-
1
-
-
0033909546
-
A general test of association for quantitative traits in nuclear families
-
Abecasis GR, Cardon LR, Cookson WO. 2000. A general test of association for quantitative traits in nuclear families. Am J Hum Genet 66:279-292.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 279-292
-
-
Abecasis, G.R.1
Cardon, L.R.2
Cookson, W.O.3
-
3
-
-
0023440638
-
Whole blood serotonin in autistic and normal subjects
-
Anderson GM, Freedman DX, Cohen DJ, Volkmar FR, Hoder EL, McPhedran P, Minderaa RB, Hansen CR, Young JG. 1987. Whole blood serotonin in autistic and normal subjects. J Child Psychol Psychiatry 28:885-900.
-
(1987)
J Child Psychol Psychiatry
, vol.28
, pp. 885-900
-
-
Anderson, G.M.1
Freedman, D.X.2
Cohen, D.J.3
Volkmar, F.R.4
Hoder, E.L.5
McPhedran, P.6
Minderaa, R.B.7
Hansen, C.R.8
Young, J.G.9
-
4
-
-
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, Rutter M. 1995. Autism as a strongly genetic disorder: Evidence from a British twin study. Psychol Med 25:63-77.
-
(1995)
Psychol Med
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
Rutter, M.7
-
5
-
-
18944365556
-
Replication of autism linkage: Fine-mapping peak at 17q21
-
Cantor RM, Kono N, Duvall JA, Alvarez-Retuerto A, Stone JL, Alarcon M, Nelson SF, Geschwind DH. 2005. Replication of autism linkage: Fine-mapping peak at 17q21. Am J Hum Genet 76:1050-1056.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1050-1056
-
-
Cantor, R.M.1
Kono, N.2
Duvall, J.A.3
Alvarez-Retuerto, A.4
Stone, J.L.5
Alarcon, M.6
Nelson, S.F.7
Geschwind, D.H.8
-
6
-
-
0035830310
-
-
Collaborative Linkage Study of Autism. 2001. An autosomal genomic screen for autism. Am J Med Genet 105:609-615.
-
Collaborative Linkage Study of Autism. 2001. An autosomal genomic screen for autism. Am J Med Genet 105:609-615.
-
-
-
-
7
-
-
2342520299
-
Serotonin transporter gene and autism: A haplotype analysis in an Irish autistic population
-
Conroy J, Meally E, Kearney G, Fitzgerald M, Gill M, Gallagher L. 2004. Serotonin transporter gene and autism: A haplotype analysis in an Irish autistic population. Mol Psychiatry 9:587-593.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 587-593
-
-
Conroy, J.1
Meally, E.2
Kearney, G.3
Fitzgerald, M.4
Gill, M.5
Gallagher, L.6
-
9
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook EH, Courchesne R, Lord C, Cox NJ, Yan S, Lincoln A, Haas R, Courchesne E, Leventhal BL. 1997. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry 2:247-250.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 247-250
-
-
Cook, E.H.1
Courchesne, R.2
Lord, C.3
Cox, N.J.4
Yan, S.5
Lincoln, A.6
Haas, R.7
Courchesne, E.8
Leventhal, B.L.9
-
10
-
-
33947114826
-
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels
-
Coutinho AM, Sousa I, Martins M, Correia C, Morgadinho T, Bento C, Marques C, Ataide A, Miguel TS, Moore JH, Oliveira G, Vicente AM. 2007. Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels. Hum Genet 121:243-256.
-
(2007)
Hum Genet
, vol.121
, pp. 243-256
-
-
Coutinho, A.M.1
Sousa, I.2
Martins, M.3
Correia, C.4
Morgadinho, T.5
Bento, C.6
Marques, C.7
Ataide, A.8
Miguel, T.S.9
Moore, J.H.10
Oliveira, G.11
Vicente, A.M.12
-
11
-
-
0035653670
-
Genetics of autism: Complex aetiology for a heterogeneous disorder
-
Folstein SE, Rosen-Sheidley B. 2001. Genetics of autism: Complex aetiology for a heterogeneous disorder. Nat Rev Genet 2:943-955.
