-
1
-
-
78049485263
-
-
Ferlay J, Shin H-R, Bray F, Forman D, Mathers C, et al. (2010) Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. 127: 2893–2917 doi:10.1002/ijc.25516
-
(2010)
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008
, vol.127
, pp. 2893-2917
-
-
Ferlay, J.1
Shin, H.-R.2
Bray, F.3
Forman, D.4
Mathers, C.5
-
2
-
-
84887405673
-
Gastric cancer-molecular and clinical dimensions
-
Wadhwa R, Song S, Lee J-S, Yao Y, Wei Q, et al. (2013) Gastric cancer-molecular and clinical dimensions. Nat Rev Clin Oncol 10: 643–655 doi:10.1038/nrclinonc.2013.170
-
(2013)
Nat Rev Clin Oncol
, vol.10
, pp. 643-655
-
-
Wadhwa, R.1
Song, S.2
Lee, J.-S.3
Yao, Y.4
Wei, Q.5
-
3
-
-
12644292106
-
The two histological main types of gastric carcinoma, an attempt at a histoclinical classification
-
Lauren P, (1965) The two histological main types of gastric carcinoma, an attempt at a histoclinical classification. Acta Pathol Microbiol Scand 64: 31–49.
-
(1965)
Acta Pathol Microbiol Scand
, vol.64
, pp. 31-49
-
-
Lauren, P.1
-
4
-
-
33646413672
-
The global health burden of infection-associated cancers in the year 2002
-
Parkin DM, (2006) The global health burden of infection-associated cancers in the year 2002. Int J Cancer 118: 3030–3044 doi:10.1002/ijc.21731
-
(2006)
Int J Cancer
, vol.118
, pp. 3030-3044
-
-
Parkin, D.M.1
-
6
-
-
0032568370
-
E-cadherin germline mutations in familial gastric cancer
-
Guilford P, Hopkins J, Harraway J, McLeod M, McLeod N, et al. (1998) E-cadherin germline mutations in familial gastric cancer. Nature 392: 402–405 doi:10.1038/32918
-
(1998)
Nature
, vol.392
, pp. 402-405
-
-
Guilford, P.1
Hopkins, J.2
Harraway, J.3
McLeod, M.4
McLeod, N.5
-
7
-
-
77956110372
-
Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research
-
Fitzgerald RC, Hardwick R, Huntsman D, Carneiro F, Guilford P, et al. (2010) Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research. J Med Genet 47: 436–444 doi:10.1136/jmg.2009.074237
-
(2010)
J Med Genet
, vol.47
, pp. 436-444
-
-
Fitzgerald, R.C.1
Hardwick, R.2
Huntsman, D.3
Carneiro, F.4
Guilford, P.5
-
8
-
-
0034329587
-
Report on the first meeting of the International Collaborative Group on Hereditary Gastric Cancer
-
Park J-G, Yang H-K, Kim WH, Caldas C, Yokota J, et al. (2000) Report on the first meeting of the International Collaborative Group on Hereditary Gastric Cancer. J Natl Cancer Inst 92: 1781–1782 doi:10.1093/jnci/92.21.1781
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1781-1782
-
-
Park, J.-G.1
Yang, H.-K.2
Kim, W.H.3
Caldas, C.4
Yokota, J.5
-
9
-
-
64549109715
-
Germline CDH1 deletions in hereditary diffuse gastric cancer families
-
Oliveira C, Senz J, Kaurah P, Pinheiro H, Sanges R, et al. (2009) Germline CDH1 deletions in hereditary diffuse gastric cancer families. Hum Mol Genet 18: 1545–1555 doi:10.1093/hmg/ddp046
-
(2009)
Hum Mol Genet
, vol.18
, pp. 1545-1555
-
-
Oliveira, C.1
Senz, J.2
Kaurah, P.3
Pinheiro, H.4
Sanges, R.5
-
10
-
-
65449146296
-
ASK1 and ASK2 differentially regulate the counteracting roles of apoptosis and inflammation in tumorigenesis
-
Iriyama T, Takeda K, Nakamura H, Morimoto Y, Kuroiwa T, et al. (2009) ASK1 and ASK2 differentially regulate the counteracting roles of apoptosis and inflammation in tumorigenesis. The EMBO Journal 28: 843–853 doi:10.1038/emboj.2009.32
