Nancy Uhrhammer

2.8k total citations
62 papers, 1.6k citations indexed

About

Nancy Uhrhammer is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Nancy Uhrhammer has authored 62 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 27 papers in Genetics and 20 papers in Pathology and Forensic Medicine. Recurrent topics in Nancy Uhrhammer's work include BRCA gene mutations in cancer (23 papers), DNA Repair Mechanisms (18 papers) and Genetic factors in colorectal cancer (17 papers). Nancy Uhrhammer is often cited by papers focused on BRCA gene mutations in cancer (23 papers), DNA Repair Mechanisms (18 papers) and Genetic factors in colorectal cancer (17 papers). Nancy Uhrhammer collaborates with scholars based in France, Tunisia and United States. Nancy Uhrhammer's co-authors include Yves‐Jean Bignon, Yannick Bidet, Carmen Rodrı́guez, Arja Jukkola‐Vuorinen, Magali Olivier, Rosette Lidereau, Charles Theillet, Jennifer M. Varley, Dieter Niederacher and Anne-Lise B√∏rresen-Dale and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Nancy Uhrhammer

60 papers receiving 1.6k citations

Peers

Countries citing papers authored by Nancy Uhrhammer

Since Specialization

Citations

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

Fields of papers citing papers by Nancy Uhrhammer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Uhrhammer

