-
1
-
-
44349132708
-
Common and rare variants in multifactorial susceptibility to common diseases
-
Bodmer, W., & Bonilla, C. Common and rare variants in multifactorial susceptibility to common diseases. Nat. Genet. 40, 695-701 (2008
-
(2008)
Nat. Genet.
, vol.40
, pp. 695-701
-
-
Bodmer, W.1
Bonilla, C.2
-
2
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch, N., & Merikangas, K. The future of genetic studies of complex human diseases. Science 273, 1516-1517 (1996
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
3
-
-
84884892198
-
Distilling pathophysiology from complex disease genetics
-
Chakravarti, A., Clark, A.G., & Mootha, V.K. Distilling pathophysiology from complex disease genetics. Cell 155, 21-26 (2013
-
(2013)
Cell
, vol.155
, pp. 21-26
-
-
Chakravarti, A.1
Clark, A.G.2
Mootha, V.K.3
-
4
-
-
79958035893
-
Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses
-
Gilman, S.R. et al. Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron 70, 898-907 (2011
-
(2011)
Neuron
, vol.70
, pp. 898-907
-
-
Gilman, S.R.1
-
5
-
-
67651205715
-
Identifying relationships among genomic disease regions: Predicting genes at pathogenic snp associations and rare deletions
-
Raychaudhuri, S. et al. Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions. PLoS Genet. 5, e1000534 (2009
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000534
-
-
Raychaudhuri, S.1
-
6
-
-
79851502150
-
Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology
-
Rossin, E.J. et al. Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology. PLoS Genet. 7, e1001273 (2011
-
(2011)
PLoS Genet.
, vol.7
, pp. e1001273
-
-
Rossin, E.J.1
-
7
-
-
84890307080
-
Integrating gwass and human protein interaction networks identifies a gene subnetwork underlying alcohol dependence
-
Han, S. et al. Integrating GWASs and human protein interaction networks identifies a gene subnetwork underlying alcohol dependence. Am. J. Hum. Genet. 93, 1027-1034 (2013
-
(2013)
Am. J. Hum. Genet.
, vol.93
, pp. 1027-1034
-
-
Han, S.1
-
8
-
-
76749134818
-
Associating genes and protein complexes with disease via network propagation
-
Vanunu, O., Magger, O., Ruppin, E., Shlomi, T., & Sharan, R. Associating genes and protein complexes with disease via network propagation. PLoS Comput. Biol. 6, e1000641 (2010
-
(2010)
PLoS Comput. Biol.
, vol.6
, pp. e1000641
-
-
Vanunu, O.1
Magger, O.2
Ruppin, E.3
Shlomi, T.4
Sharan, R.5
-
9
-
-
84864376672
-
Hint high-quality protein interactomes and their applications in understanding human disease
-
Das, J., & Yu, H. HINT: high-quality protein interactomes and their applications in understanding human disease. BMC Syst. Biol. 6, 92 (2012
-
(2012)
BMC Syst. Biol.
