-
1
-
-
26844498125
-
Sequence variants in SLITRK1 are associated with Tourette's syndrome
-
Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, Dure LS4th, Kurlan R, Singer HS, Gilbert DL, Farhi A, Louvi A, Lifton RP, Sestan N, State MW. 2005. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 310: 317-320.
-
(2005)
Science
, vol.310
, pp. 317-320
-
-
Abelson, J.F.1
Kwan, K.Y.2
O'Roak, B.J.3
Baek, D.Y.4
Stillman, A.A.5
Morgan, T.M.6
Mathews, C.A.7
Pauls, D.L.8
Rasin, M.R.9
Gunel, M.10
Davis, N.R.11
Ercan-Sencicek, A.G.12
Guez, D.H.13
Spertus, J.A.14
Leckman, J.F.15
Dure 4th, L.S.16
Kurlan, R.17
Singer, H.S.18
Gilbert, D.L.19
Farhi, A.20
Louvi, A.21
Lifton, R.P.22
Sestan, N.23
State, M.W.24
more..
-
2
-
-
0031031639
-
Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE
-
Abrams MT, Doheny KF, Mazzocco MM, Knight SJ, Baumgardner TL, Freund LS, Davies KE, Reiss AL. 1997. Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE. Am J Med Genet 74: 73-81.
-
(1997)
Am J Med Genet
, vol.74
, pp. 73-81
-
-
Abrams, M.T.1
Doheny, K.F.2
Mazzocco, M.M.3
Knight, S.J.4
Baumgardner, T.L.5
Freund, L.S.6
Davies, K.E.7
Reiss, A.L.8
-
3
-
-
0027621699
-
-
Mining association rules between sets of items in large databases. In Proc. of the ACM SIGMOD Conference on Management of Data, Washington, DC
-
Agrawal R, Imielinski T, Swami A. 1993. Mining association rules between sets of items in large databases. In Proc. of the ACM SIGMOD Conference on Management of Data, Washington, DC, p 207-216
-
(1993)
, pp. 207-216
-
-
Agrawal, R.1
Imielinski, T.2
Swami, A.3
-
4
-
-
84862804707
-
-
Fast algorithms for mining association rules. Proceedings of the VLDB Conference, Santiago, Chile, September, 1994. Expanded version available as IBM Research Report RJ9839.
-
Agrawal R, Srikant R. Fast algorithms for mining association rules. 1994. In: Proceedings of the VLDB Conference, Santiago, Chile, September, 1994. Expanded version available as IBM Research Report RJ9839.
-
(1994)
-
-
Agrawal, R.1
Srikant, R.2
-
5
-
-
77954559471
-
A text-mining technique for extracting gene-disease associations from the biomedical literature
-
Al-Mubaid H, Singh RK. 2010. A text-mining technique for extracting gene-disease associations from the biomedical literature. Int J Bioinform Res Appl 6: 270-286.
-
(2010)
Int J Bioinform Res Appl
, vol.6
, pp. 270-286
-
-
Al-Mubaid, H.1
Singh, R.K.2
-
6
-
-
58149178561
-
AutDB: a gene reference resource for autism research
-
Basu SN, Kollu R, Banerjee-Basu S. 2009. AutDB: a gene reference resource for autism research. Nucleic Acids Res 37( Database issue): D832-D836.
-
(2009)
Nucleic Acids Res
, vol.37
, Issue.DATABASE ISSUE
-
-
Basu, S.N.1
Kollu, R.2
Banerjee-Basu, S.3
-
7
-
-
29644444985
-
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample
-
International Molecular Genetic Study of Autism Consortium (IMGSAC)
-
Blasi F, Bacchelli E, Carone S, Toma C, Monaco AP, Bailey AJ, Maestrini E, International Molecular Genetic Study of Autism Consortium (IMGSAC). 2006. SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. Eur J Hum Genet 14: 123-126.
