Jean‐Baptiste Rivière

6.4k total citations
36 papers, 1.2k citations indexed

About

Jean‐Baptiste Rivière is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Jean‐Baptiste Rivière has authored 36 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 20 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Jean‐Baptiste Rivière's work include Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and RNA regulation and disease (6 papers). Jean‐Baptiste Rivière is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and RNA regulation and disease (6 papers). Jean‐Baptiste Rivière collaborates with scholars based in Canada, France and United States. Jean‐Baptiste Rivière's co-authors include Judith St‐Onge, Guy A. Rouleau, Brian J. O’Roak, Susan L. Christian, William B. Dobyns, Julien Thévenon, Laurence Faivre, Christel Thauvin‐Robinet, Yannis Duffourd and Jeffrey G. Ojemann and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Jean‐Baptiste Rivière

35 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jean‐Baptiste Rivière Canada	18	591	575	145	141	136	36	1.2k
Anneke T. Vulto-van Silfhout Netherlands	4	656 1.1×	959 1.7×	129 0.9×	129 0.9×	73 0.5×	4	1.3k
Gökhan Uyanık Germany	17	731 1.2×	424 0.7×	240 1.7×	252 1.8×	167 1.2×	42	1.2k
Chihiro Ohba Japan	16	563 1.0×	341 0.6×	252 1.7×	102 0.7×	53 0.4×	26	922
Muhammad Mahajnah Israel	16	391 0.7×	281 0.5×	117 0.8×	126 0.9×	59 0.4×	55	831
Lysanne Patry Canada	14	671 1.1×	480 0.8×	138 1.0×	91 0.6×	66 0.5×	16	1.0k
Alexandre Dionne‐Laporte Canada	15	436 0.7×	391 0.7×	115 0.8×	68 0.5×	69 0.5×	32	905
Alice Goldenberg France	20	678 1.1×	565 1.0×	124 0.9×	75 0.5×	91 0.7×	49	1.1k
Alissa M. D’Gama United States	12	753 1.3×	565 1.0×	104 0.7×	48 0.3×	109 0.8×	30	1.2k
Alexandra Afenjar France	16	521 0.9×	621 1.1×	106 0.7×	96 0.7×	113 0.8×	42	1.0k
Tyler Mark Pierson United States	21	737 1.2×	454 0.8×	400 2.8×	138 1.0×	48 0.4×	42	1.3k

Countries citing papers authored by Jean‐Baptiste Rivière

Since Specialization

Citations

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

Fields of papers citing papers by Jean‐Baptiste Rivière

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jean‐Baptiste Rivière. 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 Jean‐Baptiste Rivière. The network helps show where Jean‐Baptiste Rivière may publish in the future.

Co-authorship network of co-authors of Jean‐Baptiste Rivière

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

All Works

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20 of 20 papers shown

Anastasio, Natascia, et al.. (2024). Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis. European Journal of Human Genetics. 32(9). 1184–1189.

Rivière, Jean‐Baptiste, et al.. (2023). Routine Clinically Detected Increased ROS1 Transcripts Are Related With ROS1 Expression by Immunohistochemistry and Associated With EGFR Mutations in Lung Adenocarcinoma. JTO Clinical and Research Reports. 4(7). 100530–100530. 1 indexed citations

Ravel, Jean‐Marie, Natacha Dreumont, Desirée E.C. Smith, et al.. (2021). A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever. Human Mutation. 42(12). 1576–1583. 6 indexed citations

Ezer, Nicole, Hangjun Wang, Pierre Fiset, et al.. (2021). Integrating NGS-derived mutational profiling in the diagnosis of multiple lung adenocarcinomas. Cancer Treatment and Research Communications. 29. 100484–100484. 10 indexed citations

Watkins, David, et al.. (2019). Genome and RNA sequencing in patients with methylmalonic aciduria of unknown cause. Genetics in Medicine. 22(2). 432–436. 3 indexed citations

Accogli, Andrea, Laura Russell, Guillaume Sébire, et al.. (2019). Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia. Neurogenetics. 20(2). 103–108. 13 indexed citations

McCuaïg, Catherine, Jérôme Coulombe, Afshin Hatami, et al.. (2019). Patterned cutaneous hypopigmentation phenotype characterization: A retrospective study in 106 children. Pediatric Dermatology. 36(6). 869–875. 3 indexed citations

Mau‐Them, Frédéric Tran, Julien Thévenon, Thomas Guignard, et al.. (2018). LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters. European Journal of Medical Genetics. 62(3). 161–166. 19 indexed citations

Yauy, Kévin, Frédéric Tran Mau‐Them, Marjolaine Willems, et al.. (2017). B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation. Genetics in Medicine. 20(2). 269–274. 21 indexed citations

10.

Amos, J., Linda Huang, Julien Thévenon, et al.. (2016). Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping. Clinical Genetics. 91(1). 92–99. 16 indexed citations

11.

Li, Chunmei, Victor L. Jensen, Kwangjin Park, et al.. (2016). MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone. PLoS Biology. 14(3). e1002416–e1002416. 95 indexed citations

12.

Jansen, Laura A., Ghayda Mirzaa, Gisele E. Ishak, et al.. (2015). PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia. Brain. 138(6). 1613–1628. 237 indexed citations

13.

Chevrier, Véronique, Ange‐Line Bruel, Teunis J. P. van Dam, et al.. (2015). OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome. Human Molecular Genetics. 25(3). 497–513. 35 indexed citations

14.

Elalaoui, Siham Chafai, Laurence Duplomb, Jean‐Baptiste Rivière, et al.. (2014). Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma. European Journal of Human Genetics. 23(7). 957–962. 37 indexed citations

15.

Rivière, Jean‐Baptiste, Masoud Shekarabi, Janet Laganière, et al.. (2011). Transit Defect of Potassium-Chloride Co-transporter 3 Is a Major Pathogenic Mechanism in Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum. Journal of Biological Chemistry. 286(32). 28456–28465. 20 indexed citations

16.

Xiong, Lan, Аnastasia Levchenko, Jacques Montplaisir, et al.. (2007). Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians. Sleep Medicine. 9(3). 273–282. 4 indexed citations

17.

El‐Maarri, Osman, Muhieddine Seoud, Jean‐Baptiste Rivière, et al.. (2005). Patients with familial biparental hydatidiform moles have normal methylation at imprinted genes. European Journal of Human Genetics. 13(4). 486–490. 17 indexed citations

18.

Rivière, Jean‐Baptiste, Dominique J. Verlaan, Masoud Shekarabi, et al.. (2004). A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family. Annals of Neurology. 56(4). 572–575. 35 indexed citations

19.

Xiong, Lan, Guy A. Rouleau, Lynn E. DeLisi, et al.. (2004). CAA insertion polymorphism in the 3′UTR of Nogo gene on 2p14 is not associated with schizophrenia. Molecular Brain Research. 133(1). 153–156. 10 indexed citations

20.

Joober, Ridha, Jean‐Baptiste Rivière, Yves Dion, et al.. (2003). Association between 7q31 markers and tourette syndrome. American Journal of Medical Genetics Part A. 127A(1). 17–20. 24 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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