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For: Ekulu PM, Nkoy AB, Adebayo OC, Kazadi OK, Aloni MN, Arcolino FO, Ngiyulu RM, Gini JE, Lepira FB, Van den Heuvel LP, Levtchenko EN. A focus on the association of Apol1 with kidney disease in children. Pediatr Nephrol 2021;36:777-88. [PMID: 32253519 DOI: 10.1007/s00467-020-04553-z] [Cited by in Crossref: 11] [Cited by in F6Publishing: 5] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Pollak MR, Friedman DJ. APOL1-Associated Kidney Disease. Emery and Rimoin' s Principles and Practice of Medical Genetics and Genomics 2023. [DOI: 10.1016/b978-0-12-812534-2.00007-2] [Reference Citation Analysis]
2 Beng-Ongey H, Robinson JS, Moxey-Mims M. Chronic kidney disease emerging trends in children and what to do about it. J Natl Med Assoc 2022;114:S50-5. [PMID: 35660045 DOI: 10.1016/j.jnma.2022.05.002] [Reference Citation Analysis]
3 Gbadegesin R, Saleem M, Lipska-ziętkiewicz BS, Boyer O. Genetic Basis of Nephrotic Syndrome. Pediatric Nephrology 2022. [DOI: 10.1007/978-3-030-52719-8_90] [Reference Citation Analysis]
4 Boyer O, Gbadegesin R, Waters A. Clinical Aspects of Genetic Forms of Nephrotic Syndrome. Pediatric Nephrology 2022. [DOI: 10.1007/978-3-030-52719-8_91] [Reference Citation Analysis]
5 Vastrad B, Vastrad C. Screening key genes and signaling pathways in COVID-19 infection and its associated complications by integrated bioinformatics analysis.. [DOI: 10.1101/2021.09.24.461631] [Reference Citation Analysis]
6 Adebayo OC, Betukumesu DK, Nkoy AB, Adesoji OM, Ekulu PM, Van den Heuvel LP, Levtchenko EN, Labarque V. Clinical and genetic factors are associated with kidney complications in African children with sickle cell anaemia. Br J Haematol 2021. [PMID: 34545573 DOI: 10.1111/bjh.17832] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
7 Ekulu PM, Adebayo OC, Decuypere JP, Bellucci L, Elmonem MA, Nkoy AB, Mekahli D, Bussolati B, van den Heuvel LP, Arcolino FO, Levtchenko EN. Novel Human Podocyte Cell Model Carrying G2/G2 APOL1 High-Risk Genotype. Cells 2021;10:1914. [PMID: 34440683 DOI: 10.3390/cells10081914] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Adebayo OC, Van den Heuvel LP, Olowu WA, Levtchenko EN, Labarque V. Sickle cell nephropathy: insights into the pediatric population. Pediatr Nephrol 2021. [PMID: 34050806 DOI: 10.1007/s00467-021-05126-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Esoh K, Wonkam A. Evolutionary history of sickle-cell mutation: implications for global genetic medicine. Hum Mol Genet 2021;30:R119-28. [PMID: 33461216 DOI: 10.1093/hmg/ddab004] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
10 Boyer O, Gbadegesin R, Waters A. Clinical Aspects of Genetic Forms of Nephrotic Syndrome. Pediatric Nephrology 2021. [DOI: 10.1007/978-3-642-27843-3_91-1] [Reference Citation Analysis]
11 Gbadegesin R, Saleem M, Lipska-ziętkiewicz BS, Boyer O. Genetic Basis of Nephrotic Syndrome. Pediatric Nephrology 2021. [DOI: 10.1007/978-3-642-27843-3_90-1] [Reference Citation Analysis]