-
(2001)
Nat Rev Genet
, vol.2
, pp. 943-955
-
-
Folstein, S.E.1
Rosen-Sheidley, B.2
-
12
-
-
0017530988
-
Infantile autism:Agenetic study of 21 twin pairs
-
RutterM
-
Folstein S, RutterM.1977. Infantile autism:Agenetic study of 21 twin pairs. J Child Psychol Psychiatry 18:297-321.
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.1
-
13
-
-
0027158571
-
-
Gordon CT, State RC, Nelson JE, Hamburger SD, Rapoport JL. 1993. A double-blind comparison of clomipramine, desipramine, and placebo in the treatment of autistic disorder. Arch Gen Psychiatry 50:441-447.
-
Gordon CT, State RC, Nelson JE, Hamburger SD, Rapoport JL. 1993. A double-blind comparison of clomipramine, desipramine, and placebo in the treatment of autistic disorder. Arch Gen Psychiatry 50:441-447.
-
-
-
-
14
-
-
0037433052
-
Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions
-
Hahn LW, Ritchie MD, Moore JH. 2003. Multifactor dimensionality reduction software for detecting gene-gene and gene-environment interactions. Bioinformatics 19:376-382.
-
(2003)
Bioinformatics
, vol.19
, pp. 376-382
-
-
Hahn, L.W.1
Ritchie, M.D.2
Moore, J.H.3
-
15
-
-
51449089163
-
Autism and serotonin transporter gene polymorphisms:Asystematic review and meta-analysis.AmJ Med Genet B
-
Huang CH, Santangelo SL. 2008. Autism and serotonin transporter gene polymorphisms:Asystematic review and meta-analysis.AmJ Med Genet B Neuropsychiatr Genet 147B:903-913.
-
(2008)
Neuropsychiatr Genet
, vol.147 B
, pp. 903-913
-
-
Huang, C.H.1
Santangelo, S.L.2
-
16
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium IMGSAC
-
International Molecular Genetic Study of Autism Consortium (IMGSAC). 1998. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 7:571-578.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 571-578
-
-
-
17
-
-
0035871209
-
Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium IMGSAC
-
International Molecular Genetic Study of Autism Consortium (IMGSAC). 2001a. Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q. Hum Mol Genet 10:973-982.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 973-982
-
-
-
18
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
International Molecular Genetic Study of Autism Consortium IMGSAC
-
International Molecular Genetic Study of Autism Consortium (IMGSAC). 2001b. A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 69:570-581.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 570-581
-
-
-
19
-
-
85047695697
-
Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder
-
Kim SJ, Cox N, Courchesne R, Lord C, Corsello C, Akshoomoff N, Guter S, Leventhal BL, Courchesne E, Cook EH Jr. 2002. Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder. Mol Psychiatry 7:278-288.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 278-288
-
-
Kim, S.J.1
Cox, N.2
Courchesne, R.3
Lord, C.4
Corsello, C.5
Akshoomoff, N.6
Guter, S.7
Leventhal, B.L.8
Courchesne, E.9
Cook Jr., E.H.10
-
20
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with Autism?
-
Klauck SM, Poustka F, Benner A, Lesch KP, Poustka A. 1997. Serotonin transporter (5-HTT) gene variants associated with Autism? Hum Mol Genet 6:2233-2238.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2233-2238
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
Lesch, K.P.4
Poustka, A.5
-
21
-
-
24044520963
-
Sequence analysis of the serotonin transporter and associations with antidepressant response
-
Kraft JB, Slager SL, McGrath PJ, Hamilton SP. 2005. Sequence analysis of the serotonin transporter and associations with antidepressant response. Biol Psychiatry 58:374-381.
-
(2005)
Biol Psychiatry
, vol.58
, pp. 374-381
-
-
Kraft, J.B.1
Slager, S.L.2
McGrath, P.J.3
Hamilton, S.P.4
-
25
-
-
0034920299
-
-
Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P,HohJ, Ott J, Gilliam TC. 2001.Agenomewide screen for autism susceptibility loci. Am J Hum Genet 69:327-340.
-
Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P,HohJ, Ott J, Gilliam TC. 2001.Agenomewide screen for autism susceptibility loci. Am J Hum Genet 69:327-340.
