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Kristin Bosse

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
2020 · GEMO Study Collaborators, Laura Fachal, et al. · Nature Genetics · 173
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Psychological Distress, Anxiety, and Depression of Cancer‐Affected BRCA1/2 Mutation Carriers: a Systematic Review
2016 · Johanna Ringwald, Christina Wochnowski, et al. · Journal of Genetic Counseling · 122
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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 · 108
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DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation
2007 · H. Engels, A. Brockschmidt, et al. · Neurology · 91
Screening for ovarian cancer by transvaginal ultrasound and serum CA125 measurement in women with a familial predisposition: A prospective cohort study
2006 · Kristin Bosse, Kerstin Rhiem, et al. · Gynecologic Oncology · 58
Congenital Disorder of Glycosylation Type Id: Clinical Phenotype, Molecular Analysis, Prenatal Diagnosis, and Glycosylation of Fetal Proteins
2005 · Jonas Denecke, Christian Kranz, et al. · Pediatric Research · 49
HBOC multi-gene panel testing: comparison of two sequencing centers
2015 · Christopher Schroeder, Ulrike Faust, et al. · Breast Cancer Research and Treatment · 47
Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36
2000 · Kristin Bosse, Regina C. Betz, et al. · The American Journal of Human Genetics · 47
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
2003 · Gabriela Chavarria Soley, Kristin A. Bosse, et al. · Journal of Glaucoma · 33
23-Year-Old Female with an Inflammatory Myofibroblastic Tumour of the Breast: A Case Report and a Review of the Literature
2014 · K. Bosse, C. Ott, et al. · Geburtshilfe und Frauenheilkunde · 32
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Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations
2002 · Hartmut Engels, Kristin Bosse, et al. · American Journal of Medical Genetics · 26
Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women
2019 · Ilnaz Sepahi, Ulrike Faust, et al. · BMC Cancer · 24
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Supplemental screening ultrasound increases cancer detection yield in BRCA1 and BRCA2 mutation carriers
2013 · Kristin Bosse, Monika Graeser, et al. · Archives of Gynecology and Obstetrics · 24
Platinum Sensitivity in a BRCA1 Mutation Carrier with Advanced Breast Cancer
2009 · K. Rhiem, B. Wappenschmidt, et al. · Clinical Oncology · 24
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)
2005 · Susanne Zahn, Antje Ehrbrecht, et al. · American Journal of Medical Genetics Part A · 20
Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation
2003 · Hartmut Engels, Antje Ehrbrecht, et al. · European Journal of Human Genetics · 16
Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literature
2016 · C. Kasparis, D. Reid, et al. · Clinical and Experimental Dermatology · 12
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Communicating BRCA1 and BRCA2 Genetic Test Results
2006 · Dorothea Gadzicki, Luzie U. Wingen, et al. · Journal of Clinical Oncology · 11
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Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q
2005 · Thomas Eggermann, Ulrike Gamerdinger, et al. · American Journal of Medical Genetics Part A · 11
Childhood, adolescent, and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers
2024 · Shuai Li, Laura Madanat-Harjuoja, et al. · JNCI Journal of the National Cancer Institute · 10
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Increased risk of cervical cancer in high-risk families with and without mutations in the BRCA1 and BRCA2 genes
2007 · K. Rhiem, C. Fischer, et al. · Journal of Clinical Oncology · 8
Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?
2008 · Mahim Jain, Deeann Wallis, et al. · American Journal of Medical Genetics Part A · 6
Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletions
2004 · K. Bosse, T. Eggermann, et al. · Annales de Génétique · 6
First report of a partial trisomy 3q12-q23 de novo—FISH breakpoint determination and phenotypic characterization
2005 · Ulrike Gamerdinger, Kristin Bosse, et al. · European Journal of Medical Genetics · 5
Clinical genome sequencing in patients with hereditary breast and ovarian cancer: Concept, implementation and benefits
2025 · Dennis Witt, Marc Sturm, et al. · The Breast · 4
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Works count: 75
Citation count: 973
H-index: 16
I10-index: 20
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