Andreas Winterpacht - Concepedia

Author

Andreas Winterpacht

Johannes Gutenberg University Mainz

Also Known As

A Winterpacht, A. Winterpacht, ANDREAS WINTERPACHT, Andreas Winterpacht, Winterpacht, Andreas

122

Publications

5.4K

Citations

H-Index

136

Concepts

All Affiliations

Johannes Gutenberg University Mainz Friedrich-Alexander-Universität Erlangen-Nürnberg Universitätsklinikum Erlangen Baylor College of Medicine University of Applied Sciences Mainz

About

Andreas Winterpacht is an author at Johannes Gutenberg University Mainz specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	48	3.4K
2	Natural Sciences	9	9	407
3	Public Health	3	3	101
4	Engineering	2	2	87
5	Health Sciences	2	2	46

Andreas Winterpacht

Publications

Citations

H-Index

Page 1

	Year	Citations
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome Sandra D. Dreyer, Guang Zhou, Antonio Baldini, Nature Genetics Renal DysplasiaMendelian DisorderGenetic DisorderGeneticsPathology	1998	526
Nuclear localization of the protein encoded by the Wilms’ tumor gene <i>WT1</i> in embryonic and adult tissues Stefan Mundlos, Jerry Pelletier, André Darveau, Development GeneticsRenal PathologyMolecular GeneticsWt1 ProteinEmbryology	1993	315
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome) Martin Zenker, Julia Mayerle, Markus M. Lerch, Nature Genetics Protein Quality ControlAutoimmune DiseaseGeneticsPathologyJohanson-blizzard Syndrome	2005	270
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene Bärbel Dittrich, Karin Buiting, Bernd Korn, Nature Genetics ChromatinTranscriptional RegulationDevelopmental BiologyDevelopmental GeneticsGenetics	1996	257
<i>PAX8</i>, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms’ tumors Andrej Poleev, Helmut Fickenscher, Stefan Mundlos, Development	1992	227
Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome Roy Morello, Guang Zhou, Sandra D. Dreyer, Nature Genetics GlomerulonephritisLmx1b ContributesUrologyRenal DiseaseMedicine	2001	209
LETM1, deleted in Wolf Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability Kai Stefan Dimmer, Francesca Navoni, Alberto Casarin, Human Molecular Genetics	2007	188
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defect Andreas Winterpacht, Matthias Hilbert, Ulrike Schwarze, Nature Genetics Stickler Dysplasia PhenotypesFibrosisMendelian DisorderGenetic DisorderGenetics	1993	186
Mutation Analysis of LMX1B Gene in Nail-Patella Syndrome Patients Iain McIntosh, Sandra D. Dreyer, Mark V. Clough, The American Journal of Human Genetics	1998	171
LETM1, A Novel Gene Encoding a Putative EF-Hand Ca2+-Binding Protein, Flanks the Wolf–Hirschhorn Syndrome (WHS) Critical Region and Is Deleted in Most WHS Patients Sabine Endele, M. Fuhry, Sang-Jin Pak, Genomics Genetic DisorderGeneticsPathologyMolecular GeneticsMost Whs Patients	1999	154

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