The DOI matches its Crossref record; 98 of the 103 references it cites were found in a registry or an index.
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
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In the citing paper
“Similarly, cytogenetic abnormalities have been reported for almost every chromosome [for a review, see Ref. (3–7) and http://projects.tcag.ca/autism/].”
From Gene × Environment Interactions in Autism Spectrum Disorders: Role of Epigenetic Mechanisms (2014) · cites this paper as [4]
In the citing paper
“A subset of the genetic region associated with PWS is also associated with an increased risk for ASD, as maternally inherited duplications of the 15q11–13 region are associated with 1–3% of ASD cases (Bolton et al., 2001; Cook et al., 1997; Vorstman et al., 2006).”
From Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (2014) · cites this paper as Vorstman et al., 2006
In the citing paper
“Karyotyping studies suggested that on the order of 5% of ASD cases have one of a large number of rare but relatively gross chromosomal abnormalities. 14,78”
From Genetic architectures of psychiatric disorders: the emerging picture and its implications (2012) · cites this paper as [14]
In the citing paper
“microduplications or microdeletions of the region 15qllql3, which is subject to parental imprinting, have been repeatedly reported in subjects with autism”
From Autism risk factors: genes, environment, and gene-environment interactions (2012) · cites this paper as [71]
Citations
Cites
1 retracted
Wakefield, A., Murch, S., Anthony, A., Linnell, J., Casson, D., Malik, M., Berelowitz, M., Dhillon, A., Thomson, M., Harvey, P., et al. (1998) · The Lancet · doi:10.1016/s0140-6736(97)11096-0 · Cited by 3,006
RetractedDiagnostic and Statistical Manual of Mental Disorders
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The Future of Genetic Studies of Complex Human Diseases
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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
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Finishing the euchromatic sequence of the human genome
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Detection of large-scale variation in the human genome
Iafrate, A. J., Feuk, L., Rivera, M. N., Listewnik, M. L., Donahoe, P. K., Qi, Y., Scherer, S. W., & Lee, C. (2004) · Nature Genetics · doi:10.1038/ng1416 · Cited by 2,892
Large-scale copy number polymorphism in the human genome
Sebat, J., Lakshmi, B., Troge, J., Alexander, J., Young, J., Lundin, P., Månér, S., Massa, H., Walker, M., Chi, M., et al. (2004) · Science · doi:10.1126/science.1098918 · Cited by 2,557
Autism as a strongly genetic disorder: evidence from a British twin study
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Flagged first, then by citations
5 of the 103 references couldn’t be matched to a known paper.
Research works printed but not linked: 2
- Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Conciatori M et al. Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples. Am J Med Genet 2000; 96: 123–127. · DOI
- Salmon B, Hallmayer J, Rogers T, Kalaydjieva L, Petersen PB, Nicholas P et al. Absence of linkage and linkage disequilibrium to chromosome 15q11–q13 markers in 139 multiplex families with autism. Am J Med Genet 1999; 88: 551–556. · DOI
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Sorted by citations
Items 301–352 of 352
Genome-Wide Association Studies of Copy Number Variation in Autism Spectrum Disorder
Hu, H., & Chung, Y. (2011) · InTech eBooks · doi:10.5772/22207 · Cited by 1
“Cytogenetic alterations were detected in 7.4% of ASD (Vorstman et al., 2006), and some of them have been suggested as causative factors of neurodevelopmental disorders (Merikangas et al., 2009).”
BackgroundInfluentialBarnand, G., & Monaco, A. J. (2007) · Cambridge University Press eBooks · doi:10.1017/cbo9780511543555.032 · Cited by 1
Milovančević, M., Vesic, M., Jelisavcic, M., Nikšić, S., Radivojevic-Pilic, G., & Mandić-Maravić, V. (2012) · Srpski arhiv za celokupno lekarstvo · doi:10.2298/sarh1212760p · Cited by 1
Autism and X-linked hypophosphatemia: A possible association?
