Christine Maugard

2.9k total citations
32 papers, 824 citations indexed

About

Christine Maugard is a scholar working on Genetics, Oncology and Molecular Biology. According to data from OpenAlex, Christine Maugard has authored 32 papers receiving a total of 824 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 14 papers in Oncology and 7 papers in Molecular Biology. Recurrent topics in Christine Maugard's work include BRCA gene mutations in cancer (15 papers), Genetic factors in colorectal cancer (6 papers) and Nutrition, Genetics, and Disease (6 papers). Christine Maugard is often cited by papers focused on BRCA gene mutations in cancer (15 papers), Genetic factors in colorectal cancer (6 papers) and Nutrition, Genetics, and Disease (6 papers). Christine Maugard collaborates with scholars based in France, Canada and Italy. Christine Maugard's co-authors include Christine Chevreau, Yves‐Jean Bignon, Axel Le Cesne, Pierre Biron, Alain Ravaud, Catherine Sebban, Isabelle Ray‐Coquard, Jean‐Yves Blay, Catherine Noguès and Parviz Ghadirian and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Christine Maugard

31 papers receiving 794 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Christine Maugard France	15	409	312	247	148	109	32	824
Anna Felberg United States	13	439 1.1×	231 0.7×	209 0.8×	94 0.6×	171 1.6×	21	748
K. Tricker United Kingdom	11	118 0.3×	306 1.0×	333 1.3×	100 0.7×	105 1.0×	13	704
Kaylene Ready United States	15	486 1.2×	163 0.5×	180 0.7×	112 0.8×	268 2.5×	27	705
M J Worsham United States	12	210 0.5×	262 0.8×	203 0.8×	63 0.4×	182 1.7×	18	566
Peter Moosmann Switzerland	15	110 0.3×	392 1.3×	264 1.1×	63 0.4×	50 0.5×	23	938
Michael R. Milam United States	19	125 0.3×	177 0.6×	197 0.8×	79 0.5×	79 0.7×	58	1.2k
Monica Barile Italy	16	427 1.0×	359 1.2×	219 0.9×	121 0.8×	184 1.7×	26	794
Philip Law United Kingdom	15	161 0.4×	323 1.0×	183 0.7×	182 1.2×	140 1.3×	31	718
Iordanis Navrozoglou Greece	15	110 0.3×	98 0.3×	200 0.8×	84 0.6×	115 1.1×	49	861
Jennifer L. Geurts United States	9	290 0.7×	245 0.8×	136 0.6×	41 0.3×	102 0.9×	27	505

Countries citing papers authored by Christine Maugard

Since Specialization

Citations

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

Fields of papers citing papers by Christine Maugard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Maugard

This figure shows the co-authorship network connecting the top 25 collaborators of Christine Maugard. A scholar is included among the top collaborators of Christine Maugard 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 Christine Maugard. Christine Maugard 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

Leman, Raphaël, Laurent Castéra, Virginie Bernard, et al.. (2025). Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing. Familial Cancer. 24(1). 21–21.

Dhooge, Marion, Stéphanie Baert‐Desurmont, Carole Corsini, et al.. (2020). National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract. European Journal of Medical Genetics. 63(12). 104080–104080. 10 indexed citations

Fleury, Audrey, et al.. (2018). Breast cancer and ovarian tissue cryopreservation: Review of the literature. Journal of Gynecology Obstetrics and Human Reproduction. 47(8). 351–357. 12 indexed citations

Bougeard, Gaëlle, Mériam Koob, Marie Pierre Chenard, et al.. (2016). MSI detection and its pitfalls in CMMRD syndrome in a family with a bi-allelic MLH1 mutation. Familial Cancer. 15(4). 571–577. 9 indexed citations

Grandval, Philippe, Aurélie Fabre, Pascaline Gaildrat, et al.. (2014). Genomic variations integrated database for MUTYH-associated adenomatous polyposis. Journal of Medical Genetics. 52(1). 25–27. 2 indexed citations

Shatenstein, Bryna, et al.. (2009). Risk of Breast Cancer Among French-Canadian Women, Noncarriers of More FrequentBRCA1/2Mutations and Consumption of Total Energy, Coffee, and Alcohol. The Breast Journal. 15. S63–S71. 19 indexed citations

