-
2
-
-
0037218815
-
The prevalence of autism
-
Fombonne E. The prevalence of autism. J Am Med Assoc 289 (2003) 87
-
(2003)
J Am Med Assoc
, vol.289
, pp. 87
-
-
Fombonne, E.1
-
4
-
-
0032804766
-
The epidemiology of autism. a review
-
Fombonne E. The epidemiology of autism. a review. Psychol Med 29 (1999) 769
-
(1999)
Psychol Med
, vol.29
, pp. 769
-
-
Fombonne, E.1
-
6
-
-
28644434943
-
Effects of familial risk factors and place of birth on the risk of autism. a nationwide register-based study
-
Lauritsen M.B., Pedersen C.B., and Mortensen P.B. Effects of familial risk factors and place of birth on the risk of autism. a nationwide register-based study. J. Child Psychol Psychiatry 46 (2005) 963
-
(2005)
J. Child Psychol Psychiatry
, vol.46
, pp. 963
-
-
Lauritsen, M.B.1
Pedersen, C.B.2
Mortensen, P.B.3
-
7
-
-
0021934562
-
Familial heterogeneity in infantile autism
-
Baird T.D., and August G.J. Familial heterogeneity in infantile autism. J Autism Dev Disord 15 (1985) 315
-
(1985)
J Autism Dev Disord
, vol.15
, pp. 315
-
-
Baird, T.D.1
August, G.J.2
-
8
-
-
0028359950
-
A case-control family history study of autism
-
Bolton P., Macdonald H., Pickles A., Rios P., Goode S., Crowson M., Bailey A., and Rutter M. A case-control family history study of autism. J Child Psychol Psychiatry 35 (1994) 877
-
(1994)
J Child Psychol Psychiatry
, vol.35
, pp. 877
-
-
Bolton, P.1
Macdonald, H.2
Pickles, A.3
Rios, P.4
Goode, S.5
Crowson, M.6
Bailey, A.7
Rutter, M.8
-
9
-
-
0026596805
-
Siblings and parents of children with autism. a controlled population-based study
-
Gillberg C., Gillberg I.C., and Steffenburg S. Siblings and parents of children with autism. a controlled population-based study. Dev Med Child Neurol 34 (1992) 389
-
(1992)
Dev Med Child Neurol
, vol.34
, pp. 389
-
-
Gillberg, C.1
Gillberg, I.C.2
Steffenburg, S.3
-
10
-
-
0024336203
-
The UCLA-University of Utah epidemiologic survey of autism. recurrence risk estimates and genetic counseling
-
Ritvo E.R., Jorde L.B., Mason-Brothers A., Freeman B.J., Pingree C., Jones M.B., McMahon W.M., Petersen P.B., Jenson W.R., and Mo A. The UCLA-University of Utah epidemiologic survey of autism. recurrence risk estimates and genetic counseling. Am J Psychiatry 146 (1989) 1032
-
(1989)
Am J Psychiatry
, vol.146
, pp. 1032
-
-
Ritvo, E.R.1
Jorde, L.B.2
Mason-Brothers, A.3
Freeman, B.J.4
Pingree, C.5
Jones, M.B.6
McMahon, W.M.7
Petersen, P.B.8
Jenson, W.R.9
Mo, A.10
-
11
-
-
0027438546
-
Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders
-
Szatmari P., Jones M.B., Tuff L., Bartolucci G., Fisman S., and Mahoney W. Lack of cognitive impairment in first-degree relatives of children with pervasive developmental disorders. J Am Acad Child Adolesc Psychiatry 32 (1993) 1264
-
(1993)
J Am Acad Child Adolesc Psychiatry
, vol.32
, pp. 1264
-
-
Szatmari, P.1
Jones, M.B.2
Tuff, L.3
Bartolucci, G.4
Fisman, S.5
Mahoney, W.6
-
12
-
-
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., and Rutter M. Autism as a strongly genetic disorder. evidence from a British twin study. Psychol Med 25 (1995) 63
-
(1995)
Psychol Med
, vol.25
, pp. 63
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
Bolton, P.4
Simonoff, E.5
Yuzda, E.6
Rutter, M.7
-
13
-
-
0017530988
-
Infantile autism. a genetic study of 21 twin pairs
-
Folstein S., and Rutter M. Infantile autism. a genetic study of 21 twin pairs. J Child Psychol Psychiatry 18 (1977) 297
