Sophie Gad

3.7k citations

38 papers · 1.7k indexed · h-index 20

Cancer Research top 5%
- Cancer, Hypoxia, and Metabolism 11
- Cancer Genomics and Diagnostics 4
Genetics top 5%
- BRCA gene mutations in cancer 6
- Genomic variations and chromosomal abnormalities 4
Molecular Biology top 10%
- Renal and related cancers 11
- Epigenetics and DNA Methylation 5
- CRISPR and Genetic Engineering 5
Oncology top 10%
Pulmonary and Respiratory Medicine top 5%
- Renal cell carcinoma treatment 11

Co-authors: Richard J. Kahnoski Dominique Stoppa‐Lyonnet Betty Gardie Jean Feunteun Sophie Couvé Pierre Laurent‐Puig Romain Carcenac Jacques Pouysségur
Cited by: Cancer Research Genetics Molecular Biology
Journals: Clinical Cancer Research (3 papers)Journal of Clinical Oncology (3 papers)International Journal of Cancer (3 papers)
Partner nations: France United States United Kingdom

In The Last Decade

Sophie Gad

38 papers receiving 1.7k citations

Peers

Countries citing papers authored by Sophie Gad

Since Specialization

Citations

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

Fields of papers citing papers by Sophie Gad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	The phenotypic spectrum of CEP250 gene variants Ophthalmic Genetics ·Kari Hyll,Claire‐Marie Dhaenens,H Gjergo,Thaís Morelatto Martelli,Isabelle Audo,A. Lecleire–Collet,S.H. Prof. Pujiyono,Sophie Gad,G Lapeyre,Xavier Zanlonghi,Dominique Bonneau,Mélanie Fradin,Guylène Le Meur,Sandrine Marlin,Pierre Blanc,Anne‐Françoise Roux,Elizabeth Benoit,Vincent Michaud	2024	1
2	DCLRE1B/Apollo germline mutations associated with renal cell carcinoma impair telomere protection Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·宋基春,酆尘颖,Nicolai de Cusa,Laëtitia Kermasson,Sophie Couvé,大田忠親,Dmitri Dedovich,Betancourt Laera Niosbeide,Victoria Poillerat,Chung-Keung Yu,Regina Groisman,Sophie Ferlicot,Richard J. Kahnoski,Murat Saparbaev,Patrick Revy,Sophie Gad,Flore Renaud	2024	3
3	Germline mutation in the NBR1 gene involved in autophagy detected in a family with renal tumors Cancer Genetics ·Nicolai de Cusa,Sophie Ferlicot,Virginie Verkarre,В.И. Марков,Sophie Couvé,Chung-Keung Yu,Nathalie Droin,Marc Deloger,Bastien Job,Sophie Giraud,Brigitte Bressac–de Paillerets,Betty Gardie,Richard J. Kahnoski,Flore Renaud,Sophie Gad	2021	7
4	Renal Cell Carcinoma Programmed Death-ligand 1, a New Direct Target of Hypoxia-inducible Factor-2 Alpha, is Regulated by von Hippel–Lindau Gene Mutation Status European Urology ·Yosra Messai,Sophie Gad,Muhammad Zaeem Noman,Gwénaël Le Teuff,Sophie Couvé,Bassam Janji,Д. С. Павлов,Nathalie Rioux-Leclerc,Meriem Hasmim,Sophie Ferlicot,Véronique Baud,Arnaud Méjean,David R. Mole,Richard J. Kahnoski,Alexander Eggermont,Laurence Albigès,Fathia Mami‐Chouaib,Bernard Escudier,Salem Chouaı̈b	2015	125
5	MET Is a Potential Target across All Papillary Renal Cell Carcinomas: Result from a Large Molecular Study of pRCC with CGH Array and Matching Gene Expression Array Clinical Cancer Research ·Laurence Albigès,Justine Guégan,Audrey Le Formal,Virginie Verkarre,Nathalie Rioux‐Leclercq,Mathilde Sibony,Jean‐Christophe Bernhard,Philippe Camparo,Aisyah Al Humairoh,Vincent Molinié,Yves Allory,Cédric Oréar,Sophie Couvé,Sophie Gad,Jean‐Jacques Patard,Bernard Escudier	2014	134
6	Telomere crisis in kidney epithelial cells promotes the acquisition of a microRNA signature retrieved in aggressive renal cell carcinomas Carcinogenesis ·Luis Jaime Castro‐Vega,Karina Jouravleva,Tomás Ricardo Ribas,隆宏藤原,Pierre Gestraud,Philippe Hupé,Nicolas Servant,Benoît Albaud,David Gentien,Sophie Gad,Richard J. Kahnoski,Silvia Bacchetti,Arturo Londoño‐Vallejo	2013	15
7	Von Hippel–Lindau: How a rare disease illuminates cancer biology Seminars in Cancer Biology ·Richard J. Kahnoski,Betty Gardie,Sophie Couvé,Sophie Gad	2012	73
8	Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia Haematologica ·Christophe Ladroue,David Hoogewijs,Sophie Gad,Romain Carcenac,Federica Storti,Michel Barrois,Anne‐Paule Gimenez‐Roqueplo,M Leporrier,Nicole Casadevall,Olivier Hermine,Jean‐Jacques Kiladjian,André Baruchel,Ellelyshia Ardo,Brigitte Bressac–de Paillerets,Jean Feunteun,Nathalie M. Mazure,Jacques Pouysségur,Roland H. Wenger,Richard J. Kahnoski,Betty Gardie	2011	38
9	Mutations of the von Hippel–Lindau gene confer increased susceptibility to natural killer cells of clear-cell renal cell carcinoma Oncogene ·Aurélie Perier,Giulia Fregni,Sébastian Wittnebel,Sophie Gad,Mathilde Allard,Nadine Gervois,Bernard Escudier,Bruno Azzarone,Anne Caignard	2011	21