This figure shows the co-authorship network connecting the top 25 collaborators of Nancy Uhrhammer. A scholar is included among the top collaborators of Nancy Uhrhammer 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 Nancy Uhrhammer. Nancy Uhrhammer 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	Detection Rate and Spectrum of Pathogenic Variations in a Cohort of 83 Patients with Suspected Hereditary Risk of Kidney Cancer 2023 ·Genes ·(unknown), (unknown), (unknown), (unknown), Nancy Uhrhammer, (unknown), Yannick Bidet, Maud Privat, (unknown)	1
2	Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature 2023 ·BMC Medical Genomics ·(unknown), (unknown), (unknown), Virginie Bubien, Nancy Uhrhammer, Maud Privat, (unknown), (unknown), (unknown), (unknown), Natalie Jones, Yannick Bidet, Nicolas Sévenet, Yves‐Jean Bignon	6
3	Case Series of 11 CDH1 Families (47 Carriers) Including Incidental Findings, Signet Ring Cell Colon Cancer and Review of the Literature 2023 ·Genes ·(unknown), Nancy Uhrhammer, Maud Privat, (unknown), Myriam Kossaï, Julien Scanzi, (unknown), (unknown), Yannick Bidet, (unknown)	0
4	Feedback of extended panel sequencing in 1530 patients referred for suspicion of hereditary predisposition to adult cancers 2020 ·Clinical Genetics ·(unknown), Nancy Uhrhammer, Maud Privat, (unknown), (unknown), (unknown), (unknown), Yannick Bidet, Yves‐Jean Bignon	8
5	Is BRCA2 involved in early onset colorectal cancer risk? 2019 ·Clinical Genetics ·(unknown), Maud Privat, Alexandra Martins, Sandrine M. Caputo, Céline Pebrel‐Richard, (unknown), (unknown), Carole Corsini, (unknown), Nicolas Barnich, Yannick Bidet, Nancy Uhrhammer, Yves‐Jean Bignon	6
6	Early Onset Multiple Primary Tumors in Atypical Presentation of Cowden Syndrome Identified by Whole-Exome-Sequencing 2018 ·Frontiers in Genetics ·(unknown), (unknown), Nancy Uhrhammer, (unknown), (unknown), Maud Privat, Yannick Bidet, Yves‐Jean Bignon	14
7	Involvement of IL17A, IL17F and IL23R Polymorphisms in Colorectal Cancer Therapy 2015 ·PLoS ONE ·(unknown), (unknown), (unknown), (unknown), (unknown), Nejla Stambouli, (unknown), Nadia Kourda, Yves‐Jean Bignon, Nancy Uhrhammer, Amel Mézlini, Karim Bougatef, Amel Benammar-Elgaaïed	22
8	BRCA Mutations Increase Fertility in Families at Hereditary Breast/Ovarian Cancer Risk 2015 ·PLoS ONE ·Fabrice Kwiatkowski, (unknown), Yannick Bidet, (unknown), Nancy Uhrhammer, Yves‐Jean Bignon	36
9	Significant association between interleukin-17A polymorphism and colorectal cancer 2014 ·Tumor Biology ·(unknown), Raja Marrakchi, (unknown), Amel Mézlini, (unknown), (unknown), Nejla Stambouli, Nadia Kourda, (unknown), Nancy Uhrhammer, Karim Bougatef, Yves‐Jean Bignon, Amel Benammar-Elgaaïed	43
10	Significant association between IL23R and IL17F polymorphisms and clinical features of colorectal cancer 2014 ·Immunology Letters ·(unknown), (unknown), Karim Bougatef, Amel Mézlini, Ahmed Abidi, (unknown), Nejla Stambouli, (unknown), Nadia Kourda, Nancy Uhrhammer, Yves Jean Bignon, Amel Benammar Elgaaïed, Raja Marrakchi	33
11	Thymidylate synthase polymorphism in sporadic colorectal and gastric cancer in Tunisian population: a predictive role in 5-fluorouracil based chemotherapy treatment 2014 ·Medical Oncology ·(unknown), (unknown), (unknown), (unknown), Amel Mézlini, (unknown), Sami Guermazi, (unknown), (unknown), Nancy Uhrhammer, Yves Jean Bignon, Amel Benammar Elgaaïed, Karim Bougatef	5
12	Wild-type genotypes of BRCA1 gene SNPs combined with micro-RNA over-expression in mammary tissue leading to familial breast cancer with an increased risk of distant metastases’ occurrence 2014 ·Medical Oncology ·(unknown), (unknown), Nejla Stambouli, Houssein Khodjet‐El‐Khil, (unknown), (unknown), (unknown), Nancy Uhrhammer, Maud Privat, Amel Mézlini, Farhat Ben Ayed, Khaled Ben Romdhane, Sylvie Mader, (unknown), Amel Benammar Elgaaïed	12
13	Positive link between variant Toll-like receptor 4 (Asp299Gly and Thr399Ile) and colorectal cancer patients with advanced stage and lymph node metastasis 2013 ·Tumor Biology ·(unknown), (unknown), Nadia Kourda, Yves‐Jean Bignon, Nancy Uhrhammer, Alexis Desrichard, (unknown), (unknown), Nejla Stambouli, Amel Mézlini, (unknown), Raja Marrakchi, (unknown), Karim Bougatef	29
14	Mutation Screening of the BRCA1 Gene in Early Onset and Familial Breast/Ovarian Cancer in Moroccan Population 2013 ·International Journal of Medical Sciences ·Abdelilah Laraqui, Nancy Uhrhammer, (unknown), (unknown), Jamila El Baghdadi, (unknown), (unknown), Mohamed Ichou, Yassir Sbitti, (unknown), (unknown), Yves‐Jean Bignon	53
15	Complete BRCA mutation screening in breast and ovarian cancer predisposition families from a North-Eastern Romanian population 2010 ·Familial Cancer ·(unknown), Nancy Uhrhammer, (unknown), (unknown), E Carasevici, Yves‐Jean Bignon	16
16	Werner syndrome and mutations of theWRNandLMNAgenes in France 2006 ·Human Mutation ·Nancy Uhrhammer, (unknown), (unknown), Anna Domaszewska-Szostek, (unknown), Yong Yang, S. Aractingi, D. Bessis, Yves‐Jean Bignon	36
17	Seventh International Workshop on Ataxia-Telangiectasia. 1998 ·PubMed ·Nancy Uhrhammer, J.-O. Bay, Y. J. Bignon	17
18	CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1 1997 ·Mammalian Genome ·(unknown), Lan Yang, Nitin Udar, Teresa Liang, Nancy Uhrhammer, Shunbin Xu, Jacques‐Olivier Bay, Zhijun Wang, (unknown), (unknown), I Klisak, Milhan Telatar, Huanming Yang, Patrick Concannon, Richard A. Gatti	15
19	New localization of NCAM, proximal to DRD2 at Chromosome 11q23 1995 ·Mammalian Genome ·Milhan Telatar, Ethan M. Lange, Nancy Uhrhammer, Richard A. Gatti	1
20	A Pulsed-Field Gel Electrophoresis Map in the Ataxia-Telangiectasia Region of Chromosome 11q22.3 1994 ·Genomics ·Nancy Uhrhammer, Patrick Concannon, (unknown), Yusuke Nakamura, Richard A. Gatti	7

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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