-
(1977)
J Child Psychol Psychiatry
, vol.18
, pp. 297
-
-
Folstein, S.1
Rutter, M.2
-
14
-
-
0032904445
-
Quasi-autistic patterns following severe early global privation
-
English and Romanian Adoptees (ERA) Study Team
-
Rutter M., Andersen-Wood L., Beckett C., Bredenkamp D., Castle J., Groothues C., Kreppner J., Keaveney L., Lord C., O'Connor T.G., and English and Romanian Adoptees (ERA) Study Team. Quasi-autistic patterns following severe early global privation. J Child Psychol Psychiatry 40 (1999) 537
-
(1999)
J Child Psychol Psychiatry
, vol.40
, pp. 537
-
-
Rutter, M.1
Andersen-Wood, L.2
Beckett, C.3
Bredenkamp, D.4
Castle, J.5
Groothues, C.6
Kreppner, J.7
Keaveney, L.8
Lord, C.9
O'Connor, T.G.10
-
15
-
-
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 C.H., and Rutter M. 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 (1995) 717
-
(1995)
Am J Hum Genet
, vol.57
, pp. 717
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
Bailey, A.4
Le Couteur, A.5
Sim, C.H.6
Rutter, M.7
-
16
-
-
0000138295
-
Autism. a genetic perspective, in neurodevelopmental disorders
-
Tager-Flushberg H. (Ed), MIT Press, Cambridge (MA)
-
Santangelo S., and Folstein S. Autism. a genetic perspective, in neurodevelopmental disorders. In: Tager-Flushberg H. (Ed). Neurodevelopmental disorders. contributions to a new framework from the cognitive neurosciences (1999), MIT Press, Cambridge (MA) 431
-
(1999)
Neurodevelopmental disorders. contributions to a new framework from the cognitive neurosciences
, pp. 431
-
-
Santangelo, S.1
Folstein, S.2
-
17
-
-
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., Petersen P.B., Pingree C., McMahon W., Wong D.L., Cavalli-Sforza L.L., Kraemer H.C., and Myers R.M. A genomic screen of autism. evidence for a multilocus etiology. Am J Hum Genet 65 2 (1999) 493
-
(1999)
Am J Hum Genet
, vol.65
, Issue.2
, pp. 493
-
-
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
Petersen, P.B.25
Pingree, C.26
McMahon, W.27
Wong, D.L.28
Cavalli-Sforza, L.L.29
Kraemer, H.C.30
Myers, R.M.31
more..
-
18
-
-
26444469579
-
Complex interactions among MHC haplotypes in multiple sclerosis. susceptibility and resistance
-
Epub 2005 Jun 1
-
Dyment D.A., Herrera B.M., Cader M.Z., Willer C.J., Lincoln M.R., Sadovnick A.D., Risch N., and Ebers G.C. Complex interactions among MHC haplotypes in multiple sclerosis. susceptibility and resistance. Hum Mol Genet 14 (2005) 2019 Epub 2005 Jun 1
-
(2005)
Hum Mol Genet
, vol.14
, pp. 2019
-
-
Dyment, D.A.1
Herrera, B.M.2
Cader, M.Z.3
Willer, C.J.4
Lincoln, M.R.5
Sadovnick, A.D.6
Risch, N.7
Ebers, G.C.8
-
19
-
-
20944445879
-
MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
-
Epub 2005 Apr 10
-
Swanberg M., Lidman O., Padyukov L., Eriksson P., Akesson E., Jagodic M., Lobell A., Khademi M., Borjesson O., Lindgren C.M., Lundman P., Brookes A.J., Kere J., Luthman H., Alfredsson L., Hillert J., Klareskog L., Hamsten A., Piehl F., and Olsson T. MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction. Nat Genet 37 (2005) 486 Epub 2005 Apr 10
-
(2005)
Nat Genet
, vol.37
, pp. 486
-
-
Swanberg, M.1
Lidman, O.2
Padyukov, L.3
Eriksson, P.4
Akesson, E.5
Jagodic, M.6
Lobell, A.7
Khademi, M.8
Borjesson, O.9
Lindgren, C.M.10
Lundman, P.11
Brookes, A.J.12
Kere, J.13
Luthman, H.14
Alfredsson, L.15
Hillert, J.16
Klareskog, L.17
Hamsten, A.18
Piehl, F.19
Olsson, T.20
more..
