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For: Saelaert M, Mertes H, Moerenhout T, De Baere E, Devisch I. Criteria for reporting incidental findings in clinical exome sequencing - a focus group study on professional practices and perspectives in Belgian genetic centres. BMC Med Genomics 2019;12:123. [PMID: 31429751 DOI: 10.1186/s12920-019-0561-0] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
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1 Cospain A, Dubourg C, Gastineau S, Pichard S, Gandemer V, Bonneau J, de Tayrac M, Moreau C, Odent S, Pasquier L, Damaj L, Lavillaureix A. Incidental diagnosis of mucopolysaccharidosis type I in an infant with chronic intestinal pseudoobstruction by exome sequencing. Mol Genet Metab Rep 2020;24:100621. [PMID: 32670797 DOI: 10.1016/j.ymgmr.2020.100621] [Reference Citation Analysis]
2 Castleman JS, Wall E, Allen S, Williams D, Doyle S, Kilby MD. The prenatal exome - a door to prenatal diagnostics? Expert Rev Mol Diagn 2021;21:465-74. [PMID: 33877000 DOI: 10.1080/14737159.2021.1920398] [Reference Citation Analysis]
3 Murrell JR, Nesbitt AMI, Baker SW, Pechter KB, Balciuniene J, Zhao X, Denenberg EH, DeChene ET, Wu C, Jayaraman P, Cao K, Gonzalez M, Devoto M, Testori A, Monos JD, Dulik MC, Conlin LK, Luo M, McDonald Gibson K, Guan Q, Sarmady M, Bhoj E, Helbig I, Zackai EH, Bedoukian EC, Wilkens A, Tarpinian J, Izumi K, Skraban CM, Deardorff MA, Medne L, Krantz ID, Krock BL, Santani AB. Molecular Diagnostic Outcomes from 700 Cases: What Can We Learn from a Retrospective Analysis of Clinical Exome Sequencing? J Mol Diagn 2022;24:274-86. [PMID: 35065284 DOI: 10.1016/j.jmoldx.2021.12.002] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Esteban-bueno G, Díaz-anadón LR, Rodríguez González A, Navarro Cabrero M, Berenguel Hernández AM. Protocolo genético en Atención Primaria para enfermedades raras: el síndrome de Wolfram como prototipo. Atención Primaria 2022;54:102285. [DOI: 10.1016/j.aprim.2022.102285] [Reference Citation Analysis]
5 Spies G, Mokaya J, Steadman J, Schuitmaker N, Kidd M, Hemmings SMJ, Carr JA, Kuivaniemi H, Seedat S; SHARED ROOTS Group. Attitudes among South African university staff and students towards disclosing secondary genetic findings. J Community Genet 2021;12:171-84. [PMID: 33219499 DOI: 10.1007/s12687-020-00494-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Saelaert M, Mertes H, Moerenhout T, De Baere E, Devisch I. Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study. BMC Med Ethics 2020;21:9. [PMID: 32000764 DOI: 10.1186/s12910-020-0452-0] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]