Kristin Bosse

982 total citations
24 papers, 526 citations indexed

About

Kristin Bosse is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Kristin Bosse has authored 24 papers receiving a total of 526 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 11 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in Kristin Bosse's work include Genomic variations and chromosomal abnormalities (9 papers), BRCA gene mutations in cancer (7 papers) and Chromosomal and Genetic Variations (4 papers). Kristin Bosse is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), BRCA gene mutations in cancer (7 papers) and Chromosomal and Genetic Variations (4 papers). Kristin Bosse collaborates with scholars based in Germany, United States and United Kingdom. Kristin Bosse's co-authors include Hartmut Engels, Peter Propping, Martin Teufel, Norbert Schäffeler, Stephan Zipfel, Katrin Elisabeth Giel, Barbara Wappenschmidt, Alexander Hoischen, Regina C. Betz and Ruthild G. Weber and has published in prestigious journals such as Journal of Clinical Oncology, Neurology and The American Journal of Human Genetics.

In The Last Decade

Kristin Bosse

23 papers receiving 515 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Kristin Bosse Germany 14 312 244 64 62 57 24 526
Beike Leegte Netherlands 11 428 1.4× 189 0.8× 58 0.9× 118 1.9× 63 1.1× 15 531
C. B. van der Hagen Norway 12 259 0.8× 261 1.1× 92 1.4× 70 1.1× 14 0.2× 22 535
Mariana F.A. Funari Brazil 17 400 1.3× 368 1.5× 52 0.8× 91 1.5× 57 1.0× 35 736
Marie T. Mulcahy Australia 13 210 0.7× 193 0.8× 49 0.8× 150 2.4× 52 0.9× 25 472
Walter Zumkeller Germany 11 218 0.7× 228 0.9× 38 0.6× 67 1.1× 25 0.4× 17 497
Jodi D. Hoffman United States 18 365 1.2× 215 0.9× 23 0.4× 119 1.9× 44 0.8× 33 654
Sara Benito‐Sanz Spain 14 501 1.6× 395 1.6× 17 0.3× 29 0.5× 19 0.3× 22 637
Philip N. Mowrey United States 11 232 0.7× 162 0.7× 35 0.5× 134 2.2× 14 0.2× 22 436
Giuseppe Calabrese Italy 14 173 0.6× 257 1.1× 77 1.2× 154 2.5× 145 2.5× 45 711
E Montali Italy 13 105 0.3× 145 0.6× 35 0.5× 38 0.6× 46 0.8× 28 387

Countries citing papers authored by Kristin Bosse

Since Specialization
Citations

This map shows the geographic impact of Kristin Bosse's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kristin Bosse with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kristin Bosse more than expected).

Fields of papers citing papers by Kristin Bosse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kristin Bosse. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kristin Bosse. The network helps show where Kristin Bosse may publish in the future.