-
20
-
-
14844311971
-
Disparate MHC class II haplotypes in myelin oligodendrocyte glycoprotein- and myelin basic protein-induced experimental autoimmune encephalomyelitis
-
Muhallab S., Dahlman I., and Wallstrom E. Disparate MHC class II haplotypes in myelin oligodendrocyte glycoprotein- and myelin basic protein-induced experimental autoimmune encephalomyelitis. J Neuroimmunol 161 (2005) 155
-
(2005)
J Neuroimmunol
, vol.161
, pp. 155
-
-
Muhallab, S.1
Dahlman, I.2
Wallstrom, E.3
-
21
-
-
0029120604
-
Increased frequency of the extended or ancestral haplotype B44-SC30-DR4 in autism
-
Daniels W.W., Warren R.P., Odell J.D., Maciulis A., Burger R.A., Warren W.L., and Torres A.R. Increased frequency of the extended or ancestral haplotype B44-SC30-DR4 in autism. Neuropsychobiology 32 (1995) 120
-
(1995)
Neuropsychobiology
, vol.32
, pp. 120
-
-
Daniels, W.W.1
Warren, R.P.2
Odell, J.D.3
Maciulis, A.4
Burger, R.A.5
Warren, W.L.6
Torres, A.R.7
-
22
-
-
0036228660
-
The transmission disequilibrium test suggests that HLA-DR4 and DR13 are linked to autism spectrum disorder
-
Torres A.R., Maciulis A., Stubbs E.G., Cutler A., and Odell D. The transmission disequilibrium test suggests that HLA-DR4 and DR13 are linked to autism spectrum disorder. Hum Immunol 63 (2002) 311
-
(2002)
Hum Immunol
, vol.63
, pp. 311
-
-
Torres, A.R.1
Maciulis, A.2
Stubbs, E.G.3
Cutler, A.4
Odell, D.5
-
23
-
-
0032797155
-
Esclusion of Linkage to HLA Region in Ninety Multiple sibships with Autism
-
Rogers T., Kalaydjieva L., Hallmayer J., Petersen P.B., Nicholas P., Pingree C., McMahon W.M., Spiker D., Lotspeich L., Kraemer H., McCague P., Dimiceli S., Nouri N., Peachy T., Yang J., Hinds D., Risch N., and Myers R.M. Esclusion of Linkage to HLA Region in Ninety Multiple sibships with Autism. I Aut Dev Dis 25 (1999) 195
-
(1999)
I Aut Dev Dis
, vol.25
, pp. 195
-
-
Rogers, T.1
Kalaydjieva, L.2
Hallmayer, J.3
Petersen, P.B.4
Nicholas, P.5
Pingree, C.6
McMahon, W.M.7
Spiker, D.8
Lotspeich, L.9
Kraemer, H.10
McCague, P.11
Dimiceli, S.12
Nouri, N.13
Peachy, T.14
Yang, J.15
Hinds, D.16
Risch, N.17
Myers, R.M.18
-
25
-
-
0027281184
-
Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder
-
Cook Jr. E.H., Arora R.C., Anderson G.M., Berry-Kravis E.M., Yan S.Y., Yeoh H.C., Skllena P.J., Charak D.A., and Leventhal B.L. Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder. Life Sci 52 (1993) 2005
-
(1993)
Life Sci
, vol.52
, pp. 2005
-
-
Cook Jr., E.H.1
Arora, R.C.2
Anderson, G.M.3
Berry-Kravis, E.M.4
Yan, S.Y.5
Yeoh, H.C.6
Skllena, P.J.7
Charak, D.A.8
Leventhal, B.L.9
-
26
-
-
0033556513
-
Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives
-
Leboyer M., Philippe A., Bouvard M., Guilloud-Bataille M., Bondoux D., Tabuteau F., Feingold J., Mouren-Simeoni M.C., and Launay J.M. Whole blood serotonin and plasma beta-endorphin in autistic probands and their first-degree relatives. Biol Psychiatry 45 (1999) 158
-
(1999)
Biol Psychiatry
, vol.45
, pp. 158
-
-
Leboyer, M.1
Philippe, A.2
Bouvard, M.3
Guilloud-Bataille, M.4
Bondoux, D.5
Tabuteau, F.6
Feingold, J.7
Mouren-Simeoni, M.C.8
Launay, J.M.9
-
27
-
-
0025244988
-
Relationships of whole blood serotonin and plasma norepinephrine within families of autistic children
-
