-
1
-
-
23744471663
-
Quantitative genome scan and ordered-subsets analysis of autism endophenotypes support language QTLs
-
doi:10.1038/sj.mp.4001666
-
Alarcon, M., Yonan, A. L., Gilliam, T. C., Cantor, R. M., & Geschwind, D. H. (2005). Quantitative genome scan and ordered-subsets analysis of autism endophenotypes support language QTLs. Molecular Psychiatry, 10, 747-757. doi:10.1038/sj.mp.4001666
-
(2005)
Molecular Psychiatry
, vol.10
, pp. 747-757
-
-
Alarcon, M.1
Yonan, A.L.2
Gilliam, T.C.3
Cantor, R.M.4
Geschwind, D.H.5
-
2
-
-
39949083749
-
Neuroanatomy of autism
-
doi:10.1016/j.tins.2007.12.005
-
Amaral, D. G., Schumann, C. M., & Nordahl, C. W. (2008). Neuroanatomy of autism. Trends in Neuroscience, 31, 137-145. doi:10.1016/j.tins.2007.12.005
-
(2008)
Trends in Neuroscience
, vol.31
, pp. 137-145
-
-
Amaral, D.G.1
Schumann, C.M.2
Nordahl, C.W.3
-
3
-
-
84872904213
-
-
American Psychiatric Association. New proposed changes posted for leading manual of mental disorders. Retrieved March 22, 2010, from
-
American Psychiatric Association. (2010). New proposed changes posted for leading manual of mental disorders. Retrieved March 22, 2010, from http://www.dsm5.org/Pages/Default.aspx
-
(2010)
-
-
-
4
-
-
79851468862
-
Synthetic associations are unlikely to account for many common disease genome-wide association signals
-
doi:10.1371/journal.pbio.1000580
-
Anderson, C. A., Soranzo, N., Zeggini, E., & Barrett, J. C. (2011). Synthetic associations are unlikely to account for many common disease genome-wide association signals. PLoS Biology, 9, e1000580. doi:10.1371/journal.pbio.1000580
-
(2011)
PLoS Biology
, vol.9
-
-
Anderson, C.A.1
Soranzo, N.2
Zeggini, E.3
Barrett, J.C.4
-
5
-
-
77954902187
-
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
-
doi:10.1038/mp.2010.6
-
Arcos-Burgos, M., Jain, M., Acosta, M. T., Shively, S., Stanescu, H., Wallis, D., et al. (2010). A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication. Molecular Psychiatry, 15, 1053-1066. doi:10.1038/mp.2010.6
-
(2010)
Molecular Psychiatry
, vol.15
, pp. 1053-1066
-
-
Arcos-Burgos, M.1
Jain, M.2
Acosta, M.T.3
Shively, S.4
Stanescu, H.5
Wallis, D.6
-
6
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Autism Genome Project Consortium, doi:10.1038/ng1985
-
Autism Genome Project Consortium, Szatmari, P., Paterson, A. D., Zwaigenbaum, L., Roberts, W., Brian, J., et al. (2007). Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics, 39, 319-28. doi:10.1038/ng1985
-
(2007)
Nature Genetics
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
Roberts, W.4
Brian, J.5
-
7
-
-
0028906338
-
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., et al. (1995). Autism as a strongly genetic disorder: Evidence from a British twin study. Psychological Medicine, 25, 63-77.
-
(1995)
Psychological Medicine
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
-
8
-
-
33745818375
-
Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: The Special Needs and Autism Project (SNAP)
-
doi:10.1016/s0140-6736(06)69041-7
-
Baird, G., Simonoff, E., Pickles, A., Chandler, S., Loucas, T., Meldrum, D., et al. (2006). Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: The Special Needs and Autism Project (SNAP). Lancet, 368, 210-215. doi:10.1016/s0140-6736(06)69041-7
-
(2006)
Lancet
, vol.368
, pp. 210-215
-
-
Baird, G.1
Simonoff, E.2
Pickles, A.3
Chandler, S.4
Loucas, T.5
Meldrum, D.6
-
9
-
-
0034659234
-
Distribution and activation of voltage-gated potassium channels in cell-attached and outside-out patches from large layer 5 cortical pyramidal neurons of the rat
-
Bekkers, J. M. (2000a). Distribution and activation of voltage-gated potassium channels in cell-attached and outside-out patches from large layer 5 cortical pyramidal neurons of the rat. Journal of Physiology, 525, 611-620.
-
(2000)
Journal of Physiology
, vol.525
, pp. 611-620
-
-
Bekkers, J.M.1
-
10
-
-
0034659423
-
Properties of voltage-gated potassium currents in nucleated patches from large layer 5 cortical pyramidal neurons of the rat
-
Bekkers, J. M. (2000b). Properties of voltage-gated potassium currents in nucleated patches from large layer 5 cortical pyramidal neurons of the rat. Journal of Physiology, 525, 593-609.
-
(2000)
Journal of Physiology
, vol.525
, pp. 593-609
-
-
Bekkers, J.M.1
-
11
-
-
33846186440
-
Impaired sadness recognition is linked to social interaction deficit in autism
-
doi:10.1016/j.neuropsychologia.2006.11.010
-
Boraston, Z., Blakemore, S. J., Chilvers, R., & Skuse, D. (2007). Impaired sadness recognition is linked to social interaction deficit in autism. Neuropsychologia, 45, 1501-1510. doi:10.1016/j.neuropsychologia.2006.11.010
-
(2007)
Neuropsychologia
, vol.45
, pp. 1501-1510
-
-
Boraston, Z.1
Blakemore, S.J.2
Chilvers, R.3
Skuse, D.4
-
12
-
-
67651233780
-
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
-
doi:10.1371/journal.pgen.1000536
-
Bucan, M., Abrahams, B. S., Wang, K., Glessner, J. T., Herman, E. I., Sonnenblick, L. I., et al. (2009). Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genetics, 5, e1000536. doi:10.1371/journal.pgen.1000536
-
(2009)
PLoS Genetics
, vol.5
-
-
Bucan, M.1
Abrahams, B.S.2
Wang, K.3
Glessner, J.T.4
Herman, E.I.5
Sonnenblick, L.I.6
-
13
-
-
0030905586
-
Amphiphysin II (SH3P9; BIN1), a member of the amphiphysin/Rvs family, is concentrated in the cortical cytomatrix of axon initial segments and nodes of Ranvier in brain and around T tubules in skeletal muscle
-
Butler, M. H., David, C., Ochoa, G. C., Freyberg, Z., Daniell, L., Grabs, D., et al. (1997). Amphiphysin II (SH3P9; BIN1), a member of the amphiphysin/Rvs family, is concentrated in the cortical cytomatrix of axon initial segments and nodes of Ranvier in brain and around T tubules in skeletal muscle. Journal of Cell Biology, 137, 1355-1367.
