Dominique Smeets

8.4k total citations
112 papers, 4.9k citations indexed

About

Dominique Smeets is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Dominique Smeets has authored 112 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Genetics, 57 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Dominique Smeets's work include Genomic variations and chromosomal abnormalities (40 papers), Genetics and Neurodevelopmental Disorders (27 papers) and Prenatal Screening and Diagnostics (17 papers). Dominique Smeets is often cited by papers focused on Genomic variations and chromosomal abnormalities (40 papers), Genetics and Neurodevelopmental Disorders (27 papers) and Prenatal Screening and Diagnostics (17 papers). Dominique Smeets collaborates with scholars based in Netherlands, United States and Germany. Dominique Smeets's co-authors include Ad Geurts van Kessel, Joris A. Veltman, Conny M.A. van Ravenswaaij‐Arts, Irene M. Janssen, Eric Schoenmakers, Gerard Merkx, Bert B.A. de Vries, Han G. Brunner, Daniël Olde Weghuis and Erik Huys and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Dominique Smeets

112 papers receiving 4.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Dominique Smeets Netherlands	38	2.7k	2.6k	824	776	658	112	4.9k
Lidia Larizza Italy	43	2.3k 0.9×	3.7k 1.4×	780 0.9×	407 0.5×	573 0.9×	271	6.3k
Erik A. Sistermans Netherlands	37	2.7k 1.0×	2.9k 1.1×	1.0k 1.2×	518 0.7×	475 0.7×	123	5.6k
Veronica J. Buckle United Kingdom	47	2.1k 0.8×	4.6k 1.7×	359 0.4×	1.3k 1.7×	476 0.7×	91	6.5k
Eric Schoenmakers Belgium	34	2.1k 0.8×	2.5k 0.9×	490 0.6×	499 0.6×	705 1.1×	76	5.2k
Ankita Patel United States	42	4.1k 1.5×	2.8k 1.1×	1.7k 2.0×	744 1.0×	313 0.5×	143	6.5k
Anita Rauch Germany	48	3.4k 1.3×	4.4k 1.7×	679 0.8×	459 0.6×	332 0.5×	194	7.5k
Hirofumi Ohashi Japan	36	2.5k 0.9×	3.1k 1.2×	500 0.6×	380 0.5×	243 0.4×	165	4.8k
Lisenka E.L.M. Vissers Netherlands	39	5.1k 1.9×	3.6k 1.4×	943 1.1×	790 1.0×	586 0.9×	98	7.7k
Maj Hultén United Kingdom	39	2.4k 0.9×	2.8k 1.0×	1.2k 1.5×	1.1k 1.4×	350 0.5×	145	4.8k
Serge Romana France	29	1.3k 0.5×	1.6k 0.6×	515 0.6×	271 0.3×	580 0.9×	108	4.4k

Countries citing papers authored by Dominique Smeets

Since Specialization

Citations

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

Fields of papers citing papers by Dominique Smeets

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dominique Smeets

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

All Works

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20 of 20 papers shown

Oud, Manon S., Dominique Smeets, Liliana Ramos, et al.. (2024). Innovative all‐in‐one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10‐month experience. Andrology. 13(5). 1078–1092. 2 indexed citations

Boer, Elke de, Carlo Marcelis, Kornelia Neveling, et al.. (2023). A complex structural variant near SOX3 causes X-linked split-hand/foot malformation. Human Genetics and Genomics Advances. 4(3). 100200–100200. 1 indexed citations

Peek, Ronald, Dominique Smeets, Alessandra Camboni, et al.. (2023). Assessment of folliculogenesis in ovarian tissue from young patients with Turner syndrome using a murine xenograft model. Fertility and Sterility. 120(2). 371–381. 11 indexed citations

Graaf, Gert de, Michel E. Weijerman, Mariëtte J.V. Hoffer, et al.. (2021). Does non‐invasive prenatal testing affect the livebirth prevalence of Down syndrome in the Netherlands? A population‐based register study. Prenatal Diagnosis. 41(10). 1351–1359. 12 indexed citations

