Radu Wirth - Concepedia

Concepedia

Author

Radu Wirth

University of Cologne

Also Known As

R Wirth, Radu Wirth

7

Publications

1.6K

Citations

6

H-Index

32

Concepts

All Affiliations

University of Cologne University of Würzburg RWTH Aachen University University Hospital Cologne Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases

RW

About

Radu Wirth is an author at University of Cologne specializing in medicine, developmental biology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	1.4K
2	Cell Biology	2	2	255
3	Health Sciences	1	1	222
4	Social Sciences	1	1	33
5	Biostatistics	1	1	994

Radu Wirth

×

6

Publications

1.6K

Citations

6

H-Index

	Year	Citations
Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy Markus Feldkötter, Verena Schwarzer, Radu Wirth, The American Journal of Human Genetics Real-time Lightcycler PcrKinesiologyMedicineDiagnosisBiostatistics	2002	994
Attenuated BMP1 Function Compromises Osteogenesis, Leading to Bone Fragility in Humans and Zebrafish P. V. Asharani, Katharina Keupp, Oliver Semler, The American Journal of Human Genetics MechanobiologyBone FragilityDevelopmental BiologySclerostinBone Morphogenic Protein	2012	222
Congenital heart disease is a feature of severe infantile spinal muscular atrophy Sabine Rudnik‐Schöneborn, Raoul Heller, C Berg, Journal of Medical Genetics	2008	193
Recessive TRAPPC11 Mutations Cause a Disease Spectrum of Limb Girdle Muscular Dystrophy and Myopathy with Movement Disorder and Intellectual Disability Nina Bögershausen, Nassim Shahrzad, Jessica X. Chong, The American Journal of Human Genetics Genetic DisorderMedicineGeneticsPathologyDisease Spectrum	2013	118
Genotype–phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counselling Sabine Rudnik‐Schöneborn, C Berg, Klaus Zerres, Clinical Genetics	2009	80
Neuronal-Specific Deficiency of the Splicing Factor Tra2b Causes Apoptosis in Neurogenic Areas of the Developing Mouse Brain Markus Storbeck, Kristina Hupperich, John Antonydas Gaspar, PLoS ONE SpermatogenesisBrain DevelopmentGeneticsCell DeathEpigenetics	2014	33

Page 1