These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
169 related articles for article (PubMed ID: 35128755)
21. A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants. Cakici JA; Dimmock DP; Caylor SA; Gaughran M; Clarke C; Triplett C; Clark MM; Kingsmore SF; Bloss CS Am J Hum Genet; 2020 Nov; 107(5):953-962. PubMed ID: 33157008 [TBL] [Abstract][Full Text] [Related]
22. Caregivers' perception of and experience with variants of uncertain significance from whole exome sequencing for children with undiagnosed conditions. Li X; Nusbaum R; Smith-Hicks C; Jamal L; Dixon S; Mahida S J Genet Couns; 2019 Apr; 28(2):304-312. PubMed ID: 30680845 [TBL] [Abstract][Full Text] [Related]
23. Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders. Rosell AM; Pena LD; Schoch K; Spillmann R; Sullivan J; Hooper SR; Jiang YH; Mathey-Andrews N; Goldstein DB; Shashi V J Genet Couns; 2016 Oct; 25(5):1019-31. PubMed ID: 26868367 [TBL] [Abstract][Full Text] [Related]
24. Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing. Rego S; Dagan-Rosenfeld O; Bivona SA; Snyder MP; Ormond KE J Genet Couns; 2019 Apr; 28(2):428-437. PubMed ID: 30835913 [TBL] [Abstract][Full Text] [Related]
25. Parents' understanding of genome and exome sequencing for pediatric health conditions: a systematic review. Gereis J; Hetherington K; Ha L; Robertson EG; Ziegler DS; Barlow-Stewart K; Tucker KM; Marron JM; Wakefield CE Eur J Hum Genet; 2022 Nov; 30(11):1216-1225. PubMed ID: 35999452 [TBL] [Abstract][Full Text] [Related]
26. Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions. Ungar WJ; Hayeems RZ; Marshall CR; Gillespie MK; Szuto A; Chisholm C; James Stavropoulos D; Huang L; Jarinova O; Wu V; Tsiplova K; Lau L; Lee W; Venkataramanan V; Sawyer S; Mendoza-Londono R; Somerville MJ; Boycott KM; Clin Ther; 2023 Aug; 45(8):702-709. PubMed ID: 37453830 [TBL] [Abstract][Full Text] [Related]
28. Somatic mosaicism detected by genome-wide sequencing in 500 parent-child trios with suspected genetic disease: clinical and genetic counseling implications. Cook CB; Armstrong L; Boerkoel CF; Clarke LA; du Souich C; Demos MK; Gibson WT; Gill H; Lopez E; Patel MS; Selby K; Abu-Sharar Z; ; Elliott AM; Friedman JM Cold Spring Harb Mol Case Stud; 2021 Dec; 7(6):. PubMed ID: 34697084 [TBL] [Abstract][Full Text] [Related]
29. Genome-Wide Sequencing for Unexplained Developmental Disabilities or Multiple Congenital Anomalies: A Health Technology Assessment. Ontario Health (Quality) Ont Health Technol Assess Ser; 2020; 20(11):1-178. PubMed ID: 32194879 [TBL] [Abstract][Full Text] [Related]
30. Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact. Wynn J; Ottman R; Duong J; Wilson AL; Ahimaz P; Martinez J; Rabin R; Rosen E; Webster R; Au C; Cho MT; Egan C; Guzman E; Primiano M; Shaw JE; Sisson R; Klitzman RL; Appelbaum PS; Lichter-Konecki U; Anyane-Yeboa K; Iglesias A; Chung WK Clin Genet; 2018 May; 93(5):1039-1048. PubMed ID: 29266212 [TBL] [Abstract][Full Text] [Related]
31. The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders. Dragojlovic N; van Karnebeek CDM; Ghani A; Genereaux D; Kim E; Birch P; ; Elliott AM; Friedman JM; Lynd LD Genet Med; 2020 Feb; 22(2):292-300. PubMed ID: 31462755 [TBL] [Abstract][Full Text] [Related]
32. Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research. Middleton A; Morley KI; Bragin E; Firth HV; Hurles ME; Wright CF; Parker M; Eur J Hum Genet; 2016 Jan; 24(1):21-9. PubMed ID: 25920556 [TBL] [Abstract][Full Text] [Related]
33. Where there is no genetic counselor: An online decision-aid supports the majority of parents' diagnostic genomic testing choices for their children. Birch P; Beauchesne R; Bansback N; Boelman C; Connolly M; Demos M; Friedman JM; Race S; Stockler S; ; Elliott AM; Adam S Genet Med; 2024 Sep; 26(9):101173. PubMed ID: 38828700 [TBL] [Abstract][Full Text] [Related]
34. Offering and Returning Secondary Findings in the Context of Exome Sequencing for Hearing Loss: Clinicians' Views and Experiences. Notini L; Gaff C; Savulescu J; Vears DF AJOB Empir Bioeth; 2023; 14(2):74-83. PubMed ID: 36595590 [TBL] [Abstract][Full Text] [Related]
35. A qualitative study of Latinx parents' experiences of clinical exome sequencing. Luksic D; Sukhu R; Koval C; Cho MT; Espinal A; Rufino K; Loarte TV; Chung WK; Wynn J J Genet Couns; 2020 Aug; 29(4):574-586. PubMed ID: 32298033 [TBL] [Abstract][Full Text] [Related]
36. Parental motivations for and adaptation to trio-exome sequencing in a prospective prenatal testing cohort: Beyond the diagnosis. Talati AN; Gilmore KL; Hardisty EE; Lyerly AD; Rini C; Vora NL Prenat Diagn; 2022 May; 42(6):775-782. PubMed ID: 35132674 [TBL] [Abstract][Full Text] [Related]
37. Opt-in for secondary findings as part of diagnostic whole-exome sequencing: Real-life experience from an international diagnostic laboratory. Brunfeldt M; Kaare M; Saarinen I; Koskenvuo J; Kääriäinen H Mol Genet Genomic Med; 2023 Aug; 11(8):e2180. PubMed ID: 37025058 [TBL] [Abstract][Full Text] [Related]
38. "We don't know her history, her background": adoptive parents' perspectives on whole genome sequencing results. Crouch J; Yu JH; Shankar AG; Tabor HK J Genet Couns; 2015 Feb; 24(1):67-77. PubMed ID: 25011977 [TBL] [Abstract][Full Text] [Related]
39. Parental experiences of ultrarapid genomic testing for their critically unwell infants and children. Brett GR; Martyn M; Lynch F; de Silva MG; Ayres S; Gallacher L; Boggs K; Baxendale A; Schenscher S; King-Smith S; Fowles L; Springer A; Lunke S; Vasudevan A; Krzesinski E; Pinner J; Sandaradura SA; Barnett C; Patel C; Wilson M; Stark Z Genet Med; 2020 Dec; 22(12):1976-1985. PubMed ID: 32719395 [TBL] [Abstract][Full Text] [Related]
40. Health Care Costs After Genome-Wide Sequencing for Children With Rare Diseases in England and Canada. Weymann D; Buckell J; Fahr P; Loewen R; Ehman M; Pollard S; Friedman JM; Stockler-Ipsiroglu S; Elliott AM; Wordsworth S; Buchanan J; Regier DA JAMA Netw Open; 2024 Jul; 7(7):e2420842. PubMed ID: 38985473 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]