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
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
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
Williams, J. B. W., & First, M. B. (2013) · Oxford University Press eBooks · doi:10.1093/acrefore/9780199975839.013.104 · Cited by 109,845
Lord, C., Rutter, M., & Le Couteur, A. (1994) · Journal of Autism and Developmental Disorders · doi:10.1007/bf02172145 · Cited by 9,065
Lord, C., Risi, S., Lambrecht, L., Cook, E. H., Leventhal, B. L., DiLavore, P. C., Pickles, A., & Rutter, M. (2000) · Journal of Autism and Developmental Disorders · doi:10.1023/a:1005592401947 · Cited by 7,520
The Future of Genetic Studies of Complex Human Diseases
Risch, N., & Merikangas, K. (1996) · Science · doi:10.1126/science.273.5281.1516 · Cited by 5,355
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
Lander, E. S., & Kruglyak, L. (1995) · Nature Genetics · doi:10.1038/ng1195-241 · Cited by 5,236
Finishing the euchromatic sequence of the human genome
International Human Genome Sequencing Consortium (2004) · Nature · doi:10.1038/nature03001 · Cited by 4,971
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
Bailey, A., Le Couteur, A., Gottesman, I., Bolton, P., Simonoff, E., Yuzda, E., & Rutter, M. (1995) · Psychological Medicine · doi:10.1017/s0033291700028099 · Cited by 2,461
Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS)
Schopler, E., Reichler, R. J., DeVellis, R. F., & Daly, K. (1980) · Journal of Autism and Developmental Disorders · doi:10.1007/bf02408436 · Cited by 2,432
Pinkel, D., Segraves, R., Sudar, D., Clark, S. M., Poole, I., Kowbel, D., Collins, C. C., Kuo, W.-L., Chen, C., Zhai, Y., et al. (1998) · Nature Genetics · doi:10.1038/2524 · Cited by 2,238
Prevalence of Autism in a US Metropolitan Area
Yeargin-Allsopp, M., Rice, C., Karapurkar, T., Doernberg, N., Boyle, C., & Murphy, C. (2003) · JAMA · doi:10.1001/jama.289.1.49 · Cited by 1,248
Genetic analysis of genome-wide variation in human gene expression
Morley, M. P., Molony, C. M., Weber, T. M., Devlin, J. L., Ewens, K. G., Spielman, R. S., & Cheung, V. G. (2004) · Nature · doi:10.1038/nature02797 · Cited by 1,212
Ryan, A. K., Goodship, J. A., Wilson, D. I., Philip, N., Levy, A., Seidel, H., Schuffenhauer, S., Oechsler, H., Belohradsky, B. H., Prieur, M., et al. (1997) · Journal of Medical Genetics · doi:10.1136/jmg.34.10.798 · Cited by 1,192
Pervasive Developmental Disorders in preschool children
Chakrabarti, S. (2001) · JAMA · doi:10.1001/jama.285.24.3093 · Cited by 1,132
High rates of schizophrenia in adults with velo-cardio-facial syndrome
Murphy, K. C., Jones, L. A., & Owen, M. J. (1999) · Archives of General Psychiatry · doi:10.1001/archpsyc.56.10.940 · Cited by 1,024
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
Solinas‐Toldo, S., Lampel, S., Stilgenbauer, S., Nickolenko, J., Benner, A., Döhner, H., Cremer, T. J., & Lichter, P. (1997) · Genes Chromosomes and Cancer · doi:10.1002/(sici)1098-2264(199712)20:4 · Cited by 1,002
The epidemiology of autism: a review
FOMBONNE, E. (1999) · Psychological Medicine · doi:10.1017/s0033291799008508 · Cited by 981
Genetics of austim: complex aetiology for a heterogeneous disorder
Folstein, S. E., & Rosen-Sheidley, B. (2001) · Nature Reviews Genetics · doi:10.1038/35103559 · Cited by 771
A population-based study of measles, mumps, and rubella vaccination and autism.
