-
1
-
-
0028906338
-
Autism as a strongly genetic disorder: Evidence from a British twin study
-
Bailey A, Le Couteur A, Gottesman I, et al: Autism as a strongly genetic disorder: Evidence from a British twin study. Psychol Med 1995;25:63-77.
-
(1995)
Psychol. Med.
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
-
2
-
-
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, et al: 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 1995;57:717-726.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 717-726
-
-
Pickles, A.1
Bolton, P.2
Macdonald, H.3
-
3
-
-
0033362024
-
A genomic screen of autism: Evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L, et al: A genomic screen of autism: Evidence for a multilocus etiology. Am J Hum Genet 1999;65: 493-507.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 493-507
-
-
Risch, N.1
Spiker, D.2
Lotspeich, L.3
-
4
-
-
6844251000
-
A full genome screen for autism with evidence for linkage to a region on chromosome 7q
-
International Molecular Genetic Study of Autism Consortium
-
International Molecular Genetic Study of Autism Consortium. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 1998;7:571-578.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 571-578
-
-
-
5
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes
-
Paris Autism Research International Sibpair Study
-
Philippe A, Martinez M, Guilloud-Bataille M, et al: Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum Mol Genet 1999;8:805-812.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
-
6
-
-
0032729834
-
Genetic studies of autistic disorder and chromosome 7
-
Ashley-Koch A, Wolpert CM, Menold MM, et al: Genetic studies of autistic disorder and chromosome 7. Genomics 1999;61:227-236.
-
(1999)
Genomics
, vol.61
, pp. 227-236
-
-
Ashley-Koch, A.1
Wolpert, C.M.2
Menold, M.M.3
-
7
-
-
0034920299
-
A genomewide screen for autism susceptibility loci
-
Liu J, Nyholt DR, Magnussen P, et al: A genomewide screen for autism susceptibility loci. Am J Hum Genet 2001;69:327-340.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 327-340
-
-
Liu, J.1
Nyholt, D.R.2
Magnussen, P.3
-
8
-
-
0033573212
-
An autosomal genomic screen for autism. Collaborative linkage study of autism
-
Barrett S, Beck JC, Bernier R, et al: An autosomal genomic screen for autism. Collaborative linkage study of autism. Am J Med Genet 1999;88:609-615.
-
(1999)
Am. J. Med. Genet.
, vol.88
, pp. 609-615
-
-
Barrett, S.1
Beck, J.C.2
Bernier, R.3
-
9
-
-
37649026213
-
Genomic screen and follow-up analysis for autistic disorder
-
Shao Y, Wolpert CM, Raiford KL, et al: Genomic screen and follow-up analysis for autistic disorder. Am J Med Genet 2002; 114:99-105.
-
(2002)
Am. J. Med. Genet.
, vol.114
, pp. 99-105
-
-
Shao, Y.1
Wolpert, C.M.2
Raiford, K.L.3
-
10
-
-
0034757723
-
Prevalence of autism in a United States population: The Brick Township, New Jersey, investigation
-
Bertrand J, Mars A, Boyle C, et al: Prevalence of autism in a United States population: The Brick Township, New Jersey, investigation. Pediatrics 2001;108:1155-1161.
-
(2001)
Pediatrics
, vol.108
, pp. 1155-1161
-
-
Bertrand, J.1
Mars, A.2
Boyle, C.3
-
11
-
-
0032975478
-
Autism: Not an extremely rare disorder
-
Gillberg C, Wing L: Autism: Not an extremely rare disorder. Acta Psychiatr Scand 1999;99:399-406.
-
(1999)
Acta Psychiatr. Scand.
, vol.99
, pp. 399-406
-
-
Gillberg, C.1
Wing, L.2
-
12
-
-
0030027841
-
Autism in immigrants: A population-based study from Swedish rural and urban areas
-
Gillberg IC, Gillberg C: Autism in immigrants: A population-based study from Swedish rural and urban areas. J Intellect Disabil Res 1996;40(Pt 1):24-31.