-
(1997)
Journal of Cell Biology
, vol.137
, pp. 1355-1367
-
-
Butler, M.H.1
David, C.2
Ochoa, G.C.3
Freyberg, Z.4
Daniell, L.5
Grabs, D.6
-
14
-
-
0038626842
-
Identification of MeCP2 mutations in a series of females with autistic disorder
-
Carney, R. M., Wolpert, C. M., Ravan, S. A., Shahbazian, M., Ashley-Koch, A., Cuccaro, M. L., et al. (2003). Identification of MeCP2 mutations in a series of females with autistic disorder. Pediatric Neurology, 28, 205-211.
-
(2003)
Pediatric Neurology
, vol.28
, pp. 205-211
-
-
Carney, R.M.1
Wolpert, C.M.2
Ravan, S.A.3
Shahbazian, M.4
Ashley-Koch, A.5
Cuccaro, M.L.6
-
15
-
-
76649142079
-
Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation
-
doi:10.1212/WNL.0b013e3181cef7f9
-
Claeys, K. G., Maisonobe, T., Bohm, J., Laporte, J., Hezode, M., Romero, N. B., et al. (2010). Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation. Neurology, 74, 519-521. doi:10.1212/WNL.0b013e3181cef7f9
-
(2010)
Neurology
, vol.74
, pp. 519-521
-
-
Claeys, K.G.1
Maisonobe, T.2
Bohm, J.3
Laporte, J.4
Hezode, M.5
Romero, N.B.6
-
16
-
-
10744221938
-
Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism
-
doi:10.1016/j.biopsych.2003.10.005
-
Conciatori, M., Stodgell, C. J., Hyman, S. L., O'Bara, M., Militerni, R., Bravaccio, C., et al. (2004). Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism. Biological Psychiatry, 55, 413-419. doi:10.1016/j.biopsych.2003.10.005
-
(2004)
Biological Psychiatry
, vol.55
, pp. 413-419
-
-
Conciatori, M.1
Stodgell, C.J.2
Hyman, S.L.3
O'Bara, M.4
Militerni, R.5
Bravaccio, C.6
-
17
-
-
0141539482
-
Validation of a brief quantitative measure of autistic traits: Comparison of the social responsiveness scale with the autism diagnostic interview-revised
-
Constantino, J. N., Davis, S. A., Todd, R. D., Schindler, M. K., Gross, M. M., Brophy, S. L., et al. (2003). Validation of a brief quantitative measure of autistic traits: Comparison of the social responsiveness scale with the autism diagnostic interview-revised. Journal of Autism and Developmental Disorders, 33, 427-433.
-
(2003)
Journal of Autism and Developmental Disorders
, vol.33
, pp. 427-433
-
-
Constantino, J.N.1
Davis, S.A.2
Todd, R.D.3
Schindler, M.K.4
Gross, M.M.5
Brophy, S.L.6
-
18
-
-
36349029123
-
Rapid quantitative assessment of autistic social impairment by classroom teachers
-
doi:10.1097/chi.0b013e318157cb23
-
Constantino, J. N., Lavesser, P. D., Zhang, Y., Abbacchi, A. M., Gray, T., & Todd, R. D. (2007). Rapid quantitative assessment of autistic social impairment by classroom teachers. Journal of American Academy of Child and Adolescent Psychiatry, 46, 1668-1676. doi:10.1097/chi.0b013e318157cb23
-
(2007)
Journal of American Academy of Child and Adolescent Psychiatry
, vol.46
, pp. 1668-1676
-
-
Constantino, J.N.1
Lavesser, P.D.2
Zhang, Y.3
Abbacchi, A.M.4
Gray, T.5
Todd, R.D.6
-
19
-
-
54049144653
-
Copy-number variations associated with neuropsychiatric conditions
-
doi:10.1038/nature07458
-
Cook, E. H., Jr., & Scherer, S. W. (2008). Copy-number variations associated with neuropsychiatric conditions. Nature, 455, 919-923. doi:10.1038/nature07458
-
(2008)
Nature
, vol.455
, pp. 919-923
-
-
Cook Jr., E.H.1
Scherer, S.W.2
-
20
-
-
20544449602
-
Epilepsy in young adults with autism: A prospective population-based follow-up study of 120 individuals diagnosed in childhood
-
doi:10.1111/j.1528-1167.2005.57504.x
-
Danielsson, S., Gillberg, I. C., Billstedt, E., Gillberg, C., & Olsson, I. (2005). Epilepsy in young adults with autism: A prospective population-based follow-up study of 120 individuals diagnosed in childhood. Epilepsia, 46, 918-923. doi:10.1111/j.1528-1167.2005.57504.x
-
(2005)
Epilepsia
, vol.46
, pp. 918-923
-
-
Danielsson, S.1
Gillberg, I.C.2
Billstedt, E.3
Gillberg, C.4
Olsson, I.5
-
21
-
-
3543049569
-
Interrelationship between Autism Diagnostic Observation Schedule-Generic (ADOS-G), Autism Diagnostic Interview-Revised (ADI-R), and the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) classification in children and adolescents with mental retardation
-
de Bildt, A., Sytema, S., Ketelaars, C., Kraijer, D., Mulder, E., Volkmar, F., et al. (2004). Interrelationship between Autism Diagnostic Observation Schedule-Generic (ADOS-G), Autism Diagnostic Interview-Revised (ADI-R), and the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) classification in children and adolescents with mental retardation. Journal of Autism and Developmental Disorders, 34, 129-137.
-
(2004)
Journal of Autism and Developmental Disorders
, vol.34
, pp. 129-137
-
-
de Bildt, A.1
Sytema, S.2
Ketelaars, C.3
Kraijer, D.4
Mulder, E.5
Volkmar, F.6
-
22
-
-
70449708068
-
Imitation and communication skills development in children with pervasive developmental disorders
-
De Giacomo, A., Portoghese, C., Martinelli, D., Fanizza, I., L'Abate, L., & Margari, L. (2009). Imitation and communication skills development in children with pervasive developmental disorders. Neuropsychiatric Disease Treatment, 5, 355-362.