Madsen, K. M., Hviid, A., Vestergaard, M., Schendel, D., Wohlfahrt, J., Thorsen, P., Olsen, J., & Melbye, M. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa021134 · Cited by 710
Fombonne, E. (2003) · JAMA · doi:10.1001/jama.289.1.87 · Cited by 604
Shaikh, T. H. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.4.489 · Cited by 531
CONCEPTS OF AUTISM: A REVIEW OF RESEARCH*
Rutter, M. L. (1968) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.1968.tb02204.x · Cited by 502
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
Biology of the Autistic Syndromes
Coleman, M., & Cillberg, C. (1994) · Pediatric Physical Therapy · doi:10.1097/00001577-199400610-00026 · Cited by 468
A Broader Phenotype of Autism: The Clinical Spectrum in Twins
Couteur, A. S. L., Bailey, A. J., Goode, S., Pickles, A. R., Gottesman, I. I., Robertson, S., & Rutter, M. L. (1996) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.1996.tb01475.x · Cited by 457
AUTISM IN THALIDOMIDE EMBRYOPATHY: A POPULATION STUDY
Strömland, K., Nordin, V., Miller, M. T., Åkerström, B., & Gillberg, C. (1994) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.1994.tb11856.x · Cited by 453
A Genomewide Screen for Autism: Strong Evidence for Linkage to Chromosomes 2q, 7q, and 16p
(2001) · The American Journal of Human Genetics · doi:10.1086/323264 · Cited by 453
Lucito, R., Healy, J., Alexander, J., Reiner, A., Esposito, D., Chi, M., Rodgers, L., Brady, A., Sebat, J., Troge, J., et al. (2003) · Genome Research · doi:10.1101/gr.1349003 · Cited by 445
The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
McDonald‐McGinn, D. M., Kirschner, R. E., Goldmuntz, E., Sullivan, K. E., Eicher, P. S., Gerdes, M., Moss, E., Solot, C. B., Wang, P., Jacobs, I. N., et al. (1999) · PubMed · Cited by 435
Fetal valproate syndrome and autism: additional evidence of an association
Williams, G., King, J. O., Cunningham, M. L., Stephan, M., Kerr, B. A., & Hersh, J. H. (2001) · Developmental Medicine & Child Neurology · doi:10.1017/s001216220100038x · Cited by 431
Evidence of linkage between the serotonin transporter and autistic disorder
Cook, E., Yeung-Courchesne, R., Lord, C., Cox, N. J., Yan, S., Lincoln, A. J., Haas, R., Courchesne, E., & LEVENTHAL, B. L. (1997) · Molecular Psychiatry · doi:10.1038/sj.mp.4000266 · Cited by 426
Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives
Pulver, A. E., Nestadt, G., Goldberg, R. B., Shprintzen, R. J., Lamacz, M., Wolyniec, P. S., Morrow, B. E., Karayiorgou, M., Antonarakis, S. E., Housman, D. E., et al. (1994) · The Journal of Nervous and Mental Disease · doi:10.1097/00005053-199408000-00010 · Cited by 421
Pickles, A. R., Bolton, P., Macdonald, H., Bailey, A., Couteur, A. S. L., Sim, C. H., & Rutter, M. L. (1995) · Europe PMC (PubMed Central) · Cited by 388
Position effect in human genetic disease
Kleinjan, D. A. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.10.1611 · Cited by 370
Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
Cook, E. H., Courchesne, R. Y., Cox, N. J., Lord, C., Gonen, D., Guter, S. J., Lincoln, A., Nix, K., Haas, R., Leventhal, B. L., et al. (1998) · The American Journal of Human Genetics · doi:10.1086/301832 · Cited by 369
Taylor, B. (2002) · BMJ · doi:10.1136/bmj.324.7334.393 · Cited by 345
Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder
