-
1
-
-
77957735529
-
A genomewide scan for common alleles affecting risk for autism
-
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, et al. 2010. A genomewide scan for common alleles affecting risk for autism. Hum Mol Genet 19: 4072-4082.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4072-4082
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Regan, R.4
Conroy, J.5
Magalhaes, T.R.6
Correia, C.7
Abrahams, B.S.8
Sykes, N.9
Pagnamenta, A.T.10
-
2
-
-
84867829870
-
Individual common variants exert weak effects on the risk for autism spectrum disorder
-
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bolte S, Bolton PF, Bourgeron T, et al. 2012. Individual common variants exert weak effects on the risk for autism spectrum disorder. Hum Mol Genet 21: 4781-4792.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4781-4792
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Almeida, J.4
Bacchelli, E.5
Baird, G.6
Bolshakova, N.7
Bolte, S.8
Bolton, P.F.9
Bourgeron, T.10
-
3
-
-
62649155943
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals
-
Browning BL, Browning SR. 2009. A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. Am J Hum Genet 84: 210-223.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 210-223
-
-
Browning, B.L.1
Browning, S.R.2
-
4
-
-
79959938953
-
Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients
-
Buizer-Voskamp JE, Muntjewerff JW, Strengman E, Sabatti C, Stefansson H, Vorstman JA, Ophoff RA. 2011. Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients. Biol Psychiatry 70: 655-662.
-
(2011)
Biol Psychiatry
, vol.70
, pp. 655-662
-
-
Buizer-Voskamp, J.E.1
Muntjewerff, J.W.2
Strengman, E.3
Sabatti, C.4
Stefansson, H.5
Vorstman, J.A.6
Ophoff, R.A.7
-
5
-
-
77950329947
-
Evidence for polygenic susceptibility to multiple sclerosis-The shape of things to come
-
Bush WS, Sawcer SJ, De Jager PL, Oksenberg JR, McCauley JL, Pericak-Vance MA, Haines JL. 2010. Evidence for polygenic susceptibility to multiple sclerosis-The shape of things to come. Am J Hum Genet 86: 621-625.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 621-625
-
-
Bush, W.S.1
Sawcer, S.J.2
De Jager, P.L.3
Oksenberg, J.R.4
McCauley, J.L.5
Pericak-Vance, M.A.6
Haines, J.L.7
-
6
-
-
66149185456
-
Genomewide association studies: History, rationale, and prospects for psychiatric disorders
-
Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, et al. 2009. Genomewide association studies: History, rationale, and prospects for psychiatric disorders. Am J Psychiatry 166: 540-556.
-
(2009)
Am J Psychiatry
, vol.166
, pp. 540-556
-
-
Cichon, S.1
Craddock, N.2
Daly, M.3
Faraone, S.V.4
Gejman, P.V.5
Kelsoe, J.6
Lehner, T.7
Levinson, D.F.8
Moran, A.9
Sklar, P.10
-
7
-
-
76749157485
-
The Kraepelinian dichotomy-Going, going. But still not gone
-
Craddock N, Owen MJ. 2010. The Kraepelinian dichotomy-Going, going. But still not gone. Br J Psychiatry 196: 92-95.
-
(2010)
Br J Psychiatry
, vol.196
, pp. 92-95
-
-
Craddock, N.1
Owen, M.J.2
-
8
-
-
45449089030
-
Psychosis and autism as diametrical disorders of the social brain
-
Crespi B, Badcock C. 2008. Psychosis and autism as diametrical disorders of the social brain. Behav Brain Sci 31: 241-261.
-
(2008)
Behav Brain Sci
, vol.31
, pp. 241-261
-
-
Crespi, B.1
Badcock, C.2
-
9
-
-
44449090109
-
Parental psychiatric disorders associated with autism spectrum disorders in the offspring
-
Daniels JL, Forssen U, Hultman CM, Cnattingius S, Savitz DA, Feychting M, Sparen P. 2008. Parental psychiatric disorders associated with autism spectrum disorders in the offspring. Pediatrics 121: e1357-e1362.