-
(2009)
Neuropsychiatric Disease Treatment
, vol.5
, pp. 355-362
-
-
De Giacomo, A.1
Portoghese, C.2
Martinelli, D.3
Fanizza, I.4
L'Abate, L.5
Margari, L.6
-
23
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
doi:10.1371/journal.pbio.1000294
-
Dickson, S. P., Wang, K., Krantz, I., Hakonarson, H., & Goldstein, D. B. (2010). Rare variants create synthetic genome-wide associations. PLoS Biology, 8, e1000294. doi:10.1371/journal.pbio.1000294
-
(2010)
PLoS Biology
, vol.8
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
24
-
-
0041852863
-
Developmental changes of autistic symptoms
-
Fecteau, S., Mottron, L., Berthiaume, C., & Burack, J. A. (2003). Developmental changes of autistic symptoms. Autism, 7, 255-268.
-
(2003)
Autism
, vol.7
, pp. 255-268
-
-
Fecteau, S.1
Mottron, L.2
Berthiaume, C.3
Burack, J.A.4
-
25
-
-
50449089356
-
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder
-
doi:10.1038/ng.209
-
Ferreira, M. A., O'Donovan, M. C., Meng, Y. A., Jones, I. R., Ruderfer, D. M., Jones, L., et al. (2008). Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Nature Genetics, 40, 1056-1058. doi:10.1038/ng.209
-
(2008)
Nature Genetics
, vol.40
, pp. 1056-1058
-
-
Ferreira, M.A.1
O'Donovan, M.C.2
Meng, Y.A.3
Jones, I.R.4
Ruderfer, D.M.5
Jones, L.6
-
26
-
-
67049118065
-
Epidemiology of pervasive developmental disorders
-
doi:10.1203/PDR.0b013e31819e7203
-
Fombonne, E. (2009). Epidemiology of pervasive developmental disorders. Pediatric Research, 65, 591-598. doi:10.1203/PDR.0b013e31819e7203
-
(2009)
Pediatric Research
, vol.65
, pp. 591-598
-
-
Fombonne, E.1
-
27
-
-
37249034766
-
Systematic association mapping identifies NELL1 as a novel IBD disease gene
-
Franke, A., Hampe, J., Rosenstiel, P., Becker, C., Wagner, F., Häsler, R., et al. (2007). Systematic association mapping identifies NELL1 as a novel IBD disease gene. PLoS One, 8(8), e691.
-
(2007)
PLoS One
, vol.8
, Issue.8
-
-
Franke, A.1
Hampe, J.2
Rosenstiel, P.3
Becker, C.4
Wagner, F.5
Häsler, R.6
-
28
-
-
69949085780
-
Autism: A world changing too fast for a mis-wired brain?
-
Gepner, B., & Féron, F. (2009). Autism: A world changing too fast for a mis-wired brain?Neuroscience & Biobehavioral Reviews, 33, 1227-1242.
-
(2009)
Neuroscience & Biobehavioral Reviews
, vol.33
, pp. 1227-1242
-
-
Gepner, B.1
Féron, F.2
-
29
-
-
0034916325
-
The Autism Genetic Resource Exchange: A resource for the study of autism and related neuropsychiatric conditions
-
doi:10.1086/321292
-
Geschwind, D. H., Sowinski, J., Lord, C., Iversen, P., Shestack, J., Jones, P., et al. (2001). The Autism Genetic Resource Exchange: A resource for the study of autism and related neuropsychiatric conditions. American Journal of Human Genetics, 69, 463-466. doi:10.1086/321292
-
(2001)
American Journal of Human Genetics
, vol.69
, pp. 463-466
-
-
Geschwind, D.H.1
Sowinski, J.2
Lord, C.3
Iversen, P.4
Shestack, J.5
Jones, P.6
-
30
-
-
84856818976
-
Common variants in polygenic schizophrenia
-
doi:10.1186/gb-2009-10-9-236
-
Glessner, J. T., & Hakonarson, H. (2009). Common variants in polygenic schizophrenia. Genome Biology, 10, 236. doi:10.1186/gb-2009-10-9-236
-
(2009)
Genome Biology
, vol.10
, pp. 236
-
-
Glessner, J.T.1
Hakonarson, H.2
-
31
-
-
77953776675
-
Strong synaptic transmission impact by copy number variations in schizophrenia
-
doi:10.1073/pnas.1000274107
-
Glessner, J. T., Reilly, M. P., Kim, C. E., Takahashi, N., Albano, A., Hou, C., et al. (2010). Strong synaptic transmission impact by copy number variations in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America, 107, 10584-10589. doi:10.1073/pnas.1000274107
-
(2010)
Proceedings of the National Academy of Sciences of the United States of America
, vol.107
, pp. 10584-10589
-
-
Glessner, J.T.1
Reilly, M.P.2
Kim, C.E.3
Takahashi, N.4
Albano, A.5
Hou, C.6
-
32
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
Glessner, J. T., Wang, K., Cai, G., Korvatska, O., Kim, C. E., Wood, S., et al. (2009). Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature, 459(7246), 569-573.
