Thomas Rio Frio

3.2k citations

20 papers · 1.2k indexed · h-index 14

Cancer Research top 5%
- Cancer Genomics and Diagnostics 6
Molecular Biology
- Advanced biosensing and bioanalysis techniques 4
- Retinal Development and Disorders 4
- RNA regulation and disease 3
- CRISPR and Genetic Engineering 3
Pathology and Forensic Medicine top 10%
- Genetic factors in colorectal cancer 4
Ophthalmology top 5%
Pulmonary and Respiratory Medicine top 10%
Surgery
- Congenital Diaphragmatic Hernia Studies 2
Genetics
- Genomic variations and chromosomal abnormalities 2

Co-authors: Carlo Rivolta Eliot L. Berson J. Beckmann Adriana Ransijn Maud Kamal Christophe Le Tourneau Terri L. McGee Nicholas M. Wade
Cited by: Cancer Research Molecular Biology Pathology and Forensic Medicine
Partner nations: France United States Switzerland

In The Last Decade

Thomas Rio Frio

19 papers receiving 1.1k citations

Peers

Countries citing papers authored by Thomas Rio Frio

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Rio Frio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas Rio Frio. 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 Thomas Rio Frio. The network helps show where Thomas Rio Frio may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Exome sequencing reveals aberrant signalling pathways as hallmark of treatment-naive anal squamous cell carcinoma Wulfran Cacheux,Virginie Dangles-Marie,Étienne Rouleau,Julien Lazartigues,Elodie Girard,Adrien Briaux,Pascale Mariani,Sophie Richon,Sophie Vacher,Bruno Buecher,Marion Richard‐Molard,Emmanuelle Jeannot,Nicolas Servant,Fereshteh Farkhondeh,Odette Mariani,Thomas Rio Frio,Sergio Roman‐Roman,Emmanuel Mitry,Ivan Bièche,Astrid Lièvre	2017	19
2	Frequent Somatic Mutation in Adult Intestinal Stem Cells Drives Neoplasia and Genetic Mosaicism during Aging Katarzyna Siudeja,Sonya Nassari,Louis Gervais,Patricia Skorski,Sonia Lameiras,Donato Stolfa,Maria Zande,Virginie Bernard,Thomas Rio Frio,Allison J. Bardin	2015	63
3	Abstract PD3-8: Circulating tumor DNA and circulating tumor cells in metastatic triple negative breast cancer patients François‐Clément Bidard,Jordan Madic,Anna Kiialainen,Fabian Birzele,Guillemette Ramey,Quentin Leroy,Thomas Rio Frio,Virginie Raynal,Virginie Bernard,Alban Lermine,Inga Clausen,Nicolas Giroud,Roland Schmucki,Carsten Horn,Olivia Spleiss,Olivier Lantz,Marc‐Henri Stern,Maja Weisser,Ronald Lebofsky,Jean‐Yves Pierga	2015	2
4	Circulating tumor DNA as a non‐invasive substitute to metastasis biopsy for tumor genotyping and personalized medicine in a prospective trial across all tumor types Ronald Lebofsky,Charles Decraene,Virginie Bernard,Maud Kamal,Anthony Blin,Quentin Leroy,Thomas Rio Frio,Gaëlle Pierron,Céline Callens,Ivan Bièche,Adrien Saliou,Jordan Madic,Étienne Rouleau,François‐Clément Bidard,Olivier Lantz,Marc‐Henri Stern,Christophe Le Tourneau,Jean‐Yves Pierga	2014	216
5	A scoring strategy combining statistics and functional genomics supports a possible role for common polygenic variation in autism Jérôme Carayol,Gerard D. Schellenberg,Beth A. Dombroski,Claire Amiet,Bérengère Génin,Karine Fontaine,Francis Rousseau,Céline Vazart,David Cohen,Thomas Frazier,Antonio Y. Hardan,Géraldine Dawson,Thomas Rio Frio	2014	7
6	Multi-factor data normalization enables the detection of copy number aberrations in amplicon sequencing data Valentina Boeva,Tatiana Popova,Maxime Liénard,Sébastien Toffoli,Maud Kamal,Christophe Le Tourneau,David Gentien,Nicolas Servant,Pierre Gestraud,Thomas Rio Frio,Philippe Hupé,Emmanuel Barillot,Jean‐François Laes	2014	93
7	Randomized Phase II Trial Comparing Therapy Based on Tumor Molecular Profiling Versus Conventional Therapy in Refractory Cancer Patients: Shiva Design C. Le Tourneau,Maud Kamal,Olivier Trédan,C. Gomez-Roca,Mario Campone,A. Gonçalves,Nicolás Isambert,Céline Gavoille,David Gentien,Nicolas Servant,Thomas Rio Frio,Xavier Paolettí	2013	0
