-
1
-
-
34248205140
-
Pharmacological inhibition of glucosylceramide synthase enhances insulin sensitivity
-
J.M. Aerts, R. Ottenhoff, A.S. Powlson, A. Grefhorst, M. van Eijk, P.F. Dubbelhuis, J. Aten, F. Kuipers, M.J. Serlie, T. Wennekes, and et al. Pharmacological inhibition of glucosylceramide synthase enhances insulin sensitivity Diabetes 56 2007 1341 1349
-
(2007)
Diabetes
, vol.56
, pp. 1341-1349
-
-
Aerts, J.M.1
Ottenhoff, R.2
Powlson, A.S.3
Grefhorst, A.4
Van Eijk, M.5
Dubbelhuis, P.F.6
Aten, J.7
Kuipers, F.8
Serlie, M.J.9
Wennekes, T.10
-
2
-
-
79955589687
-
Genetic modifiers of liver injury in hereditary liver disease
-
A. Ala, and M. Schilsky Genetic modifiers of liver injury in hereditary liver disease Semin. Liver Dis. 31 2011 208 214
-
(2011)
Semin. Liver Dis.
, vol.31
, pp. 208-214
-
-
Ala, A.1
Schilsky, M.2
-
3
-
-
84906242439
-
Boolean modeling: A logic-based dynamic approach for understanding signaling and regulatory networks and for making useful predictions
-
R. Albert, and J. Thakar Boolean modeling: a logic-based dynamic approach for understanding signaling and regulatory networks and for making useful predictions Wiley Interdiscip. Rev. Syst. Biol. Med. 6 2014 353 369
-
(2014)
Wiley Interdiscip. Rev. Syst. Biol. Med.
, vol.6
, pp. 353-369
-
-
Albert, R.1
Thakar, J.2
-
4
-
-
84884530651
-
Characterization of variants in the glucosylceramide synthase gene and their association with type 1 Gaucher disease severity
-
P. Alfonso, J. Navascués, S. Navarro, P. Medina, A. Bolado-Carrancio, V. Andreu, P. Irún, J.C. Rodríguez-Rey, M. Pocoví, F. España, and P. Giraldo Characterization of variants in the glucosylceramide synthase gene and their association with type 1 Gaucher disease severity Hum. Mutat. 34 2013 1396 1403
-
(2013)
Hum. Mutat.
, vol.34
, pp. 1396-1403
-
-
Alfonso, P.1
Navascués, J.2
Navarro, S.3
Medina, P.4
Bolado-Carrancio, A.5
Andreu, V.6
Irún, P.7
Rodríguez-Rey, J.C.8
Pocoví, M.9
España, F.10
Giraldo, P.11
-
5
-
-
0034985656
-
Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: Identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency
-
B.S. Andresen, S.F. Dobrowolski, L. O'Reilly, J. Muenzer, S.E. McCandless, D.M. Frazier, S. Udvari, P. Bross, I. Knudsen, R. Banas, and et al. Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency Am. J. Hum. Genet. 68 2001 1408 1418
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1408-1418
-
-
Andresen, B.S.1
Dobrowolski, S.F.2
O'Reilly, L.3
Muenzer, J.4
McCandless, S.E.5
Frazier, D.M.6
Udvari, S.7
Bross, P.8
Knudsen, I.9
Banas, R.10
-
6
-
-
84866420982
-
Systems genetics of metabolism: The use of the BXD murine reference panel for multiscalar integration of traits
-
P.A. Andreux, E.G. Williams, H. Koutnikova, R.H. Houtkooper, M.F. Champy, H. Henry, K. Schoonjans, R.W. Williams, and J. Auwerx Systems genetics of metabolism: the use of the BXD murine reference panel for multiscalar integration of traits Cell 150 2012 1287 1299
-
(2012)
Cell
, vol.150
, pp. 1287-1299
-
-
Andreux, P.A.1
Williams, E.G.2
Koutnikova, H.3
Houtkooper, R.H.4
Champy, M.F.5
Henry, H.6
Schoonjans, K.7
Williams, R.W.8
Auwerx, J.9
-
7
-
-
33644877806
-
Mouse phenogenomics: The fast track to "systems metabolism"
-
C.A. Argmann, P. Chambon, and J. Auwerx Mouse phenogenomics: the fast track to "systems metabolism" Cell Metab. 2 2005 349 360
-
(2005)
Cell Metab.
, vol.2
, pp. 349-360
-
-
Argmann, C.A.1
Chambon, P.2
Auwerx, J.3
-
8
-
-
74249092870
-
Ppargamma2 is a key driver of longevity in the mouse
-
C. Argmann, R. Dobrin, S. Heikkinen, A. Auburtin, L. Pouilly, T.A. Cock, H. Koutnikova, J. Zhu, E.E. Schadt, and J. Auwerx Ppargamma2 is a key driver of longevity in the mouse PLoS Genet. 5 2009 e1000752
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000752
-
-
Argmann, C.1
Dobrin, R.2
Heikkinen, S.3
Auburtin, A.4
Pouilly, L.5
Cock, T.A.6
Koutnikova, H.7
Zhu, J.8
Schadt, E.E.9
Auwerx, J.10
-
9
-
-
80054746492
-
Exome sequencing as a tool for Mendelian disease gene discovery
-
M.J. Bamshad, S.B. Ng, A.W. Bigham, H.K. Tabor, M.J. Emond, D.A. Nickerson, and J. Shendure Exome sequencing as a tool for Mendelian disease gene discovery Nat. Rev. Genet. 12 2011 745 755
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 745-755
-
-
Bamshad, M.J.1
Ng, S.B.2
Bigham, A.W.3
Tabor, H.K.4
Emond, M.J.5
Nickerson, D.A.6
Shendure, J.7
-
10
-
-
84908256041
-
Gaucher disease: The metabolic defect, pathophysiology, phenotypes and natural history
-
H.N. Baris, I.J. Cohen, and P.K. Mistry Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history Pediatr. Endocrinol. Rev. 12 Suppl 1 2014 72 81
-
(2014)
Pediatr. Endocrinol. Rev.
, vol.12
, pp. 72-81
-
-
Baris, H.N.1
Cohen, I.J.2
Mistry, P.K.3
-
11
-
-
84887574376
-
Glucocerebrosidase mutations and the pathogenesis of Parkinson disease
-
M.S. Beavan, and A.H. Schapira Glucocerebrosidase mutations and the pathogenesis of Parkinson disease Ann. Med. 45 2013 511 521
-
(2013)
Ann. Med.
, vol.45
, pp. 511-521
-
-
Beavan, M.S.1
Schapira, A.H.2
-
12
-
-
84930211598
-
A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease
-
K. Bečanović, A. Nørremølle, S.J. Neal, C. Kay, J.A. Collins, D. Arenillas, T. Lilja, G. Gaudenzi, S. Manoharan, C.N. Doty, et al. REGISTRY Investigators of the European Huntington's Disease Network A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease Nat. Neurosci. 18 2015 807 816
-
(2015)
Nat. Neurosci.