-
(2008)
Pediatrics
, vol.121
-
-
Daniels, J.L.1
Forssen, U.2
Hultman, C.M.3
Cnattingius, S.4
Savitz, D.A.5
Feychting, M.6
Sparen, P.7
-
10
-
-
79952310364
-
Do common variants play a role in risk for autism? Evidence and theoretical musings
-
Devlin B, Melhem N, Roeder K. 2011. Do common variants play a role in risk for autism? Evidence and theoretical musings. Brain Res 1380: 78-84.
-
(2011)
Brain Res
, vol.1380
, pp. 78-84
-
-
Devlin, B.1
Melhem, N.2
Roeder, K.3
-
11
-
-
17644415376
-
A family history study of Asperger syndrome
-
Ghaziuddin M. 2005. A family history study of Asperger syndrome. J Autism Dev Disord 35: 177-182.
-
(2005)
J Autism Dev Disord
, vol.35
, pp. 177-182
-
-
Ghaziuddin, M.1
-
12
-
-
78650808443
-
Phenotypic variability and genetic susceptibility to genomic disorders
-
Girirajan S, Eichler EE. 2010. Phenotypic variability and genetic susceptibility to genomic disorders. Hum Mol Genet 19: R176-R187.
-
(2010)
Hum Mol Genet
, vol.19
-
-
Girirajan, S.1
Eichler, E.E.2
-
13
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium. 2008. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455: 237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
14
-
-
0014375651
-
Autistic disturbances of affective contact
-
Kanner L. 1968. Autistic disturbances of affective contact. Acta Paedopsychiatr 35: 100-136.
-
(1968)
Acta Paedopsychiatr
, vol.35
, pp. 100-136
-
-
Kanner, L.1
-
15
-
-
0035261266
-
Autistic disorder and schizophrenia: Diagnostic overlaps
-
Konstantareas MM, Hewitt T. 2001. Autistic disorder and schizophrenia: Diagnostic overlaps. J Autism Dev Disord 31: 19-28.
-
(2001)
J Autism Dev Disord
, vol.31
, pp. 19-28
-
-
Konstantareas, M.M.1
Hewitt, T.2
-
16
-
-
18544369453
-
Risk factors for autism: Perinatal factors, parental psychiatric history, and socioeconomic status
-
Larsson HJ, Eaton WW, Madsen KM, Vestergaard M, Olesen AV, Agerbo E, Schendel D, Thorsen P, Mortensen PB. 2005. Risk factors for autism: Perinatal factors, parental psychiatric history, and socioeconomic status. Am J Epidemiol 161: 916-925.
-
(2005)
Am J Epidemiol
, vol.161
, pp. 916-925
-
-
Larsson, H.J.1
Eaton, W.W.2
Madsen, K.M.3
Vestergaard, M.4
Olesen, A.V.5
Agerbo, E.6
Schendel, D.7
Thorsen, P.8
Mortensen, P.B.9
-
17
-
-
77953867567
-
Genomic analysis of mental illness: A changing landscape
-
McClellan J, King MC. 2010. Genomic analysis of mental illness: A changing landscape. JAMA 303: 2523-2524.
-
(2010)
JAMA
, vol.303
, pp. 2523-2524
-
-
McClellan, J.1
King, M.C.2
-
18
-
-
70449724778
-
Copy-number variants in neurodevelopmental disorders: Promises and challenges
-
Merikangas AK, Corvin AP, Gallagher L. 2009. Copy-number variants in neurodevelopmental disorders: Promises and challenges. Trends Genet 25: 536-544.
-
(2009)
Trends Genet
, vol.25
, pp. 536-544
-
-
Merikangas, A.K.1
Corvin, A.P.2
Gallagher, L.3
-
19
-
-
37749023493
-
Psychiatric disorders in adults diagnosed as children with atypical autism. A case control study
-
Mouridsen SE, Rich B, Isager T. 2008a. Psychiatric disorders in adults diagnosed as children with atypical autism. A case control study. J Neural Transm 115: 135-138.
-
(2008)
J Neural Transm
, vol.115
, pp. 135-138
-
-
Mouridsen, S.E.1
Rich, B.2
Isager, T.3
-
20
-
-
38549109454
-
Psychiatric disorders in individuals diagnosed with infantile autism as children: A case control study
-
Mouridsen SE, Rich B, Isager T, Nedergaard NJ. 2008b. Psychiatric disorders in individuals diagnosed with infantile autism as children: A case control study. J Psychiatr Pract 14: 5-12.
