-
1
-
-
84870469320
-
-
APA 4th edn, text revision (DSM-IV-TR) edn. American Psychiatric Association: Washington, DC
-
APA. Diagnostic and Statistical Manual of Mental Disorders, 4th edn, text revision (DSM-IV-TR) edn. American Psychiatric Association: Washington, DC 2000.
-
(2000)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
2
-
-
79957609175
-
Tourette syndrome: Evolving concepts
-
Jankovic J, Kurlan R. Tourette syndrome: evolving concepts. Mov Disord 2011; 26: 1149-1156.
-
(2011)
Mov Disord
, vol.26
, pp. 1149-1156
-
-
Jankovic, J.1
Kurlan, R.2
-
3
-
-
70449383317
-
Genetics of tic disorders
-
Rimoin DL, Connor JM, Pyeritz RE, Korf BR (eds) 5th edn Churchill Livingstone/Elsevier: Philadelphia
-
Scharf JM, Pauls DL. Genetics of tic disorders. In: Rimoin DL, Connor JM, Pyeritz RE, Korf BR (eds) Emery and Rimoin's Principles and Practices of Medical Genetics, 5th edn Churchill Livingstone/Elsevier: Philadelphia, 2007 pp 2737-2754.
-
(2007)
Emery and Rimoin's Principles and Practices of Medical Genetics
, pp. 2737-2754
-
-
Scharf, J.M.1
Pauls, D.L.2
-
4
-
-
53749095172
-
The prevalence and epidemiology of Gilles de la Tourette syndrome. Part 1: The epidemiological and prevalence studies
-
Robertson MM. The prevalence and epidemiology of Gilles de la Tourette syndrome. Part 1: the epidemiological and prevalence studies. J Psychosom Res 2008; 65: 461-472.
-
(2008)
J Psychosom Res
, vol.65
, pp. 461-472
-
-
Robertson, M.M.1
-
5
-
-
0033917041
-
An international perspective on Tourette syndrome: Selected findings from 3500 individuals in 22 countries
-
Freeman RD, Fast DK, Burd L, Kerbeshian J, Robertson MM, Sandor P. An international perspective on Tourette syndrome: selected findings from 3500 individuals in 22 countries. Dev Med Child Neurol 2000; 42: 436-447.
-
(2000)
Dev Med Child Neurol
, vol.42
, pp. 436-447
-
-
Freeman, R.D.1
Fast, D.K.2
Burd, L.3
Kerbeshian, J.4
Robertson, M.M.5
Sandor, P.6
-
10
-
-
33846632694
-
Genome scan for Tourette disorder in affected-sibling-pair and multi-generational families
-
TSAICG.
-
TSAICG. Genome scan for Tourette disorder in affected-sibling-pair and multi-generational families. Am J Hum Genet 2007; 80: 265-272.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 265-272
-
-
-
11
-
-
0038278610
-
CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder
-
Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA. CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics 2003; 82: 1-9.
-
(2003)
Genomics
, vol.82
, pp. 1-9
-
-
Verkerk, A.J.1
Mathews, C.A.2
Joosse, M.3
Eussen, B.H.4
Heutink, P.5
Oostra, B.A.6
-
12
-
-
26844498125
-
Sequence variants in SLITRK1 are associated with Tourette's syndrome
-
Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM et al. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 2005; 310: 317-320.
-
(2005)
Science
, vol.310
, pp. 317-320
-
-
Abelson, J.F.1
Kwan, K.Y.2
O'Roak, B.J.3
Baek, D.Y.4
Stillman, A.A.5
Morgan, T.M.6
-
13
-
-
77952629167
-
L-histidine decarboxylase and Tourette's syndrome
-
Ercan-Sencicek AG, Stillman AA, Ghosh AK, Bilguvar K, O'Roak BJ, Mason CE et al. L-histidine decarboxylase and Tourette's syndrome. N Engl J Med 2010; 362: 1901-1908.
-
(2010)
N Engl J Med
, vol.362
, pp. 1901-1908
-
-
Ercan-Sencicek, A.G.1
Stillman, A.A.2
Ghosh, A.K.3
Bilguvar, K.4
O'Roak, B.J.5
Mason, C.E.6
-
14
-
-
42049101407
-
Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample
-
Scharf JM, Moorjani P, Fagerness J, Platko JV, Illmann C, Galloway B et al. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample. Neurology 2008; 70(16 Pt 2): 1495-1496.