Leventhal B.L., Cook Jr. E.H., Morford J., Ravitz A., and Freedman D.X. Relationships of whole blood serotonin and plasma norepinephrine within families of autistic children. J. Autism Dev Disord 20 (1990) 499
-
(1990)
J. Autism Dev Disord
, vol.20
, pp. 499
-
-
Leventhal, B.L.1
Cook Jr., E.H.2
Morford, J.3
Ravitz, A.4
Freedman, D.X.5
-
28
-
-
0025973054
-
Platelet serotonin, a possible marker for familial autism
-
Piven J., Tsai G.C., Nehme E., Coyle J.T., Chase G.A., and Folstein S.E. Platelet serotonin, a possible marker for familial autism. J Autism Dev Disord 21 (1991) 51
-
(1991)
J Autism Dev Disord
, vol.21
, pp. 51
-
-
Piven, J.1
Tsai, G.C.2
Nehme, E.3
Coyle, J.T.4
Chase, G.A.5
Folstein, S.E.6
-
29
-
-
8244234472
-
Evidence of linkage between the serotonin transporter and autistic disorder
-
Cook Jr. E.H., Courchesne R., Lord C., Cox N.J., Yan S., Lincoln A., Haas R., Courchesne E., and Leventhal B.L. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry 2 (1997) 247
-
(1997)
Mol Psychiatry
, vol.2
, pp. 247
-
-
Cook Jr., 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
-
30
-
-
23744490895
-
Population-based and family-based studies on the serotonin transporter gene polymorphisms and bipolar disorder. a systematic review and meta-analysis
-
Cho H.J., Meira-Lima I., Cordeiro Q., Michelon L., Sham P., Vallada H., and Collier D.A. Population-based and family-based studies on the serotonin transporter gene polymorphisms and bipolar disorder. a systematic review and meta-analysis. Mol Psychiatry 10 (2005) 771
-
(2005)
Mol Psychiatry
, vol.10
, pp. 771
-
-
Cho, H.J.1
Meira-Lima, I.2
Cordeiro, Q.3
Michelon, L.4
Sham, P.5
Vallada, H.6
Collier, D.A.7
-
31
-
-
0030830590
-
Serotonin transporter (5-HTT) gene variants associated with autism?
-
Klauck S.M., Poustka F., Benner A., Lesch K.P., and Poustka A. Serotonin transporter (5-HTT) gene variants associated with autism?. Hum Mol Genet 6 (1997) 2233
-
(1997)
Hum Mol Genet
, vol.6
, pp. 2233
-
-
Klauck, S.M.1
Poustka, F.2
Benner, A.3
Lesch, K.P.4
Poustka, A.5
-
32
-
-
0023728919
-
Free serotonin in plasma. autistic children and their first-degree relatives
-
Cook Jr. E.H., Leventhal B.L., and Freedman D.X. Free serotonin in plasma. autistic children and their first-degree relatives. Biol Psychiatry 24 (1988) 488
-
(1988)
Biol Psychiatry
, vol.24
, pp. 488
-
-
Cook Jr., E.H.1
Leventhal, B.L.2
Freedman, D.X.3
-
33
-
-
2342520299
-
Serotonin transporter gene and autism. a haplotype analysis in an Irish autistic population
-
Conroy J., Meally E., Kearney G., Fitzgerald M., Gill M., and Gallagher L. Serotonin transporter gene and autism. a haplotype analysis in an Irish autistic population. Mol Psychiatry 9 (2004) 587
-
(2004)
Mol Psychiatry
, vol.9
, pp. 587
-
-
Conroy, J.1
Meally, E.2
Kearney, G.3
Fitzgerald, M.4
Gill, M.5
Gallagher, L.6
-
34
-
-
0034987571
-
Role of the serotonin transporter gene in the behavioural expression of autism
-
Tordjman S., Gutknecht L., Carlier M., Spitz E., Antoine C., Slama F., Carsalade V., Cohen D.J., Ferrari P., Roubertoux P.L., and Anderson G.M. Role of the serotonin transporter gene in the behavioural expression of autism. Mol Psychiatry 6 (2001) 434
-
(2001)
Mol Psychiatry
, vol.6
, pp. 434
-
-
Tordjman, S.1
