Eric Smeets

2.8k total citations
62 papers, 1.2k citations indexed

About

Eric Smeets is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Eric Smeets has authored 62 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 20 papers in Molecular Biology and 20 papers in Cognitive Neuroscience. Recurrent topics in Eric Smeets's work include Genetics and Neurodevelopmental Disorders (35 papers), Autism Spectrum Disorder Research (20 papers) and Genomic variations and chromosomal abnormalities (17 papers). Eric Smeets is often cited by papers focused on Genetics and Neurodevelopmental Disorders (35 papers), Autism Spectrum Disorder Research (20 papers) and Genomic variations and chromosomal abnormalities (17 papers). Eric Smeets collaborates with scholars based in Netherlands, Belgium and United States. Eric Smeets's co-authors include Leopold Curfs, Herman Van den Berghe, J. P. Fryns, Karine Pelc, Bernard Dan, Ute Moog, J. Herbergs, Connie Schrander‐Stumpel, C. T. R. M. Schrander‐Stumpel and Susan L. Coort and has published in prestigious journals such as The Lancet, The American Journal of Human Genetics and Epilepsia.

In The Last Decade

Eric Smeets

62 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric Smeets Netherlands 22 902 517 411 261 89 62 1.2k
Anne Moncla France 24 1.3k 1.5× 343 0.7× 1.1k 2.6× 52 0.2× 185 2.1× 38 1.9k
Alison D. Archibald Australia 21 545 0.6× 317 0.6× 194 0.5× 103 0.4× 245 2.8× 55 978
Genila Bibat United States 20 495 0.5× 351 0.7× 552 1.3× 111 0.4× 28 0.3× 35 925
Laia Rodríguez‐Revenga Spain 23 1.4k 1.5× 455 0.9× 873 2.1× 78 0.3× 356 4.0× 87 1.9k
Abdul Noor Canada 20 620 0.7× 145 0.3× 823 2.0× 43 0.2× 118 1.3× 42 1.4k
Deqiong Ma United States 18 580 0.6× 339 0.7× 430 1.0× 39 0.1× 73 0.8× 29 1.3k
Angela Barnicoat United Kingdom 19 1.2k 1.4× 469 0.9× 947 2.3× 55 0.2× 184 2.1× 43 1.6k
Jeff M. Milunsky United States 22 822 0.9× 252 0.5× 704 1.7× 37 0.1× 204 2.3× 70 1.7k
Jorge Saraiva Portugal 20 866 1.0× 118 0.2× 690 1.7× 84 0.3× 277 3.1× 73 1.6k
Karl‐Henrik Gustavson Sweden 20 587 0.7× 260 0.5× 498 1.2× 40 0.2× 149 1.7× 57 1.3k

Countries citing papers authored by Eric Smeets

Since Specialization
Citations

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

Fields of papers citing papers by Eric Smeets

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Smeets

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Smeets. A scholar is included among the top collaborators of Eric Smeets 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 Eric Smeets. Eric Smeets 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.
Gupta, Neerja, Kees E. P. van Roozendaal, Savita Sapra, et al.. (2020). Spectrum of MECP2 mutations in Indian females with Rett Syndrome - a large cohort study. Research Publications (Maastricht University). 3 indexed citations
2.
Ehrhart, Friederike, Susan L. Coort, Lars Eijssen, et al.. (2019). Integrated analysis of human transcriptome data for Rett syndrome finds a network of involved genes. The World Journal of Biological Psychiatry. 21(10). 712–725. 20 indexed citations
3.
Snoeijen‐Schouwenaars, Francesca M., Judith Verhoeven, Petra van Mierlo, et al.. (2018). Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability. Epilepsia. 60(1). 155–164. 60 indexed citations
4.
Ehrhart, Friederike, Susan L. Coort, Elisa Cirillo, et al.. (2016). New insights in Rett syndrome using pathway analysis for transcriptomics data. Wiener Medizinische Wochenschrift. 166(11-12). 346–352. 8 indexed citations
5.
Ehrhart, Friederike, Susan L. Coort, Elisa Cirillo, et al.. (2016). Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes. Orphanet Journal of Rare Diseases. 11(1). 158–158. 53 indexed citations
6.
Smeets, Eric, Peter O.O. Julu, Ingegerd Witt‐Engerström, et al.. (2016). Neurophysiology versus clinical genetics in Rett syndrome: A multicenter study. American Journal of Medical Genetics Part A. 170(9). 2301–2309. 13 indexed citations
7.
Smeets, Eric, Kees E. P. van Roozendaal, C. T. R. M. Schrander‐Stumpel, et al.. (2011). Genotype–phenotype relationships as prognosticators in Rett syndrome should be handled with care in clinical practice. American Journal of Medical Genetics Part A. 158A(2). 340–350. 32 indexed citations
8.
Smeets, Eric, Karine Pelc, & Bernard Dan. (2011). Rett syndrome: clinical and genetic features. Clinical Dysmorphology. 2. 113–127. 1 indexed citations
9.
Smeets, Eric, Jörgen Bierau, I. Keularts, et al.. (2011). Altered Carbon Dioxide Metabolism and Creatine Abnormalities in Rett Syndrome. JIMD Reports. 3. 117–124. 5 indexed citations
10.
Smeets, Eric, Karine Pelc, & Bernard Dan. (2011). Rett Syndrome. Molecular Syndromology. 2(3-5). 113–127. 70 indexed citations
11.
Smeets, Eric, et al.. (2009). Rett syndrome and long‐term disorder profile. American Journal of Medical Genetics Part A. 149A(2). 199–205. 25 indexed citations
12.
Bebbington, Ami, Alan K. Percy, John Christodoulou, et al.. (2009). Updating the profile of C-terminal MECP2 deletions in Rett syndrome. Journal of Medical Genetics. 47(4). 242–248. 54 indexed citations
13.
Julu, Peter O.O., Ingegerd Witt Engerström, Stig Hansen, et al.. (2008). Cardiorespiratory challenges in Rett's syndrome. The Lancet. 371(9629). 1981–1983. 48 indexed citations
14.
Stauder, Johannes, et al.. (2006). The development of visual- and auditory processing in Rett syndrome: An ERP study. Brain and Development. 28(8). 487–494. 44 indexed citations
15.
Moog, Ute, Kees van Roozendaal, Eric Smeets, et al.. (2006). MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients. Brain and Development. 28(5). 305–310. 18 indexed citations
16.
Smeets, Eric, Els Schollen, Ute Moog, et al.. (2003). Rett syndrome in adolescent and adult females: Clinical and molecular genetic findings. American Journal of Medical Genetics Part A. 122A(3). 227–233. 44 indexed citations
17.
Schollen, Els, et al.. (2002). Gross rearrangements in the MECP2 gene in two patients with Rett syndrome. The American Journal of Human Genetics. 71(4). 550–550. 2 indexed citations
18.
Smeets, Eric, J. P. Fryns, & Herman Van den Berghe. (1994). Melkersson‐Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation. Clinical Genetics. 45(6). 323–324. 50 indexed citations
19.
Brichard, Bénédicte, Eric Smeets, Y. Gillerot, et al.. (1990). Tracheal agenesis: An exceptional cause of neonatal respiratory distress. Pediatric Pulmonology. 9(2). 119–120. 4 indexed citations
20.
Borghgraef, Martine, et al.. (1988). The 49,XXXXY syndrome. Clinical and psychological follow‐up data. Clinical Genetics. 33(6). 429–434. 21 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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