, vol.6
, pp. 92
-
-
Das, J.1
Yu, H.2
-
10
-
-
58149305794
-
An empirical framework for binary interactome mapping
-
Venkatesan, K. et al. An empirical framework for binary interactome mapping. Nat. Methods 6, 83-90 (2009
-
(2009)
Nat. Methods
, vol.6
, pp. 83-90
-
-
Venkatesan, K.1
-
11
-
-
84911474471
-
A proteome-scale map of the human interactome network
-
Rolland, T. et al. A Proteome-scale map of the human interactome network. Cell 159, 1212-1226 (2014
-
(2014)
Cell
, vol.159
, pp. 1212-1226
-
-
Rolland, T.1
-
12
-
-
65949124249
-
Genomewide association studies-illuminating biologic pathways
-
Hirschhorn, J.N. Genomewide association studies-illuminating biologic pathways. N. Engl. J. Med. 360, 1699-1701 (2009
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 1699-1701
-
-
Hirschhorn, J.N.1
-
13
-
-
73149103718
-
Prioritizing gwas results: A review of statistical methods and recommendations for their application
-
Cantor, R.M., Lange, K., & Sinsheimer, J.S. Prioritizing GWAS results: a review of statistical methods and recommendations for their application. Am. J. Hum. Genet. 86, 6-22 (2010
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 6-22
-
-
Cantor, R.M.1
Lange, K.2
Sinsheimer, J.S.3
-
14
-
-
9444239213
-
A probabilistic functional network of yeast genes
-
Lee, I., Date, S.V., Adai, A.T., & Marcotte, E.M. A probabilistic functional network of yeast genes. Science 306, 1555-1558 (2004
-
(2004)
Science
, vol.306
, pp. 1555-1558
-
-
Lee, I.1
Date, S.V.2
Adai, A.T.3
Marcotte, E.M.4
-
15
-
-
77957242540
-
It's the machine that matters: Predicting gene function and phenotype from protein networks
-
Wang, P.I., & Marcotte, E.M. It's the machine that matters: predicting gene function and phenotype from protein networks. J. Proteomics 73, 2277-2289 (2010
-
(2010)
J. Proteomics
, vol.73
, pp. 2277-2289
-
-
Wang, P.I.1
Marcotte, E.M.2
-
16
-
-
80052394788
-
Systematic prediction of gene function in arabidopsis thaliana using a probabilistic functional gene network
-
Hwang, S., Rhee, S.Y., Marcotte, E.M., & Lee, I. Systematic prediction of gene function in Arabidopsis thaliana using a probabilistic functional gene network. Nat. Protoc. 6, 1429-1442 (2011
-
(2011)
Nat. Protoc.
, vol.6
, pp. 1429-1442
-
-
Hwang, S.1
Rhee, S.Y.2
Marcotte, E.M.3
Lee, I.4
-
17
-
-
47549116997
-
A critical assessment of mus musculus gene function prediction using integrated genomic evidence
-
Peña-Castillo, L. et al. A critical assessment of Mus musculus gene function prediction using integrated genomic evidence. Genome Biol. 9 (suppl. 1), S2 (2008
-
(2008)
Genome Biol.
, vol.9
, pp. S2
-
-
Peña-Castillo, L.1
-
18
-
-
77954309042
-
Fast integration of heterogeneous data sources for predicting gene function with limited annotation
-
Mostafavi, S., & Morris, Q. Fast integration of heterogeneous data sources for predicting gene function with limited annotation. Bioinformatics 26, 1759-1765 (2010
-
(2010)
Bioinformatics
, vol.26
, pp. 1759-1765
-
-
Mostafavi, S.1
Morris, Q.2
-
19
-
-
84882860336
-
A resource of quantitative functional annotation for homo sapiens genes
-
Taşan, M. et al. A resource of quantitative functional annotation for Homo sapiens genes. G3 (Bethesda) 2, 223-233 (2012
-
(2012)
G3 (Bethesda)
, vol.2
, pp. 223-233
-
-
Taşan, M.1
-
20
-
-
66449120271
-
Exploring the human genome with functional maps
-
Huttenhower, C. et al. Exploring the human genome with functional maps. Genome Res. 19, 1093-1106 (2009
-
(2009)
Genome Res.
, vol.19
, pp. 1093-1106
-
-
Huttenhower, C.1
-
21
-
-
33646884801
-
Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes
-
Franke, L. et al. Reconstruction of a functional human gene network, with an application for prioritizing positional candidate genes. Am. J. Hum. Genet. 78, 1011-1025 (2006
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 1011-1025
-
-
Franke, L.1
-
22
-
-
79959898376
-
Prioritizing candidate disease genes by network-based boosting of genome-wide association data
-
Lee, I., Blom, U.M., Wang, P.I., Shim, J.E., & Marcotte, E.M. Prioritizing candidate disease genes by network-based boosting of genome-wide association data. Genome Res. 21, 1109-1121 (2011
-
(2011)
Genome Res.
, vol.21
, pp. 1109-1121
-
-
Lee, I.1
Blom, U.M.2
Wang, P.I.3
Shim, J.E.4
Marcotte, E.M.5
-
23
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff, L.A. et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl. Acad. Sci. USA 106, 9362-9367 (2009
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
-
24
-
-
77954269901
-
The genemania prediction server: Biological network integration for gene prioritization and predicting gene function
-
Warde-Farley, D. et al. The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function. Nucleic Acids Res. 38, W214-W220 (2010
-
(2010)
Nucleic Acids Res.
