-
1
-
-
84859394070
-
Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States
-
CDC
-
Prevalence of autism spectrum disorders-Autism and Developmental Disabilities Monitoring Network, United States. CDC, Morb Mortal Wkly Rep Surveill Summ 2012 61 1 19
-
(2012)
Morb Mortal Wkly Rep Surveill Summ
, vol.61
, pp. 1-19
-
-
-
2
-
-
78649322790
-
Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome
-
10.1016/j.bbi.2010.08.003 20705131
-
Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome. Ashwood P, Krakowiak P, Hertz-Picciotto I, Hansen R, Pessah I, Van de Water J, Brain Behav Immun 2011 25 40 45 10.1016/j.bbi.2010.08.003 20705131
-
(2011)
Brain Behav Immun
, vol.25
, pp. 40-45
-
-
Ashwood, P.1
Krakowiak, P.2
Hertz-Picciotto, I.3
Hansen, R.4
Pessah, I.5
Van De Water, J.6
-
3
-
-
80052864423
-
Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytes
-
10.1016/j.jneuroim.2011.07.001 21803429
-
Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytes. Jyonouchi H, Geng L, Streck DL, Toruner GA, J Neuroimmunol 2011 238 73 80 10.1016/j.jneuroim.2011.07.001 21803429
-
(2011)
J Neuroimmunol
, vol.238
, pp. 73-80
-
-
Jyonouchi, H.1
Geng, L.2
Streck, D.L.3
Toruner, G.A.4
-
4
-
-
84857190395
-
The role of immune dysfunction in the pathophysiology of autism
-
10.1016/j.bbi.2011.08.007 21906670
-
The role of immune dysfunction in the pathophysiology of autism. Onore C, Careaga M, Ashwood P, Brain Behav Immun 2012 26 383 392 10.1016/j.bbi.2011.08. 007 21906670
-
(2012)
Brain Behav Immun
, vol.26
, pp. 383-392
-
-
Onore, C.1
Careaga, M.2
Ashwood, P.3
-
5
-
-
67849088550
-
Identification of new SLE-associated genes with a two-step Bayesian study design
-
10.1038/gene.2009.38 19440200
-
Identification of new SLE-associated genes with a two-step Bayesian study design. Armstrong DL, Reiff A, Myones BL, Quismorio FP, Klein-Gitelman M, McCurdy D, Wagner-Weiner L, Silverman E, Ojwang JO, Kaufman KM, Kelly JA, Merrill JT, Harley JB, Bae SC, Vyse TJ, Gilkeson GS, Gaffney PM, Moser KL, Putterman C, Edberg JC, Brown EE, Ziegler J, Langefeld CD, Zidovetzki R, Jacob CO, Genes Immun 2009 10 446 456 10.1038/gene.2009.38 19440200
-
(2009)
Genes Immun
, vol.10
, pp. 446-456
-
-
Armstrong, D.L.1
Reiff, A.2
Myones, B.L.3
Quismorio, F.P.4
Klein-Gitelman, M.5
McCurdy, D.6
Wagner-Weiner, L.7
Silverman, E.8
Ojwang, J.O.9
Kaufman, K.M.10
Kelly, J.A.11
Merrill, J.T.12
Harley, J.B.13
Bae, S.C.14
Vyse, T.J.15
Gilkeson, G.S.16
Gaffney, P.M.17
Moser, K.L.18
Putterman, C.19
Edberg, J.C.20
Brown, E.E.21
Ziegler, J.22
Langefeld, C.D.23
Zidovetzki, R.24
Jacob, C.O.25
more..
-
6
-
-
58149333713
-
Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes
-
10.2337/db07-1731 18678618
-
Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes. Gaulton KJ, Willer CJ, Li Y, Scott LJ, Conneely KN, Jackson AU, Duren WL, Chines PS, Narisu N, Bonnycastle LL, Luo J, Tong M, Sprau AG, Pugh EW, Doheny KF, Valle TT, Abecasis GR, Tuomilehto J, Bergman RN, Collins FS, Boehnke M, Mohlke KL, Diabetes 2008 57 3136 3144 10.2337/db07-1731 18678618
-
(2008)
Diabetes
, vol.57
, pp. 3136-3144
-
-
Gaulton, K.J.1
Willer, C.J.2
Li, Y.3
Scott, L.J.4
Conneely, K.N.5
Jackson, A.U.6
Duren, W.L.7
Chines, P.S.8
Narisu, N.9
Bonnycastle, L.L.10
Luo, J.11
Tong, M.12
Sprau, A.G.13
Pugh, E.W.14
Doheny, K.F.15
Valle, T.T.16
Abecasis, G.R.17
Tuomilehto, J.18
Bergman, R.N.19
Collins, F.S.20
Boehnke, M.21
Mohlke, K.L.22
more..
