Sigmar Stricker - Concepedia

Author

Sigmar Stricker

Max Planck Institute for Molecular Genetics ORCID

Also Known As

S Stricker, S. Stricker, Shawna L. Stricker, Sigmar Stricker, Sigmar Stricker (42596), Stricker, Sigmar

118

Publications

5.6K

Citations

H-Index

109

Concepts

All Affiliations

Max Planck Institute for Molecular Genetics Charité - Universitätsmedizin Berlin Freie Universität Berlin Inserm Centre National de la Recherche Scientifique

About

Sigmar Stricker is an author at Max Planck Institute for Molecular Genetics specializing in medicine, developmental biology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	34	3.2K
2	Natural Sciences	7	7	313
3	Biochemistry	2	2	119
4	Health Sciences	1	1	67
5	Social Sciences	1	1	19

Sigmar Stricker

Publications

5.1K

Citations

H-Index

Page 1

	Year	Citations
BMP signaling controls muscle mass Roberta Sartori, Elija Schirwis, Bert Blaauw, Nature Genetics Muscle FunctionSignal TransductionMolecular PhysiologySkeletal MusclePhysiology	2013	440
Role of Runx Genes in Chondrocyte Differentiation Sigmar Stricker, Reinald Fundele, Andrea Vortkamp, Developmental Biology Developmental BiologyOsteoarthritisMorphogenesisRunx GenesMedicine	2002	235
Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation Florian Witte, Janine Dokas, Franziska Neuendorf, Gene Expression Patterns Knockout MouseMusculoskeletal ResearchDevelopmental BiologyBone Morphogenic ProteinGenetics	2009	200
PDE3A mutations cause autosomal dominant hypertension with brachydactyly Philipp G. Maass, Friedrich C. Luft, Carolin Schächterle, Nature Genetics HypertensionPde3a MutationsGenetic DisorderAntihypertensive TherapyGenetics	2015	169
Mutations in <i>bone morphogenetic protein receptor 1B</i> cause brachydactyly type A2 Katarina Lehmann, Petra Seemann, Sigmar Stricker, Proceedings of the National Academy of Sciences	2003	164
Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome C. Geoffrey Woods, Sigmar Stricker, Petra Seemann, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2006	158
Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit Katrin Hoffmann, Juliane Müller, Sigmar Stricker, The American Journal of Human Genetics Developmental BiologyPhysiologyEscobar SyndromePrenatal MyastheniaMedicine	2006	151
A molecular pathogenesis for transcription factor associated poly-alanine tract expansions Andrea N. Albrecht, Uwe Kornak, Annett Böddrich, Human Molecular Genetics	2004	147
Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders Anne Michalk, Sigmar Stricker, Jutta Becker, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2008	139
Multiple roles for neurofibromin in skeletal development and growth Mateusz Kolanczyk, Nadine Kossler, Jirko Kühnisch, Human Molecular Genetics	2007	134

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