-
(2009)
Nature
, vol.459
, Issue.7246
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
Korvatska, O.4
Kim, C.E.5
Wood, S.6
-
33
-
-
67349117273
-
Standardizing ADOS scores for a measure of severity in autism spectrum disorders
-
doi:10.1007/s10803-008-0674-3
-
Gotham, K., Pickles, A., & Lord, C. (2009). Standardizing ADOS scores for a measure of severity in autism spectrum disorders. Journal of Autism and Developmental Disorders, 39, 693-705. doi:10.1007/s10803-008-0674-3
-
(2009)
Journal of Autism and Developmental Disorders
, vol.39
, pp. 693-705
-
-
Gotham, K.1
Pickles, A.2
Lord, C.3
-
34
-
-
34147123692
-
The Autism Diagnostic Observation Schedule: Revised algorithms for improved diagnostic validity
-
doi:10.1007/s10803-006-0280-1
-
Gotham, K., Risi, S., Pickles, A., & Lord, C. (2007). The Autism Diagnostic Observation Schedule: Revised algorithms for improved diagnostic validity. Journal of Autism and Developmental Disorders, 37, 613-627. doi:10.1007/s10803-006-0280-1
-
(2007)
Journal of Autism and Developmental Disorders
, vol.37
, pp. 613-627
-
-
Gotham, K.1
Risi, S.2
Pickles, A.3
Lord, C.4
-
35
-
-
41049102728
-
Using the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule with young children with developmental delay: Evaluating diagnostic validity
-
doi:10.1007/s10803-007-0432-y
-
Gray, K. M., Tonge, B. J., & Sweeney, D. J. (2008). Using the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule with young children with developmental delay: Evaluating diagnostic validity. Journal of Autism and Developmental Disorders, 38, 657-667. doi:10.1007/s10803-007-0432-y
-
(2008)
Journal of Autism and Developmental Disorders
, vol.38
, pp. 657-667
-
-
Gray, K.M.1
Tonge, B.J.2
Sweeney, D.J.3
-
36
-
-
39649108872
-
Genome-wide significance for dense SNP and resequencing data
-
doi:10.1002/gepi.20292
-
Hoggart, C. J., Clark, T. G., De Iorio, M., Whittaker, J. C., & Balding, D. J. (2008). Genome-wide significance for dense SNP and resequencing data. Genetic Epidemiology, 32, 179-185. doi:10.1002/gepi.20292
-
(2008)
Genetic Epidemiology
, vol.32
, pp. 179-185
-
-
Hoggart, C.J.1
Clark, T.G.2
De Iorio, M.3
Whittaker, J.C.4
Balding, D.J.5
-
37
-
-
66349137661
-
Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism
-
Hu, V. W., Sarachana, T., Kim, K. S., Nguyen, A., Kulkarni, S., & Steinberg, M.E., et al. (2009). Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism. Autism Research, 2(2), 78-97.
-
(2009)
Autism Research
, vol.2
, Issue.2
, pp. 78-97
-
-
Hu, V.W.1
Sarachana, T.2
Kim, K.S.3
Nguyen, A.4
Kulkarni, S.5
Steinberg, M.E.6
-
38
-
-
66349105641
-
Novel clustering of items from the Autism Diagnostic Interview-Revised to define phenotypes within autism spectrum disorders
-
doi:10.1002/aur.72
-
Hu, V. W., & Steinberg, M. E. (2009). Novel clustering of items from the Autism Diagnostic Interview-Revised to define phenotypes within autism spectrum disorders. Autism Research, 2, 67-77. doi:10.1002/aur.72
-
(2009)
Autism Research
, vol.2
, pp. 67-77
-
-
Hu, V.W.1
Steinberg, M.E.2
-
39
-
-
79959524146
-
A haplotype map of the human genome
-
International HapMap Consortium. ., doi:10.1038/nature04226
-
International HapMap Consortium. (2005). A haplotype map of the human genome. Nature, 437, 1299-1320. doi:10.1038/nature04226
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
40
-
-
0034162944
-
Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA)
-
doi:10.1006/geno.2000.6117
-
Isbrandt, D., Leicher, T., Waldschutz, R., Zhu, X., Luhmann, U., Michel, U., et al. (2000). Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA). Genomics, 64, 144-154. doi:10.1006/geno.2000.6117
-
(2000)
Genomics
, vol.64
, pp. 144-154
-
-
Isbrandt, D.1
Leicher, T.2
Waldschutz, R.3
Zhu, X.4
Luhmann, U.5
Michel, U.6
-
41
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
doi:10.1038/ng1136
-
Jamain, S., Quach, H., Betancur, C., Rastam, M., Colineaux, C., Gillberg, I. C., et al. (2003). Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nature Genetics, 34, 27-29. doi:10.1038/ng1136
-
(2003)
Nature Genetics
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Rastam, M.4
Colineaux, C.5
Gillberg, I.C.6
-
42
-
-
0042855814
-
Cognitive profiles and social-communicative functioning in children with autism spectrum disorder
-
Joseph, R. M., Tager-Flusberg, H., & Lord, C. (2002). Cognitive profiles and social-communicative functioning in children with autism spectrum disorder. Journal of Child Psychology & Psychiatry, 43, 807-821.
-
(2002)
Journal of Child Psychology & Psychiatry
, vol.43
, pp. 807-821
-
-
Joseph, R.M.1
Tager-Flusberg, H.2
Lord, C.3
-
43
-
-
76049110842
-
Neuroendocrine pathways altered in autism. Special role of reelin
-
Kelemenova, S., & Ostatnikova, D. (2009). Neuroendocrine pathways altered in autism. Special role of reelin. Neuroendocrinology Letters, 30, 429-436.
