L. Clarke - Concepedia

Author

L. Clarke

Also Known As

CLARKE L,, Clarke, L, Craigen, William J., D Burke, E. Roussou, Joji Decolongon, Jones, Simon, L A Clarke, L CLARKE, L Clarke

269

Publications

8.8K

Citations

H-Index

161

Concepts

All Affiliations

University of British Columbia Child and Family Research Institute BC Children's Hospital University of Reading Imperial College London

About

L. Clarke is an author at University of British Columbia specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	39	2.8K
2	Health Sciences	8	8	241
3	Natural Sciences	5	5	156
4	Engineering	2	2	46
5	Education	1	1	20

L. Clarke

103

Publications

7.5K

Citations

H-Index

Page 1

	Year	Citations
Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human α-L-iduronidase (laronidase) J. E. Wraith, L. Clarke, Michael Beck, The Journal of Pediatrics Enzyme Replacement TherapyRecombinant Human α-L-iduronidasePathologyNeurologyMultinational Study	2004	540
Mucopolysaccharidosis I: Management and Treatment Guidelines Joseph Muenzer, J. E. Wraith, L. Clarke PEDIATRICS	2008	451
Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm Håkan Telenius, Berry Kremer, Y. Paul Goldberg, Nature Genetics SpermatogenesisGenetic DisorderGeneticsGameteMolecular Genetics	1994	449
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. Maximilian Muenke, Karen W. Gripp, Donna M. McDonald‐McGinn, PubMed	1997	394
Long-term Efficacy and Safety of Laronidase in the Treatment of Mucopolysaccharidosis I L. Clarke, J. E. Wraith, Michael Beck, PEDIATRICS	2008	335
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes Gary A. Bellus, Karin Gaudenz, Elaine H. Zackai, Nature Genetics SclerostinBone Morphogenic ProteinGeneticsIdentical MutationsCraniofacial Anomalies	1996	320
Characterization of Fabry Disease in 352 Pediatric Patients in the Fabry Registry Robert J. Hopkin, John J. Bissler, Maryam Banikazemi, Pediatric Research Fabry DiseaseMendelian DisorderPediatric PatientsPediatricsPathology	2008	297
Exome Sequencing Identifies <i>SMAD3</i> Mutations as a Cause of Familial Thoracic Aortic Aneurysm and Dissection With Intracranial and Other Arterial Aneurysms Ellen S. Regalado, Dongchuan Guo, Carlos Villamizar, Circulation Research	2011	288
Murine mucopolysaccharidosis type I: targeted disruption of the murine alpha-L-iduronidase gene L. Clarke Human Molecular Genetics	1997	175
Porcine models for the metabolic syndrome, digestive and bone disorders: a general overview J.C. Litten-Brown, A.M. Corson, L. Clarke animal	2010	157

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