Velden, Janielle van der, et al.. (2020). Why are some patients with 45,X Turner syndrome fertile? A young girl with classical 45,X Turner syndrome and a cryptic mosaicism in the ovary. Fertility and Sterility. 115(5). 1280–1287. 18 indexed citations

Duijnhouwer, Anthonie L., Livia Kapusta, Marlies Kempers, et al.. (2018). Phenotype in girls and women with Turner syndrome: Association between dysmorphic features, karyotype and cardio-aortic malformations. European Journal of Medical Genetics. 61(6). 301–306. 18 indexed citations

Oud, Manon S., Liliana Ramos, Moira K. O’Bryan, et al.. (2017). Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia. Human Mutation. 38(11). 1592–1605. 44 indexed citations

Smeets, Dominique, et al.. (2015). SQUAMOUS CELL CARCINOMA OF THE HEAD AND NECK: NEW AVENUES OF TREATMENT?. SHILAP Revista de lepidopterología. 2 indexed citations

Freriks, Kim, Henri Timmers, Romana T. Netea‐Maier, et al.. (2013). Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome. European Journal of Medical Genetics. 56(9). 497–501. 40 indexed citations

10.

Smeets, Dominique, Willy M. Nillesen, Tri Indah Winarni, et al.. (2012). Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversion. Gene. 511(2). 451–454. 16 indexed citations

11.

Feenstra, Ilse, et al.. (2006). Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature. European Journal of Medical Genetics. 49(5). 384–395. 23 indexed citations

12.

Veltman, Joris A., Yvonne M.H. Versleijen‐Jonkers, Irene M. Janssen, et al.. (2003). Definition of a Critical Region on Chromosome 18 for Congenital Aural Atresia by ArrayCGH. The American Journal of Human Genetics. 72(6). 1578–1584. 83 indexed citations

13.

Vissers, Lisenka E.L.M., Bert B.A. de Vries, Kazutoyo Osoegawa, et al.. (2003). Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities. The American Journal of Human Genetics. 73(6). 1261–1270. 348 indexed citations

14.

Matsuura, Shinya, Hiroshi Tauchi, Asako Nakamura, et al.. (1998). \nPositional cloning of the gene for Nijmegen breakage syndrome. Radboud Repository (Radboud University). 242 indexed citations

15.

Wijmenga, Cisca, Lambert P.W.J. van den Heuvel, Eric Strengman, et al.. (1998). Localization of the ICF Syndrome to Chromosome 20 by Homozygosity Mapping. The American Journal of Human Genetics. 63(3). 803–809. 42 indexed citations

16.

Smeets, Dominique, Ben C.J. Hamel, Marcel Nelen, et al.. (1992). Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15. New England Journal of Medicine. 326(12). 807–811. 105 indexed citations

17.

Semmekrot, Ben A., Ásgeir Haraldsson, Corry M.R. Weemaes, et al.. (1992). Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis. American Journal of Medical Genetics. 42(5). 736–740. 2 indexed citations

18.

Smits, Arie P.T., Bernard A. van Oost, Anton F. J. de Haan, et al.. (1992). Penetrance of Fra(X) gene: Influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male. American Journal of Medical Genetics. 43(1-2). 365–372. 7 indexed citations

19.

Slater, Rosalyn, Dominique Smeets, A Hagemeijer, et al.. (1990). Update of the Cytogenetic Study of Childhood Non-High-Risk Acute Lymphocytic Leukemia at Diagnosis in Protocol VI of the Dutch Childhood Leukemia Study Group. Hämatologie und Bluttransfusion. 33. 169–173. 5 indexed citations

20.

Hulsebos, Theo J.M., B. Wieringa, Ron Hochstenbach, et al.. (1986). Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosome. Cytogenetic and Genome Research. 43(1-2). 47–56. 30 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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