-
1
-
-
0036164143
-
A factor analysis of tic symptoms in Gilles de la Tourette's syndrome
-
Alsobrook JP, Pauls DL. A factor analysis of tic symptoms in Gilles de la Tourette's syndrome. Am J Psychiatry 2002;159:291-6.
-
(2002)
Am J Psychiatry
, vol.159
, pp. 291-296
-
-
Alsobrook, J.P.1
Pauls, D.L.2
-
2
-
-
0033588323
-
Genome scan for linkage to Gilles de la Tourette syndrome
-
Barr CL, Wigg KG, Pakstis AJ, Kurlan R, Pauls DL, Kidd KK, Tsui L-C, Sandor P. Genome scan for linkage to Gilles de la Tourette syndrome. Am J Med Genet 1999;88:437-45.
-
(1999)
Am J Med Genet
, vol.88
, pp. 437-445
-
-
Barr, C.L.1
Wigg, K.G.2
Pakstis, A.J.3
Kurlan, R.4
Pauls, D.L.5
Kidd, K.K.6
Tsui, L.-C.7
Sandor, P.8
-
3
-
-
0032748329
-
Cathechol-O-methyltransferase and Gilles de la Tourette syndrome
-
Barr CL, Wigg KG, Sandor P. Cathechol-O-methyltransferase and Gilles de la Tourette syndrome. Mol Psychiatry 1999;4(5):492-5.
-
(1999)
Mol Psychiatry
, vol.4
, Issue.5
, pp. 492-495
-
-
Barr, C.L.1
Wigg, K.G.2
Sandor, P.3
-
4
-
-
0031014917
-
Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome
-
Barr CL, Wigg KG, Zovko E, Sandor P, Tsui L-C. Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome. Am J Med Genet (Neuropsychiatr Genet) 1997;74:58-61.
-
(1997)
Am J Med Genet (Neuropsychiatr Genet)
, vol.74
, pp. 58-61
-
-
Barr, C.L.1
Wigg, K.G.2
Zovko, E.3
Sandor, P.4
Tsui, L.-C.5
-
5
-
-
0029931471
-
No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families
-
Barr CL, Wigg KG, Zovko E, Sandor P, Tsui L-C. No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families. Am J Med Genet (Neuropsychiatr Genet) 1996;67:301-5.
-
(1996)
Am J Med Genet (Neuropsychiatr Genet)
, vol.67
, pp. 301-305
-
-
Barr, C.L.1
Wigg, K.G.2
Zovko, E.3
Sandor, P.4
Tsui, L.-C.5
-
6
-
-
0028986830
-
Exclusions of the 5-HT1A seratonin neuroreceptor and tryptophan oxygenase genes in a large British kindered multiply affected with Tourette's syndrome, chronic motor tics, and obssessive-compulsive behavior
-
Brett P, Curtis D, Robertson M, Gurling H. Exclusions of the 5-HT1A seratonin neuroreceptor and tryptophan oxygenase genes in a large British kindered multiply affected with Tourette's syndrome, chronic motor tics, and obssessive-compulsive behavior. Am J Psychiatry 1995;152:437-40.
-
(1995)
Am J Psychiatry
, vol.152
, pp. 437-440
-
-
Brett, P.1
Curtis, D.2
Robertson, M.3
Gurling, H.4
-
7
-
-
0029806344
-
Linkage analysis and exclusion of regions of chromosomes 3 and 8 in Gilles de la Tourette syndrome following the identification of a balanced reciprocal translocation 46 XY, t(3:8)(p21.3 q24.1) in a case of Tourette syndrome
-
Brett PM, Curtis D, Robertson MM, Dahlitz M, Gurling HM. Linkage analysis and exclusion of regions of chromosomes 3 and 8 in Gilles de la Tourette syndrome following the identification of a balanced reciprocal translocation 46 XY, t(3:8)(p21.3 q24.1) in a case of Tourette syndrome. Psychiatr Genet 1996;6:99-105.
-
(1996)
Psychiatr Genet
, vol.6
, pp. 99-105
-
-
Brett, P.M.1
Curtis, D.2
Robertson, M.M.3
Dahlitz, M.4
Gurling, H.M.5
-
8
-
-
0030667412
-
Neuroreceptor subunit genes and the genetic susceptibility to Gilles de la Tourette syndrome
-
Brett PM, Curtis D, Robertson MM, Gurling HM. Neuroreceptor subunit genes and the genetic susceptibility to Gilles de la Tourette syndrome. Biol Psychiatry 1997;42:941-7.
