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For: Knoppers BM, Senecal K, Borry P, Avard D. Whole-Genome Sequencing in Newborn Screening Programs. Science Translational Medicine 2014;6:229cm2-229cm2. [DOI: 10.1126/scitranslmed.3008494] [Cited by in Crossref: 44] [Cited by in F6Publishing: 38] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
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3 Modell SM, Citrin T, Kardia SLR. Laying Anchor: Inserting Precision Health into a Public Health Genetics Policy Course. Healthcare (Basel) 2018;6:E93. [PMID: 30081448 DOI: 10.3390/healthcare6030093] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
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6 Foulkes WD, Knoppers BM, Turnbull C. Population genetic testing for cancer susceptibility: founder mutations to genomes. Nat Rev Clin Oncol 2016;13:41-54. [PMID: 26483301 DOI: 10.1038/nrclinonc.2015.173] [Cited by in Crossref: 63] [Cited by in F6Publishing: 54] [Article Influence: 9.0] [Reference Citation Analysis]
7 Ismail IT, Showalter MR, Fiehn O. Inborn Errors of Metabolism in the Era of Untargeted Metabolomics and Lipidomics. Metabolites 2019;9:E242. [PMID: 31640247 DOI: 10.3390/metabo9100242] [Cited by in Crossref: 25] [Cited by in F6Publishing: 19] [Article Influence: 8.3] [Reference Citation Analysis]
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10 Hale AT, Akinnusotu O, He J, Wang J, Hibshman N, Shannon CN, Naftel RP. Genome-Wide Association Study Identifies Genetic Risk Factors for Spastic Cerebral Palsy. Neurosurgery 2021:nyab184. [PMID: 34098570 DOI: 10.1093/neuros/nyab184] [Reference Citation Analysis]
11 Chaudhari BP, Manickam K, McBride KL. A pediatric perspective on genomics and prevention in the twenty-first century. Pediatr Res 2020;87:338-44. [PMID: 31578042 DOI: 10.1038/s41390-019-0597-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
12 Chan K, Petros M. Simple Test, Complex System: Multifaceted Views of Newborn Screening Science, Technology, and Policy. Glob Pediatr Health 2019;6:2333794X19894812. [PMID: 31903414 DOI: 10.1177/2333794X19894812] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
13 Kerruish NJ, Healey DM, Gray AR. Psychosocial effects in parents and children 12 years after newborn genetic screening for type 1 diabetes. Eur J Hum Genet 2017;25:397-403. [PMID: 28120838 DOI: 10.1038/ejhg.2016.190] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
14 Ayuso C, Millan JM, Dal-re R. Management and return of incidental genomic findings in clinical trials. Pharmacogenomics J 2015;15:1-5. [DOI: 10.1038/tpj.2014.62] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 0.6] [Reference Citation Analysis]
15 Bodian DL, Klein E, Iyer RK, Wong WS, Kothiyal P, Stauffer D, Huddleston KC, Gaither AD, Remsburg I, Khromykh A, Baker RL, Maxwell GL, Vockley JG, Niederhuber JE, Solomon BD. Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates. Genet Med 2016;18:221-30. [PMID: 26334177 DOI: 10.1038/gim.2015.111] [Cited by in Crossref: 59] [Cited by in F6Publishing: 51] [Article Influence: 8.4] [Reference Citation Analysis]
16 Park KJ, Park S, Lee E, Park JH, Park JH, Park HD, Lee SY, Kim JW. A Population-Based Genomic Study of Inherited Metabolic Diseases Detected Through Newborn Screening. Ann Lab Med 2016;36:561-72. [PMID: 27578510 DOI: 10.3343/alm.2016.36.6.561] [Cited by in Crossref: 12] [Cited by in F6Publishing: 10] [Article Influence: 2.4] [Reference Citation Analysis]
17 Knoppers BM, Zawati MH, Sénécal K. Return of genetic testing results in the era of whole-genome sequencing. Nat Rev Genet 2015;16:553-9. [PMID: 26239711 DOI: 10.1038/nrg3960] [Cited by in Crossref: 98] [Cited by in F6Publishing: 88] [Article Influence: 14.0] [Reference Citation Analysis]
