-
1
-
-
73149102059
-
Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006
-
Autism and Developmental Disabilities Monitoring Network
-
Autism and Developmental Disabilities Monitoring Network: Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006. MMWR Surveill Summ 2009, 58:1-20.
-
(2009)
MMWR Surveill Summ
, vol.58
, pp. 1-20
-
-
-
2
-
-
1042303581
-
Autism and pervasive developmental disorders
-
14959806
-
Volkmar FR, Lord C, Bailey A, Schultz RT, Klin A: Autism and pervasive developmental disorders. J Child Psychol Psychiatry 2004, 45:135-170.
-
(2004)
J Child Psychol Psychiatry
, vol.45
, pp. 135-170
-
-
Volkmar, F.R.1
Lord, C.2
Bailey, A.3
Schultz, R.T.4
Klin, A.5
-
3
-
-
84867829870
-
Individual common variants exert weak effects on the risk for autism spectrum disorders
-
3471395 1:CAS:528:DC%2BC38XhsFCgsLnP 22843504
-
Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, Corsello C, Crawford EL, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Gilbert J, Gillberg C, Glessner JT, Green A, et al.: Individual common variants exert weak effects on the risk for autism spectrum disorders. Hum Mol Genet 2012, 21:4781-4792.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 4781-4792
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Almeida, J.4
Bacchelli, E.5
Baird, G.6
Bolshakova, N.7
Bölte, S.8
Bolton, P.F.9
Bourgeron, T.10
Brennan, S.11
Brian, J.12
Casey, J.13
Conroy, J.14
Correia, C.15
Corsello, C.16
Crawford, E.L.17
De Jonge, M.18
Delorme, R.19
Duketis, E.20
Duque, F.21
Estes, A.22
Farrar, P.23
Fernandez, B.A.24
Folstein, S.E.25
Fombonne, E.26
Gilbert, J.27
Gillberg, C.28
Glessner, J.T.29
Green, A.30
more..
-
4
-
-
67349112868
-
Common genetic variants on 5p14.1 associate with autism spectrum disorders
-
2943511 1:CAS:528:DC%2BD1MXlt1Sku7g%3D 19404256
-
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.: Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature 2009, 459:528-533.
-
(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..
-
5
-
-
70349956425
-
A genome-wide linkage and association scan reveals novel loci for autism
-
2772655 1:CAS:528:DC%2BD1MXht1CisLvI 19812673
-
Weiss LA, Arking DE, Daly MJ, Chakravarti A: A genome-wide linkage and association scan reveals novel loci for autism. Nature 2009, 461:802-808.
-
(2009)
Nature
, vol.461
, pp. 802-808
-
-
Weiss, L.A.1
Arking, D.E.2
Daly, M.J.3
Chakravarti, A.4
-
6
-
-
77957735529
-
A genome-wide scan for common alleles affecting risk for autism
-
2947401 1:CAS:528:DC%2BC3cXht1eqtL3F 20663923
-
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Carson AR, Casallo G, Casey J, Chu SH, Cochrane L, Corsello C, Crawford EL, Crossett A, et al.: A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet 2010, 19:4072-4082.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 4072-4082
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Regan, R.4
Conroy, J.5
Magalhaes, T.R.6
Correia, C.7
Abrahams, B.S.8
Sykes, N.9
Pagnamenta, A.T.10
Almeida, J.11
Bacchelli, E.12
Bailey, A.J.13
Baird, G.14
Battaglia, A.15
Berney, T.16
Bolshakova, N.17
Bölte, S.18
Bolton, P.F.19
Bourgeron, T.20
Brennan, S.21
Brian, J.22
Carson, A.R.23
Casallo, G.24
Casey, J.25
Chu, S.H.26
Cochrane, L.27
Corsello, C.28
Crawford, E.L.29
Crossett, A.30
more..
-
7
-
-
84862493260
-
Genetic architecture in autism spectrum disorder
-
1:CAS:528:DC%2BC38XltVaktbY%3D 22463983
-
Devlin B, Scherer SW: Genetic architecture in autism spectrum disorder. Curr Opin Genet Dev 2012, 22:229-237.
-
(2012)
Curr Opin Genet Dev
, vol.22
, pp. 229-237
-
-
Devlin, B.1
Scherer, S.W.2
-
8
-
-
84872696957
-
Using whole-exome sequencing to identify inherited causes of autism
-
3694430 1:CAS:528:DC%2BC3sXhs1egtb0%3D 23352163
-
Yu TW, Chahrour MH, Coulter ME, Jiralerspong S, Okamura-Ikeda K, Ataman B, Schmitz-Abe K, Harmin DA, Adli M, Malik AN, D'Gama AM, Lim ET, Sanders SJ, Mochida GH, Partlow JN, Sunu CM, Felie JM, Rodriguez J, Nasir RH, Ware J, Joseph RM, Hill RS, Kwan BY, Al-Saffar M, Mukaddes NM, Hashmi A, Balkhy S, Gascon GG, Hisama FM, LeClair E, et al.: Using whole-exome sequencing to identify inherited causes of autism. Neuron 2013, 77:259-273.
-
(2013)
Neuron
, vol.77
, pp. 259-273
-
-
Yu, T.W.1
Chahrour, M.H.2
Coulter, M.E.3
Jiralerspong, S.4
Okamura-Ikeda, K.5
Ataman, B.6
Schmitz-Abe, K.7
Harmin, D.A.8
Adli, M.9
Malik, A.N.10
D'Gama, A.M.11
Lim, E.T.12
Sanders, S.J.13
Mochida, G.H.14
Partlow, J.N.15
Sunu, C.M.16
Felie, J.M.17
Rodriguez, J.18
Nasir, R.H.19
Ware, J.20
Joseph, R.M.21
Hill, R.S.22
Kwan, B.Y.23
Al-Saffar, M.24
Mukaddes, N.M.25
Hashmi, A.26
Balkhy, S.27
Gascon, G.G.28
Hisama, F.M.29
LeClair, E.30
more..
