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For: Singh A, Jindal AK, Joshi V, Anjani G, Rawat A. An updated review on phenocopies of primary immunodeficiency diseases. Genes Dis 2020;7:12-25. [PMID: 32181272 DOI: 10.1016/j.gendis.2019.09.007] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Rey-jurado E, Poli MC. Functional genetics in inborn errors of immunity. Future Rare Diseases 2021;1:FRD11. [DOI: 10.2217/frd-2020-0003] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Singh S, Zhao X, Zhang H. Primary Immune Deficiencies - A rapidly emerging area of basic and clinical research. Genes Dis 2020;7:1-2. [PMID: 32181270 DOI: 10.1016/j.gendis.2020.01.006] [Reference Citation Analysis]
3 Cos Esquius ML, López Montesinos I, Gimeno Martinez R, Eguía Núñez J, Caballero-Rabasco MA, Sánchez González B, López García A, Mellibovsky L. Severe COVID-19 pneumonia in Good syndrome with a favorable outcome. Clin Immunol 2021;:108789. [PMID: 34197951 DOI: 10.1016/j.clim.2021.108789] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 Aluri J, Cooper MA. Genetic Mosaicism as a Cause of Inborn Errors of Immunity. J Clin Immunol 2021;41:718-28. [PMID: 33864184 DOI: 10.1007/s10875-021-01037-z] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Abraham RS, Butte MJ. The New "Wholly Trinity" in the Diagnosis and Management of Inborn Errors of Immunity. J Allergy Clin Immunol Pract 2021;9:613-25. [PMID: 33551037 DOI: 10.1016/j.jaip.2020.11.044] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
6 Becherucci F, Landini S, Cirillo L, Mazzinghi B, Romagnani P. Look Alike, Sound Alike: Phenocopies in Steroid-Resistant Nephrotic Syndrome. Int J Environ Res Public Health 2020;17:E8363. [PMID: 33198123 DOI: 10.3390/ijerph17228363] [Reference Citation Analysis]
7 van der Made CI, Potjewijd J, Hoogstins A, Willems HPJ, Kwakernaak AJ, de Sevaux RGL, van Daele PLA, Simons A, Heijstek M, Beck DB, Netea MG, van Paassen P, Elizabeth Hak A, van der Veken LT, van Gijn ME, Hoischen A, van de Veerdonk FL, Leavis HL, Rutgers A. Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS. J Allergy Clin Immunol 2021:S0091-6749(21)00819-8. [PMID: 34048852 DOI: 10.1016/j.jaci.2021.05.014] [Cited by in Crossref: 19] [Cited by in F6Publishing: 12] [Article Influence: 19.0] [Reference Citation Analysis]
8 Sreedharanunni S, Jamwal M, Balakrishnan A, Aravindan AV, Sharma R, Singh N, Rajpal S, Singla S, Khadwal AR, Ahluwalia J, Malhotra P, Das R. Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation-An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlap. Leuk Res 2021;112:106753. [PMID: 34856508 DOI: 10.1016/j.leukres.2021.106753] [Reference Citation Analysis]
9 Mohtashami M, Razavi A, Abolhassani H, Aghamohammadi A, Yazdani R. Primary Immunodeficiency and Thrombocytopenia. Int Rev Immunol 2021;:1-43. [PMID: 33464134 DOI: 10.1080/08830185.2020.1868454] [Reference Citation Analysis]
10 Casamayor-Polo L, López-Nevado M, Paz-Artal E, Anel A, Rieux-Laucat F, Allende LM. Immunologic evaluation and genetic defects of apoptosis in patients with autoimmune lymphoproliferative syndrome (ALPS). Crit Rev Clin Lab Sci 2021;58:253-74. [PMID: 33356695 DOI: 10.1080/10408363.2020.1855623] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]