Jacques Rochette

2.6k total citations
59 papers, 1.4k citations indexed

About

Jacques Rochette is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Jacques Rochette has authored 59 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 22 papers in Molecular Biology and 21 papers in Hematology. Recurrent topics in Jacques Rochette's work include Hemoglobinopathies and Related Disorders (24 papers), Iron Metabolism and Disorders (16 papers) and Prenatal Screening and Diagnostics (8 papers). Jacques Rochette is often cited by papers focused on Hemoglobinopathies and Related Disorders (24 papers), Iron Metabolism and Disorders (16 papers) and Prenatal Screening and Diagnostics (8 papers). Jacques Rochette collaborates with scholars based in France, United Kingdom and India. Jacques Rochette's co-authors include Jamie E. Craig, Swee Lay Thein, Catherine Dodé, Janette Lamb, Florence Démenais, G.M. Lathrop, SL Thein, Pierre Szepetowski, Chris Fisher and D. J. Weatherall and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Blood.

In The Last Decade

Jacques Rochette

59 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacques Rochette France 20 687 583 474 256 226 59 1.4k
Lars Palmqvist Sweden 23 243 0.4× 666 1.1× 722 1.5× 150 0.6× 117 0.5× 67 1.6k
SJ Lauer United States 16 153 0.2× 321 0.6× 586 1.2× 283 1.1× 168 0.7× 19 1.6k
S. S. Zail South Africa 17 119 0.2× 151 0.3× 377 0.8× 196 0.8× 88 0.4× 43 1.0k
P. A. Bolhuis Netherlands 24 159 0.2× 548 0.9× 1.2k 2.5× 16 0.1× 102 0.5× 60 2.1k
Yamin Shen United States 16 205 0.3× 201 0.3× 314 0.7× 39 0.2× 82 0.4× 20 1.2k
Lewis Waber United States 14 95 0.1× 84 0.1× 552 1.2× 174 0.7× 135 0.6× 20 1.7k
P Guibaud France 19 100 0.1× 74 0.1× 548 1.2× 131 0.5× 138 0.6× 60 1.1k
M. Ueda Japan 18 126 0.2× 495 0.8× 549 1.2× 62 0.2× 136 0.6× 47 1.4k
Jacqueline Hagège France 18 95 0.1× 188 0.3× 491 1.0× 41 0.2× 62 0.3× 32 1.2k

Countries citing papers authored by Jacques Rochette

Since Specialization
Citations

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

Fields of papers citing papers by Jacques Rochette

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacques Rochette

This figure shows the co-authorship network connecting the top 25 collaborators of Jacques Rochette. A scholar is included among the top collaborators of Jacques Rochette 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 Jacques Rochette. Jacques Rochette is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Meuth, Valérie Metzinger‐Le, et al.. (2024). A proteomic study of the downregulation of TRIM37 on chondrocytes: Implications for the MULIBREY syndrome. Bone. 187. 117205–117205. 2 indexed citations
2.
Callebaut, Isabelle, Serge Pissard, Caroline Kannengiesser, et al.. (2014). Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients. Human Molecular Genetics. 23(17). 4479–4490. 35 indexed citations
3.
Anbazhagan, Kolandaswamy, et al.. (2013). Human pre‐B cell receptor signal transduction: evidence for distinct roles of PI3kinase and MAP‐kinase signalling pathways. Immunity Inflammation and Disease. 1(1). 26–36. 9 indexed citations
4.
Coppo, Paul, et al.. (2013). Clinical significance of autoantibodies to the pericentromeric heterochromatin protein 1a protein. European Journal of Internal Medicine. 24(8). 868–871. 3 indexed citations
5.
Jouanolle, Anne‐Marie, V. Gérolami, Cécile Ged, et al.. (2012). Molecular diagnosis of HFE mutations in routine laboratories. Results of a survey from reference laboratories in France. Annales de biologie clinique. 70(3). 305–313. 3 indexed citations
6.
Rochette, Jacques, Gérald Le Gac, Kaı̈ss Lassoued, Claude Férec, & Kathryn Robson. (2010). Factors influencing disease phenotype and penetrance in HFE haemochromatosis. Human Genetics. 128(3). 233–248. 29 indexed citations
7.
Roll, Patrice, Damien Sanlaville, Audrey Labalme, et al.. (2010). Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11. PLoS ONE. 5(10). e13750–e13750. 10 indexed citations
8.
Pointon, Jennifer J., et al.. (2009). A novel HFE mutation (c.del478) results in nonsense-mediated decay of the mutant transcript in a hemochromatosis patient. Blood Cells Molecules and Diseases. 43(2). 194–198. 7 indexed citations
9.
Rochette, Jacques, Patrice Roll, & Pierre Szepetowski. (2008). Genetics of infantile seizures with paroxysmal dyskinesia: the infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes. Journal of Medical Genetics. 45(12). 773–779. 20 indexed citations
10.
Maurice, Pascal, Ludovic Waeckel, Pascal Sonnet, et al.. (2005). The platelet receptor for type III collagen (TIIICBP) is present in platelet membrane lipid microdomains (rafts). Histochemistry and Cell Biology. 125(4). 407–417. 16 indexed citations
11.
Gizard, Florence, Carole Amant, Olivier Barbier, et al.. (2005). PPARα inhibits vascular smooth muscle cell proliferation underlying intimal hyperplasia by inducing the tumor suppressor p16INK4a. Journal of Clinical Investigation. 115(11). 3228–3238. 134 indexed citations
12.
Capron, Dominique, Sabrina Crépin, S Arlot, et al.. (2003). A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis. Journal of Internal Medicine. 253(2). 217–224. 19 indexed citations
13.
Caraballo, Roberto, Sylvana Pavek, Arnaud Lemainque, et al.. (2001). Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome. The American Journal of Human Genetics. 68(3). 788–794. 92 indexed citations
14.
Gamé, Laurence, James Close, Steve Best, et al.. (2000). An Integrated Map of Human 6q22.3–q24 Including a 3-Mb High-Resolution BAC/PAC Contig Encompassing a QTL for Fetal Hemoglobin. Genomics. 64(3). 264–276. 10 indexed citations
15.
Rees, David C., Nicola H. Chapman, Matthew T. Webster, et al.. (1999). Born to clot: the European burden. British Journal of Haematology. 105(2). 564–566. 52 indexed citations
16.
Craig, Jamie E., Jacques Rochette, Chris Fisher, et al.. (1996). Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach. Nature Genetics. 12(1). 58–64. 133 indexed citations
17.
Ho, P. Joy, Jacques Rochette, David C. Rees, et al.. (1996). Hb Sun Prairie: Diagnostic Pitfalls in Thalassemic Hemoglobinopathies. Hemoglobin. 20(2). 103–112. 17 indexed citations
18.
Dodé, Catherine, et al.. (1993). Rapid analysis of ‐α3.7 thalassaemia and αααanti 3.7 triplication by enzymatic amplification analysis. British Journal of Haematology. 83(1). 105–111. 126 indexed citations
19.
Vinet, Marie Claude, et al.. (1989). Autosomal dominant polycystic kidney disease and ??4.2 thalassemia in a Caucasian family. Human Genetics. 83(1). 55–57. 3 indexed citations
20.
Dodé, Catherine, et al.. (1987). Haemoglobin Disorders among Southeast-Asian Refugees in France. Acta Haematologica. 78(2-3). 135–136. 3 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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