-
1
-
-
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. JPsychosom Res. 2008;65(5):461-472
-
(2008)
JPsychosom Res
, vol.65
, Issue.5
, pp. 461-472
-
-
Robertson, M.M.1
-
2
-
-
0027433824
-
Definitions and classification of tic disorders
-
The Tourette Syndrome Classification Study Group
-
Definitions and classification of tic disorders. The Tourette Syndrome Classification Study Group. Arch Neurol. 1993;50 (10):1013-1016
-
(1993)
Arch Neurol
, vol.50
, Issue.10
, pp. 1013-1016
-
-
-
3
-
-
0035000925
-
Prospective, longitudinal study of tic, obsessive-compulsive, and attention-deficit/ hyperactivity disorders in an epidemiological sample
-
Peterson BS, Pine DS, Cohen P, Brook JS. Prospective, longitudinal study of tic, obsessive-compulsive, and attention-deficit/ hyperactivity disorders in an epidemiological sample. JAm Acad Child Adolesc Psychiatry. 2001;40(6):685-695
-
(2001)
JAm Acad Child Adolesc Psychiatry
, vol.40
, Issue.6
, pp. 685-695
-
-
Peterson, B.S.1
Pine, D.S.2
Cohen, P.3
Brook, J.S.4
-
4
-
-
0033983916
-
Tourette syndrome, associated conditions and the complexities of treatment
-
Robertson MM. Tourette syndrome, associated conditions and the complexities of treatment. Brain. 2000;123(Pt 3):425-462
-
(2000)
Brain
, vol.123
, Issue.3
, pp. 425-462
-
-
Robertson, M.M.1
-
5
-
-
0019469312
-
Familial pattern and transmission of Gilles de la Tourette syndrome and multiple tics
-
Pauls DL, Cohen DJ, Heimbuch R, Detlor J, Kidd KK. Familial pattern and transmission of Gilles de la Tourette syndrome and multiple tics. Arch Gen Psychiatry. 1981;38(10):1091-1093
-
(1981)
Arch Gen Psychiatry
, vol.38
, Issue.10
, pp. 1091-1093
-
-
Pauls, D.L.1
Cohen, D.J.2
Heimbuch, R.3
Detlor, J.4
Kidd, K.K.5
-
6
-
-
0021971622
-
A twin study of Tourette syndrome
-
Price RA, Kidd KK, Cohen DJ, Pauls DL, Leckman JF. A twin study of Tourette syndrome. Arch Gen Psychiatry. 1985;42(8):815-820
-
(1985)
Arch Gen Psychiatry
, vol.42
, Issue.8
, pp. 815-820
-
-
Price, R.A.1
Kidd, K.K.2
Cohen, D.J.3
Pauls, D.L.4
Leckman, J.F.5
-
7
-
-
0031963425
-
Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse
-
Gade R, Muhleman D, Blake H, MacMurray J, Johnson P, Verde R, et al. Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse. Mol Psychiatry. 1998;3(1):50-60.