-
(2009)
The EMBO Journal
, vol.28
, pp. 843-853
-
-
Iriyama, T.1
Takeda, K.2
Nakamura, H.3
Morimoto, Y.4
Kuroiwa, T.5
-
11
-
-
78651403369
-
Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing
-
Zang ZJ, Ong CK, Cutcutache I, Yu W, Zhang SL, et al. (2011) Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing. Cancer Res 71: 29–39 doi:10.1158/0008-5472.CAN-10-1749
-
(2011)
Cancer Res
, vol.71
, pp. 29-39
-
-
Zang, Z.J.1
Ong, C.K.2
Cutcutache, I.3
Yu, W.4
Zhang, S.L.5
-
12
-
-
0036338150
-
Merlin–rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR, (2002) Merlin–rapid analysis of dense genetic maps using sparse gene flow trees. Nature Genetics 30: 97–101 doi:10.1038/ng786
-
(2002)
Nature Genetics
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
13
-
-
78651330430
-
COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
-
Forbes SA, Bindal N, Bamford S, Cole C, Kok CY, et al. (2011) COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer. Nucleic Acids Res 39: D945–D950 doi:10.1093/nar/gkq929
-
(2011)
Nucleic Acids Res
, vol.39
, pp. D945-D950
-
-
Forbes, S.A.1
Bindal, N.2
Bamford, S.3
Cole, C.4
Kok, C.Y.5
-
14
-
-
34147186130
-
Apoptosis signal-regulating kinase (ASK) 2 functions as a mitogen-activated protein kinase kinase kinase in a heteromeric complex with ASK1
-
Takeda K, Shimozono R, Noguchi T, Umeda T, Morimoto Y, et al. (2007) Apoptosis signal-regulating kinase (ASK) 2 functions as a mitogen-activated protein kinase kinase kinase in a heteromeric complex with ASK1. Journal of Biological Chemistry 282: 7522–7531 doi:10.1074/jbc.M607177200
-
(2007)
Journal of Biological Chemistry
, vol.282
, pp. 7522-7531
-
-
Takeda, K.1
Shimozono, R.2
Noguchi, T.3
Umeda, T.4
Morimoto, Y.5
-
15
-
-
65349155170
-
Mitogen-activated protein 3 kinase 6 mediates angiogenic and tumorigenic effects via vascular endothelial growth factor expression
-
Eto N, Miyagishi M, Inagi R, Fujita T, Nangaku M, (2009) Mitogen-activated protein 3 kinase 6 mediates angiogenic and tumorigenic effects via vascular endothelial growth factor expression. Am J Pathol 174: 1553–1563 doi:10.2353/ajpath.2009.080190
-
(2009)
Am J Pathol
, vol.174
, pp. 1553-1563
-
-
Eto, N.1
Miyagishi, M.2
Inagi, R.3
Fujita, T.4
Nangaku, M.5
-
16
-
-
0034744639
-
Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer
-
Baylin SB, Esteller M, Rountree MR, Bachman KE, Schuebel K, et al. (2001) Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer. Hum Mol Genet 10: 687–692 doi:10.1093/hmg/10.7.687
-
(2001)
Hum Mol Genet
, vol.10
, pp. 687-692
-
-
Baylin, S.B.1
Esteller, M.2
Rountree, M.R.3
Bachman, K.E.4
Schuebel, K.5
-
17
-
-
84865393828
-
Genome-scale DNA methylation pattern profiling of human bone marrow mesenchymal stem cells in long-term culture
-
Choi MR, In Y-H, Park J, Park T, Jung KH, et al. (2012) Genome-scale DNA methylation pattern profiling of human bone marrow mesenchymal stem cells in long-term culture. Exp Mol Med 44: 503 doi:10.3858/emm.2012.44.8.057
-
(2012)
Exp Mol Med
, vol.44
, pp. 503
-
-
Choi, M.R.1
In, Y.-H.2
Park, J.3
Park, T.4
Jung, K.H.5
-
18
-
-
0345603004
-
The CpG island searcher: a new WWW resource
-
Takai D, Jones PA, (2003) The CpG island searcher: a new WWW resource. In silico biology 3: 235–240.
