-
1
-
-
41849136862
-
Biorepositories--at the bleeding edge
-
Manolio, T. A. Biorepositories--at the bleeding edge. Int J Epidemiol 37, 231–233 (2008).
-
(2008)
Int J Epidemiol
, vol.37
, pp. 231-233
-
-
Manolio, T.A.1
-
3
-
-
85012110172
-
INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES
-
Verma, A. et al. INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES. Pac Symp Biocomput 21, 168–179 (2016).
-
(2016)
Pac Symp Biocomput
, vol.21
, pp. 168-179
-
-
Verma, A.1
-
4
-
-
84927518293
-
Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis
-
Namjou, B. et al. Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis. Front Genet 5, (2014).
-
(2014)
Front Genet
, vol.5
-
-
Namjou, B.1
-
5
-
-
84928601920
-
Extracting research-quality phenotypes from electronic health records to support precision medicine
-
Wei, W.-Q. & Denny, J. C. Extracting research-quality phenotypes from electronic health records to support precision medicine. Genome Med 7, (2015).
-
(2015)
Genome Med
, vol.7
-
-
Wei, W.-Q.1
Denny, J.C.2
-
6
-
-
77958522275
-
A Genome-Wide Association Study of Red Blood Cell Traits Using the Electronic Medical Record
-
Kullo, I. J., Ding, K., Jouni, H., Smith, C. Y. & Chute, C. G. A Genome-Wide Association Study of Red Blood Cell Traits Using the Electronic Medical Record. PLoS One 5, (2010).
-
(2010)
Plos One
, vol.5
-
-
Kullo, I.J.1
Ding, K.2
Jouni, H.3
Smith, C.Y.4
Chute, C.G.5
-
7
-
-
84892389710
-
EMR-linked GWAS study: Investigation of variation landscape of loci for body mass index in children
-
Namjou, B. et al. EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. Front Genet 4, (2013).
-
(2013)
Front Genet
, vol.4
-
-
Namjou, B.1
-
8
-
-
71249132095
-
A multilevel linear mixed model of the association between candidate genes and weight and body mass index using the Framingham longitudinal family data
-
Luan, J. ’an et al. A multilevel linear mixed model of the association between candidate genes and weight and body mass index using the Framingham longitudinal family data. BMC Proc 3 Suppl 7, S115 (2009).
-
(2009)
BMC Proc
, vol.3
, pp. S115
-
-
Luan, J.1
-
9
-
-
84984945132
-
The Geisinger MyCode community health initiative: An electronic health record-linked biobank for precision medicine research
-
Carey, D. J. et al. The Geisinger MyCode community health initiative: an electronic health record-linked biobank for precision medicine research. Genet Med (2016). doi:10.1038/gim.2015.187
-
(2016)
Genet Med
-
-
Carey, D.J.1
-
10
-
-
79952742395
-
Finding unique filter sets in PLATO: A precursor to efficient interaction analysis in GWAS data
-
Grady, B. J. et al. Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data. Pac Symp Biocomput 315–326 (2010).
-
(2010)
Pac Symp Biocomput
, pp. 315-326
-
-
Grady, B.J.1
-
11
-
-
33749524440
-
Association between the UGT1A1*28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study
-
Lin, J.-P. et al. Association between the UGT1A1*28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study. Circulation 114, 1476–1481 (2006).
-
(2006)
Circulation
, vol.114
, pp. 1476-1481
-
-
Lin, J.-P.1
-
12
-
-
84864370842
-
UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. Neonatal hyperbilirubinemia: Is there an association?
-
de Azevedo, L. A. et al. UGT1A1, SLCO1B1, and SLCO1B3 polymorphisms vs. neonatal hyperbilirubinemia: is there an association? Pediatr Res 72, 169–173 (2012).
-
(2012)
Pediatr Res
, vol.72
, pp. 169-173
-
-
de Azevedo, L.A.1
-
13
-
-
77956154650
-
Genome-wide association of serum bilirubin levels in Korean population
-
Kang, T.-W. et al. Genome-wide association of serum bilirubin levels in Korean population. Hum. Mol. Genet. 19, 3672–3678 (2010).