-
-
-
-
26
-
-
0027997172
-
Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
Lord C, RutterM,LeCouteur A. 1994. Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 24:659-685.
-
(1994)
J Autism Dev Disord
, vol.24
, pp. 659-685
-
-
Lord, C.1
RutterM2
LeCouteur, A.3
-
27
-
-
0033006510
-
Familial factors influence level of functioning in pervasive developmental disorder
-
MacLean JE, Szatmari P, Jones MB, Bryson SE, Mahoney WJ, Bartolucci G, Tuff L. 1999. Familial factors influence level of functioning in pervasive developmental disorder. J Am Acad Child Adolesc Psychiatry 38:746-753.
-
(1999)
J Am Acad Child Adolesc Psychiatry
, vol.38
, pp. 746-753
-
-
MacLean, J.E.1
Szatmari, P.2
Jones, M.B.3
Bryson, S.E.4
Mahoney, W.J.5
Bartolucci, G.6
Tuff, L.7
-
28
-
-
0033569931
-
-
Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A, Cook EH, Weeks DE, Monaco AP. 1999. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.AmJMed Genet 88:492-496.
-
Maestrini E, Lai C, Marlow A, Matthews N, Wallace S, Bailey A, Cook EH, Weeks DE, Monaco AP. 1999. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.AmJMed Genet 88:492-496.
-
-
-
-
29
-
-
0034615152
-
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
-
Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. 2000. Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder. Am J Med Genet 96:43-48.
-
(2000)
Am J Med Genet
, vol.96
, pp. 43-48
-
-
Martin, E.R.1
Menold, M.M.2
Wolpert, C.M.3
Bass, M.P.4
Donnelly, S.L.5
Ravan, S.A.6
Zimmerman, A.7
Gilbert, J.R.8
Vance, J.M.9
Maddox, L.O.10
Wright, H.H.11
Abramson, R.K.12
DeLong, G.R.13
Cuccaro, M.L.14
Pericak-Vance, M.A.15
-
30
-
-
0035076031
-
Correcting for a potential bias in the pedigree disequilibrium test
-
Martin ER, Bass MP, Kaplan NL. 2001. Correcting for a potential bias in the pedigree disequilibrium test. Am J Hum Genet 68:1065-1067.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1065-1067
-
-
Martin, E.R.1
Bass, M.P.2
Kaplan, N.L.3
-
31
-
-
0142094699
-
Genotype-based association test for general pedigrees: The genotype-PDT
-
Martin ER, Bass MP, Gilbert JR, Pericak-Vance MA, Hauser ER. 2003. Genotype-based association test for general pedigrees: The genotype-PDT. Genet Epidemiol 25:203-213.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 203-213
-
-
Martin, E.R.1
Bass, M.P.2
Gilbert, J.R.3
Pericak-Vance, M.A.4
Hauser, E.R.5
-
32
-
-
28444496622
-
Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data
-
Mei H, Ma D, Ashley-Koch A, Martin ER. 2005. Extension of multifactor dimensionality reduction for identifying multilocus effects in the GAW14 simulated data. BMC Genet 6(Suppl 1): S145.
-
(2005)
BMC Genet
, vol.6
, Issue.SUPPL. 1
-
-
Mei, H.1
Ma, D.2
Ashley-Koch, A.3
Martin, E.R.4
-
33
-
-
36749015065
-
Multifactor dimensionality reduction-phenomics: A novel method to capture genetic heterogeneity with use of phenotypic variables
-
Mei H, Cuccaro ML, Martin ER. 2007. Multifactor dimensionality reduction-phenomics: A novel method to capture genetic heterogeneity with use of phenotypic variables. Am J Hum Genet 81:1251-1261.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 1251-1261
-
-
Mei, H.1
Cuccaro, M.L.2
Martin, E.R.3
-
35
-
-
0033974338
-
The human serotonin transporter gene linked polymorphism (5-HTTLPR) shows ten novel allelic variants
-
Nakamura M, Ueno S, Sano A, Tanabe H. 2000. The human serotonin transporter gene linked polymorphism (5-HTTLPR) shows ten novel allelic variants. Mol Psychiatry 5:32-38.