-
(2008)
J Psychiatr Pract
, vol.14
, pp. 5-12
-
-
Mouridsen, S.E.1
Rich, B.2
Isager, T.3
Nedergaard, N.J.4
-
21
-
-
80052366179
-
Recurrence risk for autism spectrum disorders: A baby siblings research consortium study
-
Ozonoff S, Young GS, Carter A, Messinger D, Yirmiya N, Zwaigenbaum L, Bryson S, Carver LJ, Constantino JN, Dobkins K, et al. 2011. Recurrence risk for autism spectrum disorders: A baby siblings research consortium study. Pediatrics 128: e488-e495.
-
(2011)
Pediatrics
, vol.128
-
-
Ozonoff, S.1
Young, G.S.2
Carter, A.3
Messinger, D.4
Yirmiya, N.5
Zwaigenbaum, L.6
Bryson, S.7
Carver, L.J.8
Constantino, J.N.9
Dobkins, K.10
-
22
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, et al. 2010. Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466: 368-372.
-
(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
Conroy, J.7
Magalhaes, T.R.8
Correia, C.9
Abrahams, B.S.10
-
23
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, et al. 2007. PLINK: A tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
-
24
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P. 2009. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460: 748-752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'Donovan, M.C.5
Sullivan, P.F.6
Sklar, P.7
-
25
-
-
80052055926
-
A family-based study of common polygenic variation and risk of schizophrenia
-
Ruderfer DM, Kirov G, Chambert K, Moran JL, Owen MJ, O'Donovan MC, Sklar P, Purcell SM. 2011. A family-based study of common polygenic variation and risk of schizophrenia. Mol Psychiatry 16: 887-888.
-
(2011)
Mol Psychiatry
, vol.16
, pp. 887-888
-
-
Ruderfer, D.M.1
Kirov, G.2
Chambert, K.3
Moran, J.L.4
Owen, M.J.5
O'Donovan, M.C.6
Sklar, P.7
Purcell, S.M.8
-
26
-
-
84980128273
-
Concepts of autism: A review of research
-
Rutter M. 1968. Concepts of autism: A review of research. J Child Psychol Psychiatry 9: 1-25.
-
(1968)
J Child Psychol Psychiatry
, vol.9
, pp. 1-25
-
-
Rutter, M.1
-
27
-
-
34250463641
-
Childhood schizophrenia reconsidered
-
Rutter M. 1972. Childhood schizophrenia reconsidered. J Autism Child Schizophr 2: 315-337.
-
(1972)
J Autism Child Schizophr
, vol.2
, pp. 315-337
-
-
Rutter, M.1
-
28
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region are strongly associated with autism
-
Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, et al. 2011. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region are strongly associated with autism. Neuron 70: 863-885.
-
(2011)
Neuron
, vol.70
, pp. 863-885
-
-
Sanders, S.J.1
Ercan-Sencicek, A.G.2
Hus, V.3
Luo, R.4
Murtha, M.T.5
Moreno-De-Luca, D.6
Chu, S.H.7
Moreau, M.P.8
Gupta, A.R.9
Thomson, S.A.10
-
29
-
-
79958023253
-
The benefit of directly comparing autism and schizophrenia for revealing mechanisms of social cognitive impairment
-
Sasson NJ, Pinkham AE, Carpenter KL, Belger A. 2011. The benefit of directly comparing autism and schizophrenia for revealing mechanisms of social cognitive impairment. J Neurodev Disord 3: 87-100.
-
(2011)
J Neurodev Disord
, vol.3
, pp. 87-100
-
-
Sasson, N.J.1
Pinkham, A.E.2
Carpenter, K.L.3
Belger, A.4
-
30
-
-
0035173378
-
dbSNP: The NCBI database of genetic variation
-
Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, Smigielski EM, Sirotkin K. 2001. dbSNP: The NCBI database of genetic variation. Nucleic Acids Res 29: 308-311.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
Smigielski, E.M.6
Sirotkin, K.7
-
31
-
-
70350700468
-
Psychosis, affective disorders and anxiety in autistic spectrum disorder: Prevalence and nosological considerations
-
Skokauskas N, Gallagher L. 2010. Psychosis, affective disorders and anxiety in autistic spectrum disorder: Prevalence and nosological considerations. Psychopathology 43: 8-16.
