-
1
-
-
65949104586
-
Genomewide association studies and human disease
-
Hardy J, Singleton A. Genomewide association studies and human disease. N Engl J Med 2009;360:1759-68.
-
(2009)
N Engl J Med
, vol.360
, pp. 1759-1768
-
-
Hardy, J.1
Singleton, A.2
-
2
-
-
42349112088
-
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
-
McCarthy MI, Abecasis GR, Cardon LR, et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet 2008;9:356-69.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
-
3
-
-
34147186908
-
Understanding autism: parents and pediatricians in historical perspective
-
Silverman C, Brosco JP. Understanding autism: parents and pediatricians in historical perspective. Arch Pediatr Adolesc Med 2007;161:392- 8.
-
(2007)
Arch Pediatr Adolesc Med
, vol.161
, pp. 392-398
-
-
Silverman, C.1
Brosco, J.P.2
-
4
-
-
0000984981
-
Autistic disturbances of affective contact
-
Kanner L. Autistic disturbances of affective contact. Nervous Child 1943;2:217-50.
-
(1943)
Nervous Child
, vol.2
, pp. 217-250
-
-
Kanner, L.1
-
6
-
-
0017138765
-
The genetics, if any, of infantile autism and childhood schizophrenia
-
Hanson DR, Gottesman II. The genetics, if any, of infantile autism and childhood schizophrenia. J Autism Child Schizophr 1976;6:209-34.
-
(1976)
J Autism Child Schizophr
, vol.6
, pp. 209-234
-
-
Hanson, D.R.1
Gottesman, I.I.2
-
7
-
-
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
-
8
-
-
33744462332
-
Genetics of autism spectrum disorder
-
Klauck SM. Genetics of autism spectrum disorder. Eur J Hum Genet 2006;14:714-20.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 714-720
-
-
Klauck, S.M.1
-
9
-
-
33847327313
-
Autism Genome Project, Consortium., Mapping autism risk loci using genetic linkage and chromosomal, rearrangements
-
Autism Genome Project Consortium. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat Genet 2007;39:319-28.
-
(2007)
Nat Genet
, vol.39
, pp. 319-328
-
-
-
10
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J, Lakshmi B, Malhotra D, et al. Strong association of de novo copy number mutations with autism. Science 2007;316:445-9.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
-
11
-
-
42349095075
-
Advances in autism genetics: on the threshold of a new neurobiology
-
Abrahams BS, Geschwind DH. Advances in autism genetics: on the threshold of a new neurobiology. Nat Rev Genet 2008;9:341-55.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 341-355
-
-
Abrahams, B.S.1
Geschwind, D.H.2
-
13
-
-
77958113119
-
-
Wellcome Trust Centre for Human Genetics. Neurogenetics & Psychiatric Disorders Accessed 4 June 2010
-
Wellcome Trust Centre for Human Genetics. Neurogenetics & Psychiatric Disorders. http://www.well.ox.ac.uk/monaco/autism/autism_links.shtml (Accessed 4 June 2010).
-
-
-
-
14
-
-
27144517182
-
Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism
-
Philippi A, Roschmann E, Tores F, et al. Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autism. Mol Psychiatry 2005;10:950-60.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 950-960
-
-
Philippi, A.1
Roschmann, E.2
Tores, F.3
-
15
-
-
33845683734
-
Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population
-
Yang MS, Cochrane L, Conroy J, et al. Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population. Psychiatr Genet 2007;17:39-41.
-
(2007)
Psychiatr Genet
, vol.17
, pp. 39-41
-
-
Yang, M.S.1
Cochrane, L.2
Conroy, J.3
-
16
-
-
67649387094
-
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression
-
Lintas C, Sacco R, Garbett K, et al. Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression. Mol Psychiatry 2009;14:705-18.
-
(2009)
Mol Psychiatry
, vol.14
, pp. 705-718
-
-
Lintas, C.1
Sacco, R.2
Garbett, K.3
-
17
-
-
38949210771
-
Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis
-
Philippi A, Tores F, Carayol J, et al. Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis. BMC Med Genet 2007;8:74.
-
(2007)
BMC Med Genet
, vol.8
, pp. 74
-
-
Philippi, A.1
Tores, F.2
Carayol, J.3
-
18
-
-
48349101819
-
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism
-
Maussion G, Carayol J, Lepagnol-Bestel AM, et al. Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism. Hum Mol Genet 2008;17:2541-51.
-
(2008)
Hum Mol Genet
, vol.17
, pp. 2541-2551
-
-
Maussion, G.1
Carayol, J.2
Lepagnol-Bestel, A.M.3
-
19
-
-
27144491428
-
Demandez le test de l'autisme! [Autism test on sale!]
-
Jordan B. Demandez le test de l'autisme! [Autism test on sale!]. Med Sci (Paris) 2005;21:886-7.
-
(2005)
Med Sci (Paris)
, vol.21
, pp. 886-887
-
-
Jordan, B.1
-
20
-
-
33847216876
-
L'autisme d'une entreprise [The autism of a company]
-
Jordan B. L'autisme d'une entreprise [The autism of a company]. Med Sci (Paris) 2007;23:215-16.
-
(2007)
Med Sci (Paris)
, vol.23
, pp. 215-216
-
-
Jordan, B.1
-
21
-
-
34249749922
-
Génétique et business: défendons la liberté de critique! [Genetics and business: in defence of free speech!]
-
Jordan B, Favre M, Barthelemy C, et al. Génétique et business: défendons la liberté de critique! [Genetics and business: in defence of free speech!]. Med Sci (Paris) 2007;23:545-6.
-
(2007)
Med Sci (Paris)
, vol.23
, pp. 545-546
-
-
Jordan, B.1
Favre, M.2
Barthelemy, C.3
-
22
-
-
77958097590
-
-
23andMe Democratizes Personal Genetics Accessed 4 June 2010
-
23andMe Democratizes Personal Genetics. https://www.23andme.com/about/press/20080909b/ (Accessed 4 June 2010).
-
-
-
-
23
-
-
50549102055
-
The contractual genome: how direct-to-consumer genomic services may help patients take ownership of their DNA
-
Accessed 4 June 2010
-
Foster MW, Sharp RR. The contractual genome: how direct-to-consumer genomic services may help patients take ownership of their DNA. Person Med 2008;5:399-404. http://www.futuremedicine.com/doi/full/10.2217/17410541.5.4.399 (Accessed 4 June 2010).
-
(2008)
Person Med
, vol.5
, pp. 399-404
-
-
Foster, M.W.1
Sharp, R.R.2
-
24
-
-
67650459886
-
Biomarkers in psychiatry
-
Singh l, Rose N. Biomarkers in psychiatry. Nature 2009;460:202-7.
-
(2009)
Nature
, vol.460
, pp. 202-207
-
-
Singh, l.1
Rose, N.2
-
25
-
-
35348957507
-
ASHG social issues committee ASHG statement on direct-to-consumer genetic testing in the United States
-
Hudson K, Javitt G, Burke W, et al. ASHG social issues committee. ASHG statement on direct-to-consumer genetic testing in the United States. Am J Hum Genet 2007;81:635-7.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 635-637
-
-
Hudson, K.1
Javitt, G.2
Burke, W.3
|