-
8
-
-
84877093663
-
-
http://discover.nci.nih.gov/matchminer/index.jsp
-
MatchMiner. http://discover.nci.nih.gov/matchminer/index.jsp
-
MatchMiner
-
-
-
10
-
-
65449184161
-
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1
-
10.1111/j.1469-1809.2009.00523.x 19456320
-
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, Martin ER, Hussman JP, Gilbert JR, Cuccaro ML, Haines JL, Pericak-Vance MA, Ann Hum Genet 2009 73 263 273 10.1111/j.1469-1809.2009.00523.x 19456320
-
(2009)
Ann Hum Genet
, vol.73
, pp. 263-273
-
-
Ma, D.1
Salyakina, D.2
Jaworski, J.M.3
Konidari, I.4
Whitehead, P.L.5
Andersen, A.N.6
Hoffman, J.D.7
Slifer, S.H.8
Hedges, D.J.9
Cukier, H.N.10
Griswold, A.J.11
McCauley, J.L.12
Beecham, G.W.13
Wright, H.H.14
Abramson, R.K.15
Martin, E.R.16
Hussman, J.P.17
Gilbert, J.R.18
Cuccaro, M.L.19
Haines, J.L.20
Pericak-Vance, M.A.21
more..
-
11
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
10.1038/nature07999 19404256
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders. Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, Salyakina D, Imielinski M, Bradfield JP, Sleiman PM, Kim CE, Hou C, Frackelton E, Chiavacci R, Takahashi N, Sakurai T, Rappaport E, Lajonchere CM, Munson J, Estes A, Korvatska O, Piven J, Sonnenblick LI, Alvarez Retuerto AI, Herman EI, Dong H, Hutman T, Sigman M, Ozonoff S, Klin A, et al. Nature 2009 459 528 533 10.1038/nature07999 19404256
-
(2009)
Nature
, vol.459
, pp. 528-533
-
-
Wang, K.1
Zhang, H.2
Ma, D.3
Bucan, M.4
Glessner, J.T.5
Abrahams, B.S.6
Salyakina, D.7
Imielinski, M.8
Bradfield, J.P.9
Sleiman, P.M.10
Kim, C.E.11
Hou, C.12
Frackelton, E.13
Chiavacci, R.14
Takahashi, N.15
Sakurai, T.16
Rappaport, E.17
Lajonchere, C.M.18
Munson, J.19
Estes, A.20
Korvatska, O.21
Piven, J.22
Sonnenblick, L.I.23
Alvarez Retuerto, A.I.24
Herman, E.I.25
Dong, H.26
Hutman, T.27
Sigman, M.28
Ozonoff, S.29
Klin, A.30
more..