18 Wade CH, Elliott KR. Young adults' attitudes toward pediatric whole-genome sequencing. Per Med 2016;13:541-52. [PMID: 29754547 DOI: 10.2217/pme-2016-0066] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
19 Boemer F, Fasquelle C, d'Otreppe S, Josse C, Dideberg V, Segers K, Guissard V, Capraro V, Debray FG, Bours V. A next-generation newborn screening pilot study: NGS on dried blood spots detects causal mutations in patients with inherited metabolic diseases. Sci Rep 2017;7:17641. [PMID: 29247206 DOI: 10.1038/s41598-017-18038-x] [Cited by in Crossref: 15] [Cited by in F6Publishing: 11] [Article Influence: 3.0] [Reference Citation Analysis]
20 Sabatello M, Appelbaum PS. Behavioral Genetics in Criminal and Civil Courts. Harv Rev Psychiatry 2017;25:289-301. [PMID: 29117024 DOI: 10.1097/HRP.0000000000000141] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 1.4] [Reference Citation Analysis]
21 Bert F, van der Star A, Scaioli G. Next generation of public health professionals: networks and the EUPHAnxtintegration approach. The European Journal of Public Health 2014;24:876-876. [DOI: 10.1093/eurpub/cku128] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
22 Ulm E, Feero WG, Dineen R, Charrow J, Wicklund C. Genetics professionals' opinions of whole-genome sequencing in the newborn period. J Genet Couns 2015;24:452-63. [PMID: 25348082 DOI: 10.1007/s10897-014-9779-3] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.1] [Reference Citation Analysis]
23 Wendler DS, Rid A. Genetic research on biospecimens poses minimal risk. Trends Genet 2015;31:11-5. [PMID: 25530152 DOI: 10.1016/j.tig.2014.10.003] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
24 Therrell BL, Padilla CD, Loeber JG, Kneisser I, Saadallah A, Borrajo GJ, Adams J. Current status of newborn screening worldwide: 2015. Semin Perinatol 2015;39:171-87. [PMID: 25979780 DOI: 10.1053/j.semperi.2015.03.002] [Cited by in Crossref: 226] [Cited by in F6Publishing: 185] [Article Influence: 37.7] [Reference Citation Analysis]
25 Boccia S, Mc Kee M, Adany R, Boffetta P, Burton H, Cambon-Thomsen A, Cornel MC, Gray M, Jani A, Knoppers BM, Khoury MJ, Meslin EM, Van Duijn CM, Villari P, Zimmern R, Cesario A, Puggina A, Colotto M, Ricciardi W. Beyond public health genomics: proposals from an international working group. Eur J Public Health 2014;24:877-9. [PMID: 25168910 DOI: 10.1093/eurpub/cku142] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 1.9] [Reference Citation Analysis]
26 Borry P, Bentzen HB, Budin-Ljøsne I, Cornel MC, Howard HC, Feeney O, Jackson L, Mascalzoni D, Mendes Á, Peterlin B, Riso B, Shabani M, Skirton H, Sterckx S, Vears D, Wjst M, Felzmann H. The challenges of the expanded availability of genomic information: an agenda-setting paper. J Community Genet 2018;9:103-16. [PMID: 28952070 DOI: 10.1007/s12687-017-0331-7] [Cited by in Crossref: 19] [Cited by in F6Publishing: 13] [Article Influence: 3.8] [Reference Citation Analysis]
27 Karki R, Pandya D, Elston RC, Ferlini C. Defining "mutation" and "polymorphism" in the era of personal genomics. BMC Med Genomics 2015;8:37. [PMID: 26173390 DOI: 10.1186/s12920-015-0115-z] [Cited by in Crossref: 62] [Cited by in F6Publishing: 55] [Article Influence: 8.9] [Reference Citation Analysis]
28 Iskrov G, Ivanov S, Wrenn S, Stefanov R. Whole-Genome Sequencing in Newborn Screening-Attitudes and Opinions of Bulgarian Pediatricians and Geneticists. Front Public Health 2017;5:308. [PMID: 29250518 DOI: 10.3389/fpubh.2017.00308] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
29 Jansen ME, Lister KJ, van Kranen HJ, Cornel MC. Policy Making in Newborn Screening Needs a Structured and Transparent Approach. Front Public Health 2017;5:53. [PMID: 28377917 DOI: 10.3389/fpubh.2017.00053] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.2] [Reference Citation Analysis]