Gutknecht, L.2
Carlier, M.3
Spitz, E.4
Antoine, C.5
Slama, F.6
Carsalade, V.7
Cohen, D.J.8
Ferrari, P.9
Roubertoux, P.L.10
Anderson, G.M.11
-
35
-
-
0035826536
-
Evidence for an association with the serotonin transporter promoter region polymorphism and autism
-
Yirmiya N., Pilowsky T., Nemanov L., Arbelle S., Feinsilver T., Fried I., and Ebstein R.P. Evidence for an association with the serotonin transporter promoter region polymorphism and autism. Am J Med Genet 105 (2001) 381
-
(2001)
Am J Med Genet
, vol.105
, pp. 381
-
-
Yirmiya, N.1
Pilowsky, T.2
Nemanov, L.3
Arbelle, S.4
Feinsilver, T.5
Fried, I.6
Ebstein, R.P.7
-
36
-
-
0034615162
-
Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples
-
Persico A.M., Militerni R., Bravaccio C., Schneider C., Melmed R., Conciatori M., Damiani V., Baldi A., and Keller F. Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples. Am J Med Genet 96 (2000) 123
-
(2000)
Am J Med Genet
, vol.96
, pp. 123
-
-
Persico, A.M.1
Militerni, R.2
Bravaccio, C.3
Schneider, C.4
Melmed, R.5
Conciatori, M.6
Damiani, V.7
Baldi, A.8
Keller, F.9
-
37
-
-
0033569931
-
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
-
Maestrini E., Lai C., Marlow A., Matthews N., Wallace S., Bailey A., Cook E.H., Weeks D.E., and Monaco A.P. 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. Am J Med Genet 88 (1999) 492
-
(1999)
Am J Med Genet
, vol.88
, pp. 492
-
-
Maestrini, E.1
Lai, C.2
Marlow, A.3
Matthews, N.4
Wallace, S.5
Bailey, A.6
Cook, E.H.7
Weeks, D.E.8
Monaco, A.P.9
-
38
-
-
21044453735
-
Lack of evidence for association between the serotonin transporter gene (SLC6A4) polymorphisms and autism in the Chinese trios
-
Wu S., Guo Y., Jia M., Ruan Y., Shuang M., Liu J., Gong X., Zhang Y., Yang J., Yang X., and Zhang D. Lack of evidence for association between the serotonin transporter gene (SLC6A4) polymorphisms and autism in the Chinese trios. Neurosci Lett 381 (2005) 1
-
(2005)
Neurosci Lett
, vol.381
, pp. 1
-
-
Wu, S.1
Guo, Y.2
Jia, M.3
Ruan, Y.4
Shuang, M.5
Liu, J.6
Gong, X.7
Zhang, Y.8
Yang, J.9
Yang, X.10
Zhang, D.11
-
39
-
-
22544446444
-
Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors
-
Sutcliffe J.S., Delahanty R.J., Prasad H.C., McCauley J.L., Han Q., Jiang L., Li C., Folstein S.E., and Blakely R.D. Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors. Am J Hum Genet 77 (2005) 265
-
(2005)
Am J Hum Genet
, vol.77
, pp. 265
-
-
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
-
40
-
-
0037739218
-
Reconstruction of human evolution. bringing together genetic, archaeological, and linguistic data
-
Cavalli-Sforza L.L., Piazza A., Menozzi P., and Mountain J. Reconstruction of human evolution. bringing together genetic, archaeological, and linguistic data. Proc Natl Acad Sci USA 85 (1988) 6002
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 6002
-
-
Cavalli-Sforza, L.L.1
Piazza, A.2
Menozzi, P.3
Mountain, J.4
-
41
-
-
0021997657
-
Genetic and population structure of four Sardinian villages
-
Piazza A., Mayr W.R., Contu L., Amoroso A., Borelli I., Curtoni E.S., Marcello C., Moroni A., Olivetti E., Richiardi P., et al. Genetic and population structure of four Sardinian villages. Ann Hum Genet 49 (1985) 47
-
(1985)
Ann Hum Genet
, vol.49
, pp. 47
-