-
(1997)
Biol Psychiatry
, vol.42
, pp. 941-947
-
-
Brett, P.M.1
Curtis, D.2
Robertson, M.M.3
Gurling, H.M.4
-
9
-
-
0034096555
-
Social and emotional adjustment in children affected with Gilles de la Tourette's syndrome: Associations with ADHD and family functioning
-
Carter AS, O'Donnell DA, Schultz RT, Scahill L, Leckman JF, Pauls DL. Social and emotional adjustment in children affected with Gilles de la Tourette's syndrome: Associations with ADHD and family functioning. J Child Psychol Psychiatry Allied Discipl 2000;41:215-23.
-
(2000)
J Child Psychol Psychiatry Allied Discipl
, vol.41
, pp. 215-223
-
-
Carter, A.S.1
O'Donnell, D.A.2
Schultz, R.T.3
Scahill, L.4
Leckman, J.F.5
Pauls, D.L.6
-
11
-
-
0034722923
-
An association study 5-HTTLPR polymorphism, COMT polymorphism, and Tourette's syndrome
-
Cavallini MC, Di Bella D, Catalano M, Bellodi L. An association study 5-HTTLPR polymorphism, COMT polymorphism, and Tourette's syndrome. Psychiatry Res 2000;97(2-3):93-100.
-
(2000)
Psychiatry Res
, vol.97
, Issue.2-3
, pp. 93-100
-
-
Cavallini, M.C.1
Di Bella, D.2
Catalano, M.3
Bellodi, L.4
-
12
-
-
0002046974
-
Evidence the Tourette syndrome gene is at 18q22.1
-
Comings D, Comings B, Dietz G, et al. Evidence the Tourette syndrome gene is at 18q22.1. Proceedings of the VIIth International Congress of Human Genetics, Berlin, vol. 620, 1986.
-
(1986)
Proceedings of the VIIth International Congress of Human Genetics, Berlin
, vol.620
-
-
Comings, D.1
Comings, B.2
Dietz, G.3
-
13
-
-
0023623378
-
A controlled study of Tourette syndrome
-
Comings DE, Comings BG. A controlled study of Tourette syndrome. Am J Hum Genet 1987;41:701-838.
-
(1987)
Am J Hum Genet
, vol.41
, pp. 701-838
-
-
Comings, D.E.1
Comings, B.G.2
-
14
-
-
0025925207
-
The dopamine D2 receptor locus as a modifying gene in neuropsychiatric disorders
-
Comings DE, Comings BG, Muhleman D, Dietz G, Shahbahrami B, Tast D, Knell E, Kocsis P, Baumgarten R, Kovacs BW. The dopamine D2 receptor locus as a modifying gene in neuropsychiatric disorders. JAMA 1991;266:1793-800.
-
(1991)
JAMA
, vol.266
, pp. 1793-1800
-
-
Comings, D.E.1
Comings, B.G.2
Muhleman, D.3
Dietz, G.4
Shahbahrami, B.5
Tast, D.6
Knell, E.7
Kocsis, P.8
Baumgarten, R.9
Kovacs, B.W.10
-
15
-
-
0032714352
-
Genomic control for association studies
-
Devlin B, Roeder K. Genomic control for association studies. Biometrics 1999;55:997-1004.
-
(1999)
Biometrics
, vol.55
, pp. 997-1004
-
-
Devlin, B.1
Roeder, K.2
-
16
-
-
0025237053
-
Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome
-
Devor EJ, Grandy DK, Civelli O, Litt M, Burgess AK, Isenberg KE, Van De Wetering BJ, Oostra B. Genetic linkage is excluded for the D2-dopamine receptor lambda HD2G1 and flanking loci on chromosome 11q22-q23 in Tourette syndrome. Hum Hered 1990:40(2):105-8.
-
(1990)
Hum Hered
, vol.40
, Issue.2
, pp. 105-108
-
-
Devor, E.J.1
Grandy, D.K.2
Civelli, O.3
Litt, M.4
Burgess, A.K.5
Isenberg, K.E.6
Van De Wetering, B.J.7
Oostra, B.8
-
17
-
-
0027318629
-
Evidence for autosomal dominant transmission in Tourette's syndrome - United Kingdom Cohort Study
-
Eapen V, Pauls DL, Robertson MM. Evidence for autosomal dominant transmission in Tourette's syndrome - United Kingdom Cohort Study. Br J Psychiatry 1993;162:593-6.