Cavallone, Luca, Suzanna L. Arcand, Christine Maugard, et al.. (2008). Haplotype analysis of TP53 polymorphisms, Arg72Pro and Ins16, in BRCA1 and BRCA2 mutation carriers of French Canadian descent. BMC Cancer. 8(1). 96–96. 18 indexed citations

Metcalfe, Kelly, William D. Foulkes, Charmaine Kim‐Sing, et al.. (2008). Family history as a predictor of uptake of cancer preventive procedures by women with a BRCA1 or BRCA2 mutation. Clinical Genetics. 73(5). 474–479. 40 indexed citations

Metcalfe, Kelly, Parviz Ghadirian, Barry P. Rosen, et al.. (2007). Variation in Rates of Uptake of Preventive Options in BRCA1 and BRCA2 Mutation Carriers Across Canada. 1(2). 92–98. 8 indexed citations

10.

Metcalfe, Kelly, Parviz Ghadirian, Barry P. Rosen, et al.. (2007). Variation in rates of uptake of preventive options by Canadian women carrying the BRCA1 or BRCA2 genetic mutation.. PubMed. 1(2). e92–8. 36 indexed citations

11.

Vogl, Florian D., Emanuela Taioli, Christine Maugard, et al.. (2004). Glutathione S-transferases M1, T1, and P1 and Breast Cancer: A Pooled Analysis. Cancer Epidemiology Biomarkers & Prevention. 13(9). 1473–1479. 93 indexed citations

12.

Tournier, Isabelle, Brigitte Bressac–de Paillerets, Dominique Stoppa-Lyonnet, et al.. (2004). Significant Contribution of Germline BRCA2 Rearrangements in Male Breast Cancer Families. Cancer Research. 64(22). 8143–8147. 81 indexed citations

13.

Tournier, Isabelle, Brigitte Bressac–de Paillerets, H. Sobol, et al.. (2004). Significant contribution of germline BRCA2 rearrangements in male breast cancer families. HAL (Le Centre pour la Communication Scientifique Directe). 7 indexed citations

14.

Toquet, Claire, Jean Néel, Louis Guillou, et al.. (2002). Elevated (≥10%) MIB-1 Proliferative Index Correlates with Poor Outcome in Gastric Stromal Tumor Patients: A Study of 35 Cases. Digestive Diseases and Sciences. 47(10). 2247–2253. 40 indexed citations

15.

Gad, Sophie, Virginie Caux‐Moncoutier, Sabine Pagès-Berhouet, et al.. (2002). Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families. Oncogene. 21(44). 6841–6847. 115 indexed citations

16.

Chevreau, Christine, Binh Bui, Bernard Chevallier, et al.. (1999). Phase I-II Trial of Intensification of the MAID Regimen With Support of Lenograstim (rHuG-CSF) in Patients With Advanced Soft-Tissue Sarcoma (STS). American Journal of Clinical Oncology. 22(3). 267–272. 9 indexed citations

17.

Essioux, Laurent, Olga M. Sinilnikova, François Eisinger, et al.. (1998). Marker segregation information in breast/ovarian cancer genetic counseling: Is it still useful?. American Journal of Medical Genetics. 79(3). 175–183. 4 indexed citations

18.

Julian‐Reynier, Claire, François Eisinger, F Chabal, et al.. (1998). Cancer genetic clinics: why do women who already have cancer attend?. European Journal of Cancer. 34(10). 1549–1553. 38 indexed citations

19.

Vaurs‐Barrière, Catherine, Valérie Vidal, Frédérique Penault‐Llorca, et al.. (1998). Pathology of sporadic breast tumors with LOH at the BRCA1 locus: correlation with histopathological features specific to familial BRCA1 tumors and absence of microsatellite instability.. International Journal of Oncology. 12(6). 1373–8. 7 indexed citations

20.

Jumas‐Bilak, Estelle, Christine Maugard, Sylvie Michaux‐Charachon, et al.. (1995). Study of the organization of the genomes of Escherichia coli, Brucella melitensis and Agrobacterium tumefaciens by insertion of a unique restriction site. Microbiology. 141(10). 2425–2432. 28 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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