, vol.18
, pp. 807-816
-
-
Bečanović, K.1
Nørremølle, A.2
Neal, S.J.3
Kay, C.4
Collins, J.A.5
Arenillas, D.6
Lilja, T.7
Gaudenzi, G.8
Manoharan, S.9
Doty, C.N.10
-
13
-
-
72949117677
-
Modulation of glycosphingolipid metabolism significantly improves hepatic insulin sensitivity and reverses hepatic steatosis in mice
-
N. Bijl, M. Sokolović, C. Vrins, M. Langeveld, P.D. Moerland, R. Ottenhoff, C.P. van Roomen, N. Claessen, R.G. Boot, J. Aten, and et al. Modulation of glycosphingolipid metabolism significantly improves hepatic insulin sensitivity and reverses hepatic steatosis in mice Hepatology 50 2009 1431 1441
-
(2009)
Hepatology
, vol.50
, pp. 1431-1441
-
-
Bijl, N.1
Sokolović, M.2
Vrins, C.3
Langeveld, M.4
Moerland, P.D.5
Ottenhoff, R.6
Van Roomen, C.P.7
Claessen, N.8
Boot, R.G.9
Aten, J.10
-
14
-
-
84884890589
-
A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk
-
D.R. Blair, C.S. Lyttle, J.M. Mortensen, C.F. Bearden, A.B. Jensen, H. Khiabanian, R. Melamed, R. Rabadan, E.V. Bernstam, S. Brunak, and et al. A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk Cell 155 2013 70 80
-
(2013)
Cell
, vol.155
, pp. 70-80
-
-
Blair, D.R.1
Lyttle, C.S.2
Mortensen, J.M.3
Bearden, C.F.4
Jensen, A.B.5
Khiabanian, H.6
Melamed, R.7
Rabadan, R.8
Bernstam, E.V.9
Brunak, S.10
-
15
-
-
84892788440
-
Constraint-based models predict metabolic and associated cellular functions
-
A. Bordbar, J.M. Monk, Z.A. King, and B.O. Palsson Constraint-based models predict metabolic and associated cellular functions Nat. Rev. Genet. 15 2014 107 120
-
(2014)
Nat. Rev. Genet.
, vol.15
, pp. 107-120
-
-
Bordbar, A.1
Monk, J.M.2
King, Z.A.3
Palsson, B.O.4
-
16
-
-
0022549920
-
A receptor-mediated pathway for cholesterol homeostasis
-
M.S. Brown, and J.L. Goldstein A receptor-mediated pathway for cholesterol homeostasis Science 232 1986 34 47
-
(1986)
Science
, vol.232
, pp. 34-47
-
-
Brown, M.S.1
Goldstein, J.L.2
-
18
-
-
84971280514
-
Causal inference in biology networks with integrated belief propagation
-
R. Chang, J.R. Karr, and E.E. Schadt Causal inference in biology networks with integrated belief propagation Pac. Symp. Biocomput. 2015 359 370
-
(2015)
Pac. Symp. Biocomput.
, pp. 359-370
-
-
Chang, R.1
Karr, J.R.2
Schadt, E.E.3
-
19
-
-
40749105508
-
Variations in DNA elucidate molecular networks that cause disease
-
Y. Chen, J. Zhu, P.Y. Lum, X. Yang, S. Pinto, D.J. MacNeil, C. Zhang, J. Lamb, S. Edwards, S.K. Sieberts, and et al. Variations in DNA elucidate molecular networks that cause disease Nature 452 2008 429 435
-
(2008)
Nature
, vol.452
, pp. 429-435
-
-
Chen, Y.1
Zhu, J.2
Lum, P.Y.3
Yang, X.4
Pinto, S.5
MacNeil, D.J.6
Zhang, C.7
Lamb, J.8
Edwards, S.9
Sieberts, S.K.10
-
20
-
-
84890546613
-
Systems genetics approaches to understand complex traits
-
M. Civelek, and A.J. Lusis Systems genetics approaches to understand complex traits Nat. Rev. Genet. 15 2014 34 48
-
(2014)
Nat. Rev. Genet.
, vol.15
, pp. 34-48
-
-
Civelek, M.1
Lusis, A.J.2
-
21
-
-
78650404224
-
Modifier genes in Mendelian disorders: The example of cystic fibrosis
-
G.R. Cutting Modifier genes in Mendelian disorders: the example of cystic fibrosis Ann. N Y Acad. Sci. 1214 2010 57 69
-
(2010)
Ann. N y Acad. Sci.
, vol.1214
, pp. 57-69
-
-
Cutting, G.R.1
-
22
-
-
84862189804
-
Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration
-
B. Dehay, A. Ramirez, M. Martinez-Vicente, C. Perier, M.H. Canron, E. Doudnikoff, A. Vital, M. Vila, C. Klein, and E. Bezard Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration Proc. Natl. Acad. Sci. USA 109 2012 9611 9616
-
(2012)
Proc. Natl. Acad. Sci. USA
, vol.109
, pp. 9611-9616
-
-
Dehay, B.1
Ramirez, A.2
Martinez-Vicente, M.3
Perier, C.4
Canron, M.H.5
Doudnikoff, E.6
Vital, A.7
Vila, M.8
Klein, C.9
Bezard, E.10
-
23
-
-
0033799531
-
Modifier genes convert "simple" Mendelian disorders to complex traits
-
K.M. Dipple, and E.R. McCabe Modifier genes convert "simple" Mendelian disorders to complex traits Mol. Genet. Metab. 71 2000 43 50
-
(2000)
Mol. Genet. Metab.
, vol.71
, pp. 43-50
-
-
Dipple, K.M.1
McCabe, E.R.2
-
24
-
-
0033911995
-
Phenotypes of patients with "simple" Mendelian disorders are complex traits: Thresholds, modifiers, and systems dynamics
-
K.M. Dipple, and E.R. McCabe Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics Am. J. Hum. Genet. 66 2000 1729 1735
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 1729-1735
-
-
Dipple, K.M.1
McCabe, E.R.2
-
25
-
-
0034788710
-
Consequences of complexity within biological networks: Robustness and health, or vulnerability and disease
-
K.M. Dipple, J.K. Phelan, and E.R. McCabe Consequences of complexity within biological networks: robustness and health, or vulnerability and disease Mol. Genet. Metab. 74 2001 45 50
-
(2001)
Mol. Genet. Metab.