-
(2003)
In silico biology
, vol.3
, pp. 235-240
-
-
Takai, D.1
Jones, P.A.2
-
19
-
-
84866111524
-
Evolutionary diagnosis method for variants in personal exomes
-
Kumar S, Sanderford M, Gray VE, Ye J, Liu L, (2012) Evolutionary diagnosis method for variants in personal exomes. Nat Methods 9: 855–856 doi:10.1038/nmeth.2147
-
(2012)
Nat Methods
, vol.9
, pp. 855-856
-
-
Kumar, S.1
Sanderford, M.2
Gray, V.E.3
Ye, J.4
Liu, L.5
-
20
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, et al. (2010) A method and server for predicting damaging missense mutations. Nat Methods 7: 248–249 doi:10.1038/nmeth0410-248
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
-
21
-
-
0043122919
-
SIFT: Predicting amino acid changes that affect protein function
-
Ng PC, Henikoff S, (2003) SIFT: Predicting amino acid changes that affect protein function. Nucleic Acids Res 31: 3812–3814 doi:10.1093/nar/gkg509
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 3812-3814
-
-
Ng, P.C.1
Henikoff, S.2
-
22
-
-
84884759753
-
Intragenic DNA methylation in transcriptional regulation, normal differentiation and cancer
-
Kulis M, Queirós AC, Beekman R, Martín-Subero JI, (2013) Intragenic DNA methylation in transcriptional regulation, normal differentiation and cancer. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms 1829: 1161–1174 doi:10.1016/j.bbagrm.2013.08.001
-
(2013)
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms
, vol.1829
, pp. 1161-1174
-
-
Kulis, M.1
Queirós, A.C.2
Beekman, R.3
Martín-Subero, J.I.4
-
24
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
Greenman C, Stephens P, Smith R, Dalgliesh GL, Hunter C, et al. (2007) Patterns of somatic mutation in human cancer genomes. Nature 446: 153–158 doi:10.1038/nature05610
-
(2007)
Nature
, vol.446
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
Dalgliesh, G.L.4
Hunter, C.5
-
25
-
-
33749993417
-
The consensus coding sequences of human breast and colorectal cancers
-
Sjöblom T, Jones S, Wood LD, Parsons DW, Lin J, et al. (2006) The consensus coding sequences of human breast and colorectal cancers. Science 314: 268–274 doi:10.1126/science.1133427
-
(2006)
Science
, vol.314
, pp. 268-274
-
-
Sjöblom, T.1
Jones, S.2
Wood, L.D.3
Parsons, D.W.4
Lin, J.5
-
26
-
-
69849112388
-
Clinical implications of the colorectal cancer risk associated with MUTYH mutation
-
Lubbe SJ, Di Bernardo MC, Chandler IP, Houlston RS, (2009) Clinical implications of the colorectal cancer risk associated with MUTYH mutation. Journal of Clinical Oncology 27: 3975–3980 doi:10.1200/JCO.2008.21.6853
-
(2009)
Journal of Clinical Oncology
, vol.27
, pp. 3975-3980
-
-
Lubbe, S.J.1
Di Bernardo, M.C.2
Chandler, I.P.3
Houlston, R.S.4
-
27
-
-
62949228316
-
Germline MutY Human Homologue Mutations and Colorectal Cancer: A Multisite Case-Control Study
-
Cleary SP, Cotterchio M, Jenkins MA, Kim H, Bristow R, et al. (2009) Germline MutY Human Homologue Mutations and Colorectal Cancer: A Multisite Case-Control Study. Gastroenterology 136: 1251–1260 doi:10.1053/j.gastro.2008.12.050
-
(2009)
Gastroenterology
, vol.136
, pp. 1251-1260
-
-
Cleary, S.P.1
Cotterchio, M.2
Jenkins, M.A.3
Kim, H.4
Bristow, R.5
-
28
-
-
78650005336
-
A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants
-