-
(1993)
Br J Psychiatry
, vol.162
, pp. 593-596
-
-
Eapen, V.1
Pauls, D.L.2
Robertson, M.M.3
-
18
-
-
0030750082
-
Obsessive compulsive symptoms in Gilles de la Tourette's syndrome and obsessive compulsive disorder: Differences by diagnosis and family history
-
Eapen V, Robertson MM, Alsobrook JP, Pauls DL. Obsessive compulsive symptoms in Gilles de la Tourette's syndrome and obsessive compulsive disorder: Differences by diagnosis and family history. Am J Med Genet (Neuropsychiatr Genet) 1997;74:432-8.
-
(1997)
Am J Med Genet (Neuropsychiatr Genet)
, vol.74
, pp. 432-438
-
-
Eapen, V.1
Robertson, M.M.2
Alsobrook, J.P.3
Pauls, D.L.4
-
19
-
-
0023235253
-
Haplotype relative risks: An easy reliable way to construct a proper control sample for risk calculations
-
Falk C, Rubinstein P. Haplotype relative risks: An easy reliable way to construct a proper control sample for risk calculations. Ann Hum Genet 1987;51:227-33.
-
(1987)
Ann Hum Genet
, vol.51
, pp. 227-233
-
-
Falk, C.1
Rubinstein, P.2
-
20
-
-
0027503132
-
Exclusion of close linkage of Gilles de la Tourette syndrome to D1 dopamine receptor
-
Gelernter J, Kennedy J, Grandy D, Civelli O, Pauls DL, Pakstis A, Kurlan R, Sunahara RK, Niznik HB, Seeman P, O'Dowd B, Kidd KK. Exclusion of close linkage of Gilles de la Tourette syndrome to D1 dopamine receptor. Am J Psychiatry 1993;150:449-53.
-
(1993)
Am J Psychiatry
, vol.150
, pp. 449-453
-
-
Gelernter, J.1
Kennedy, J.2
Grandy, D.3
Civelli, O.4
Pauls, D.L.5
Pakstis, A.6
Kurlan, R.7
Sunahara, R.K.8
Niznik, H.B.9
Seeman, P.10
O'Dowd, B.11
Kidd, K.K.12
-
21
-
-
0025167818
-
Gilles de la Tourette syndrome is not linked to D2 dopamine receptor
-
Gelernter J, Pakstis AJ, Pauls DL, Kurlan R, Gancher ST, Civelli O, Grandy D, Kidd KK. Gilles de la Tourette syndrome is not linked to D2 dopamine receptor. Arch Gen Psychiatry 1990;47:1073-7.
-
(1990)
Arch Gen Psychiatry
, vol.47
, pp. 1073-1077
-
-
Gelernter, J.1
Pakstis, A.J.2
Pauls, D.L.3
Kurlan, R.4
Gancher, S.T.5
Civelli, O.6
Grandy, D.7
Kidd, K.K.8
-
22
-
-
0028178293
-
D2 dopamine receptor (DRD2) alleles do not influence severity of Tourette's syndrome: Results from four large kindreds
-
Gelernter J, Pauls DL, Leckman J, Kidd KK, Kurlan R. D2 dopamine receptor (DRD2) alleles do not influence severity of Tourette's syndrome: Results from four large kindreds. Arch Neurol 1994; 51: 397-400.
-
(1994)
Arch Neurol
, vol.51
, pp. 397-400
-
-
Gelernter, J.1
Pauls, D.L.2
Leckman, J.3
Kidd, K.K.4
Kurlan, R.5
-
23
-
-
0028902430
-
Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome
-
Gelernter J, Rao PA, Pauls DL, Hamblin MW, Sibley DR, Kidd KK. Assignment of the 5HT7 receptor gene (HTR7) to chromosome 10q and exclusion of genetic linkage with Tourette syndrome. Genomics 1995;26:207-9.
-
(1995)
Genomics
, vol.26
, pp. 207-209
-
-
Gelernter, J.1
Rao, P.A.2
Pauls, D.L.3
Hamblin, M.W.4
Sibley, D.R.5
Kidd, K.K.6
-
24
-
-
19244363371
-
Linkage disequilibrium between an allele at the dopamine D4 receptor locus with Tourette's syndrome by the transmission disequilibrium test
-
Grice DE, Leckman JF, Pauls DL, Kurlan R, Kidd KK, Pakstis AJ, Chang FM, Cohen DJ, Gelernter J. Linkage disequilibrium between an allele at the dopamine D4 receptor locus with Tourette's syndrome by the transmission disequilibrium test. Am J Hum Genet 1996;59:644-52.
