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Cited by in F6Publishing
For: Khan NM, Hussain B, Zheng C, Khan A, Masoud MS, Gu Q, Qiu L, Malik NA, Qasim M, Tariq M, Chang J. Updates on Clinical and Genetic Heterogeneity of ASPM in 12 Autosomal Recessive Primary Microcephaly Families in Pakistani Population. Front Pediatr 2021;9:695133. [PMID: 34295862 DOI: 10.3389/fped.2021.695133] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Skarp S, Korvala J, Kotimäki J, Sorri M, Männikkö M, Hietikko E. New Genetic Variants in CYP2B6 and SLC6A Support the Role of Oxidative Stress in Familial Ménière’s Disease. Genes 2022;13:998. [DOI: 10.3390/genes13060998] [Reference Citation Analysis]
2 Fatumo S, Chikowore T, Choudhury A, Ayub M, Martin AR, Kuchenbaecker K. A roadmap to increase diversity in genomic studies. Nat Med 2022. [PMID: 35145307 DOI: 10.1038/s41591-021-01672-4] [Cited by in Crossref: 29] [Cited by in F6Publishing: 36] [Article Influence: 29.0] [Reference Citation Analysis]
3 Naqvi SF, Shabbir RMK, Tolun A, Basit S, Malik S. A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family. Genet Test Mol Biomarkers 2022;26:37-42. [PMID: 35089071 DOI: 10.1089/gtmb.2021.0231] [Reference Citation Analysis]