-
(2008)
Neurology
, vol.70
, Issue.16 PART 2
, pp. 1495-1496
-
-
Scharf, J.M.1
Moorjani, P.2
Fagerness, J.3
Platko, J.V.4
Illmann, C.5
Galloway, B.6
-
15
-
-
77951878282
-
Additional support for the association of SLITRK1 var321 and Tourette syndrome
-
O'Roak BJ, Morgan TM, Fishman DO, Saus E, Alonso P, Gratacos M et al. Additional support for the association of SLITRK1 var321 and Tourette syndrome. Mol Psychiatry 2010; 15: 447-450.
-
(2010)
Mol Psychiatry
, vol.15
, pp. 447-450
-
-
O'Roak, B.J.1
Morgan, T.M.2
Fishman, D.O.3
Saus, E.4
Alonso, P.5
Gratacos, M.6
-
16
-
-
0027433824
-
Definitions and classification of tic disorders
-
TSCSG.
-
TSCSG. Definitions and classification of tic disorders. Arch Neurol 1993; 50: 1013-1016.
-
(1993)
Arch Neurol
, vol.50
, pp. 1013-1016
-
-
-
17
-
-
0042351172
-
Defining alcohol-related phenotypes in humans. The Collaborative Study on the genetics of alcoholism
-
Bierut LJ, Saccone NL, Rice JP, Goate A, Foroud T, Edenberg H et al. Defining alcohol-related phenotypes in humans. The Collaborative Study on the genetics of alcoholism. Alcohol Res Health 2002; 26: 208-213.
-
(2002)
Alcohol Res Health
, vol.26
, pp. 208-213
-
-
Bierut, L.J.1
Saccone, N.L.2
Rice, J.P.3
Goate, A.4
Foroud, T.5
Edenberg, H.6
-
18
-
-
33846536406
-
Novel genes identified in a high-density genome wide association study for nicotine dependence
-
Bierut LJ, Madden PA, Breslau N, Johnson EO, Hatsukami D, Pomerleau OF et al. Novel genes identified in a high-density genome wide association study for nicotine dependence. Hum Mol Genet 2007; 16: 24-35.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 24-35
-
-
Bierut, L.J.1
Madden, P.A.2
Breslau, N.3
Johnson, E.O.4
Hatsukami, D.5
Pomerleau, O.F.6
-
19
-
-
40649119407
-
Drug use and dependence in cocaine dependent subjects, community-based individuals, and their siblings
-
Bierut LJ, Strickland JR, Thompson JR, Afful SE, Cottler LB. Drug use and dependence in cocaine dependent subjects, community-based individuals, and their siblings. Drug Alcohol Depend 2008; 95: 14-22.
-
(2008)
Drug Alcohol Depend
, vol.95
, pp. 14-22
-
-
Bierut, L.J.1
Strickland, J.R.2
Thompson, J.R.3
Afful, S.E.4
Cottler, L.B.5
-
20
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D et al. Common variants conferring risk of schizophrenia. Nature 2009; 460: 744-747.
-
(2009)
Nature
, vol.460
, pp. 744-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
Andreassen, O.A.4
Cichon, S.5
Rujescu, D.6
-
21
-
-
0038143616
-
Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica
-
Carvajal-Carmona LG, Ophoff R, Service S, Hartiala J, Molina J, Leon P et al. Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica. Hum Genet 2003; 112: 534-541.
-
(2003)
Hum Genet
, vol.112
, pp. 534-541
-
-
Carvajal-Carmona, L.G.1
Ophoff, R.2
Service, S.3
Hartiala, J.4
Molina, J.5
Leon, P.6
-
22
-
-
33646375453
-
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies
-
Service S, DeYoung J, Karayiorgou M, Roos JL, Pretorious H, Bedoya G et al. Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies. Nat Genet 2006; 38: 556-560.
-
(2006)
Nat Genet
, vol.38
, pp. 556-560
-
-
Service, S.1
Deyoung, J.2
Karayiorgou, M.3
Roos, J.L.4
Pretorious, H.5
Bedoya, G.6
-
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 et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 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
-
24
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D. Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006; 38: 904-909.
-
(2006)
Nat Genet
, 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
-
25
-
-
84879418465
-
Genome-wide association study of obsessive-compulsive disorder
-
in press
-
Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD et al. Genome-wide association study of obsessive-compulsive disorder. Mol Psychiatry (in press).