Theodoratou E, Campbell H, Tenesa A, Houlston R, Webb E, et al. (2010) A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants. Br J Cancer 103: 1875–1884 doi:10.1038/sj.bjc.6605966
-
(2010)
Br J Cancer
, vol.103
, pp. 1875-1884
-
-
Theodoratou, E.1
Campbell, H.2
Tenesa, A.3
Houlston, R.4
Webb, E.5
-
29
-
-
84907365915
-
Nonpenetrance of the Most Frequent Autosomal Recessive Leber Congenital Amaurosis Mutation in NMNAT1
-
Siemiatkowska AM, Schuurs-Hoeijmakers JHM, Bosch DGM, Boonstra FN, Riemslag FCC, et al. (2014) Nonpenetrance of the Most Frequent Autosomal Recessive Leber Congenital Amaurosis Mutation in NMNAT1. JAMA Ophthalmol 132: 1002–4 doi:10.1001/jamaophthalmol.2014.983
-
(2014)
JAMA Ophthalmol
, vol.132
, pp. 1002-1004
-
-
Siemiatkowska, A.M.1
Schuurs-Hoeijmakers, J.H.M.2
Bosch, D.G.M.3
Boonstra, F.N.4
Riemslag, F.C.C.5
-
30
-
-
84861121701
-
Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression
-
Baradaran-Heravi A, Cho KS, Tolhuis B, Sanyal M, Morozova O, et al. (2012) Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression. Hum Mol Genet 21: 2572–2587 doi:10.1093/hmg/dds083
-
(2012)
Hum Mol Genet
, vol.21
, pp. 2572-2587
-
-
Baradaran-Heravi, A.1
Cho, K.S.2
Tolhuis, B.3
Sanyal, M.4
Morozova, O.5
-
31
-
-
84867135409
-
BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome
-
Estrada-Cuzcano A, Koenekoop RK, Senechal A, De Baere EBW, de Ravel T, et al. (2012) BBS1 Mutations in a Wide Spectrum of Phenotypes Ranging From Nonsyndromic Retinitis Pigmentosa to Bardet-Biedl Syndrome. Arch Ophthalmol 130: 1425–1432 doi:10.1001/archophthalmol.2012.2434
-
(2012)
Arch Ophthalmol
, vol.130
, pp. 1425-1432
-
-
Estrada-Cuzcano, A.1
Koenekoop, R.K.2
Senechal, A.3
De Baere, E.B.W.4
De Ravel, T.5
-
32
-
-
0038744241
-
Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome
-
Beales PL, Badano JL, Ross AJ, Ansley SJ, (2003) Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome. Am J Hum Gen doi:10.1086/375178
-
(2003)
Am J Hum Gen
-
-
Beales, P.L.1
Badano, J.L.2
Ross, A.J.3
Ansley, S.J.4
-
33
-
-
34548205302
-
Heteromeric complex formation of ASK2 and ASK1 regulates stress-induced signaling
-
Ortner E, Moelling K, (2007) Heteromeric complex formation of ASK2 and ASK1 regulates stress-induced signaling. Biochemical and Biophysical Research Communications 362: 454–459 doi:10.1016/j.bbrc.2007.08.006
-
(2007)
Biochemical and Biophysical Research Communications
, vol.362
, pp. 454-459
-
-
Ortner, E.1
Moelling, K.2
-
34
-
-
0344437796
-
Increasing Prevalence of Helicobacter pylori Infection with Age: Continuous Risk of Infection in Adults Rather than Cohort Effect
-
van Zanten SJOV, Pollak PT, Best LM, Bezanson GS, Marrie T, (1994) Increasing Prevalence of Helicobacter pylori Infection with Age: Continuous Risk of Infection in Adults Rather than Cohort Effect. J Infect Dis 169: 434–437 doi:10.1093/infdis/169.2.434
-
(1994)
J Infect Dis
, vol.169
, pp. 434-437
-
-
Van Zanten, S.J.O.V.1
Pollak, P.T.2
Best, L.M.3
Bezanson, G.S.4
Marrie, T.5
-
35
-
-
43549096178
-
Helicobacter pylori infection in Canadian and related Arctic Aboriginal populations
-
Goodman KJ, Jacobson K, Veldhuyzen van Zanten S, (2008) Helicobacter pylori infection in Canadian and related Arctic Aboriginal populations. Can J Gastroenterol 22: 289–295.
