Robert S. Wildin - Concepedia

Author

Robert S. Wildin

Oregon Health & Science University ORCID

Also Known As

R S WILDIN, R S Wildin, R. S. Wildin, R. Wildin, Robert S Wildin, Robert S. Wildin, Robert Wildin, Wildin, Robert

Publications

4.6K

Citations

H-Index

Concepts

All Affiliations

Oregon Health & Science University University of Washington St. Luke's Children's Hospital National Institutes of Health Baylor College of Medicine

About

Robert S. Wildin is an author at Oregon Health & Science University specializing in medicine, pathology, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	13	2.8K
2	Public Health	3	3	82
3	Health Sciences	2	2	1.9K
4	Allergy	1	1	20
5	Biology	1	1	63

Robert S. Wildin

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy Robert S. Wildin, Fred Ramsdell, Jane Peake, Nature Genetics Knockout MouseMetabolic SyndromeHuman EquivalentXenotransplantationGrowth Hormone	2001	1.9K
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 Jan Kazenwadel, Genevieve A. Secker, Yajuan J. Liu, Blood	2011	276
Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation Olivier Baud, Olivier Goulet, Danielle Canioni, New England Journal of Medicine ImmunodeficienciesImmunologyGenetic EpidemiologyPathologyX-linked Syndrome	2001	259
A retrovirus vector expressing the putative mammary oncogene int-1 causes partial transformation of a mammary epithelial cell line Anthony M.C. Brown, Robert S. Wildin, Thomas J. Prendergast, Cell Viral ReplicationPathogenesisImmunologyRetrovirus VectorPutative Mammary Oncogene	1986	189
Developmental regulation of lck gene expression in T lymphocytes. Robert S. Wildin, Alex M. Garvin, Shashi Singh Pawar, The Journal of Experimental Medicine Lymphocyte DevelopmentT-regulatory CellImmunologyPathologyAntigen Processing	1991	118
Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , which Encode Subcomponents C1r and C1s of Complement Ines Kapferer‐Seebacher, Melanie Pepin, Roland Werner, The American Journal of Human Genetics	2016	116
Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm Luke Boyd, Joseph S. Livingston, Michael G. Brown, American Journal of Medical Genetics Part A	2005	83
Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome Ephrat Levy‐Lahad, Robert S. Wildin The Journal of Pediatrics Endocrine DiseaseDiabetesHematologyPediatricsPathology	2001	81
Sequences on the human Y chromosome homologous to the autosomal gene for argininosuccinate synthetase S.P. Daiger, Robert S. Wildin, T S Su Nature BiologyHuman Y ChromosomeAutosomal GeneGeneticsGenome Structure	1982	63
Identification of novel candidate disease genes from de novo exonic copy number variants Tomasz Gambin, Bo Yuan, Weimin Bi, Genome Medicine	2017	62

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