-
Mol Psychiatry
-
-
Stewart, S.E.1
Yu, D.2
Scharf, J.M.3
Neale, B.M.4
Fagerness, J.A.5
Mathews, C.A.6
Arnold, P.D.7
-
26
-
-
77955894071
-
METAL: Fast and efficient meta-analysis of genomewide association scans
-
Willer CJ, Li Y, Abecasis GR. METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 2010; 26: 2190-2191.
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
27
-
-
79952269948
-
A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci
-
Gamazon ER, Nicolae DL, Cox NJ. A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci. PLoS Genet 2011; 7: e1001292.
-
(2011)
PLoS Genet
, vol.7
-
-
Gamazon, E.R.1
Nicolae, D.L.2
Cox, N.J.3
-
28
-
-
77953223693
-
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
-
Gibbs JR, van der Brug MP, Hernandez DG, Traynor BJ, Nalls MA, Lai SL et al. Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain. PLoS Genet 2010; 6: e1000952.
-
(2010)
PLoS Genet
, vol.6
-
-
Gibbs, J.R.1
Van Der Brug, M.P.2
Hernandez, D.G.3
Traynor, B.J.4
Nalls, M.A.5
Lai, S.L.6
-
29
-
-
84884212298
-
Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants
-
advance online publication 3 January 2012; doi:10.1038/mp.2011.174
-
Gamazon ER, Badner JA, Cheng L, Zhang C, Zhang D, Cox NJ et al. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Mol Psychiatry; advance online publication, 3 January 2012; doi:10.1038/mp.2011.174.
-
Mol Psychiatry
-
-
Gamazon, E.R.1
Badner, J.A.2
Cheng, L.3
Zhang, C.4
Zhang, D.5
Cox, N.J.6
-
30
-
-
77649204292
-
Genetic control of individual differences in gene-specific methylation in human brain
-
Zhang D, Cheng L, Badner JA, Chen C, Chen Q, Luo W et al. Genetic control of individual differences in gene-specific methylation in human brain. Am J Hum Genet 2010; 86: 411-419.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 411-419
-
-
Zhang, D.1
Cheng, L.2
Badner, J.A.3
Chen, C.4
Chen, Q.5
Luo, W.6
-
31
-
-
67651222400
-
A flexible and accurate genotype imputation method for the next generation of genome-wide association studies
-
Howie BN, Donnelly P, Marchini J. A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 2009; 5: e1000529.
-
(2009)
PLoS Genet
, vol.5
-
-
Howie, B.N.1
Donnelly, P.2
Marchini, J.3
-
32
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project.
-
1000 Genomes Project. A map of human genome variation from population-scale sequencing. Nature 2010; 467: 1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
33
-
-
43249125992
-
Estimation of the multiple testing burden for genomewide association studies of nearly all common variants
-
Pe'er I, Yelensky R, Altshuler D, Daly MJ. Estimation of the multiple testing burden for genomewide association studies of nearly all common variants. Genet Epidemiol 2008; 32: 381-385.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 381-385
-
-
Pe'Er, I.1
Yelensky, R.2
Altshuler, D.3
Daly, M.J.4
-
34
-
-
42249087793
-
Estimation of significance thresholds for genomewide association scans
-
Dudbridge F, Gusnanto A. Estimation of significance thresholds for genomewide association scans. Genet Epidemiol 2008; 32: 227-234.
-
(2008)
Genet Epidemiol
, vol.32
, pp. 227-234
-
-
Dudbridge, F.1
Gusnanto, A.2
-
35
-
-
77957914609
-
The psychiatric GWAS consortium: Big science comes to psychiatry
-
Sullivan PF. The psychiatric GWAS consortium: big science comes to psychiatry. Neuron 2010; 68: 182-186.
-
(2010)
Neuron
, vol.68
, pp. 182-186
-
-
Sullivan, P.F.1
-
36
-
-
33646376925
-
Neurobiology of basal ganglia and Tourette syndrome: Basal ganglia circuits and thalamocortical outputs
-
Mink JW. Neurobiology of basal ganglia and Tourette syndrome: basal ganglia circuits and thalamocortical outputs. Adv Neurol 2006; 99: 89-98.
