Stefanie Vogt - Concepedia

Author

Stefanie Vogt

Also Known As

Noel Muridzo, S Vogt, S. L. Vogt, S. Vogt, S.L. Vogt, Stefanie L Vogt, Stefanie L. Vogt, Stefanie Vogt, Stefanie Vogt, MD, Vogt, Stefanie L.

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

University of Bonn University of Alberta University of British Columbia Canada's Michael Smith Genome Sciences Centre Cardiff University

About

Stefanie Vogt is an author at University of Bonn specializing in medicine, microbiology, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	1K
2	Natural Sciences	3	3	126
3	Engineering	1	1	64
4	Biochemistry	1	1	44
5	Biology	1	1	69

Stefanie Vogt

Publications

Citations

H-Index

Page 1

	Year	Citations
Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis Stefanie Vogt, Natalie Jones, Daria Christian, Gastroenterology Tumor BiologyTumoral PathologyMedicineSurgical PathologyPathology	2009	343
High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Journal of Medical Genetics	2007	244
Analysis of MUTYH Genotypes and Colorectal Phenotypes in Patients With MUTYH-Associated Polyposis Maartje Nielsen, Mirjam C. Joerink - van de Beld, Natalie Jones, Gastroenterology GeneticsGenetic EpidemiologyGastroenterologyPathologyMutyh Genotypes	2008	171
Frequency and phenotypic spectrum of germline mutations in <scp><i>POLE</i></scp> and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas Isabel Spier, Stefanie Holzapfel, Janine Altmüller, International Journal of Cancer	2014	137
Increased Colorectal Cancer Incidence in Obligate Carriers of Heterozygous Mutations in MUTYH Natalie Jones, Stefanie Vogt, Maartje Nielsen, Gastroenterology Somatic VariantMedicineGeneticsColorectal Cancer IncidencePathology	2009	133
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation J. Seidel, Simone Schiller, Christina Kelbova, Clinical Genetics	2001	83
Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures Ellen Knierim, Hiromi Hirata, Nicole I. Wolf, The American Journal of Human Genetics Spinal Cord InjuryDevelopmental BiologyBone Morphogenic ProteinGenetic DisorderGenetics	2016	72
Deep intronic<i>APC</i>mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis Isabel Spier, Sukanya Horpaopan, Stefanie Vogt, Human Mutation	2012	71
The Stringent Response Is Essential for Pseudomonas aeruginosa Virulence in the Rat Lung Agar Bead and Drosophila melanogaster Feeding Models of Infection Stefanie Vogt, Christopher Green, Katarzyna M. Stevens, Infection and Immunity Pathogenic MicrobiologyBacteriologyMolecular BiologyBacterial PathogenesisMedical Microbiology	2011	69
Genome‐wide CNV analysis in 221 unrelated patients and targeted high‐throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis Sukanya Horpaopan, Isabel Spier, Alexander M. Zink, International Journal of Cancer Unrelated PatientsEngineeringGenome‐wide Cnv AnalysisGeneticsPathology	2014	64

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