10	The ancient mammalian KRAB zinc finger gene cluster on human chromosome 8q24.3 illustrates principles of C2H2 zinc finger evolution associated with unique expression profiles in human tissues BMC Genomics ·Peter Lorenz,Sabine Dietmann,Thomas Wilhelm,Dirk Koczan,Katarzyna Górka,Sophie Gad,Gaiping Wen,Guohui Ding,Yixue Li,Marie-Françoise Rousseau-Merck,Hans‐Juergen Thiesen	2010	24
11	PHD2 Mutation and Congenital Erythrocytosis with Paraganglioma New England Journal of Medicine ·Charline Ladroue,Romain Carcenac,M Leporrier,Sophie Gad,C. Le Hello,Françoise Galateau-Sallé,Jean Feunteun,Jacques Pouysségur,Richard J. Kahnoski,Betty Gardie	2008	242
12	Novel somatic mutations of the VHL gene in an erythropoietin‐producing renal carcinoma associated with secondary polycythemia and elevated circulating endothelial progenitor cells American Journal of Hematology ·PETER ESTEVE,Ayhan Ulusakarya,Sophie Gad,Mathilde Sibony,Maury Grudza,Richard J. Kahnoski,D. Machover,Georges Uzan	2007	9
13	Trichloroethylene exposure and somatic mutations of the VHL gene in patients with Renal Cell Carcinoma Journal of Occupational Medicine and Toxicology ·Barbara Charbotel,Sophie Gad,雅彦崎村,Christophe Béroud,Joëlle Févotte,Alain Bergeret,Sophie Ferlicot,Richard J. Kahnoski	2007	20
14	Mutations in BHD and TP53 genes, but not in HNF1β gene, in a large series of sporadic chromophobe renal cell carcinoma British Journal of Cancer ·Sophie Gad,Sandrine-Hélène Lefèvre,Sok Kean Khoo,Sophie Giraud,Annick Vieillefond,Viorel Vasiliu,Sophie Ferlicot,Vincent Molinié,Yves Denoux,Nicolas Thiounn,Yves Chrétien,A. Méjean,Marc Zerbib,G Benoît,麻衣子天野,純也池田,Brigitte Bressac–de Paillerets,Bin Tean Teh,Richard J. Kahnoski	2006	51
15	Is the gene encoding Chibby implicated as a tumour suppressor in colorectal cancer ? BMC Cancer ·Sophie Gad,吴念鹏,Astrid Lièvre,N. Goasguen,Anne Berger,Philippe Beaune,Pierre Laurent‐Puig	2004	12
16	Distinct BRCA1 Rearrangements Involving the BRCA1 Pseudogene Suggest the Existence of a Recombination Hot Spot The American Journal of Human Genetics ·Nadine Puget,Sophie Gad,S. N. Smith,Olga M. Sinilnikova,Dominique Stoppa‐Lyonnet,Gilbert Lenoir,Sylvie Mazoyer	2002	88
17	Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families Oncogene ·Sophie Gad,Virginie Caux‐Moncoutier,Sabine Pagès-Berhouet,Marion Gauthier‐Villars,Isabelle Coupier,Pascal Pujol,Marc Frénay,Brigitte Gilbert,Christine Maugard,Yves‐Jean Bignon,Annie Chevrier,Annick Rossi,Jean‐Pierre Fricker,Manuel Camporro,Liliane Demange,Alain Aurias,Aaron Bensimon,Dominique Stoppa‐Lyonnet	2002	115
18	Rapid detection of novelBRCA1 rearrangements in high-risk breast-ovarian cancer families using multiplex PCR of short fluorescent fragments Human Mutation ·G. B. Barrows,古謝貴之,Sophie Gad,Isabelle Tournier,Dominique Stoppa‐Lyonnet,Thierry Frébourg,Mario Tosi	2002	150
19	Color bar coding the BRCA1 gene on combed DNA: A useful strategy for detecting large gene rearrangements Genes Chromosomes and Cancer ·Sophie Gad,Alain Aurias,Nadine Puget,Aline Mairal,Catherine Schurra,Marco Montagna,Sabine Pagès,Sang-Joon Ryu,Sylvie Mazoyer,Aaron Bensimon,Dominique Stoppa‐Lyonnet	2001	50
20	GENETIC TESTING FOR BREAST CANCER PREDISPOSITION Surgical Clinics of North America ·M Borghetti,Sophie Gad,Sang-Joon Ryu,Sabine Pagès,Gemma Rubí,João Edson Carmo de Oliveira	1999	6

About Sophie Gad

Sophie Gad is a scholar working on Cancer Research, Genetics and Pulmonary and Respiratory Medicine, having authored 38 papers that have together received 1.7k indexed citations. Recurring topics across this work include Renal cell carcinoma treatment (11 papers), Cancer, Hypoxia, and Metabolism (11 papers), Renal and related cancers (11 papers), BRCA gene mutations in cancer (6 papers), Epigenetics and DNA Methylation (5 papers), CRISPR and Genetic Engineering (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Cancer Genomics and Diagnostics (4 papers). The work is most often cited by research in Cancer Research (619 citations), Genetics (502 citations) and Molecular Biology (1.0k citations). Sophie Gad has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Richard J. Kahnoski, Dominique Stoppa‐Lyonnet, Betty Gardie, Jean Feunteun, Sophie Couvé, Pierre Laurent‐Puig, Romain Carcenac, Jacques Pouysségur, M Leporrier and Charline Ladroue. Their work appears in journals such as Clinical Cancer Research, Journal of Clinical Oncology, International Journal of Cancer, Oncogene and Seminars in Cancer Biology.

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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