E. Vámos

788 total citations
23 papers, 420 citations indexed

About

E. Vámos is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, E. Vámos has authored 23 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 8 papers in Genetics and 6 papers in Surgery. Recurrent topics in E. Vámos's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Congenital Anomalies and Fetal Surgery (3 papers). E. Vámos is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Congenital Anomalies and Fetal Surgery (3 papers). E. Vámos collaborates with scholars based in Belgium, France and Hong Kong. E. Vámos's co-authors include Winnie Courtens, Nicole Van Regemorter, J Flament-Durand, Marc Abramowicz, Willy Lissens, F Rodesch, Jasmine Parma, L Duprez, E. Dupont and Marc Andrien and has published in prestigious journals such as Journal of Clinical Investigation, Neuroscience and The Journal of Pediatrics.

In The Last Decade

E. Vámos

23 papers receiving 399 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Vámos Belgium 11 205 156 111 78 65 23 420
J. W. E. Oorthuys Netherlands 12 345 1.7× 211 1.4× 87 0.8× 66 0.8× 51 0.8× 25 558
Osamu Shinohara Japan 12 107 0.5× 137 0.9× 140 1.3× 44 0.6× 41 0.6× 30 477
Alicia S. Martínez Argentina 10 256 1.2× 238 1.5× 75 0.7× 40 0.5× 43 0.7× 16 582
C Y Hayashida Brazil 12 295 1.4× 309 2.0× 58 0.5× 180 2.3× 34 0.5× 18 873
Esther Vamos Belgium 15 179 0.9× 286 1.8× 85 0.8× 28 0.4× 8 0.1× 21 533
Wee Teik Keng Malaysia 11 183 0.9× 183 1.2× 45 0.4× 100 1.3× 15 0.2× 20 420
Eri Imagawa Japan 13 170 0.8× 250 1.6× 29 0.3× 41 0.5× 33 0.5× 30 418
Philippe Parent France 14 208 1.0× 130 0.8× 118 1.1× 48 0.6× 10 0.2× 35 518
Elisabeth Steichen Austria 9 197 1.0× 255 1.6× 41 0.4× 100 1.3× 19 0.3× 13 447
Naoya Morisada Japan 15 205 1.0× 367 2.4× 59 0.5× 45 0.6× 17 0.3× 46 585

Countries citing papers authored by E. Vámos

Since Specialization
Citations

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

Fields of papers citing papers by E. Vámos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Vámos