-
9
-
-
84872722295
-
Rare complete knockouts in humans: Population distribution and significant role in autism spectrum disorders
-
3613849 1:CAS:528:DC%2BC3sXhs1Chtb4%3D 23352160
-
Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, Muzny D, Reid JG, Hawes A, Newsham I, Wu Y, Lewis L, Dinh H, Gross S, Wang LS, Lin CF, Valladares O, Gabriel SB, de Pristo M, Altshuler DM, Purcell SM, et al.: Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron 2013, 77:235-242.
-
(2013)
Neuron
, vol.77
, pp. 235-242
-
-
Lim, E.T.1
Raychaudhuri, S.2
Sanders, S.J.3
Stevens, C.4
Sabo, A.5
MacArthur, D.G.6
Neale, B.M.7
Kirby, A.8
Ruderfer, D.M.9
Fromer, M.10
Lek, M.11
Liu, L.12
Flannick, J.13
Ripke, S.14
Nagaswamy, U.15
Muzny, D.16
Reid, J.G.17
Hawes, A.18
Newsham, I.19
Wu, Y.20
Lewis, L.21
Dinh, H.22
Gross, S.23
Wang, L.S.24
Lin, C.F.25
Valladares, O.26
Gabriel, S.B.27
De Pristo, M.28
Altshuler, D.M.29
Purcell, S.M.30
more..
-
10
-
-
47249088331
-
Identifying autism loci and genes by tracing recent shared ancestry
-
2586171 1:CAS:528:DC%2BD1cXot1entbc%3D 18621663
-
Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA: Identifying autism loci and genes by tracing recent shared ancestry. Science 2008, 321:218-223.
-
(2008)
Science
, vol.321
, pp. 218-223
-
-
Morrow, E.M.1
Yoo, S.Y.2
Flavell, S.W.3
Kim, T.K.4
Lin, Y.5
Hill, R.S.6
Mukaddes, N.M.7
Balkhy, S.8
Gascon, G.9
Hashmi, A.10
Al-Saad, S.11
Ware, J.12
Joseph, R.M.13
Greenblatt, R.14
Gleason, D.15
Ertelt, J.A.16
Apse, K.A.17
Bodell, A.18
Partlow, J.N.19
Barry, B.20
Yao, H.21
Markianos, K.22
Ferland, R.J.23
Greenberg, M.E.24
Walsh, C.A.25
more..
-
11
-
-
84860564877
-
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism
-
ARRA Autism Sequencing Collaboration 3325173 1:CAS:528:DC%2BC38XmtFGiur8%3D 22511880
-
Chahrour MH, Yu TW, Lim ET, Ataman B, Coulter ME, Hill RS, Stevens CR, Schubert CR, Greenberg ME, Gabriel SB, Walsh CA, ARRA Autism Sequencing Collaboration: Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. PLoS Genet 2012, 8:e1002635.
-
(2012)
PLoS Genet
, vol.8
, pp. e1002635
-
-
Chahrour, M.H.1
Yu, T.W.2
Lim, E.T.3
Ataman, B.4
Coulter, M.E.5
Hill, R.S.6
Stevens, C.R.7
Schubert, C.R.8
Greenberg, M.E.9
Gabriel, S.B.10
Walsh, C.A.11
-
12
-
-
84860879137
-
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
-
3303079 21996756
-
Casey JP, Magalhaes T, Conroy JM, Regan R, Shah N, Anney R, Shields DC, Abrahams BS, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bolton PF, Bourgeron T, Brennan S, Cali P, Correia C, Corsello C, Coutanche M, Dawson G, de Jonge M, Delorme R, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, et al.: A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Hum Genet 2012, 131:565-579.
-
(2012)
Hum Genet
, vol.131
, pp. 565-579
-
-
Casey, J.P.1
Magalhaes, T.2
Conroy, J.M.3
Regan, R.4
Shah, N.5
Anney, R.6
Shields, D.C.7
Abrahams, B.S.8
Almeida, J.9
Bacchelli, E.10
Bailey, A.J.11
Baird, G.12
Battaglia, A.13
Berney, T.14
Bolshakova, N.15
Bolton, P.F.16
Bourgeron, T.17
Brennan, S.18
Cali, P.19
Correia, C.20
Corsello, C.21
Coutanche, M.22
Dawson, G.23
De Jonge, M.24
Delorme, R.25
Duketis, E.26
Duque, F.27
Estes, A.28
Farrar, P.29
Fernandez, B.A.30
more..
-
13
-
-
84899918742
-
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
-
4067558 1:CAS:528:DC%2BC2cXntVCjsr0%3D 24768552
-
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JAS, Thompson A, Regan R, Pilorge M, Pellecchia G, Pagnamenta AT, Oliveira B, Marshall CR, Magalhaes TR, Lowe JK, Howe JL, Griswold AJ, Gilbert J, Duketis E, Dombroski BA, De Jonge MV, Cuccaro M, Crawford EL, Correia CT, Conroy J, et al.: Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. Am J Hum Genet 2014, 94:677-694.
-
(2014)
Am J Hum Genet
, vol.94
, pp. 677-694
-
-
Pinto, D.1
Delaby, E.2
Merico, D.3
Barbosa, M.4
Merikangas, A.5
Klei, L.6
Thiruvahindrapuram, B.7
Xu, X.8
Ziman, R.9
Wang, Z.10
Vorstman, J.A.S.11
Thompson, A.12
Regan, R.13
Pilorge, M.14
Pellecchia, G.15
Pagnamenta, A.T.16
Oliveira, B.17
Marshall, C.R.18
Magalhaes, T.R.19
Lowe, J.K.20
Howe, J.L.21
Griswold, A.J.22
Gilbert, J.23
Duketis, E.24
Dombroski, B.A.25
De Jonge, M.V.26
Cuccaro, M.27
Crawford, E.L.28
Correia, C.T.29
Conroy, J.30
more..
