Thiébaut-Noël Willig
Association Française de Pédiatrie Ambulatoire(FR)Clinique Ambroise Paré(FR)
Publications by Year
Research Areas
RNA modifications and cancer, Cancer-related gene regulation, Epigenetics and DNA Methylation, Attention Deficit Hyperactivity Disorder, Infant Development and Preterm Care
Most-Cited Works
- → The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia(1999)784 cited
- Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression.(1999)
- → Identification of New Prognosis Factors from the Clinical and Epidemiologic Analysis of a Registry of 229 Diamond-Blackfan Anemia Patients(1999)182 cited
- → Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind α5 chain-containing human laminin with high affinity(2001)129 cited
- → Diamond-Blackfan anemia(2001)113 cited
- → Identification of Microdeletions Spanning the Diamond-Blackfan Anemia Locus on 19q13 and Evidence for Genetic Heterogeneity(1998)77 cited
- → Ribosomal protein S19 expression during erythroid differentiation(2002)67 cited
- → Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes---a new syndrome?(2001)55 cited
- → High adenosine deaminase level among healthy probands of Diamond Blackfan anemia (DBA) cosegregates with the DBA gene region on chromosome 19q13. The DBA Working Group of Société d'Immunologie Pédiatrique (SHIP).(1998)40 cited