-
(1996)
Am J Hum Genet
, vol.59
, 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
Chang, F.M.7
Cohen, D.J.8
Gelernter, J.9
-
25
-
-
0037209076
-
Analytical methods applied to psychiatric genetics
-
In: Leboyer M, Bellivier F, editors; Totowa (NJ): Humana Press
-
Grigorenko EL, Pauls DL. Analytical methods applied to psychiatric genetics. In: Leboyer M, Bellivier F, editors. Psychiatry Genetics: Methods and Protocols. Totowa (NJ): Humana Press. pp. 23-61.
-
Psychiatry Genetics: Methods and Protocols
, pp. 23-61
-
-
Grigorenko, E.L.1
Pauls, D.L.2
-
26
-
-
0029135426
-
Intermediate inheritance of Tourette syndrome, assuming assortative mating
-
Hasstedt SJ, Leppert M, Filoux F, Van De Wetering BJM, McMahon Wm. Intermediate inheritance of Tourette syndrome, assuming assortative mating. Am J Hum Genet 1995;57:682-9.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 682-689
-
-
Hasstedt, S.J.1
Leppert, M.2
Filoux, F.3
Van De Wetering, B.J.M.4
McMahon, Wm.5
-
27
-
-
0030762997
-
Rates for tic disorders and obsessive compulsive symptomatology in families of children and adolescents with Gilles de la Tourette syndrome
-
Hebebrand J, Klug B, Fimmers R, Seuchter SA, Wettke-Schafer R, Deget F, Camps A, Lisch S, Hebebrand K, Von Gontard A, Lehmkuhl G, Poustka F, SChmidt M, Baur MP, Remschmidt H. Rates for tic disorders and obsessive compulsive symptomatology in families of children and adolescents with Gilles de la Tourette syndrome. J Psychiatr Res 1997;31:519-30.
-
(1997)
J Psychiatr Res
, vol.31
, pp. 519-530
-
-
Hebebrand, J.1
Klug, B.2
Fimmers, R.3
Seuchter, S.A.4
Wettke-Schafer, R.5
Deget, F.6
Camps, A.7
Lisch, S.8
Hebebrand, K.9
Von Gontard, A.10
Lehmkuhl, G.11
Poustka, F.12
Schmidt, M.13
Baur, M.P.14
Remschmidt, H.15
-
28
-
-
0027288020
-
Tourette's syndrome and homozygosity for the dopamine D3 receptor gene. German Tourette's Syndrome Collaborative Research Group
-
Hebebrand J, Nöthen MM, Lehmkuhl G, Poustka F, Schmidt M, Propping P, Remschmidt H. Tourette's syndrome and homozygosity for the dopamine D3 receptor gene. German Tourette's Syndrome Collaborative Research Group. Lancet 1993;341:1483-4.
-
(1993)
Lancet
, vol.341
, pp. 1483-1484
-
-
Hebebrand, J.1
Nöthen, M.M.2
Lehmkuhl, G.3
Poustka, F.4
Schmidt, M.5
Propping, P.6
Remschmidt, H.7
-
29
-
-
0025358973
-
No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosome 7 and 18
-
Heutink P, Van De Wetering BJM, Breedfeld G, Weber J, Sandkuyl LA, Devor EJ, Heiberg A, Niermeijer MF, Oostra BA. No evidence for genetic linkage of Gilles de la Tourette syndrome on chromosome 7 and 18. J Med Genet 1990;27:433-6.
-
(1990)
J Med Genet
, vol.27
, pp. 433-436
-
-
Heutink, P.1
Van De Wetering, B.J.M.2
Breedfeld, G.3
Weber, J.4
Sandkuyl, L.A.5
Devor, E.J.6
Heiberg, A.7
Niermeijer, M.F.8
Oostra, B.A.9
-
30
-
-
0028999118
-
Linkage studies on Gilles de la Tourette syndrome: What is the strategy of choice?
-
Heutink P, Van De Wetering BJM, Pakstis AJ, Kurlan R, Sandor P, Oostra BA, Sandkuijl LA. Linkage studies on Gilles de la Tourette syndrome: What is the strategy of choice? Am Hum Genet 1995;57(2):465-73.
