Arie P.T. Smits - Concepedia

Author

Arie P.T. Smits

Also Known As

A P T Smits, A Smits, A. P.T. Smits, A.P.T. Smits, Arie P T Smits, Arie P. T. Smits, Arie P.T. Smits, Arie PT Smits, Arie Smits

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Erasmus University Rotterdam Institute of Human Genetics Rijnstate Hospital

About

Arie P.T. Smits is an author at Radboud University Nijmegen specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	21	1.3K
2	Public Health	9	9	688
3	Natural Sciences	2	2	149
4	Biology	2	2	67
5	Biochemistry	1	1	20

Arie P.T. Smits

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 Dominique Smeets, Ben C.J. Hamel, Marcel Nelen, New England Journal of Medicine Chromosomes 6GeneticsGenetic EpidemiologyPathologyMolecular Genetics	1992	192
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease? Y.M. van Kasteren, Rubin D.L. Hundscheid, Arie P.T. Smits, Human Reproduction Family MedicineFertilityGeneticsReproductive HealthGenetic Epidemiology	1999	162
Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis Brigitte H. W. Faas, I. van der Bürgt, Angelique J. A. Kooper, Journal of Medical Genetics	2010	144
Imprinting Effect in Premature Ovarian Failure Confined to Paternally Inherited Fragile X Premutations Rubin D.L. Hundscheid, Erik A. Sistermans, Chris M.G. Thomas, The American Journal of Human Genetics InfertilityDevelopmental BiologyFertilityPremature Ovarian FailureGenetics	2000	130
CGG-Repeat Expansion in the DIP2B Gene Is Associated with the Fragile Site FRA12A on Chromosome 12q13.1 Birgitta Winnepenninckx, Kim Debacker, Jacqueline Ramsay, The American Journal of Human Genetics ChromatinGenome InstabilityFragile Site Fra12aChromatin StructureGenetic Disorder	2007	129
Widespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice Michael R. Hunsaker, Claudia Greco, Marian A. Spath, Acta Neuropathologica Cgg Knock-in MiceFragile X SpectrumNeurologyNeuroscienceNeuropathology	2011	106
Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27 Hans van Bokhoven, Martin Jung, Arie P.T. Smits, The American Journal of Human Genetics Developmental AnomalyThumb HypoplasiaDevelopmental BiologyMendelian DisorderLimb Mammary Syndrome	1999	105
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site Gregory J. Riggins, Stephanie L. Sherman, Ben A. Oostra, American Journal of Medical Genetics	1992	86
Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives Rubin D.L. Hundscheid, D.D.M. Braat, Lambertus A. Kiemeney, Human Reproduction Hormonal ContraceptiveFertilityOral ContraceptiveReproductive HealthSerum Fsh	2001	82
Noninvasive Test for Fragile X Syndrome, Using Hair Root Analysis Rob Willemsen, Burcu Anar, Yolanda de Diego‐Otero, The American Journal of Human Genetics PediatricsFragile X SpectrumDiagnosisNoninvasive TestMedicine	1999	72

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