-
14
-
-
67651233780
-
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
-
2695001 19557195
-
Bucan M, Abrahams BS, Wang K, Glessner JT, Herman EI, Sonnenblick LI, Alvarez Retuerto AI, Imielinski M, Hadley D, Bradfield JP, Kim C, Gidaya NB, Lindquist I, Hutman T, Sigman M, Kustanovich V, Lajonchere CM, Singleton A, Kim J, Wassink TH, McMahon WM, Owley T, Sweeney JA, Coon H, Nurnberger JI, Li M, Cantor RM, Minshew NJ, Sutcliffe JS, Cook EH, et al.: Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet 2009, 5:e1000536.
-
(2009)
PLoS Genet
, vol.5
, pp. e1000536
-
-
Bucan, M.1
Abrahams, B.S.2
Wang, K.3
Glessner, J.T.4
Herman, E.I.5
Sonnenblick, L.I.6
Alvarez Retuerto, A.I.7
Imielinski, M.8
Hadley, D.9
Bradfield, J.P.10
Kim, C.11
Gidaya, N.B.12
Lindquist, I.13
Hutman, T.14
Sigman, M.15
Kustanovich, V.16
Lajonchere, C.M.17
Singleton, A.18
Kim, J.19
Wassink, T.H.20
McMahon, W.M.21
Owley, T.22
Sweeney, J.A.23
Coon, H.24
Nurnberger, J.I.25
Li, M.26
Cantor, R.M.27
Minshew, N.J.28
Sutcliffe, J.S.29
Cook, E.H.30
more..
-
15
-
-
67649400549
-
The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders
-
1:CAS:528:DC%2BD1MXotFCisLs%3D 19541375
-
Betancur C, Sakurai T, Buxbaum JD: The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders. Trends Neurosci 2009, 32:402-412.
-
(2009)
Trends Neurosci
, vol.32
, pp. 402-412
-
-
Betancur, C.1
Sakurai, T.2
Buxbaum, J.D.3
-
16
-
-
78650866712
-
Cell adhesion molecules and their involvement in autism spectrum disorder
-
1:CAS:528:DC%2BC3MXisVajt7Y%3D 21212702
-
Ye H, Liu J, Wu JY: Cell adhesion molecules and their involvement in autism spectrum disorder. Neurosignals 2010, 18:62-71.
-
(2010)
Neurosignals
, vol.18
, pp. 62-71
-
-
Ye, H.1
Liu, J.2
Wu, J.Y.3
-
17
-
-
79958074870
-
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism
-
3939065 1:CAS:528:DC%2BC3MXnsVyrt7Y%3D 21658581
-
Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, Davis L, Wright NR, Dhodapkar RM, DiCola M, DiLullo NM, Fernandez TV, Fielding-Singh V, Fishman DO, Frahm S, Garagaloyan R, Goh GS, Kammela S, Klei L, Lowe JK, Lund SC, et al.: Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011, 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
Moreno-De-Luca, D.6
Chu, S.H.7
Moreau, M.P.8
Gupta, A.R.9
Thomson, S.A.10
Mason, C.E.11
Bilguvar, K.12
Celestino-Soper, P.B.13
Choi, M.14
Crawford, E.L.15
Davis, L.16
Wright, N.R.17
Dhodapkar, R.M.18
DiCola, M.19
DiLullo, N.M.20
Fernandez, T.V.21
Fielding-Singh, V.22
Fishman, D.O.23
Frahm, S.24
Garagaloyan, R.25
Goh, G.S.26
Kammela, S.27
Klei, L.28
Lowe, J.K.29
Lund, S.C.30
more..
-
18
-
-
79958032110
-
Rare de novo and transmitted copy-number variation in autistic spectrum disorders
-
1:CAS:528:DC%2BC3MXnsVyrt7c%3D 21658582
-
Levy D, Ronemus M, Yamrom B, Lee YH, Leotta A, Kendall J, Marks S, Lakshmi B, Pai D, Ye K, Buja A, Krieger A, Yoon S, Troge J, Rodgers L, Iossifov I, Wigler M: Rare de novo and transmitted copy-number variation in autistic spectrum disorders. Neuron 2011, 70:886-897.
-
(2011)
Neuron
, vol.70
, pp. 886-897
-
-
Levy, D.1
Ronemus, M.2
Yamrom, B.3
Lee, Y.H.4
Leotta, A.5
Kendall, J.6
Marks, S.7
Lakshmi, B.8
Pai, D.9
Ye, K.10
Buja, A.11
Krieger, A.12
Yoon, S.13
Troge, J.14
Rodgers, L.15
Iossifov, I.16
Wigler, M.17
-
19
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
3350576 22495309
-
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, Reilly B, Akey JM, Borenstein E, Rieder MJ, Nickerson DA, Bernier R, Shendure J, Eichler EE: Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature 2012, 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
Coe, B.P.6
Levy, R.7
Ko, A.8
Lee, C.9
Smith, J.D.10
Turner, E.H.11
Stanaway, I.B.12
Vernot, B.13
Malig, M.14
Baker, C.15
Reilly, B.16
Akey, J.M.17
Borenstein, E.18
Rieder, M.J.19
Nickerson, D.A.20
Bernier, R.21
Shendure, J.22
Eichler, E.E.23
more..
-
20
-
-
84883171661
-
A discovery resource of rare copy number variations in individuals with autism spectrum disorder
-
1:CAS:528:DC%2BC3sXksVyhsw%3D%3D
-
Prasad A, Merico D, Thiruvahindrapuram B, Wei J, Lionel AC, Sato D, Rickaby J, Lu C, Szatmari P, Roberts W, Fernandez BA, Marshall CR, Hatchwell E, Eis PS, Scherer SW: A discovery resource of rare copy number variations in individuals with autism spectrum disorder. G3 (Bethesda) 2012, 2:1665-1685.
