Kristin Bosse - Concepedia

Author

Kristin Bosse

University Hospital Cologne

Also Known As

Bosse, Kristin, K BOSSE, K Bosse, K. Bosse, Kristin A. Bosse, Kristin Bosse, Natalia V. Bogdanova

Publications

972

Citations

H-Index

Concepts

All Affiliations

University Hospital Cologne University of Cologne University of Bonn Max Planck Institute for Molecular Genetics University of Tübingen

About

Kristin Bosse is an author at University Hospital Cologne specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	379
2	Public Health	2	2	70
3	Health Sciences	1	1	24
4	Natural Sciences	1	1	51
5	Biology	1	1	18

Kristin Bosse

Publications

542

Citations

H-Index

Page 1

	Year	Citations
Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis Eva Klopocki, Silke B. Lohan, Francesco Brancati, The American Journal of Human Genetics Developmental BiologyGenetic DisorderCopy-number VariationsGeneticsMolecular Genetics	2010	105
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation Hartmut Engels, Antje Brockschmidt, Alexander Hoischen, Neurology	2007	92
Screening for ovarian cancer by transvaginal ultrasound and serum CA125 measurement in women with a familial predisposition: A prospective cohort study Kristin Bosse, Kerstin Rhiem, Barbara Wappenschmidt, Gynecologic Oncology Transvaginal UltrasoundRadiologyCancer DetectionCancer ScreeningMedicine	2006	57
Congenital Disorder of Glycosylation Type Id: Clinical Phenotype, Molecular Analysis, Prenatal Diagnosis, and Glycosylation of Fetal Proteins Jonas Denecke, Christian Kranz, Juergen Ch Von Kleist-Retzow, Pediatric Research GlycoproteomicsProtein GlycosylationDevelopmental AnomalyDevelopmental BiologyMendelian Disorder	2005	51
Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36 Kristin Bosse, Regina C. Betz, Young‐Ae Lee, The American Journal of Human Genetics ChromatinSyndactyly Type 1CytogeneticsGenetic DisorderGenetics	2000	46
HBOC multi-gene panel testing: comparison of two sequencing centers Christopher Schroeder, Ulrike Faust, Marc Sturm, Breast Cancer Research and Treatment MedicineGeneticsNext-generation SequencingSequencing CentersMolecular Genetics	2015	43
Primary Congenital Glaucoma: A Novel Single-Nucleotide Deletion and Varying Phenotypic Expression for the 1546???1555dup Mutation in the GLC3A (CYP1B1) Gene in 2 Families of Different Ethnic Origin Gabriela Chavarría‐Soley, Kristin Bosse, David Flikier, Journal of Glaucoma	2003	33
Supplemental screening ultrasound increases cancer detection yield in BRCA1 and BRCA2 mutation carriers Kristin Bosse, Monika Graeser, Axel Goßmann, Archives of Gynecology and Obstetrics Brca2 Mutation CarriersCancer DetectionCancer ScreeningMedicineMolecular Diagnostics	2013	24
Platinum Sensitivity in a BRCA1 Mutation Carrier with Advanced Breast Cancer Kerstin Rhiem, Barbara Wappenschmidt, Kristin Bosse, Clinical Oncology Advanced Breast CancerBrca1 Mutation CarrierOncologyBreast OncologyMedicine	2009	22
Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1) Susanne Zahn, Antje Ehrbrecht, Kristin Bosse, American Journal of Medical Genetics Part A	2005	19

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