; Anna Materna-Kiryluk; Francesca Lugani; Gianluca Caridi; Luca Rampoldi; Aditya Mattoo; Chad A Newton; Maya K Rao; Jai Radhakrishnan; Wooin Ahn; Pietro A Canetta; Andrew S Bomback; Gerald B Appel; Corinne Antignac; Glen S Markowitz; Christine K Garcia; Krzysztof Kiryluk; Simone Sanna-Cherchi; Ali G Gharavi
Journal:  Ann Intern Med       Date:  2017-12-05       Impact factor: 25.391

6.  A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data.

Authors:  Zornitza Stark; Harriet Dashnow; Sebastian Lunke; Tiong Y Tan; Alison Yeung; Simon Sadedin; Natalie Thorne; Ivan Macciocca; Clara Gaff; Alicia Oshlack; Susan M White; Paul A James
Journal:  Eur J Hum Genet       Date:  2017-08-23       Impact factor: 4.246

Review 7.  A Review of Recent Advances in Translational Bioinformatics: Bridges from Biology to Medicine.

Authors:  J Vamathevan; E Birney
Journal:  Yearb Med Inform       Date:  2017-09-11

Review 8.  Paediatric genomics: diagnosing rare disease in children.

Authors:  Caroline F Wright; David R FitzPatrick; Helen V Firth
Journal:  Nat Rev Genet       Date:  2018-02-05       Impact factor: 53.242

Review 9.  A primer to clinical genome sequencing.

Authors:  James R Priest
Journal:  Curr Opin Pediatr       Date:  2017-10       Impact factor: 2.856

10.  Exome sequencing disclosures in pediatric cancer care: Patterns of communication among oncologists, genetic counselors, and parents.

Authors:  Sarah Scollon; Mary A Majumder; Katie Bergstrom; Tao Wang; Amy L McGuire; Jill O Robinson; Amanda M Gutierrez; Caroline H Lee; Susan G Hilsenbeck; Sharon E Plon; D Williams Parsons; Richard L Street
Journal:  Patient Educ Couns       Date:  2018-11-12
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