-
1
-
-
77958500315
-
Genomic copy number variation in disorders of cognitive development
-
Morrow EM, (2010) Genomic copy number variation in disorders of cognitive development. J Am Acad Child Adolesc Psychiatry 49: 1091-1104.
-
(2010)
J Am Acad Child Adolesc Psychiatry
, vol.49
, pp. 1091-1104
-
-
Morrow, E.M.1
-
2
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, et al. (2010) Functional impact of global rare copy number variation in autism spectrum disorders. Nature 466: 368-372.
-
(2010)
Nature
, vol.466
, pp. 368-372
-
-
Pinto, D.1
Pagnamenta, A.T.2
Klei, L.3
Anney, R.4
Merico, D.5
-
3
-
-
84861234329
-
Human genetics: Fruits of exome sequencing for autism
-
Muers M, (2012) Human genetics: Fruits of exome sequencing for autism. Nat Rev Genet 13: 377.
-
(2012)
Nat Rev Genet
, vol.13
, pp. 377
-
-
Muers, M.1
-
4
-
-
84862493260
-
Genetic architecture in autism spectrum disorder
-
Devlin B, Scherer SW, (2012) Genetic architecture in autism spectrum disorder. Curr Opin Genet Dev 22: 229-237.
-
(2012)
Curr Opin Genet Dev
, vol.22
, pp. 229-237
-
-
Devlin, B.1
Scherer, S.W.2
-
5
-
-
84877695008
-
Environmental factors in autism
-
Grabrucker AM, (2012) Environmental factors in autism. Front Psychiatry 3: 118.
-
(2012)
Front Psychiatry
, vol.3
, pp. 118
-
-
Grabrucker, A.M.1
-
6
-
-
84859508516
-
Epigenetics in autism and other neurodevelopmental diseases
-
Miyake K, Hirasawa T, Koide T, Kubota T, (2012) Epigenetics in autism and other neurodevelopmental diseases. Adv Exp Med Biol 724: 91-98.
-
(2012)
Adv Exp Med Biol
, vol.724
, pp. 91-98
-
-
Miyake, K.1
Hirasawa, T.2
Koide, T.3
Kubota, T.4
-
7
-
-
84866309634
-
Brain transcriptional and epigenetic associations with autism
-
Ginsberg MR, Rubin RA, Falcone T, Ting AH, Natowicz MR, (2012) Brain transcriptional and epigenetic associations with autism. PLoS One 7: e44736.
-
(2012)
PLoS One
, vol.7
-
-
Ginsberg, M.R.1
Rubin, R.A.2
Falcone, T.3
Ting, A.H.4
Natowicz, M.R.5
-
8
-
-
84863247768
-
Epigenetic signatures of autism: trimethylated H3K4 landscapes in prefrontal neurons
-
Shulha HP, Cheung I, Whittle C, Wang J, Virgil D, et al. (2012) Epigenetic signatures of autism: trimethylated H3K4 landscapes in prefrontal neurons. Arch Gen Psychiatry 69: 314-324.
-
(2012)
Arch Gen Psychiatry
, vol.69
, pp. 314-324
-
-
Shulha, H.P.1
Cheung, I.2
Whittle, C.3
Wang, J.4
Virgil, D.5
-
9
-
-
84897111264
-
Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits
-
Wong CC, Meaburn EL, Ronald A, Price TS, Jeffries AR, et al. (2014) Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits. Mol Psychiatry 19: 495-503.
-
(2014)
Mol Psychiatry
, vol.19
, pp. 495-503
-
-
Wong, C.C.1
Meaburn, E.L.2
Ronald, A.3
Price, T.S.4
Jeffries, A.R.5
-
10
-
-
84905024735
-
Common DNA methylation alterations in multiple brain regions in autism
-
doi: 10.1038/mp.2013.114
-
Ladd-Acosta C, Hansen KD, Briem E, Fallin MD, Kaufmann WE, et al. (2013) Common DNA methylation alterations in multiple brain regions in autism. Mol Psychiatry doi: 10.1038/mp.2013.114.