Persico, A. M., D'Agruma, L., Maiorano, N., Totaro, A., Militerni, R., Bravaccio, C., Wassink, T. H., Schneider, C., Melmed, R., Trillo, S., et al. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000850 · Cited by 337
Structure of Chromosomal Duplicons and their Role in Mediating Human Genomic DisordersPreprint
Ji, Y., Eichler, E. E., Schwartz, S., & Nicholls, R. D. (2000) · Genome Research · doi:10.1101/gr.10.5.597 · Cited by 327
Association between a GABRB3 polymorphism and autism
Buxbaum, J. D., Silverman, J. M., Smith, C. J. W., Greenberg, D. A., Kilifarski, M., Reichert, J. G., Cook, E. H., Fang, Y., Song, C.-Y., & Vitale, R. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001011 · Cited by 322
Segmental duplications: an 'expanding' role in genomic instability and disease
Emanuel, B. S., & Shaikh, T. H. (2001) · Nature Reviews Genetics · doi:10.1038/35093500 · Cited by 303
AUTISM AS A PARADIGMATIC COMPLEX GENETIC DISORDER
Veenstra-VanderWeele, J. M., Christian, S. L., & Cook, E. H. (2004) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.5.061903.180050 · Cited by 282
Christian, S. L. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.6.1025 · Cited by 272
Serotonin transporter (5-HTT) gene variants associated with autism?
Klauck, S. M. (1997) · Human Molecular Genetics · doi:10.1093/hmg/6.13.2233 · Cited by 259
Auranen, M., Vanhala, R., Varilo, T., Ayers, K. L., Kempas, E., Ylisaukko‐oja, T., Sinsheimer, J. S., Peltonen, L., & Järvelä, I. E. (2002) · The American Journal of Human Genetics · doi:10.1086/342720 · Cited by 241
Chromosomal disorders and autism
Gillberg, C. (1998) · Journal of Autism and Developmental Disorders · doi:10.1023/a:1026004505764 · Cited by 237
Juul-Dam, N., Townsend, J., & Courchesne, E. (2001) · PEDIATRICS · doi:10.1542/peds.107.4.e63 · Cited by 232
Epidemiological trends in rates of autism
Fombonne, E. J. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001162 · Cited by 231
Molecular genetics of autism spectrum disorder
Veenstra-VanderWeele, J. M., & Cook, E. H. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001505 · Cited by 224
Cytogenetic abnormalities and fragile-x syndrome in Autism Spectrum Disorder
Reddy, K. S. (2005) · BMC Medical Genetics · doi:10.1186/1471-2350-6-3 · Cited by 222
Gribble, S. M., Prigmore, E., Burford, D. C., Porter, K. M., Ng, B. L., Douglas, E. J., Fiegler, H., Carr, P., Kalaitzopoulos, D., Clegg, S., et al. (2005) · Journal of Medical Genetics · doi:10.1136/jmg.2004.024141 · Cited by 217
Human Chromosome 7: DNA Sequence and Biology
Scherer, S. W., Cheung, J., MacDonald, J. R., Osborne, L. R., Nakabayashi, K., Herbrick, J.-A., Carson, A. R., Parker-Katiraee, L., Skaug, J., Khaja, R., et al. (2003) · Science · doi:10.1126/science.1083423 · Cited by 215
Pfeifer, D., Kist, R., Dewar, K., Devon, K. L., Lander, E. S., Birren, B. W., Korniszewski, L., Back, E., & Scherer, G. (1999) · The American Journal of Human Genetics · doi:10.1086/302455 · Cited by 213
Evidence supporting WNT2 as an autism susceptibility gene
Wassink, T. H., Piven, J., Vieland, V. J., Huang, J., Swiderski, R. E., Pietila, J., Braun, T. A., Beck, G. E., Folstein, S. E., Haines, J. L., et al. (2001) · American Journal of Medical Genetics · doi:10.1002/ajmg.1401 · Cited by 208
Analysis of the RELN gene as a genetic risk factor for autism
Skaar, D. A., Shao, Y., Haines, J. L., Stenger, J. E., Jaworski, J. M., Martin, E. R., DeLong, G. R., Moore, J. H., McCauley, J. L., Sutcliffe, J. S., et al. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001614 · Cited by 204
