The DOI matches its Crossref record; 75 of the 75 references it cites were found in a registry or an index.
Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands
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Citations
Cites
International System for Human Cytogenetic Nomenclature
National Cancer Institute (2020) · Definitions · doi:10.32388/78qroa · Cited by 6,840
Schouten, J. P. (2002) · Nucleic Acids Research · doi:10.1093/nar/gnf056 · Cited by 2,699
Nielsen, J., & Wohlert, M. (1991) · Human Genetics · doi:10.1007/bf01213097 · Cited by 1,193
Chromosome Abnormalities and Genetic Counseling
Gardner, R. J. M., Sutherland, G. R., & Shaffer, L. G. (2011) · Oxford University Press eBooks · doi:10.1093/med/9780195375336.001.0001 · Cited by 857
Shevell, M., Ashwal, S., Donley, D., Flint, J., Gingold, M., Hirtz, D., Majnemer, A., Noetzel, M., & Sheth, R. D. (2003) · Neurology · doi:10.1212/01.wnl.0000031431.81555.16 · Cited by 829
Catalogue of Unbalanced Chromosome Aberrations in Man
Schinzel, A. (1983) · De Gruyter eBooks · doi:10.1515/9783112329047 · Cited by 758
Diagnostic genome profiling in mental retardation
de Vries, B. B. A., Pfundt, R., Leisink, M., Koolen, D. A., Vissers, L. E. L. M., Janssen, I. M., Reijmersdal, S. V., Nillesen, W. M., Huys, E. H. L. P. G., Leeuw, N. D., et al. (2005) · The American Journal of Human Genetics · doi:10.1086/491719 · Cited by 605
Self-citationShaw-Smith, C., Redon, R., Rickman, L., Rio, M., Willatt, L., Fiegler, H., Firth, H., Sanlaville, D., Winter, R., Colleaux, L., et al. (2004) · Journal of Medical Genetics · doi:10.1136/jmg.2003.017731 · Cited by 513
Vissers, L. E. L. M., de Vries, B. B. A., Osoegawa, K., Janssen, I. M., Feuth, T., Choy, C. O., Straatman, H., van der Vliet, W., Huys, E. H. L. P. G., van Rijk, A., et al. (2003) · The American Journal of Human Genetics · doi:10.1086/379977 · Cited by 469 · cited 1×
“[72] 2003 BAC 3569 1.”
Self-citationThe new cytogenetics: blurring the boundaries with molecular biology
Speicher, M. R., & Carter, N. P. (2005) · Nature Reviews Genetics · doi:10.1038/nrg1692 · Cited by 458
Cited by
Miller, D. T., Adam, M. P., Aradhya, S., Biesecker, L. G., Brothman, A. R., Carter, N. P., Church, D. M., Crolla, J. A., Eichler, E. E., Epstein, C. J., et al. (2010) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2010.04.006 · Cited by 2,882
Diagnostic exome sequencing in persons with severe intellectual disability
de Ligt, J., Willemsen, M. H., van Bon, B. W. M., Kleefstra, T., Yntema, H. G., Kroes, T., Vulto-van Silfhout, A. T., Koolen, D. A., de Vries, P., Gilissen, C., et al. (2012) · New England Journal of Medicine · doi:10.1056/nejmoa1206524 · Cited by 1,546
Genetic and Epigenetic Networks in Intellectual Disabilities
van Bokhoven, H. (2011) · Annual Review of Genetics · doi:10.1146/annurev-genet-110410-132512 · Cited by 382
Cognitive and behavioral characterization of 16p11.2 deletion syndrome
Hanson, E., Nasir, R. H., Fong, A., Lian, A., Hundley, R., Shen, Y., Wu, B.-L., Holm, I. A., & Miller, D. T. (2010) · Journal of Developmental & Behavioral Pediatrics · doi:10.1097/dbp.0b013e3181ea50ed · Cited by 125
Oneda, B., Baldinger, R., Reissmann, R., Reshetnikova, I., Krejci, P., Masood, R., Ochsenbein‐Kölble, N., Bartholdi, D., Steindl, K., Morotti, D., et al. (2014) · Prenatal Diagnosis · doi:10.1002/pd.4342 · Cited by 53
Metadata
- Authors
- Hochstenbach, R., van Binsbergen, E., Engelen, J., Nieuwint, A., Polstra, A., Poddighe, P., Ruivenkamp, C., Sikkema-Raddatz, B., Smeets, D., & Poot, M.
- Venue
- European Journal of Medical Genetics
- Publisher
- Elsevier BV
- Published
- 2009-07
- Volume
- 52
- Issue
- 4
- Pages
- 161-169
- ISSN
- 1769-7212 (ISSN-L)
- OpenAlex
- W2158094580
- Cited by
- 284
- References
- 75
- FWCI
- 17.29
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands. https://app.cochat.ai/papers/10.1016/j.ejmg.2009.03.015
- The paper
- Hochstenbach, R., van Binsbergen, E., Engelen, J., Nieuwint, A., Polstra, A., Poddighe, P., Ruivenkamp, C., Sikkema-Raddatz, B., Smeets, D., & Poot, M. (2009). Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands. European Journal of Medical Genetics. https://doi.org/10.1016/j.ejmg.2009.03.015
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