, vol.38
, pp. W214-W220
-
-
Warde-Farley, D.1
-
26
-
-
84885425093
-
Prognostication of oct4 isoform expression in prostate cancer
-
de Resende, M.F. et al. Prognostication of OCT4 isoform expression in prostate cancer. Tumour Biol. 34, 2665-2673 (2013
-
(2013)
Tumour Biol.
, vol.34
, pp. 2665-2673
-
-
De Resende, M.F.1
-
27
-
-
84876896778
-
Hnf1b is involved in prostate cancer risk via modulating androgenic hormone effects and coordination with other genes
-
Hu, Y.L. et al. HNF1b is involved in prostate cancer risk via modulating androgenic hormone effects and coordination with other genes. Genet. Mol. Res. 12, 1327-1335 (2013
-
(2013)
Genet. Mol. Res.
, vol.12
, pp. 1327-1335
-
-
Hu, Y.L.1
-
28
-
-
1542515338
-
A census of human cancer genes
-
Futreal, P.A. et al. A census of human cancer genes. Nat. Rev. Cancer 4, 177-183 (2004
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 177-183
-
-
Futreal, P.A.1
-
29
-
-
70449477656
-
Next generation software for functional trend analysis
-
Berriz, G.F., Beaver, J.E., Cenik, C., Tasan, M., & Roth, F.P. Next generation software for functional trend analysis. Bioinformatics 25, 3043-3044 (2009
-
(2009)
Bioinformatics
, vol.25
, pp. 3043-3044
-
-
Berriz, G.F.1
Beaver, J.E.2
Cenik, C.3
Tasan, M.4
Roth, F.P.5
-
30
-
-
36649036989
-
Enhanced paracrine fgf10 expression promotes formation of multifocal prostate adenocarcinoma and an increase in epithelial androgen receptor
-
Memarzadeh, S. et al. Enhanced paracrine FGF10 expression promotes formation of multifocal prostate adenocarcinoma and an increase in epithelial androgen receptor. Cancer Cell 12, 572-585 (2007
-
(2007)
Cancer Cell
, vol.12
, pp. 572-585
-
-
Memarzadeh, S.1
-
31
-
-
2342558431
-
Androgen receptor in prostate cancer
-
Heinlein, C.A., & Chang, C. Androgen receptor in prostate cancer. Endocr. Rev. 25, 276-308 (2004
-
(2004)
Endocr. Rev.
, vol.25
, pp. 276-308
-
-
Heinlein, C.A.1
Chang, C.2
-
32
-
-
0033561173
-
Roles for nkx3.1 in prostate development and cancer
-
Bhatia-Gaur, R. et al. Roles for Nkx3.1 in prostate development and cancer. Genes Dev. 13, 966-977 (1999
-
(1999)
Genes Dev.
, vol.13
, pp. 966-977
-
-
Bhatia-Gaur, R.1
-
33
-
-
78649330542
-
Androgen receptor as a therapeutic target
-
Gao, W. Androgen receptor as a therapeutic target. Adv. Drug Deliv. Rev. 62, 1277-1284 (2010
-
(2010)
Adv. Drug Deliv. Rev.
, vol.62
, pp. 1277-1284
-
-
Gao, W.1
-
34
-
-
84895057195
-
Fgf receptors: Cancer biology and therapeutics
-
Katoh, M., & Nakagama, H. FGF receptors: cancer biology and therapeutics. Med. Res. Rev. 34, 280-300 (2014
-
(2014)
Med. Res. Rev.
