Paola Griseri
Istituto Giannina Gaslini(IT)
Publications by Year
Research Areas
Congenital gastrointestinal and neural anomalies, Congenital Anomalies and Fetal Surgery, Intestinal Malrotation and Obstruction Disorders, Digestive system and related health, Cancer-related molecular mechanisms research
Most-Cited Works
- → Hirschsprung disease, associated syndromes and genetics: a review(2007)1,197 cited
- → Differential Contributions of Rare and Common, Coding and Noncoding Ret Mutations to Multifactorial Hirschsprung Disease Liability(2010)243 cited
- → Functional Loss of Semaphorin 3C and/or Semaphorin 3D and Their Epistatic Interaction with Ret Are Critical to Hirschsprung Disease Liability(2015)147 cited
- → Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model(2013)128 cited
- → Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes(2017)91 cited
- → Double Heterozygosity for a RET Substitution Interfering with Splicing and an EDNRB Missense Mutation in Hirschsprung Disease(1999)90 cited
- → A synonymous polymorphism of the Tristetraprolin (TTP) gene, an AU-rich mRNA-binding protein, affects translation efficiency and response to Herceptin treatment in breast cancer patients(2011)75 cited
- → Constitutive ERK activity induces downregulation of tristetraprolin, a major protein controlling interleukin8/CXCL8 mRNA stability in melanoma cells(2011)67 cited
- → Induction of RET Dependent and Independent Pro-Inflammatory Programs in Human Peripheral Blood Mononuclear Cells from Hirschsprung Patients(2013)55 cited
- → FHIT andp53 gene abnormalities in bronchioloalveolar carcinomas. Correlations with clinicopathological data and K-ras mutations(1998)50 cited