Martine Sinico

928 total citations
12 papers, 279 citations indexed

About

Martine Sinico is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Martine Sinico has authored 12 papers receiving a total of 279 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Martine Sinico's work include Fetal and Pediatric Neurological Disorders (2 papers), Cleft Lip and Palate Research (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Martine Sinico is often cited by papers focused on Fetal and Pediatric Neurological Disorders (2 papers), Cleft Lip and Palate Research (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Martine Sinico collaborates with scholars based in France, United States and Netherlands. Martine Sinico's co-authors include Férechté Encha‐Razavi, Claude Danan, Anne‐Lise Delezoide, Marc Lombès, Pascal Boileau, J Valayer, C Kalifa, Frédéric Gauthier, Sophie Prévôt and Say Viengchareun and has published in prestigious journals such as Brain Research, Endocrinology and The Journal of Pediatrics.

In The Last Decade

Martine Sinico

12 papers receiving 273 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martine Sinico France 9 139 64 62 58 52 12 279
Yoshihiko Ueta Japan 11 137 1.0× 41 0.6× 43 0.7× 32 0.6× 220 4.2× 26 389
Ivana Pela Italy 10 279 2.0× 47 0.7× 31 0.5× 49 0.8× 35 0.7× 19 473
Charles Kresge United States 12 225 1.6× 61 1.0× 121 2.0× 40 0.7× 10 0.2× 16 500
Stefano Lavaroni Italy 9 141 1.0× 22 0.3× 36 0.6× 11 0.2× 180 3.5× 16 379
Zesergio Melo Mexico 12 255 1.8× 92 1.4× 37 0.6× 11 0.2× 27 0.5× 21 403
H Küntziger France 9 137 1.0× 57 0.9× 32 0.5× 24 0.4× 12 0.2× 20 338
Takefumi Narikiyo Japan 10 380 2.7× 195 3.0× 37 0.6× 27 0.5× 90 1.7× 14 477
Roger Belusa Sweden 9 225 1.6× 116 1.8× 36 0.6× 38 0.7× 47 0.9× 12 323
Amarilis Sanchez‐Valle United States 12 289 2.1× 40 0.6× 96 1.5× 82 1.4× 32 0.6× 26 642

Countries citing papers authored by Martine Sinico

Since Specialization
Citations

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

Fields of papers citing papers by Martine Sinico

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martine Sinico

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

All Works

12 of 12 papers shown
1.
Spaggiari, Emmanuel, Azzedine Aboura, Martine Sinico, et al.. (2012). Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre–Chotzen syndrome. European Journal of Medical Genetics. 55(8-9). 498–501. 4 indexed citations
2.
Durrmeyer, Xavier, Gilles Kayem, Martine Sinico, et al.. (2011). Perinatal Risk Factors for Bronchopulmonary Dysplasia in Extremely Low Gestational Age Infants: A Pregnancy Disorder–Based Approach. The Journal of Pediatrics. 160(4). 578–583.e2. 33 indexed citations
3.
Boer, Karin, Férechté Encha‐Razavi, Martine Sinico, & Eleonora Aronica. (2010). Differential distribution of group I metabotropic glutamate receptors in developing human cortex. Brain Research. 1324. 24–33. 25 indexed citations
4.
Sinico, Martine, Guillaume Bassez, Claudine Touboul, et al.. (2010). Excess of Neuromuscular Spindles in a Fetus with Costello Syndrome: A Clinicopathological Report. Pediatric and Developmental Pathology. 14(3). 218–223. 5 indexed citations
5.
Martinerie, Laëtitia, Say Viengchareun, Anne‐Lise Delezoide, et al.. (2009). Low Renal Mineralocorticoid Receptor Expression at Birth Contributes to Partial Aldosterone Resistance in Neonates. Endocrinology. 150(9). 4414–4424. 66 indexed citations
6.
Encha‐Razavi, Férechté, Marie Gonzalès, Annie Laquerrière, et al.. (2008). A practical approach to the examination of the malformed fetal brain: impact on genetic counselling. Pathology. 40(2). 180–187. 3 indexed citations
7.
Jonard, Laurence, Delphine Feldmann, Martine Sinico, et al.. (2007). A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45E. European Journal of Medical Genetics. 51(1). 35–43. 49 indexed citations
8.
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
9.
Hertz‐Pannier, Lucie, M Déchaux, Martine Sinico, et al.. (2005). Congenital disorders of glycosylation type I: a rare but new cause of hyperechoic kidneys in infants and children due to early microcystic changes. Pediatric Radiology. 36(2). 108–114. 13 indexed citations
10.
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
11.
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
12.
Gauthier, Frédéric, et al.. (1986). Hepatoblastoma and hepatocarcinoma in children: Analysis of a series of 29 cases. Journal of Pediatric Surgery. 21(5). 424–429. 37 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Yoshihiko Ueta Breakdown of academic impact, for papers by Ivana Pela Breakdown of academic impact, for papers by Charles Kresge Breakdown of academic impact, for papers by Stefano Lavaroni Breakdown of academic impact, for papers by Zesergio Melo Breakdown of academic impact, for papers by H Küntziger Breakdown of academic impact, for papers by Takefumi Narikiyo Breakdown of academic impact, for papers by Roger Belusa Breakdown of academic impact, for papers by Amarilis Sanchez‐Valle
Rankless by CCL
2026