Arie P.T. Smits

1.9k citations

43 papers · 1.2k indexed · h-index 21

Genetics top 2%
Molecular Biology
Pediatrics, Perinatology and Child Health top 5%
Cognitive Neuroscience top 5%
Public Health, Environmental and Occupational Health

Co-authors: Ben C.J. Hamel Dominique Smeets D.D.M. Braat Chris M.G. Thomas Hans‐Hilger Ropers Angelique J. A. Kooper Lambertus A. Kiemeney Bernard A. van Oost
Topics: Genetics and Neurodevelopmental Disorders (24 papers)Genomic variations and chromosomal abnormalities (15 papers)Prenatal Screening and Diagnostics (12 papers)
Cited by: Genetics Developmental Biology Cognitive Neuroscience
Journals: New England Journal of Medicine The American Journal of Human Genetics Clinical Chemistry
Partner nations: Netherlands Poland Germany

In The Last Decade

Arie P.T. Smits

42 papers receiving 1.2k citations

Peers

Countries citing papers authored by Arie P.T. Smits

Since Specialization

Citations

This map shows the geographic impact of Arie P.T. Smits'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 Arie P.T. Smits with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Arie P.T. Smits more than expected).

Fields of papers citing papers by Arie P.T. Smits

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Arie P.T. Smits. 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 Arie P.T. Smits. The network helps show where Arie P.T. Smits may publish in the future.