-
(2013)
Mol Psychiatry
-
-
Ladd-Acosta, C.1
Hansen, K.D.2
Briem, E.3
Fallin, M.D.4
Kaufmann, W.E.5
-
11
-
-
84884669130
-
Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism
-
Ben-David E, Shifman S, (2013) Combined analysis of exome sequencing points toward a major role for transcription regulation during brain development in autism. Mol Psychiatry 18: 1054-1056.
-
(2013)
Mol Psychiatry
, vol.18
, pp. 1054-1056
-
-
Ben-David, E.1
Shifman, S.2
-
12
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, et al. (2012) Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 485: 246-250.
-
(2012)
Nature
, vol.485
, pp. 246-250
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
Karakoc, E.4
Krumm, N.5
-
13
-
-
84865208871
-
Rate of de novo mutations and the importance of father's age to disease risk
-
Kong A, Frigge ML, Masson G, Besenbacher S, Sulem P, et al. (2012) Rate of de novo mutations and the importance of father's age to disease risk. Nature 488: 471-475.
-
(2012)
Nature
, vol.488
, pp. 471-475
-
-
Kong, A.1
Frigge, M.L.2
Masson, G.3
Besenbacher, S.4
Sulem, P.5
-
14
-
-
84860223780
-
Advancing maternal age is associated with increasing risk for autism: a review and meta-analysis
-
Sandin S, Hultman CM, Kolevzon A, Gross R, MacCabe JH, et al. (2012) Advancing maternal age is associated with increasing risk for autism: a review and meta-analysis. J Am Acad Child Adolesc Psychiatry 51: 477-486 e471.
-
(2012)
J Am Acad Child Adolesc Psychiatry
, vol.51
, pp. 477-486
-
-
Sandin, S.1
Hultman, C.M.2
Kolevzon, A.3
Gross, R.4
MacCabe, J.H.5
-
15
-
-
26244463373
-
Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes
-
Pellestor F, Anahory T, Hamamah S, (2005) Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes. Cytogenet Genome Res 111: 206-212.
-
(2005)
Cytogenet Genome Res
, vol.111
, pp. 206-212
-
-
Pellestor, F.1
Anahory, T.2
Hamamah, S.3
-
16
-
-
84862979818
-
Distinct DNA methylomes of newborns and centenarians
-
Heyn H, Li N, Ferreira HJ, Moran S, Pisano DG, et al. (2012) Distinct DNA methylomes of newborns and centenarians. Proc Natl Acad Sci U S A 109: 10522-10527.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, pp. 10522-10527
-
-
Heyn, H.1
Li, N.2
Ferreira, H.J.3
Moran, S.4
Pisano, D.G.5
-
17
-
-
79960556965
-
Epigenome-wide association studies for common human diseases
-
Rakyan VK, Down TA, Balding DJ, Beck S, (2011) Epigenome-wide association studies for common human diseases. Nat Rev Genet 12: 529-541.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 529-541
-
-
Rakyan, V.K.1
Down, T.A.2
Balding, D.J.3
Beck, S.4
-
18
-
-
84860637797
-
DNA methylation arrays as surrogate measures of cell mixture distribution
-
Houseman EA, Accomando WP, Koestler DC, Christensen BC, Marsit CJ, et al. (2012) DNA methylation arrays as surrogate measures of cell mixture distribution. BMC Bioinformatics 13: 86.
-
(2012)
BMC Bioinformatics
, vol.13
, pp. 86
-
-
Houseman, E.A.1
Accomando, W.P.2
Koestler, D.C.3
Christensen, B.C.4
Marsit, C.J.5
-
19
-
-
84863230488
-
IMA: an R package for high-throughput analysis of Illumina's 450K Infinium methylation data
-
Wang D, Yan L, Hu Q, Sucheston LE, Higgins MJ, et al. (2012) IMA: an R package for high-throughput analysis of Illumina's 450K Infinium methylation data. Bioinformatics 28: 729-730.