-
(2012)
G3 (Bethesda)
, vol.2
, pp. 1665-1685
-
-
Prasad, A.1
Merico, D.2
Thiruvahindrapuram, B.3
Wei, J.4
Lionel, A.C.5
Sato, D.6
Rickaby, J.7
Lu, C.8
Szatmari, P.9
Roberts, W.10
Fernandez, B.A.11
Marshall, C.R.12
Hatchwell, E.13
Eis, P.S.14
Scherer, S.W.15
-
21
-
-
84867172514
-
Phenotypic heterogeneity of genomic disorders and rare copy-number variants
-
3494411 1:CAS:528:DC%2BC38XhsFWksLrK 22970919
-
Girirajan S, Rosenfeld JA, Coe BP, Parikh S, Friedman N, Goldstein A, Filipink RA, McConnell JS, Angle B, Meschino WS, Nezarati MM, Asamoah A, Jackson KE, Gowans GC, Martin JA, Carmany EP, Stockton DW, Schnur RE, Penney LS, Martin DM, Raskin S, Leppig K, Thiese H, Smith R, Aberg E, Niyazov DM, Escobar LF, El-Khechen D, Johnson KD, Lebel RR, et al.: Phenotypic heterogeneity of genomic disorders and rare copy-number variants. N Engl J Med 2012, 367:1321-1331.
-
(2012)
N Engl J Med
, vol.367
, pp. 1321-1331
-
-
Girirajan, S.1
Rosenfeld, J.A.2
Coe, B.P.3
Parikh, S.4
Friedman, N.5
Goldstein, A.6
Filipink, R.A.7
McConnell, J.S.8
Angle, B.9
Meschino, W.S.10
Nezarati, M.M.11
Asamoah, A.12
Jackson, K.E.13
Gowans, G.C.14
Martin, J.A.15
Carmany, E.P.16
Stockton, D.W.17
Schnur, R.E.18
Penney, L.S.19
Martin, D.M.20
Raskin, S.21
Leppig, K.22
Thiese, H.23
Smith, R.24
Aberg, E.25
Niyazov, D.M.26
Escobar, L.F.27
El-Khechen, D.28
Johnson, K.D.29
Lebel, R.R.30
more..
-
22
-
-
0035710746
-
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method
-
1:CAS:528:DC%2BD38XhtFelt7s%3D 11846609
-
Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 2001, 25:402-408.
-
(2001)
Methods
, vol.25
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
23
-
-
77954657070
-
Functional impact of global rare copy number variation in autism spectrum disorders
-
3021798 1:CAS:528:DC%2BC3cXntF2msbk%3D 20531469
-
Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, et al.: Functional impact of global rare copy number variation in autism spectrum disorders. Nature 2010, 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
Regan, R.6
Conroy, J.7
Magalhaes, T.R.8
Correia, C.9
Abrahams, B.S.10
Almeida, J.11
Bacchelli, E.12
Bader, G.D.13
Bailey, A.J.14
Baird, G.15
Battaglia, A.16
Berney, T.17
Bolshakova, N.18
Bölte, S.19
Bolton, P.F.20
Bourgeron, T.21
Brennan, S.22
Brian, J.23
Bryson, S.E.24
Carson, A.R.25
Casallo, G.26
Casey, J.27
Chung, B.H.28
Cochrane, L.29
Corsello, C.30
more..
-
24
-
-
77950497675
-
Gene, environment association studies consortium. A genome-wide association study of alcohol dependence
-
2841942 1:CAS:528:DC%2BC3cXjvFaqtbY%3D 20202923
-
Bierut LJ, Agrawal A, Bucholz KK, Doheny KF, Laurie C, Pugh E, Fisher S, Fox L, Howells W, Bertelsen S, Hinrichs AL, Almasy L, Breslau N, Culverhouse RC, Dick DM, Edenberg HJ, Foroud T, Grucza RA, Hatsukami D, Hesselbrock V, Johnson EO, Kramer J, Krueger RF, Kuperman S, Lynskey M, Mann K, Neuman RJ, Nöthen MM, Nurnberger JI Jr, Porjesz B, et al.: Gene, environment association studies consortium. A genome-wide association study of alcohol dependence. Proc Natl Acad Sci U S A 2010, 107:5082-5087.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 5082-5087
-
-
Bierut, L.J.1
Agrawal, A.2
Bucholz, K.K.3
Doheny, K.F.4
Laurie, C.5
Pugh, E.6
Fisher, S.7
Fox, L.8
Howells, W.9
Bertelsen, S.10
Hinrichs, A.L.11
Almasy, L.12
Breslau, N.13
Culverhouse, R.C.14
Dick, D.M.15
Edenberg, H.J.16
Foroud, T.17
Grucza, R.A.18
Hatsukami, D.19
Hesselbrock, V.20
Johnson, E.O.21
Kramer, J.22
Krueger, R.F.23
Kuperman, S.24
Lynskey, M.25
Mann, K.26
Neuman, R.J.27
Nöthen, M.M.28
Nurnberger, J.I.29
Porjesz, B.30
more..
-
25
-
-
33344470090
-
PopGen: Population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships
-
16490960
-
Krawczak M, Nikolaus S, von Eberstein H, Croucher PJ, El Mokhtari NE, Schreiber S: PopGen: population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships. Community Genet 2006, 9:55-61.
-
(2006)
Community Genet
, vol.9
, pp. 55-61
-
-
Krawczak, M.1
Nikolaus, S.2
Von Eberstein, H.3
Croucher, P.J.4
El Mokhtari, N.E.5
Schreiber, S.6
-
26
-
-
64049119620
-
Kinesin family member 6 variant Trp719Arg does not associate with angiographically defined coronary artery disease in the Ottawa Heart Genomics Study
-
1:CAS:528:DC%2BD1MXkslGqtb0%3D 19371834
-
Stewart AF, Dandona S, Chen L, Assogba O, Belanger M, Ewart G, LaRose R, Doelle H, Williams K, Wells GA, McPherson R, Roberts R: Kinesin family member 6 variant Trp719Arg does not associate with angiographically defined coronary artery disease in the Ottawa Heart Genomics Study. J Am Coll Cardiol 2009, 53:1471-1472.
