Barbara Wappenschmidt

10.2k citations

62 papers · 1.7k indexed · h-index 27

Co-authors: Barbara Burwinkel Claus R. Bartram Kari Hemminki Peter Bugert Christian Sutter Alfons Meindl Rita K. Schmutzler Dieter Niederacher
Topics: BRCA gene mutations in cancer (32 papers)DNA Repair Mechanisms (15 papers)Cancer Genomics and Diagnostics (11 papers)
Cited by: Cancer Research Genetics Molecular Biology
Journals: Journal of Clinical Oncology PLoS ONE The Journal of Clinical Endocrinology & Metabolism
Partner nations: Germany Sweden United States

In The Last Decade

Barbara Wappenschmidt

60 papers receiving 1.6k citations

Peers

Countries citing papers authored by Barbara Wappenschmidt

Since Specialization

Citations

This map shows the geographic impact of Barbara Wappenschmidt'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 Barbara Wappenschmidt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Wappenschmidt more than expected).

Fields of papers citing papers by Barbara Wappenschmidt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara Wappenschmidt. 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 Barbara Wappenschmidt. The network helps show where Barbara Wappenschmidt may publish in the future.

Co-authorship network of co-authors of Barbara Wappenschmidt

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Wappenschmidt. A scholar is included among the top collaborators of Barbara Wappenschmidt 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 Barbara Wappenschmidt. Barbara Wappenschmidt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Implementing mainstream genetic counseling within the area‐wide network of the German Consortium Hereditary Breast and Ovarian Cancer (GC‐HBOC): Satisfaction of primary care providers with the provided state‐of‐the‐art training by the Cologne Center 2024 ·Journal of Genetic Counseling ·N Herold,(unknown),Corinna Ernst,(unknown),Britta Blümcke,Anke Waha,(unknown),Jan Hauke,Barbara Wappenschmidt,Eric Hahnen,Rita K. Schmutzler,Kerstin Rhiem	1
2	Phenotype analysis of families with TP53 germline variants at the Center for Familial Breast and Ovarian Cancer, Cologne 2024 ·Cancer Medicine ·Karin Kast,Kerstin Rhiem,(unknown),Barbara Wappenschmidt,Rita K. Schmutzler	1
3	Satisfaction and Quality of Life of Healthy and Unilateral Diseased BRCA1/2 Pathogenic Variant Carriers after Risk-Reducing Mastectomy and Reconstruction Using the BREAST-Q Questionnaire 2022 ·Genes ·N Herold,Martin Hellmich,(unknown),Beyhan Ataseven,(unknown),Barbara Wappenschmidt,Rita K. Schmutzler,Kerstin Rhiem	6
4	A tandem duplication of BRCA1 exons 1–19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndrome 2018 ·Breast Cancer Research and Treatment ·(unknown),(unknown),Barbara Wappenschmidt,(unknown),Brigitte Pabst,Saki Chan,Han Cao,Susanne Morlot,Caroline Scholz,Bernd Auber,Kerstin Rhiem,Rita K. Schmutzler,Thomas Illig,Brigitte Schlegelberger,Doris Steinemann	11
5	Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer 2011 ·Human Mutation ·Heide Hellebrand,Christian Sutter,Ellen Honisch,Eva Groß,Barbara Wappenschmidt,Christian Schem,Helmut Deißler,Nina Ditsch,(unknown),Marion Kiechle,Claus R. Bartram,(unknown),Dieter Niederacher,Norbert Arnold,Alfons Meindl	36
6	Risk-reducing salpingo-oophorectomy in BRCA1 and BRCA2 mutation carriers 2010 ·Archives of Gynecology and Obstetrics ·Kerstin Rhiem,Dolores Foth,Barbara Wappenschmidt,Heidrun Gevensleben,Reinhard Büttner,U. Ulrich,Rita K. Schmutzler	24
7	Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk 2009 ·Breast Cancer Research and Treatment ·Rongxi Yang,Bowang Chen,Kari Hemminki,Barbara Wappenschmidt,Christoph Engel,Christian Sutter,Nina Ditsch,Bernhard H. F. Weber,Dieter Niederacher,Norbert Arnold,Alfons Meindl,Claus R. Bartram,Rita K. Schmutzler,Barbara Burwinkel	5
8	MLPA screening in theBRCA1gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases 2008 ·Human Mutation ·Stefanie Engert,Barbara Wappenschmidt,Beate Betz,Karin Kast,Michael Kutsche,Heide Hellebrand,Timm O. Goecke,Marion Kiechle,Dieter Niederacher,Rita K. Schmutzler,Alfons Meindl	74
9	Polymorphisms in the Janus kinase 2 (JAK)/signal transducer and activator of transcription (STAT) genes: putative association of the STAT gene region with familial breast cancer 2007 ·Endocrine Related Cancer ·(unknown),Justo Lorenzo Bermejo,Rita K. Schmutzler,Christian Sutter,Barbara Wappenschmidt,Alfons Meindl,Marion Kiechle,Norbert Arnold,Bernhard H. F. Weber,Dieter Niederacher,Barbara Burwinkel,Claus R. Bartram,Kari Hemminki,Asta Försti	33
