-
1
-
-
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
-
2
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard, J.K. Are rare variants responsible for susceptibility to complex diseases? Am. J. Hum. Genet. 69, 124-137 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
3
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol
-
Cohen, J.C. et al. Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science 305, 869-872 (2004).
-
(2004)
Science
, vol.305
, pp. 869-872
-
-
Cohen, J.C.1
-
4
-
-
84944358132
-
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
-
Yang, J. et al. Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index. Nat. Genet. 47, 1114-1120 (2015).
-
(2015)
Nat. Genet.
, vol.47
, pp. 1114-1120
-
-
Yang, J.1
-
5
-
-
84856405512
-
The mystery of missing heritability: Genetic interactions create phantom heritability
-
Zuk, O., Hechter, E., Sunyaev, S.R. & Lander, E.S. The mystery of missing heritability: Genetic interactions create phantom heritability. Proc. Natl. Acad. Sci. USA 109, 1193-1198 (2012).
-
(2012)
Proc. Natl. Acad. Sci. USA
, vol.109
, pp. 1193-1198
-
-
Zuk, O.1
Hechter, E.2
Sunyaev, S.R.3
Lander, E.S.4
-
6
-
-
0036912779
-
Variance components models for gene-environment interaction in twin analysis
-
Purcell, S. Variance components models for gene-environment interaction in twin analysis. Twin Res. 5, 554-571 (2002).
-
(2002)
Twin Res.
, vol.5
, pp. 554-571
-
-
Purcell, S.1
-
7
-
-
84867237275
-
Twins and the mystery of missing heritability: The contribution of gene-environment interactions
-
Kaprio, J. Twins and the mystery of missing heritability: the contribution of gene-environment interactions. J. Intern. Med. 272, 440-448 (2012).
-
(2012)
J. Intern. Med.
, vol.272
, pp. 440-448
-
-
Kaprio, J.1
-
8
-
-
84910134758
-
Missing heritability of common diseases and treatments outside the protein-coding exome
-
Sadee, W. et al. Missing heritability of common diseases and treatments outside the protein-coding exome. Hum. Genet. 133, 1199-1215 (2014).
-
(2014)
Hum. Genet.
, vol.133
, pp. 1199-1215
-
-
Sadee, W.1
-
9
-
-
79953174333
-
Genomics and drug response
-
Wang, L., McLeod, H.L. & Weinshilboum, R.M. Genomics and drug response. N. Engl. J. Med. 364, 1144-1153 (2011).
-
(2011)
N. Engl. J. Med.
, vol.364
, pp. 1144-1153
-
-
Wang, L.1
McLeod, H.L.2
Weinshilboum, R.M.3
-
10
-
-
16044373004
-
Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene
-
Samson, M. et al. Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene. Nature 382, 722-725 (1996).
-
(1996)
Nature
, vol.382
, pp. 722-725
-
-
Samson, M.1
-
11
-
-
84919332432
-
Interactions between ultraviolet light and MC1R and OCA2 variants are determinants of childhood nevus and freckle phenotypes
-
Baron, A.E. et al. Interactions between ultraviolet light and MC1R and OCA2 variants are determinants of childhood nevus and freckle phenotypes. Cancer Epidemiol. Biomarkers Prev. 23, 2829-2839 (2014).
-
(2014)
Cancer Epidemiol. Biomarkers Prev.
, vol.23
, pp. 2829-2839
-
-
Baron, A.E.1
-
12
-
-
85013838557
-
The importance of gene-environment interactions in human obesity
-
Reddon, H., Gueant, J.L. & Meyre, D. The importance of gene-environment interactions in human obesity. Clin. Sci. (Lond.) 130, 1571-1597 (2016).
-
(2016)
Clin. Sci. (Lond.)
, vol.130
, pp. 1571-1597
-
-
Reddon, H.1
Gueant, J.L.2
Meyre, D.3
-
13
-
-
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
-
14
-
-
0034969437
-
Are rare variants responsible for susceptibility to complex diseases?