-
(2009)
J Am Coll Cardiol
, vol.53
, pp. 1471-1472
-
-
Stewart, A.F.1
Dandona, S.2
Chen, L.3
Assogba, O.4
Belanger, M.5
Ewart, G.6
LaRose, R.7
Doelle, H.8
Williams, K.9
Wells, G.A.10
McPherson, R.11
Roberts, R.12
-
27
-
-
69749121852
-
High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications
-
2752118 1:CAS:528:DC%2BD1MXhtFCjsLjM 19592680
-
Shaikh TH, Gai X, Perin JC, Glessner JT, Xie H, Murphy K, O'Hara R, Casalunovo T, Conlin LK, D'Arcy M, Frackelton EC, Geiger EA, Haldeman-Englert C, Imielinski M, Kim CE, Medne L, Annaiah K, Bradfield JP, Dabaghyan E, Eckert A, Onyiah CC, Ostapenko S, Otieno FG, Santa E, Shaner JL, Skraban R, Smith RM, Elia J, Goldmuntz E, Spinner NB, et al.: High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications. Genome Res 2009, 19:1682-1690.
-
(2009)
Genome Res
, vol.19
, pp. 1682-1690
-
-
Shaikh, T.H.1
Gai, X.2
Perin, J.C.3
Glessner, J.T.4
Xie, H.5
Murphy, K.6
O'Hara, R.7
Casalunovo, T.8
Conlin, L.K.9
D'Arcy, M.10
Frackelton, E.C.11
Geiger, E.A.12
Haldeman-Englert, C.13
Imielinski, M.14
Kim, C.E.15
Medne, L.16
Annaiah, K.17
Bradfield, J.P.18
Dabaghyan, E.19
Eckert, A.20
Onyiah, C.C.21
Ostapenko, S.22
Otieno, F.G.23
Santa, E.24
Shaner, J.L.25
Skraban, R.26
Smith, R.M.27
Elia, J.28
Goldmuntz, E.29
Spinner, N.B.30
more..
-
28
-
-
79955780907
-
Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: Results from a genome-wide association study
-
3089660 21357381
-
Figueiredo JC, Lewinger JP, Song C, Campbell PT, Conti DV, Edlund CK, Duggan DJ, Rangrej J, Lemire M, Hudson T, Zanke B, Cotterchio M, Gallinger S, Jenkins M, Hopper J, Haile R, Newcomb P, Potter J, Baron JA, Le Marchand L, Casey G: Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: results from a genome-wide association study. Cancer Epidemiol Biomarkers Prev 2011, 20:758-766.
-
(2011)
Cancer Epidemiol Biomarkers Prev
, vol.20
, pp. 758-766
-
-
Figueiredo, J.C.1
Lewinger, J.P.2
Song, C.3
Campbell, P.T.4
Conti, D.V.5
Edlund, C.K.6
Duggan, D.J.7
Rangrej, J.8
Lemire, M.9
Hudson, T.10
Zanke, B.11
Cotterchio, M.12
Gallinger, S.13
Jenkins, M.14
Hopper, J.15
Haile, R.16
Newcomb, P.17
Potter, J.18
Baron, J.A.19
Le Marchand, L.20
Casey, G.21
more..
-
29
-
-
84863684047
-
Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women
-
3349734 1:CAS:528:DC%2BC38XnslOlt70%3D 22589738
-
Fox CS, Liu Y, White CC, Feitosa M, Smith AV, Heard-Costa N, Lohman K, Consortium GIANT, Consortium MAGIC, Consortium GLGC, Johnson AD, Foster MC, Greenawalt DM, Griffin P, Ding J, Newman AB, Tylavsky F, Miljkovic I, Kritchevsky SB, Launer L, Garcia M, Eiriksdottir G, Carr JJ, Gudnason V, Harris TB, Cupples LA, Borecki IB: Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. PLoS Genet 2012, 8:e1002695.
-
(2012)
PLoS Genet
, vol.8
, pp. e1002695
-
-
Fox, C.S.1
Liu, Y.2
White, C.C.3
Feitosa, M.4
Smith, A.V.5
Heard-Costa, N.6
Lohman, K.7
Consortium, G.I.A.N.T.8
Consortium, M.A.G.I.C.9
Consortium, G.L.G.C.10
Johnson, A.D.11
Foster, M.C.12
Greenawalt, D.M.13
Griffin, P.14
Ding, J.15
Newman, A.B.16
Tylavsky, F.17
Miljkovic, I.18
Kritchevsky, S.B.19
Launer, L.20
Garcia, M.21
Eiriksdottir, G.22
Carr, J.J.23
Gudnason, V.24
Harris, T.B.25
Cupples, L.A.26
Borecki, I.B.27
more..
-
30
-
-
0034741031
-
Alpha T-catenin a novel tissue-specific beta-catenin-binding protein mediating strong cell-cell adhesion
-
1:CAS:528:DC%2BD3MXnsFOhu7w%3D 11590244
-
Janssens B, Goossens S, Staes K, Gilbert B, van Hengel J, Colpaert C, Bruyneel E, Mareel M, van Roy F: Alpha T-catenin a novel tissue-specific beta-catenin-binding protein mediating strong cell-cell adhesion. J Cell Sci 2001, 114:3177-3188.
-
(2001)
J Cell Sci
, vol.114
, pp. 3177-3188
-
-
Janssens, B.1
Goossens, S.2
Staes, K.3
Gilbert, B.4
Van Hengel, J.5
Colpaert, C.6
Bruyneel, E.7
Mareel, M.8
Van Roy, F.9
-
31
-
-
70350776635
-
Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture
-
1:CAS:528:DC%2BD1MXhtFagsbnJ 19578123
-
Vissers LE, Bhatt SS, Janssen IM, Xia Z, Lalani SR, Pfundt R, Derwinska K, de Vries BB, Gilissen C, Hoischen A, Nesteruk M, Wisniowiecka-Kowalnik B, Smyk M, Brunner HG, Cheung SW, van Kessel AG, Veltman JA, Stankiewicz P: Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture. Hum Mol Genet 2009, 18:3579-3593.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 3579-3593
-
-
Vissers, L.E.1
Bhatt, S.S.2
Janssen, I.M.3
Xia, Z.4
Lalani, S.R.5
Pfundt, R.6
Derwinska, K.7
De Vries, B.B.8
Gilissen, C.9
Hoischen, A.10
Nesteruk, M.11
Wisniowiecka-Kowalnik, B.12
Smyk, M.13
Brunner, H.G.14
Cheung, S.W.15
Van Kessel, A.G.16
Veltman, J.A.17
Stankiewicz, P.18
-
32
-
-
30144442771
-
Common fragile sites, extremely large genes, neural development and cancer
-
1:CAS:528:DC%2BD28XjsF2jtg%3D%3D 16221525
-
Smith DI, Zhu Y, McAvoy S, Kuhn R: Common fragile sites, extremely large genes, neural development and cancer. Cancer Lett 2006, 232:48-57.
