Élodie Manié

2.4k citations

18 papers · 1.3k indexed · h-index 12

Cancer Research top 5%
- Cancer Genomics and Diagnostics 7
Oncology top 5%
- Cancer-related Molecular Pathways 2
- PARP inhibition in cancer therapy 2
- Pancreatic and Hepatic Oncology Research 1
Genetics top 5%
- BRCA gene mutations in cancer 8
- Genomic variations and chromosomal abnormalities 7
Reproductive Medicine top 5%
Molecular Biology top 10%
- DNA Repair Mechanisms 5
- Gene expression and cancer classification 2

Co-authors: Marc‐Henri Stern Dominique Stoppa‐Lyonnet Tatiana Popova Anne Vincent‐Salomon Xavier Sastre‐Garau Olivier Delattre Emmanuel Barillot Brigitte Sigal‐Zafrani
Cited by: Cancer Research Oncology Genetics
Journals: Blood (1 paper)Bioinformatics (1 paper)Cancer Research (4 papers)
Partner nations: France Mali Morocco

In The Last Decade

Élodie Manié

18 papers receiving 1.3k citations

Peers

Countries citing papers authored by Élodie Manié

Since Specialization

Citations

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

Fields of papers citing papers by Élodie Manié

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Élodie Manié, 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 Élodie Manié Line = papers co-authored together Élodie Manié links everyone, so they are left out of the graph.