This figure shows the co-authorship network connecting the top 25 collaborators of E. Vámos. A scholar is included among the top collaborators of E. Vámos 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 E. Vámos. E. Vámos 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.
Tudor, Elizabeth L., Clare Galtrey, Michael S. Perkinton, et al.. (2010). Amyotrophic lateral sclerosis mutant vesicle-associated membrane protein-associated protein-B transgenic mice develop TAR-DNA-binding protein-43 pathology. Neuroscience. 167(3). 774–785. 63 indexed citations
2.
Kumps, Alain, et al.. (2004). Assessment of an electron‐impact GC‐MS method for organic acids and glycine conjugates in amniotic fluid. Journal of Inherited Metabolic Disease. 27(5). 567–579. 8 indexed citations
3.
Vassart, Gilbert, Marc Abramowicz, Pascale Cochaux, et al.. (2002). [Medical genetics service].. PubMed. 23 Suppl 2. 63–7. 2 indexed citations
4.
Courtens, Winnie, Wiebren Tjalma, Ludwine Messiaen, et al.. (1998). Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly. American Journal of Medical Genetics. 77(3). 188–197. 24 indexed citations
5.
Courtens, Winnie, E. Vámos, Catherine Christophe, & Albert Schinzel. (1997). Acrocallosal syndrome in Algerian boy born to consanguineous parents: Review of the literature and further delineation of the syndrome. American Journal of Medical Genetics. 69(1). 17–22. 27 indexed citations
6.
Courtens, Winnie, et al.. (1996). CHARGE association in a neonate exposed in utero to carbon monoxide.. PubMed. 30(1). 407–12. 2 indexed citations
7.
Neyns, Bart, Erik Teugels, Willy Lissens, et al.. (1995). Frequent deletion of chromosome 19 and a rare rearrangement of 19p13.3 involving the insulin receptor gene in human ovarian cancer.. PubMed. 11(2). 351–8. 20 indexed citations
8.
Abramowicz, Marc, Marc Andrien, E. Dupont, et al.. (1994). Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus.. Journal of Clinical Investigation. 94(1). 418–421. 67 indexed citations
9.
Courtens, Winnie, Michael B. Petersen, J.C. Noël, et al.. (1994). Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies. American Journal of Medical Genetics. 51(3). 260–265. 32 indexed citations
10.
Heimann, Pierre, E. Vámos, Alina Ferster, & Eric Sariban. (1994). Granulocytic sarcoma showing chromosomal changes other than the t(8;21). Cancer Genetics and Cytogenetics. 74(1). 59–61. 10 indexed citations
11.
Donner, Catherine, et al.. (1992). [Collection of fetal cord blood for karyotyping].. PubMed. 21(2). 241–5. 1 indexed citations
12.
Pierquin, Geneviève, Nicole Van Regemorter, Catherine Fourneau, et al.. (1991). Two unrelated children with partial trisomy 1q and monosomy 6p, presenting with the phenotype of the Larsen syndrome. Human Genetics. 87(5). 587–591. 29 indexed citations
13.
Meirleir, Linda J. De, Willy Lissens, E. Vámos, & I. Liebærs. (1991). Pyruvate dehydrogenase deficiency due to a mutation of the E1 α subunit. Journal of Inherited Metabolic Disease. 14(3). 301–304. 9 indexed citations
14.
Regemorter, Nicole Van, E. Vámos, Sabine Lévi, et al.. (1986). Pathological Pregnancies: Results of amniotic fluid studies and fetal outcome. Acta Obstetricia Et Gynecologica Scandinavica. 65(1). 27–32. 5 indexed citations
15.
Vámos, E., et al.. (1985). Prenatal diagnosis and fetal pathology of partial trisomy 20p–monosomy 4p resulting from paternal translocation. Prenatal Diagnosis. 5(3). 209–214. 9 indexed citations
16.
Bosson, D., et al.. (1985). 126 GENERALIZED MINERALOCORTICOID UNRESPONSIVENESS FAMILIAL RECESSIVE PSEUDOHYPOALDOSTERONISM. Pediatric Research. 19(6). 624–624. 1 indexed citations
17.
Regemorter, Nicole Van, et al.. (1984). Congenital malformations in 10,000 consecutive births in a university hospital: Need for genetic counseling and prenatal diagnosis. The Journal of Pediatrics. 104(3). 386–390. 41 indexed citations
18.
Regemorter, Nicole Van, et al.. (1983). Alphafetoprotein (AFP), concanavalin A non-reactive AFP and specific acetylcholinesterase in amniotic fluid from pathological pregnancies. Predictive values for open spina bifida. European Journal of Obstetrics & Gynecology and Reproductive Biology. 16(1). 9–18. 5 indexed citations
19.
Vámos, E., et al.. (1983). Partial trisomy 3p in two siblings: Clinical and pathological findings. European Journal of Pediatrics. 141(1). 53–56. 17 indexed citations
20.
Libert, Jacques, et al.. (1981). Unusual early manifestation of multiple sulfatase deficiency.. PubMed. 24(1). 43–8. 7 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 J. W. E. Oorthuys Breakdown of academic impact, for papers by Osamu Shinohara Breakdown of academic impact, for papers by Alicia S. Martínez Breakdown of academic impact, for papers by C Y Hayashida Breakdown of academic impact, for papers by Esther Vamos Breakdown of academic impact, for papers by Wee Teik Keng Breakdown of academic impact, for papers by Eri Imagawa Breakdown of academic impact, for papers by Philippe Parent Breakdown of academic impact, for papers by Elisabeth Steichen Breakdown of academic impact, for papers by Naoya Morisada
Rankless by CCL
2026