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For: Chinn IK, Sanders RP, Stray-Pedersen A, Coban-Akdemir ZH, Kim VH, Dadi H, Roifman CM, Quigg T, Lupski JR, Orange JS, Hanson IC. Novel Combined Immune Deficiency and Radiation Sensitivity Blended Phenotype in an Adult with Biallelic Variations in ZAP70 and RNF168. Front Immunol 2017;8:576. [PMID: 28603521 DOI: 10.3389/fimmu.2017.00576] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Béziat V. Human genetic dissection of papillomavirus-driven diseases: new insight into their pathogenesis. Hum Genet 2020;139:919-39. [PMID: 32435828 DOI: 10.1007/s00439-020-02183-x] [Cited by in Crossref: 10] [Cited by in F6Publishing: 13] [Article Influence: 5.0] [Reference Citation Analysis]
2 Béziat V, Casanova JL, Jouanguy E. Human genetic and immunological dissection of papillomavirus-driven diseases: new insights into their pathogenesis. Curr Opin Virol 2021;51:9-15. [PMID: 34555675 DOI: 10.1016/j.coviro.2021.09.002] [Reference Citation Analysis]
3 Pilania RK, Anjani G, Saini AG, Jain R, Suri D, Rawat A. X-Linked Thrombocytopenia and Vanishing White Matter Disease in a Child: Double Tragedy. J Clin Immunol 2020;40:1176-80. [PMID: 32865661 DOI: 10.1007/s10875-020-00858-8] [Reference Citation Analysis]
4 Ebstein F, Küry S, Papendorf JJ, Krüger E. Neurodevelopmental Disorders (NDD) Caused by Genomic Alterations of the Ubiquitin-Proteasome System (UPS): the Possible Contribution of Immune Dysregulation to Disease Pathogenesis. Front Mol Neurosci 2021;14:733012. [PMID: 34566579 DOI: 10.3389/fnmol.2021.733012] [Reference Citation Analysis]
5 Moore R, Puniya BL, Powers R, Guda C, Bayles KW, Berkowitz DB, Helikar T. Integrative network analyses of transcriptomics data reveal potential drug targets for acute radiation syndrome. Sci Rep 2021;11:5585. [PMID: 33692493 DOI: 10.1038/s41598-021-85044-5] [Reference Citation Analysis]
6 Rae W, Ward D, Mattocks C, Pengelly RJ, Eren E, Patel SV, Faust SN, Hunt D, Williams AP. Clinical efficacy of a next-generation sequencing gene panel for primary immunodeficiency diagnostics. Clin Genet 2018;93:647-55. [PMID: 29077208 DOI: 10.1111/cge.13163] [Cited by in Crossref: 30] [Cited by in F6Publishing: 28] [Article Influence: 7.5] [Reference Citation Analysis]
7 Pietrucha B, Heropolitańska-Pliszka E, Geffers R, Enßen J, Wieland B, Bogdanova NV, Dörk T. Clinical and Biological Manifestation of RNF168 Deficiency in Two Polish Siblings. Front Immunol 2017;8:1683. [PMID: 29255463 DOI: 10.3389/fimmu.2017.01683] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 1.4] [Reference Citation Analysis]
8 Sharifinejad N, Jamee M, Zaki-Dizaji M, Lo B, Shaghaghi M, Mohammadi H, Jadidi-Niaragh F, Shaghaghi S, Yazdani R, Abolhassani H, Aghamohammadi A, Azizi G. Clinical, Immunological, and Genetic Features in 49 Patients With ZAP-70 Deficiency: A Systematic Review. Front Immunol 2020;11:831. [PMID: 32431715 DOI: 10.3389/fimmu.2020.00831] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
9 Purzycka-Bohdan D, Nowicki RJ, Herms F, Casanova JL, Fouéré S, Béziat V. The Pathogenesis of Giant Condyloma Acuminatum (Buschke-Lowenstein Tumor): An Overview. Int J Mol Sci 2022;23:4547. [PMID: 35562936 DOI: 10.3390/ijms23094547] [Reference Citation Analysis]
10 Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol 2021:S0198-8859(21)00061-6. [PMID: 33715910 DOI: 10.1016/j.humimm.2021.02.011] [Reference Citation Analysis]
11 Gruber C, Bogunovic D. Incomplete penetrance in primary immunodeficiency: a skeleton in the closet. Hum Genet 2020;139:745-57. [PMID: 32067110 DOI: 10.1007/s00439-020-02131-9] [Cited by in Crossref: 22] [Cited by in F6Publishing: 16] [Article Influence: 11.0] [Reference Citation Analysis]