, vol.74
, pp. 45-50
-
-
Dipple, K.M.1
Phelan, J.K.2
McCabe, E.R.3
-
26
-
-
41349095280
-
Genetics of gene expression and its effect on disease
-
V. Emilsson, G. Thorleifsson, B. Zhang, A.S. Leonardson, F. Zink, J. Zhu, S. Carlson, A. Helgason, G.B. Walters, S. Gunnarsdottir, and et al. Genetics of gene expression and its effect on disease Nature 452 2008 423 428
-
(2008)
Nature
, vol.452
, pp. 423-428
-
-
Emilsson, V.1
Thorleifsson, G.2
Zhang, B.3
Leonardson, A.S.4
Zink, F.5
Zhu, J.6
Carlson, S.7
Helgason, A.8
Walters, G.B.9
Gunnarsdottir, S.10
-
27
-
-
84901610068
-
Translational genomics. Clues from the resilient
-
S.H. Friend, and E.E. Schadt Translational genomics. Clues from the resilient Science 344 2014 970 972
-
(2014)
Science
, vol.344
, pp. 970-972
-
-
Friend, S.H.1
Schadt, E.E.2
-
28
-
-
84907483796
-
Lysosomal stress in obese adipose tissue macrophages contributes to MITF-dependent Gpnmb induction
-
T.L. Gabriel, M.J. Tol, R. Ottenhof, C. van Roomen, J. Aten, N. Claessen, B. Hooibrink, B. de Weijer, M.J. Serlie, C. Argmann, and et al. Lysosomal stress in obese adipose tissue macrophages contributes to MITF-dependent Gpnmb induction Diabetes 63 2014 3310 3323
-
(2014)
Diabetes
, vol.63
, pp. 3310-3323
-
-
Gabriel, T.L.1
Tol, M.J.2
Ottenhof, R.3
Van Roomen, C.4
Aten, J.5
Claessen, N.6
Hooibrink, B.7
De Weijer, B.8
Serlie, M.J.9
Argmann, C.10
-
29
-
-
84862832272
-
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California
-
N.M. Gallant, K. Leydiker, H. Tang, L. Feuchtbaum, F. Lorey, R. Puckett, J.L. Deignan, J. Neidich, N. Dorrani, E. Chang, and et al. Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California Mol. Genet. Metab. 106 2012 55 61
-
(2012)
Mol. Genet. Metab.
, vol.106
, pp. 55-61
-
-
Gallant, N.M.1
Leydiker, K.2
Tang, H.3
Feuchtbaum, L.4
Lorey, F.5
Puckett, R.6
Deignan, J.L.7
Neidich, J.8
Dorrani, N.9
Chang, E.10
-
30
-
-
84904318867
-
Disease-modifying genes and monogenic disorders: Experience in cystic fibrosis
-
S. Gallati Disease-modifying genes and monogenic disorders: experience in cystic fibrosis Appl. Clin. Genet. 7 2014 133 146
-
(2014)
Appl. Clin. Genet.
, vol.7
, pp. 133-146
-
-
Gallati, S.1
-
31
-
-
0029790367
-
The incidence of alkaptonuria: A study in chemical individuality. 1902
-
A.E. Garrod The incidence of alkaptonuria: a study in chemical individuality. 1902 Mol. Med. 2 1996 274 282
-
(1996)
Mol. Med.
, vol.2
, pp. 274-282
-
-
Garrod, A.E.1
-
32
-
-
55749096378
-
Identifying modifier genes of monogenic disease: Strategies and difficulties
-
E. Génin, J. Feingold, and F. Clerget-Darpoux Identifying modifier genes of monogenic disease: strategies and difficulties Hum. Genet. 124 2008 357 368
-
(2008)
Hum. Genet.
, vol.124
, pp. 357-368
-
-
Génin, E.1
Feingold, J.2
Clerget-Darpoux, F.3
-
33
-
-
34547140875
-
The human disease network
-
K.I. Goh, M.E. Cusick, D. Valle, B. Childs, M. Vidal, and A.L. Barabási The human disease network Proc. Natl. Acad. Sci. USA 104 2007 8685 8690
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 8685-8690
-
-
Goh, K.I.1
Cusick, M.E.2
Valle, D.3
Childs, B.4
Vidal, M.5
Barabási, A.L.6
-
34
-
-
84929001104
-
Human genomics. the Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans
-
GTEx Consortium Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans Science 348 2015 648 660
-
(2015)
Science
, vol.348
, pp. 648-660
-
-
-
35
-
-
0000729228
-
The relative importance of principal and modifying genes in determining some human diseases
-
J. Haldane The relative importance of principal and modifying genes in determining some human diseases J. Genet. 41 1941 147 157
-
(1941)
J. Genet.
, vol.41
, pp. 147-157
-
-
Haldane, J.1
-
36
-
-
84887896439
-
Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects
-
S.M. Houten, H. Herrema, H. Te Brinke, S. Denis, J.P. Ruiter, T.H. van Dijk, C.A. Argmann, R. Ottenhoff, M. Müller, A.K. Groen, and et al. Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects Hum. Mol. Genet. 22 2013 5249 5261
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 5249-5261
-
-
Houten, S.M.1
Herrema, H.2
Te Brinke, H.3
Denis, S.4
Ruiter, J.P.5
Van Dijk, T.H.6
Argmann, C.A.7
Ottenhoff, R.8
Müller, M.9
Groen, A.K.10
-
37
-
-
84906836553
-
Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia
-
S.M. Houten, S. Denis, H. Te Brinke, A. Jongejan, A.H. van Kampen, E.J. Bradley, F. Baas, R.C. Hennekam, D.S. Millington, S.P. Young, and et al. Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia Hum. Mol. Genet. 23 2014 5009 5016
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 5009-5016
-
-
Houten, S.M.1
Denis, S.2
Te Brinke, H.3
Jongejan, A.4
Van Kampen, A.H.5
Bradley, E.J.6
Baas, F.7
Hennekam, R.C.8
Millington, D.S.9
Young, S.P.10
-
38
-
-
26244445000
-
The lysosomal cysteine proteases in MHC class II antigen presentation
-
L.C. Hsing, and A.Y. Rudensky The lysosomal cysteine proteases in MHC class II antigen presentation Immunol. Rev. 207 2005 229 241
-
(2005)
Immunol. Rev.
