Charalambos Papapetrou
Great Ormond Street Hospital(GB)University College London(GB)
Publications by Year
Research Areas
Congenital heart defects research, Congenital Anomalies and Fetal Surgery, Genomics and Chromatin Dynamics, Congenital gastrointestinal and neural anomalies, Folate and B Vitamins Research
Most-Cited Works
- → Mutation Analysis and Embryonic Expression of the HLXB9 Currarino Syndrome Gene(2000)137 cited
- → Susceptibility to spina bifida; an association study of five candidate genes(1998)117 cited
- → Methylenetetrahydrofolate reductase and neural tube defects(1996)100 cited
- → A genetic study of the human T gene and its exclusion as a major candidate gene for sacral agenesis with anorectal atresia(1999)37 cited
- → Mutations of UFD1L Are Not Responsible for the Majority of Cases of DiGeorge Syndrome/Velocardiofacial Syndrome without Deletions within Chromosome 22q11(1999)36 cited
- → The T transcription factor functions as a dimer and exhibits a common human polymorphism Gly‐177‐Asp in the conserved DNA‐binding domain(1997)34 cited
- → The HumanTBX6Gene: Cloning and Assignment to Chromosome 16p11.2(1999)18 cited
- The human T transcription factor : a study of genetics and function.(1999)
- → The T transcription factor functions as a dimer and exhibits a common polymorphism in the conserved DNA binding domain of the human protein(1998)