30 Yang L, Chen J, Shen B. Newborn Screening in the Era of Precision Medicine. In: Shen B, editor. Translational Informatics in Smart Healthcare. Singapore: Springer; 2017. pp. 47-61. [DOI: 10.1007/978-981-10-5717-5_3] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
31 Wolf SM, Burke W, Koenig BA. Mapping the Ethics of Translational Genomics: Situating Return of Results and Navigating the Research-Clinical Divide. J Law Med Ethics 2015;43:486-501. [PMID: 26479558 DOI: 10.1111/jlme.12291] [Cited by in Crossref: 16] [Cited by in F6Publishing: 27] [Article Influence: 3.2] [Reference Citation Analysis]
32 Knoppers BM, Nguyen MT, Sénécal K, Tassé AM, Zawati MH. Next-Generation Sequencing and the Return of Results. Cold Spring Harb Perspect Med 2016;6:a026724. [PMID: 27599532 DOI: 10.1101/cshperspect.a026724] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
33 Sabatello M, Appelbaum S. Psychiatric Genetics in Child Custody Proceedings: Ethical, Legal, and Social Issues. Curr Genet Med Rep 2016;4:98-106. [PMID: 27695660 DOI: 10.1007/s40142-016-0093-2] [Cited by in Crossref: 4] [Article Influence: 0.7] [Reference Citation Analysis]
34 Modell SM, Citrin T, Burmeister M, Kardia SLR, Beil A, Raisky J; Genetics and Faith Dialogue Group. When Genetics Meets Religion: What Scientists and Religious Leaders Can Learn from Each Other. Public Health Genomics 2019;22:174-88. [PMID: 31801151 DOI: 10.1159/000504261] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
35 Howard HC, Knoppers BM, Cornel MC, Wright Clayton E, Sénécal K, Borry P; European Society of Human Genetics., P3G International Paediatric Platform., Human Genome Organisation; and the PHG Foundation. Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes. Eur J Hum Genet 2015;23:1593-600. [PMID: 25626707 DOI: 10.1038/ejhg.2014.289] [Cited by in Crossref: 56] [Cited by in F6Publishing: 44] [Article Influence: 8.0] [Reference Citation Analysis]
36 Wu C, Tsai C, Hung C, Lin Y, Lin Y, Huang F, Tsao P, Su Y, Lee YL, Hsieh W, Hsu C. Newborn genetic screening for hearing impairment: a population-based longitudinal study. Genet Med 2017;19:6-12. [DOI: 10.1038/gim.2016.66] [Cited by in Crossref: 30] [Cited by in F6Publishing: 27] [Article Influence: 5.0] [Reference Citation Analysis]
37 Fisher E, Achilles S, Tönnies H, Schmidtke J. [Concepts for the return of secondary genetic findings in medical diagnostics and research]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 2015;58:166-73. [PMID: 25487853 DOI: 10.1007/s00103-014-2096-z] [Reference Citation Analysis]
38 Sabatello M. A Genomically Informed Education System? Challenges for Behavioral Genetics. J Law Med Ethics 2018;46:130-44. [PMID: 29805246 DOI: 10.1177/1073110518766027] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
39 Ashton-Prolla P, Goldim JR, Vairo FP, da Silveira Matte U, Sequeiros J. Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil. J Community Genet 2015;6:275-83. [PMID: 26040235 DOI: 10.1007/s12687-015-0238-0] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 1.4] [Reference Citation Analysis]
40 Kamp M, Krause A, Ramsay M. Has translational genomics come of age in Africa? Hum Mol Genet 2021:ddab180. [PMID: 34240178 DOI: 10.1093/hmg/ddab180] [Reference Citation Analysis]
41 Goldenberg AJ, Ponsaran R, Gaviglio A, Simancek D, Tarini BA. Genomics and Newborn Screening: Perspectives of Public Health Programs. IJNS 2022;8:11. [DOI: 10.3390/ijns8010011] [Reference Citation Analysis]
42 Mollison L, Berg JS. Genetic screening: birthright or earned with age? Expert Rev Mol Diagn 2017;17:735-8. [PMID: 28641021 DOI: 10.1080/14737159.2017.1346473] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]