Joel, V., Hellemans, H., & Deboutte, D. (2010) · Indian journal of human genetics · doi:10.4103/0971-6866.64937 · Cited by 1
As Perturbações do Espectro do Autismo – Avanços da Biologia Molecular
Ribeiro, I. P., Freitas, M. M., & Teles, N. O. (2017) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) · doi:10.25753/birthgrowthmj.v22.i1.12894 · Cited by 1
Curran, S. R., & Bolton, P. (2009) · Springer eBooks · doi:10.1007/978-0-387-76727-7_27 · Cited by 1
“Another approach has been to study genes disrupted in the cases of autism with rare co-occurring cytogenetic abnormalities (Castermans, Wilquet, Parthoens et al., 2003; Vorstman et al., 2006).”
Chromosomal Abnormalities and Putative Susceptibility Genes in Autism Spectrum Disorders
Gilling, M. (2015) · Cited by 1
Research Progress on Autism Spectrum Disorders and Current Situations in Western China
Yang, H., Mao, M., Zhang, L., WenXu, Y. A. N. G., & JiaZhi, Q. U. (2015) · Scientia Sinica Vitae · doi:10.1360/052010-363 · Cited by 1
A case of Nablus mask-like facial syndrome with autism spectrum disorders
Akaltun, İ., & Kara, T. (2018) · Psychiatric Genetics · doi:10.1097/ypg.0000000000000198 · Cited by 1
“Chromosomal anomalies such as deletion, duplication, inversion or translocation are estimated to be capable of detection in ∼ 3% of ASDs (Vorstman et al., 2006).”
BackgroundCoexistence of Autism and Ring Chromosome 22
Sizer, E., Yüksel, T., & Oral, D. (2019) · Eastern Journal Of Medicine · doi:10.5505/ejm.2019.52714 · Cited by 1
Bolivar, V. J. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781107360556.012 · Cited by 1
Prevalence of Autism Spectrum Disorder (ASD) in Offspring’s of Consanguineous Marriages
Yousuf, F., Asif, A., qui, S., Husain, S., & Rafiq, R. (2023) · Journal of BioMed Research and Reports · doi:10.59657/2837-4681.brs.23.014 · Cited by 1
Brusco, A., & Ferrero, G. B. (2019) · Springer eBooks · doi:10.1007/978-3-030-26276-1_2 · Cited by 2
Specific Functions of ERK/MAPK Signaling in Brain Development and Neurocognition
Holter, M. C. (2019) · Cited by 1
Genetic heterogeneity in autism spectrum disorders in a population isolate
Rehnström, K. (2009) · Työväentutkimus Vuosikirja · Cited by 1
Transtornos do espectro autista: progredindo para melhorias em sua farmacoterapia
Suzuki, Â. M. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.41.2013.tde-26072013-144026 · Cited by 1
A posterior probability of linkage & association study of 111 autism candidate genes
Chen, F. (2009) · Rutgers University Community Repository (Rutgers University) · doi:10.7282/t3bp030b · Cited by 1
Estudos de comorbidades e dos aspectos genéticos de pacientes com transtorno do espectro autista
Moreira, D. D. P. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.41.2012.tde-15102012-101307 · Cited by 1
Comparative Genomic Hybridization in the Study of Human Disease
Cheung, S. W., & Pursley, A. N. (2011) · Wiley eBooks · doi:10.1002/9780470015902.a0005955.pub2 · Cited by 1
CHARACTERIZATION AND TREATMENT OF A NOVEL MOUSE MODEL OF TSC-ASSOCIATED AUTISM
Reith, R. M. (2012) · Digital Commons-TMC (Texas Medical Center)
Identificação de genes e vias associadas aos transtornos do espectro autista
Oliveira, K. G. (2011) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2011.tde-23092011-162004
Rivera, C. C. (2007) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Yang, S.-Y., Yim, S., Hu, H., Kim, S.-A., Yoo, H., & Chung, Y. (2010) · Genomics & Informatics · doi:10.5808/gi.2010.8.2.076
“4% of ASDs (Vorstman et al., 2006), and some alterations have been suggested as causative factors of neurodevelopmental disorders (Merikangas et al.”
