Eric Smeets

2.8k citations

62 papers · 1.2k indexed · h-index 22

Impact in

Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research

Papers in ⓘ

Genetics 53
- Genetics and Neurodevelopmental Disorders 35
- Genomic variations and chromosomal abnormalities 17
- Connective tissue disorders research 4
Cognitive Neuroscience 20
- Autism Spectrum Disorder Research 20

Co-authors: Leopold Curfs (20 shared papers)Herman Van den Berghe (8 shared papers)J. P. Fryns (8 shared papers)Bernard Dan (2 shared papers)Karine Pelc (2 shared papers)Ute Moog (4 shared papers)J. Herbergs (3 shared papers)Connie Schrander‐Stumpel (3 shared papers)
Journals: Clinical Genetics (4 papers)Journal of Developmental and Physical Disabilities (4 papers)Journal of Medical Genetics (3 papers)Brain and Development (3 papers)European Journal of Paediatric Neurology (2 papers)
Partner nations: Netherlands Belgium United States

In The Last Decade

Eric Smeets

62 papers receiving 1.2k citations

Peers

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-authors

The 25 scholars most cited alongside Eric Smeets, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eric Smeets Line = papers co-authored together Eric Smeets links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 62 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2) European Journal of Paediatric Neurology ·Ute Moog, Eric Smeets, Kees EP van Roozendaal, Sam Schoenmakers, J. Herbergs, A Schoonbrood-Lenssen, Connie Schrander‐Stumpel	2003	71
2	Rett Syndrome Molecular Syndromology ·Eric Smeets, Karine Pelc, Bernard Dan	2011	70
3	Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability Epilepsia ·Francesca M. Snoeijen‐Schouwenaars, Jans S. van Ool, Judith Verhoeven, Petra van Mierlo, Hilde M. H. Braakman, Eric Smeets, Joost Nicolai, Jeroen Schoots, Mariël W.A. Teunissen, Rob P.W. Rouhl, Francis Tan, Helger G. Yntema, Han G. Brunner, Rolph Pfundt, Alexander P.A. Stegmann, Erik‐Jan Kamsteeg, Helenius J. Schelhaas, Marjolein H. Willemsen	2018	60
4	Communication in Individuals with Rett Syndrome: an Assessment of Forms and Functions Journal of Developmental and Physical Disabilities ·Robert Didden, Hubert Korzilius, Eric Smeets, Vanessa A. Green, Russell Lang, Giulio E. Lancioni, Leopold Curfs	2009	60
5	Updating the profile of C-terminal MECP2 deletions in Rett syndrome Journal of Medical Genetics ·Ami Bebbington, Alan K. Percy, John Christodoulou, David Ravine, Gladys Ho, Peter Jacoby, Alison Anderson, M. Pineda, Bruria Ben Zeev, Nadia Bahi‐Buisson, Eric Smeets, Helen Leonard	2009	54
6	Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes Orphanet Journal of Rare Diseases ·Friederike Ehrhart, Susan L. Coort, Elisa Cirillo, Eric Smeets, Chris T. Evelo, Leopold Curfs	2016	53
7	Melkersson‐Rosenthal syndrome and de novo autosomal t(9;21)(p11;p11) translocation Clinical Genetics ·Eric Smeets, J. P. Fryns, Herman Van den Berghe	1994	50
8	Cardiorespiratory challenges in Rett's syndrome The Lancet ·Peter O.O. Julu, Ingegerd Witt Engerström, Stig Hansen, Flora Apartopoulos, Bengt Engerström, Giorgio Pini, R. Shane Delamont, Eric Smeets	2008	48
9	MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions American Journal of Medical Genetics Part A ·Servi J.C. Stevens, Conny M.A. van Ravenswaaij‐Arts, Jannie W.H. Janssen, Jolien S. Klein Wassink‐Ruiter, Anthonie J. van Essen, Trijnie Dijkhuizen, Jeroen van Rheenen, Regina Heuts‐Vijgen, Alexander P.A. Stegmann, Eric Smeets, J.J.M. Engelen	2011	48
10	Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations Genes Chromosomes and Cancer ·Ellen Denayer, Koenraad Devriendt, Thomy de Ravel, Griet Van Buggenhout, Eric Smeets, Inge François, Yves Sznajer, Margarita Craen, Georgios Leventopoulos, Léon Mutesa, W. Vandecasseye, Guy Massa, Hülya Kayserili, Raf Sciot, J P Fryns, Eric Legius	2009	46
11	Rett syndrome in adolescent and adult females: Clinical and molecular genetic findings American Journal of Medical Genetics Part A ·Eric Smeets, Els Schollen, Ute Moog, Gert Matthijs, J. Herbergs, H. Smeets, Leopold Curfs, C. T. R. M. Schrander‐Stumpel, J. P. Fryns	2003	44
