Marion Gérard‐Blanluet

752 total citations
24 papers, 399 citations indexed

About

Marion Gérard‐Blanluet is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marion Gérard‐Blanluet has authored 24 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marion Gérard‐Blanluet's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and Kidney Cyst Diseases (4 papers). Marion Gérard‐Blanluet is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic and Kidney Cyst Diseases (4 papers). Marion Gérard‐Blanluet collaborates with scholars based in France, United States and Belgium. Marion Gérard‐Blanluet's co-authors include Alain Verloès, Alexis Arzimanoglou, Francis Renault, Aga Lewelt, Matthew Sweney, Kathryn J. Swoboda, Kenneth Silver, Sandra P. Reyna, Anne‐Lise Delezoide and Férechté Encha‐Razavi and has published in prestigious journals such as PEDIATRICS, Annals of the Rheumatic Diseases and American Journal of Medical Genetics.

In The Last Decade

Marion Gérard‐Blanluet

24 papers receiving 388 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marion Gérard‐Blanluet France 13 200 158 72 61 33 24 399
Magdalena Badura‐Stronka Poland 12 183 0.9× 141 0.9× 41 0.6× 77 1.3× 22 0.7× 32 357
Agata Polizzi Italy 15 183 0.9× 190 1.2× 63 0.9× 117 1.9× 56 1.7× 36 590
G. Fekete Hungary 12 281 1.4× 173 1.1× 75 1.0× 39 0.6× 47 1.4× 32 490
Marie McDonald United States 8 308 1.5× 207 1.3× 53 0.7× 42 0.7× 103 3.1× 13 505
Donal Brosnahan Ireland 13 105 0.5× 124 0.8× 63 0.9× 30 0.5× 29 0.9× 25 421
Virginia Fano Argentina 15 206 1.0× 395 2.5× 123 1.7× 83 1.4× 62 1.9× 55 634
Mariet W. Elting Netherlands 13 95 0.5× 171 1.1× 77 1.1× 25 0.4× 36 1.1× 23 772
Sevcan Tuğ Bozdoğan Türkiye 10 86 0.4× 77 0.5× 33 0.5× 40 0.7× 16 0.5× 35 296
Laurence Perrin France 10 141 0.7× 149 0.9× 29 0.4× 67 1.1× 33 1.0× 28 366
Nina B. Gold United States 10 186 0.9× 220 1.4× 76 1.1× 34 0.6× 12 0.4× 37 457

Countries citing papers authored by Marion Gérard‐Blanluet

Since Specialization
Citations

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

Fields of papers citing papers by Marion Gérard‐Blanluet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marion Gérard‐Blanluet. 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 Marion Gérard‐Blanluet. The network helps show where Marion Gérard‐Blanluet may publish in the future.

