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Cited by in F6Publishing
For: Mu W, Schiess N, Orthmann-Murphy JL, El-Hattab AW. The utility of whole exome sequencing in diagnosing neurological disorders in adults from a highly consanguineous population. J Neurogenet 2019;33:21-6. [PMID: 30724636 DOI: 10.1080/01677063.2018.1555249] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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1 Ahuja AS, Selvam P, Vadlamudi C, Chopra H, Richter JE Jr, Macklin SK, Samreen A, Helmi H, Mohammaad AN, Hines S, Davila MC, Atwal PS, Caulfield TR. Genomics combined with a protein informatics platform to assess a novel pathogenic variant c.1024 A>G (p.K342E) in OPA1 in a patient with autosomal dominant optic atrophy. Ophthalmic Genet 2020;41:563-9. [PMID: 32940104 DOI: 10.1080/13816810.2020.1814344] [Reference Citation Analysis]
2 Muthaffar OY. The Utility of Whole Exome Sequencing in Diagnosing Pediatric Neurological Disorders. Balkan J Med Genet 2020;23:17-24. [PMID: 33816068 DOI: 10.2478/bjmg-2020-0028] [Reference Citation Analysis]
3 Sun S, Chen L, Wang Y, Wang J, Li N, Wang X. Further delineation of autosomal recessive intellectual disability syndrome caused by homozygous variant of the NSUN2 gene in a chinese pedigree. Mol Genet Genomic Med 2020;8:e1518. [PMID: 33002343 DOI: 10.1002/mgg3.1518] [Reference Citation Analysis]