Co-authorship network of co-authors of Arie P.T. Smits

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Is routine karyotyping required in prenatal samples with a molecular or metabolic referral? 2012 ·Molecular Cytogenetics ·Angelique J. A. Kooper,(unknown),Brigitte H. W. Faas,Lies H. Hoefsloot,Ineke van der Burgt,H.A. Zondervan,Arie P.T. Smits	2
2	Predictors and risk model development for menopausal age in fragile X premutation carriers 2011 ·Genetics in Medicine ·Marian A. Spath,Ton Feuth,Arie P.T. Smits,Helger G. Yntema,D.D.M. Braat,Chris M.G. Thomas,Ad Geurts van Kessel,Stephanie L. Sherman,Emily G. Allen	28
3	Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice 2011 ·Acta Neuropathologica ·Michael R. Hunsaker,Claudia Greco,Marian A. Spath,Arie P.T. Smits,(unknown),Flora Tassone,Johan M. Kros,(unknown),Elizabeth Berry‐Kravis,Robert F. Berman,Paul J. Hagerman,Rob Willemsen,Randi J. Hagerman,Renate K. Hukema	75
4	Economic evaluation of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis: a cost-minimization analysis 2011 ·Archives of Gynecology and Obstetrics ·(unknown),Erwin Birnie,Mariëtte J.V. Hoffer,Merryn Macville,Robert‐Jan Galjaard,G. Heleen Schuring‐Blom,(unknown),(unknown),Arie P.T. Smits,J. M. M. van Lith	4
5	X chromosome inactivation does not define the development of premature ovarian failure in fragile X premutation carriers 2010 ·American Journal of Medical Genetics Part A ·Marian A. Spath,(unknown),Arie P.T. Smits,Ton Feuth,D.D.M. Braat,Ad Geurts van Kessel,Helger G. Yntema	22
6	CGG-Repeat Expansion in the DIP2B Gene Is Associated with the Fragile Site FRA12A on Chromosome 12q13.1 2007 ·The American Journal of Human Genetics ·Birgitta Winnepenninckx,(unknown),Jacqueline Ramsay,Dominique Smeets,Arie P.T. Smits,David Fitzpatrick,R. Frank Kooy	72
7	Lysosomal storage diseases in non-immune hydrops fetalis pregnancies 2006 ·Clinica Chimica Acta ·Angelique J. A. Kooper,Pim M.W. Janssens,A.N.J.A. de Groot,(unknown),(unknown),(unknown),Paul P. van den Berg,Emilia K. Bijlsma,Arie P.T. Smits,Ron A. Wevers	35
8	Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defects 2006 ·Prenatal Diagnosis ·Angelique J. A. Kooper,Dagmar de Bruijn,(unknown),Brigitte H. W. Faas,(unknown),Chris M.G. Thomas,Arie P.T. Smits	21
9	A new locus for postaxial polydactyly type A/B on chromosome 7q21–q34 2003 ·European Journal of Human Genetics ·Robert‐Jan H. Galjaard,Arie P.T. Smits,J.H.A.M. Tuerlings,Aagje G. Bais,(unknown),Guido J. Breedveld,Esther de Graaff,Ben A. Oostra,Peter Heutink	30
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	Reply to the Letters from Murray et al. and Vianna-Morgante and Costa 2000 ·The American Journal of Human Genetics ·(unknown),Chris M.G. Thomas,Didi D.M. Braat,Ben A. Oostra,Arie P.T. Smits	5
12	Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27 1999 ·The American Journal of Human Genetics ·Hans van Bokhoven,Martin Jung,Arie P.T. Smits,Sylvia E. C. van Beersum,Franz Rüschendorf,Maurice A. M. Van Steensel,(unknown),J.H.A.M. Tuerlings,Edwin C.M. Mariman,Han G. Brunner,Thomas F. Wienker,André Reis,Hans‐Hilger Ropers,Ben C.J. Hamel	72
13	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
14	Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease? 1999 ·Human Reproduction ·Y.M. van Kasteren,(unknown),Arie P.T. Smits,Frans P.M. Cremers,(unknown),D.D.M. Braat	111
15	Psychometric assessment of families with X-linked mental retardation 1999 ·American Journal of Medical Genetics ·(unknown),Arie P.T. Smits,Geert Thoonen,Ben C.J. Hamel,(unknown),F.J.M. Gabreëls	1
16	Noninvasive Test for Fragile X Syndrome, Using Hair Root Analysis 1999 ·The American Journal of Human Genetics ·Rob Willemsen,Burcu Anar,Yolanda de Diego‐Otero,Bert B.A. de Vries,Yvonne Hilhorst‐Hofstee,Arie P.T. Smits,(unknown),Patrick J. Willems,H. Galjaard,Ben A. Oostra	45
17	Linkage analysis in a Dutch family with X-linked recessive congenital stationary night blindness (XL-CSNB) 1995 ·Human Genetics ·Wolfgang Berger,Gerard van Duijnhoven,A. Pinckers,Arie P.T. Smits,Hans‐Hilger Ropers,Frans P.M. Cremers	5
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	Validation of linkage‐based DNA‐diagnosis of fragile X gene carriers with the CGG repeat probe 1992 ·American Journal of Medical Genetics ·Bernard A. van Oost,Arie P.T. Smits,Jos Dreesen,Ans M.W. van den Ouweland,Ben A. Oostra	4
20	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 1992 ·American Journal of Medical Genetics ·Arie P.T. Smits,Bernard A. van Oost,Anton F. J. de Haan,Ben C.J. Hamel,Jos Dreesen,Dominique Smeets	7

About Arie P.T. Smits

Arie P.T. Smits is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 43 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (24 papers), Genomic variations and chromosomal abnormalities (15 papers) and Prenatal Screening and Diagnostics (12 papers). The work is most often cited by research in Genetics (858 citations), Developmental Biology (41 citations) and Cognitive Neuroscience (279 citations). Arie P.T. Smits has collaborated with scholars based in Netherlands, Poland and Germany. Frequent co-authors include Ben C.J. Hamel, Dominique Smeets, D.D.M. Braat, Chris M.G. Thomas, Hans‐Hilger Ropers, Angelique J. A. Kooper, Lambertus A. Kiemeney, Bernard A. van Oost, Brigitte H. W. Faas and Edwin C.M. Mariman. Their work appears in journals such as New England Journal of Medicine, The American Journal of Human Genetics and Clinical Chemistry.

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