-
(2006)
Adv Neurol
, vol.99
, pp. 89-98
-
-
Mink, J.W.1
-
38
-
-
0344088437
-
Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1
-
Pace JM, Corrado M, Missero C, Byers PH. Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1. Matrix Biol 2003; 22: 3-14.
-
(2003)
Matrix Biol
, vol.22
, pp. 3-14
-
-
Pace, J.M.1
Corrado, M.2
Missero, C.3
Byers, P.H.4
-
39
-
-
50849107027
-
Novel roles for collagens in wiring the vertebrate nervous system
-
Fox MA. Novel roles for collagens in wiring the vertebrate nervous system. Curr Opin Cell Biol 2008; 20: 508-513.
-
(2008)
Curr Opin Cell Biol
, vol.20
, pp. 508-513
-
-
Fox, M.A.1
-
40
-
-
36549073601
-
The expanding RNA polymerase III transcriptome
-
Dieci G, Fiorino G, Castelnuovo M, Teichmann M, Pagano A. The expanding RNA polymerase III transcriptome. Trends Genet 2007; 23: 614-622.
-
(2007)
Trends Genet
, vol.23
, pp. 614-622
-
-
Dieci, G.1
Fiorino, G.2
Castelnuovo, M.3
Teichmann, M.4
Pagano, A.5
-
41
-
-
81155128530
-
Mutations in POLR3A and POLR3B encoding RNA Polymerase III subunits cause an autosomal-recessive hypomyelinating leukoencephalopathy
-
Saitsu H, Osaka H, Sasaki M, Takanashi J, Hamada K, Yamashita A et al. Mutations in POLR3A and POLR3B encoding RNA Polymerase III subunits cause an autosomal-recessive hypomyelinating leukoencephalopathy. Am J Hum Genet 2011; 89: 644-651.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 644-651
-
-
Saitsu, H.1
Osaka, H.2
Sasaki, M.3
Takanashi, J.4
Hamada, K.5
Yamashita, A.6
-
42
-
-
80955151659
-
Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophy
-
Tetreault M, Choquet K, Orcesi S, Tonduti D, Balottin U, Teichmann M et al. Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophy. Am J Hum Genet 2011; 89: 652-655.
-
(2011)
Am J Hum Genet
, vol.89
, pp. 652-655
-
-
Tetreault, M.1
Choquet, K.2
Orcesi, S.3
Tonduti, D.4
Balottin, U.5
Teichmann, M.6
-
43
-
-
0034687097
-
Human nectin3/PRR3: A novel member of the PVR/PRR/nectin family that interacts with afadin
-
Reymond N, Borg JP, Lecocq E, Adelaide J, Campadelli-Fiume G, Dubreuil P et al. Human nectin3/PRR3: a novel member of the PVR/PRR/nectin family that interacts with afadin. Gene 2000; 255: 347-355.
-
(2000)
Gene
, vol.255
, pp. 347-355
-
-
Reymond, N.1
Borg, J.P.2
Lecocq, E.3
Adelaide, J.4
Campadelli-Fiume, G.5
Dubreuil, P.6
-
44
-
-
73649085461
-
Thrombospondin type i domain containing 7A (THSD7A) mediates endothelial cell migration and tube formation
-
Wang CH, Su PT, Du XY, Kuo MW, Lin CY, Yang CC et al. Thrombospondin type I domain containing 7A (THSD7A) mediates endothelial cell migration and tube formation. J Cell Physiol 2010; 222: 685-694.
-
(2010)
J Cell Physiol
, vol.222
, pp. 685-694
-
-
Wang, C.H.1
Su, P.T.2
Du, X.Y.3
Kuo, M.W.4
Lin, C.Y.5
Yang, C.C.6
-
45
-
-
77649136250
-
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
-
Van Deerlin VM, Sleiman PM, Martinez-Lage M, Chen-Plotkin A, Wang LS, Graff-Radford NR et al. Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nat Genet 2010; 42: 234-239.
-
(2010)
Nat Genet
, vol.42
, pp. 234-239
-
-
Van Deerlin, V.M.1
Sleiman, P.M.2
Martinez-Lage, M.3
Chen-Plotkin, A.4
Wang, L.S.5
Graff-Radford, N.R.6
-
46
-
-
66649096211
-
Association of SLITRK1 to Gilles de la Tourette Syndrome
-
Miranda DM, Wigg K, Kabia EM, Feng Y, Sandor P, Barr CL. Association of SLITRK1 to Gilles de la Tourette Syndrome. Am J Med Genet B Neuropsychiatr Genet 2009; 150B: 483-486.