-
(2006)
Cancer Lett
, vol.232
, pp. 48-57
-
-
Smith, D.I.1
Zhu, Y.2
McAvoy, S.3
Kuhn, R.4
-
33
-
-
84875269728
-
Role of DNA secondary structures in fragile site breakage along human chromosome 10
-
3596854 1:CAS:528:DC%2BC3sXktFSjs7w%3D 23297364
-
Dillon LW, Pierce LC, Ng MC, Wang YH: Role of DNA secondary structures in fragile site breakage along human chromosome 10. Hum Mol Genet 2013, 22:1443-1456.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 1443-1456
-
-
Dillon, L.W.1
Pierce, L.C.2
Ng, M.C.3
Wang, Y.H.4
-
34
-
-
8844267643
-
Differential downregulation of alphaT-catenin expression in placenta: Trophoblast cell type-dependent imprinting of the CTNNA3 gene
-
1:CAS:528:DC%2BD2cXptl2lsrY%3D 15533819
-
van Dijk M, Mulders J, Könst A, Janssens B, van Roy F, Blankenstein M, Oudejans C: Differential downregulation of alphaT-catenin expression in placenta: trophoblast cell type-dependent imprinting of the CTNNA3 gene. Gene Expr Patterns 2004, 5:61-65.
-
(2004)
Gene Expr Patterns
, vol.5
, pp. 61-65
-
-
Van Dijk, M.1
Mulders, J.2
Könst, A.3
Janssens, B.4
Van Roy, F.5
Blankenstein, M.6
Oudejans, C.7
-
35
-
-
0025752664
-
The 102 kDa cadherin-associated protein: Similarity to vinculin and posttranscriptional regulation of expression
-
1:CAS:528:DyaK38XnvVOnsQ%3D%3D 1904011
-
Nagafuchi A, Takeichi M, Tsukita S: The 102 kDa cadherin-associated protein: similarity to vinculin and posttranscriptional regulation of expression. Cell 1991, 65:849-857.
-
(1991)
Cell
, vol.65
, pp. 849-857
-
-
Nagafuchi, A.1
Takeichi, M.2
Tsukita, S.3
-
36
-
-
0026630994
-
Identification of a neural alpha-catenin as a key regulator of cadherin function and multicellular organization
-
1:CAS:528:DyaK3sXkt1aqtLk%3D 1638632
-
Hirano S, Kimoto N, Shimoyama Y, Hirohashi S, Takeichi M: Identification of a neural alpha-catenin as a key regulator of cadherin function and multicellular organization. Cell 1992, 70:293-301.
-
(1992)
Cell
, vol.70
, pp. 293-301
-
-
Hirano, S.1
Kimoto, N.2
Shimoyama, Y.3
Hirohashi, S.4
Takeichi, M.5
-
37
-
-
34347364710
-
A unique and specific interaction between alphaT-catenin and plakophilin-2 in the area composita, the mixed-type junctional structure of cardiac intercalated discs
-
1:CAS:528:DC%2BD2sXnvVamtLk%3D 17535849
-
Goossens S, Janssens B, Bonné S, De Rycke R, Braet F, van Hengel J, van Roy F: A unique and specific interaction between alphaT-catenin and plakophilin-2 in the area composita, the mixed-type junctional structure of cardiac intercalated discs. J Cell Sci 2007, 120:2126-2136.
-
(2007)
J Cell Sci
, vol.120
, pp. 2126-2136
-
-
Goossens, S.1
Janssens, B.2
Bonné, S.3
De Rycke, R.4
Braet, F.5
Van Hengel, J.6
Van Roy, F.7
-
38
-
-
0034703979
-
Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees
-
1:CAS:528:DC%2BD3cXptFSms7g%3D 11125143
-
Ertekin-Taner N, Graff-Radford N, Younkin LH, Eckman C, Baker M, Adamson J, Ronald J, Blangero J, Hutton M, Younkin SG: Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. Science 2000, 290:2303-2304.
-
(2000)
Science
, vol.290
, pp. 2303-2304
-
-
Ertekin-Taner, N.1
Graff-Radford, N.2
Younkin, L.H.3
Eckman, C.4
Baker, M.5
Adamson, J.6
Ronald, J.7
Blangero, J.8
Hutton, M.9
Younkin, S.G.10
-
39
-
-
0344668728
-
Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees
-
2836540 1:CAS:528:DC%2BD3sXptVSntL0%3D 14559775
-
Ertekin-Taner N, Ronald J, Asahara H, Younkin L, Hella M, Jain S, Gnida E, Younkin S, Fadale D, Ohyagi Y, Singleton A, Scanlin L, de Andrade M, Petersen R, Graff-Radford N, Hutton M, Younkin S: Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees. Hum Mol Genet 2003, 12:3133-3143.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3133-3143
-
-
Ertekin-Taner, N.1
Ronald, J.2
Asahara, H.3
Younkin, L.4
Hella, M.5
Jain, S.6
Gnida, E.7
Younkin, S.8
Fadale, D.9
Ohyagi, Y.10
Singleton, A.11
Scanlin, L.12
De Andrade, M.13
Petersen, R.14
Graff-Radford, N.15
Hutton, M.16
Younkin, S.17
-
40
-
-
26944473203
-
Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease
-
1735932 1:CAS:528:DC%2BD2MXhtFyhu7fJ 16199552
-
Martin ER, Bronson PG, Li YJ, Wall N, Chung RH, Schmechel DE, Small G, Xu PT, Bartlett J, Schnetz-Boutaud N, Haines JL, Gilbert JR, Pericak-Vance MA: Interaction between the alpha-T catenin gene (VR22) and APOE in Alzheimer's disease. J Med Genet 2005, 42:787-792.
