Ans van den Ouweland

Author

Erasmus University Rotterdam

Also Known As

A Van Den Ouweland, A van den Ouweland, A. van den Ouweland, Ans van den Ouweland

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

Erasmus University Rotterdam Erasmus MC University Medical Center Utrecht Leiden University University College London

About

Ans van den Ouweland is an author at Erasmus University Rotterdam specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	976
2	Cell Biology	3	3	103
3	Natural Sciences	1	1	42
4	Public Health	1	1	52
5	Biostatistics	1	1	52

Ans van den Ouweland

Publications

3.5K

Citations

H-Index

Page 1

	Year	Citations
Identification of the Tuberous Sclerosis Gene <i>TSC1</i> on Chromosome 9q34 Marjon van Slegtenhorst, Ronald De Hoogt, Caroline Hermans, Science	1997	1.7K
Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex Őzgür Sancak, Mark Nellist, Miriam Goedbloed, European Journal of Human Genetics Tuberous Sclerosis ComplexMolecular Diagnostic TechniquesDiagnostic Dna TechniquesGenetic DisorderMedicine	2005	481
Cognitive impairment in tuberous sclerosis complex is a multifactorial condition Floor E. Jansen, Koen L. Vincken, Ale Algra, Neurology	2007	206
A Cystic Fibrosis Mutation Associated with Mild Lung Disease K. H. Gan, Henk J. Veeze, Ans van den Ouweland, New England Journal of Medicine	1995	177
Common C-to-T Substitution at Position −480 of the Hepatic Lipase Promoter Associated With a Lowered Lipase Activity in Coronary Artery Disease Patients Hans Jansen, Adrie J.M. Verhoeven, Lilian Weeks, Arteriosclerosis Thrombosis and Vascular Biology	1997	164
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation Marjon van Slegtenhorst, Senno Verhoef, A.M.P. Tempelaars, Journal of Medical Genetics Tuberous Sclerosis ComplexTsc2 GeneMendelian DisorderGenetic DisorderGenetics	1999	136
Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique Rob Willemsen, Arie Smits, Serieta Mohkamsing, Human Genetics Fragile X SyndromeRapid Antibody TestDiagnosisFragile X SpectrumPathology	1997	121
Overlapping neurologic and cognitive phenotypes in patients with <i>TSC1</i> or <i>TSC2</i> mutations Floor E. Jansen, Olga Braams, Koen L. Vincken, Neurology	2007	121
Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations Mark Nellist, Rutger W. W. Brouwer, Christel Kockx, BMC Medical Genetics	2015	82
Functional assessment of TSC1 missense variants identified in individuals with tuberous sclerosis complex Marianne Hoogeveen‐Westerveld, Rosemary Ekong, Sue Povey, Human Mutation	2011	54

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