-
(2012)
Bioinformatics
, vol.28
, pp. 729-730
-
-
Wang, D.1
Yan, L.2
Hu, Q.3
Sucheston, L.E.4
Higgins, M.J.5
-
20
-
-
69449084444
-
The relationship of DNA methylation with age, gender and genotype in twins and healthy controls
-
Boks MP, Derks EM, Weisenberger DJ, Strengman E, Janson E, et al. (2009) The relationship of DNA methylation with age, gender and genotype in twins and healthy controls. PLoS One 4: e6767.
-
(2009)
PLoS One
, vol.4
-
-
Boks, M.P.1
Derks, E.M.2
Weisenberger, D.J.3
Strengman, E.4
Janson, E.5
-
21
-
-
84860572791
-
Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population
-
Bell JT, Tsai PC, Yang TP, Pidsley R, Nisbet J, et al. (2012) Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population. PLoS Genet 8: e1002629.
-
(2012)
PLoS Genet
, vol.8
-
-
Bell, J.T.1
Tsai, P.C.2
Yang, T.P.3
Pidsley, R.4
Nisbet, J.5
-
22
-
-
23944437199
-
Sex differential in methylation patterns of selected genes in Singapore Chinese
-
Sarter B, Long TI, Tsong WH, Koh WP, Yu MC, et al. (2005) Sex differential in methylation patterns of selected genes in Singapore Chinese. Hum Genet 117: 402-403.
-
(2005)
Hum Genet
, vol.117
, pp. 402-403
-
-
Sarter, B.1
Long, T.I.2
Tsong, W.H.3
Koh, W.P.4
Yu, M.C.5
-
23
-
-
79960688508
-
DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines
-
Bell JT, Pai AA, Pickrell JK, Gaffney DJ, Pique-Regi R, et al. (2011) DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines. Genome Biol 12: R10.
-
(2011)
Genome Biol
, vol.12
-
-
Bell, J.T.1
Pai, A.A.2
Pickrell, J.K.3
Gaffney, D.J.4
Pique-Regi, R.5
-
24
-
-
77953223693
-
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
-
Gibbs JR, van der Brug MP, Hernandez DG, Traynor BJ, Nalls MA, et al. (2010) Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain. PLoS Genet 6: e1000952.
-
(2010)
PLoS Genet
, vol.6
-
-
Gibbs, J.R.1
van der Brug, M.P.2
Hernandez, D.G.3
Traynor, B.J.4
Nalls, M.A.5
-
25
-
-
80052306947
-
Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation
-
Gertz J, Varley KE, Reddy TE, Bowling KM, Pauli F, et al. (2011) Analysis of DNA methylation in a three-generation family reveals widespread genetic influence on epigenetic regulation. PLoS Genet 7: e1002228.
-
(2011)
PLoS Genet
, vol.7
-
-
Gertz, J.1
Varley, K.E.2
Reddy, T.E.3
Bowling, K.M.4
Pauli, F.5
-
26
-
-
77949533111
-
An epigenetic signature in peripheral blood predicts active ovarian cancer
-
Teschendorff AE, Menon U, Gentry-Maharaj A, Ramus SJ, Gayther SA, et al. (2009) An epigenetic signature in peripheral blood predicts active ovarian cancer. PLoS One 4: e8274.
-
(2009)
PLoS One
, vol.4
-
-
Teschendorff, A.E.1
Menon, U.2
Gentry-Maharaj, A.3
Ramus, S.J.4
Gayther, S.A.5
-
27
-
-
79955946158
-
A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data
-
Gonzalez JR, Rodriguez-Santiago B, Caceres A, Pique-Regi R, Rothman N, et al. (2011) A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data. BMC Bioinformatics 12: 166.
