Tamim H. Shaikh
University of Pennsylvania(US)University of Colorado Denver(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Congenital heart defects research, Genomics and Rare Diseases, Chromosomal and Genetic Variations, Prenatal Screening and Diagnostics
Most-Cited Works
- → Microduplications of 16p11.2 are associated with schizophrenia(2009)732 cited
- → A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay(2010)671 cited
- → Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes(2009)530 cited
- → Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis(2000)529 cited
- → Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations(2009)527 cited
- → High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications(2009)389 cited