Constanze Pagenstecher

2.4k citations

27 papers · 1.7k indexed · h-index 22

Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer 25
Cancer Research top 5%
- Cancer Genomics and Diagnostics 12
Oncology top 5%
- Colorectal Cancer Screening and Detection 11
- Colorectal Cancer Treatments and Studies 8
Genetics top 10%
Molecular Biology
- DNA Repair Mechanisms 3
- RNA Research and Splicing 3
- RNA modifications and cancer 2
Surgery
- Cholangiocarcinoma and Gallbladder Cancer Studies 2

Co-authors: Elisabeth Mangold Waltraut Friedl Peter Propping Stefan Aretz Gabriela Möslein Siegfried Uhlhaas Hans K. Schackert Christoph Engel
Cited by: Pathology and Forensic Medicine Cancer Research Oncology
Journals: Journal of Clinical Oncology (2 papers)Gastroenterology (1 paper)Oncogene (1 paper)
Partner nations: Germany France Poland

In The Last Decade

Constanze Pagenstecher

27 papers receiving 1.7k citations

Peers

Countries citing papers authored by Constanze Pagenstecher

Since Specialization

Citations

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

Fields of papers citing papers by Constanze Pagenstecher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Constanze Pagenstecher, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Constanze Pagenstecher Line = papers co-authored together Constanze Pagenstecher links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1 Cancer Letters ·Stefan Krüger,Christoph Engel,Andrea Bier,Ann-Sophie Silber,Heike Görgens,Elisabeth Mangold,Constanze Pagenstecher,Elke Holinski‐Feder,Magnus von Knebel Doeberitz,Brigitte Royer‐Pokora,Stefan Dechant,Christian Pox,Nils Rahner,A. Hermann Müller,Hans K. Schackert	2007	15
2	A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification Journal of Molecular Diagnostics ·Constanze Pagenstecher,Dorothea Gadzicki,Dietlinde Stienen,Siegfried Uhlhaas,Elisabeth Mangold,Nils Rahner,Mine Arslan‐Kirchner,Peter Propping,Waltraut Friedl,Stefan Aretz	2007	7
3	Microsatellite Stable Colorectal Cancers in Clinically Suspected Hereditary Nonpolyposis Colorectal Cancer Patients without Vertical Transmission of Disease Are Unlikely to Be Caused by Biallelic Germline Mutations in MYH Journal of Molecular Diagnostics ·Heike Görgens,Stefan Krüger,Eberhard Kuhlisch,Constanze Pagenstecher,Ruth Höhl,Hans K. Schackert,A. Hermann Müller	2006	14
4	MSH6 mutation in Muir?Torre syndrome: could this be a rare finding? British Journal of Dermatology ·Elisabeth Mangold,Nils Rahner,Nicolaus Friedrichs,Reinhard Buettner,Constanze Pagenstecher,Stefan Aretz,Waltraut Friedl,Thomas Ruzicka,Peter Propping,Arno Rütten,Roland Kruse	2006	26
5	Microsatellite instability did not predict individual survival of unselected patients with colorectal cancer International Journal of Colorectal Disease ·C. Lamberti,Sara Lundin,M. Bogdanow,Constanze Pagenstecher,Nicolaus Friedrichs,Reinhard Büttner,Tilman Sauerbruch	2006	51
6	Frequency of Hereditary Non-Polyposis Colorectal Cancer among Unselected Patients with Colorectal Cancer in Germany Digestion ·C. Lamberti,Elisabeth Mangold,Constanze Pagenstecher,Matthias Jungck,Dave Schwering,Magdolna Bollmann,J. Vogel,D Kindermann,R. Nikorowitsch,Nicolaus Friedrichs,Björn Schneider,F. Houshdaran,I G Schmidt-Wolf,Waltraut Friedl,Peter Propping,Tilman Sauerbruch,Reinhard Büttner,Micaela Mathiak	2006	23
7	Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer International Journal of Cancer ·Christoph Engel,Jochen Forberg,Elke Holinski‐Feder,Constanze Pagenstecher,Jens Plaschke,Matthias Kloor,Christopher Poremba,Christian Pox,Josef Rüschoff,Gisela Keller,Wolfgang Dietmaier,Petra Rümmele,Nicolaus Friedrichs,Elisabeth Mangold,Reinhard Buettner,Hans K. Schackert,Peter Kienle,Susanne Stemmler,Gabriela Möslein,Markus Loeffler	2005	71
8	N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC) Cancer Letters ·Steffen Pistorius,Heike Görgens,Stefan Krüger,Christoph Engel,Elisabeth Mangold,Constanze Pagenstecher,Elke Holinski‐Feder,Gabriela Möslein,Magnus von Knebel Doeberitz,Josef Rüschoff,Judith Karner‐Hanusch,Hans-Detlev Saeger,Hans K. Schackert	2005	4
9	Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study The Lancet Oncology ·Stefan Krüger,Ann-Sophie Silber,Christoph Engel,Heike Görgens,Elisabeth Mangold,Constanze Pagenstecher,Elke Holinski‐Feder,Magnus von Knebel Doeberitz,Gabriela Möslein,Wolfgang Dietmaier,Susanne Stemmler,Waltraut Friedl,Josef Rüschoff,Hans K. Schackert	2005	37