-
(2011)
BMC Bioinformatics
, vol.12
, pp. 166
-
-
Gonzalez, J.R.1
Rodriguez-Santiago, B.2
Caceres, A.3
Pique-Regi, R.4
Rothman, N.5
-
28
-
-
84863386102
-
Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies
-
Jaffe AE, Murakami P, Lee H, Leek JT, Fallin MD, et al. (2012) Bump hunting to identify differentially methylated regions in epigenetic epidemiology studies. Int J Epidemiol 41: 200-209.
-
(2012)
Int J Epidemiol
, vol.41
, pp. 200-209
-
-
Jaffe, A.E.1
Murakami, P.2
Lee, H.3
Leek, J.T.4
Fallin, M.D.5
-
29
-
-
84874353239
-
Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray
-
Chen YA, Lemire M, Choufani S, Butcher DT, Grafodatskaya D, et al. (2013) Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray. Epigenetics 8: 203-209.
-
(2013)
Epigenetics
, vol.8
, pp. 203-209
-
-
Chen, Y.A.1
Lemire, M.2
Choufani, S.3
Butcher, D.T.4
Grafodatskaya, D.5
-
30
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, et al. (2011) Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 70: 863-885.
-
(2011)
Neuron
, vol.70
, pp. 863-885
-
-
Sanders, S.J.1
Ercan-Sencicek, A.G.2
Hus, V.3
Luo, R.4
Murtha, M.T.5
-
31
-
-
80054993342
-
Spatio-temporal transcriptome of the human brain
-
Kang HJ, Kawasawa YI, Cheng F, Zhu Y, Xu X, et al. (2011) Spatio-temporal transcriptome of the human brain. Nature 478: 483-489.
-
(2011)
Nature
, vol.478
, pp. 483-489
-
-
Kang, H.J.1
Kawasawa, Y.I.2
Cheng, F.3
Zhu, Y.4
Xu, X.5
-
32
-
-
79959262465
-
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
-
Voineagu I, Wang X, Johnston P, Lowe JK, Tian Y, et al. (2011) Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Nature 474: 380-384.
-
(2011)
Nature
, vol.474
, pp. 380-384
-
-
Voineagu, I.1
Wang, X.2
Johnston, P.3
Lowe, J.K.4
Tian, Y.5
-
33
-
-
84869044837
-
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects
-
van Eijk KR, de Jong S, Boks MP, Langeveld T, Colas F, et al. (2012) Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects. BMC Genomics 13: 636.
-
(2012)
BMC Genomics
, vol.13
, pp. 636
-
-
van Eijk, K.R.1
de Jong, S.2
Boks, M.P.3
Langeveld, T.4
Colas, F.5
-
34
-
-
60549111634
-
WGCNA: an R package for weighted correlation network analysis
-
Langfelder P, Horvath S, (2008) WGCNA: an R package for weighted correlation network analysis. BMC Bioinformatics 9: 559.
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 559
-
-
Langfelder, P.1
Horvath, S.2
-
35
-
-
84872586906
-
Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based study
-
Garg S, Lehtonen A, Huson SM, Emsley R, Trump D, et al. (2013) Autism and other psychiatric comorbidity in neurofibromatosis type 1: evidence from a population-based study. Dev Med Child Neurol 55: 139-145.
-
(2013)
Dev Med Child Neurol
, vol.55
, pp. 139-145
-
-
Garg, S.1
Lehtonen, A.2
Huson, S.M.3
Emsley, R.4
Trump, D.5
-
36
-
-
84880544162
-
Gene-set analysis is severely biased when applied to genome-wide methylation data
-
Geeleher P, Hartnett L, Egan LJ, Golden A, Raja Ali RA, et al. (2013) Gene-set analysis is severely biased when applied to genome-wide methylation data. Bioinformatics 29: 1851-1857.