-
(2008)
Can J Gastroenterol
, vol.22
, pp. 289-295
-
-
Goodman, K.J.1
Jacobson, K.2
Veldhuyzen Van Zanten, S.3
-
36
-
-
84881280396
-
Crystal structures of ASK1-inhibtor complexes provide a platform for structure-based drug design
-
Singh O, Shillings A, Craggs P, Wall I, Rowland P, et al. (2013) Crystal structures of ASK1-inhibtor complexes provide a platform for structure-based drug design. Protein Science 22: 1071–1077 doi:10.1002/pro.2298
-
(2013)
Protein Science
, vol.22
, pp. 1071-1077
-
-
Singh, O.1
Shillings, A.2
Craggs, P.3
Wall, I.4
Rowland, P.5
-
37
-
-
84880648928
-
-
Jin L, Li D, Lee JS, Elf S, Alesi GN, et al. (2013) p90 RSK2 Mediates Antianoikis Signals by both Transcription-Dependent and-Independent Mechanisms. … and cellular biology. doi:10.1128/MCB.01677-12
-
(2013)
p90 RSK2 Mediates Antianoikis Signals by both Transcription-Dependent and-Independent Mechanisms. … and cellular biology
-
-
Jin, L.1
Li, D.2
Lee, J.S.3
Elf, S.4
Alesi, G.N.5
-
38
-
-
84878427065
-
ER stress and ASK1-JNK activation contribute to oridonin-induced apoptosis and growth inhibition in cultured human hepatoblastoma HuH-6 cells
-
Cai D-T, Jin H, Xiong Q-X, Liu W-G, Gao Z-G, et al. (2013) ER stress and ASK1-JNK activation contribute to oridonin-induced apoptosis and growth inhibition in cultured human hepatoblastoma HuH-6 cells. Mol Cell Biochem 379: 161–169 doi:10.1007/s11010-013-1638-2
-
(2013)
Mol Cell Biochem
, vol.379
, pp. 161-169
-
-
Cai, D.-T.1
Jin, H.2
Xiong, Q.-X.3
Liu, W.-G.4
Gao, Z.-G.5
-
40
-
-
8844250042
-
Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis
-
Huang Q, Shete S, Amos CI, (2004) Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis. Am J Hum Gen 75: 1106–1112 doi:10.1086/426000
-
(2004)
Am J Hum Gen
, vol.75
, pp. 1106-1112
-
-
Huang, Q.1
Shete, S.2
Amos, C.I.3
-
41
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MAR, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Gen 81: 559–575 doi:10.1086/519795
-
(2007)
Am J Hum Gen
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.R.5
-
42
-
-
0028301661
-
A class of tests for linkage using affected pedigree members
-
Whittemore AS, Halpern J, (1994) A class of tests for linkage using affected pedigree members. Biometrics 50: 118–127.
-
(1994)
Biometrics
, vol.50
, pp. 118-127
-
-
Whittemore, A.S.1
Halpern, J.2
-
43
-
-
0030728925
-
Allele-sharing models: LOD scores and accurate linkage tests
-
Kong A, Cox NJ, (1997) Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Gen 61: 1179–1188 doi:10.1086/301592
-
(1997)
Am J Hum Gen
, vol.61
, pp. 1179-1188
-
-
Kong, A.1
Cox, N.J.2
-
44
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
Altshuler DM, Gibbs RA, Peltonen L, Dermitzakis E, International HapMap 3 Consortium (2010) et al. (2010) Integrating common and rare genetic variation in diverse human populations. Nature 467: 52–58 doi:10.1038/nature09298
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
Altshuler, D.M.1
Gibbs, R.A.2
Peltonen, L.3
Dermitzakis, E.4
-
45
-
-
80052565471
-
-
Alfares A, Nunez LD, Al-Thihli K, Mitchell J, Melançon S, et al. (2011) Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype. 48: 602–605 doi:10.1136/jmedgenet-2011-100230
-
(2011)
Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype
, vol.48
, pp. 602-605
-
-
Alfares, A.1
Nunez, L.D.2
Al-Thihli, K.3
Mitchell, J.4
Melançon, S.5
-
46
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R, (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25: 1754–1760 doi:10.1093/bioinformatics/btp324
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
47
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, et al. (2010) The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Research 20: 1297–1303 doi:10.1101/gr.107524.110
-
(2010)
Genome Research
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
-
48
-
-
84862506964
-
