Dominique Smeets

8.4k citations

112 papers · 4.9k indexed · h-index 38

Genetics top 0.5%
Molecular Biology top 2%
Pediatrics, Perinatology and Child Health top 1%
Plant Science top 5%
Cancer Research top 2%

Co-authors: 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
Topics: Genomic variations and chromosomal abnormalities (40 papers)Genetics and Neurodevelopmental Disorders (27 papers)Prenatal Screening and Diagnostics (17 papers)
Cited by: Genetics Cancer Research Pediatrics, Perinatology and Child Health
Journals: New England Journal of MedicineSHILAP Revista de lepidopterologíaBlood
Partner nations: Netherlands United States Germany

In The Last Decade

Dominique Smeets

112 papers receiving 4.7k citations

Peers

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

#	Work	Indexed citations
1	Innovative all‐in‐one exome sequencing strategy for diagnostic genetic testing in male infertility: Validation and 10‐month experience 2024 ·Andrology ·Manon S. Oud,(unknown),Dominique Smeets,Liliana Ramos,Godfried W. van der Heijden,(unknown),Maartje van de Vorst,Tom Hofste,Marlies Kempers,Marijn F. Stokman,Kathleen D’Hauwers,Brigitte H. W. Faas,Dineke Westra	2
2	Assessment of folliculogenesis in ovarian tissue from young patients with Turner syndrome using a murine xenograft model 2023 ·Fertility and Sterility ·Ronald Peek,(unknown),(unknown),(unknown),Dominique Smeets,(unknown),Alessandra Camboni,D.D.M. Braat,Janielle van der Velden,Jacques Donnez,Kathrin Fleischer,Marie‐Madeleine Dolmans	11
3	A complex structural variant near SOX3 causes X-linked split-hand/foot malformation 2023 ·Human Genetics and Genomics Advances ·Elke de Boer,Carlo Marcelis,Kornelia Neveling,Ellen van Beusekom,Alexander Hoischen,Willemijn M. Klein,Nicole de Leeuw,Tuomo Mantere,Uirá Souto Melo,Jeroen van Reeuwijk,Dominique Smeets,Malte Spielmann,Tjitske Kleefstra,Hans van Bokhoven,Lisenka E.L.M. Vissers	1
4	Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping 2021 ·The American Journal of Human Genetics ·Kornelia Neveling,Tuomo Mantere,(unknown),Michiel Oorsprong,Ronald van Beek,Ellen Kater‐Baats,Marc Pauper,(unknown),Dominique Smeets,Daniël Olde Weghuis,Marian Stevens‐Kroef,Alexander Hoischen	110
5	Phenotype in girls and women with Turner syndrome: Association between dysmorphic features, karyotype and cardio-aortic malformations 2018 ·European Journal of Medical Genetics ·(unknown),Anthonie L. Duijnhouwer,Livia Kapusta,Marlies Kempers,Nel Roeleveld,Michiel Schokking,Dominique Smeets,Kim Freriks,Henri Timmers,(unknown)	18
6	Mosaic maternal 10qter deletions are associated with FRA10B expansions and may cause false-positive noninvasive prenatal screening results 2018 ·Genetics in Medicine ·Karin Huijsdens–van Amsterdam,Roy Straver,Merel C. van Maarle,Alida C. Knegt,Diane Van Opstal,Frank Sleutels,Dominique Smeets,Erik A. Sistermans	13
7	Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia 2017 ·Human Mutation ·Manon S. Oud,Liliana Ramos,Moira K. O’Bryan,Robert I. McLachlan,Özlem Okutman,Stéphane Viville,Petra F. de Vries,Dominique Smeets,Dorien Lugtenberg,Jayne Y. Hehir‐Kwa,Christian Gilissen,(unknown),Lisenka E.L.M. Vissers,Alexander Hoischen,(unknown),Kathrin Fleischer,Joris A. Veltman,Michiel J. Noordam	44
8	SQUAMOUS CELL CARCINOMA OF THE HEAD AND NECK: NEW AVENUES OF TREATMENT? 2015 ·SHILAP Revista de lepidopterología ·(unknown),(unknown),Dominique Smeets,(unknown)	2
9	ICF syndrome: High variability of the chromosomal phenotype and association with classical Hodgkin lymphoma 2007 ·American Journal of Medical Genetics Part A ·Catharina Schuetz,Gotthold Barbi,Thomas F.E. Barth,Manfred Hoenig,Ansgar Schulz,Peter Möeller,Dominique Smeets,Jessica C. de Greef,Silvère M. van der Maarel,Walther Vogel,Klaus‐Michael Debatin,W Friedrich	12
