Wayne A. Cabral - Concepedia

Author

Wayne A. Cabral

Eunice Kennedy Shriver National Institute of Child Health and Human Development ORCID

Also Known As

Chen, Yulong, W A Cabral, W CABRAL, W. Cabral, W.A. Cabral, W.A. Cabral⁎, Wayne A Cabral, Wayne A. Cabral, Wayne Cabral, Yamauchi, Mitsuo

Publications

5.7K

Citations

H-Index

Concepts

All Affiliations

Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health University of Washington National Human Genome Research Institute Hanusch Hospital

About

Wayne A. Cabral is an author at Eunice Kennedy Shriver National Institute of Child Health and Human Development specializing in medicine, developmental biology, and osteogenesis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	22	2.2K
2	Natural Sciences	5	5	241
3	Engineering	2	2	64
4	Health Sciences	1	1	14
5	Social Sciences	1	1	33

Wayne A. Cabral

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta Wayne A. Cabral, Weizhong Chang, Aileen M. Barnes, Nature Genetics Bone DiseaseDevelopmental BiologyProlyl 3-Hydroxylase 1Lethal/severe Osteogenesis ImperfectaMetabolic Bone Disease	2007	477
In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice Luke W. Koblan, Michael R. Erdos, Christopher Wilson, Nature Knockout MouseDevelopmental BiologyDegenerative DiseaseVivo BaseMedicine	2021	467
Deficiency of Cartilage-Associated Protein in Recessive Lethal Osteogenesis Imperfecta Aileen M. Barnes, Weizhong Chang, Roy Morello, New England Journal of Medicine Developmental BiologyBone Morphogenic ProteinMedicineGeneticsSevere Osteoporosis	2006	346
Candidate Cell and Matrix Interaction Domains on the Collagen Fibril, the Predominant Protein of Vertebrates Shawn M. Sweeney, Joseph Orgel, Andrzej Fertala, Journal of Biological Chemistry	2008	290
Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding Aileen M. Barnes, Erin M. Carter, Wayne A. Cabral, New England Journal of Medicine Bone FragilityCollagen FoldingNormal Collagen FoldingGeneticsOsteogenesis	2010	175
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta Uschi Lindert, Wayne A. Cabral, Surasawadee Ausavarat, Nature Communications	2016	141
Mutations Near Amino End of α1(I) Collagen Cause Combined Osteogenesis Imperfecta/Ehlers-Danlos Syndrome by Interference with N-propeptide Processing Wayne A. Cabral, Elena Makareeva, Alain Colige, Journal of Biological Chemistry	2005	131
Abnormal Type I Collagen Post-translational Modification and Crosslinking in a Cyclophilin B KO Mouse Model of Recessive Osteogenesis Imperfecta Wayne A. Cabral, Irina Perdivara, MaryAnn Weis, PLoS Genetics	2014	124
Mapping of SPARC/BM-40/Osteonectin-binding Sites on Fibrillar Collagens Camilla Giudici, Nicolas Raynal, Hanna Wiedemann, Journal of Biological Chemistry	2008	100
Absence of<i>FKBP10</i>in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix Aileen M. Barnes, Wayne A. Cabral, MaryAnn Weis, Human Mutation	2012	97

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