Johannes G. Dauwerse

Author

Leiden University

Also Known As

J Dauwerse, J G Dauwerse, J. G. Dauwerse, J.G. Dauwerse, Johannes G Dauwerse, Johannes G. Dauwerse

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Leiden University Leiden University Medical Center Centre for Human Drug Research Erasmus University Rotterdam Radboud University Nijmegen

About

Johannes G. Dauwerse is an author at Leiden University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	2K
2	Natural Sciences	3	3	515
3	Cell Biology	3	3	387
4	Health Sciences	1	1	68
5	Biology	1	1	125

Johannes G. Dauwerse

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
A Unifying Genetic Model for Facioscapulohumeral Muscular Dystrophy Richard J.L.F. Lemmers, Patrick J. van der Vliet, Rinse Klooster, Science Facioscapulohumeral Muscular DystrophyDevelopmental BiologyMendelian DisorderFshd PatientsGenetic Disorder	2010	756
Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome Johannes G. Dauwerse, Jill Dixon, Saskia Seland, Nature Genetics Mendelian DisorderTreacher CollinsRna PolymerasesGenetic DisorderNatural Sciences	2010	364
Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease Irma S Lantinga‐van Leeuwen, Johannes G. Dauwerse, Hans J. Baelde, Human Molecular Genetics Pkd1 ExpressionPathologyNephrologyGlomerulonephritisRenal Function	2004	350
High-resolution <i>in situ</i> hybridization using DNA halo preparations J. Wiegant, Wouter Kalle, L.H.F. Mullenders, Human Molecular Genetics	1992	173
Multiple colors by fluorescence <i>in situ</i> hybridization using ratio-labelled DNA probes create a molecular karyotype Johannes G. Dauwerse, J. Wiegant, Anton K. Raap, Human Molecular Genetics CytogeneticsRatio-labelled Dna ProbesGeneticsDna AnalysisMolecular Biology	1992	125
Broad phenotype of cysteine-altering <i>NOTCH3</i> variants in UK Biobank Julie W. Rutten, Remco J. Hack, Marco Duering, Neurology	2020	92
De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16). Janette Lamb, Peter C. Harris, Andrew O.M. Wilkie, PubMed	1993	90
Variation in microdeletions of the cyclic AMP-responsive element-binding protein gene at chromosome band 16p13.3 in the Rubinstein-Taybi syndrome Ruthann I. Blough, Fred Petrij, Johannes G. Dauwerse, American Journal of Medical Genetics Rubinstein-taybi SyndromeGeneticsTotal Cbp DeletionGenetic EpidemiologyGenomic Mechanism	2000	74
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1). M.H. Breuning, F.G.M. Snijdewint, HG Brunner, Journal of Medical Genetics CytogeneticsGeneticsHuman PolymorphismPathologyMolecular Biology	1990	72
Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p Johannes G. Dauwerse, Tim Kievits, G.C. Beverstock, Cytogenetic and Genome Research CytogeneticsMixed-phenotype Acute LeukemiaGeneticsPathologyEpigenetics	1990	68

Page 1