, vol.207
, pp. 229-241
-
-
Hsing, L.C.1
Rudensky, A.Y.2
-
39
-
-
84902096048
-
Development and applications of CRISPR-Cas9 for genome engineering
-
P.D. Hsu, E.S. Lander, and F. Zhang Development and applications of CRISPR-Cas9 for genome engineering Cell 157 2014 1262 1278
-
(2014)
Cell
, vol.157
, pp. 1262-1278
-
-
Hsu, P.D.1
Lander, E.S.2
Zhang, F.3
-
42
-
-
0142052944
-
A Bayesian networks approach for predicting protein-protein interactions from genomic data
-
R. Jansen, H. Yu, D. Greenbaum, Y. Kluger, N.J. Krogan, S. Chung, A. Emili, M. Snyder, J.F. Greenblatt, and M. Gerstein A Bayesian networks approach for predicting protein-protein interactions from genomic data Science 302 2003 449 453
-
(2003)
Science
, vol.302
, pp. 449-453
-
-
Jansen, R.1
Yu, H.2
Greenbaum, D.3
Kluger, Y.4
Krogan, N.J.5
Chung, S.6
Emili, A.7
Snyder, M.8
Greenblatt, J.F.9
Gerstein, M.10
-
43
-
-
84868336049
-
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
-
L. Jostins, S. Ripke, R.K. Weersma, R.H. Duerr, D.P. McGovern, K.Y. Hui, J.C. Lee, L.P. Schumm, Y. Sharma, C.A. Anderson, et al. International IBD Genetics Consortium (IIBDGC) Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease Nature 491 2012 119 124
-
(2012)
Nature
, vol.491
, pp. 119-124
-
-
Jostins, L.1
Ripke, S.2
Weersma, R.K.3
Duerr, R.H.4
McGovern, D.P.5
Hui, K.Y.6
Lee, J.C.7
Schumm, L.P.8
Sharma, Y.9
Anderson, C.A.10
-
44
-
-
0019869334
-
The molecular basis of dominance
-
H. Kacser, and J.A. Burns The molecular basis of dominance Genetics 97 1981 639 666
-
(1981)
Genetics
, vol.97
, pp. 639-666
-
-
Kacser, H.1
Burns, J.A.2
-
45
-
-
13044277575
-
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
-
D.M. Kurtz, P. Rinaldo, W.J. Rhead, L. Tian, D.S. Millington, J. Vockley, D.A. Hamm, A.E. Brix, J.R. Lindsey, C.A. Pinkert, and et al. Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation Proc. Natl. Acad. Sci. USA 95 1998 15592 15597
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 15592-15597
-
-
Kurtz, D.M.1
Rinaldo, P.2
Rhead, W.J.3
Tian, L.4
Millington, D.S.5
Vockley, J.6
Hamm, D.A.7
Brix, A.E.8
Lindsey, J.R.9
Pinkert, C.A.10
-
46
-
-
79960000200
-
Predictive genes in adjacent normal tissue are preferentially altered by sCNV during tumorigenesis in liver cancer and may rate limiting
-
J.R. Lamb, C. Zhang, T. Xie, K. Wang, B. Zhang, K. Hao, E. Chudin, H.B. Fraser, J. Millstein, M. Ferguson, and et al. Predictive genes in adjacent normal tissue are preferentially altered by sCNV during tumorigenesis in liver cancer and may rate limiting PLoS ONE 6 2011 e20090
-
(2011)
PLoS ONE
, vol.6
, pp. e20090
-
-
Lamb, J.R.1
Zhang, C.2
Xie, T.3
Wang, K.4
Zhang, B.5
Hao, K.6
Chudin, E.7
Fraser, H.B.8
Millstein, J.9
Ferguson, M.10
-
47
-
-
33646893457
-
Inborn errors of metabolism: The flux from Mendelian to complex diseases
-
B. Lanpher, N. Brunetti-Pierri, and B. Lee Inborn errors of metabolism: the flux from Mendelian to complex diseases Nat. Rev. Genet. 7 2006 449 460
-
(2006)
Nat. Rev. Genet.
, vol.7
, pp. 449-460
-
-
Lanpher, B.1
Brunetti-Pierri, N.2
Lee, B.3
-
48
-
-
84874104942
-
Maternal ABCA1 genotype is associated with severity of Smith-Lemli-Opitz syndrome and with viability of patients homozygous for null mutations
-
B. Lanthaler, E. Steichen-Gersdorf, B. Kollerits, J. Zschocke, and M. Witsch-Baumgartner Maternal ABCA1 genotype is associated with severity of Smith-Lemli-Opitz syndrome and with viability of patients homozygous for null mutations Eur. J. Hum. Genet. 21 2013 286 293
-
(2013)
Eur. J. Hum. Genet.
, vol.21
, pp. 286-293
-
-
Lanthaler, B.1
Steichen-Gersdorf, E.2
Kollerits, B.3
Zschocke, J.4
Witsch-Baumgartner, M.5
-
49
-
-
84923687677
-
Quantitative and logic modelling of molecular and gene networks
-
N. Le Novère Quantitative and logic modelling of molecular and gene networks Nat. Rev. Genet. 16 2015 146 158
-
(2015)
Nat. Rev. Genet.
, vol.16
, pp. 146-158
-
-
Le Novère, N.1
-
50
-
-
9444239213
-
A probabilistic functional network of yeast genes
-
I. Lee, S.V. Date, A.T. Adai, and E.M. Marcotte A probabilistic functional network of yeast genes Science 306 2004 1555 1558
-
(2004)
Science
, vol.306
, pp. 1555-1558
-
-
Lee, I.1
Date, S.V.2
Adai, A.T.3
Marcotte, E.M.4
-
51
-
-
84877135776
-
The search for genetic modifiers of disease severity in the β-hemoglobinopathies
-
G. Lettre The search for genetic modifiers of disease severity in the β-hemoglobinopathies Cold Spring Harb. Perspect. Med. 2 2012 10.1101/cshperspect.a015032
-
(2012)
Cold Spring Harb. Perspect. Med.
, vol.2
-
-
Lettre, G.1
-
52
-
-
84879121718
-
Targeted exome sequencing of suspected mitochondrial disorders
-
D.S. Lieber, S.E. Calvo, K. Shanahan, N.G. Slate, S. Liu, S.G. Hershman, N.B. Gold, B.A. Chapman, D.R. Thorburn, G.T. Berry, and et al. Targeted exome sequencing of suspected mitochondrial disorders Neurology 80 2013 1762 1770
-
(2013)
Neurology
, vol.80
, pp. 1762-1770
-
-
Lieber, D.S.1
Calvo, S.E.2
Shanahan, K.3
Slate, N.G.4
Liu, S.5
Hershman, S.G.6
Gold, N.B.7
Chapman, B.A.8
Thorburn, D.R.9
Berry, G.T.10
-
53
-
-
84861217290
-
Phenotype diversity in type 1 Gaucher disease: Discovering the genetic basis of Gaucher disease/hematologic malignancy phenotype by individual genome analysis
-
S.M. Lo, M. Choi, J. Liu, D. Jain, R.G. Boot, W.W. Kallemeijn, J.M. Aerts, F. Pashankar, G.M. Kupfer, S. Mane, and et al. Phenotype diversity in type 1 Gaucher disease: discovering the genetic basis of Gaucher disease/hematologic malignancy phenotype by individual genome analysis Blood 119 2012 4731 4740
-
(2012)
Blood
, vol.119
, pp. 4731-4740
-
-
Lo, S.M.1
Choi, M.2
Liu, J.3
Jain, D.4
Boot, R.G.5
Kallemeijn, W.W.6
Aerts, J.M.7
Pashankar, F.8
Kupfer, G.M.9
Mane, S.10
-
54
-
-
80053549439
-
Clan genomics and the complex architecture of human disease
-
J.R. Lupski, J.W. Belmont, E. Boerwinkle, and R.A. Gibbs Clan genomics and the complex architecture of human disease Cell 147 2011 32 43
-
(2011)
Cell
, vol.147
, pp. 32-43
-
-
Lupski, J.R.1
Belmont, J.W.2
Boerwinkle, E.3
Gibbs, R.A.4
-
55
-
-
84896739948
-
Single cell genomics: Advances and future perspectives
-
I.C. Macaulay, and T. Voet Single cell genomics: advances and future perspectives PLoS Genet. 10 2014 e1004126
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004126
-
-
Macaulay, I.C.1
Voet, T.2
-
56
-
-
31544470891
-
Targeted disruption of glycerol kinase gene in mice: Expression analysis in liver shows alterations in network partners related to glycerol kinase activity
-
N.K. MacLennan, L. Rahib, C. Shin, Z. Fang, S. Horvath, J. Dean, J.C. Liao, E.R. McCabe, and K.M. Dipple Targeted disruption of glycerol kinase gene in mice: expression analysis in liver shows alterations in network partners related to glycerol kinase activity Hum. Mol. Genet. 15 2006 405 415
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 405-415
-
-
MacLennan, N.K.1
Rahib, L.2
Shin, C.3
Fang, Z.4
Horvath, S.5
Dean, J.6
Liao, J.C.7
McCabe, E.R.8
Dipple, K.M.9
-
57
-
-
84882415756
-
Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia
-
I. Manoli, J.R. Sysol, L. Li, P. Houillier, C. Garone, C. Wang, P.M. Zerfas, K. Cusmano-Ozog, S. Young, N.S. Trivedi, and et al. Targeting proximal tubule mitochondrial dysfunction attenuates the renal disease of methylmalonic acidemia Proc. Natl. Acad. Sci. USA 110 2013 13552 13557
-
(2013)
Proc. Natl. Acad. Sci. USA
, vol.110
, pp. 13552-13557
-
-
Manoli, I.1
Sysol, J.R.2
Li, L.3
Houillier, P.4
Garone, C.5
Wang, C.6
Zerfas, P.M.7
Cusmano-Ozog, K.8
Young, S.9
Trivedi, N.S.10
-
58
-
-
84945462763
-
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism
-
M.J. Miller, A.D. Kennedy, A.D. Eckhart, L.C. Burrage, J.E. Wulff, L.A. Miller, M.V. Milburn, J.A. Ryals, A.L. Beaudet, Q. Sun, and et al. Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism J. Inherit. Metab. Dis. 38 2015 1029 1039
-
(2015)