-
(2000)
Mol Psychiatry
, vol.5
, pp. 32-38
-
-
Nakamura, M.1
Ueno, S.2
Sano, A.3
Tanabe, H.4
-
36
-
-
0242552619
-
Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype
-
Ozaki N, Goldman D, Kaye WH, Plotnicov K, Greenberg BD, Lappalainen J, Rudnick G, Murphy DL. 2003. Serotonin transporter missense mutation associated with a complex neuropsychiatric phenotype. Mol Psychiatry 8:933-936.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 933-936
-
-
Ozaki, N.1
Goldman, D.2
Kaye, W.H.3
Plotnicov, K.4
Greenberg, B.D.5
Lappalainen, J.6
Rudnick, G.7
Murphy, D.L.8
-
37
-
-
0036373349
-
Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children
-
Persico AM, Pascucci T, Puglisi-Allegra S, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S, Montecchi F, Palermo M, Rabinowitz D, Reichelt KL, Conciatori M, Marino R, Keller F. 2002. Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children. Mol Psychiatry 7:795-800.
-
(2002)
Mol Psychiatry
, vol.7
, pp. 795-800
-
-
Persico, A.M.1
Pascucci, T.2
Puglisi-Allegra, S.3
Militerni, R.4
Bravaccio, C.5
Schneider, C.6
Melmed, R.7
Trillo, S.8
Montecchi, F.9
Palermo, M.10
Rabinowitz, D.11
Reichelt, K.L.12
Conciatori, M.13
Marino, R.14
Keller, F.15
-
38
-
-
0029134874
-
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error:A twin and family history study of autism
-
Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim CH, Rutter M. 1995. Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error:A twin and family history study of autism. Am J Hum Genet 57:717-726.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
Bailey, A.4
Le Couteur, A.5
Sim, C.H.6
Rutter, M.7
-
39
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard JK. 2001. Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69:124-137.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
40
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T, Nguyen L, Yang J, Harper C, Thorpe D, Vermeer S, Young H, Hebert J, Lin A, Ferguson J, Chiotti C, Wiese-Slater S, Rogers T, Salmon B, Nicholas P, Myers RM. 1999. A genomic screen of autism: Evidence for a multilocus etiology. Am J Hum Genet 65:493-507.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
Nouri, N.4
Hinds, D.5
Hallmayer, J.6
Kalaydjieva, L.7
McCague, P.8
Dimiceli, S.9
Pitts, T.10
Nguyen, L.11
Yang, J.12
Harper, C.13
Thorpe, D.14
Vermeer, S.15
Young, H.16
Hebert, J.17
Lin, A.18
Ferguson, J.19
Chiotti, C.20
Wiese-Slater, S.21
Rogers, T.22
Salmon, B.23
Nicholas, P.24
Myers, R.M.25
more..
-
41
-
-
0034973569
-
Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer
-
Ritchie MD, Hahn LW, Roodi N, Bailey LR, Dupont WD, Parl FF, Moore JH. 2001. Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. Am J Hum Genet 69:138-147.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 138-147
-
-
Ritchie, M.D.1
Hahn, L.W.2
Roodi, N.3
Bailey, L.R.4
Dupont, W.D.5
Parl, F.F.6
Moore, J.H.7
-
42
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimaki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, ChungW,Warburton D, KingMC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M. 2007. Strong association of de novo copy number mutations with autism. Science 316:445-449.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
Yamrom, B.7
Yoon, S.8
Krasnitz, A.9
Kendall, J.10
Leotta, A.11
Pai, D.12
Zhang, R.13
Lee, Y.H.14
Hicks, J.15
Spence, S.J.16
Lee, A.T.17
Puura, K.18
Lehtimaki, T.19
Ledbetter, D.20
Gregersen, P.K.21
Bregman, J.22
Sutcliffe, J.S.23
Jobanputra, V.24
Chung, W.25
Warburton, D.26
King, M.C.27
Skuse, D.28
Geschwind, D.H.29
Gilliam, T.C.30
Ye, K.31
Wigler, M.32
more..