, vol.34
, pp. 280-300
-
-
Katoh, M.1
Nakagama, H.2
-
35
-
-
84885735554
-
Mutational landscape and significance across 12 major cancer types
-
Kandoth, C. et al. Mutational landscape and significance across 12 major cancer types. Nature 502, 333-339 (2013
-
(2013)
Nature
, vol.502
, pp. 333-339
-
-
Kandoth, C.1
-
36
-
-
1542272766
-
Predicting phenotype from patterns of annotation
-
King, O.D. et al. Predicting phenotype from patterns of annotation. Bioinformatics 19 (suppl. 1), i183-i189 (2003
-
(2003)
Bioinformatics
, vol.19
, pp. i183-i189
-
-
King, O.D.1
-
37
-
-
77955064853
-
A versatile gene-based test for genome-wide association studies
-
Liu, J.Z. et al. A versatile gene-based test for genome-wide association studies. Am. J. Hum. Genet. 87, 139-145 (2010
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 139-145
-
-
Liu, J.Z.1
-
38
-
-
48249158278
-
The implications of human metabolic network topology for disease comorbidity
-
Lee, D.-S. et al. The implications of human metabolic network topology for disease comorbidity. Proc. Natl. Acad. Sci. USA 105, 9880-9885 (2008
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, pp. 9880-9885
-
-
Lee, D.-S.1
-
39
-
-
84856532705
-
De novo discovery of mutated driver pathways in cancer
-
Vandin, F., Upfal, E., & Raphael, B.J. De novo discovery of mutated driver pathways in cancer. Genome Res. 22, 375-385 (2012
-
(2012)
Genome Res.
, vol.22
, pp. 375-385
-
-
Vandin, F.1
Upfal, E.2
Raphael, B.J.3
-
40
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio, T.A. et al. Finding the missing heritability of complex diseases. Nature 461, 747-753 (2009
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
-
41
-
-
58149189856
-
Mckusick's online mendelian inheritance in man (omim
-
Amberger, J., Bocchini, C.A., Scott, A.F., & Hamosh, A. McKusick's Online Mendelian Inheritance in Man (OMIM). Nucleic Acids Res. 37, D793-D796 (2009
-
(2009)
Nucleic Acids Res.
, vol.37
, pp. D793-D796
-
-
Amberger, J.1
Bocchini, C.A.2
Scott, A.F.3
Hamosh, A.4
-
42
-
-
84858602406
-
Interpro in 2011: New developments in the family and domain prediction database
-
Hunter, S. et al. InterPro in 2011: new developments in the family and domain prediction database. Nucleic Acids Res. 40, D306-D312 (2012
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. D306-D312
-
-
Hunter, S.1
-
43
-
-
0347755544
-
Rnaidb and phenoblast: Web tools for genome-wide phenotypic mapping projects
-
Gunsalus, K.C., Yueh, W.-C., MacMenamin, P., & Piano, F. RNAiDB and PhenoBlast: web tools for genome-wide phenotypic mapping projects. Nucleic Acids Res. 32, D406-D410 (2004
-
(2004)
Nucleic Acids Res.
, vol.32
, pp. D406-D410
-
-
Gunsalus, K.C.1
Yueh, W.-C.2
Macmenamin, P.3
Piano, F.4
-
44
-
-
84891771466
-
The ucsc genome browser database: 2014 update
-
Karolchik, D. et al. The UCSC Genome Browser database: 2014 update. Nucleic Acids Res. 42, D764-D770 (2014
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. D764-D770
-
-
Karolchik, D.1
-
45
-
-
75549086594
-
Inparanoid 7: New algorithms and tools for eukaryotic orthology analysis
-
Östlund, G. et al. InParanoid 7: new algorithms and tools for eukaryotic orthology analysis. Nucleic Acids Res. 38, D196-D203 (2010
-
(2010)
Nucleic Acids Res.
, vol.38
, pp. D196-D203
-
-
Östlund, G.1
-
46
-
-
11144358198
-
A gene atlas of the mouse and human protein-encoding transcriptomes
-
Su, A.I. et al. A gene atlas of the mouse and human protein-encoding transcriptomes. Proc. Natl. Acad. Sci. USA 101, 6062-6067 (2004
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 6062-6067
-
-
Su, A.I.1
-
47
-
-
0035478854
-
Random forests
-
Breiman, L. Random Forests. Mach. Learn. 45, 5-32 (2001
-
(2001)
Mach. Learn.