-
(1998)
Mol Psychiatry
, vol.3
, Issue.1
, pp. 50-60
-
-
Gade, R.1
Muhleman, D.2
Blake, H.3
MacMurray, J.4
Johnson, P.5
Verde, R.6
-
8
-
-
19244363371
-
Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmissiondisequilibrium test
-
Grice DE, Leckman JF, Pauls DL, Kurlan R, Kidd KK, Pakstis AJ, et al. Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmissiondisequilibrium test. Am JHum Genet. 1996;59(3):644-652
-
(1996)
Am JHum Genet
, vol.59
, Issue.3
, pp. 644-652
-
-
Grice, D.E.1
Leckman, J.F.2
Pauls, D.L.3
Kurlan, R.4
Kidd, K.K.5
Pakstis, A.J.6
-
9
-
-
1942502214
-
Tourette syndrome and dopaminergic genes: A family-based association study in the French Canadian founder population
-
Diaz-Anzaldua A, Joober R, Riviere JB, Dion Y, Lesperance P, Richer F, et al. Tourette syndrome and dopaminergic genes: a family-based association study in the French Canadian founder population. Mol Psychiatry. 2004;9(3):272-277
-
(2004)
Mol Psychiatry
, vol.9
, Issue.3
, pp. 272-277
-
-
Diaz-Anzaldua, A.1
Joober, R.2
Riviere, J.B.3
Dion, Y.4
Lesperance, P.5
Richer, F.6
-
10
-
-
0028986830
-
Exclusion of the 5-HT1A serotonin neuroreceptor and tryptophan oxygenase genes in a large British kindred multiply affected with Tourette's syndrome, chronic motor tics, and obsessive-compulsive behavior
-
Brett PM, Curtis D, Robertson MM, Gurling HM. Exclusion of the 5-HT1A serotonin neuroreceptor and tryptophan oxygenase genes in a large British kindred multiply affected with Tourette's syndrome, chronic motor tics, and obsessive-compulsive behavior. Am JPsychiatry . 1995;152(3):437-440
-
(1995)
Am JPsychiatry
, vol.152
, Issue.3
, pp. 437-440
-
-
Brett, P.M.1
Curtis, D.2
Robertson, M.M.3
Gurling, H.M.4
-
11
-
-
0030747149
-
Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome
-
Hebebrand J, Nothen MM, Ziegler A, Klug B, Neidt H, Eggermann K, et al. Nonreplication of linkage disequilibrium between the dopamine D4 receptor locus and Tourette syndrome. Am JHum Genet. 1997;61(1):238-239
-
(1997)
Am J Hum Genet
, vol.61
, Issue.1
, pp. 238-239
-
-
Hebebrand, J.1
Nothen, M.M.2
Ziegler, A.3
Klug, B.4
Neidt, H.5
Eggermann, K.6
-
12
-
-
0033588059
-
Studies of the 48 bp repeat polymorphism of the DRD4 gene in impulsive, compulsive, addictive behaviors: Tourette syndrome, ADHD, pathological gambling, and substance abuse
-
Comings DE, Gonzalez N,Wu S, Gade R, Muhleman D, Saucier G, et al. Studies of the 48 bp repeat polymorphism of the DRD4 gene in impulsive, compulsive, addictive behaviors: Tourette syndrome, ADHD, pathological gambling, and substance abuse. Am JM ed Genet. 1999;88(4):358-368
-
(1999)
Am JM Ed Genet
, vol.88
, Issue.4
, pp. 358-368
-
-
Comings, D.E.1
Gonzalez, N.2
Wu, S.3
Gade, R.4
Muhleman, D.5
Saucier, G.6
-
13
-
-
2542446307
-
Isolates and their potential use in complex gene mapping efforts
-
Varilo T, Peltonen L. Isolates and their potential use in complex gene mapping efforts. Curr Opin Genet Dev. 2004;14(3):316-323
-
(2004)
Curr Opin Genet Dev
, vol.14
, Issue.3
, pp. 316-323
-
-
Varilo, T.1
Peltonen, L.2
-
14
-
-
31344432937
-
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
-
Lesage S, Durr A, Tazir M, Lohmann E, Leutenegger AL, Janin S, et al. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. N Engl JMed. 2006;354(4):422-423
-
(2006)
N Engl JMed
, vol.354
, Issue.4
, pp. 422-423
-
-
Lesage, S.1
Durr, A.2
Tazir, M.3
Lohmann, E.4
Leutenegger, A.L.5
Janin, S.6
-
15
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
Ozelius LJ, Senthil G, Saunders-Pullman R, Ohmann E, Deligtisch A, Tagliati M, et al. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N Engl J Med. 2006;354(4):424-425
-
(2006)
N Engl J Med
, vol.354
, Issue.4
, pp. 424-425
-
-
Ozelius, L.J.1
Senthil, G.2
Saunders-Pullman, R.3
Ohmann, E.4
Deligtisch, A.5
Tagliati, M.6
-
16
-
-
0032231382
-
Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families
-
Tonin PN, Mes-Masson AM, Futreal PA, Morgan K, Mahon M, Foulkes WD, et al. Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families. Am JHum Genet. 1998;63(5):1341-1351
-
(1998)
Am JHum Genet
, vol.63
, Issue.5
, pp. 1341-1351
-
-
Tonin, P.N.1
Mes-Masson, A.M.2
Futreal, P.A.3
Morgan, K.4
Mahon, M.5
Foulkes, W.D.6
-
17
-
-
0028940272
-
Variability of the genetic contribution of Quebec population founders associated to some deleterious genes
-
Heyer E, Tremblay M. Variability of the genetic contribution of Quebec population founders associated to some deleterious genes. Am JHum Genet. 1995;56(4):970-978
-
(1995)
Am JHum Genet
, vol.56
, Issue.4
, pp. 970-978
-
-
Heyer, E.1
Tremblay, M.2
-
18
-
-
0024435153
-
The yale-brown obsessive compulsive scale. I.Development, use, and reliability
-
Goodman WK, Price LH, Rasmussen SA, Mazure C, Fleischmann RL, Hill CL, et al. The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability. Arch Gen Psychiatry. 1989;46(11):1006-1011
-
(1989)
Arch Gen Psychiatry
, vol.46
, Issue.11
, pp. 1006-1011
-
-
Goodman, W.K.1
Price, L.H.2
Rasmussen, S.A.3
Mazure, C.4
Fleischmann, R.L.5
Hill, C.L.6
-
19
-
-
0033814928
-
Implementing a unified approach to family-based tests of association
-
Laird NM, Horvath S, Xu X. Implementing a unified approach to family-based tests of association. Genet Epidemiol. 2000;19 Suppl 1:S36-42.
-
(2000)
Genet Epidemiol
, vol.19
, Issue.SUPPL. 1
-
-
Laird, N.M.1
Horvath, S.2
Xu, X.3
-
20
-
-
0034054165
-
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information
-
Rabinowitz D, Laird N. A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information. Hum Hered. 2000;50(4):211-223
-
(2000)
Hum Hered
, vol.50
, Issue.4
, pp. 211-223
-
-
Rabinowitz, D.1
Laird, N.2
-
21
-
-
0035055544
-
The family based association test method: Strategies for studying general genotype--phenotype associations
-
Horvath S, Xu X, Laird NM. The family based association test method: strategies for studying general genotype--phenotype associations. Eur JHum Genet. 2001;9(4):301-306
-
(2001)
Eur JHum Genet
, vol.9
, Issue.4
, pp. 301-306
-
-
Horvath, S.1
Xu, X.2
Laird, N.M.3
-
22
-
-
0034929626
-
A general and accurate approach for computing the statistical power of the transmission disequilibrium test for complex disease genes
-
Chen WM, Deng HW. A general and accurate approach for computing the statistical power of the transmission disequilibrium test for complex disease genes. Genet Epidemiol. 2001;21(1):53-67.
-
(2001)
Genet Epidemiol
, vol.21
, Issue.1
, pp. 53-67
-
-
Chen, W.M.1
Deng, H.W.2
-
23
-
-
0033365190
-
A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. The tourette syndrome association international consortium for genetics
-
A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. The Tourette Syndrome Association International Consortium for Genetics. Am JHum Genet. 1999;65(5):1428-1436
-
(1999)
Am JHum Genet
, vol.65
, Issue.5
, pp. 1428-1436
-
-
-
24
-
-
33846632694
-
Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families
-
Genome scan for Tourette disorder in affected-sibling-pair and multigenerational families.Am JHum Genet. 2007;80(2):265-272
-
(2007)
Am JHum Genet
, vol.80
, Issue.2
, pp. 265-272
-
-
-
25
-
-
0029911803
-
Bilineal transmission and phenotypic variation of Tourette's disorder in a large pedigree
-
McMahon WM, van de Wetering BJ, Filloux F, Betit K, Coon H, Leppert M. Bilineal transmission and phenotypic variation of Tourette's disorder in a large pedigree. JAm Acad Child Adolesc Psychiatry. 1996;35(5):672-680
-
(1996)
J Am Acad Child Adolesc Psychiatry
, vol.35
, Issue.5
, pp. 672-680
-
-
McMahon, W.M.1
Van De Wetering, B.J.2
Filloux, F.3
Betit, K.4
Coon, H.5
Leppert, M.6
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