-
Piazza, A.1
Mayr, W.R.2
Contu, L.3
Amoroso, A.4
Borelli, I.5
Curtoni, E.S.6
Marcello, C.7
Moroni, A.8
Olivetti, E.9
Richiardi, P.10
-
42
-
-
0034634349
-
The genetic legacy of Paleolithic homo sapiens sapiens in extant Europeans. a Y chromosome perspective
-
Semino O., Passarino G., Oefner P.J., Lin A.A., Arbuzova S., Beckman L.E., De Benedictis G., Francalacci P., Kouvatsi A., Limborska S., Marcikiae M., Mika A., Mika B., Primorac D., Santachiara-Benerecetti A.S., Cavalli-Sforza L.L., and Underhill P.A. The genetic legacy of Paleolithic homo sapiens sapiens in extant Europeans. a Y chromosome perspective. Science 290 (2000) 1155
-
(2000)
Science
, vol.290
, pp. 1155
-
-
Semino, O.1
Passarino, G.2
Oefner, P.J.3
Lin, A.A.4
Arbuzova, S.5
Beckman, L.E.6
De Benedictis, G.7
Francalacci, P.8
Kouvatsi, A.9
Limborska, S.10
Marcikiae, M.11
Mika, A.12
Mika, B.13
Primorac, D.14
Santachiara-Benerecetti, A.S.15
Cavalli-Sforza, L.L.16
Underhill, P.A.17
-
43
-
-
0033762701
-
Y chromosome sequence variation and the history of human population
-
Underhill P.A., Shen P., Lin A.A., Jin L., Passarino G., Yang W.H., Kauffman E., Bonne-Tamir B., Bertranpetit J., Francalacci P., Ibrahim M., Jenkins T., Kidd J.R., Mehdi S.Q., Seielstad M.T., Wells R.S., Piazza A., Davis R.W., Feldman M.W., Cavalli-Sforza L.L., and Oefner P.J. Y chromosome sequence variation and the history of human population. Nat Genet 26 (2000) 358
-
(2000)
Nat Genet
, vol.26
, pp. 358
-
-
Underhill, P.A.1
Shen, P.2
Lin, A.A.3
Jin, L.4
Passarino, G.5
Yang, W.H.6
Kauffman, E.7
Bonne-Tamir, B.8
Bertranpetit, J.9
Francalacci, P.10
Ibrahim, M.11
Jenkins, T.12
Kidd, J.R.13
Mehdi, S.Q.14
Seielstad, M.T.15
Wells, R.S.16
Piazza, A.17
Davis, R.W.18
Feldman, M.W.19
Cavalli-Sforza, L.L.20
Oefner, P.J.21
more..
-
44
-
-
0029118078
-
Genes and language in Europe. an analysis of mitochondrial lineages
-
Sajantila A., Lahermo P., Anttinen T., Lukka M., Sistonen P., Savontaus M.L., Aula P., Beckman L., Tranebjaerg L., Gedde-Dahl T., Issel-Tarver L., DiRienzo A., and Paabo S. Genes and language in Europe. an analysis of mitochondrial lineages. Genome Res 5 (1995) 42
-
(1995)
Genome Res
, vol.5
, pp. 42
-
-
Sajantila, A.1
Lahermo, P.2
Anttinen, T.3
Lukka, M.4
Sistonen, P.5
Savontaus, M.L.6
Aula, P.7
Beckman, L.8
Tranebjaerg, L.9
Gedde-Dahl, T.10
Issel-Tarver, L.11
DiRienzo, A.12
Paabo, S.13
-
46
-
-
0017255909
-
Immunoglobulin allotypes in Sardinia
-
Piazza A., van Loghem E., de Lange G., Curtoni E.S., Ulizzi L., and Terrenato L. Immunoglobulin allotypes in Sardinia. Am J Hum Genet 28 (1976) 77
-
(1976)
Am J Hum Genet
, vol.28
, pp. 77
-
-
Piazza, A.1
van Loghem, E.2
de Lange, G.3
Curtoni, E.S.4
Ulizzi, L.5
Terrenato, L.6
-
47
-
-
0026499555
-
HLA structure of the Sardinian population. a haplotype study of 551 families
-
Contu L., Arras M., Carcassi C., La Nasa G., and Mulargia M. HLA structure of the Sardinian population. a haplotype study of 551 families. Tissue Antigens 40 (1992) 165
-
(1992)
Tissue Antigens
, vol.40
, pp. 165
-
-
Contu, L.1
Arras, M.2
Carcassi, C.3
La Nasa, G.4
Mulargia, M.5
-
48
-
-
0035692034
-
West Mediterranean islands (Corsica, Balearic islands, Sardinia) and the Basque population. contribution of HLA class I molecular markers to their evolutionary history
