G. Wildhardt - Concepedia

Author

G. Wildhardt

Johannes Gutenberg University Mainz

Also Known As

G Wildhardt, G. WILDHARDT, G. Wildhardt, GABI WILDHARDT, Gabi Wildhardt

Publications

823

Citations

H-Index

Concepts

All Affiliations

Johannes Gutenberg University Mainz Heidelberg University

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	157
2	Public Health	2	2	46
3	Biology	1	1	46
4	Endocrinology	1	1	11
5	Epidemiology	1	1	14

G. Wildhardt

Publications

775

Citations

H-Index

Page 1

	Year	Citations
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes Christian P. Kratz, Lude Franke, Harm Peters, British Journal of Cancer	2015	207
Enhancer deletions of the <i>SHOX</i> gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain J Chen, G. Wildhardt, Zeyan Zhong, Journal of Medical Genetics	2009	130
Correlation of germ-line mutations and two-hit inactivation of the <i>WT1</i> gene with Wilms tumors of stromal–predominant histology Valerié Schumacher, Susanne A. Schneider, A. Figge, Proceedings of the National Academy of Sciences	1997	130
Three α‐amylase genes of <i>Aspergillus oryzae</i> exhibit identical intron‐exon organization Stefan G. R. Wirsel, Astrid Lachmund, G. Wildhardt, Molecular Microbiology	1989	73
Ten novel mutations found in aniridia Matthias T. F. Wolf, Birgit Lorenz, Andreas Winterpacht, Human Mutation Ocular DiseaseGeneticsMolecular GeneticsDisease Gene IdentificationGenomics	1998	46
Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations Susanne A. Schneider, G. Wildhardt, R. Ludwig, Human Genetics Genome InstabilitySomatic VariantMendelian DisorderGenetic DisorderMedicine	1993	43
Spondyloperipheral dysplasia is caused by truncating mutations in the C‐propeptide of COL2A1 Andreas Zankl, Bernhard Zabel, Katja Hilbert, American Journal of Medical Genetics Part A	2004	42
RNA polymerase chain reaction detects different levels of four alternatively spliced WT1 transcripts in Wilms' tumors. Bernhard Brenner, G. Wildhardt, Susanne A. Schneider, PubMed	1992	36
A familial case of achondrogenesis type II caused by a dominant <i>COL2A1</i> mutation and “patchy” expression in the mosaic father Francesca Forzano, Mario Lituania, V. Superti‐Furga, American Journal of Medical Genetics Part A CytogeneticsGeneticsPathologyAchondrogenesis Type IiMolecular Genetics	2007	32
Mutation screening for the prothrombin variant G20210A by melting point analysis with the Light Cycler system: atypical results, detection of the variant C20209T and possible clinical implications C. WYLENZEK, J. TRUBENBACH, Peter Gohl, Clinical & Laboratory Haematology GeneticsFactor VGenetic EpidemiologyMolecular BiologyPathology	2005	14

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