Role of the serotonin transporter gene in the behavioral expression of autism
Tordjman, S., Gutknecht, L., Carlier, M., Spitz, E., Antoine, C., Slama, F., Carsalade, V, Cohen, D. J., Ferrari, P., Roubertoux, P. L., et al. (2001) · Molecular Psychiatry · doi:10.1038/sj.mp.4000873 · Cited by 196
Velagaleti, G. V. N., Bien-Willner, G. A., Northup, J. K., Lockhart, L. H., Hawkins, J. C., Jalal, S. M., Withers, M. A., Lupski, J. R., & Stankiewicz, P. (2005) · The American Journal of Human Genetics · doi:10.1086/429252 · Cited by 183
Association Analysis of Chromosome 15 GABAAReceptor Subunit Genes in Autistic Disorder
Menold, M. M., Shao, Y., Wolpert, C. M., Donnelly, S. L., Raiford, K. L., Martin, E. R., Ravan, S. A., Abramson, R. K., Wright, H. H., DeLong, G. R., et al. (2001) · Journal of Neurogenetics · doi:10.3109/01677060109167380 · Cited by 181
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q
International Molecular Genetic Study of Autism Consortium (2001) · Human Molecular Genetics · doi:10.1093/hmg/10.9.973 · Cited by 176
Evidence for an association with the serotonin transporter promoter region polymorphism and autism
Yirmiya, N., Pilowsky, T., Nemanov, L., Arbelle, S., Feinsilver, T., Fried, I., & Ebstein, R. P. (2001) · American Journal of Medical Genetics · doi:10.1002/ajmg.1365 · Cited by 171
Reelin gene alleles and susceptibility to autism spectrum disorders
Zhang, H., Liu, X., Zhang, C., Mundo, E., Macciardi, F. M., Grayson, D. R., Guidotti, A. R., & Holden, J. J. A. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001124 · Cited by 168
Psychiatric Disorders of Children With Congenital Rubella
Schwartz, A. H. (1972) · JAMA · doi:10.1001/jama.1972.03200150063038 · Cited by 163
Neuropsychiatric disorders in the 22q11 deletion syndrome
Niklasson, L., Rasmussen, P., Óskarsdóttir, S., & Gillberg, C. (2001) · Genetics in Medicine · doi:10.1097/00125817-200101000-00017 · Cited by 160
Linkage Disequilibrium at the Angelman Syndrome Gene UBE3A in Autism Families
Nurmi, E. L., Bradford, Y., Chen, Y.-H., Hall, J. L., Arnone, B., Gardiner, M., Hutcheson, H. B., Gilbert, J. R., Pericak‐Vance, M. A., Copeland‐Yates, S. A., et al. (2001) · Genomics · doi:10.1006/geno.2001.6617 · Cited by 157
Kim, S.-J., Cox, N. J., Yeung-Courchesne, R., Lord, C., Corsello, C. M., Akshoomoff, N., Guter, S. J., LEVENTHAL, B. L., Courchesne, E., & Cook, E. H. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001033 · Cited by 152
Psychiatric disorders of children with congenital rubella
Chess, S., KORN, S. J., & Fernandez, P. (1971) · Medical Entomology and Zoology · Cited by 150
Buxbaum, J. D., Silverman, J. M., Keddache, M. A., Smith, C. J. W., Hollander, E., Ramoz, N., & Reichert, J. G. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001465 · Cited by 143
Analysis of reelin as a candidate gene for autism
Bonora, E., Beyer, K. S., Lamb, J. A., Parr, J. R., Klauck, S. M., Benner, A., Paolucci, M., Abbott, A., Ragoussis, J., Poustka, A., et al. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001310 · Cited by 132
The role of mercury in the pathogenesis of autism
Bernard, S., Enayati, A., Roger, H., Binstock, T., & Redwood, L. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001177 · Cited by 124
Molecular karyotyping using an SNP array for genomewide genotyping