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 3672-3678
-
-
Kang, T.-W.1
-
14
-
-
67649838598
-
Genome-wide association meta-analysis for total serum bilirubin levels
-
Johnson, A. D. et al. Genome-wide association meta-analysis for total serum bilirubin levels. Hum. Mol. Genet. 18, 2700–2710 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 2700-2710
-
-
Johnson, A.D.1
-
15
-
-
70350638919
-
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels
-
Chambers, J. C. et al. Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. Nat Genet 41, 1170–1172 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 1170-1172
-
-
Chambers, J.C.1
-
16
-
-
84871464519
-
Seventy-five genetic loci influencing the human red blood cell
-
van der Harst, P. et al. Seventy-five genetic loci influencing the human red blood cell. Nature 492, 369–375 (2012).
-
(2012)
Nature
, vol.492
, pp. 369-375
-
-
van der Harst, P.1
-
17
-
-
70350628958
-
Common variants in TMPRSS6 are associated with iron status and erythrocyte volume
-
Benyamin, B. et al. Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nat Genet 41, 1173–1175 (2009).
-
(2009)
Nat Genet
, vol.41
, pp. 1173-1175
-
-
Benyamin, B.1
-
18
-
-
84884957730
-
Genome-wide association study on serum alkaline phosphatase levels in a Chinese population
-
Li, J. et al. Genome-wide association study on serum alkaline phosphatase levels in a Chinese population. BMC Genomics 14, 684 (2013).
-
(2013)
BMC Genomics
, vol.14
, pp. 684
-
-
Li, J.1
-
19
-
-
84910112211
-
Genetics of calcium homeostasis in humans: Continuum between monogenic diseases and continuous phenotypes
-
Bonny, O. & Bochud, M. Genetics of calcium homeostasis in humans: continuum between monogenic diseases and continuous phenotypes. Nephrol. Dial. Transplant. 29, iv55–iv62 (2014).
-
(2014)
Nephrol. Dial. Transplant.
, vol.29
, pp. iv55-iv62
-
-
Bonny, O.1
Bochud, M.2
-
20
-
-
77957376468
-
Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene
-
Kapur, K. et al. Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene. PLOS Genet 6, e1001035 (2010).
-
(2010)
PLOS Genet
, vol.6
-
-
Kapur, K.1
-
21
-
-
78649468820
-
The genetics of type 2 diabetes: What have we learned from GWAS?
-
Billings, L. K. & Florez, J. C. The genetics of type 2 diabetes: what have we learned from GWAS? Ann N Y Acad Sci 1212, 59–77 (2010).
-
(2010)
Ann N Y Acad Sci
, vol.1212
, pp. 59-77
-
-
Billings, L.K.1
Florez, J.C.2
-
22
-
-
84885453095
-
Visualizing genomic information across chromosomes with PhenoGram
-
Wolfe, D., Dudek, S., Ritchie, M. D. & Pendergrass, S. A. Visualizing genomic information across chromosomes with PhenoGram. BioData Min 6, 18 (2013).
-
(2013)
Biodata Min
, vol.6
, pp. 18
-
-
Wolfe, D.1
Dudek, S.2
Ritchie, M.D.3
Pendergrass, S.A.4
-
23
-
-
53049090077
-
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes
-
Yuan, X. et al. Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. Am. J. Hum. Genet. 83, 520–528 (2008).
-
(2008)
Am. J. Hum. Genet.
, vol.83
, pp. 520-528
-
-
Yuan, X.1
-
24
-
-
84859224216
-
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans
-
Qayyum, R. et al. A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. PLoS Genet. 8, e1002491 (2012).