Co-authorship network of co-authors of Marion Gérard‐Blanluet

This figure shows the co-authorship network connecting the top 25 collaborators of Marion Gérard‐Blanluet. A scholar is included among the top collaborators of Marion Gérard‐Blanluet 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 Marion Gérard‐Blanluet. Marion Gérard‐Blanluet 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.
Chaste, Pauline, Catalina Betancur, Marion Gérard‐Blanluet, et al.. (2012). High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters. Molecular Autism. 3(1). 5–5. 12 indexed citations
2.
Colin, Estelle, Renaud Touraine, J.‐M. Levaillant, et al.. (2011). Binder phenotype in mothers affected with autoimmune disorders. The Journal of Maternal-Fetal & Neonatal Medicine. 25(8). 1413–1418. 11 indexed citations
3.
Gérard‐Blanluet, Marion, Véronique Lambert, Suonavy Khung‐Savatovsky, et al.. (2011). Aphallia, Lung Agenesis and Multiple Defects of Blastogenesis. Fetal and Pediatric Pathology. 30(1). 22–26. 9 indexed citations
4.
Gérard‐Blanluet, Marion, et al.. (2010). Unilateral agenesis of the abdominal wall musculature: An early muscle deficiency. American Journal of Medical Genetics Part A. 152A(11). 2870–2874. 5 indexed citations
5.
Levaillant, J. M., Martine Bucourt, Lydie Bürglen, et al.. (2009). Binder phenotype: clinical and etiological heterogeneity of the so‐called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature. Prenatal Diagnosis. 29(2). 140–150. 24 indexed citations
6.
Gérard‐Blanluet, Marion, Stéphane Serero, Clarisse Baumann, et al.. (2008). Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome. American Journal of Medical Genetics Part A. 146A(14). 1871–1874. 9 indexed citations
7.
Messiaen, Claude, Loïc Le Mignot, Ana Rath, et al.. (2008). CEMARA: a Web dynamic application within a N-tier architecture for rare diseases.. PubMed. 136. 51–6. 18 indexed citations
8.
Mignot, Loïc Le, Ana Rath, Jean‐Baptiste Richard, et al.. (2008). Cemara : épidémiologie des maladies rares et système d’information. Revue d Épidémiologie et de Santé Publique. 56(1). 48–49. 1 indexed citations
9.
Keren, Boris, Oscar Suzuki, Marion Gérard‐Blanluet, et al.. (2007). CNS malformations in Knobloch syndrome with splice mutation in COL18A1 gene. American Journal of Medical Genetics Part A. 143A(13). 1514–1518. 31 indexed citations
10.
Levaillant, J. M., et al.. (2007). Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic images. Prenatal Diagnosis. 27(3). 222–227. 17 indexed citations
11.
Pipiras, Eva, Cyril Touboul, Férechté Encha‐Razavi, et al.. (2007). De novo Subtelomeric Deletion Additional to an Inherited Apparently Balanced Reciprocal Translocation. Fetal Diagnosis and Therapy. 22(4). 306–312. 3 indexed citations
12.
Gérard‐Blanluet, Marion, Volney Sheen, Jason Neal, et al.. (2006). Bilateral periventricular heterotopias in an X‐linked dominant transmission in a family with two affected males. American Journal of Medical Genetics Part A. 140A(10). 1041–1046. 20 indexed citations
13.
Tchernitchko, Dimitri, Marion Gérard‐Blanluet, Marie Legendre, et al.. (2006). Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever. Annals of the Rheumatic Diseases. 65(9). 1154–1157. 19 indexed citations
14.
Deffert, Christine, Florence Niel, Fanny Mochel, et al.. (2006). Recurrent insertional polydactyly and situs inversus in a Bardet‐Biedl syndrome family. American Journal of Medical Genetics Part A. 143A(2). 208–213. 6 indexed citations
15.
Brémond‐Gignac, Dominique, Marion Gérard‐Blanluet, Henri Copin, et al.. (2005). Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins. American Journal of Medical Genetics Part A. 134A(4). 422–425. 13 indexed citations
16.
Levaillant, J. M., et al.. (2005). Prenatal forehead edema in 4p- deletion: the ‘Greek warrior helmet’ profile revisited. Prenatal Diagnosis. 25(12). 1150–1155. 15 indexed citations
17.
Gérard‐Blanluet, Marion, Serge Romana, Marc Le Lorc’h, et al.. (2004). Classical West “syndrome” phenotype with a subtelomeric 4p trisomy. American Journal of Medical Genetics Part A. 130A(3). 299–302. 10 indexed citations
18.
Sinico, Martine, Claudine Touboul, Bassam Haddad, et al.. (2004). Giant omphalocele and “prune belly” sequence as components of the Beckwith–Wiedemann syndrome. American Journal of Medical Genetics Part A. 129A(2). 198–200. 12 indexed citations
19.
Gérard‐Blanluet, Marion, Claude Danan, Martine Sinico, et al.. (2002). Mosaic trisomy 9 and lobar holoprosencephaly. American Journal of Medical Genetics. 111(3). 295–300. 12 indexed citations
20.
Gérard‐Blanluet, Marion, et al.. (2001). Mosaic trisomy 15 and hemihypertrophy. Annales de Génétique. 44(3). 143–148. 5 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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