Co-authorship network of co-authors of Kristin Bosse

This figure shows the co-authorship network connecting the top 25 collaborators of Kristin Bosse. A scholar is included among the top collaborators of Kristin Bosse based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kristin Bosse. Kristin Bosse is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Bosse, Kristin, et al.. (2016). Psychological Distress, Anxiety, and Depression of Cancer‐Affected BRCA1/2 Mutation Carriers: a Systematic Review. Journal of Genetic Counseling. 25(5). 880–891. 74 indexed citations
2.
Wilson, Neil, Volkan Okur, Christian Cole, et al.. (2016). Isolated recessive nail dysplasia caused byFZD6mutations: report of three families and review of the literature. Clinical and Experimental Dermatology. 41(8). 884–889. 8 indexed citations
3.
Faust, Ulrike, Marc Sturm, Karl Hackmann, et al.. (2015). HBOC multi-gene panel testing: comparison of two sequencing centers. Breast Cancer Research and Treatment. 152(1). 129–136. 35 indexed citations
4.
Bosse, Kristin, Claudia Ott, Thorsten Biegner, et al.. (2014). 23-Year-Old Female with an Inflammatory Myofibroblastic Tumour of the Breast: A Case Report and a Review of the Literature. Geburtshilfe und Frauenheilkunde. 74(2). 167–170. 17 indexed citations
5.
Bosse, Kristin, Monika Graeser, Axel Goßmann, et al.. (2013). Supplemental screening ultrasound increases cancer detection yield in BRCA1 and BRCA2 mutation carriers. Archives of Gynecology and Obstetrics. 289(3). 663–670. 17 indexed citations
6.
Klopocki, Eva, Silke B. Lohan, Francesco Brancati, et al.. (2010). Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis. The American Journal of Human Genetics. 88(1). 70–75. 67 indexed citations
7.
Graeser, Monika, et al.. (2009). Association of hormone receptor status with grading, age of onset, and tumor size in BRCA1-associated breast cancer. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 454(5). 519–524. 5 indexed citations
8.
Rhiem, Kerstin, Barbara Wappenschmidt, Kristin Bosse, et al.. (2009). Platinum Sensitivity in a BRCA1 Mutation Carrier with Advanced Breast Cancer. Clinical Oncology. 21(6). 448–450. 16 indexed citations
9.
Jain, Mahim, Deeann Wallis, Nathaniel H. Robin, et al.. (2008). Locus homogeneity between syndactyly type 1A and craniosynostosis Philadelphia type?. American Journal of Medical Genetics Part A. 146A(17). 2308–2311. 4 indexed citations
10.
Bosse, Kristin, Kerstin Rhiem, Barbara Wappenschmidt, et al.. (2006). Screening for ovarian cancer by transvaginal ultrasound and serum CA125 measurement in women with a familial predisposition: A prospective cohort study. Gynecologic Oncology. 103(3). 1077–1082. 41 indexed citations
11.
Eggermann, Thomas, Ulrike Gamerdinger, Kristin Bosse, et al.. (2005). Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q. American Journal of Medical Genetics Part A. 134A(3). 305–308. 7 indexed citations
12.
Gamerdinger, Ulrike, Kristin Bosse, Thomas Eggermann, et al.. (2005). First report of a partial trisomy 3q12-q23 de novo—FISH breakpoint determination and phenotypic characterization. European Journal of Medical Genetics. 49(3). 225–234. 4 indexed citations
13.
Denecke, Jonas, Christian Kranz, Kristin Bosse, et al.. (2005). Congenital Disorder of Glycosylation Type Id: Clinical Phenotype, Molecular Analysis, Prenatal Diagnosis, and Glycosylation of Fetal Proteins. Pediatric Research. 58(2). 248–253. 40 indexed citations
14.
Zahn, Susanne, Kristin Bosse, Vera M. Kalscheuer, et al.. (2005). 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). American Journal of Medical Genetics Part A. 139A(1). 19–24. 15 indexed citations
15.
Bosse, Kristin, et al.. (2004). Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletions. Annales de Génétique. 47(2). 191–197. 5 indexed citations
16.
Chavarría‐Soley, Gabriela, Kristin Bosse, Jorge Azofeifa, et al.. (2003). 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. Journal of Glaucoma. 12(1). 27–30. 25 indexed citations
17.
Engels, Hartmut, Susanne Zahn, Kristin Bosse, et al.. (2003). Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation. European Journal of Human Genetics. 11(9). 643–651. 13 indexed citations
18.
Engels, Hartmut, Kristin Bosse, Susanne Zahn, et al.. (2002). Further case of Cantú syndrome: Exclusion of cryptic subtelomeric chromosome aberrations. American Journal of Medical Genetics. 111(2). 205–209. 17 indexed citations
19.
Bosse, Kristin, Regina C. Betz, Young‐Ae Lee, et al.. (2000). Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36. The American Journal of Human Genetics. 67(2). 492–497. 32 indexed citations
20.
Bosse, Kristin. (1966). [Comparative studies of the physiology and pathology of hair shedding with special reference to its synchronization. I. Introduction and problem presentation].. PubMed. 17(12). 541–6. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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