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K. Bosse · SciRah

Researcher profile · Semantic Scholar

K. Bosse

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K. Bosse — researcher profile on SciRah

h-index: 15
Works: 36
Citations: 783

Most-cited papers

Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.
E. Klopocki, Silke Lohan, F. Brancati, R. Koll +15 more
2011American Journal of Human Genetics104 citations Open access
Semantic Scholar
Psychological Distress, Anxiety, and Depression of Cancer-Affected BRCA1/2 Mutation Carriers: a Systematic Review
J. Ringwald, Christina Wochnowski, K. Bosse, K. Giel +3 more
2016Journal of Genetic Counseling101 citations Open access
Semantic Scholar
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation
H. Engels, Antje Brockschmidt, A. Hoischen, C. Landwehr +7 more
2007Neurology98 citations
Semantic Scholar
Screening for ovarian cancer by transvaginal ultrasound and serum CA125 measurement in women with a familial predisposition: a prospective cohort study.
K. Bosse, K. Rhiem, B. Wappenschmidt, M. Hellmich +4 more
2006Gynecologic Oncology60 citations
Semantic Scholar
Congenital Disorder of Glycosylation Type Id: Clinical Phenotype, Molecular Analysis, Prenatal Diagnosis, and Glycosylation of Fetal Proteins
J. Denecke, C. Kranz, J. von Kleist-Retzow, K. Bosse +4 more
2005Pediatric Research54 citations Open access
Semantic Scholar
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.
K. Bosse, R. Betz, Young-ae Lee, T. Wienker +5 more
2000American Journal of Human Genetics48 citations Open access
Semantic Scholar
HBOC multi-gene panel testing: comparison of two sequencing centers
C. Schroeder, U. Faust, M. Sturm, K. Hackmann +16 more
2015Breast Cancer Research and Treatment45 citations
Semantic Scholar
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, K. Bosse, D. Flikier, Paul Flikier +5 more
2003Journal of glaucoma39 citations Open access
Semantic Scholar
23-Year-Old Female with an Inflammatory Myofibroblastic Tumour of the Breast: A Case Report and a Review of the Literature.
K. Bosse, C. Ott, T. Biegner, F. Fend +3 more
2014Geburtshilfe und Frauenheilkunde28 citations Open access
Semantic Scholar
Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.
H. Engels, K. Bosse, Antje Ehrbrecht, Susanne Zahn +4 more
2002American journal of medical genetics25 citations
Semantic Scholar
Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation
H. Engels, Antje Ehrbrecht, Susanne Zahn, K. Bosse +9 more
2003European Journal of Human Genetics23 citations
Semantic Scholar
Supplemental screening ultrasound increases cancer detection yield in BRCA1 and BRCA2 mutation carriers
K. Bosse, M. Graeser, A. Gossmann, M. Hackenbroch +2 more
2014Archives of Gynecology and Obstetrics22 citations
Semantic Scholar
Platinum sensitivity in a BRCA1 mutation carrier with advanced breast cancer.
K. Rhiem, B. Wappenschmidt, K. Bosse, H. Köppler +2 more
2009Clinics in oncology21 citations
Semantic Scholar
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, K. Bosse, V. Kalscheuer +4 more
2005American Journal of Medical Genetics. Part A21 citations
Semantic Scholar
Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women
I. Sepahi, U. Faust, M. Sturm, K. Bosse +23 more
2019BMC Cancer20 citations Open access
Semantic Scholar
Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literature
C. Kasparis, D. Reid, N. Wilson, V. Okur +6 more
2016Clincal and Experimental Dermatology12 citations Open access
Semantic Scholar
Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q
T. Eggermann, U. Gamerdinger, K. Bosse, C. Heidrich-Kaul +6 more
2005American Journal of Medical Genetics. Part A11 citations
Semantic Scholar
Communicating BRCA1 and BRCA2 genetic test results.
D. Gadzicki, L. Wingen, Birgitta Teige, D. Horn +13 more
2006Journal of Clinical Oncology10 citations Open access
Semantic Scholar