-
(2012)
Plos Genet
, vol.8
-
-
Qayyum, R.1
-
25
-
-
84978368209
-
A comparative study of serum aminotransferases in chronic kidney disease with and without end-stage renal disease: Need for new reference ranges
-
Ray, L., Nanda, S. K., Chatterjee, A., Sarangi, R. & Ganguly, S. A comparative study of serum aminotransferases in chronic kidney disease with and without end-stage renal disease: Need for new reference ranges. Int J Appl Basic Med Res 5, 31–35 (2015).
-
(2015)
Int J Appl Basic Med Res
, vol.5
, pp. 31-35
-
-
Ray, L.1
Nanda, S.K.2
Chatterjee, A.3
Sarangi, R.4
Ganguly, S.5
-
26
-
-
77957326576
-
Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones— Role of Age and Comorbid Diseases
-
Gudbjartsson, D. F. et al. Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones— Role of Age and Comorbid Diseases. PLOS Genet 6, e1001039 (2010).
-
(2010)
PLOS Genet
, vol.6
-
-
Gudbjartsson, D.F.1
-
27
-
-
84865653405
-
UMOD as a susceptibility gene for end-stage renal disease
-
Reznichenko, A. et al. UMOD as a susceptibility gene for end-stage renal disease. BMC Medical Genetics 13, 78 (2012).
-
(2012)
BMC Medical Genetics
, vol.13
, pp. 78
-
-
Reznichenko, A.1
-
28
-
-
79551587720
-
Cytoscape 2.8: New features for data integration and network visualization
-
Smoot, M. E., Ono, K., Ruscheinski, J., Wang, P.-L. & Ideker, T. Cytoscape 2.8: new features for data integration and network visualization. Bioinformatics 27, 431–432 (2011).
-
(2011)
Bioinformatics
, vol.27
, pp. 431-432
-
-
Smoot, M.E.1
Ono, K.2
Ruscheinski, J.3
Wang, P.-L.4
Ideker, T.5
-
29
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661–678 (2007).
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
30
-
-
34547702501
-
Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes
-
Lyssenko, V. et al. Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes. J. Clin. Invest. 117, 2155–2163 (2007).
-
(2007)
J. Clin. Invest.
, vol.117
, pp. 2155-2163
-
-
Lyssenko, V.1
-
31
-
-
77949425860
-
A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level
-
Pattaro, C. et al. A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. BMC Med. Genet. 11, 41 (2010).
-
(2010)
BMC Med. Genet
, vol.11
, pp. 41
-
-
Pattaro, C.1
-
32
-
-
84876430655
-
Correlation between Peripheral White Blood Cell Counts and Hyperglycemic Emergencies
-
Xu, W. et al. Correlation between Peripheral White Blood Cell Counts and Hyperglycemic Emergencies. Int J Med Sci 10, 758–765 (2013).
-
(2013)
Int J Med Sci
, vol.10
, pp. 758-765
-
-
Xu, W.1
-
33
-
-
84873841370
-
White Blood Cells Count and Incidence of Type 2 Diabetes in Young Men
-
Twig, G. et al. White Blood Cells Count and Incidence of Type 2 Diabetes in Young Men. Diabetes Care 36, 276–282 (2013).
-
(2013)
Diabetes Care
, vol.36
, pp. 276-282
-
-
Twig, G.1
-
34
-
-
36849012027
-
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
-
Nejentsev, S. et al. Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A. Nature 450, 887–892 (2007).
-
(2007)
Nature
, vol.450
, pp. 887-892
-
-
Nejentsev, S.1
-
35
-
-
0035863759
-
Type 1 Diabetes-Predisposing MHC Alleles Influence the Selection of Glutamic Acid Decarboxylase (GAD) 65-Specific T Cells in a Transgenic Model
-
Abraham, R. S., Wen, L., Marietta, E. V. & David, C. S. Type 1 Diabetes-Predisposing MHC Alleles Influence the Selection of Glutamic Acid Decarboxylase (GAD) 65-Specific T Cells in a Transgenic Model. J Immunol 166, 1370–1379 (2001).
-
(2001)
J Immunol
, vol.166
, pp. 1370-1379
-
-
Abraham, R.S.1
Wen, L.2
Marietta, E.V.3
David, C.S.4
|