-
(2013)
Bioinformatics
, vol.29
, pp. 1851-1857
-
-
Geeleher, P.1
Hartnett, L.2
Egan, L.J.3
Golden, A.4
Raja Ali, R.A.5
-
38
-
-
77954269901
-
The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function
-
Warde-Farley D, Donaldson SL, Comes O, Zuberi K, Badrawi R, et al. (2010) The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function. Nucleic Acids Res 38: W214-220.
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Warde-Farley, D.1
Donaldson, S.L.2
Comes, O.3
Zuberi, K.4
Badrawi, R.5
-
39
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, et al. (2012) Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature 485: 242-245.
-
(2012)
Nature
, vol.485
, pp. 242-245
-
-
Neale, B.M.1
Kou, Y.2
Liu, L.3
Ma'ayan, A.4
Samocha, K.E.5
-
40
-
-
79959464683
-
DADA: Degree-Aware Algorithms for Network-Based Disease Gene Prioritization
-
Erten S, Bebek G, Ewing RM, Koyuturk M, (2011) DADA: Degree-Aware Algorithms for Network-Based Disease Gene Prioritization. BioData Min 4: 19.
-
(2011)
BioData Min
, vol.4
, pp. 19
-
-
Erten, S.1
Bebek, G.2
Ewing, R.M.3
Koyuturk, M.4
-
41
-
-
84859098571
-
The sva package for removing batch effects and other unwanted variation in high-throughput experiments
-
Leek JT, Johnson WE, Parker HS, Jaffe AE, Storey JD, (2012) The sva package for removing batch effects and other unwanted variation in high-throughput experiments. Bioinformatics 28: 882-883.
-
(2012)
Bioinformatics
, vol.28
, pp. 882-883
-
-
Leek, J.T.1
Johnson, W.E.2
Parker, H.S.3
Jaffe, A.E.4
Storey, J.D.5
-
42
-
-
77956671613
-
A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation
-
Abu-Amero KK, Hellani AM, Salih MA, Seidahmed MZ, Elmalik TS, et al. (2010) A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation. BMC Med Genet 11: 135.
-
(2010)
BMC Med Genet
, vol.11
, pp. 135
-
-
Abu-Amero, K.K.1
Hellani, A.M.2
Salih, M.A.3
Seidahmed, M.Z.4
Elmalik, T.S.5
-
43
-
-
84864422706
-
Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder
-
Chen CP, Lin SP, Su JW, Lee MS, Wang W, (2012) Phenotypic features associated with mosaic tetrasomy 9p in a 20-year-old female patient include autism spectrum disorder. Genet Couns 23: 335-338.
-
(2012)
Genet Couns
, vol.23
, pp. 335-338
-
-
Chen, C.P.1
Lin, S.P.2
Su, J.W.3
Lee, M.S.4
Wang, W.5
-
44
-
-
84870242862
-
Developmental and behavioral characteristics of individuals with Pallister-Killian syndrome
-
Kostanecka A, Close LB, Izumi K, Krantz ID, Pipan M, (2012) Developmental and behavioral characteristics of individuals with Pallister-Killian syndrome. Am J Med Genet A 158A: 3018-3025.
-
(2012)
Am J Med Genet A
, vol.158 A
, pp. 3018-3025
-
-
Kostanecka, A.1
Close, L.B.2
Izumi, K.3
Krantz, I.D.4
Pipan, M.5
-
45
-
-
84879756120
-
Somatic mutation, genomic variation, and neurological disease
-
Poduri A, Evrony GD, Cai X, Walsh CA, (2013) Somatic mutation, genomic variation, and neurological disease. Science 341: 1237758.
-
(2013)
Science
, vol.341
, pp. 1237758
-
-
Poduri, A.1
Evrony, G.D.2
Cai, X.3
Walsh, C.A.4
-
46
-
-
84861628224
-
Detectable clonal mosaicism and its relationship to aging and cancer
-
Jacobs KB, Yeager M, Zhou W, Wacholder S, Wang Z, et al. (2012) Detectable clonal mosaicism and its relationship to aging and cancer. Nat Genet 44: 651-658.