-
43
-
-
0037371673
-
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
-
Shao Y, Cuccaro ML, Hauser ER, Raiford KL, Menold MM, Wolpert CM, Ravan SA, Elston L, Decena K, Donnelly SL, Abramson RK, Wright HH, DeLong GR, Gilbert JR, Pericak-Vance MA. 2003. Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes. Am J Hum Genet 72:539-548.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 539-548
-
-
Shao, Y.1
Cuccaro, M.L.2
Hauser, E.R.3
Raiford, K.L.4
Menold, M.M.5
Wolpert, C.M.6
Ravan, S.A.7
Elston, L.8
Decena, K.9
Donnelly, S.L.10
Abramson, R.K.11
Wright, H.H.12
DeLong, G.R.13
Gilbert, J.R.14
Pericak-Vance, M.A.15
-
44
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway, and Sweden
-
Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G, Bohman M. 1989. A twin study of autism in Denmark, Finland, Iceland, Norway, and Sweden. J Child Psychol Psychiatry 30:405-416.
-
(1989)
J Child Psychol Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
Andersson, L.4
Gillberg, I.C.5
Jakobsson, G.6
Bohman, M.7
-
45
-
-
8844244724
-
Evidence for sex-specific risk alleles in autism spectrum disorder
-
Stone JL, Merriman B, Cantor RM, Yonan AL, Gilliam TC, Geschwind DH, Nelson SF. 2004. Evidence for sex-specific risk alleles in autism spectrum disorder. Am J Hum Genet 75:1117-1123.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 1117-1123
-
-
Stone, J.L.1
Merriman, B.2
Cantor, R.M.3
Yonan, A.L.4
Gilliam, T.C.5
Geschwind, D.H.6
Nelson, S.F.7
-
46
-
-
22544446444
-
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigidcompulsive behaviors
-
Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD. 2005. Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigidcompulsive behaviors. Am J Hum Genet 77:265-279.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 265-279
-
-
Sutcliffe, J.S.1
Delahanty, R.J.2
Prasad, H.C.3
McCauley, J.L.4
Han, Q.5
Jiang, L.6
Li, C.7
Folstein, S.E.8
Blakely, R.D.9
-
47
-
-
0029813328
-
High phenotypic correlations among siblings with autism and pervasive developmental disorders
-
Szatmari P, Jones MB, Holden J, Bryson S, Mahoney W, Tuff L, MacLean J, White B, Bartolucci G, Schutz C, Robinson P, Hoult L. 1996. High phenotypic correlations among siblings with autism and pervasive developmental disorders. Am J Med Genet 67:354-360.
-
(1996)
Am J Med Genet
, vol.67
, pp. 354-360
-
-
Szatmari, P.1
Jones, M.B.2
Holden, J.3
Bryson, S.4
Mahoney, W.5
Tuff, L.6
MacLean, J.7
White, B.8
Bartolucci, G.9
Schutz, C.10
Robinson, P.11
Hoult, L.12
-
48
-
-
0002121803
-
The collection of biological samples for DNA analysis
-
Haines JL, Pericak-Vance MA, editors, New York: Wiley-Liss. pp
-
Vance JM. 1998. The collection of biological samples for DNA analysis. In: Haines JL, Pericak-Vance MA, editors. Approaches to gene mapping in complex human diseases. New York: Wiley-Liss. pp 201-211.
-
(1998)
Approaches to gene mapping in complex human diseases
, pp. 201-211
-
-
Vance, J.M.1
-
49
-
-
0037302791
-
Role of selective serotonin reuptake inhibitors in psychiatric disorders: Acomprehensive review
-
Vaswani M, Linda FK, Ramesh S. 2003. Role of selective serotonin reuptake inhibitors in psychiatric disorders: Acomprehensive review. Prog Neuropsychopharmacol Biol Psychiatry 27:85-102.
-
(2003)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.27
, pp. 85-102
-
-
Vaswani, M.1
Linda, F.K.2
Ramesh, S.3
-
51
-
-
7744229124
-
Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin
-
Weiss LA, Veenstra-VanderWeele J, Newman DL, Kim SJ, Dytch H, McPeek MS, Cheng S, Ober C, Cook EH, Abney M. 2004. Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin. Eur J Hum Genet 12:949-954.