-
(2005)
J Med Genet
, vol.42
, pp. 787-792
-
-
Martin, E.R.1
Bronson, P.G.2
Li, Y.J.3
Wall, N.4
Chung, R.H.5
Schmechel, D.E.6
Small, G.7
Xu, P.T.8
Bartlett, J.9
Schnetz-Boutaud, N.10
Haines, J.L.11
Gilbert, J.R.12
Pericak-Vance, M.A.13
-
41
-
-
79958035893
-
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
-
3607702 1:CAS:528:DC%2BC3MXnsVyrtL4%3D 21658583
-
Gilman SR, Iossifov I, Levy D, Ronemus M, Wigler M, Vitkup D: Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron 2011, 70:898-907.
-
(2011)
Neuron
, vol.70
, pp. 898-907
-
-
Gilman, S.R.1
Iossifov, I.2
Levy, D.3
Ronemus, M.4
Wigler, M.5
Vitkup, D.6
-
42
-
-
1842612444
-
Stability of dendritic spines and synaptic contacts is controlled by alpha N-catenin
-
1:CAS:528:DC%2BD2cXisFCisLs%3D 15034585
-
Abe K, Chisaka O, Van Roy F, Takeichi M: Stability of dendritic spines and synaptic contacts is controlled by alpha N-catenin. Nat Neurosci 2004, 7:357-363.
-
(2004)
Nat Neurosci
, vol.7
, pp. 357-363
-
-
Abe, K.1
Chisaka, O.2
Van Roy, F.3
Takeichi, M.4
-
43
-
-
2342574965
-
Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease
-
1:CAS:528:DC%2BD2cXjvFChsrw%3D 15075440
-
Busby V, Goossens S, Nowotny P, Hamilton G, Smemo S, Harold D, Turic D, Jehu L, Myers A, Womick M, Woo D, Compton D, Doil LM, Tacey KM, Lau KF, Al-Saraj S, Killick R, Pickering-Brown S, Moore P, Hollingworth P, Archer N, Foy C, Walter S, Lendon C, Iwatsubo T, Morris JC, Norton J, Mann D, Janssens B, Hardy J, et al.: Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease. Neuromolecular Med 2004, 5:133-146.
-
(2004)
Neuromolecular Med
, vol.5
, pp. 133-146
-
-
Busby, V.1
Goossens, S.2
Nowotny, P.3
Hamilton, G.4
Smemo, S.5
Harold, D.6
Turic, D.7
Jehu, L.8
Myers, A.9
Womick, M.10
Woo, D.11
Compton, D.12
Doil, L.M.13
Tacey, K.M.14
Lau, K.F.15
Al-Saraj, S.16
Killick, R.17
Pickering-Brown, S.18
Moore, P.19
Hollingworth, P.20
Archer, N.21
Foy, C.22
Walter, S.23
Lendon, C.24
Iwatsubo, T.25
Morris, J.C.26
Norton, J.27
Mann, D.28
Janssens, B.29
Hardy, J.30
more..
-
44
-
-
84868616944
-
A review of the evidence for the canonical Wnt pathway in autism spectrum disorders
-
3492093 1:CAS:528:DC%2BC38XhslOiurvL 23083465
-
Kalkman HO: A review of the evidence for the canonical Wnt pathway in autism spectrum disorders. Mol Autism 2012, 3:10.
-
(2012)
Mol Autism
, vol.3
, pp. 10
-
-
Kalkman, H.O.1
-
45
-
-
84873060273
-
Autism recurrence in half siblings: Strong support for genetic mechanisms of transmission in ASD
-
1:STN:280:DC%2BC38vksFansQ%3D%3D 22371046
-
Constantino JN, Todorov A, Hilton C, Law P, Zhang Y, Molloy E, Fitzgerald R, Geschwind D: Autism recurrence in half siblings: strong support for genetic mechanisms of transmission in ASD. Mol Psychiatry 2013, 18:137-138.
-
(2013)
Mol Psychiatry
, vol.18
, pp. 137-138
-
-
Constantino, J.N.1
Todorov, A.2
Hilton, C.3
Law, P.4
Zhang, Y.5
Molloy, E.6
Fitzgerald, R.7
Geschwind, D.8
-
46
-
-
30344476413
-
Low-frequency common fragile sites: Link to neuropsychiatric disorders?
-
1:CAS:528:DC%2BD28XjsF2jtw%3D%3D 16298041
-
Savelyeva L, Sagulenko E, Schmitt JG, Schwab M: Low-frequency common fragile sites: link to neuropsychiatric disorders? Cancer Lett 2006, 232:58-69.
-
(2006)
Cancer Lett
, vol.232
, pp. 58-69
-
-
Savelyeva, L.1
Sagulenko, E.2
Schmitt, J.G.3
Schwab, M.4
-
47
-
-
78650019788
-
Genomic and epigenomic instability, fragile sites, schizophrenia and autism
-
3018726 1:CAS:528:DC%2BC3cXhtFyks7jO 21358990
-
Smith CL, Bolton A, Nguyen G: Genomic and epigenomic instability, fragile sites, schizophrenia and autism. Curr Genomics 2010, 11:447-469.
-
(2010)
Curr Genomics
, vol.11
, pp. 447-469
-
-
Smith, C.L.1
Bolton, A.2
Nguyen, G.3
-
48
-
-
84896071049
-
Origin and loss of nested LRRTM/α-catenin genes during vertebrate evolution
-
3933685 24587117
-
Uvarov P, Kajander T, Airaksinen MS: Origin and loss of nested LRRTM/α-catenin genes during vertebrate evolution. PLoS One 2014, 9:e89910.
