Jean‐Marie Rival

618 total citations
24 papers, 370 citations indexed

About

Jean‐Marie Rival is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jean‐Marie Rival has authored 24 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jean‐Marie Rival's work include Prenatal Screening and Diagnostics (6 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Jean‐Marie Rival is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Jean‐Marie Rival collaborates with scholars based in France and Switzerland. Jean‐Marie Rival's co-authors include Cédric Le Caignec, Albert David, Madeleine Joubert, Norbert Winer, Philippe Loget, Sylvie Nguyen The Tich, Nicole M. Le Douarin, Marie‐Claire Vincent, Chloé Quēlin and Véronique David and has published in prestigious journals such as Developmental Biology, Human Reproduction and Fertility and Sterility.

In The Last Decade

Jean‐Marie Rival

24 papers receiving 351 citations

Peers

Jean‐Marie Rival

GENET

PPCH

SURGE

Elizabeth Bhoj United States

P. Wieacker Germany

Barbara Delle Chiaie Belgium

Janice Zunich United States

Didier Theophile France

Rina Schmidt United States

M. J. E. Harrod United States

Emilia K. Bijlsma Netherlands

I. López Pajares Spain

G. Wildhardt Germany

Elizabeth Bhoj United States

Jean‐Marie Rival

356 ×1.9

286 ×1.5

GENET

67 ×0.9

PPCH

84 ×1.2

SURGE

16 ×0.4

Citations per year, relative to Jean‐Marie Rival Jean‐Marie Rival (= 1×) peers Elizabeth Bhoj

Countries citing papers authored by Jean‐Marie Rival

Since Specialization

Citations

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

Fields of papers citing papers by Jean‐Marie Rival

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jean‐Marie Rival

This figure shows the co-authorship network connecting the top 25 collaborators of Jean‐Marie Rival. A scholar is included among the top collaborators of Jean‐Marie Rival 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‐Marie Rival. Jean‐Marie Rival 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

Dreux, Sophie, Agnès Guichet, Jean‐Marie Rival, et al.. (2012). Relationship of non‐visualization of the fetal gallbladder and amniotic fluid digestive enzymes analysis to outcome. Prenatal Diagnosis. 32(5). 423–426. 21 indexed citations

Caignec, Cédric Le, Jean‐Marie Rival, Claudine Le Vaillant, et al.. (2009). Grossesses gémellaires monozygotes hétérocaryotes : diagnostic et prise en charge prénatale. La Presse Médicale. 38(7-8). 1170–1173. 1 indexed citations

Monnot, Sophie, Bernadette Chadefaux-Vekemans, Joëlle Aupetit, et al.. (2009). Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiency. Human Mutation. 30(5). 734–740. 25 indexed citations

Gloan, Laurianne Le, Olivier Pichon, Bertrand Isidor, et al.. (2008). A 8.26 Mb deletion in 6q16 and a 4.95 Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff–Parkinson–White syndrome. European Journal of Medical Genetics. 51(6). 651–657. 16 indexed citations

Isidor, Bertrand, Martine Le Cunff, Pierre Boisseau, et al.. (2008). Complex constitutional subtelomeric 1p36.3 deletion/duplication in a mentally retarded child with neonatal neuroblastoma. European Journal of Medical Genetics. 51(6). 679–684. 17 indexed citations

Quēlin, Chloé, Claude Bendavid, Christèle Dubourg, et al.. (2008). Twelve new patients with 13q deletion syndrome: Genotype–phenotype analyses in progress. European Journal of Medical Genetics. 52(1). 41–46. 69 indexed citations

Caignec, Cédric Le, Capucine Delnatte, Joris Vermeesch, et al.. (2007). Complete sex reversal in a WAGR syndrome patient. American Journal of Medical Genetics Part A. 143A(22). 2692–2695. 19 indexed citations

Caignec, C. Le, Christine Gicquel, Marie-Claire Gübler, et al.. (2004). Sonographic findings in Beckwith–Wiedemann syndrome related to H19 hypermethylation. Prenatal Diagnosis. 24(3). 165–168. 6 indexed citations

Caignec, Cédric Le, P. De Mas, Marie‐Claire Vincent, et al.. (2004). Subtelomeric 6p deletion: Clinical, FISH, and array CGH characterization of two cases. American Journal of Medical Genetics Part A. 132A(2). 175–180. 32 indexed citations

10.

Caignec, Cédric Le, Norbert Winer, Capucine Delnatte, et al.. (2003). Prenatal diagnosis of sacrococcygeal teratoma with constitutional partial monosomy 7q/trisomy 2p. Prenatal Diagnosis. 23(12). 981–984. 26 indexed citations

11.

Caignec, Cédric Le, et al.. (2003). Inherited ring chromosome 8 without loss of subtelomeric sequences. Annales de Génétique. 47(3). 289–296. 32 indexed citations

12.

Caignec, C. Le, et al.. (2003). Prenatal diagnosis of a small supernumerary, XIST‐negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetus. Prenatal Diagnosis. 23(2). 143–145. 8 indexed citations

13.

Winer, Norbert, Cédric Le Caignec, M.P. Quéré, et al.. (2003). Prenatal diagnosis of a cleidocranial dysplasia‐like phenotype associated with a de novo balanced t(2q;6q)(q36;q16) translocation. Ultrasound in Obstetrics and Gynecology. 22(6). 648–651. 5 indexed citations

14.

Caignec, Cédric Le, S. Baron, Ken McElreavey, et al.. (2002). 46,XY gonadal dysgenesis: Evidence for autosomal dominant transmission in a large kindred. American Journal of Medical Genetics Part A. 116A(1). 37–43. 20 indexed citations

15.

Winer, Norbert, Albert David, Philippe Le Conte, et al.. (2001). Amniocentesis and amnioinfusion during pregnancy. European Journal of Obstetrics & Gynecology and Reproductive Biology. 100(1). 108–111. 9 indexed citations

16.

Winer, Norbert, Michael Lefevre, Jean‐Marie Rival, et al.. (1998). Persisting Spongy Myocardium. Fetal Diagnosis and Therapy. 13(4). 227–232. 22 indexed citations

17.

Rival, Jean‐Marie, et al.. (1998). Characterization of two add(4qter) chromosomes by comparative genomic hybridization.. PubMed. 41(2). 83–6. 5 indexed citations

18.

Jean, M., et al.. (1997). Prenatal diagnosis of ring chromosome 14 after intracytoplasmic sperm injection. Fertility and Sterility. 67(1). 164–165. 6 indexed citations

19.

Jean, M., et al.. (1997). P-056. ICSI without polyvinylpyrrolidone: report of a series of 305 consecutive treatment cycles. Human Reproduction. 12(Suppl_2). 146–146. 1 indexed citations

20.

David, Albert, et al.. (1996). Nosology of fetal hypokinesia sequence based on CNS abnormalities: is there an Aase‐Smith syndrome?. Clinical Genetics. 50(4). 251–254. 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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