Increased risk of cervical cancer in high-risk families with and without mutations in the BRCA1 and BRCA2 genes
K. Rhiem, C. Fischer, K. Bosse, B. Wappenschmidt +1 more
20078 citations
Semantic Scholar
Childhood, adolescent and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers.
Shuai Li, Laura Madanat-Harjuoja, Goska Leslie, D. Barnes +45 more
2024Journal of the National Cancer Institute7 citations Open access
Semantic Scholar
First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
U. Gamerdinger, K. Bosse, T. Eggermann, V. Kalscheuer +2 more
2006European Journal of Medical Genetics7 citations Open access
Semantic Scholar
Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletions.
K. Bosse, T. Eggermann, K. van der Ven, R. Raff +2 more
2004Annales de Genetique7 citations
Semantic Scholar
Locus Homogeneity Between Syndactyly Type 1A and Craniosynostosis Philadelphia Type?
Mahim Jain, Deeann Wallis, Nathaniel H. Robin, Fabienne Wavrant de Vrieze +7 more
2008American Journal of Medical Genetics. Part A5 citations Open access
Semantic Scholar
Association of hormone receptor status with grading, age of onset, and tumor size in BRCA1-associated breast cancer
M. Graeser, K. Bosse, M. Brosig, C. Engel +2 more
2009Virchows Archiv4 citations
Semantic Scholar
Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits
Dennis Witt, M. Sturm, Antje Stäbler, Benita Menden +18 more
2025Breast2 citations Open access
Semantic Scholar
Neoadjuvant, biweekly, dose-dense chemotherapy with epirubicin (E) and cyclophosphamide (C) followed by docetaxel (T) in primary breast cancer (BC).
E. Cramer, C. Moers, V. Zarghooni, K. Bosse +2 more
2005Journal of Clinical Oncology2 citations
Semantic Scholar
Beyond BRCA1 and BRCA2 – evaluation of 123 carriers of pathogenic variants in other HBOC associated genes
K. Bosse, L. Ruisinger, Ann-Kathrin Uhde, U. Faust +16 more
2022Senologie - Zeitschrift für Mammadiagnostik und -therapie0 citations
Semantic Scholar
Genome sequencing of HBOC patients in routine diagnostics
D. Witt, T. Haack, U. Faust, A. Stäbler +6 more
202264. Kongress der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe e. V.0 citations
Semantic Scholar
Truncating variants in DNA-repair genes and their effect on AAO of hereditary breast cancer
I. Sepahi, U. Faust, M. Sturm, K. Bosse +22 more
2018Senologie - Zeitschrift für Mammadiagnostik und -therapie0 citations
Semantic Scholar
Breast cancer growth rates in BRCA1/2 mutation carriers
K. Bosse, A. Goβmann, K. Rhiem, M. Warm +1 more
20160 citations
Semantic Scholar
The Value of Breast Ultrasound inBRCA1 andBRCA2 Mutation Carriers.
K. Bosse, M. Graeser, K. Rhiem, A. Gossmann +4 more
20090 citations
Semantic Scholar
Combination of oncolytic adenoviral therapy with chemotherapy for enhanced breast cancer cell killing.
M. Stoff-Khalili, A. Nedeljkovic-Kurepa, JS Jung, Bv Glover +7 more
20090 citations
Semantic Scholar
Other cancer types besides breast and ovarian cancer in 266 families with a proven BRCA1/2 mutation or a high probability for an autosomal dominant gene
K. Bosse, K. Weinhold, K. Rhiem, V. Hübbel +3 more
20050 citations
Semantic Scholar
P5: Genome-wide array-CGH screening of 52 patients with idiopathic mental retardation – Detection of two cases with de novo imbalances and two cases with causative imbalances inherited from a parent
Antje Ehrbrecht, A. Hoischen, M. Ehrler, K. Bosse +8 more
20050 citations
Semantic Scholar
Congenital disorders of glycosylation – a second patient of CDG type Id deficiency: different clinical phenotype, molecular analysis and prenatal diagnosis
J. von Kleist-Retzow, P. Herkenrath, K. Bosse, O. Debus +3 more
20050 citations
Semantic Scholar
P3 Prospective incidence rates of breast cancer and efficacy of a structured surveillance program in proven or suspected carriers of BRCAl/2 gene mutations
R. Schmutzler, P. Breuer, K. Rhiem, V. Hbbel +2 more
20040 citations
Semantic Scholar

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