-
(2006)
Eur J Hum Genet
, vol.14
, pp. 123-126
-
-
Blasi, F.1
Bacchelli, E.2
Carone, S.3
Toma, C.4
Monaco, A.P.5
Bailey, A.J.6
Maestrini, E.7
-
8
-
-
38549117309
-
The HGNC Database in 2008: a resource for the human genome
-
Bruford EA, Lush MJ, Wright MW, Sneddon TP, Povey S, Birney E. 2008. The HGNC Database in 2008: a resource for the human genome. Nucleic Acids Res 36( Database issue): D445-D448.
-
(2008)
Nucleic Acids Res
, vol.36
, Issue.DATABASE ISSUE
-
-
Bruford, E.A.1
Lush, M.J.2
Wright, M.W.3
Sneddon, T.P.4
Povey, S.5
Birney, E.6
-
9
-
-
65249185072
-
Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT
-
Cai G, Edelmann L, Goldsmith JE, Cohen N, Nakamine A, Reichert JG, Hoffman EJ, Zurawiecki DM, Silverman JM, Hollander E, Soorya L, Anagnostou E, Betancur C, Buxbaum JD. 2008. Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT. BMC Med Genomics 1: 50.
-
(2008)
BMC Med Genomics
, vol.1
, pp. 50
-
-
Cai, G.1
Edelmann, L.2
Goldsmith, J.E.3
Cohen, N.4
Nakamine, A.5
Reichert, J.G.6
Hoffman, E.J.7
Zurawiecki, D.M.8
Silverman, J.M.9
Hollander, E.10
Soorya, L.11
Anagnostou, E.12
Betancur, C.13
Buxbaum, J.D.14
-
10
-
-
48449088232
-
PolySearch: a web-based text mining system for extracting relationships between human diseases, genes, mutations, drugs and metabolites
-
Cheng D, Knox C, Young N, Stothard P, Damaraju S, Wishart DS. 2008. PolySearch: a web-based text mining system for extracting relationships between human diseases, genes, mutations, drugs and metabolites. Nucleic Acids Res 36( Web Server issue): W399-W405.
-
(2008)
Nucleic Acids Res
, vol.36
, Issue.WEB SERVER ISSUE
-
-
Cheng, D.1
Knox, C.2
Young, N.3
Stothard, P.4
Damaraju, S.5
Wishart, D.S.6
-
11
-
-
0037245822
-
Mining gene expression databases for association rules
-
Creighton C, Hanash S. 2003. Mining gene expression databases for association rules. Bioinformatics 19: 79-86.
-
(2003)
Bioinformatics
, vol.19
, pp. 79-86
-
-
Creighton, C.1
Hanash, S.2
-
12
-
-
77954658446
-
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals
-
E-pub 18 November 2009.
-
Cukier HN, Rabionet R, Konidari I, Rayner-Evans MY, Baltos ML, Wright HH, Abramson RK, Martin ER, Cuccaro ML, Pericak-Vance MA, Gilbert JR. 2010. Novel variants identified in methyl-CpG-binding domain genes in autistic individuals. Neurogenetics 11: 291-303. E-pub 18 November 2009.
-
(2010)
Neurogenetics
, vol.11
, pp. 291-303
-
-
Cukier, H.N.1
Rabionet, R.2
Konidari, I.3
Rayner-Evans, M.Y.4
Baltos, M.L.5
Wright, H.H.6
Abramson, R.K.7
Martin, E.R.8
Cuccaro, M.L.9
Pericak-Vance, M.A.10
Gilbert, J.R.11
-
15
-
-
0035653670
-
Genetics of autism: complex aetiology for a heterogeneous disorder
-
review].
-
Folstein SE, Rosen-Sheidley B. 2000. Genetics of autism: complex aetiology for a heterogeneous disorder [review]. Nat Rev Genet 2: 943-955.
-
(2000)
Nat Rev Genet
, vol.2
, pp. 943-955
-
-
Folstein, S.E.1
Rosen-Sheidley, B.2
-
16
-
-
0037656313
-
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
-
Paris Autism Research International Sibpair Study.