-
(1995)
Am Hum Genet
, vol.57
, Issue.2
, pp. 465-473
-
-
Heutink, P.1
Van De Wetering, B.J.M.2
Pakstis, A.J.3
Kurlan, R.4
Sandor, P.5
Oostra, B.A.6
Sandkuijl, L.A.7
-
31
-
-
0035827823
-
A family study of Tourette syndrome in Japan
-
Kano Y, Ohta M, Nagai Y, Pauls DL, Leckman JF. A family study of Tourette syndrome in Japan. Am J Med Genet 2001;105(5):414-21.
-
(2001)
Am J Med Genet
, vol.105
, Issue.5
, pp. 414-421
-
-
Kano, Y.1
Ohta, M.2
Nagai, Y.3
Pauls, D.L.4
Leckman, J.F.5
-
32
-
-
0025219093
-
The perinatal factors in the expression of Tourette's syndrome
-
Leckman JF, Dolnansky ES, Hardin M, Clubb M, Walkup JT, Stevenson J, Pauls DL. The perinatal factors in the expression of Tourette's syndrome. J Am Acad Child Adolesc Psychiatry 1990:29:220-6.
-
(1990)
J Am Acad Child Adolesc Psychiatry
, vol.29
, pp. 220-226
-
-
Leckman, J.F.1
Dolnansky, E.S.2
Hardin, M.3
Clubb, M.4
Walkup, J.T.5
Stevenson, J.6
Pauls, D.L.7
-
33
-
-
18344413003
-
Birth-weights of monozygotic twins discordant for Tourette's syndrome
-
Leckman JF, Price RA, Walkup JT, Ort S, Pauls DL, Cohen DJ. Birth-weights of monozygotic twins discordant for Tourette's syndrome. Arch Gen Psychiatry 1987;44:100.
-
(1987)
Arch Gen Psychiatry
, vol.44
, pp. 100
-
-
Leckman, J.F.1
Price, R.A.2
Walkup, J.T.3
Ort, S.4
Pauls, D.L.5
Cohen, D.J.6
-
34
-
-
0033710786
-
Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome
-
Matsumoto N, David DE, Johnson EW, Konecki D, Burmester JK, Ledbetter DH, Weber JL. Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome. Eur J Hum Genet 2000;8:87-83.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 875-883
-
-
Matsumoto, N.1
David, D.E.2
Johnson, E.W.3
Konecki, D.4
Burmester, J.K.5
Ledbetter, D.H.6
Weber, J.L.7
-
35
-
-
0033804566
-
Significant linkange for Tourette syndrome in a large French Canadian family
-
Merette C, Brassard A, Potvin A, Bouvier H, Rousseau F, Emond C, Bissonnette L, Roy MA, Maziade M, Ott J, Caron C. Significant linkange for Tourette syndrome in a large French Canadian family. Am J Hum Genet 2000;67(4):1008-13.
-
(2000)
Am J Hum Genet
, vol.67
, Issue.4
, pp. 1008-1013
-
-
Merette, C.1
Brassard, A.2
Potvin, A.3
Bouvier, H.4
Rousseau, F.5
Emond, C.6
Bissonnette, L.7
Roy, M.A.8
Maziade, M.9
Ott, J.10
Caron, C.11
-
36
-
-
0028107987
-
Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method
-
Nöthen MM, Hebebrand J, Knapp M, Hebebrand K, Camps A, Von Gontard A, Wettke-Schafer R, Lisch S, Cichon S, Poustka F, et al. Association analysis of the dopamine D2 receptor gene in Tourette's syndrome using the haplotype relative risk method. Am J Med Genet 1994;54:249-52.