J. Inherit. Metab. Dis.
, vol.38
, pp. 1029-1039
-
-
Miller, M.J.1
Kennedy, A.D.2
Eckhart, A.D.3
Burrage, L.C.4
Wulff, J.E.5
Miller, L.A.6
Milburn, M.V.7
Ryals, J.A.8
Beaudet, A.L.9
Sun, Q.10
-
59
-
-
0036399154
-
Pulmonary hypertension in type 1 Gaucher's disease: Genetic and epigenetic determinants of phenotype and response to therapy
-
P.K. Mistry, S. Sirrs, A. Chan, M.R. Pritzker, T.P. Duffy, M.E. Grace, D.P. Meeker, and M.E. Goldman Pulmonary hypertension in type 1 Gaucher's disease: genetic and epigenetic determinants of phenotype and response to therapy Mol. Genet. Metab. 77 2002 91 98
-
(2002)
Mol. Genet. Metab.
, vol.77
, pp. 91-98
-
-
Mistry, P.K.1
Sirrs, S.2
Chan, A.3
Pritzker, M.R.4
Duffy, T.P.5
Grace, M.E.6
Meeker, D.P.7
Goldman, M.E.8
-
60
-
-
78650614891
-
Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage
-
P.K. Mistry, J. Liu, M. Yang, T. Nottoli, J. McGrath, D. Jain, K. Zhang, J. Keutzer, W.L. Chuang, W.Z. Mehal, and et al. Glucocerebrosidase gene-deficient mouse recapitulates Gaucher disease displaying cellular and molecular dysregulation beyond the macrophage Proc. Natl. Acad. Sci. USA 107 2010 19473 19478
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 19473-19478
-
-
Mistry, P.K.1
Liu, J.2
Yang, M.3
Nottoli, T.4
McGrath, J.5
Jain, D.6
Zhang, K.7
Keutzer, J.8
Chuang, W.L.9
Mehal, W.Z.10
-
61
-
-
84875283093
-
Gaucher disease and malignancy: A model for cancer pathogenesis in an inborn error of metabolism
-
P.K. Mistry, T. Taddei, S. vom Dahl, and B.E. Rosenbloom Gaucher disease and malignancy: a model for cancer pathogenesis in an inborn error of metabolism Crit. Rev. Oncog. 18 2013 235 246
-
(2013)
Crit. Rev. Oncog.
, vol.18
, pp. 235-246
-
-
Mistry, P.K.1
Taddei, T.2
Vom Dahl, S.3
Rosenbloom, B.E.4
-
63
-
-
84866361701
-
Circuitry and dynamics of human transcription factor regulatory networks
-
S. Neph, A.B. Stergachis, A. Reynolds, R. Sandstrom, E. Borenstein, and J.A. Stamatoyannopoulos Circuitry and dynamics of human transcription factor regulatory networks Cell 150 2012 1274 1286
-
(2012)
Cell
, vol.150
, pp. 1274-1286
-
-
Neph, S.1
Stergachis, A.B.2
Reynolds, A.3
Sandstrom, R.4
Borenstein, E.5
Stamatoyannopoulos, J.A.6
-
64
-
-
84881604631
-
A genome-scale modeling approach to study inborn errors of liver metabolism: Toward an in silico patient
-
R. Pagliarini, and D. di Bernardo A genome-scale modeling approach to study inborn errors of liver metabolism: toward an in silico patient J. Comput. Biol. 20 2013 383 397
-
(2013)
J. Comput. Biol.
, vol.20
, pp. 383-397
-
-
Pagliarini, R.1
Di Bernardo, D.2
-
65
-
-
84952715180
-
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6
-
I. Ratbi, K.D. Falkenberg, M. Sommen, N. Al-Sheqaih, S. Guaoua, G. Vandeweyer, J.E. Urquhart, K.E. Chandler, S.G. Williams, N.A. Roberts, and et al. Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 Am. J. Hum. Genet. 97 2015 535 545
-
(2015)
Am. J. Hum. Genet.
, vol.97
, pp. 535-545
-
-
Ratbi, I.1
Falkenberg, K.D.2
Sommen, M.3
Al-Sheqaih, N.4
Guaoua, S.5
Vandeweyer, G.6
Urquhart, J.E.7
Chandler, K.E.8
Williams, S.G.9
Roberts, N.A.10
-
66
-
-
84925031191
-
Methods of integrating data to uncover genotype-phenotype interactions
-
M.D. Ritchie, E.R. Holzinger, R. Li, S.A. Pendergrass, and D. Kim Methods of integrating data to uncover genotype-phenotype interactions Nat. Rev. Genet. 16 2015 85 97
-
(2015)
Nat. Rev. Genet.
, vol.16
, pp. 85-97
-
-
Ritchie, M.D.1
Holzinger, E.R.2
Li, R.3
Pendergrass, S.A.4
Kim, D.5
-
68
-
-
70249134919
-
Molecular networks as sensors and drivers of common human diseases
-
E.E. Schadt Molecular networks as sensors and drivers of common human diseases Nature 461 2009 218 223
-
(2009)
Nature
, vol.461
, pp. 218-223
-
-
Schadt, E.E.1
-
69
-
-
22844446947
-
An integrative genomics approach to infer causal associations between gene expression and disease
-
E.E. Schadt, J. Lamb, X. Yang, J. Zhu, S. Edwards, D. Guhathakurta, S.K. Sieberts, S. Monks, M. Reitman, C. Zhang, and et al. An integrative genomics approach to infer causal associations between gene expression and disease Nat. Genet. 37 2005 710 717
-
(2005)
Nat. Genet.