-
Jamain S, Quach H, Betancur C, Råstam M, Colineaux C, Gillberg IC, Soderstrom H, Giros B, Leboyer M, Gillberg C, Bourgeron T, Paris Autism Research International Sibpair Study. 2003. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism. Nat Genet 34: 27-29.
-
(2003)
Nat Genet
, vol.34
, pp. 27-29
-
-
Jamain, S.1
Quach, H.2
Betancur, C.3
Råstam, M.4
Colineaux, C.5
Gillberg, I.C.6
Soderstrom, H.7
Giros, B.8
Leboyer, M.9
Gillberg, C.10
Bourgeron, T.11
-
17
-
-
78649632841
-
Evolving role of MeCP2 in Rett syndrome and autism
-
Lasalle JM, Yasui DH. 2009. Evolving role of MeCP2 in Rett syndrome and autism. Epigenomics 1: 119-130.
-
(2009)
Epigenomics
, vol.1
, pp. 119-130
-
-
Lasalle, J.M.1
Yasui, D.H.2
-
19
-
-
77954311004
-
Multi-way association extraction and visualization from biological text documents using hyper-graphs: applications to genetic association studies for diseases
-
Mukhopadhyay S, Palakal M, Maddu K. 2010. Multi-way association extraction and visualization from biological text documents using hyper-graphs: applications to genetic association studies for diseases. Artif Intell Med 49: 145-154.
-
(2010)
Artif Intell Med
, vol.49
, pp. 145-154
-
-
Mukhopadhyay, S.1
Palakal, M.2
Maddu, K.3
-
20
-
-
33947106896
-
Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism
-
E-pub 5 Marsh 2007.
-
Nishimura K, Nakamura K, Anitha A, Yamada K, Tsujii M, Iwayama Y, Hattori E, Toyota T, Takei N, Miyachi T, Iwata Y, Suzuki K, Matsuzaki H, Kawai M, Sekine Y, Tsuchiya K, Sugihara G, Suda S, Ouchi Y, Sugiyama T, Yoshikawa T, Mori N. 2007. Genetic analyses of the brain-derived neurotrophic factor (BDNF) gene in autism. Biochem Biophys Res Commun 356: 200-206. E-pub 5 Marsh 2007.
-
(2007)
Biochem Biophys Res Commun
, vol.356
, pp. 200-206
-
-
Nishimura, K.1
Nakamura, K.2
Anitha, A.3
Yamada, K.4
Tsujii, M.5
Iwayama, Y.6
Hattori, E.7
Toyota, T.8
Takei, N.9
Miyachi, T.10
Iwata, Y.11
Suzuki, K.12
Matsuzaki, H.13
Kawai, M.14
Sekine, Y.15
Tsuchiya, K.16
Sugihara, G.17
Suda, S.18
Ouchi, Y.19
Sugiyama, T.20
Yoshikawa, T.21
Mori, N.22
more..
-
21
-
-
46249127253
-
Identifying gene-disease associations using centrality on a literature mined gene-interaction network
-
Ozgür A, Vu T, Erkan G, Radev DR. 2008. Identifying gene-disease associations using centrality on a literature mined gene-interaction network. Bioinformatics 24: i277-i285.
-
(2008)
Bioinformatics
, vol.24
-
-
Ozgür, A.1
Vu, T.2
Erkan, G.3
Radev, D.R.4
-
22
-
-
33746314832
-
Searching for ways out of the autism maze: genetic, epigenetic and environmental clues
-
Persico AM, Bourgeron T. 2006. Searching for ways out of the autism maze: genetic, epigenetic and environmental clues. Trends Neurosci 29: 349-358.
-
(2006)
Trends Neurosci
, vol.29
, pp. 349-358
-
-
Persico, A.M.1
Bourgeron, T.2
-
23
-
-
0035675794
-
The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders
-
Rogers SJ, Wehner DE, Hagerman R. 2001. The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. J Dev Behav Pediatr 22: 409-417.