-
Grimaldi M.C., Crouau-Roy B., Amoros J.P., Cambon-Thomsen A., Carcassi C., Orru S., Viader C., and Contu L. West Mediterranean islands (Corsica, Balearic islands, Sardinia) and the Basque population. contribution of HLA class I molecular markers to their evolutionary history. Tissue Antigens 58 (2001) 281
-
(2001)
Tissue Antigens
, vol.58
, pp. 281
-
-
Grimaldi, M.C.1
Crouau-Roy, B.2
Amoros, J.P.3
Cambon-Thomsen, A.4
Carcassi, C.5
Orru, S.6
Viader, C.7
Contu, L.8
-
49
-
-
0034642303
-
The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseases
-
Lampis R., Morelli L., Congia M., Macis M.D., Mulargia A., Loddo M., De Virgiliis S., Marrosu M.G., Todd J.A., and Cucca F. The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseases. Hum Mol Genet 9 (2000) 2959
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2959
-
-
Lampis, R.1
Morelli, L.2
Congia, M.3
Macis, M.D.4
Mulargia, A.5
Loddo, M.6
De Virgiliis, S.7
Marrosu, M.G.8
Todd, J.A.9
Cucca, F.10
-
50
-
-
0026691249
-
HLA -DR typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours. an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation
-
Olerup O., and Zitterquist H. HLA -DR typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours. an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation. Tissue Antigens 39 (1992) 225
-
(1992)
Tissue Antigens
, vol.39
, pp. 225
-
-
Olerup, O.1
Zitterquist, H.2
-
51
-
-
0029895783
-
Allelic variation of human serotonin transporter gene expression
-
Heils A., Teufel A., Petri S., Strober G., Riaderer P., Bengel D., and Lesch K.P. Allelic variation of human serotonin transporter gene expression. J Neurochem 66 (1996) 2621
-
(1996)
J Neurochem
, vol.66
, pp. 2621
-
-
Heils, A.1
Teufel, A.2
Petri, S.3
Strober, G.4
Riaderer, P.5
Bengel, D.6
Lesch, K.P.7
-
53
-
-
0027377799
-
Transmission test for linkage disequilibrium. the insuline gene region and insulin- dependent diabetes mellitus (IDDM)
-
Spielman R.S., McGinnis R.E., and Ewens W.J. Transmission test for linkage disequilibrium. the insuline gene region and insulin- dependent diabetes mellitus (IDDM). Am J Hum Gent 52 (1993) 506
-
(1993)
Am J Hum Gent
, vol.52
, pp. 506
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
54
-
-
0026071479
-
Increased frequency of the null allele at the complement C4b locus in autism
-
Warren R.P., Singh V.K., Cole P., Odell J.D., Pingree C.B., Warren W.L., and White E. Increased frequency of the null allele at the complement C4b locus in autism. Clin Exp Immunol 83 (1991) 438
-
(1991)
Clin Exp Immunol
, vol.83
, pp. 438
-
-
Warren, R.P.1
Singh, V.K.2
Cole, P.3
Odell, J.D.4
Pingree, C.B.5
Warren, W.L.6
White, E.7
-
56
-
-
0141892769
-
Significant association of HLA A2-DR11 with CD4 naive decrease in autistic children
-
Ferrante P., Saresella M., Guerini F.R., Marzorati M., Musetti M.C., and Cazzullo A.G. Significant association of HLA A2-DR11 with CD4 naive decrease in autistic children. Biomed Pharmacother 57 (2003) 372
-
(2003)
Biomed Pharmacother
, vol.57
, pp. 372
-
-
Ferrante, P.1
Saresella, M.2
Guerini, F.R.3
Marzorati, M.4
Musetti, M.C.5
Cazzullo, A.G.6
-
57
-
-
17844380266
-
What is known about autism. genes, brain, and behavior
-