-
(2009)
Neuroendocrinology Letters
, vol.30
, pp. 429-436
-
-
Kelemenova, S.1
Ostatnikova, D.2
-
44
-
-
61449115868
-
Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios
-
doi:10.1002/ajmg.b.30798
-
Kim, H. W., Cho, S. C., Kim, J. W., Cho, I. H., Kim, S. A., Park, M., et al. (2009). Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios. AmericanJournal of MedicalGeneticsPartB:Neuropsychiatric Genetics, 150B, 300-306. doi:10.1002/ajmg.b.30798
-
(2009)
AmericanJournal of MedicalGeneticsPartB:Neuropsychiatric Genetics
, vol.150 B
, pp. 300-306
-
-
Kim, H.W.1
Cho, S.C.2
Kim, J.W.3
Cho, I.H.4
Kim, S.A.5
Park, M.6
-
45
-
-
28244434047
-
Kv4 potassium channel subunits control action potential repolarization and frequency-dependent broadening in rat hippocampal CA1 pyramidal neurones
-
doi:10.1113/jphysiol.2005.095042
-
Kim, J., Wei, D. S., & Hoffman, D. A. (2005). Kv4 potassium channel subunits control action potential repolarization and frequency-dependent broadening in rat hippocampal CA1 pyramidal neurones. Journal of Physiology, 569, 41-57. doi:10.1113/jphysiol.2005.095042
-
(2005)
Journal of Physiology
, vol.569
, pp. 41-57
-
-
Kim, J.1
Wei, D.S.2
Hoffman, D.A.3
-
46
-
-
33744957290
-
Skin conductance responses to another person's gaze in children with autism
-
doi:10.1007/s10803-006-0091-4
-
Kylliainen, A., & Hietanen, J. K. (2006). Skin conductance responses to another person's gaze in children with autism. Journal of Autism and Developmental Disorders, 36, 517-525. doi:10.1007/s10803-006-0091-4
-
(2006)
Journal of Autism and Developmental Disorders
, vol.36
, pp. 517-525
-
-
Kylliainen, A.1
Hietanen, J.K.2
-
47
-
-
67651033371
-
Changes in the developmental trajectories of striatum in autism
-
doi:10.1016/j.biopsych.2009.03.017
-
Langen, M., Schnack, H. G., Nederveen, H., Bos, D., Lahuis, B. E., de Jonge, M. V., et al. (2009). Changes in the developmental trajectories of striatum in autism. Biological Psychiatry, 66, 327-333. doi:10.1016/j.biopsych.2009.03.017
-
(2009)
Biological Psychiatry
, vol.66
, pp. 327-333
-
-
Langen, M.1
Schnack, H.G.2
Nederveen, H.3
Bos, D.4
Lahuis, B.E.5
de Jonge, M.V.6
-
48
-
-
28644434943
-
Effects of familial risk factors and place of birth on the risk of autism: A nationwide register-based study
-
doi:10.1111/j.1469-7610.2004.00391.x
-
Lauritsen, M. B., Pedersen, C. B., & Mortensen, P. B. (2005). Effects of familial risk factors and place of birth on the risk of autism: A nationwide register-based study. Journal of Child Psychology & Psychiatry, 46, 963-971. doi:10.1111/j.1469-7610.2004.00391.x
-
(2005)
Journal of Child Psychology & Psychiatry
, vol.46
, pp. 963-971
-
-
Lauritsen, M.B.1
Pedersen, C.B.2
Mortensen, P.B.3
-
49
-
-
52049086907
-
Emotional regulation, or: How I learned to stop worrying and love the nucleus accumbens
-
doi:10.1016/j.neuron.2008.09.007
-
Lebrecht, S., & Badre, D. (2008). Emotional regulation, or: How I learned to stop worrying and love the nucleus accumbens. Neuron, 59, 841-843. doi:10.1016/j.neuron.2008.09.007
-
(2008)
Neuron
, vol.59
, pp. 841-843
-
-
Lebrecht, S.1
Badre, D.2
-
50
-
-
79960077354
-
Pilocarpine-induced status epilepticus alters hippocampal PKC expression in mice
-
Liu, J. X., Liu, Y., & Tang, F. R. (2011). Pilocarpine-induced status epilepticus alters hippocampal PKC expression in mice. Acta Neurobiologiae Experimentalis (Warsaw), 71(2), 220-232.
-
(2011)
Acta Neurobiologiae Experimentalis (Warsaw)
, vol.71
, Issue.2
, pp. 220-232
-
-
Liu, J.X.1
Liu, Y.2
Tang, F.R.3
-
51
-
-
0033802632
-
The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism
-
Lord, C., Risi, S., Lambrecht, L., Cook, E. H., Jr, Leventhal, B. L., DiLavore, P. C., et al. (2000). The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. Journal of Autism and Developmental Disorders, 30, 205-223.
-
(2000)
Journal of Autism and Developmental Disorders
, vol.30
, pp. 205-223
-
-
Lord, C.1
Risi, S.2
Lambrecht, L.3
Cook Jr., E.H.4
Leventhal, B.L.5
DiLavore, P.C.6
-
52
-
-
0003428096
-
-
Los Angeles, CA: Western Psychological Services.
-
Lord, C., Rutter, M., DiLavore, P. C., & Risi, S. (1999). Autism Diagnostic Observation Schedule-WPS (ADOS-WPS). Los Angeles, CA: Western Psychological Services.
-
(1999)
Autism Diagnostic Observation Schedule-WPS (ADOS-WPS)
-
-
Lord, C.1
Rutter, M.2
DiLavore, P.C.3
Risi, S.4
-
53
-
-
0003428096
-
-
Los Angeles, CA: Western Psychological Services.
-
Lord, C., Rutter, M., DiLavore, P. C., & Risi, S. (2002). Autism Diagnostic Observation Schedule. Los Angeles, CA: Western Psychological Services.
-
(2002)
Autism Diagnostic Observation Schedule
-
-
Lord, C.1
Rutter, M.2
DiLavore, P.C.3
Risi, S.4
-
54
-
-
0027997172
-
Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
Lord, C., Rutter, M., & Le Couteur, A. (1994). Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. Journal of Autism and Developmental Disorders, 24, 659-685.