, vol.37
, pp. 710-717
-
-
Schadt, E.E.1
Lamb, J.2
Yang, X.3
Zhu, J.4
Edwards, S.5
Guhathakurta, D.6
Sieberts, S.K.7
Monks, S.8
Reitman, M.9
Zhang, C.10
-
70
-
-
45149108420
-
Mapping the genetic architecture of gene expression in human liver
-
E.E. Schadt, C. Molony, E. Chudin, K. Hao, X. Yang, P.Y. Lum, A. Kasarskis, B. Zhang, S. Wang, C. Suver, and et al. Mapping the genetic architecture of gene expression in human liver PLoS Biol. 6 2008 e107
-
(2008)
PLoS Biol.
, vol.6
, pp. e107
-
-
Schadt, E.E.1
Molony, C.2
Chudin, E.3
Hao, K.4
Yang, X.5
Lum, P.Y.6
Kasarskis, A.7
Zhang, B.8
Wang, S.9
Suver, C.10
-
71
-
-
84921718446
-
Evolving toward a human-cell based and multiscale approach to drug discovery for CNS disorders
-
E.E. Schadt, S. Buchanan, K.J. Brennand, and K.M. Merchant Evolving toward a human-cell based and multiscale approach to drug discovery for CNS disorders Front. Pharmacol. 5 2014 252
-
(2014)
Front. Pharmacol.
, vol.5
, pp. 252
-
-
Schadt, E.E.1
Buchanan, S.2
Brennand, K.J.3
Merchant, K.M.4
-
72
-
-
0037639877
-
Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: Results, outcome, and implications
-
A. Schulze, M. Lindner, D. Kohlmüller, K. Olgemöller, E. Mayatepek, and G.F. Hoffmann Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implications Pediatrics 111 2003 1399 1406
-
(2003)
Pediatrics
, vol.111
, pp. 1399-1406
-
-
Schulze, A.1
Lindner, M.2
Kohlmüller, D.3
Olgemöller, K.4
Mayatepek, E.5
Hoffmann, G.F.6
-
73
-
-
0033168957
-
Monogenic traits are not simple: Lessons from phenylketonuria
-
C.R. Scriver, and P.J. Waters Monogenic traits are not simple: lessons from phenylketonuria Trends Genet. 15 1999 267 272
-
(1999)
Trends Genet.
, vol.15
, pp. 267-272
-
-
Scriver, C.R.1
Waters, P.J.2
-
74
-
-
84901686870
-
An atlas of genetic influences on human blood metabolites
-
S.Y. Shin, E.B. Fauman, A.K. Petersen, J. Krumsiek, R. Santos, J. Huang, M. Arnold, I. Erte, V. Forgetta, T.P. Yang, et al. Multiple Tissue Human Expression Resource (MuTHER) Consortium An atlas of genetic influences on human blood metabolites Nat. Genet. 46 2014 543 550
-
(2014)
Nat. Genet.
, vol.46
, pp. 543-550
-
-
Shin, S.Y.1
Fauman, E.B.2
Petersen, A.K.3
Krumsiek, J.4
Santos, R.5
Huang, J.6
Arnold, M.7
Erte, I.8
Forgetta, V.9
Yang, T.P.10
-
75
-
-
66249132328
-
Predicting metabolic biomarkers of human inborn errors of metabolism
-
T. Shlomi, M.N. Cabili, and E. Ruppin Predicting metabolic biomarkers of human inborn errors of metabolism Mol. Syst. Biol. 5 2009 263
-
(2009)
Mol. Syst. Biol.
, vol.5
, pp. 263
-
-
Shlomi, T.1
Cabili, M.N.2
Ruppin, E.3
-
76
-
-
34548427938
-
Moving toward a system genetics view of disease
-
S.K. Sieberts, and E.E. Schadt Moving toward a system genetics view of disease Mamm. Genome 18 2007 389 401
-
(2007)
Mamm. Genome
, vol.18
, pp. 389-401
-
-
Sieberts, S.K.1
Schadt, E.E.2
-
77
-
-
0042266280
-
Minimum birth prevalence of mitochondrial respiratory chain disorders in children
-
D. Skladal, J. Halliday, and D.R. Thorburn Minimum birth prevalence of mitochondrial respiratory chain disorders in children Brain 126 2003 1905 1912
-
(2003)
Brain
, vol.126
, pp. 1905-1912
-
-
Skladal, D.1
Halliday, J.2
Thorburn, D.R.3
-
78
-
-
25144498379
-
A human protein-protein interaction network: A resource for annotating the proteome
-
U. Stelzl, U. Worm, M. Lalowski, C. Haenig, F.H. Brembeck, H. Goehler, M. Stroedicke, M. Zenkner, A. Schoenherr, S. Koeppen, and et al. A human protein-protein interaction network: a resource for annotating the proteome Cell 122 2005 957 968
-
(2005)
Cell
, vol.122
, pp. 957-968
-
-
Stelzl, U.1
Worm, U.2
Lalowski, M.3
Haenig, C.4
Brembeck, F.H.5
Goehler, H.6
Stroedicke, M.7
Zenkner, M.8
Schoenherr, A.9
Koeppen, S.10
-
79
-
-
84877315835
-
A community-driven global reconstruction of human metabolism
-
I. Thiele, N. Swainston, R.M. Fleming, A. Hoppe, S. Sahoo, M.K. Aurich, H. Haraldsdottir, M.L. Mo, O. Rolfsson, M.D. Stobbe, and et al. A community-driven global reconstruction of human metabolism Nat. Biotechnol. 31 2013 419 425
-
(2013)
Nat. Biotechnol.
, vol.31
, pp. 419-425
-
-
Thiele, I.1
Swainston, N.2
Fleming, R.M.3
Hoppe, A.4
Sahoo, S.5
Aurich, M.K.6
Haraldsdottir, H.7
Mo, M.L.8
Rolfsson, O.9
Stobbe, M.D.10
-
80
-
-
79960888804
-
Inferring causal genomic alterations in breast cancer using gene expression data
-
L.M. Tran, B. Zhang, Z. Zhang, C. Zhang, T. Xie, J.R. Lamb, H. Dai, E.E. Schadt, and J. Zhu Inferring causal genomic alterations in breast cancer using gene expression data BMC Syst. Biol. 5 2011 121
-
(2011)
BMC Syst. Biol.
, vol.5
, pp. 121
-
-
Tran, L.M.1
Zhang, B.2
Zhang, Z.3
Zhang, C.4
Xie, T.5
Lamb, J.R.6
Dai, H.7
Schadt, E.E.8
Zhu, J.9
-
81
-
-
84939839714
-
Inborn Errors of Metabolism: Advances in Diagnosis and Therapy
-
H.J. Vernon Inborn Errors of Metabolism: Advances in Diagnosis and Therapy JAMA Pediatr. 169 2015 778 782
-
(2015)
JAMA Pediatr.