-
(2014)
PLoS One
, vol.9
, pp. e89910
-
-
Uvarov, P.1
Kajander, T.2
Airaksinen, M.S.3
-
49
-
-
61549142067
-
An unbiased expression screen for synaptogenic proteins identifies the LRRTM protein family as synaptic organizers
-
2746109 1:CAS:528:DC%2BD1MXlt1Klt7c%3D 19285470
-
Linhoff MW, Laurén J, Cassidy RM, Dobie FA, Takahashi H, Nygaard HB, Airaksinen MS, Strittmatter SM, Craig AM: An unbiased expression screen for synaptogenic proteins identifies the LRRTM protein family as synaptic organizers. Neuron 2009, 61:734-749.
-
(2009)
Neuron
, vol.61
, pp. 734-749
-
-
Linhoff, M.W.1
Laurén, J.2
Cassidy, R.M.3
Dobie, F.A.4
Takahashi, H.5
Nygaard, H.B.6
Airaksinen, M.S.7
Strittmatter, S.M.8
Craig, A.M.9
-
50
-
-
80053634855
-
The neurexin ligands, neuroligins and leucine-rich repeat transmembrane proteins, perform convergent and divergent synaptic functions in vivo
-
3189075 1:CAS:528:DC%2BC3MXhtlWksrrE 21953696
-
Soler-Llavina GJ, Fuccillo MV, Ko J, Sudhof TC, Malenka RC: The neurexin ligands, neuroligins and leucine-rich repeat transmembrane proteins, perform convergent and divergent synaptic functions in vivo. Proc Natl Acad Sci U S A 2011, 108:16502-16509.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 16502-16509
-
-
Soler-Llavina, G.J.1
Fuccillo, M.V.2
Ko, J.3
Sudhof, T.C.4
Malenka, R.C.5
-
51
-
-
0037380873
-
A novel gene family encoding leucine-rich repeat transmembrane proteins differentially expressed in the nervous system
-
12676565
-
Laurén J, Airaksinen MS, Saarma M, Timmusk T: A novel gene family encoding leucine-rich repeat transmembrane proteins differentially expressed in the nervous system. Genomics 2003, 81:411-421.
-
(2003)
Genomics
, vol.81
, pp. 411-421
-
-
Laurén, J.1
Airaksinen, M.S.2
Saarma, M.3
Timmusk, T.4
-
52
-
-
33845202373
-
LRRTM3 promotes processing of amyloid-precursor protein by BACE1 and is a positional candidate gene for late-onset Alzheimer's disease
-
1635650 1:CAS:528:DC%2BD28Xht1Kmsr7E 17098871
-
Majercak J, Ray WJ, Espeseth A, Simon A, Shi XP, Wolffe C, Getty K, Marine S, Stec E, Ferrer M, Strulovici B, Bartz S, Gates A, Xu M, Huang Q, Ma L, Shughrue P, Burchard J, Colussi D, Pietrak B, Kahana J, Beher D, Rosahl T, Shearman M, Hazuda D, Sachs AB, Koblan KS, Seabrook GR, Stone DJ: LRRTM3 promotes processing of amyloid-precursor protein by BACE1 and is a positional candidate gene for late-onset Alzheimer's disease. Proc Natl Acad Sci U S A 2006, 103:17967-17972.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 17967-17972
-
-
Majercak, J.1
Ray, W.J.2
Espeseth, A.3
Simon, A.4
Shi, X.P.5
Wolffe, C.6
Getty, K.7
Marine, S.8
Stec, E.9
Ferrer, M.10
Strulovici, B.11
Bartz, S.12
Gates, A.13
Xu, M.14
Huang, Q.15
Ma, L.16
Shughrue, P.17
Burchard, J.18
Colussi, D.19
Pietrak, B.20
Kahana, J.21
Beher, D.22
Rosahl, T.23
Shearman, M.24
Hazuda, D.25
Sachs, A.B.26
Koblan, K.S.27
Seabrook, G.R.28
Stone, D.J.29
more..
-
53
-
-
77954646843
-
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
-
International Molecular Genetic Study of Autism Consortium (IMGSAC) 2913944 20678249
-
Sousa I, Clark TG, Holt R, Pagnamenta AT, Mulder EJ, Minderaa RB, Bailey AJ, Battaglia A, Klauck SM, Poustka F, Monaco AP, International Molecular Genetic Study of Autism Consortium (IMGSAC): Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. Mol Autism 2010, 1:7.
-
(2010)
Mol Autism
, vol.1
, pp. 7
-
-
Sousa, I.1
Clark, T.G.2
Holt, R.3
Pagnamenta, A.T.4
Mulder, E.J.5
Minderaa, R.B.6
Bailey, A.J.7
Battaglia, A.8
Klauck, S.M.9
Poustka, F.10
Monaco, A.P.11
-
54
-
-
84861211989
-
Loss of αt-catenin alters the hybrid adhering junctions in the heart and leads to dilated cardiomyopathy and ventricular arrhythmia following acute ischemia
-
3311935 1:CAS:528:DC%2BC38Xmsl2nu7Y%3D 22421363
-
Li J, Goossens S, van Hengel J, Gao E, Cheng L, Tyberghein K, Shang X, De Rycke R, van Roy F, Radice GL: Loss of αT-catenin alters the hybrid adhering junctions in the heart and leads to dilated cardiomyopathy and ventricular arrhythmia following acute ischemia. J Cell Sci 2012, 125:1058-1067.
-
(2012)
J Cell Sci
, vol.125
, pp. 1058-1067
-
-
Li, J.1
Goossens, S.2
Van Hengel, J.3
Gao, E.4
Cheng, L.5
Tyberghein, K.6
Shang, X.7
De Rycke, R.8
Van Roy, F.9
Radice, G.L.10
-
55
-
-
77953800799
-
Behavioural phenotyping assays for mouse models of autism
-
3087436 1:CAS:528:DC%2BC3cXns1Gis7k%3D 20559336
-
Silverman JL, Yang M, Lord C, Crawley JN: Behavioural phenotyping assays for mouse models of autism. Nat Rev Neurosci 2010, 11:490-502.
-
(2010)
Nat Rev Neurosci
, vol.11
, pp. 490-502
-
-
Silverman, J.L.1
Yang, M.2
Lord, C.3
Crawley, J.N.4
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