-
(1994)
Journal of Autism and Developmental Disorders
, vol.24
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Le Couteur, A.3
-
55
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., et al. (2009). Finding the missing heritability of complex diseases. Nature, 461, 747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
-
56
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
doi:10.1016/j.ajhg.2007.12.009
-
Marshall, C. R., Noor, A., Vincent, J. B., Lionel, A. C., Feuk, L., Skaug, J., et al. (2008). Structural variation of chromosomes in autism spectrum disorder. American Journal of Human Genetics, 82, 477-488. doi:10.1016/j.ajhg.2007.12.009
-
(2008)
American Journal of Human Genetics
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
Lionel, A.C.4
Feuk, L.5
Skaug, J.6
-
57
-
-
42349112088
-
Genome-wide association studies for complex traits: Consensus, uncertainty and challenges
-
doi:10.1038/nrg2344
-
McCarthy, M. I., Abecasis, G. R., Cardon, L. R., Goldstein, D. B., Little, J., Ioannidis, J. P., et al. (2008). Genome-wide association studies for complex traits: Consensus, uncertainty and challenges. Nature Reviews Genetics, 9, 356-369. doi:10.1038/nrg2344
-
(2008)
Nature Reviews Genetics
, vol.9
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
Goldstein, D.B.4
Little, J.5
Ioannidis, J.P.6
-
58
-
-
36749040875
-
Contribution of SHANK3 mutations to autism spectrum disorder
-
doi:10.1086/522590
-
Moessner, R., Marshall, C. R., Sutcliffe, J. S., Skaug, J., Pinto, D., Vincent, J., et al. (2007). Contribution of SHANK3 mutations to autism spectrum disorder. American Journal of Human Genetics, 81, 1289-1297. doi:10.1086/522590
-
(2007)
American Journal of Human Genetics
, vol.81
, pp. 1289-1297
-
-
Moessner, R.1
Marshall, C.R.2
Sutcliffe, J.S.3
Skaug, J.4
Pinto, D.5
Vincent, J.6
-
59
-
-
49949152363
-
Stability of the autism diagnostic interview-revised from pre-school to elementary school age in children with autism spectrum disorders
-
doi:10.1007/s10803-007-0487-9
-
Moss, J., Magiati, I., Charman, T., & Howlin, P. (2008). Stability of the autism diagnostic interview-revised from pre-school to elementary school age in children with autism spectrum disorders. Journal of Autism and Developmental Disorders, 38, 1081-1091. doi:10.1007/s10803-007-0487-9
-
(2008)
Journal of Autism and Developmental Disorders
, vol.38
, pp. 1081-1091
-
-
Moss, J.1
Magiati, I.2
Charman, T.3
Howlin, P.4
-
60
-
-
27644556286
-
Enhanced perceptual functioning in autism: An update, and eight principles of autistic perception
-
doi:10.1007/s10803-005-0040-7
-
Mottron, L., Dawson, M., Soulieres, I., Hubert, B., & Burack, J. (2006). Enhanced perceptual functioning in autism: An update, and eight principles of autistic perception. Journal of Autism and Developmental Disorders, 36, 27-43. doi:10.1007/s10803-005-0040-7
-
(2006)
Journal of Autism and Developmental Disorders
, vol.36
, pp. 27-43
-
-
Mottron, L.1
Dawson, M.2
Soulieres, I.3
Hubert, B.4
Burack, J.5
-
61
-
-
3442894480
-
The genetics of autism
-
Muhle, R., Trentacoste, S. V., & Rapin, I. (2004). The genetics of autism. Pediatrics, 113, e472-486.
-
(2004)
Pediatrics
, vol.113
-
-
Muhle, R.1
Trentacoste, S.V.2
Rapin, I.3
-
62
-
-
79960240142
-
Underconnected, but how? A survey of functional connectivity MRI studies in autism spectrum disorders
-
Müller, R. A., Shih, P., Keehn, B., Deyoe, J. R., Leyden, K. M., & Shukla, D. K. (2011). Underconnected, but how? A survey of functional connectivity MRI studies in autism spectrum disorders. Cerebral Cortex, 21, 2233-2243.
-
(2011)
Cerebral Cortex
, vol.21
, pp. 2233-2243
-
-
Müller, R.A.1
Shih, P.2
Keehn, B.3
Deyoe, J.R.4
Leyden, K.M.5
Shukla, D.K.6
-
63
-
-
34249735268
-
The epidemiology of autism spectrum disorders
-
doi:10.1146/annurev.publhealth.28.021406.144007
-
Newschaffer, C. J., Croen, L. A., Daniels, J., Giarelli, E., Grether, J. K., Levy, S. E., et al. (2007). The epidemiology of autism spectrum disorders. Annual Review of Public Health, 28, 235-258. doi:10.1146/annurev.publhealth.28.021406.144007
-
(2007)
Annual Review of Public Health
, vol.28
, pp. 235-258
-
-
Newschaffer, C.J.1
Croen, L.A.2
Daniels, J.3
Giarelli, E.4
Grether, J.K.5
Levy, S.E.6
-
64
-
-
72449123165
-
Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals
-
doi:10.1038/ajh.2009.190
-
Oguri, M., Kato, K., Yokoi, K., Yoshida, T., Watanabe, S., Metoki, N., et al. (2010). Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals. American Journal of Hypertension, 23, 70-77. doi:10.1038/ajh.2009.190
-
(2010)
American Journal of Hypertension
, vol.23
, pp. 70-77
-
-
Oguri, M.1
Kato, K.2
Yokoi, K.3
Yoshida, T.4
Watanabe, S.5
Metoki, N.6
-
65
-
-
77955883755
-
Improved diagnostic validity of the ADOS revised algorithms: A replication study in an independent sample
-
doi:10.1007/s10803-009-0915-0
-
Oosterling, I., Roos, S., de Bildt, A., Rommelse, N., de Jonge, M., Visser, J., et al. (2010). Improved diagnostic validity of the ADOS revised algorithms: A replication study in an independent sample. Journal of Autism and Developmental Disorders, 40, 689-703. doi:10.1007/s10803-009-0915-0
-
(2010)
Journal of Autism and Developmental Disorders
, vol.40
, pp. 689-703
-
-
Oosterling, I.1
Roos, S.2
de Bildt, A.3
Rommelse, N.4
de Jonge, M.5
Visser, J.6
-
66
-
-
77956229776
-
Epilepsy and EEG paroxysmal abnormalities in autism spectrum disorders
-
doi:10.1016/j.braindev.2010.07.003
-
Parmeggiani, A., Barcia, G., Posar, A., Raimondi, E., Santucci, M., & Scaduto, M. C. (2010). Epilepsy and EEG paroxysmal abnormalities in autism spectrum disorders. Brain Development, 32, 783-789. doi:10.1016/j.braindev.2010.07.003
-
(2010)
Brain Development
, vol.32
, pp. 783-789
-
-
Parmeggiani, A.1
Barcia, G.2
Posar, A.3
Raimondi, E.4
Santucci, M.5
Scaduto, M.C.6
-
67
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
doi:10.1038/nature09146
-
Pinto, D., Pagnamenta, A. T., Klei, L., Anney, R., Merico, D., Regan, R., et al. (2010). Functional impact of global rare copy number variation in autism spectrum disorders. Nature, 466, 368-372. doi:10.1038/nature09146
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
Pagnamenta, A.T.2
Klei, L.3
Anney, R.4
Merico, D.5
Regan, R.6
-
68
-
-
0031035019
-
Broader autism phenotype: Evidence from a family history study of multiple-incidence autism families
-
Piven, J., Palmer, P., Jacobi, D., Childress, D., & Arndt, S. (1997). Broader autism phenotype: Evidence from a family history study of multiple-incidence autism families. American Journal Psychiatry, 15, 185-190.