, vol.45
, pp. 5-32
-
-
Breiman, L.1
-
48
-
-
47549116753
-
An en masse phenotype and function prediction system for mus musculus
-
Taşan, M. et al. An en masse phenotype and function prediction system for Mus musculus. Genome Biol. 9 (suppl. 1), S8 (2008
-
(2008)
Genome Biol.
, vol.9
, pp. S8
-
-
Taşan, M.1
-
49
-
-
47549107689
-
Genemania a real-time multiple association network integration algorithm for predicting gene function
-
Mostafavi, S., Ray, D., Warde-Farley, D., Grouios, C., & Morris, Q. GeneMANIA: a real-time multiple association network integration algorithm for predicting gene function. Genome Biol. 9 (suppl. 1), S4 (2008
-
(2008)
Genome Biol.
, vol.9
, pp. S4
-
-
Mostafavi, S.1
Ray, D.2
Warde-Farley, D.3
Grouios, C.4
Morris, Q.5
-
50
-
-
84890453567
-
Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafish
-
Musso, G. et al. Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafish. Development 141, 224-235 (2014
-
(2014)
Development
, vol.141
, pp. 224-235
-
-
Musso, G.1
-
51
-
-
47549104748
-
Combining guilt-by-Association and guilt-by-profiling to predict saccharomyces cerevisiae gene function
-
Tian, W. et al. Combining guilt-by-Association and guilt-by-profiling to predict Saccharomyces cerevisiae gene function. Genome Biol. 9 (suppl. 1), S7 (2008
-
(2008)
Genome Biol.
, vol.9
, pp. S7
-
-
Tian, W.1
-
52
-
-
79959524146
-
A haplotype map of the human genome
-
The International HapMap Consortium
-
The International HapMap Consortium. A haplotype map of the human genome. Nature 437, 1299-1320 (2005
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
53
-
-
77957947562
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height
-
Lango Allen, H. et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467, 832-838 (2010
-
(2010)
Nature
, vol.467
, pp. 832-838
-
-
Lango Allen, H.1
-
54
-
-
4444357184
-
Beta regression for modelling rates and proportions
-
Ferrari, S., & Cribari-Neto, F. Beta regression for modelling rates and proportions. J. Appl. Stat. 31, 799-815 (2004
-
(2004)
J. Appl. Stat.
, vol.31
, pp. 799-815
-
-
Ferrari, S.1
Cribari-Neto, F.2
-
55
-
-
33646226097
-
Linkage disequilibrium in finite populations
-
Hill, W.G., & Robertson, A. Linkage disequilibrium in finite populations. Theor. Appl. Genet. 38, 226-231 (1968
-
(1968)
Theor. Appl. Genet.
, vol.38
, pp. 226-231
-
-
Hill, W.G.1
Robertson, A.2
-
56
-
-
0015070635
-
Linkage disequilibrium and homozygosity of chromosome segments in finite populations
-
Sved, J.A. Linkage disequilibrium and homozygosity of chromosome segments in finite populations. Theor. Popul. Biol. 2, 125-141 (1971
-
(1971)
Theor. Popul. Biol.
, vol.2
, pp. 125-141
-
-
Sved, J.A.1
-
57
-
-
84876515907
-
String v9.1: Protein-protein interaction networks, with increased coverage and integration
-
Franceschini, A. et al. STRING v9.1: protein-protein interaction networks, with increased coverage and integration. Nucleic Acids Res. 41, D808-D815 (2013
-
(2013)
Nucleic Acids Res.
, vol.41
, pp. D808-D815
-
-
Franceschini, A.1
-
58
-
-
77954143522
-
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
-
Voight, B.F. et al. Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat. Genet. 42, 579-589 (2010
-
(2010)
Nat. Genet.
