Astrid Speer - Concepedia

Author

Astrid Speer

Humboldt-Universität zu Berlin

Also Known As

Astrid Speer

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Humboldt-Universität zu Berlin Berliner Hochschule für Technik Charité - Universitätsmedizin Berlin Max Delbrück Center Universität Hamburg

About

Astrid Speer is an author at Humboldt-Universität zu Berlin specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	658
2	Public Health	3	3	161
3	Engineering	1	1	76
4	Health Sciences	1	1	25
5	Natural Sciences	1	1	169

Astrid Speer

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Apoptotic neurodegeneration following trauma is markedly enhanced in the immature brain Petra Bittigau, Marco Sifringer, Daniela Pohl, Annals of Neurology	1999	247
Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis Susan Kenwrick, Mark Patterson, Astrid Speer, Cell Muscle FunctionBiochemistrySkeletal MuscleNatural SciencesMolecular Analysis	1987	169
Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients Uwe Lenk, R. Hanke, Hannelore Thiele, Human Molecular Genetics Neurodegenerative DiseasesRare DiseasesDmd PatientsPoint MutationsPsychiatry	1993	120
DMA polymorphisms in adhesion molecule genes ? a new risk factor for early atherosclerosis Katrin Wenzel, Monika Ernst, Klaus Rohde, Human Genetics Vascular DiseaseAdhesion Molecule GenesGeneticsGenetic EpidemiologyImmunology	1996	117
E-selectin polymorphism and atherosclerosis: an association study Katrin Wenze, Stephan B. Felix, Franz X. KIeberi, Human Molecular Genetics	1994	107
Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European study Anthonie J. van Essen, Stephen Abbs, Montserrat Baiget, Human Genetics Developmental BiologyDystrophin GeneGenetic DisorderGeneticsGermline Mosaicism	1992	98
Modularization of biochemical networks based on classification of Petri net t-invariants Eva Grafahrend‐Belau, Falk Schreiber, Monika Heiner, BMC Bioinformatics	2008	86
Petri net modelling of gene regulation of the Duchenne muscular dystrophy Stefanie Grunwald, Astrid Speer, Jörg Ackermann, Biosystems EngineeringSkeletal MuscleDuchenne Muscular DystrophyGeneticsComputational Biology	2008	76
Treatment of ataxia in isolated vitamin E deficiency caused by α-tocopherol transfer protein deficiency Markus Schuelke, Ertan Mayatepek, Markus Inter, The Journal of Pediatrics MedicineTranslational MedicineClinical Nutrition	1999	71
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophy Birgit Kerst, Detlev Mennerich, Markus Schuelke, Neuromuscular Disorders Mitochondrial MyopathySevere CourseMendelian DisorderGenetic DisorderGenetics	2000	56

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