-
(1997)
American Journal Psychiatry
, vol.15
, pp. 185-190
-
-
Piven, J.1
Palmer, P.2
Jacobi, D.3
Childress, D.4
Arndt, S.5
-
69
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
doi:10.1038/ng1847
-
Price, A. L., Patterson, N. J., Plenge, R. M., Weinblatt, M. E., Shadick, N. A., & Reich, D. (2006). Principal components analysis corrects for stratification in genome-wide association studies. Nature Genetics, 38, 904-909. doi:10.1038/ng1847
-
(2006)
Nature Genetics
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
70
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N., & Merikangas, K. (1996). The future of genetic studies of complex human diseases. Science, 273, 1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
71
-
-
33748417617
-
Combining information from multiple sources in the diagnosis of autism spectrum disorders
-
doi:10.1097/01.chi.0000227880.42780.0e
-
Risi, S., Lord, C., Gotham, K., Corsello, C., Chrysler, C., Szatmari, P., et al. (2006). Combining information from multiple sources in the diagnosis of autism spectrum disorders. Journal of the American Academy of Child and Adolescent Psychiatry, 45, 1094-103. doi:10.1097/01.chi.0000227880.42780.0e
-
(2006)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.45
, pp. 1094-1103
-
-
Risi, S.1
Lord, C.2
Gotham, K.3
Corsello, C.4
Chrysler, C.5
Szatmari, P.6
-
72
-
-
77249176699
-
MEG detection of delayed auditory evoked responses in autism spectrum disorders: Towards an imaging biomarker for autism
-
doi:10.1002/aur.111
-
Roberts, T. P., Khan, S. Y., Rey, M., Monroe, J. F., Cannon, K., Blaskey, L., et al. (2010). MEG detection of delayed auditory evoked responses in autism spectrum disorders: Towards an imaging biomarker for autism. Autism Research, 3, 8-18. doi:10.1002/aur.111
-
(2010)
Autism Research
, vol.3
, pp. 8-18
-
-
Roberts, T.P.1
Khan, S.Y.2
Rey, M.3
Monroe, J.F.4
Cannon, K.5
Blaskey, L.6
-
73
-
-
0037613764
-
-
Los Angeles, CA: Western Psychological Services.
-
Rutter, M., Le Couteur, A., & Lord, C. (2003). Autism Diagnostic Interview-Revised. Los Angeles, CA: Western Psychological Services.
-
(2003)
Autism Diagnostic Interview-Revised
-
-
Rutter, M.1
Le Couteur, A.2
Lord, C.3
-
74
-
-
34447628063
-
Rethinking the nature of genetic vulnerability to autistic spectrum disorders
-
doi:10.1016/j.tig.2007.06.003
-
Skuse, D. H. (2007). Rethinking the nature of genetic vulnerability to autistic spectrum disorders. Trends Genetics, 23, 387-395. doi:10.1016/j.tig.2007.06.003
-
(2007)
Trends Genetics
, vol.23
, pp. 387-395
-
-
Skuse, D.H.1
-
75
-
-
0037297040
-
Stability and change among high-functioning children with pervasive developmental disorders: A 2-year outcome study
-
Starr, E., Szatmari, P., Bryson, S., & Zwaigenbaum, L. (2003). Stability and change among high-functioning children with pervasive developmental disorders: A 2-year outcome study. Journal of Autism and Developmental Disorders, 33, 15-22.
-
(2003)
Journal of Autism and Developmental Disorders
, vol.33
, pp. 15-22
-
-
Starr, E.1
Szatmari, P.2
Bryson, S.3
Zwaigenbaum, L.4
-
76
-
-
77951880837
-
Response to Mitchell and Porteus
-
doi:10.1038/mp.2009.106
-
Sullivan, P. F., & Gejman, P. V. (2010). Response to Mitchell and Porteus. Molecular Psychiatry, 15, 450-452. doi:10.1038/mp.2009.106
-
(2010)
Molecular Psychiatry
, vol.15
, pp. 450-452
-
-
Sullivan, P.F.1
Gejman, P.V.2
-
77
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
doi:10.1038/nature09270
-
Teslovich, T. M., Musunuru, K., Smith, A. V., Edmondson, A. C., Stylianou, I. M., Koseki, M., et al. (2010). Biological, clinical and population relevance of 95 loci for blood lipids. Nature, 466, 707-713. doi:10.1038/nature09270
-
(2010)
Nature
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
Musunuru, K.2
Smith, A.V.3
Edmondson, A.C.4
Stylianou, I.M.5
Koseki, M.6
-
78
-
-
0032925143
-
Human NELL-1 expressed in unilateral coronal synostosis
-
doi:10.1359/jbmr.1999.14.1.80
-
Ting, K., Vastardis, H., Mulliken, J. B., Soo, C., Tieu, A., Do, H., et al. (1999). Human NELL-1 expressed in unilateral coronal synostosis. Journal of Bone and Mineral Research, 14, 80-89. doi:10.1359/jbmr.1999.14.1.80
-
(1999)
Journal of Bone and Mineral Research
, vol.14
, pp. 80-89
-
-
Ting, K.1
Vastardis, H.2
Mulliken, J.B.3
Soo, C.4
Tieu, A.5
Do, H.6
-
79
-
-
0025889717
-
Autistic and dysphasic children. II: Epilepsy
-
Tuchman, R. F., Rapin, I., & Shinnar, S. (1991). Autistic and dysphasic children. II: Epilepsy. Pediatrics, 88, 1219-1225.
-
(1991)
Pediatrics
, vol.88
, pp. 1219-1225
-
-
Tuchman, R.F.1
Rapin, I.2
Shinnar, S.3
-
80
-
-
0025848462
-
Abnormal electrodermal reactivity to novel visual stimuli in autistic children
-
van Engeland, H, Roelofs, J.W, Verbaten, M.N, & Slangen, J.L. (1991). Abnormal electrodermal reactivity to novel visual stimuli in autistic children. Psychiatry Research, 38, 27-38.
-
(1991)
Psychiatry Research
, vol.38
, pp. 27-38
-
-
van Engeland, H.1
Roelofs, J.W.2
Verbaten, M.N.3
Slangen, J.L.4
-
81
-
-
33847621680
-
Differentiating between autism spectrum disorders and other developmental disabilities in children who failed a screening instrument for ASD
-
Ventola, P., Kleinman, J., Pandey, J., Wilson, L., Esser, E., Fein, D. (2007). Differentiating between autism spectrum disorders and other developmental disabilities in children who failed a screening instrument for ASD. Journal of Autism and Developmental Disorders, 37, 425-436.