, vol.169
, pp. 778-782
-
-
Vernon, H.J.1
-
82
-
-
84864208657
-
Systems analysis of eleven rodent disease models reveals an inflammatome signature and key drivers
-
I.M. Wang, B. Zhang, X. Yang, J. Zhu, S. Stepaniants, C. Zhang, Q. Meng, M. Peters, Y. He, C. Ni, and et al. Systems analysis of eleven rodent disease models reveals an inflammatome signature and key drivers Mol. Syst. Biol. 8 2012 594
-
(2012)
Mol. Syst. Biol.
, vol.8
, pp. 594
-
-
Wang, I.M.1
Zhang, B.2
Yang, X.3
Zhu, J.4
Stepaniants, S.5
Zhang, C.6
Meng, Q.7
Peters, M.8
He, Y.9
Ni, C.10
-
83
-
-
84902087268
-
Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies
-
G. Wang, M.L. McCain, L. Yang, A. He, F.S. Pasqualini, A. Agarwal, H. Yuan, D. Jiang, D. Zhang, L. Zangi, and et al. Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies Nat. Med. 20 2014 616 623
-
(2014)
Nat. Med.
, vol.20
, pp. 616-623
-
-
Wang, G.1
McCain, M.L.2
Yang, L.3
He, A.4
Pasqualini, F.S.5
Agarwal, A.6
Yuan, H.7
Jiang, D.8
Zhang, D.9
Zangi, L.10
-
85
-
-
0037685217
-
Screening newborns for inborn errors of metabolism by tandem mass spectrometry
-
B. Wilcken, V. Wiley, J. Hammond, and K. Carpenter Screening newborns for inborn errors of metabolism by tandem mass spectrometry N. Engl. J. Med. 348 2003 2304 2312
-
(2003)
N. Engl. J. Med.
, vol.348
, pp. 2304-2312
-
-
Wilcken, B.1
Wiley, V.2
Hammond, J.3
Carpenter, K.4
-
86
-
-
84862979366
-
Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness
-
S.B. Wortmann, F.M. Vaz, T. Gardeitchik, L.E. Vissers, G.H. Renkema, J.H. Schuurs-Hoeijmakers, W. Kulik, M. Lammens, C. Christin, L.A. Kluijtmans, and et al. Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness Nat. Genet. 44 2012 797 802
-
(2012)
Nat. Genet.
, vol.44
, pp. 797-802
-
-
Wortmann, S.B.1
Vaz, F.M.2
Gardeitchik, T.3
Vissers, L.E.4
Renkema, G.H.5
Schuurs-Hoeijmakers, J.H.6
Kulik, W.7
Lammens, M.8
Christin, C.9
Kluijtmans, L.A.10
-
87
-
-
84908077262
-
Multilayered genetic and omics dissection of mitochondrial activity in a mouse reference population
-
Y. Wu, E.G. Williams, S. Dubuis, A. Mottis, V. Jovaisaite, S.M. Houten, C.A. Argmann, P. Faridi, W. Wolski, Z. Kutalik, and et al. Multilayered genetic and omics dissection of mitochondrial activity in a mouse reference population Cell 158 2014 1415 1430
-
(2014)
Cell
, vol.158
, pp. 1415-1430
-
-
Wu, Y.1
Williams, E.G.2
Dubuis, S.3
Mottis, A.4
Jovaisaite, V.5
Houten, S.M.6
Argmann, C.A.7
Faridi, P.8
Wolski, W.9
Kutalik, Z.10
-
88
-
-
84889663497
-
Obesity activates a program of lysosomal-dependent lipid metabolism in adipose tissue macrophages independently of classic activation
-
X. Xu, A. Grijalva, A. Skowronski, M. van Eijk, M.J. Serlie, and A.W. Ferrante Jr. Obesity activates a program of lysosomal-dependent lipid metabolism in adipose tissue macrophages independently of classic activation Cell Metab. 18 2013 816 830
-
(2013)
Cell Metab.
, vol.18
, pp. 816-830
-
-
Xu, X.1
Grijalva, A.2
Skowronski, A.3
Van Eijk, M.4
Serlie, M.J.5
Ferrante, A.W.6
-
89
-
-
33746681910
-
Tissue-specific expression and regulation of sexually dimorphic genes in mice
-
X. Yang, E.E. Schadt, S. Wang, H. Wang, A.P. Arnold, L. Ingram-Drake, T.A. Drake, and A.J. Lusis Tissue-specific expression and regulation of sexually dimorphic genes in mice Genome Res. 16 2006 995 1004
-
(2006)
Genome Res.
, vol.16
, pp. 995-1004
-
-
Yang, X.1
Schadt, E.E.2
Wang, S.3
Wang, H.4
Arnold, A.P.5
Ingram-Drake, L.6
Drake, T.A.7
Lusis, A.J.8
-
90
-
-
63449132586
-
Validation of candidate causal genes for obesity that affect shared metabolic pathways and networks
-
X. Yang, J.L. Deignan, H. Qi, J. Zhu, S. Qian, J. Zhong, G. Torosyan, S. Majid, B. Falkard, R.R. Kleinhanz, and et al. Validation of candidate causal genes for obesity that affect shared metabolic pathways and networks Nat. Genet. 41 2009 415 423
-
(2009)
Nat. Genet.
, vol.41
, pp. 415-423
-
-
Yang, X.1
Deignan, J.L.2
Qi, H.3
Zhu, J.4
Qian, S.5
Zhong, J.6
Torosyan, G.7
Majid, S.8
Falkard, B.9
Kleinhanz, R.R.10
-
91
-
-
68149132205
-
Late endosome/lysosome-localized Rab7b suppresses TLR9-initiated proinflammatory cytokine and type i IFN production in macrophages
-
M. Yao, X. Liu, D. Li, T. Chen, Z. Cai, and X. Cao Late endosome/lysosome-localized Rab7b suppresses TLR9-initiated proinflammatory cytokine and type I IFN production in macrophages J. Immunol. 183 2009 1751 1758
-
(2009)
J. Immunol.
, vol.183
, pp. 1751-1758
-
-
Yao, M.1
Liu, X.2
Li, D.3
Chen, T.4
Cai, Z.5
Cao, X.6
-
92
-
-
84924370678
-
Integrative analysis of DNA methylation and gene expression data identifies EPAS1 as a key regulator of COPD
-
S. Yoo, S. Takikawa, P. Geraghty, C. Argmann, J. Campbell, L. Lin, T. Huang, Z. Tu, R.F. Foronjy, A. Spira, and et al. Integrative analysis of DNA methylation and gene expression data identifies EPAS1 as a key regulator of COPD PLoS Genet. 11 2015 e1004898
-
(2015)
PLoS Genet.