10	Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15) 2001 ·Genes Chromosomes and Cancer ·Marc J. Eleveld,Daniëlle Bodmer,Gerard Merkx,(unknown),Sandra H. E. Sprenger,Marian A. J. Weterman,Marjolijn J. L. Ligtenberg,(unknown),(unknown),Judith W. M. Jeuken,Dominique Smeets,Arie P.T. Smits,Ad Geurts van Kessel	29
11	X-linked mental retardation: Evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region 1999 ·American Journal of Medical Genetics ·Helger G. Yntema,Bellinda van den Helm,Nine V.A.M. Knoers,Arie P.T. Smits,(unknown),Dominique Smeets,Edwin C.M. Mariman,Ineke van der Burgt,Hans van Bokhoven,Hans‐Hilger Ropers,Hannie Kremer,Ben C.J. Hamel	7
12	\nPositional cloning of the gene for Nijmegen breakage syndrome 1998 ·Radboud Repository (Radboud University) ·Shinya Matsuura,Hiroshi Tauchi,Asako Nakamura,Noriko Kondo,Shuichi Sakamoto,Satoru Endo,Dominique Smeets,B. Sölder,Bernd H. Belohradsky,Vazken M. Der Kaloustian,Mitsuo Oshimura,Minoru Isomura,Yusuke Nakamura,Kenshi Komatsu	242
13	Localization of the ICF Syndrome to Chromosome 20 by Homozygosity Mapping 1998 ·The American Journal of Human Genetics ·Cisca Wijmenga,Lambert P.W.J. van den Heuvel,Eric Strengman,(unknown),(unknown),Ronald de Groot,Dominique Smeets,Jos Draaisma,Jacques J. M. van Dongen,Ronney A. De Abreu,P. Pearson,Lodewijk A. Sandkuijl,Corry M.R. Weemaes	42
14	MISINTERPRETATION OF TRISOMY 18 AS A PSEUDOMOSAICISM AT THIRD-TRIMESTER AMNIOCENTESIS OF A CHILD WITH A MOSAIC 46,XY/47,XY,+3/48,XXY,+18 KARYOTYPE 1997 ·Prenatal Diagnosis ·Conny M.A. van Ravenswaaij‐Arts,J.H.A.M. Tuerlings,Arno van Heijst,J.G. Nijhuis,(unknown),Dominique Smeets	4
15	Genetic Mapping Using Microcell-Mediated Chromosome Transfer Suggests a Locus for Nijmegen Breakage Syndrome at Chromosome 8q21-24 1997 ·The American Journal of Human Genetics ·Shinya Matsuura,Corry M.R. Weemaes,Dominique Smeets,(unknown),Noriko Kondo,Shuichi Sakamoto,(unknown),Asako Nakamura,Hiroshi Tauchi,Satoru Endo,Mitsuo Oshimura,Kenshi Komatsu	57
16	No imprinting involved in the expression of DM-kinase m RNAs in mouse and human tissues 1993 ·Human Molecular Genetics ·Gert Jansen,(unknown),Vera M. Kalscheuer,Gerard Merkx,(unknown),Edwin C.M. Mariman,Dominique Smeets,Hans‐Hilger Ropers,(unknown)	20
17	Absent thumb, immune disorder, and congenital anemia presenting with hydrops fetalis 1992 ·American Journal of Medical Genetics ·Ben A. Semmekrot,Ásgeir Haraldsson,Corry M.R. Weemaes,Dominique Smeets,Wil B. Geven,Han G. Brunner	2
18	Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 1992 ·New England Journal of Medicine ·Dominique Smeets,Ben C.J. Hamel,Marcel Nelen,H. Smeets,J. Bollen,Arie P.T. Smits,Hans‐Hilger Ropers,Bernard A. van Oost	105
19	Marker profile of mesothelial cells versus ovarian carcinoma cells 1989 ·International Journal of Cancer ·Catharina C. van Niekerk,P. H. K. Jap,Chris M.G. Thomas,Dominique Smeets,F. C. S. Ramaekers,Lambert G. Poels	29
20	Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosome 1986 ·Cytogenetic and Genome Research ·Theo J.M. Hulsebos,B. Wieringa,Ron Hochstenbach,Dominique Smeets,Jan Schepens,Frank Oerlemans,J. Zimmer,H.-H. Ropers	30

About Dominique Smeets

Dominique Smeets is a scholar working on Genetics, Developmental Biology and Cancer Research, having authored 112 papers that have together received 4.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (40 papers), Genetics and Neurodevelopmental Disorders (27 papers) and Prenatal Screening and Diagnostics (17 papers). The work is most often cited by research in Genetics (2.7k citations), Cancer Research (658 citations) and Pediatrics, Perinatology and Child Health (824 citations). Dominique Smeets has collaborated with scholars based in Netherlands, United States and Germany. Frequent 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 Lisenka E.L.M. Vissers. Their work appears in journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Blood.

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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