-
(2004)
Eur J Hum Genet
, vol.12
, pp. 949-954
-
-
Weiss, L.A.1
Veenstra-VanderWeele, J.2
Newman, D.L.3
Kim, S.J.4
Dytch, H.5
McPeek, M.S.6
Cheng, S.7
Ober, C.8
Cook, E.H.9
Abney, M.10
-
52
-
-
20344407852
-
Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample
-
Weiss LA, Abney M, Parry R, Scanu AM, Cook EH Jr, Ober C. 2005. Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample. Hum Genet 117:81-87.
-
(2005)
Hum Genet
, vol.117
, pp. 81-87
-
-
Weiss, L.A.1
Abney, M.2
Parry, R.3
Scanu, A.M.4
Cook Jr, E.H.5
Ober, C.6
-
53
-
-
33745682011
-
Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility
-
Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS. 2006a. Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility. Eur J Hum Genet 14:923-931.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 923-931
-
-
Weiss, L.A.1
Kosova, G.2
Delahanty, R.J.3
Jiang, L.4
Cook, E.H.5
Ober, C.6
Sutcliffe, J.S.7
-
54
-
-
33745728424
-
ITGB3 shows genetic and expression interaction with SLC6A4
-
CookEHJr
-
Weiss LA, Ober C, CookEHJr. 2006b. ITGB3 shows genetic and expression interaction with SLC6A4. Hum Genet 120:93-100.
-
(2006)
Hum Genet
, vol.120
, pp. 93-100
-
-
Weiss, L.A.1
Ober, C.2
-
55
-
-
33644614818
-
Simultaneous genotyping of four functional loci of human SLC6A4, with a reappraisal of 5-HTTLPR and rs25531
-
Wendland JR, Martin BJ, Kruse MR, Lesch KP, Murphy DL. 2006. Simultaneous genotyping of four functional loci of human SLC6A4, with a reappraisal of 5-HTTLPR and rs25531. Mol Psychiatry 11:224-226.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 224-226
-
-
Wendland, J.R.1
Martin, B.J.2
Kruse, M.R.3
Lesch, K.P.4
Murphy, D.L.5
-
56
-
-
0142059641
-
A genomewide screen of 345 families for autism-susceptibility loci
-
Yonan AL, Alarcon M, Cheng R, Magnusson PKE, Spence SJ, Palmer AA, Grunn A, Juo SHH, Terwilliger JD, Liu JJ, Cantor RM, Geschwind DH, Gilliam TC. 2003. A genomewide screen of 345 families for autism-susceptibility loci. Am J Hum Genet 73:886-897.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 886-897
-
-
Yonan, A.L.1
Alarcon, M.2
Cheng, R.3
Magnusson, P.K.E.4
Spence, S.J.5
Palmer, A.A.6
Grunn, A.7
Juo, S.H.H.8
Terwilliger, J.D.9
Liu, J.J.10
Cantor, R.M.11
Geschwind, D.H.12
Gilliam, T.C.13
-
57
-
-
41149101588
-
Genetic flip-flop without an accompanying change in linkage disequilibrium
-
author reply 796-797
-
Zaykin DV, Shibata K. 2008. Genetic flip-flop without an accompanying change in linkage disequilibrium. Am J Hum Genet 82:794-796; author reply 796-797.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 794-796
-
-
Zaykin, D.V.1
Shibata, K.2
-
58
-
-
0029185482
-
Exact tests for association between alleles at arbitrary numbers of loci
-
Zaykin D, Zhivotovsky L, Weir BS. 1995. Exact tests for association between alleles at arbitrary numbers of loci. Genetica 96:169-178.
-
(1995)
Genetica
, vol.96
, pp. 169-178
-
-
Zaykin, D.1
Zhivotovsky, L.2
Weir, B.S.3
-
59
-
-
0032904498
-
5-HTTLPR variants not associated with autistic spectrum disorders
-
Zhong N, Ye L, Ju W, Brown WT, Tsiouris J, Cohen I. 1999. 5-HTTLPR variants not associated with autistic spectrum disorders. Neurogenetics 2:129-131.
-
(1999)
Neurogenetics
, vol.2
, pp. 129-131
-
-
Zhong, N.1
Ye, L.2
Ju, W.3
Brown, W.T.4
Tsiouris, J.5
Cohen, I.6
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