10	Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining The Journal of Pathology ·Elisabeth Mangold,Constanze Pagenstecher,Waltraut Friedl,Hans‐Peter Fischer,Sabine Merkelbach‐Bruse,Maike Ohlendorf,Nicolaus Friedrichs,Stefan Aretz,Reinhard Buettner,Peter Propping,Micaela Mathiak	2005	82
11	Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes European Journal of Human Genetics ·Maria Wehner,Elisabeth Mangold,Marlies Sengteller,Nicolaus Friedrichs,Stefan Aretz,Waltraut Friedl,Peter Propping,Constanze Pagenstecher	2005	30
12	HNPCC-associated small bowel cancer: Clinical and molecular characteristics Gastroenterology ·Karsten Schulmann,Frank Brasch,Erdmute Kunstmann,Christoph Engel,Constanze Pagenstecher,H. Vogelsang,Stefan Krüger,Tilman Vogel,Hanns-Peter Knaebel,Josef Rüschoff,Stephan A. Hahn,Magnus von Knebel Doeberitz,Gabriela Möslein,Stephen J. Meltzer,Hans K. Schackert,Christiane Tympner,Elisabeth Mangold,Wolff Schmiegel	2005	132
13	Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer Cancer Letters ·Stefan Krüger,Christoph Engel,Andrea Bier,Elisabeth Mangold,Constanze Pagenstecher,Magnus von Knebel Doeberitz,Elke Holinski‐Feder,Gabriela Möslein,Gisela Keller,Erdmute Kunstmann,Waltraut Friedl,Jens Plaschke,Josef Rüschoff,Hans K. Schackert	2005	27
14	The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC) Journal of Medical Genetics ·Stefan Krüger,August Bier,Christoph Engel,Elisabeth Mangold,Constanze Pagenstecher,Magnus von Knebel Doeberitz,Elke Holinski‐Feder,Gabriela Möslein,Karsten Schulmann,Jens Plaschke,Josef Rüschoff,Hans K. Schackert	2005	30
15	High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome Human Mutation ·Stefan Aretz,Dietlinde Stienen,Siegfried Uhlhaas,Steffan Loff,Walter Back,Constanze Pagenstecher,D. Ross McLeod,Gail E. Graham,Elisabeth Mangold,René Santer,Peter Propping,Waltraut Friedl	2005	174
16	Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants Human Genetics ·Constanze Pagenstecher,Maria Wehner,Waltraut Friedl,Nils Rahner,Stefan Aretz,Nicolaus Friedrichs,Marlies Sengteller,Wolfram Henn,Reinhard Buettner,Peter Propping,Elisabeth Mangold	2005	73
17	Spectrum and frequencies of mutations inMSH2 andMLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer International Journal of Cancer ·Elisabeth Mangold,Constanze Pagenstecher,Waltraut Friedl,Micaela Mathiak,Reinhard Buettner,Christoph Engel,Markus Loeffler,Elke Holinski‐Feder,Y Müller-Koch,Gisela Keller,Hans K. Schackert,Stefan Krüger,Timm O. Goecke,Gabriela Möslein,Matthias Kloor,Johannes Gebert,Erdmute Kunstmann,Karsten Schulmann,Josef Rüschoff,Peter Propping	2005	95
18	Familial adenomatous polyposis: Aberrant splicing due to missense or silent mutations in theAPCgene Human Mutation ·Stefan Aretz,Siegfried Uhlhaas,Yuli Sun,Constanze Pagenstecher,Elisabeth Mangold,Reiner Caspari,Gabriela Möslein,Karsten Schulmann,Peter Propping,Waltraut Friedl	2004	89
19	Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis European Journal of Human Genetics ·Stefan Aretz,Siegfried Uhlhaas,Reiner Caspari,Elisabeth Mangold,Constanze Pagenstecher,Peter Propping,Waltraut Friedl	2003	103
20	Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes International Journal of Cancer ·Yaping Wang,Waltraut Friedl,Christof Lamberti,Matthias Jungck,Micaela Mathiak,Constanze Pagenstecher,Peter Propping,Elisabeth Mangold	2002	87

About Constanze Pagenstecher

Constanze Pagenstecher is a scholar working on Pathology and Forensic Medicine, Cancer Research and Oncology, having authored 27 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (25 papers), Cancer Genomics and Diagnostics (12 papers), Colorectal Cancer Screening and Detection (11 papers), Colorectal Cancer Treatments and Studies (8 papers), DNA Repair Mechanisms (3 papers), RNA Research and Splicing (3 papers), RNA modifications and cancer (2 papers) and Cholangiocarcinoma and Gallbladder Cancer Studies (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.4k citations), Cancer Research (630 citations) and Oncology (908 citations). Constanze Pagenstecher has collaborated with scholars based in Germany, France and Poland. Frequent co-authors include Elisabeth Mangold, Waltraut Friedl, Peter Propping, Stefan Aretz, Gabriela Möslein, Siegfried Uhlhaas, Hans K. Schackert, Christoph Engel, Stefan Krüger and Karsten Schulmann. Their work appears in journals such as Journal of Clinical Oncology, Gastroenterology and Oncogene.

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