All Works

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18 of 18 papers shown

#	Work
1	Lack of evidence for CDK12 as an ovarian cancer predisposing gene Familial Cancer ·Alexandre Eeckhoutte,Mathilde Saint‐Ghislain,Manon Reverdy,Virginie Raynal,Sylvain Baulande,Guillaume Bataillon,Lisa Golmard,Dominique Stoppa‐Lyonnet,Tatiana Popova,Claude Houdayer,Élodie Manié,Marc‐Henri Stern	2020	2
2	ShallowHRD: detection of homologous recombination deficiency from shallow whole genome sequencing Bioinformatics ·Alexandre Eeckhoutte,Alexandre Houy,Élodie Manié,Manon Reverdy,Ivan Bièche,Elisabetta Marangoni,Oumou Goundiam,Anne Vincent‐Salomon,Dominique Stoppa‐Lyonnet,François‐Clément Bidard,Marc‐Henri Stern,Tatiana Popova	2020	35
3	Ovarian Cancers Harboring Inactivating Mutations in CDK12 Display a Distinct Genomic Instability Pattern Characterized by Large Tandem Duplications Cancer Research ·Tatiana Popova,Élodie Manié,Valentina Boeva,Aude Battistella,Oumou Goundiam,Nicholas K. Smith,Christopher R. Mueller,Virginie Raynal,Odette Mariani,Xavier Sastre‐Garau,Marc‐Henri Stern	2016	79
4	Genomic hallmarks of homologous recombination deficiency in invasive breast carcinomas International Journal of Cancer ·Élodie Manié,Tatiana Popova,Aude Battistella,Julien Tarabeux,Virginie Caux‐Moncoutier,Lisa Golmard,Nicholas K. Smith,Christopher R. Mueller,Odette Mariani,Brigitte Sigal‐Zafrani,Thierry Dubois,Anne Vincent‐Salomon,Claude Houdayer,Dominique Stoppa‐Lyonnet,Marc‐Henri Stern	2015	51
5	First description of a sporadic breast cancer in a woman with BRCA1 germline mutation Oncotarget ·Elsa Curtit,Vanessa Benhamo,Nadège Gruel,Tatiana Popova,Élodie Manié,Paul Cottu,Odette Mariani,Dominique Stoppa‐Lyonnet,Xavier Pivot,Marc‐Henri Stern,Anne Vincent‐Salomon	2015	7
6	Genomic Signature of Homologous Recombination Deficiency in Breast and Ovarian Cancers BIO-PROTOCOL ·Tatiana Popova,Élodie Manié,Marc‐Henri Stern	2013	2
7	Loss of heterozygosity at 13q13 and 14q32 predicts BRCA2 inactivation in luminal breast carcinomas International Journal of Cancer ·Nicolas Pécuchet,Tatiana Popova,Élodie Manié,Carlo Lucchesi,Aude Battistella,Anne Vincent‐Salomon,Virginie Caux‐Moncoutier,Marc A. Bollet,Brigitte Sigal‐Zafrani,Xavier Sastre‐Garau,Dominique Stoppa‐Lyonnet,Marc‐Henri Stern	2013	6
8	Ploidy and Large-Scale Genomic Instability Consistently Identify Basal-like Breast Carcinomas with BRCA1/2 Inactivation Cancer Research ·Tatiana Popova,Élodie Manié,Guillaume Rieunier,Virginie Caux‐Moncoutier,Carole Tirapo,Thierry Dubois,Olivier Delattre,Brigitte Sigal‐Zafrani,Marc A. Bollet,Michel Longy,Claude Houdayer,Xavier Sastre‐Garau,Anne Vincent‐Salomon,Dominique Stoppa‐Lyonnet,Marc‐Henri Stern	2012	418
9	Syntenic Relationships between Genomic Profiles of Fiber-Induced Murine and Human Malignant Mesothelioma American Journal Of Pathology ·Didier Jean,Emilie Thomas,Élodie Manié,Annie Renier,Aurélien de Reyniès,Céline Boulangé-Lecomte,Pascal Andujar,Jocelyne Fleury‐Feith,Françoise Galateau-Sallé,Marco Giovannini,Jessica Zucman‐Rossi,Marc‐Henri Stern,Marie‐Claude Jaurand	2011	36
10	Leukemic phase of follicular lymphomas: an atypical presentation Leukemia & lymphoma ·Chadi Al‐Nawakil,Olivier Kosmider,Marc‐Henri Stern,Élodie Manié,Valérie Bardet,Véronique Leblond,Sophie Park,F. Dreyfus,Didier Bouscary,Jérôme Tamburini	2011	10
11	High Frequency of TP53 Mutation in BRCA1 and Sporadic Basal-like Carcinomas but not in BRCA1 Luminal Breast Tumors Cancer Research ·Élodie Manié,Anne Vincent‐Salomon,Jacqueline Lehmann‐Che,Gaëlle Pierron,Elisabeth Turpin,Mathilde Warcoin,Nadège Gruel,Ingrid Lebigot,Xavier Sastre‐Garau,Rosette Lidereau,Audrey Remenieras,Jean Feunteun,Olivier Delattre,Hugues de Thé,Dominique Stoppa‐Lyonnet,Marc‐Henri Stern	2009	112
12	Beta‐catenin status in paediatric medulloblastomas: correlation of immunohistochemical expression with mutational status, genetic profiles, and clinical characteristics The Journal of Pathology ·Sarah Fattet,Christine Haberler,Patricia Legoix,Pascale Varlet,Arielle Lellouch‐Tubiana,Séverine Lair,Élodie Manié,Marie‐Anne Raquin,D. Bours,Sabrina Carpentier,Emmanuel Barillot,Jacques Grill,François Doz,Stéphanie Puget,Isabelle Janoueix‐Lerosey,Olivier Delattre	2009	139
13	Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays Genome biology ·Tatiana Popova,Élodie Manié,Dominique Stoppa‐Lyonnet,Guillem Rigaill,Emmanuel Barillot,Marc‐Henri Stern	2009	118
14	Genetic heterogeneity versus molecular analysis of prion susceptibility in neuroblasma N2a sublines Archives of Virology ·Stéphanie Chasseigneaux,Manuela Pastore,Janice Britton‐Davidian,Élodie Manié,Marc‐Henri Stern,Jacques Callebert,Josette Catalan,Danielle Casanova,Maxime Bélondrade,Monique Provansal,Yonghua Zhang,Alexander Bürkle,Jean Laplanche,Nicolas Sévenet,Sylvain Lehmann	2008	11
15	BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas International Journal of Cancer ·Ahmed Idbaïh,Yannick Marie,Carlo Lucchesi,Gaëlle Pierron,Élodie Manié,Virginie Raynal,Véronique Mosseri,Khê Hoang‐Xuan,M. Kujas,Isabel Martínez Brito,Karima Mokhtari,Marc Sanson,Emmanuel Barillot,Alain Aurias,Jean‐Yves Delattre,Olivier Delattre	2007	88
16	X Inactive–Specific Transcript RNA Coating and Genetic Instability of the X Chromosome in BRCA1 Breast Tumors Cancer Research ·Anne Vincent‐Salomon,Carine Ganem‐Elbaz,Élodie Manié,Virginie Raynal,Xavier Sastre‐Garau,Dominique Stoppa‐Lyonnet,Marc‐Henri Stern,Édith Heard	2007	70
17	Spatial normalization of array-CGH data BMC Bioinformatics ·Pierre Neuvial,Philippe Hupé,Isabel Martínez Brito,Stéphane Liva,Élodie Manié,Caroline Brennetot,François Radvanyi,Alain Aurias,Emmanuel Barillot	2006	64
18	In vitro identification of human pro-B cells that give rise to macrophages, natural killer cells, and T cells Blood ·Damien Reynaud,Nathalie Lefort,Élodie Manié,Laure Coulombel,Yves Lévy	2003	42

About Élodie Manié

Élodie Manié is a scholar working on Cancer Research, Genetics and Genetics, having authored 18 papers that have together received 1.3k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), Cancer Genomics and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers), DNA Repair Mechanisms (5 papers), Cancer-related Molecular Pathways (2 papers), PARP inhibition in cancer therapy (2 papers), Gene expression and cancer classification (2 papers) and Pancreatic and Hepatic Oncology Research (1 paper). The work is most often cited by research in Cancer Research (450 citations), Oncology (585 citations) and Genetics (180 citations). Élodie Manié has collaborated with scholars based in France, Mali and Morocco. Frequent co-authors include Marc‐Henri Stern, Dominique Stoppa‐Lyonnet, Tatiana Popova, Anne Vincent‐Salomon, Xavier Sastre‐Garau, Olivier Delattre, Emmanuel Barillot, Brigitte Sigal‐Zafrani, Virginie Caux‐Moncoutier and Claude Houdayer. Their work appears in journals such as Blood, Bioinformatics and Cancer Research.

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