-
(1994)
Am J Med Genet
, vol.54
, pp. 249-252
-
-
Nöthen, M.M.1
Hebebrand, J.2
Knapp, M.3
Hebebrand, K.4
Camps, A.5
Von Gontard, A.6
Wettke-Schafer, R.7
Lisch, S.8
Cichon, S.9
Poustka, F.10
-
37
-
-
0026012010
-
Progress in the search for genetic linkage with Tourette syndrome: An exclusion map covering more than 50% of the autosomal genome
-
Pakstis AJ, Heutink P, Pauls DL, Kurlan R, Van De Wetering BJM, Leckman JF, Sandkuyl LA, Kidd JR, Breedveld GJ, Castiglione CM, Weber J, Sparkes RS, Cohen DJ, Kidd KK, Oostra BA. Progress in the search for genetic linkage with Tourette syndrome: An exclusion map covering more than 50% of the autosomal genome. Am J Hum Genet 1991;48:281-94.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 281-294
-
-
Pakstis, A.J.1
Heutink, P.2
Pauls, D.L.3
Kurlan, R.4
Van De Wetering, B.J.M.5
Leckman, J.F.6
Sandkuyl, L.A.7
Kidd, J.R.8
Breedveld, G.J.9
Castiglione, C.M.10
Weber, J.11
Sparkes, R.S.12
Cohen, D.J.13
Kidd, K.K.14
Oostra, B.A.15
-
38
-
-
0005925539
-
Genetic and epidemiological analyses of the Yale Tourette's Syndrome Family Study data
-
Pauls DL, Alsobrook JP, Almasy L, Leckman JF, Cohen DJ. Genetic and epidemiological analyses of the Yale Tourette's Syndrome Family Study data. Psychiatr Genet 1991;2:28.
-
(1991)
Psychiatr Genet
, vol.2
, pp. 28
-
-
Pauls, D.L.1
Alsobrook, J.P.2
Almasy, L.3
Leckman, J.F.4
Cohen, D.J.5
-
39
-
-
0028299851
-
Evidence against a genetic relationship between Gilles de la Tourette's syndrome and anxiety, depression, panic and phobic disorders
-
Pauls DL, Leckman JF, Cohen DJ. Evidence against a genetic relationship between Gilles de la Tourette's syndrome and anxiety, depression, panic and phobic disorders. Br J Psychiatry 1994;164:215-21.
-
(1994)
Br J Psychiatry
, vol.164
, pp. 215-221
-
-
Pauls, D.L.1
Leckman, J.F.2
Cohen, D.J.3
-
40
-
-
0027221011
-
The familial relationship between Gilles de la Tourette's syndrome, attention deficit disorder, learning disabilities, speech disorders and stuttering
-
Pauls DL, Leckman JF, Cohen DJ. The familial relationship between Gilles de la Tourette's syndrome, attention deficit disorder, learning disabilities, speech disorders and stuttering. J Am Acad Child Adolesc Psychiatry 1993;32:1044-50.
-
(1993)
J Am Acad Child Adolesc Psychiatry
, vol.32
, pp. 1044-1050
-
-
Pauls, D.L.1
Leckman, J.F.2
Cohen, D.J.3
-
41
-
-
0022515798
-
The inheritance of Gilles de la Tourette's syndrome and associated behaviors: Evidence for autosomal dominant transmission
-
Pauls DL, Leckman JF. The inheritance of Gilles de la Tourette's syndrome and associated behaviors: Evidence for autosomal dominant transmission. N Engl J Med 1986;315:993-7.
-
(1986)
N Engl J Med
, vol.315
, pp. 993-997
-
-
Pauls, D.L.1
Leckman, J.F.2
-
42
-
-
0025254154
-
Segregation and linkage analyses of Tourette's syndrome and related disorders
-
Pauls DL, Pakstis AJ, Kurlan R, Kidd KK, Leckman JF, Cohen DJ, Kidd JR, et al. Segregation and linkage analyses of Tourette's syndrome and related disorders. J Am Acad Child Adolesc Psychiatry 1990;29:195-203.
-
(1990)
J Am Acad Child Adolesc Psychiatry
, vol.29
, pp. 195-203
-
-
Pauls, D.L.1
Pakstis, A.J.2
Kurlan, R.3
Kidd, K.K.4
Leckman, J.F.5
Cohen, D.J.6
Kidd, J.R.7
-
44
-
-
0027477632
-
Behavioural disorders: Lessons in linkage
-
Pauls DL. Behavioural disorders: Lessons in linkage. Nat Genet 1993;3:4-5.
-
(1993)
Nat Genet
, vol.3
, pp. 4-5
-
-
Pauls, D.L.1
-
45
-
-
0041695946
-
Emerging genetic markers and their role in potential preventive intervention strategies
-
In: Muehrer P, editor; Rockville (MD): NIMH
-
Pauls DL. Emerging genetic markers and their role in potential preventive intervention strategies. In: Muehrer P, editor. Conceptual Research Models for Preventing Mental Disorders. Rockville (MD): NIMH, 1990. pp. 184-95.