-
(1996)
J. Intellect. Disabil. Res.
, vol.40
, Issue.PART 1
, pp. 24-31
-
-
Gillberg, I.C.1
Gillberg, C.2
-
13
-
-
0031976555
-
Relation between blindness due to retinopathy of prematurity and autistic spectrum disorders: A population-based study
-
Ek U, Fernell E, Jacobson L, Gillberg C: Relation between blindness due to retinopathy of prematurity and autistic spectrum disorders: A population-based study. Dev Med Child Neurol 1998;40:297-301.
-
(1998)
Dev. Med. Child Neurol.
, vol.40
, pp. 297-301
-
-
Ek, U.1
Fernell, E.2
Jacobson, L.3
Gillberg, C.4
-
14
-
-
0033549334
-
Autism and measles, mumps, and rubella vaccine: No epidemiological evidence for a causal association
-
Taylor B, Miller E, Farrington CP, et al: Autism and measles, mumps, and rubella vaccine: No epidemiological evidence for a causal association. Lancet 1999;353:2026-2029.
-
(1999)
Lancet
, vol.353
, pp. 2026-2029
-
-
Taylor, B.1
Miller, E.2
Farrington, C.P.3
-
15
-
-
0037038217
-
A population-based study of measles, mumps, and rubella vaccination and autism
-
Madsen KM, Hviid A, Vestergaard M, et al: A population-based study of measles, mumps, and rubella vaccination and autism. N Engl J Med 2002;347:1477-1482.
-
(2002)
N. Engl. J. Med.
, vol.347
, pp. 1477-1482
-
-
Madsen, K.M.1
Hviid, A.2
Vestergaard, M.3
-
16
-
-
0042763207
-
Thimerosal and the occurrence of autism: Negative ecological evidence from Danish population-based data
-
Madsen KM, Lauritsen MB, Pedersen CB, et al: Thimerosal and the occurrence of autism: Negative ecological evidence from Danish population-based data. Pediatrics 2003;112:604-606.
-
(2003)
Pediatrics
, vol.112
, pp. 604-606
-
-
Madsen, K.M.1
Lauritsen, M.B.2
Pedersen, C.B.3
-
17
-
-
0035958295
-
Pervasive developmental disorders in preschool children
-
Chakrabarti S, Fombonne E: Pervasive developmental disorders in preschool children. JAMA 2001;285:3093-3099.
-
(2001)
JAMA
, vol.285
, pp. 3093-3099
-
-
Chakrabarti, S.1
Fombonne, E.2
-
18
-
-
0033910523
-
The developing brain and the environment: An introduction
-
Weiss B, Landrigan PJ: The developing brain and the environment: An introduction. Environ Health Perspect 2000;108(Suppl 3):373-374.
-
(2000)
Environ. Health Perspect.
, vol.108
, Issue.SUPPL. 3
, pp. 373-374
-
-
Weiss, B.1
Landrigan, P.J.2
-
19
-
-
0033911258
-
Critical periods of vulnerability for the developing nervous system: Evidence from humans and animal models
-
Rice D, Barone S Jr: Critical periods of vulnerability for the developing nervous system: Evidence from humans and animal models. Environ Health Perspect 2000;108(Suppl 3):511-533.
-
(2000)
Environ. Health Perspect.
