Gholamali Tariverdian
Publications by Year
Research Areas
Digestive system and related health, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation(2005)374 cited
- → The novel Rho-GTPase activating gene MEGAP / srGAP3 has a putative role in severe mental retardation(2002)214 cited
- → Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy(2008)148 cited
- → Kabuki make-up (Niikawa-Kuroki) syndrome(1992)106 cited
- → Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Parent-Specific Methylation in Fetuses(1997)95 cited
- → Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome(2004)86 cited
- → A monozygotic twin pair with Rett syndrome(1987)74 cited
- → Maternal uniparental disomy 7 - review and further delineation of the phenotype(2000)66 cited
- → Some problems in the genetics of X-linked mental retardation(2000)56 cited
- → Agnathia‐otocephaly complex: Report of three cases with involvement of two different Carnegie stages(2002)55 cited