Rauch, A. M., Rüschendorf, F., Huang, J., Trautmann, U., Becker, C., Thiel, C. T., Jones, K. W., Reis, A., & Nürnberg, P. (2004) · Journal of Medical Genetics · doi:10.1136/jmg.2004.022855 · Cited by 122
Prevalence of pervasive developmental disorders in children and adolescents with mental retardation
de Bildt, A. A., Sytema, S., Kraijer, D. W., & Minderaa, R. B. (2004) · Journal of Child Psychology and Psychiatry · doi:10.1111/j.1469-7610.2004.00346.x · Cited by 113
Serajee, F., Zhong, H., Nabi, R., & Huq, A. H. M. M. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.4.e42 · Cited by 109
Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons
Pujana, M. Á., Nadal, M., Guitart, M., Armengol, L., Gratacòs, M., & Estivill, X. (2002) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5200760 · Cited by 106
Serotonin transporter gene and autism: a haplotype analysis in an Irish autistic population
Conroy, J., Meally, E., Kearney, G., Fitzgerald, M., Gill, M., & Gallagher, L. (2004) · Molecular Psychiatry · doi:10.1038/sj.mp.4001459 · Cited by 105
Krebs, M., Betancur, C., Leroy, S., Bourdel, M., Gillberg, C., & Leboyer, M. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4001071 · Cited by 103
Lauritsen, M. B., Mors, O. N., Mortensen, P. B., & Ewald, H. (1999) · Journal of Child Psychology and Psychiatry · doi:10.1111/1469-7610.00451 · Cited by 99
Pregnancy and Birth Complications in Autism and Liability to the Broader Autism Phenotype
Zwaigenbaum, L., Szatmári, P., Jones, M. B., Bryson, S. E., MacLean, J. E., Mahoney, W. J., Bartolucci, G., & TUFF, L. (2002) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1097/00004583-200205000-00015 · Cited by 96
The biology of the autistic syndromes
Desombre, H. (2001) · Archives de Pédiatrie · doi:10.1016/s0929-693x(00)00234-7 · Cited by 94
Association between the FOXP2 gene and autistic disorder in Chinese population
Gong, X., Jia, M., Ruan, Y., Mei, S., Liu, J., Wu, S., Guo, Y., Yang, J., Ling, Y., Yang, X., et al. (2004) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.20162 · Cited by 89
The Biology of the Autistic Syndromes, 3rd Edition
Castelli, F. (2001) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.70.1.138k · Cited by 87
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q
Bonora, E., Lamb, J. A., Barnby, G., Sykes, N., Moberly, T., Beyer, K. S., Klauck, S. M., Poustka, F., Bacchelli, E., Blasi, F., et al. (2004) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201315 · Cited by 86
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network
Devlin, B., Bennett, P. J., Dawson, G., Figlewicz, D. A., Grigorenko, E. L., McMahon, W., Minshew, N. J., Pauls, D. L., Smith, M., Spence, M. A., et al. (2004) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.20125 · Cited by 85
Nurmi, E. L., Amin, T. T., Olson, L. M., Jacobs, M. M., McCauley, J. L., Lam, A. Y., Organ, E. L., Folstein, S. E., Haines, J. L., & Sutcliffe, J. S. (2003) · Molecular Psychiatry · doi:10.1038/sj.mp.4001283 · Cited by 74
Examination of NRCAM, LRRN3, KIAA0716, and LAMB1as autism candidate genes
Hutcheson, H. B., Olson, L. M., Bradford, Y., Folstein, S. E., Santangelo, S. L., Sutcliffe, J. S., & Haines, J. L. (2004) · BMC Medical Genetics · doi:10.1186/1471-2350-5-12 · Cited by 66
Presence of Large Deletions in Kindreds with Autism
Yu, C., Dawson, G., MUNSON, J. A., D’Souza, I., Osterling, J., Estes, A. M., Leutenegger, A., Flodman, P. L., Smith, M., Raskind, W. H., et al. (2002) · The American Journal of Human Genetics · doi:10.1086/341291 · Cited by 65