-
12
-
-
70349956425
-
A genome-wide linkage and association scan reveals novel loci for autism
-
10.1038/nature08490 19812673
-
A genome-wide linkage and association scan reveals novel loci for autism. Weiss LA, Arking DE, Daly MJ, Chakravarti A, Nature 2009 461 802 808 10.1038/nature08490 19812673
-
(2009)
Nature
, vol.461
, pp. 802-808
-
-
Weiss, L.A.1
Arking, D.E.2
Daly, M.J.3
Chakravarti, A.4
-
13
-
-
79959262465
-
Transcriptomic analysis of autistic brain reveals convergent molecular pathology
-
10.1038/nature10110 21614001
-
Transcriptomic analysis of autistic brain reveals convergent molecular pathology. Voineagu I, Wang X, Johnston P, Lowe JK, Tian Y, Horvath S, Mill J, Cantor RM, Blencowe BJ, Geschwind DH, Nature 2011 474 380 384 10.1038/nature10110 21614001
-
(2011)
Nature
, vol.474
, pp. 380-384
-
-
Voineagu, I.1
Wang, X.2
Johnston, P.3
Lowe, J.K.4
Tian, Y.5
Horvath, S.6
Mill, J.7
Cantor, R.M.8
Blencowe, B.J.9
Geschwind, D.H.10
-
14
-
-
34548292504
-
PLINK: A tool set for whole-genome association and population-based linkage analyses
-
10.1086/519795 17701901
-
PLINK: a tool set for whole-genome association and population-based linkage analyses. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC, Am J Hum Genet 2007 81 559 575 10.1086/519795 17701901
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
15
-
-
0033910787
-
A test for linkage and association in general pedigrees: The pedigree disequilibrium test
-
10.1086/302957 10825280
-
A test for linkage and association in general pedigrees: the pedigree disequilibrium test. Martin ER, Monks SA, Warren LL, Kaplan NL, Am J Hum Genet 2000 67 146 154 10.1086/302957 10825280
-
(2000)
Am J Hum Genet
, vol.67
, pp. 146-154
-
-
Martin, E.R.1
Monks, S.A.2
Warren, L.L.3
Kaplan, N.L.4
-
16
-
-
84877097132
-
-
INRICH
-
INRICH. http://atgu.mgh.harvard.edu/inrich/
-
-
-
-
17
-
-
0001677717
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Controlling the false discovery rate: a practical and powerful approach to multiple testing. Benjamini Y, Hochberg Y, J R Stat Soc B 1995 57 289 300
-
(1995)
J R Stat Soc B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
18
-
-
62649155943
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals
-
10.1016/j.ajhg.2009.01.005 19200528
-
A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. Browning BL, Browning SR, Am J Hum Genet 2009 84 210 223 10.1016/j.ajhg.2009.01.005 19200528
-
(2009)
Am J Hum Genet
, vol.84
, pp. 210-223
-
-
Browning, B.L.1
Browning, S.R.2
-
19
-
-
33846383832
-
Positive association of schizophrenia to JARID2 gene
-
10.1002/ajmg.b.30386 16967465
-
Positive association of schizophrenia to JARID2 gene. Pedrosa E, Ye K, Nolan KA, Morrell L, Okun JM, Persky AD, Saito T, Lachman HM, Am J Med Genet B Neuropsychiatr Genet 2007 144B 45 51 10.1002/ajmg.b.30386 16967465
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144
, pp. 45-51
-
-
Pedrosa, E.1
Ye, K.2
Nolan, K.A.3
Morrell, L.4
Okun, J.M.5
Persky, A.D.6
Saito, T.7
Lachman, H.M.8
-
20
-
-
71149090779
-
Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia
-
19884986
-
Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia. Liu Y, Chen G, Norton N, Liu W, Zhu H, Zhou P, Luan M, Yang S, Chen X, Carroll L, Williams NM, O'Donovan MC, Kirov G, Owen MJ, J Biomed Biotechnol 2009 2009 536918 19884986
-
(2009)
J Biomed Biotechnol
, vol.2009
, pp. 536918
-
-
Liu, Y.1
Chen, G.2
Norton, N.3
Liu, W.4
Zhu, H.5
Zhou, P.6
Luan, M.7
Yang, S.8
Chen, X.9
Carroll, L.10
Williams, N.M.11
O'Donovan, M.C.12
Kirov, G.13
Owen, M.J.14
-
21
-
-
43249102851
-
Erasing the methyl mark: Histone demethylases at the center of cellular differentiation and disease
-
10.1101/gad.1652908 18451103
-
Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease. Cloos PA, Christensen J, Agger K, Helin K, Genes Dev 2008 22 1115 1140 10.1101/gad.1652908 18451103
-
(2008)
Genes Dev
, vol.22
, pp. 1115-1140
-
-
Cloos, P.A.1
Christensen, J.2
Agger, K.3
Helin, K.4
-
22
-
-
34249079113
-
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis
-
10.1530/EJE-07-0037 17468186
-
High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis. Avbelj M, Tahirovic H, Debeljak M, Kusekova M, Toromanovic A, Krzisnik C, Battelino T, Eur J Endocrinol 2007 156 511 519 10.1530/EJE-07-0037 17468186
-
(2007)
Eur J Endocrinol
, vol.156
, pp. 511-519
-
-
Avbelj, M.1
Tahirovic, H.2
Debeljak, M.3
Kusekova, M.4
Toromanovic, A.5
Krzisnik, C.6
Battelino, T.7
|