-
(2010)
Psychopathology
, vol.43
, pp. 8-16
-
-
Skokauskas, N.1
Gallagher, L.2
-
32
-
-
3142756617
-
Bipolar disorder, schizophrenia, and other psychotic disorders in adults with childhood onset AD/HD and/or autism spectrum disorders
-
Stahlberg O, Soderstrom H, Rastam M, Gillberg C. 2004. Bipolar disorder, schizophrenia, and other psychotic disorders in adults with childhood onset AD/HD and/or autism spectrum disorders. J Neural Transm 111: 891-902.
-
(2004)
J Neural Transm
, vol.111
, pp. 891-902
-
-
Stahlberg, O.1
Soderstrom, H.2
Rastam, M.3
Gillberg, C.4
-
33
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson H, Rujescu D, Cichon S, Pietilainen OP, Ingason A, Steinberg S, Fossdal R, Sigurdsson E, Sigmundsson T, Buizer-Voskamp JE, et al. 2008. Large recurrent microdeletions associated with schizophrenia. Nature 455: 232-236.
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietilainen, O.P.4
Ingason, A.5
Steinberg, S.6
Fossdal, R.7
Sigurdsson, E.8
Sigmundsson, T.9
Buizer-Voskamp, J.E.10
-
34
-
-
84868531256
-
Family history of schizophrenia and bipolar disorder as risk factors for autism
-
Sullivan PF, Magnusson C, Reichenberg A, Boman M, Dalman C, Davidson M, Fruchter E, Hultman CM, Lundberg M, Langstrom N, et al. 2012. Family history of schizophrenia and bipolar disorder as risk factors for autism. Arch Gen Psychiatry 69: 1099-1103.
-
(2012)
Arch Gen Psychiatry
, vol.69
, pp. 1099-1103
-
-
Sullivan, P.F.1
Magnusson, C.2
Reichenberg, A.3
Boman, M.4
Dalman, C.5
Davidson, M.6
Fruchter, E.7
Hultman, C.M.8
Lundberg, M.9
Langstrom, N.10
-
35
-
-
84860151961
-
Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses
-
Visscher PM, Goddard ME, Derks EM, Wray NR. 2012. Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. Mol Psychiatry 17: 474-485.
-
(2012)
Mol Psychiatry
, vol.17
, pp. 474-485
-
-
Visscher, P.M.1
Goddard, M.E.2
Derks, E.M.3
Wray, N.R.4
-
36
-
-
0025748041
-
Comorbid association of autism and schizophrenia
-
Volkmar FR, Cohen DJ. 1991. Comorbid association of autism and schizophrenia. Am J Psychiatry 148: 1705-1707.
-
(1991)
Am J Psychiatry
, vol.148
, pp. 1705-1707
-
-
Volkmar, F.R.1
Cohen, D.J.2
-
37
-
-
32844460507
-
Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism
-
Vorstman JA, Staal WG, van Daalen E, van Engeland H, Hochstenbach PF, Franke L. 2006. Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism. Mol Psychiatry 11: 18-28.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 18-28
-
-
Vorstman, J.A.1
Staal, W.G.2
van Daalen, E.3
van Engeland, H.4
Hochstenbach, P.F.5
Franke, L.6
-
38
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, et al. 2008. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320: 539-543.
-
(2008)
Science
, vol.320
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Addington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
Nord, A.S.7
Kusenda, M.8
Malhotra, D.9
Bhandari, A.10
-
39
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR, Madden PA, Heath AC, Martin NG, Montgomery GW, et al. 2010. Common SNPs explain a large proportion of the heritability for human height. Nat Genet 42: 565-569.
-
(2010)
Nat Genet
, vol.42
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
Nyholt, D.R.6
Madden, P.A.7
Heath, A.C.8
Martin, N.G.9
Montgomery, G.W.10
|