10	Association of the BRCA1 missense variant R1699W with a malignant phyllodes tumor of the breast 2007 ·Cancer Genetics and Cytogenetics ·Kerstin Rhiem,Uta Flucke,Christoph Engel,Barbara Wappenschmidt,Axel Reinecke‐Lüthge,Reinhard Büttner,Rita K. Schmutzler	11
11	Aurora kinases A and B and familial breast cancer risk 2006 ·Cancer Letters ·Sandrine Tchatchou,Michael Wirtenberger,Kari Hemminki,Christian Sutter,Alfons Meindl,Barbara Wappenschmidt,Marion Kiechle,Peter Bugert,Rita K. Schmutzler,Claus R. Bartram,Barbara Burwinkel	49
12	Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer 2006 ·Carcinogenesis ·Michael Wirtenberger,Sandrine Tchatchou,Kari Hemminki,Joachim Schmutzhard,Christian Sutter,R Schmutzler,(unknown),Barbara Wappenschmidt,(unknown),Norbert Arnold,Bernhard H. F. Weber,Dieter Niederacher,C. R. Bartram,Barbara Burwinkel	47
13	Transcription factor 7-like 2 (TCF7L2) variant is associated with familial breast cancer risk: a case-control study 2006 ·BMC Cancer ·Barbara Burwinkel,Kalai Selvi Shanmugam,Kari Hemminki,Alfons Meindl,Rita K. Schmutzler,Christian Sutter,Barbara Wappenschmidt,Marion Kiechle,Claus R. Bartram,Bernd Frank	45
14	Outcome of a structured surveillance programme in women with a familial predisposition for breast cancer 2006 ·European Journal of Cancer Prevention ·Rita K. Schmutzler,Kerstin Rhiem,(unknown),Eva Wardelmann,Martin Lehnert,Silke Coburger,Barbara Wappenschmidt	26
15	Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer 2005 ·Carcinogenesis ·Michael Wirtenberger,Sandrine Tchatchou,Kari Hemminki,Rüdiger Klaes,Rita K. Schmutzler,Justo Lorenzo Bermejo,Bowang Chen,Barbara Wappenschmidt,Alfons Meindl,Claus R. Bartram,Barbara Burwinkel	35
16	Association of death receptor 4 haplotype 626C–683C with an increased breast cancer risk 2005 ·Carcinogenesis ·Bernd Frank,Kari Hemminki,Kalai Selvi Shanmugam,Alfons Meindl,Rüdiger Klaes,Rita K. Schmutzler,Barbara Wappenschmidt,Michael Untch,Peter Bugert,Claus R. Bartram,Barbara Burwinkel	26
17	TP53-binding protein variants and breast cancer risk: a case-control study 2005 ·Breast Cancer Research ·Bernd Frank,Kari Hemminki,Justo Lorenzo Bermejo,Rüdiger Klaes,Peter Bugert,Barbara Wappenschmidt,Rita K. Schmutzler,Barbara Burwinkel	11
18	PTEN mutations do not cause nuclear β-catenin accumulation in endometrial carcinomas 2004 ·Human Pathology ·Barbara Wappenschmidt,Eva Wardelmann,Andrea Gehrig,Thomas Schöndorf,Nicolaì Maass,G. Bonatz,A. M. Gassel,Torsten Pietsch,Peter Mallmann,Bernhard H. F. Weber,Rita K. Schmutzler	14
19	Limited relevance of the CHEK2 gene in hereditary breast cancer 2004 ·International Journal of Cancer ·Michael R. Dufault,Beate Betz,Barbara Wappenschmidt,Wera Hofmann,(unknown),Astrid Golla,(unknown),(unknown),Kerstin Rhiem,(unknown),(unknown),Peter Dall,Marion Kiechle,Michael Untch,W. Jonat,Alfons Meindl,Siegfried Scherneck,Dieter Niederacher,Rita K. Schmutzler,Norbert Arnold	70
20	Exclusion of a major role for the PTEN tumour-suppressor gene in breast carcinomas 1999 ·British Journal of Cancer ·(unknown),(unknown),(unknown),Barbara Wappenschmidt,(unknown),Yutaka Hayashi,A Meindl,D. Krebs,O. D. Wiestler,Andreas von Deimling,Rita K. Schmutzler	60

About Barbara Wappenschmidt

Barbara Wappenschmidt is a scholar working on Genetics, Aging and Cancer Research, having authored 62 papers that have together received 1.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (32 papers), DNA Repair Mechanisms (15 papers) and Cancer Genomics and Diagnostics (11 papers). The work is most often cited by research in Cancer Research (536 citations), Genetics (732 citations) and Molecular Biology (1.1k citations). Barbara Wappenschmidt has collaborated with scholars based in Germany, Sweden and United States. Frequent co-authors include Barbara Burwinkel, Claus R. Bartram, Kari Hemminki, Peter Bugert, Christian Sutter, Alfons Meindl, Rita K. Schmutzler, Dieter Niederacher, Rita K. Schmutzler and Norbert Arnold. Their work appears in journals such as Journal of Clinical Oncology, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

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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