8	Breakpoint Features of Genomic Rearrangements in Neuroblastoma with Unbalanced Translocations and Chromothripsis Valentina Boeva,Stéphanie Jouannet,Romain Daveau,Valérie Combaret,Cécile Pierre‐Eugène,Alex Cazes,Caroline Louis‐Brennetot,Gudrun Schleiermacher,Sandrine Ferrand,Gaëlle Pierron,Alban Lermine,Thomas Rio Frio,Virginie Raynal,Gilles Vassal,Emmanuel Barillot,Olivier Delattre,Isabelle Janoueix‐Lerosey	2013	28
9	Streamlined ion torrent PGM-based diagnostics: BRCA1 and BRCA2 genes as a model Julien Tarabeux,Bruno Zeitouni,Virginie Moncoutier,Henrique Tenreiro,Khadija Abidallah,Séverine Lair,Patricia Legoix-Né,Quentin Leroy,Étienne Rouleau,Lisa Golmard,Emmanuel Barillot,Marc‐Henri Stern,Thomas Rio Frio,Dominique Stoppa‐Lyonnet,Claude Houdayer	2013	46
10	Designs and challenges for personalized medicine studies in oncology: focus on the SHIVA trial Christophe Le Tourneau,Maud Kamal,Olivier Trédan,Jean‐Pierre Delord,Mario Campone,Anthony Gonçalvès,Nicolás Isambert,Thierry Conroy,David Gentien,Anne Vincent‐Salomon,Anne-Lise Pouliquen,Nicolas Servant,Marc‐Henri Stern,Anne‐Gaëlle Le Corroller,Sébastien Armanet,Thomas Rio Frio,Xavier Paolettí	2012	44
11	<emph type="ital">DICER1</emph> Mutations in Familial Multinodular Goiter With and Without Ovarian Sertoli-Leydig Cell Tumors Thomas Rio Frio	2011	224
12	Mutation analysis of the gene encoding the PALB2-binding protein MRG15 in BRCA1/2-negative breast cancer families Thomas Rio Frio,Maria K. Haanpää,Carly Pouchet,Katri Pylkäs,Mikko Vuorela,Marc Tischkowitz,Robert Winqvist,William D. Foulkes	2010	5
13	Germline DICER1 mutations and familial cystic nephroma Amin Bahubeshi,Nebıl Bal,Thomas Rio Frio,Nancy Hamel,Carly Pouchet,Ahmet Yılmaz,Dorothée Bouron‐Dal Soglio,Gretchen M. Williams,M Tischkowitz,John R. Priest,William D. Foulkes	2010	87
14	Homozygous BUB1B Mutation and Susceptibility to Gastrointestinal Neoplasia Thomas Rio Frio,Josée N. Lavoie,Nancy Hamel,Felipe C. Geyer,Yaël B. Kushner,David J. Novak,Landon Wark,Cristian Capelli,Jorge S. Reis‐Filho,Sabine Mai,Tomi Pastinen,Marc Tischkowitz,Victoria Marcus,William D. Foulkes	2010	60
15	A Single-Base Substitution Within an Intronic Repetitive Element in PRPF31 Causes Dominant Retinitis Pigmentosa With Reduced Penetrance Carlo Rivolta,Terri L. McGee,Nicholas M. Wade,Christian Iseli,J. Beckmann,Eliot L. Berson,Thomas Rio Frio	2009	6
16	A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance Thomas Rio Frio,Terri L. McGee,Nicholas M. Wade,Christian Iseli,J. Beckmann,Eliot L. Berson,Carlo Rivolta	2009	40
17	Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa. Thomas Rio Frio,Sylwia Panek,Christian Iseli,Silvio Alessandro Di Gioia,Arun Kumar,Andreas Gal,Carlo Rivolta	2009	3
18	Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay Thomas Rio Frio,Nicholas M. Wade,Adriana Ransijn,Eliot L. Berson,J. Beckmann,Carlo Rivolta	2008	87
19	Two trans-acting eQTLs modulate the penetrance of PRPF31 mutations Thomas Rio Frio,Natacha Civic,Adriana Ransijn,J. Beckmann,Carlo Rivolta	2008	43
20	Variation in retinitis pigmentosa-11 (PRPF31orRP11) gene expression between symptomatic and asymptomatic patients with dominantRP11mutations Carlo Rivolta,Terri L. McGee,Thomas Rio Frio,Roderick V. Jensen,Eliot L. Berson,Thaddeus P. Dryja	2006	85

About Thomas Rio Frio

Thomas Rio Frio is a scholar working on Aging, Cancer Research and Pathology and Forensic Medicine, having authored 20 papers that have together received 1.2k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (6 papers), Genetic factors in colorectal cancer (4 papers), Advanced biosensing and bioanalysis techniques (4 papers), Retinal Development and Disorders (4 papers), RNA regulation and disease (3 papers), CRISPR and Genetic Engineering (3 papers), Congenital Diaphragmatic Hernia Studies (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Cancer Research (369 citations), Molecular Biology (612 citations) and Pathology and Forensic Medicine (155 citations). Thomas Rio Frio has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Carlo Rivolta, Eliot L. Berson, J. Beckmann, Adriana Ransijn, Maud Kamal, Christophe Le Tourneau, Terri L. McGee, Nicholas M. Wade, Virginie Bernard and Marc‐Henri Stern.

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