The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Female with autistic disorder and monosomy X (Turner syndrome): Parent-of-origin effect of the X chromosome
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“with an increased rate of ASD diagnosis in Turner syndrome (TS, XO, ~3% ASD) [52,53,54], Klinefelter syndrome (KS, XXY, ~10% ASD) [55,56*], and 47,XYY syndrome (~20% ASD), but no increased rate in X chromosome trisomy [57,58**].”
From Sex differences in autism spectrum disorders (2013) · cites this paper as [52]
In the citing paper
“in patients with MDD, there appears to be no general association between the disease and this SNP (Desan et al., 2000).”
From Circadian genes, rhythms and the biology of mood disorders (2007) · cites this paper as Desan et al., 2000
Citations
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Mutagenesis and Mapping of a Mouse Gene, Clock , Essential for Circadian Behavior
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Cited by
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Behavioral phenotypes of impulsivity related to the ANKK1 gene are independent of an acute stressor
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Drechsler, R., Rizzo, P., & Steinhausen, H.-C. (2010) · Child Neuropsychology · doi:10.1080/09297040903190774 · Cited by 56
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From Disordered Eating to Addiction: The “Food Drug” in Bulimia Nervosa
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Martin, N. C., Levy, F., Pieka, J., & Hay, D. A. (2006) · International Journal of Disability, Development and Education · doi:10.1080/10349120500509992 · Cited by 52
NPAS2 Regulation of Anxiety-Like Behavior and GABAA Receptors
Ozburn, A. R., Kern, J., Parekh, P. K., Logan, R. W., Liu, Z., Falcon, E., Becker-Krail, D., Purohit, K., Edgar, N. M., Huang, Y., et al. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00360 · Cited by 49
Lin, A. E., Prakash, S. K., Andersen, N. H., Viuff, M. H., Levitsky, L. L., Rivera‐Davila, M., Crenshaw, M. L., Hansen, L., Colvin, M. K., Hayes, F. J., et al. (2019) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.61310 · Cited by 50
Time Perception: Does It Distinguish ADHD and RD Children in a Clinical Sample?
McGee, R., Brodeur, D., Symons, D., Andrade, B., & Fahie, C. (2004) · Journal of Abnormal Child Psychology · doi:10.1023/b:jacp.0000037778.61929.1b · Cited by 47
Pálmason, H., Moser, D., Sigmund, J., Vogler, C., Hänig, S., Schneider, A., Seitz, C., Marcus, A., Meyer, J., & Freitag, C. M. (2010) · Journal of Neural Transmission · doi:10.1007/s00702-009-0338-2 · Cited by 44
Wong, J., Duncan, C. E., Beveridge, N. J., Webster, M. J., Cairns, M. J., & Shannon Weickert, C. (2013) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr177 · Cited by 43
Bonvicini, C., Faraone, S. V., & Scassellati, C. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.128 · Cited by 42
Pan, Y.-Q., Qiao, L., Xue, X.-D., & Fu, J.-H. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.01.076 · Cited by 41
Nievergelt, C. M., Kripke, D. F., Remick, R. A., Sadovnick, A. D., McElroy, S. L., Keck, P. E., & Kelsoe, J. R. (2005) · Psychiatric Genetics · doi:10.1097/00041444-200503000-00008 · Cited by 38
Drechsler, R., Rizzo, P., & Steinhausen, H.-C. (2009) · Kindheit und Entwicklung · doi:10.1026/0942-5403.18.3.153 · Cited by 36
Gizer, I. R., & Waldman, I. D. (2012) · Journal of Abnormal Psychology · doi:10.1037/a0028225 · Cited by 36
Sethi, A., Voon, V., Critchley, H. D., Cercignani, M., & Harrison, N. A. (2018) · Brain · doi:10.1093/brain/awy048 · Cited by 36
DRD4 genotype moderates the impact of parental problems on unresolved loss or trauma
Bakermans-Kranenburg, M. J., van IJzendoorn, M. H., Caspers, K., & Philibert, R. (2011) · Attachment & Human Development · doi:10.1080/14616734.2011.562415 · Cited by 34
Williams, B. R., Strauss, E. H., Hultsch, D. F., Hunter, M. A., & Tannock, R. (2007) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803390600678020 · Cited by 34
Pennington, B. F., Willcutt, E., & Rhee, S. H. (2005) · Advances in Child Development and Behavior · doi:10.1016/s0065-2407(05)80010-2 · Cited by 31
Self-citationLasky-Su, J., Banaschewski, T., Buitelaar, J., Franke, B., Brookes, K., Sonuga-Barke, E., Ebstein, R., Eisenberg, J., Gill, M., Manor, I., et al. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.03.006 · Cited by 29
Astrocytic transporters in Alzheimer's disease
Ugbode, C., Hu, Y., Whalley, B., Peers, C., Rattray, M., & Dallas, M. L. (2017) · Biochemical Journal · doi:10.1042/bcj20160505 · Cited by 25
Association study of catechol-O-methyltransferase gene polymorphism in Korean male alcoholics
Kweon, Y.-S., Lee, H. K., Lee, C. T., & Pae, C.-U. (2005) · Psychiatric Genetics · doi:10.1097/00041444-200506000-00014 · Cited by 23
Genetic Variants and Early Cigarette Smoking and Nicotine Dependence Phenotypes in Adolescents
O'Loughlin, J., Sylvestre, M.-P., Labbe, A., Low, N. C., Roy-Gagnon, M.-H., Dugas, E. N., Karp, I., & Engert, J. C. (2014) · PLoS ONE · doi:10.1371/journal.pone.0115716 · Cited by 21
Kaya, Z., Caglayan, S., Akkiprik, M., Aral, C., Ozisik, G., Ozata, M., & Ozer, A. (2016) · Journal of Endocrinological Investigation · doi:10.1007/s40618-015-0409-1 · Cited by 19
Rizzo, P., Steinhausen, H.-C., & Drechsler, R. (2010) · ADHD Attention Deficit and Hyperactivity Disorders · doi:10.1007/s12402-010-0043-x · Cited by 16
Wigal, S. B., Maltas, S., Crinella, F., Stehli, A., Steinhoff, K., Lakes, K., & Schuck, S. (2012) · Journal of Attention Disorders · doi:10.1177/1087054710378008 · Cited by 14
Metadata
- Authors
- Donnelly, S. L., Wolpert, C. M., Menold, M. M., Bass, M. P., Gilbert, J. R., Cuccaro, M. L., Delong, G. R., & Pericak-Vance, M. A.
- Venue
- American Journal of Medical Genetics
- Published
- 2000
- References
- 49
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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.
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