Neurogenomics: at the intersection of neurobiology and genome sciences
Boguski, M. S., & Jones, A. R. (2004) · Nature Neuroscience · doi:10.1038/nn1232 · Cited by 64
Serajee, F., Nabi, R., Zhong, H., & Huq, A. H. M. M. (2003) · Journal of Medical Genetics · doi:10.1136/jmg.40.11.e119 · Cited by 60
Nordin, V., & Gillberg, C. (1996) · Developmental Medicine & Child Neurology · doi:10.1111/j.1469-8749.1996.tb12097.x · Cited by 56
Chromosomal Anomalies in Individuals with Autism
Castermans, D., Wilquet, V., Steyaert, J. G., de Ven, W. V., Fryns, J., & Devriendt, K. (2004) · Autism · doi:10.1177/1362361304042719 · Cited by 46
Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder
Vourc’h, P., Martin, I., Bonnet‐Brilhault, F., Marouillat, S., Barth�l�my, C., Müh, J. P., & Andres, C. R. (2003) · Psychiatric Genetics · doi:10.1097/00041444-200312000-00005 · Cited by 32
Deb, S. S., Prasad, K. B. G., -, H. S., & Eagles, J. (1997) · Journal of Intellectual Disability Research · doi:10.1111/j.1365-2788.1997.tb00680.x · Cited by 32
Genetic tests of biologic systems in affective disorders
Hattori, E., Liu, C., Zhu, H., & Gershon, E. S. (2005) · Molecular Psychiatry · doi:10.1038/sj.mp.4001695 · Cited by 31
Evaluation of linkage of markers on chromosome 6p with schizophrenia in Taiwanese families
Hwu, H., Lin, M., Lee, P.-C., Lee, S. F. ‐., Ouyang, W., & Liu, C. (2000) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(20000207)96:1 · Cited by 30
Souery, D., Lipp, O., Rivelli, S. K., Massat, I., Serretti, A., Cavallini, M. C., Ackenheil, M., Adolfsson, R., Aschauer, H. N., Blackwood, D., et al. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19991015)88:5 · Cited by 19
RecurrentNF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1)
Buske, A., Gewies, A., Lehmann, R., R�ther, K., Algermissen, B., N�rnberg, P., & Tinschert, S. (1999) · American Journal of Medical Genetics · doi:10.1002/(sici)1096-8628(19991008)86:4 · Cited by 15
Jonnal (2000) · doi:10.1002/1096-8628(20001204)96:6
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
Cited by
Sorted by citations
Strong association of de novo copy number mutations with autism
Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., et al. (2007) · Science · doi:10.1126/science.1138659 · Cited by 2,795
Structural Variation of Chromosomes in Autism Spectrum Disorder
Marshall, C. R., Noor, A., Vincent, J. B., Lionel, A. C., Feuk, L., Skaug, J., Shago, M., Moessner, R., Pinto, D., Ren, Y., et al. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2007.12.009 · Cited by 1,815
“2 (MIM 610883), most likely because we limited our cases to more strictly defined ASD.”
BackgroundInfluentialAdvances in autism genetics: on the threshold of a new neurobiology
Abrahams, B. S., & Geschwind, D. H. (2008) · Nature Reviews Genetics · doi:10.1038/nrg2346 · Cited by 1,866
Durand, C. M., Betancur, C., Boeckers, T. M., Bockmann, J., Chaste, P., Fauchereau, F., Nygren, G., Rastam, M., Gillberg, I. C., Anckarsäter, H., et al. (2007) · Nature Genetics · doi:10.1038/ng1933 · Cited by 1,602
Behavioural phenotyping assays for mouse models of autism
Silverman, J. L., Yang, M., Lord, C., & Crawley, J. N. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2851 · Cited by 1,462
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review