12	The development of visual- and auditory processing in Rett syndrome: An ERP study Brain and Development ·Johannes Stauder, Eric Smeets, Saskia G.M. van Mil, Leopold G.M. Curfs	2006	44
13	Eye Gaze Technology as a Form of Augmentative and Alternative Communication for Individuals with Rett Syndrome: Experiences of Families in The Netherlands Journal of Developmental and Physical Disabilities ·Gillian S. Townend, Peter B. Marschik, Eric Smeets, Raymond van de Berg, Mariёlle van den Berg, Leopold Curfs	2015	44
14	Aging in people with specific genetic syndromes: Rett syndrome American Journal of Medical Genetics Part A ·Nicky S. J. Halbach, Eric Smeets, Connie T.R.M. Schrander‐Stumpel, Henny H.J. van Schrojenstein Lantman de Valk, Marian A. Maaskant, Leopold Curfs	2008	39
15	Genotype–phenotype relationships as prognosticators in Rett syndrome should be handled with care in clinical practice American Journal of Medical Genetics Part A ·Nicky S. J. Halbach, Eric Smeets, Noortje van den Braak, Kees E. P. van Roozendaal, Rien Blok, C. T. R. M. Schrander‐Stumpel, Jean‐Pierre Frijns, Marian A. Maaskant, Leopold Curfs	2011	32
16	Strong variable clinical presentation in 3 patients with 7q terminal deletion. PubMed ·Suzanna G.M. Frints, C. T. R. M. Schrander‐Stumpel, Eric Schoenmakers, J.J.M. Engelen, Ad Reekers, Anita M. Van den Neucker, Eric Smeets, H. Devlieger, J P Fryns	1998	31
17	Rett syndrome and long‐term disorder profile American Journal of Medical Genetics Part A ·Eric Smeets, Mickey Chenault, Leopold Curfs, Connie T.R.M. Schrander‐Stumpel, Jean‐Pierre Frijns	2009	25
18	Functional characterization of the TSC2 c.3598C>T (p.R1200W) missense mutation that co‐segregates with tuberous sclerosis complex in mildly affected kindreds Clinical Genetics ·Marjolein Wentink, Mark Nellist, Marianne Hoogeveen‐Westerveld, Bernard A. Zonnenberg, DM van der Kolk, Ton van Essen, S. M. Park, Geoffrey Woods, Petra E. Cohn‐Hokke, Wim Brussel, Eric Smeets, Alice S. Brooks, Dicky Halley, Ans van den Ouweland, Anneke Maat‐Kievit	2011	24
19	Management of a severe forceful breather with Rett Syndrome using carbogen Brain and Development ·Eric Smeets, Peter O.O. Julu, Dick van Waardenburg, Ingegerd Witt Engerström, Stig Hansen, Flora Apartopoulos, Leopold Curfs, Connie Schrander‐Stumpel	2006	24
20	De novo 7q36 deletion: Breakpoint analysis and types of holoprosencephaly American Journal of Medical Genetics ·Suzanna G.M. Frints, Eric Schoenmakers, Eric Smeets, Paul Petit, Jean‐Pierre Fryns	1998	23

About Eric Smeets

Eric Smeets is a scholar working on Genetics, Cognitive Neuroscience, Developmental Biology, Structural Biology and Clinical Psychology, having authored 62 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (35 papers), Autism Spectrum Disorder Research (20 papers), Genomic variations and chromosomal abnormalities (17 papers), Family and Disability Support Research (10 papers), Prenatal Screening and Diagnostics (7 papers), Chromosomal and Genetic Variations (6 papers), RNA modifications and cancer (5 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Genetics (902 citations), Cognitive Neuroscience (517 citations), Clinical Psychology (261 citations), Developmental Biology (16 citations) and Occupational Therapy (26 citations). Eric Smeets has collaborated with scholars based in Netherlands, Belgium and United States. Frequent co-authors include Leopold Curfs, Herman Van den Berghe, J. P. Fryns, Bernard Dan, Karine Pelc, Ute Moog, J. Herbergs, Connie Schrander‐Stumpel, C. T. R. M. Schrander‐Stumpel and Chris T. Evelo. Their work appears in journals such as Clinical Genetics, Journal of Developmental and Physical Disabilities, Journal of Medical Genetics, Brain and Development and European Journal of Paediatric Neurology.

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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