Marianne Hoogeveen‐Westerveld

Author

Also Known As

Hoogeveen-Westerveld, M, M Hoogeveen-Westerveld, M Hoogeveen‐Westerveld, M. Hoogeveen-Westerveld, M. Hoogeveen‐Westerveld, M. Hoogeveen–Westerveld, Marianne Hoogeveen-Westerveld, Marianne Hoogeveen‐Westerveld

Publications

2.7K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Erasmus University Rotterdam University College London University Medical Center Utrecht Boston Children's Hospital

About

Marianne Hoogeveen‐Westerveld is an author at Erasmus MC specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	1.1K
2	Public Health	4	4	170
3	Natural Sciences	3	3	266
4	Engineering	2	2	46
5	Social Sciences	1	1	31

Marianne Hoogeveen‐Westerveld

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo Edwin Mientjes, Ingeborg M. Nieuwenhuizen, Laura Kirkpatrick, Neurobiology of Disease Knockout MouseSignal TransductionConditional Fmr1 KnockFmrp FunctionNeuroscience	2005	286
Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex. L. H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Marian A. Kroos, The EMBO Journal Lysosomal Alpha-glucosidaseBiosynthesisCellular EnzymologyBiochemistryPrimary Structure	1988	174
Characterization of the human lysosomal α-glucosidase gene Lies H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Arnold Reuser, Biochemical Journal	1990	126
Enzyme therapy and immune response in relation to CRIM status: the Dutch experience in classic infantile Pompe disease Carin M. Van Gelder, Marianne Hoogeveen‐Westerveld, Marian A. Kroos, Journal of Inherited Metabolic Disease	2014	105
Functional assessment of variants in the <i>TSC1</i> and <i>TSC2</i> genes identified in individuals with Tuberous Sclerosis Complex Marianne Hoogeveen‐Westerveld, Marjolein Wentink, Diana van den Heuvel, Human Mutation	2011	92
Effects of a higher dose of alglucosidase alfa on ventilator‐free survival and motor outcome in classic infantile Pompe disease: an open‐label single‐center study Carin M. Van Gelder, Esther Poelman, Iris Plug, Journal of Inherited Metabolic Disease	2016	83
Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations Mark Nellist, Rutger W. W. Brouwer, Christel Kockx, BMC Medical Genetics	2015	82
TORC1‐dependent epilepsy caused by acute biallelic <i>Tsc1</i> deletion in adult mice Elisabeth Abs, Susanna M. I. Goorden, Jadwiga Schreiber, Annals of Neurology	2013	79
Rheb Is Essential for Murine Development Susanna M. I. Goorden, Marianne Hoogeveen‐Westerveld, Caroline Cheng, Molecular and Cellular Biology Ras HomologMurine DevelopmentProtein FunctionSignal TransductionDevelopmental Biology	2011	76
Functional Assessment of<i>TSC</i>2 Variants Identified in Individuals with Tuberous Sclerosis Complex Marianne Hoogeveen‐Westerveld, Rosemary Ekong, Karin Mayer, Human Mutation	2012	76

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