-
(1990)
Conceptual Research Models for Preventing Mental Disorders
, pp. 184-195
-
-
Pauls, D.L.1
-
46
-
-
0035072652
-
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome
-
Petek E, Windpassinger C, Vincent JB, Cheung J, Boright AP, Scherer SW, Kroisel PM, Wagner K. Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome. Am J Hum Genet 2001;68(4):848-58.
-
(2001)
Am J Hum Genet
, vol.68
, Issue.4
, pp. 848-858
-
-
Petek, E.1
Windpassinger, C.2
Vincent, J.B.3
Cheung, J.4
Boright, A.P.5
Scherer, S.W.6
Kroisel, P.M.7
Wagner, K.8
-
47
-
-
0031667834
-
Tic disorders: New developments in Tourette syndrome and related disorders
-
Robertson MM, Stern JS. Tic disorders: New developments in Tourette syndrome and related disorders. Curr Opin Neurol 1998;11:373-80.
-
(1998)
Curr Opin Neurol
, vol.11
, pp. 373-380
-
-
Robertson, M.M.1
Stern, J.S.2
-
48
-
-
0028290494
-
Tourette syndrome: What are the influences of gender and co-morbid OCD?
-
Santangelo SL, Pauls DL, Goldstein JM, Faraone SV, Tsuang MT, Leckman JF. Tourette syndrome: What are the influences of gender and co-morbid OCD? J Am Acad Child Adolesc Psychiatry 1994;33:795-804.
-
(1994)
J Am Acad Child Adolesc Psychiatry
, vol.33
, pp. 795-804
-
-
Santangelo, S.L.1
Pauls, D.L.2
Goldstein, J.M.3
Faraone, S.V.4
Tsuang, M.T.5
Leckman, J.F.6
-
49
-
-
0029920682
-
Assessing risk for the Tourette spectrum of disorders among first degree relatives of probands with Tourette syndrome
-
Santangelo SL, Pauls DL, Lavori PL, Goldstein JM, Faraone SV, Tsuang MT. Assessing risk for the Tourette spectrum of disorders among first degree relatives of probands with Tourette syndrome. Am J Med Genet (Neuropsychiatr Genet) 1996;67:107-16.
-
(1996)
Am J Med Genet (Neuropsychiatr Genet)
, vol.67
, pp. 107-116
-
-
Santangelo, S.L.1
Pauls, D.L.2
Lavori, P.L.3
Goldstein, J.M.4
Faraone, S.V.5
Tsuang, M.T.6
-
50
-
-
0031953230
-
Visual-motor integration, visuosperceptual and fine motor functioning in children with Tourette syndrome
-
Schultz RT, Carter AS, Gladstone M, Scahill L, Leckman JF, Peterson BS, Zhang H, Cohen DJ, Pauls DL. Visual-motor integration, visuosperceptual and fine motor functioning in children with Tourette syndrome. Neuropsychology 1998;12:134-45.
-
(1998)
Neuropsychology
, vol.12
, pp. 134-145
-
-
Schultz, R.T.1
Carter, A.S.2
Gladstone, M.3
Scahill, L.4
Leckman, J.F.5
Peterson, B.S.6
Zhang, H.7
Cohen, D.J.8
Pauls, D.L.9
-
51
-
-
0033986209
-
Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome
-
Seuchter SA, Hebebrand J, Klug B, Knapp M, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Baur MP. Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome. Genet Epidemiol 2000;18(1):33-47.
-
(2000)
Genet Epidemiol
, vol.18
, Issue.1
, pp. 33-47
-
-
Seuchter, S.A.1
Hebebrand, J.2
Klug, B.3
Knapp, M.4
Lehmkuhl, G.5
Poustka, F.6
Schmidt, M.7
Remschmidt, H.8
Baur, M.P.9
-
52
-
-
0032231676
-
Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population
-
Simonic I, Gericke GS, Ott J, Weber JL. Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population. Am J Hum Gen 1998;63:839-46.
-
(1998)
Am J Hum Gen
, vol.63
, pp. 839-846
-
-
Simonic, I.1
Gericke, G.S.2
Ott, J.3
Weber, J.L.4
-
53
-
-
0035825981
-
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8p22 and 11q23-24 in South African Afrikaners
-
Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, Ledbetter DH, Ott J, Weber JL. Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8p22 and 11q23-24 in South African Afrikaners. Am J Med Genet 2001;105(32):163-7.
