Heide Ritter - Concepedia

Author

Heide Ritter

Charité - Universitätsmedizin Berlin

Also Known As

H. RITTER, H. Ritter, Heide Ritter

Publications

780

Citations

H-Index

Concepts

All Affiliations

Charité - Universitätsmedizin Berlin Max Delbrück Center Humboldt-Universität zu Berlin

About

Heide Ritter is an author at Charité - Universitätsmedizin Berlin specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	780
2	Natural Sciences	2	2	238
3	Public Health	1	1	172
4	Biochemistry	1	1	187
5	Biology	1	1	51

Heide Ritter

Publications

780

Citations

H-Index

Page 1

	Year	Citations
Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia Peter Nürnberg, Hölger Thiele, David Chandler, Nature Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderHuman Ortholog	2001	240
Loss of chondroitin 6-<i>O</i>-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement Hölger Thiele, Masahiro Sakano, Hiroshi Kitagawa, Proceedings of the National Academy of Sciences Bioorganic ChemistryDelta Hexa-galnacGlycobiologyPathologyMolecular Biology	2004	187
Evaluation of a potential epigenetic biomarker by quantitative methyl‐single nucleotide polymorphism analysis Karen Uhlmann, Anja Brinckmann, Mohammad R. Toliat, Electrophoresis Epigenetic ChangeGeneticsDna MethylationHuman PolymorphismMolecular Biology	2002	172
Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin Konstantin Miller, Brigitte Pabst, Heide Ritter, Human Genetics ChromatinGeneticsChromosome BiologyChromosome 18Chromosomal Rearrangement	2003	54
Identification of highly polymorphic microsatellites in the rhesus macaque <i>Macaca mulatta</i> by cross‐species amplification Manfred Kayser, Heide Ritter, Fred B. Bercovitch, Molecular Ecology BiologyGenetic DiversityMolecular EcologyCross‐species AmplificationMedicine	1996	51
Nearby Stop Codons in Exons of the Neurofibromatosis Type 1 Gene Are Disparate Splice Effectors Sven Hoffmeyer, Peter Nürnberg, Heide Ritter, The American Journal of Human Genetics Stop CodonsNeurogenomicsGenetic DisorderGeneticsMolecular Genetics	1998	50
Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia Peter Nürnberg, Hölger Thiele, David Chandler, Nature Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderHuman Ortholog	2001	26

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