Santangelo S.L., and Tsatsanis K. What is known about autism. genes, brain, and behavior. Am J Pharmacogenomics 5 (2005) 71
-
(2005)
Am J Pharmacogenomics
, vol.5
, pp. 71
-
-
Santangelo, S.L.1
Tsatsanis, K.2
-
58
-
-
0026680702
-
Possible association of the extended MHC haplotype B44-SC30-DR4 with autism
-
Warren R.P., Singh V.K., Cole P., Odell J.D., Pingree C.B., Warren W.L., DeWitt C.W., and McCullough M. Possible association of the extended MHC haplotype B44-SC30-DR4 with autism. Immunogenetics 36 (1992) 203
-
(1992)
Immunogenetics
, vol.36
, pp. 203
-
-
Warren, R.P.1
Singh, V.K.2
Cole, P.3
Odell, J.D.4
Pingree, C.B.5
Warren, W.L.6
DeWitt, C.W.7
McCullough, M.8
-
59
-
-
0030200135
-
Strong association of the third hypervariable region of HLA-DR beta 1 with autism
-
Warren R.P., Odell J.D., Warren W.L., Burger R.A., Maciulis A., Daniels W.W., and Torres A.R. Strong association of the third hypervariable region of HLA-DR beta 1 with autism. J Neuroimmunol 67 (1996) 97
-
(1996)
J Neuroimmunol
, vol.67
, pp. 97
-
-
Warren, R.P.1
Odell, J.D.2
Warren, W.L.3
Burger, R.A.4
Maciulis, A.5
Daniels, W.W.6
Torres, A.R.7
-
60
-
-
0029810533
-
Immunogenetic studies in autism and related disorders
-
Review
-
Warren R.P., Singh V.K., Averett R.E., Odell J.D., Maciulis A., Burger R.A., Daniels W.W., and Warren W.L. Immunogenetic studies in autism and related disorders. Review. Mol Chem Neuropathol 28 (1996) 77
-
(1996)
Mol Chem Neuropathol
, vol.28
, pp. 77
-
-
Warren, R.P.1
Singh, V.K.2
Averett, R.E.3
Odell, J.D.4
Maciulis, A.5
Burger, R.A.6
Daniels, W.W.7
Warren, W.L.8
-
61
-
-
13444293140
-
Confirmation of the association of the C4B null allelle in autism
-
Odell D., Maciulis A., Cutler A., Warren L., McMahon W.M., Coon H., Stubbs G., Henley K., and Torres A. Confirmation of the association of the C4B null allelle in autism. Hum Immunol 66 (2005) 140
-
(2005)
Hum Immunol
, vol.66
, pp. 140
-
-
Odell, D.1
Maciulis, A.2
Cutler, A.3
Warren, L.4
McMahon, W.M.5
Coon, H.6
Stubbs, G.7
Henley, K.8
Torres, A.9
-
62
-
-
0021994210
-
Gene mapping studies with the syndrome of autism
-
Spence M.A., Ritvo E.R., Marazita M.L., Funderburk S.J., Sparkes R.S., and Freeman B.J. Gene mapping studies with the syndrome of autism. Behav Genet 15 (1985) 1
-
(1985)
Behav Genet
, vol.15
, pp. 1
-
-
Spence, M.A.1
Ritvo, E.R.2
Marazita, M.L.3
Funderburk, S.J.4
Sparkes, R.S.5
Freeman, B.J.6
-
63
-
-
18244367163
-
Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia
-
Marrosu M.G., Murru R., Murru M.R., Costa G., Zavattari P., Whalen M., Cocco E., Mancosu C., Schirru L., Solla E., Fadda E., Melis C., Porru I., Rolesu M., and Cucca F. Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia. Hum Mol Genet 10 (2001) 2907
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2907
-
-
Marrosu, M.G.1
Murru, R.2
Murru, M.R.3
Costa, G.4
Zavattari, P.5
Whalen, M.6
Cocco, E.7
Mancosu, C.8
Schirru, L.9
Solla, E.10
Fadda, E.11
Melis, C.12
Porru, I.13
Rolesu, M.14
Cucca, F.15
-
64
-
-
0035653670
-
Genetics of autism. complex aetiology for a heterogeneous disorder
-
Folstein S.E., and Rosen-Sheidley B. Genetics of autism. complex aetiology for a heterogeneous disorder. Nat Rev Genet 2 (2001) 943
-
(2001)
Nat Rev Genet
, vol.2
, pp. 943
-
-
Folstein, S.E.1
Rosen-Sheidley, B.2
|