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Sigmar Stricker

BMP signaling controls muscle mass
2013 · Roberta Sartori, Elija Schirwis, et al. · Nature Genetics · 468
Role of Runx Genes in Chondrocyte Differentiation
2002 · Sigmar Stricker, Reinald Fundele, et al. · Developmental Biology · 236
Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation
2009 · Florian Witte, Janine Dokas, et al. · Gene Expression Patterns · 198
PDE3A mutations cause autosomal dominant hypertension with brachydactyly
2015 · Philipp G Maass, Atakan Aydin, et al. · Nature Genetics · 166
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Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2
2003 · Katarina Lehmann, Petra Seemann, et al. · Proceedings of the National Academy of Sciences · 166
Mutations in WNT7A Cause a Range of Limb Malformations, Including Fuhrmann Syndrome and Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome
2006 · C.G. Woods, S. Stricker, et al. · The American Journal of Human Genetics · 160
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Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit
2006 · Katrin Hoffmann, Juliane S. Müller, et al. · The American Journal of Human Genetics · 158
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A molecular pathogenesis for transcription factor associated poly-alanine tract expansions
2004 · Andrea N. Albrecht, Uwe Kornak, et al. · Human Molecular Genetics · 149
Acetylcholine Receptor Pathway Mutations Explain Various Fetal Akinesia Deformation Sequence Disorders
2008 · Anne Michalk, Sigmar Stricker, et al. · The American Journal of Human Genetics · 145
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Multiple roles for neurofibromin in skeletal development and growth
2007 · Mateusz Kolanczyk, Nadine Kossler, et al. · Human Molecular Genetics · 133
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Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development
2017 · Pedro Vallecillo-García, Mickael Orgeur, et al. · Nature Communications · 125
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Mutations in PVRL4, Encoding Cell Adhesion Molecule Nectin-4, Cause Ectodermal Dysplasia-Syndactyly Syndrome
2010 · Francesco Brancati, Paola Fortugno, et al. · The American Journal of Human Genetics · 124
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Faulty Initiation of Proteoglycan Synthesis Causes Cardiac and Joint Defects
2011 · Sevjidmaa Baasanjav, Lihadh Al-Gazali, et al. · The American Journal of Human Genetics · 123
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A misplaced lncRNA causes brachydactyly in humans
2012 · Philipp G. Maass, Andreas Rump, et al. · Journal of Clinical Investigation · 122
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Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia
2009 · Ingo Kurth, Eva Klopocki, et al. · Nature Genetics · 116
A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range
2009 · Bo Gao, Jianxin Hu, et al. · Nature · 105
Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis
2010 · Eva Klopocki, Silke Lohan, et al. · The American Journal of Human Genetics · 104
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Modulation of GDF5/BRI‐b signalling through interaction with the tyrosine kinase receptor Ror2
2004 · Marei Sammar, Sigmar Stricker, et al. · Genes to Cells · 104
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Mutations in GDF5 Reveal a Key Residue Mediating BMP Inhibition by NOGGIN
2009 · Petra Seemann, Anja Brehm, et al. · PLoS Genetics · 100
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Induction of Macrophage Chemotaxis by Aortic Extracts of the mgR Marfan Mouse Model and a GxxPG-Containing Fibrillin-1 Fragment
2006 · Gao Guo, Patrick Booms, et al. · Circulation · 98
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Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2−/− mouse model
2006 · J. Hecht, V. Seitz, et al. · Gene Expression Patterns · 93
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion
2011 · Eva Klopocki, Silke Lohan, et al. · Journal of Medical Genetics · 92
Expression of Galectin-3 in Skeletal Tissues Is Controlled by Runx2
2003 · Michael Stock, Henning Schäfer, et al. · Journal of Biological Chemistry · 83
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Regulation of cell polarity in the cartilage growth plate and perichondrium of metacarpal elements by HOXD13 and WNT5A
2013 · Pia Kuss, Katerina Kraft, et al. · Developmental Biology · 79
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Odd skipped-related 1 (Osr1) identifies muscle-interstitial fibro-adipogenic progenitors (FAPs) activated by acute injury
2018 · Jürgen Stumm, Pedro Vallecillo-García, et al. · Stem Cell Research · 78
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Works count: 119
Citation count: 5,547
H-index: 45
I10-index: 74
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