BackgroundInfluentialExpression Analysis of the Imprinted Gene Transketolase-like 1 in Mouse and Human
Friss, A. F. (2011) · OpenCommons - UConn (University of Connecticut)
Woo, J.-H., Yang, S., Yim, S., Hu, H., Shin, M.-J., Oh, E.-H., Kang, H., Park, S.-Y., & Chung, Y. (2010) · Genomics & Informatics · doi:10.5808/gi.2010.8.1.019
“…a ASD-specific BAC array named ‘MacArray Karyo Autism Prototype’ which covers a total of 27 CNV regions that have been reported to be asso- ciated with autism in previous studies including ours (Cho et al., 2009; Klauck, 2006; Schellenberg et al., 2006; Sultana et al., 2002; Vorstman et al., 2006).”
InfluentialKim, J. Y., Park, T. J., Lee, J.-S., Chun, J.-Y., Bae, J., Park, B., Cheong, H.-S., Lee, H., Kim, Y. J., & Shin, H.-D. (2010) · Genomics & Informatics · doi:10.5808/gi.2010.8.1.001
Social dysfunction and mental retardation
Pietropaolo, S., Sluyter, F., & Crusio, W. E. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781107360556.010
Genetic Basis and Neural Mechanism of Autism Spectrum Disorder*
Li, J., Zhu-Mei, L. I. N., & Zhu, L. (2012) · PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS · doi:10.3724/sp.j.1206.2011.00519
Le-Niculescu, H., Balaraman, Y., Patel, S. D., Tan, J., Paulus, M. P., Kuczenski, R. T., Niculescu, A. B., McFarland, M. J., Ca, O., Za, R., et al. (2008)
Ibrahim‐Verbaas, C. A., Schuur, M., Swieten, J. C. V., Zorkoltseva, I. V., Axenovich, T. I., van Duijn, C. M., Breteler, M. M. B., Ikram, M. A., & Verbeek, M. M. (2012)
Cytogenetic and fragile X testing in a group of Romanian autistic children.
Dronca, E., Militaru, M., Ciumărnean, L., & Pop, I. V. (2015)
A 15q11–q13 Duplication Mouse Model of Autism Spectrum Disorders
Takumi, T., Fukumoto, K., & Nomura, J. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-391924-3.00029-6
A mouse model of 15q duplication towards understanding of the pathophysiology of autism
Nakanishi, M., & 内匠, 透. (2012) · doi:10.11249/jsbpjjpp.23.4_267
Characterization of Ambra1 heterozygous mice as genetic mouse model of female-specific autism
Ju, A. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6476
Etiological Investigation of Autism Spectrum Disorders – State of The Art
Gonçalves, D., Guardiano, M., & Leão, M. (2017) · Scientific Repository of Open Access of Portugal (RCAAP) · doi:10.25753/birthgrowthmj.v27.i3.12106
Association Between HLA-B Polymorphisms and Autism Spectrum Disorder in Chinese Population
Kang, G., Kang, Q., Zhu, X., Li, R., Zhang, S., Sun, Y., Zhang, M., Chen, X., Wang, Y., Jiang, H., et al. (2020) · Iranian Journal of Pediatrics · doi:10.5812/ijp.90110
“These related genes are distributed in multiple regions, including 7th, 15th, 17th, and 22nd X chromosomes (9).”