-
(2001)
Am J Med Genet
, vol.105
, Issue.32
, pp. 163-167
-
-
Simonic, I.1
Nyholt, D.R.2
Gericke, G.S.3
Gordon, D.4
Matsumoto, N.5
Ledbetter, D.H.6
Ott, J.7
Weber, J.L.8
-
54
-
-
0029858544
-
The TDT and other family-based tests for linkage disequilibrium and association
-
Spielman R, Ewens W. The TDT and other family-based tests for linkage disequilibrium and association. Am J Hum Genet 1996;59:983-9.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 983-989
-
-
Spielman, R.1
Ewens, W.2
-
55
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993;52:506-16.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
56
-
-
0033574529
-
Tourette syndrome and the norepinephrine transporter gene: Results of a systematic mutation screening
-
Stober G, Hebebrand J, Cichon S, Bruss M, Bonisch H, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Propping P, Nothen MM. Tourette syndrome and the norepinephrine transporter gene: Results of a systematic mutation screening. Am J Med Genet 1999;88(2):158-63.
-
(1999)
Am J Med Genet
, vol.88
, Issue.2
, pp. 158-163
-
-
Stober, G.1
Hebebrand, J.2
Cichon, S.3
Bruss, M.4
Bonisch, H.5
Lehmkuhl, G.6
Poustka, F.7
Schmidt, M.8
Remschmidt, H.9
Propping, P.10
Nothen, M.M.11
-
57
-
-
0026494911
-
A haplotype-based "haplotype relative risk" approach to detecting allelic associations
-
Terwillinger JD, Ott J. A haplotype-based "haplotype relative risk" approach to detecting allelic associations. Hum Hered 1992;42:337-46.
-
(1992)
Hum Hered
, vol.42
, pp. 337-346
-
-
Terwillinger, J.D.1
Ott, J.2
-
58
-
-
0033365190
-
A complete genome screen in sib-pairs affected with the Gilles de la Tourette syndrome
-
The Tourette Syndrome Association International Consortium for Genetics. A complete genome screen in sib-pairs affected with the Gilles de la Tourette syndrome. Am J Hum Genet 1999;65:1428-36.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1428-1436
-
-
-
59
-
-
0042697782
-
A genetic study of Gilles de la Tourette syndrome in the Netherlands
-
PhD thesis
-
Van De Wetering BJM. A genetic study of Gilles de la Tourette syndrome in the Netherlands. PhD thesis, 1993.
-
(1993)
-
-
Van De Wetering, B.J.M.1
-
60
-
-
0004883390
-
Human dopamine transporter gene: Coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivity disorder populations
-
Vandenbergh DJ, Thompson MD, Cook EH, Bendahhou E, Nguyen T, Krasowski MD, Zarrabian D, Comings D, Sellers EM, Tyndale RF, George SR, O'Dowd BF, Uhl GR. Human dopamine transporter gene: Coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivity disorder populations. Mol Psychiatry 2000;5(2):283-92.
-
(2000)
Mol Psychiatry
, vol.5
, Issue.3
, pp. 283-292
-
-
Vandenbergh, D.J.1
Thompson, M.D.2
Cook, E.H.3
Bendahhou, E.4
Nguyen, T.5
Krasowski, M.D.6
Zarrabian, D.7
Comings, D.8
Sellers, E.M.9
Tyndale, R.F.10
George, S.R.11
O'Dowd, B.F.12
Uhl, G.R.13
-
61
-
-
0029759164
-
Family study and segregation analysis of Tourette syndrome: Evidence for a mixed model of inheritance
-
Walkup JT, LaBuda MC, Singer HS, Brown J, Riddle MA, Hurko O. Family study and segregation analysis of Tourette syndrome: Evidence for a mixed model of inheritance. Am J Hum Genet 1996;59:684-93.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 684-693
-
-
Walkup, J.T.1
LaBuda, M.C.2
Singer, H.S.3
Brown, J.4
Riddle, M.A.5
Hurko, O.6
-
62
-
-
0031034483
-
Improved set of short-tandem-repeat polymorphisms for screening the human genome
-
Yuan B, Vaske D, Weber JL, Beck J, Sheffield VC. Improved set of short-tandem-repeat polymorphisms for screening the human genome. Am J Hum Genet 1997;60:459-60.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 459-460
-
-
Yuan, B.1
Vaske, D.2
Weber, J.L.3
Beck, J.4
Sheffield, V.C.5
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