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Cited by in F6Publishing
For: Bolz-Johnson M, Kenny T, Le Cam Y, Hernando I. Our greatest untapped resource: our patients. J Community Genet 2021;12:241-6. [PMID: 33884523 DOI: 10.1007/s12687-021-00524-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Ward AJ, Murphy D, Marron R, Mcgrath V, Bolz-johnson M, Cullen W, Daly A, Hardiman O, Lawlor A, Lynch SA, Maclachlan M, Mcbrien J, Ni Bhriain S, O’byrne JJ, O’connell SM, Turner J, Treacy EP. Designing rare disease care pathways in the Republic of Ireland: a co-operative model. Orphanet J Rare Dis 2022;17. [DOI: 10.1186/s13023-022-02309-6] [Reference Citation Analysis]
2 Tumienė B, del Toro Riera M, Grikiniene J, Samaitienė-aleknienė R, Praninskienė R, Monavari AA, Sykut-cegielska J. Multidisciplinary Care of Patients with Inherited Metabolic Diseases and Epilepsy: Current Perspectives. JMDH 2022;Volume 15:553-66. [DOI: 10.2147/jmdh.s251863] [Reference Citation Analysis]
3 Tumiene B. Unmet psychosocial needs of parents of children with rare, complex, and severe genetic diseases. Dev Med Child Neurol 2021. [PMID: 34355798 DOI: 10.1111/dmcn.15002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Tumiene B, Kristoffersson U, Hedley V, Kääriäinen H. Rare diseases: past achievements and future prospects. J Community Genet 2021;12:205-6. [PMID: 33945116 DOI: 10.1007/s12687-021-00529-0] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]