BackgroundSCREENING PROTOCOL FOR SIGNS OF AUTISTIC SPECTRUM DISORDER FOR BABIES
SARAH Network of Neurorehabilitation (Brazil), Alcântara, C., Melo, L., & SARAH Network of Neurorehabilitation (Brazil) (2020) · Psychological applications and trends · doi:10.36315/2020inpact003
Brain organoids as a model system for human neurodevelopment in health and disease
Reiner, O., & Karzbrun, E. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00010-2
Buitelaar, J. K. (2008) · Bohn Stafleu van Loghum eBooks · doi:10.1007/978-90-313-6632-3_16
Diagnosis and Epidemiology of Pediatric Psychiatric Disorders
Robinson, E., Neale, B. M., & Daly, M. J. (2017) · Oxford University Press eBooks · doi:10.1093/med/9780190681425.003.0058
Genetics and Epigenetics of ASD
Mojarad, B. A., Qaiser, F., & Yuen, R. K. C. (2023) · Springer eBooks · doi:10.1007/978-3-031-20792-1_18 · Cited by 2
Costa, C. I. S. (2024) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2024.tde-22082024-180122
Oxytocin and Vasopressin in Autism and Genetic Syndromes
Levin‐Decanini, T., Francis, S. M., Sagar, A., Liu, W., Carter, C. S., & Jacob, S. (2015) · Contemporary clinical neuroscience · doi:10.1007/978-1-4939-2190-4_14
“A subset of the chromosomal region associated with PWS is also associated with an increased risk for ASD, as maternally inherited duplications of the 15q11-13 region are associated with 1–3 % of ASD cases (Bolton et al. 2001; Cook et al. 1997; Vorstman et al. 2006).”
BackgroundSaitovitch, A. (2014) · theses.fr (ABES) · doi:10.70675/ddd5f246z0fe4z4134z8a28z27d0a24aed40
Déterminants moteurs des troubles du spectre autistiques (TSA)
Sagheer, T. A. (2017) · theses.fr (ABES) · doi:10.70675/c5eec78az159az4adcz8f56ze9a4ebc82422
“…studies have suggested that patients with ASD almost always show a greater variability in stride length (Rinehart et al., 2006; Hallet et al., 1993, Vilensky et al., 1981), decreased step length (Verrnazza et al., 2005), as well as deficits in upper body movements (Vernazza et al., 2005; Vilensky…”
BackgroundInfluentialEstudo citogenético, regiões 2q37e 22q13.3 e condições médicas em doenças do espectro autístico
Gonçalves, A. B. (2010) · doi:10.5016/dt000624387
“After approval of the Ethics Committee, written informed consent was obtained from the 20 individuals with ASDs according to the criteria of the DSM-IV. These subjects attend the Municipal School of Autism in São José do Rio Preto ―Maria Lúcia de Oliveira‖, AMA in Ribeirão Preto and other specialized schools and clini…”
BackgroundFunction and structure of the mirror neuron system in autism
Perkins, T. J. (2014)
Metadata
- Authors
- Vorstman, J. A. S., Staal, W. G., van Daalen, E., van Engeland, H., Hochstenbach, P. F. R., & Franke, L.
- Affiliations
- Utrecht University (NL)
- University Medical Center Utrecht (NL)
- Corresponding author
- Vorstman, J A S
- Venue
- Molecular Psychiatry
- Published
- 2005-10-04
- Volume
- 11
- Issue
- 1
- Pages
- 18-28
- ISSN
- 1359-4184 (ISSN-L)
- 1476-5578
- OpenAlex
- W2134175099
- Cited by
- 353
- References
- 103
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 5 · 2023: 3 · 2022: 4 · 2021: 4 · 2020: 9 · 2019: 15 · 2018: 10 · 2017: 20 · 2016: 11 · 2015: 17 · 2014: 18 · 2013: 21 · 2012: 27
- FWCI
- 14.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Molecular Psychiatry (publishedVersion)
- University of Groningen research database (University of Groningen / Centre for Information Technology) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Autism Spectrum Disorder Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- autism spectrum disorder, chromosomal abnormalities, candidate genomic regions, chromosome 15q11-q13, chromosome 22q11.2, chromosome 2q37, chromosome 17p11.2, segmental duplication
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