, vol.108
, Issue.SUPPL. 3
, pp. 511-533
-
-
Rice, D.1
Barone Jr., S.2
-
21
-
-
0029858544
-
The TDT and other family-based tests for linkage disequilibrium and association
-
Spielman RS, Ewens WJ: The TDT and other family-based tests for linkage disequilibrium and association. Am J Hum Genet 1996;59:983-989.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 983-989
-
-
Spielman, R.S.1
Ewens, W.J.2
-
22
-
-
0034916325
-
The Autism Genetic Resource Exchange: A resource for the study of autism and related neuropsychiatric conditions
-
Geschwind DH, Sowinski J, Lord C, et al: The Autism Genetic Resource Exchange: A resource for the study of autism and related neuropsychiatric conditions. Am J Hum Genet 2001; 69:463-466.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 463-466
-
-
Geschwind, D.H.1
Sowinski, J.2
Lord, C.3
-
23
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
O'Connell JR, Weeks DE: PedCheck: A program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet 1998;63:259-266.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
24
-
-
0036338150
-
Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR: Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002;30:97-101.
-
(2002)
Nat. Genet.
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
25
-
-
0029945706
-
Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
-
Sobel E, Lange K: Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 1996;58:1323-1337.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1323-1337
-
-
Sobel, E.1
Lange, K.2
-
26
-
-
0034017850
-
GOLD - Graphical overview of linkage disequilibrium
-
Abecasis GR, Cookson WO: GOLD - Graphical overview of linkage disequilibrium. Bioinformatics 2000;16:182-183.
-
(2000)
Bioinformatics
, vol.16
, pp. 182-183
-
-
Abecasis, G.R.1
Cookson, W.O.2
-
28
-
-
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;21:53-67.
-
(2001)
Genet. Epidemiol.
, vol.21
, pp. 53-67
-
-
Chen, W.M.1
Deng, H.W.2
-
29
-
-
0033358557
-
A note on power approximations for the transmission/disequilibrium test
-
Knapp M: A note on power approximations for the transmission/disequilibrium test. Am J Hum Genet 1999;64:1177-1185.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1177-1185
-
-
Knapp, M.1
-
30
-
-
0037036433
-
Regulation of metallothionein transcription by the metal-responsive transcription factor MTF-1: Identification of signal transduction cascades that control metal-inducible transcription
-
Saydam N, Adams TK, Steiner F, et al: Regulation of metallothionein transcription by the metal-responsive transcription factor MTF-1: identification of signal transduction cascades that control metal-inducible transcription. J Biol Chem 2002;277:20438-20445.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 20438-20445
-
-
Saydam, N.1
Adams, T.K.2
Steiner, F.3
-
31
-
-
0029948054
-
A murine model of Menkes disease reveals a physiological function of metallothionein
-
Kelly EJ, Palmiter RD: A murine model of Menkes disease reveals a physiological function of metallothionein. Nat Genet 1996;13:219-222.
-
(1996)
Nat. Genet.
, vol.13
, pp. 219-222
-
-
Kelly, E.J.1
Palmiter, R.D.2
-
32
-
-
0030755366
-
Cloning and characterization of a mammalian proton-coupled metal-ion transporter
-
Gunshin H, Mackenzie B, Berger UV, et al: Cloning and characterization of a mammalian proton-coupled metal-ion transporter. Nature 1997;388:482-488.
-
(1997)
Nature
, vol.388
, pp. 482-488
-
-
Gunshin, H.1
Mackenzie, B.2
Berger, U.V.3
-
33
-
-
0036185195
-
Iron deficiency in autism and Asperger syndrome
-
Latif A, Heinz P, Cook R: Iron deficiency in autism and Asperger syndrome. Autism 2002;6:103-114.
-
(2002)
Autism
, vol.6
, pp. 103-114
-
-
Latif, A.1
Heinz, P.2
Cook, R.3
-
34
-
-
0028152793
-
Quantification of human serum paraoxonase by enzyme-linked immunoassay: Population differences in protein concentrations
-
Blatter Garin MC, Abbott C, Messmer S, et al: Quantification of human serum paraoxonase by enzyme-linked immunoassay: Population differences in protein concentrations. Biochem J 1994;304(Pt 2):549-554.
-
(1994)
Biochem. J.
, vol.304
, Issue.PART 2
, pp. 549-554
-
-
Blatter Garin, M.C.1
Abbott, C.2
Messmer, S.3
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