Robert S. Wildin
University of Vermont(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, T-cell and B-cell Immunology, BRCA gene mutations in cancer, Immune Cell Function and Interaction
Most-Cited Works
- → X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy(2001)1,872 cited
- → Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome(2002)702 cited
- → Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature(2011)277 cited
- → Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation(2001)259 cited
- → A retrovirus vector expressing the putative mammary oncogene int-1 causes partial transformation of a mammary epithelial cell line(1986)189 cited
- → IPEX and FOXP3: Clinical and research perspectives(2005)164 cited
- → Research Directions in the Clinical Implementation of Pharmacogenomics: An Overview of US Programs and Projects(2018)130 cited
- → Developmental regulation of lck gene expression in T lymphocytes.(1991)118 cited
- → Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , which Encode Subcomponents C1r and C1s of Complement(2016)116 cited
- → Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm(2005)83 cited