Jules G. Leroy - Concepedia

Author

Jules G. Leroy

Also Known As

Gibson, Kate, J.G. Leroy, JULES G. LEROY, JULES LEROY, Jules G Leroy, Jules G. Leroy, Jules Gerard Leroy, Jules Leroy, Jules G. Leroy, Leroy, Jules

156

Publications

4.7K

Citations

H-Index

136

Concepts

All Affiliations

Ghent University Hospital University of Antwerp Greenwood Genetic Center Antwerp University Hospital KU Leuven

About

Jules G. Leroy is an author at Ghent University Hospital specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	54	4K
2	Natural Sciences	5	5	205
3	Public Health	4	4	215
4	Health Sciences	3	3	102
5	Arts	1	1	32

Jules G. Leroy

Publications

4.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux Cynthia F. Bartels, Hülya Bükülmez, Pius S. Padayatti, The American Journal of Human Genetics SclerostinSignal TransductionMolecular PhysiologyBone Morphogenic ProteinGenetic Disorder	2004	363
Mutant Enzymatic and Cytological Phenotypes in Cultured Human Fibroblasts Jules G. Leroy, Robert DeMars Science FibrosisOcular DiseaseAcid PhosphataseOphthalmologyCell Specialization	1967	244
Mutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5 Margaret J. McMillin, Anita E. Beck, Jessica X. Chong, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyPathology	2014	214
I-Cell Disease: Biochemical Studies Jules G. Leroy, Mae Wan Ho, Monica C. MacBrinn, Pediatric Research Autoimmune DiseaseDisease MechanismPathogenesisI-cell DiseasePathology	1972	213
Mutations in different components of FGF signaling in LADD syndrome Edyta Rohmann, Han G. Brunner, Hülya Kayserili, Nature Genetics Developmental BiologyMendelian DisorderHuman GrowthGenetic DisorderGenetics	2006	207
Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy Pia Østergaard, Michael A. Simpson, Antonella Mendola, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyCongenital Lymphedema	2012	187
Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum Michael D. Briggs, Geert Mortier, William G. Cole, The American Journal of Human Genetics Diverse MutationsMusculoskeletal ResearchGenetic DisorderGeneticsCartilage Degeneration	1998	184
Tay-Sachs Disease: Prenatal Diagnosis John S. O’Brien, Shintaro Okada, Dorothy L. Fillerup, Science Maternal ImmunizationInfertilityDiagnosisPathologyMaternal Health	1971	174
I-cell disease: A clinical picture Jules G. Leroy, Jürgen W. Spranger, Murray Feingold, The Journal of Pediatrics Primary ImmunodeficiencyAutoimmune DiseaseHistopathologyImmunologyHematology	1971	167
Deficiency of UDP-N-acetylglucosamine: Lysosomal enzyme N-acetylglucosamine-1-phosphotransferase in organs of I-cell patients Abdül Waheed, Regina Pohlmann, Andrej Hasilík, Biochemical and Biophysical Research Communications Signal TransductionLysosomal Enzyme N-acetylglucosamine-1-phosphotransferaseGenetic DisorderMedicinePathology	1982	147

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