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
-
Cingolani P, Platts A, Wang LL, Coon M, Nguyen T, et al. (2012) A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly (Austin) 6: 80–92 doi:10.4161/fly.19695
-
(2012)
Fly (Austin)
, vol.6
, pp. 80-92
-
-
Cingolani, P.1
Platts, A.2
Wang, L.L.3
Coon, M.4
Nguyen, T.5
-
49
-
-
84880800567
-
GEMINI: integrative exploration of genetic variation and genome annotations
-
Paila U, Kirchner R, Chapman BA, Quinlan AR, (2013) GEMINI: integrative exploration of genetic variation and genome annotations. PLoS Comput Biol 9: e1003153 doi:10.1371/journal.pcbi.1003153
-
(2013)
PLoS Comput Biol
, vol.9
, pp. e1003153
-
-
Paila, U.1
Kirchner, R.2
Chapman, B.A.3
Quinlan, A.R.4
-
50
-
-
0035173378
-
dbSNP: the NCBI database of genetic variation
-
Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, et al. (2001) dbSNP: the NCBI database of genetic variation. Nucleic Acids Res 29: 308–311 doi:10.1093/nar/29.1.308
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 308-311
-
-
Sherry, S.T.1
Ward, M.H.2
Kholodov, M.3
Baker, J.4
Phan, L.5
-
51
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
The 1000 Genomes Project Consortium (2010) A map of human genome variation from population-scale sequencing. Nature 467: 1061–1073 doi:10.1038/nature09534
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
52
-
-
25144496606
-
PMUT: a web-based tool for the annotation of pathological mutations on proteins
-
Ferrer-Costa C, Gelpí JL, Zamakola L, Parraga I, la Cruz de X, et al. (2005) PMUT: a web-based tool for the annotation of pathological mutations on proteins. Bioinformatics 21: 3176–3178 doi:10.1093/bioinformatics/bti486
-
(2005)
Bioinformatics
, vol.21
, pp. 3176-3178
-
-
Ferrer-Costa, C.1
Gelpí, J.L.2
Zamakola, L.3
Parraga, I.4
La Cruz De, X.5
-
53
-
-
84878799611
-
Predicting functional effect of human missense mutations using PolyPhen-2
-
Adzhubei I, Jordan DM, Sunyaev SR, (2013) Predicting functional effect of human missense mutations using PolyPhen-2. Curr Protoc Hum Genet Chapter 7: Unit7.20–7 doi:10.1002/0471142905.hg0720s76
-
(2013)
Curr Protoc Hum Genet Chapter
, vol.7
, pp. Unit7.20-7
-
-
Adzhubei, I.1
Jordan, D.M.2
Sunyaev, S.R.3
-
54
-
-
84867301515
-
-
Choi Y, Sims GE, Murphy S, Miller JR, Chan AP, (2012) Predicting the functional effect of amino acid substitutions and indels. 7: e46688 doi:10.1371/journal.pone.0046688
-
(2012)
Predicting the functional effect of amino acid substitutions and indels
, vol.7
, pp. e46688
-
-
Choi, Y.1
Sims, G.E.2
Murphy, S.3
Miller, J.R.4
Chan, A.P.5
-
55
-
-
77955151784
-
MutationTaster evaluates disease-causing potential of sequence alterations
-
Schwarz JM, Rödelsperger C, Schuelke M, Seelow D, (2010) MutationTaster evaluates disease-causing potential of sequence alterations. Nat Methods 7: 575–576 doi:10.1038/nmeth0810-575
-
(2010)
Nat Methods
, vol.7
, pp. 575-576
-
-
Schwarz, J.M.1
Rödelsperger, C.2
Schuelke, M.3
Seelow, D.4
-
56
-
-
84871578629
-
Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models
-
Shihab HA, Gough J, Cooper DN, Stenson PD, Barker GLA, et al. (2013) Predicting the Functional, Molecular, and Phenotypic Consequences of Amino Acid Substitutions using Hidden Markov Models. Hum Mutat 34: 57–65 doi:10.1002/humu.22225
-
(2013)
Hum Mutat
, vol.34
, pp. 57-65
-
-
Shihab, H.A.1
Gough, J.2
Cooper, D.N.3
Stenson, P.D.4
Barker, G.L.A.5
-
57
-
-
84878880551
-
Predicting the functional consequences of cancer-associated amino acid substitutions
-
Shihab HA, Gough J, Cooper DN, Day INM, Gaunt TR, (2013) Predicting the functional consequences of cancer-associated amino acid substitutions. Bioinformatics 29: 1504–1510 doi:10.1093/bioinformatics/btt182
-
(2013)
Bioinformatics
, vol.29
, pp. 1504-1510
-
-
Shihab, H.A.1
Gough, J.2
Cooper, D.N.3
Day, I.N.M.4
Gaunt, T.R.5
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