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Cited by in F6Publishing
For: Cerminara M, Spirito G, Pisciotta L, Squillario M, Servetti M, Divizia MT, Lerone M, Berloco B, Boeri S, Nobili L, Vozzi D, Sanges R, Gustincich S, Puliti A. Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances. Front Genet 2021;12:625564. [PMID: 33679889 DOI: 10.3389/fgene.2021.625564] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
Number Citing Articles
1 Haavik J. Genome Guided Personalized Drug Therapy in Attention Deficit Hyperactivity Disorder. Front Psychiatry 2022;13:925442. [DOI: 10.3389/fpsyt.2022.925442] [Reference Citation Analysis]
2 Servetti M, Pisciotta L, Tassano E, Cerminara M, Nobili L, Boeri S, Rosti G, Lerone M, Divizia MT, Ronchetto P, Puliti A. Neurodevelopmental Disorders in Patients With Complex Phenotypes and Potential Complex Genetic Basis Involving Non-Coding Genes, and Double CNVs. Front Genet 2021;12:732002. [PMID: 34621295 DOI: 10.3389/fgene.2021.732002] [Reference Citation Analysis]
3 Yang L, Zhao S, Ma N, Liu L, Li D, Li X, Wang Z, Song X, Wang Y, Wang D. Novel DIP2C gene splicing variant in an individual with focal infantile epilepsy. Am J Med Genet A 2022;188:210-5. [PMID: 34617658 DOI: 10.1002/ajmg.a.62524] [Reference Citation Analysis]