-
(2012)
Nat Genet
, vol.44
, pp. 651-658
-
-
Jacobs, K.B.1
Yeager, M.2
Zhou, W.3
Wacholder, S.4
Wang, Z.5
-
48
-
-
84876903461
-
Olfaction in the autism spectrum
-
Galle SA, Courchesne V, Mottron L, Frasnelli J, (2013) Olfaction in the autism spectrum. Perception 42: 341-355.
-
(2013)
Perception
, vol.42
, pp. 341-355
-
-
Galle, S.A.1
Courchesne, V.2
Mottron, L.3
Frasnelli, J.4
-
49
-
-
63749094761
-
The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues
-
Papavassiliou P, York TP, Gursoy N, Hill G, Nicely LV, et al. (2009) The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues. Am J Med Genet A 149A: 573-583.
-
(2009)
Am J Med Genet A
, vol.149 A
, pp. 573-583
-
-
Papavassiliou, P.1
York, T.P.2
Gursoy, N.3
Hill, G.4
Nicely, L.V.5
-
50
-
-
67651225410
-
Sensitive detection of chromosomal segments of distinct ancestry in admixed populations
-
Price AL, Tandon A, Patterson N, Barnes KC, Rafaels N, et al. (2009) Sensitive detection of chromosomal segments of distinct ancestry in admixed populations. PLoS Genet 5: e1000519.
-
(2009)
PLoS Genet
, vol.5
-
-
Price, A.L.1
Tandon, A.2
Patterson, N.3
Barnes, K.C.4
Rafaels, N.5
-
51
-
-
24044440971
-
BiNGO: a Cytoscape plugin to assess overrepresentation of gene ontology categories in biological networks
-
Maere S, Heymans K, Kuiper M, (2005) BiNGO: a Cytoscape plugin to assess overrepresentation of gene ontology categories in biological networks. Bioinformatics 21: 3448-3449.
-
(2005)
Bioinformatics
, vol.21
, pp. 3448-3449
-
-
Maere, S.1
Heymans, K.2
Kuiper, M.3
-
52
-
-
68949141599
-
BSMAP: whole genome bisulfite sequence MAPping program
-
Xi Y, Li W, (2009) BSMAP: whole genome bisulfite sequence MAPping program. BMC Bioinformatics 10: 232.
-
(2009)
BMC Bioinformatics
, vol.10
, pp. 232
-
-
Xi, Y.1
Li, W.2
-
53
-
-
0033362024
-
A genomic screen of autism: evidence for a multilocus etiology
-
Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, et al. (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
-
54
-
-
79952254931
-
A population genetic approach to mapping neurological disorder genes using deep resequencing
-
Myers RA, Casals F, Gauthier J, Hamdan FF, Keebler J, et al. (2011) A population genetic approach to mapping neurological disorder genes using deep resequencing. PLoS Genet 7: e1001318.
-
(2011)
PLoS Genet
, vol.7
-
-
Myers, R.A.1
Casals, F.2
Gauthier, J.3
Hamdan, F.F.4
Keebler, J.5
-
55
-
-
32844454862
-
A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands
-
Lauritsen MB, Als TD, Dahl HA, Flint TJ, Wang AG, et al. (2006) A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands. Mol Psychiatry 11: 37-46.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 37-46
-
-
Lauritsen, M.B.1
Als, T.D.2
Dahl, H.A.3
Flint, T.J.4
Wang, A.G.5
-
56
-
-
34547731978
-
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways
-
Nishimura Y, Martin CL, Vazquez-Lopez A, Spence SJ, Alvarez-Retuerto AI, et al. (2007) Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways. Hum Mol Genet 16: 1682-1698.
-
(2007)
Hum Mol Genet
, vol.16
, pp. 1682-1698
-
-
Nishimura, Y.1
Martin, C.L.2
Vazquez-Lopez, A.3
Spence, S.J.4
Alvarez-Retuerto, A.I.5
|