-
(2007)
Journal of Autism and Developmental Disorders
, vol.37
, pp. 425-436
-
-
Ventola, P.1
Kleinman, J.2
Pandey, J.3
Wilson, L.4
Esser, E.5
Fein, D.6
-
82
-
-
33846449102
-
Endophenotype approach to developmental psychopathology: Implications for autism research
-
Viding, E., & Blakemore, S. J. (2007). Endophenotype approach to developmental psychopathology: Implications for autism research. Behavioural Genetics, 37, 51-60.
-
(2007)
Behavioural Genetics
, vol.37
, pp. 51-60
-
-
Viding, E.1
Blakemore, S.J.2
-
83
-
-
58849095405
-
CREB regulation of nucleus accumbens excitability mediates social isolation-induced behavioral deficits
-
doi:10.1038/nn.2257
-
Wallace, D. L., Han, M. H., Graham, D. L., Green, T. A., Vialou, V., Iniguez, S. D., et al. (2009). CREB regulation of nucleus accumbens excitability mediates social isolation-induced behavioral deficits. Nature Neuroscience, 12, 200-209. doi:10.1038/nn.2257
-
(2009)
Nature Neuroscience
, vol.12
, pp. 200-209
-
-
Wallace, D.L.1
Han, M.H.2
Graham, D.L.3
Green, T.A.4
Vialou, V.5
Iniguez, S.D.6
-
84
-
-
78549251736
-
Analysing biological pathways in genome-wide association studies
-
doi:10.1038/nrg2884
-
Wang, K., Li, M., & Hakonarson, H. (2010). Analysing biological pathways in genome-wide association studies. Nature Reviews Genetics, 11, 843-854. doi:10.1038/nrg2884
-
(2010)
Nature Reviews Genetics
, vol.11
, pp. 843-854
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
85
-
-
77951974619
-
Interpretation of association signals and identification of causal variants from genome-wide association studies
-
Wang, K., Samuel, P., Dickson, S. P., Stolle, C. A., Krantz, I. D., Goldstein, D. B., et al. (2010). Interpretation of association signals and identification of causal variants from genome-wide association studies. American Journal of Human Genetics, 86, 730-42.
-
(2010)
American Journal of Human Genetics
, vol.86
, pp. 730-742
-
-
Wang, K.1
Samuel, P.2
Dickson, S.P.3
Stolle, C.A.4
Krantz, I.D.5
Goldstein, D.B.6
-
86
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
doi:10.1038/nature07999
-
Wang, K., Zhang, H., Ma, D., Bucan, M., Glessner, J. T., Abrahams, B. S., et al. (2009). Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature, 459, 528-533. doi:10.1038/nature07999
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
Bucan, M.4
Glessner, J.T.5
Abrahams, B.S.6
-
87
-
-
0037617928
-
Molecular genetics of microvascular disease in diabetic retinopathy
-
doi:10.1038/sj.eye.6700348
-
Warpeha, K. M., & Chakravarthy, U. (2003). Molecular genetics of microvascular disease in diabetic retinopathy. Eye (Lond), 17, 305-311. doi:10.1038/sj.eye.6700348
-
(2003)
Eye (Lond)
, vol.17
, pp. 305-311
-
-
Warpeha, K.M.1
Chakravarthy, U.2
-
88
-
-
38549172807
-
Dscam and Sidekick proteins direct lamina-specific synaptic connections in vertebrate retina
-
doi:10.1038/nature06469
-
Yamagata, M., & Sanes, J. R. (2008). Dscam and Sidekick proteins direct lamina-specific synaptic connections in vertebrate retina. Nature, 451, 465-469. doi:10.1038/nature06469
-
(2008)
Nature
, vol.451
, pp. 465-469
-
-
Yamagata, M.1
Sanes, J.R.2
-
89
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan, A. L., Alarcon, M., Cheng, R., Magnusson, P. K., Spence, S. J., Palmer, A. A., et al. (2003). A genomewide screen of 345 families for autism-susceptibility loci. American Journal of Human Genetics, 73, 886-897.
-
(2003)
American Journal of Human Genetics
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.4
Spence, S.J.5
Palmer, A.A.6
-
90
-
-
10744226842
-
Overexpression of Nell-1, a craniosynostosis-associated gene, induces apoptosis in osteoblasts during craniofacial development
-
doi:10.1359/jbmr.2003.18.12.2126
-
Zhang, X., Carpenter, D., Bokui, N., Soo, C., Miao, S., Truong, T., et al. (2003). Overexpression of Nell-1, a craniosynostosis-associated gene, induces apoptosis in osteoblasts during craniofacial development. Journal of Bone and Mineral Research, 18, 2126-2134. doi:10.1359/jbmr.2003.18.12.2126
-
(2003)
Journal of Bone and Mineral Research
, vol.18
, pp. 2126-2134
-
-
Zhang, X.1
Carpenter, D.2
Bokui, N.3
Soo, C.4
Miao, S.5
Truong, T.6
-
91
-
-
0036738422
-
Craniosynostosis in transgenic mice overexpressing Nell-1
-
doi:10.1172/jci15375
-
Zhang, X., Kuroda, S., Carpenter, D., Nishimura, I., Soo, C., Moats, R., et al. (2002). Craniosynostosis in transgenic mice overexpressing Nell-1. Journal of Clinical Investigation, 110, 861-870. doi:10.1172/jci15375
-
(2002)
Journal of Clinical Investigation
, vol.110
, pp. 861-870
-
-
Zhang, X.1
Kuroda, S.2
Carpenter, D.3
Nishimura, I.4
Soo, C.5
Moats, R.6
-
92
-
-
0032842884
-
Characterization of human Kv4.2 mediating a rapidly-inactivating transient voltage-sensitive K+ current
-
Zhu, X. R., Wulf, A., Schwarz, M., Isbrandt, D., & Pongs, O. (1999). Characterization of human Kv4.2 mediating a rapidly-inactivating transient voltage-sensitive K+ current. Receptors and Channels, 6, 387-400.
-
(1999)
Receptors and Channels
, vol.6
, pp. 387-400
-
-
Zhu, X.R.1
Wulf, A.2
Schwarz, M.3
Isbrandt, D.4
Pongs, O.5
|