Patricia Combes

1.2k citations

22 papers · 737 indexed · h-index 15

Impact in

Molecular Biology
- RNA regulation and disease
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
- Genomics and Phylogenetic Studies
- CRISPR and Genetic Engineering
- Connexins and lens biology
Pharmacology top 10%
- Microbial Natural Products and Biosynthesis

Papers in

Physiology 2
- Telomeres, Telomerase, and Senescence 3
- Adenosine and Purinergic Signaling 2
Genetics 3
- Chronic Lymphocytic Leukemia Research 2

Co-authors: Margaret C. M. Smith Odile Boespflug‐Tanguy Rob Till Diana Rodriguez Enrico Bertini Raphael Schiffmann Matthew C. A. Smith Antonio Rodríguez‐García
Journals: Annals of Human Genetics (2 papers)Neurology (2 papers)Oncotarget (2 papers)Journal of Pharmacy and Pharmacology (1 paper)Gene (1 paper)
Partner nations: France United Kingdom United States

In The Last Decade

Patricia Combes

22 papers receiving 727 citations

Peers

Countries citing papers authored by Patricia Combes

Since Specialization

Citations

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

Fields of papers citing papers by Patricia Combes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Evidence of co-infections during Delta and Omicron SARS-CoV-2 variants co-circulation through prospective screening and sequencing Clinical Microbiology and Infection ·Patricia Combes, Maxime Bisseux, Antonin Bal, Pierre Marin, Justine Latour, Christine Archimbaud, Amélie Brebion, Hélène Chabrolles, Christel Regagnon, Jérémy Lafolie, Grégory Destras, Bruno Simon, Jacques Izopet, Laurence Josset, Cécile Henquell, Audrey Mirand	2022	28
2	TERT promoter status and gene copy number gains: effect on TERT expression and association with prognosis in breast cancer Oncotarget ·Mathilde Gay‐Bellile, Lauren Véronèse, Patricia Combes, Éléonore Eymard-Pierre, Fabrice Kwiatkowski, Marie-Mélanie Dauplat, Anne Cayre, Maud Privat, Catherine Abrial, Yves‐Jean Bignon, Marie‐Ange Mouret‐Reynier, Philippe Vago, Frédérique Penault‐Llorca, Andréï Tchirkov	2017	37
3	Telomere status in chronic lymphocytic leukemia with TP53 disruption Oncotarget ·Romain Guièze, Mélanie Pagès, Lauren Véronèse, Patricia Combes, Richard Lemal, Mathilde Gay‐Bellile, Martine Chauvet, Mary Callanan, Fabrice Kwiatkowski, Bruno Pereira, Philippe Vago, Jacques‐Olivier Bay, Olivier Tournilhac, Andréï Tchirkov	2016	15
4	Contribution of MLPA to routine diagnostic testing of recurrent genomic aberrations in chronic lymphocytic leukemia Cancer Genetics ·Lauren Véronèse, Olivier Tournilhac, Patricia Combes, Nolwen Prié, Eléonore Pierre-Eymard, Romain Guièze, Richard Veyrat‐Masson, Jacques‐Olivier Bay, Philippe Vago, Andréï Tchirkov	2013	14
5	Relevance of SOX17 Variants for Hypomyelinating Leukodystrophies and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) Annals of Human Genetics ·Patricia Combes, Vincent Planche, Éléonore Eymard-Pierre, Catherine Sarret, Diana Rodriguez, Odile Boespflug‐Tanguy, Catherine Vaurs‐Barrière	2012	5
6	Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort Journal of the Neurological Sciences ·Catherine Sarret, Mélanie Rigal, Catherine Vaurs‐Barrière, Imen Dorboz, Éléonore Eymard-Pierre, Patricia Combes, G Giraud, Ronald J. A. Wanders, Alexandra Afenjar, Christine Francannet, Odile Boespflug‐Tanguy	2011	8
7	Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant Gene ·Carole Goumy, Stéphan Kemeny, Éléonore Eymard-Pierre, Charles W. Richard, Laëtitia Gouas, Patricia Combes, Mathilde Gay‐Bellile, Denis Gallot, Andréï Tchirkov, Philippe Vago	2011	1
8	Novel neuronal proteolipid protein isoforms encoded by the human myelin proteolipid protein 1 gene Neuroscience ·Catherine Sarret, Patricia Combes, Pierre Micheau, A. Gélot, Odile Boespflug‐Tanguy, Catherine Vaurs‐Barrière	2009	23
9	PLP1splicing abnormalities identified in Pelizaeus-Merzbacher disease and SPG2 fibroblasts are associated with different types of mutations Human Mutation ·Marie‐Noëlle Bonnet‐Dupeyron, Patricia Combes, Paola Santander, Fabrice Cailloux, Odile Boespflug‐Tanguy, Catherine Vaurs‐Barrière	2008	18
10	GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease Neurology ·Marco Henneke, Patricia Combes, Simone Diekmann, Enrico Bertini, Knut Brockmann, Alessandro P. Burlina, Jens Kaiser, Andreas Ohlenbusch, Barbara Plecko, Diana Rodriguez, Odile Boespflug‐Tanguy, Jutta Gärtner	2007	59