, vol.11
, pp. e1004898
-
-
Yoo, S.1
Takikawa, S.2
Geraghty, P.3
Argmann, C.4
Campbell, J.5
Lin, L.6
Huang, T.7
Tu, Z.8
Foronjy, R.F.9
Spira, A.10
-
93
-
-
84862301385
-
Disease-drug pairs revealed by computational genomic connectivity mapping on GBA1 deficient, Gaucher disease mice
-
T. Yuen, J. Iqbal, L.L. Zhu, L. Sun, A. Lin, H. Zhao, J. Liu, P.K. Mistry, and M. Zaidi Disease-drug pairs revealed by computational genomic connectivity mapping on GBA1 deficient, Gaucher disease mice Biochem. Biophys. Res. Commun. 422 2012 573 577
-
(2012)
Biochem. Biophys. Res. Commun.
, vol.422
, pp. 573-577
-
-
Yuen, T.1
Iqbal, J.2
Zhu, L.L.3
Sun, L.4
Lin, A.5
Zhao, H.6
Liu, J.7
Mistry, P.K.8
Zaidi, M.9
-
94
-
-
84896289322
-
Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction
-
Z. Zhang, and M.J. Falk Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction Int. J. Biochem. Cell Biol. 50 2014 106 111
-
(2014)
Int. J. Biochem. Cell Biol.
, vol.50
, pp. 106-111
-
-
Zhang, Z.1
Falk, M.J.2
-
95
-
-
23944458138
-
A general framework for weighted gene co-expression network analysis
-
Published online August 12, 2005
-
B. Zhang, and S. Horvath A general framework for weighted gene co-expression network analysis Stat. Appl. Genet. Mol. Biol. 4 2005 Published online August 12, 2005
-
(2005)
Stat. Appl. Genet. Mol. Biol.
, vol.4
-
-
Zhang, B.1
Horvath, S.2
-
96
-
-
84862776523
-
Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation
-
C.K. Zhang, P.B. Stein, J. Liu, Z. Wang, R. Yang, J.H. Cho, P.K. Gregersen, J.M. Aerts, H. Zhao, G.M. Pastores, and P.K. Mistry Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation Am. J. Hematol. 87 2012 377 383
-
(2012)
Am. J. Hematol.
, vol.87
, pp. 377-383
-
-
Zhang, C.K.1
Stein, P.B.2
Liu, J.3
Wang, Z.4
Yang, R.5
Cho, J.H.6
Gregersen, P.K.7
Aerts, J.M.8
Zhao, H.9
Pastores, G.M.10
Mistry, P.K.11
-
97
-
-
84876907931
-
Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease
-
B. Zhang, C. Gaiteri, L.G. Bodea, Z. Wang, J. McElwee, A.A. Podtelezhnikov, C. Zhang, T. Xie, L. Tran, R. Dobrin, and et al. Integrated systems approach identifies genetic nodes and networks in late-onset Alzheimer's disease Cell 153 2013 707 720
-
(2013)
Cell
, vol.153
, pp. 707-720
-
-
Zhang, B.1
Gaiteri, C.2
Bodea, L.G.3
Wang, Z.4
McElwee, J.5
Podtelezhnikov, A.A.6
Zhang, C.7
Xie, T.8
Tran, L.9
Dobrin, R.10
-
98
-
-
84880850111
-
Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling network
-
Z. Zhang, M. Tsukikawa, M. Peng, E. Polyak, E. Nakamaru-Ogiso, J. Ostrovsky, S. McCormack, E. Place, C. Clarke, G. Reiner, and et al. Primary respiratory chain disease causes tissue-specific dysregulation of the global transcriptome and nutrient-sensing signaling network PLoS ONE 8 2013 e69282
-
(2013)
PLoS ONE
, vol.8
, pp. e69282
-
-
Zhang, Z.1
Tsukikawa, M.2
Peng, M.3
Polyak, E.4
Nakamaru-Ogiso, E.5
Ostrovsky, J.6
McCormack, S.7
Place, E.8
Clarke, C.9
Reiner, G.10
-
99
-
-
77950339092
-
Integrating pathway analysis and genetics of gene expression for genome-wide association studies
-
H. Zhong, X. Yang, L.M. Kaplan, C. Molony, and E.E. Schadt Integrating pathway analysis and genetics of gene expression for genome-wide association studies Am. J. Hum. Genet. 86 2010 581 591
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 581-591
-
-
Zhong, H.1
Yang, X.2
Kaplan, L.M.3
Molony, C.4
Schadt, E.E.5
-
100
-
-
3242806720
-
An integrative genomics approach to the reconstruction of gene networks in segregating populations
-
J. Zhu, P.Y. Lum, J. Lamb, D. GuhaThakurta, S.W. Edwards, R. Thieringer, J.P. Berger, M.S. Wu, J. Thompson, A.B. Sachs, and E.E. Schadt An integrative genomics approach to the reconstruction of gene networks in segregating populations Cytogenet. Genome Res. 105 2004 363 374
-
(2004)
Cytogenet. Genome Res.
, vol.105
, pp. 363-374
-
-
Zhu, J.1
Lum, P.Y.2
Lamb, J.3
GuhaThakurta, D.4
Edwards, S.W.5
Thieringer, R.6
Berger, J.P.7
Wu, M.S.8
Thompson, J.9
Sachs, A.B.10
Schadt, E.E.11
-
101
-
-
34247556038
-
Increasing the power to detect causal associations by combining genotypic and expression data in segregating populations
-
J. Zhu, M.C. Wiener, C. Zhang, A. Fridman, E. Minch, P.Y. Lum, J.R. Sachs, and E.E. Schadt Increasing the power to detect causal associations by combining genotypic and expression data in segregating populations PLoS Comput. Biol. 3 2007 e69
-
(2007)
PLoS Comput. Biol.
, vol.3
, pp. e69
-
-
Zhu, J.1
Wiener, M.C.2
Zhang, C.3
Fridman, A.4
Minch, E.5
Lum, P.Y.6
Sachs, J.R.7
Schadt, E.E.8
-
102
-
-
45149106353
-
Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks
-
J. Zhu, B. Zhang, E.N. Smith, B. Drees, R.B. Brem, L. Kruglyak, R.E. Bumgarner, and E.E. Schadt Integrating large-scale functional genomic data to dissect the complexity of yeast regulatory networks Nat. Genet. 40 2008 854 861
-
(2008)
Nat. Genet.
, vol.40
, pp. 854-861
-
-
Zhu, J.1
Zhang, B.2
Smith, E.N.3
Drees, B.4
Brem, R.B.5
Kruglyak, L.6
Bumgarner, R.E.7
Schadt, E.E.8
-
103
-
-
84859959092
-
Stitching together multiple data dimensions reveals interacting metabolomic and transcriptomic networks that modulate cell regulation
-
J. Zhu, P. Sova, Q. Xu, K.M. Dombek, E.Y. Xu, H. Vu, Z. Tu, R.B. Brem, R.E. Bumgarner, and E.E. Schadt Stitching together multiple data dimensions reveals interacting metabolomic and transcriptomic networks that modulate cell regulation PLoS Biol. 10 2012 e1001301
-
(2012)
PLoS Biol.
, vol.10
, pp. e1001301
-
-
Zhu, J.1
Sova, P.2
Xu, Q.3
Dombek, K.M.4
Xu, E.Y.5
Vu, H.6
Tu, Z.7
Brem, R.B.8
Bumgarner, R.E.9
Schadt, E.E.10
|