-
(2001)
J Dev Behav Pediatr
, vol.22
, pp. 409-417
-
-
Rogers, S.J.1
Wehner, D.E.2
Hagerman, R.3
-
24
-
-
79952607358
-
Identification of direct downstream targets of Dlx5 during early inner ear development
-
Sajan SA, Rubenstein JL, Warchol ME, Lovett M. 2001. Identification of direct downstream targets of Dlx5 during early inner ear development. Hum Mol Genet 20: 1262-1273.
-
(2001)
Hum Mol Genet
, vol.20
, pp. 1262-1273
-
-
Sajan, S.A.1
Rubenstein, J.L.2
Warchol, M.E.3
Lovett, M.4
-
25
-
-
79952117230
-
Visualization and analysis of a cardio vascular disease- and MUPP1-related biological network combining text mining and data warehouse approaches
-
doi: 10.2390/biecoll-jib-2010-148.
-
Sommer B, Tiys ES, Kormeier B, Hippe K, Janowski SJ, Ivanisenko TV, Bragin AO, Arrigo P, Demenkov PS, Kochetov AV, Ivanisenko VA, Kolchanov NA, Hofestädt R. 2010. Visualization and analysis of a cardio vascular disease- and MUPP1-related biological network combining text mining and data warehouse approaches. J Integr Bioinform 7: 148. doi: 10.2390/biecoll-jib-2010-148.
-
(2010)
J Integr Bioinform
, vol.7
, pp. 148
-
-
Sommer, B.1
Tiys, E.S.2
Kormeier, B.3
Hippe, K.4
Janowski, S.J.5
Ivanisenko, T.V.6
Bragin, A.O.7
Arrigo, P.8
Demenkov, P.S.9
Kochetov, A.V.10
Ivanisenko, V.A.11
Kolchanov, N.A.12
Hofestädt, R.13
-
26
-
-
67649125873
-
Mining association rules from clinical databases: an intelligent diagnostic process in healthcare
-
Stilou S, Bamidis PD, Maglaveras N, Pappas C. 2001. Mining association rules from clinical databases: an intelligent diagnostic process in healthcare. Stud Health Technol Inform 84: 1399-1403.
-
(2001)
Stud Health Technol Inform
, vol.84
, pp. 1399-1403
-
-
Stilou, S.1
Bamidis, P.D.2
Maglaveras, N.3
Pappas, C.4
-
27
-
-
54949111758
-
FACTA: a text search engine for finding associated biomedical concepts
-
Tsuruoka Y, Tsujii J, Ananiadou S. 2008. FACTA: a text search engine for finding associated biomedical concepts. Bioinformatics 24: 2559-2560.
-
(2008)
Bioinformatics
, vol.24
, pp. 2559-2560
-
-
Tsuruoka, Y.1
Tsujii, J.2
Ananiadou, S.3
-
28
-
-
58149512312
-
Comparative analysis of neurological disorders focuses genome-wide search for autism genes
-
Wall DP, Esteban FJ, Deluca TF, Huyck M, Monaghan T, Velez de Mendizabal N, Goñí J, Kohane IS. 2009. Comparative analysis of neurological disorders focuses genome-wide search for autism genes. Genomics 93: 120-129.
-
(2009)
Genomics
, vol.93
, pp. 120-129
-
-
Wall, D.P.1
Esteban, F.J.2
Deluca, T.F.3
Huyck, M.4
Monaghan, T.5
Velez de Mendizabal, N.6
Goñí, J.7
Kohane, I.S.8
-
29
-
-
84864040931
-
Prediction of similarities among rheumatic diseases
-
doi 10.1007/s10916-0010-9609-6.
-
Yildirim P, Ceken C, Hassanpour R, Tolun MR. 2010. Prediction of similarities among rheumatic diseases. J Med Syst doi 10.1007/s10916-0010-9609-6.
-
(2010)
J Med Syst
-
-
Yildirim, P.1
Ceken, C.2
Hassanpour, R.3
Tolun, M.R.4
|