11	PLP1 and GPM6B intragenic copy number analysis by MAPH in 262 patients with hypomyelinating leukodystrophies: identification of one partial triplication and two partial deletions of PLP1 Neurogenetics ·Patricia Combes, Marie-Noelle Bonnet-Dupeyron, Fernande Gauthier‐Barichard, Raphael Schiffmann, Enrico Bertini, Diana Rodriguez, John A.L. Armour, Odile Boespflug‐Tanguy, Catherine Vaurs‐Barrière	2006	21
12	Peptidomics and proteomics studies of transformed lymphocytes from patients mutated for the eukaryotic initiation factor 2B☆ Journal of Chromatography B ·Anne Fogli, Claire Malinverni, Lynne Thadikkaran, Patricia Combes, Florent Perret, David Crettaz, Jean‐Daniel Tissot, Odile Boespflug‐Tanguy, Reto Stöcklin, Philippe Bulet	2006	3
13	Novel missense mutation in ALS2 gene results in infantile ascending hereditary spastic paralysis Annals of Neurology ·Éléonore Eymard-Pierre, Koji Yamanaka, Martin Haeussler, Wolfram Kreß, Fernande Gauthier‐Barichard, Patricia Combes, Don W. Cleveland, Odile Boespflug‐Tanguy	2006	46
14	Golli‐MBP Copy Number Analysis by FISH, QMPSF and MAPH in 195 Patients with Hypomyelinating Leukodystrophies Annals of Human Genetics ·Catherine Vaurs‐Barrière, M‐N. Bonnet‐Dupeyron, Patricia Combes, Fernande Gauthier‐Barichard, Xavier T. Reveles, Raphael Schiffmann, Enrico Bertini, Diana Rodriguez, Philippe Vago, John A.L. Armour, Pascale Saugier-Véber, Thierry Frébourg, Robin J. Leach, Odile Boespflug‐Tanguy	2005	14
15	Natural and synthetic tetracycline-inducible promoters for use in the antibiotic-producing bacteria Streptomyces Nucleic Acids Research ·Antonio Rodríguez‐García, Patricia Combes, Rosario Pèrez‐Redondo, Matthew C. A. Smith, Margaret C. M. Smith	2005	91
16	Decreased guanine nucleotide exchange factor activity in eIF2B-mutated patients European Journal of Human Genetics ·Anne Fogli, Raphael Schiffmann, Lynne Hugendubler, Patricia Combes, Enrico Bertini, Diana Rodriguez, Scot R. Kimball, Odile Boespflug‐Tanguy	2004	73
17	The effect of genotype on the natural history of eIF2B-related leukodystrophies Neurology ·Anne Fogli, Raphael Schiffmann, Enrico Bertini, Sylvie Ughetto, Patricia Combes, Éléonore Eymard-Pierre, Christine R. Kaneski, M. Pineda, M. Troncoso, Graziella Uziel, R. Surtees, D. Pugin, M. -P. Chaunu, Diana Rodriguez, Odile Boespflug‐Tanguy	2004	117
18	The Streptomyces Genome Contains Multiple Pseudo- attB Sites for the φC31-Encoded Site-Specific Recombination System Journal of Bacteriology ·Patricia Combes, Rob Till, Sally Bee, Margaret C. M. Smith	2002	113
19	Regulation of p42/p44 mitogen-activated protein kinase by the human adenosine A3 receptor in transfected CHO cells European Journal of Pharmacology ·Graham Stuart, Patricia Combes, Magali Crumiere, Karl‐Norbert Klotz, John M. Dickenson	2001	21
20	Récidives tumorales pures des cancers labiaux: traitement de rattrapage par curiethérapie interstitielle. A propos d'une série de trente et une observations. Tim Nguyen, J Douchez, D Combes, B de Lafonan, N Daly, Patricia Combes	1982	1

About Patricia Combes

Patricia Combes is a scholar working on Physiology, Genetics, Molecular Biology, Neurology and Cell Biology, having authored 22 papers that have together received 737 indexed citations. Recurring topics across this work include RNA regulation and disease (7 papers), RNA Research and Splicing (6 papers), Telomeres, Telomerase, and Senescence (3 papers), RNA modifications and cancer (3 papers), Microbial Natural Products and Biosynthesis (2 papers), Endoplasmic Reticulum Stress and Disease (2 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Adenosine and Purinergic Signaling (2 papers). The work is most often cited by research in Molecular Biology (567 citations), Pharmacology (129 citations), Neurology (50 citations), Cell Biology (91 citations) and Biotechnology (47 citations). Patricia Combes has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Margaret C. M. Smith, Odile Boespflug‐Tanguy, Rob Till, Diana Rodriguez, Enrico Bertini, Raphael Schiffmann, Matthew C. A. Smith, Antonio Rodríguez‐García, Rosario Pèrez‐Redondo and Éléonore Eymard-Pierre. Their work appears in journals such as Annals of Human Genetics, Neurology, Oncotarget, Journal of Pharmacy and Pharmacology and Gene.

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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