Martha Kalff-Suske - Concepedia

Author

Martha Kalff-Suske

Philipps University of Marburg

Also Known As

M Kalff-Suske, M. Kalff-Suske, M. Kalff‐Suske, MARTHA KALFF‐SUSKE, Martha Kalff-Suske

Publications

735

Citations

H-Index

Concepts

All Affiliations

Philipps University of Marburg Goethe University Frankfurt University Children's Hospital Zurich Praxis für Humangenetik

About

Martha Kalff-Suske is an author at Philipps University of Marburg specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	284
2	Cell Biology	3	3	142
3	Natural Sciences	2	2	84
4	Public Health	1	1	22
5	Immunology	1	1	113

Martha Kalff-Suske

Publications

717

Citations

H-Index

Page 1

	Year	Citations
Point Mutations in Human GLI3 Cause Greig Syndrome Anja Wild, Martha Kalff-Suske, Andrea Vortkamp, Human Molecular Genetics	1997	173
Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome Martha Kalff-Suske, Anja Wild, Juliane Topp, Human Molecular Genetics	1999	147
Molecular Characterization of Human Zyxin Teresita Macalma, Jürgen Otte, Mary E. Hensler, Journal of Biological Chemistry Signal TransductionMouse ZyxinSignaling PathwayBiomedical ResearchCell Trafficking	1996	113
All Known Human H1 Histone Genes Except the H10 Gene Are Clustered on Chromosome 6 Werner Albig, Birgit Drabent, Jürgen Kunz, Genomics Histone ModificationsChromatinChromatin StructureChromatin RemodelingNatural Sciences	1993	66
All Human Genes of the Uteroglobin Family Are Localized on Chromosome 11q12.2 and Form a Dense Cluster Jian Ni, Martha Kalff-Suske, Reiner Gentz, Annals of the New York Academy of Sciences	2000	63
Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identified <i>GLI3</i> mutations Philippe Debeer, Hilde Peeters, S. Driess, American Journal of Medical Genetics Part A	2003	50
Regional Localization of 725 Human Chromosome 7-Specific Yeast Artificial Chromosome Clones Jürgen Kunz, Stephen W. Scherer, Ingrid Klawitz, Genomics ChromatinRegional LocalizationChromosome DynamicsGeneticsYeast	1994	41
Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality P. Gail Williams, Joseph H. Hersh, Frank Yen, Clinical Genetics GeneticsGenetic EpidemiologyPathologyDisease Gene IdentificationEpigenetics	1997	22
Human Sp3 Transcriptional Regulator Gene (SP3) Maps to Chromosome 2q31 Martha Kalff-Suske, Jürgen Kunz, Karl‐Heinz Grzeschik, Genomics ChromatinTranscriptional RegulationChromatin StructureNatural SciencesGenetics	1996	18
Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: Not a new syndrome, but two dominant mutations (GLI3 E543X andCOL2A1 G973R) in the same individual Diana Sobetzko, Georg Eich, Martha Kalff-Suske, American Journal of Medical Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderConnective Tissue DiseaseGenetic Disorder	2000	13

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