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.150 B
, pp. 483-486
-
-
Miranda, D.M.1
Wigg, K.2
Kabia, E.M.3
Feng, Y.4
Sandor, P.5
Barr, C.L.6
-
47
-
-
84862768792
-
Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families
-
advance online publication 15 November 2011; doi:10.1038/mp.2011.151
-
Karagiannidis I, Rizzo R, Tarnok Z, Wolanczyk T, Hebebrand J, Nothen MM et al. Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families. Mol Psychiatry; advance online publication, 15 November 2011; doi:10.1038/mp.2011.151.
-
Mol Psychiatry
-
-
Karagiannidis, I.1
Rizzo, R.2
Tarnok, Z.3
Wolanczyk, T.4
Hebebrand, J.5
Nothen, M.M.6
-
48
-
-
80053319759
-
Genetic signatures of exceptional longevity in humans
-
[Science advance online publication 1 July 2010; doi:10.1126/science. 1190532; Retraction in: Science 2011; 333: 404]
-
Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S et al. Genetic signatures of exceptional longevity in humans. Science 2010 [Science advance online publication, 1 July 2010; doi:10.1126/science.1190532; Retraction in: Science 2011; 333: 404].
-
(2010)
Science
-
-
Sebastiani, P.1
Solovieff, N.2
Puca, A.3
Hartley, S.W.4
Melista, E.5
Andersen, S.6
-
49
-
-
41949133594
-
Geographic patterns of genome admixture in Latin American Mestizos
-
Wang S, Ray N, Rojas W, Parra MV, Bedoya G, Gallo C et al. Geographic patterns of genome admixture in Latin American Mestizos. PLoS Genet 2008; 4: e1000037.
-
(2008)
PLoS Genet
, vol.4
-
-
Wang, S.1
Ray, N.2
Rojas, W.3
Parra, M.V.4
Bedoya, G.5
Gallo, C.6
-
50
-
-
77952503974
-
Tourette syndrome is associated with recurrent exonic copy number variants
-
Sundaram SK, Huq AM, Wilson BJ, Chugani HT. Tourette syndrome is associated with recurrent exonic copy number variants. Neurology 2010; 74: 1583-1590.
-
(2010)
Neurology
, vol.74
, pp. 1583-1590
-
-
Sundaram, S.K.1
Huq, A.M.2
Wilson, B.J.3
Chugani, H.T.4
-
51
-
-
79955409459
-
Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder
-
Sundaram SK, Huq AM, Sun Z, Yu W, Bennett L, Wilson BJ et al. Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder. Ann Neurol 2011; 69: 901-904.
-
(2011)
Ann Neurol
, vol.69
, pp. 901-904
-
-
Sundaram, S.K.1
Huq, A.M.2
Sun, Z.3
Yu, W.4
Bennett, L.5
Wilson, B.J.6
-
52
-
-
84858737859
-
Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism
-
Fernandez TV, Sanders SJ, Yurkiewicz IR, Ercan-Sencicek AG, Kim YS, Fishman DO et al. Rare copy number variants in Tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biol Psychiatry 2012; 71: 392-402.
-
(2012)
Biol Psychiatry
, vol.71
, pp. 392-402
-
-
Fernandez, T.V.1
Sanders, S.J.2
Yurkiewicz, I.R.3
Ercan-Sencicek, A.G.4
Kim, Y.S.5
Fishman, D.O.6
-
53
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium.
-
International Schizophrenia Consortium. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
54
-
-
84862777863
-
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs
-
Lee SH, DeCandia TR, Ripke S, Yang J, Sullivan PF, Goddard ME et al. Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet 2012; 44: 247-250.
-
(2012)
Nat Genet
, vol.44
, pp. 247-250
-
-
Lee, S.H.1
Decandia, T.R.2
Ripke, S.3
Yang, J.4
Sullivan, P.F.5
Goddard, M.E.6
-
55
-
-
84855348536
-
Don't give up on GWAS
-
Sullivan P. Don't give up on GWAS. Mol Psychiatry 2012; 17: 2-3.
-
(2012)
Mol Psychiatry
, vol.17
, pp. 2-3
-
-
Sullivan, P.1
|