, vol.42
, pp. 579-589
-
-
Voight, B.F.1
-
59
-
-
84893716900
-
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
-
THE SIGMA Type 2 Diabetes Consortium
-
THE SIGMA Type 2 Diabetes Consortium. Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico. Nature 506, 97-101 (2014
-
(2014)
Nature
, vol.506
, pp. 97-101
-
-
-
60
-
-
84890397941
-
Genome-wide association study identifies three novel loci for type 2 diabetes
-
Hara, K. et al. Genome-wide association study identifies three novel loci for type 2 diabetes. Hum. Mol. Genet. 23, 239-246 (2014
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 239-246
-
-
Hara, K.1
-
61
-
-
84871596296
-
Diabetes risk gene and wnt effector tcf7l2/tcf4 controls hepatic response to perinatal and adult metabolic demand
-
Boj, S.F. et al. Diabetes risk gene and Wnt effector Tcf7l2/TCF4 controls hepatic response to perinatal and adult metabolic demand. Cell 151, 1595-1607 (2012
-
(2012)
Cell
, vol.151
, pp. 1595-1607
-
-
Boj, S.F.1
-
62
-
-
80052527283
-
Alterations in tcf7l2 expression define its role as a key regulator of glucose metabolism
-
Savic, D. et al. Alterations in TCF7L2 expression define its role as a key regulator of glucose metabolism. Genome Res. 21, 1417-1425 (2011
-
(2011)
Genome Res.
, vol.21
, pp. 1417-1425
-
-
Savic, D.1
-
63
-
-
8344272048
-
Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1?
-
Bingham, C., & Hattersley, A.T. Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1?. Nephrol. Dial. Transplant. 19, 2703-2708 (2004
-
(2004)
Nephrol. Dial. Transplant.
, vol.19
, pp. 2703-2708
-
-
Bingham, C.1
Hattersley, A.T.2
-
64
-
-
44149120984
-
Molecular determinants of brown adipocyte formation and function
-
Farmer, S.R. Molecular determinants of brown adipocyte formation and function. Genes Dev. 22, 1269-1275 (2008
-
(2008)
Genes Dev.
, vol.22
, pp. 1269-1275
-
-
Farmer, S.R.1
-
65
-
-
84866076374
-
Leptin revisited: Its mechanism of action and potential for treating diabetes
-
Coppari, R., & Bjørbaek, C. Leptin revisited: its mechanism of action and potential for treating diabetes. Nat. Rev. Drug Discov. 11, 692-708 (2012
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 692-708
-
-
Coppari, R.1
Bjørbaek, C.2
-
66
-
-
84898914052
-
The diabetes gene hhex maintains ?-cell differentiation and islet function
-
Zhang, J., McKenna, L.B., Bogue, C.W., & Kaestner, K.H. The diabetes gene Hhex maintains ?-cell differentiation and islet function. Genes Dev. 28, 829-834 (2014
-
(2014)
Genes Dev.
, vol.28
, pp. 829-834
-
-
Zhang, J.1
McKenna, L.B.2
Bogue, C.W.3
Kaestner, K.H.4
-
67
-
-
77949507153
-
Rna-seq gene expression estimation with read mapping uncertainty
-
Li, B., Ruotti, V., Stewart, R.M., Thomson, J.A., & Dewey, C.N. RNA-Seq gene expression estimation with read mapping uncertainty. Bioinformatics 26, 493-500 (2010
-
(2010)
Bioinformatics
, vol.26
, pp. 493-500
-
-
Li, B.1
Ruotti, V.2
Stewart, R.M.3
Thomson, J.A.4
Dewey, C.N.5
-
68
-
-
75249087100
-
Edger: A bioconductor package for differential expression analysis of digital gene expression data
-
Robinson, M.D., McCarthy, D.J., & Smyth, G.K. edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics 26, 139-140 (2010
-
(2010)
Bioinformatics
, vol.26
, pp. 139-140
-
-
Robinson, M.D.1
McCarthy, D.J.2
Smyth, G.K.3
-
69
-
-
84961945798
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Benjamini, Y., & Hochberg, Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J. R. Stat. Soc. Series B Stat. Methodol. 57, 289-300 (1995
-
(1995)
J. R. Stat. Soc. Series B Stat. Methodol.
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
70
-
-
78651317908
-
Entrez gene: Gene-centered information at ncbi
-
Maglott, D., Ostell, J., Pruitt, K.D., & Tatusova, T. Entrez Gene: gene-centered information at NCBI. Nucleic Acids Res. 39, D52-D57 (2011).
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. D52-D57
-
-
Maglott, D.1
Ostell, J.2
Pruitt, K.D.3
Tatusova, T.4
|