-
Pritchard, J.K. Are rare variants responsible for susceptibility to complex diseases? Am. J. Hum. Genet. 69, 124-137 (2001).
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 124-137
-
-
Pritchard, J.K.1
-
15
-
-
3843056691
-
Multiple rare alleles contribute to low plasma levels of HDL cholesterol
-
Cohen, J.C. et al. Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science 305, 869-872 (2004).
-
(2004)
Science
, vol.305
, pp. 869-872
-
-
Cohen, J.C.1
-
16
-
-
84944358132
-
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
-
Yang, J. et al. Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index. Nat. Genet. 47, 1114-1120 (2015).
-
(2015)
Nat. Genet.
, vol.47
, pp. 1114-1120
-
-
Yang, J.1
-
17
-
-
84856405512
-
The mystery of missing heritability: Genetic interactions create phantom heritability
-
Zuk, O., Hechter, E., Sunyaev, S.R. & Lander, E.S. The mystery of missing heritability: Genetic interactions create phantom heritability. Proc. Natl. Acad. Sci. USA 109, 1193-1198 (2012).
-
(2012)
Proc. Natl. Acad. Sci. USA
, vol.109
, pp. 1193-1198
-
-
Zuk, O.1
Hechter, E.2
Sunyaev, S.R.3
Lander, E.S.4
-
18
-
-
0036912779
-
Variance components models for gene-environment interaction in twin analysis
-
Purcell, S. Variance components models for gene-environment interaction in twin analysis. Twin Res. 5, 554-571 (2002).
-
(2002)
Twin Res.
, vol.5
, pp. 554-571
-
-
Purcell, S.1
-
19
-
-
84867237275
-
Twins and the mystery of missing heritability: The contribution of gene-environment interactions
-
Kaprio, J. Twins and the mystery of missing heritability: the contribution of gene-environment interactions. J. Intern. Med. 272, 440-448 (2012).
-
(2012)
J. Intern. Med.
, vol.272
, pp. 440-448
-
-
Kaprio, J.1
-
20
-
-
84910134758
-
Missing heritability of common diseases and treatments outside the protein-coding exome
-
Sadee, W. et al. Missing heritability of common diseases and treatments outside the protein-coding exome. Hum. Genet. 133, 1199-1215 (2014).
-
(2014)
Hum. Genet.
, vol.133
, pp. 1199-1215
-
-
Sadee, W.1
-
21
-
-
79953174333
-
Genomics and drug response
-
Wang, L., McLeod, H.L. & Weinshilboum, R.M. Genomics and drug response. N. Engl. J. Med. 364, 1144-1153 (2011).
-
(2011)
N. Engl. J. Med.
, vol.364
, pp. 1144-1153
-
-
Wang, L.1
McLeod, H.L.2
Weinshilboum, R.M.3
-
22
-
-
16044373004
-
Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene
-
Samson, M. et al. Resistance to HIV-1 infection in Caucasian individuals bearing mutant alleles of the CCR-5 chemokine receptor gene. Nature 382, 722-725 (1996).
-
(1996)
Nature
, vol.382
, pp. 722-725
-
-
Samson, M.1
-
23
-
-
84919332432
-
Interactions between ultraviolet light and MC1R and OCA2 variants are determinants of childhood nevus and freckle phenotypes
-
Baron, A.E. et al. Interactions between ultraviolet light and MC1R and OCA2 variants are determinants of childhood nevus and freckle phenotypes. Cancer Epidemiol. Biomarkers Prev. 23, 2829-2839 (2014).
-
(2014)
Cancer Epidemiol. Biomarkers Prev.
, vol.23
, pp. 2829-2839
-
-
Baron, A.E.1
-
24
-
-
85013838557
-
The importance of gene-environment interactions in human obesity
-
Reddon, H., Gueant, J.L. & Meyre, D. The importance of gene-environment interactions in human obesity. Clin. Sci. (Lond.) 130, 1571-1597 (2016).
-
(2016)
Clin. Sci. (Lond.)
, vol.130
, pp. 1571-1597
-
-
Reddon, H.1
Gueant, J.L.2
Meyre, D.3
-
26
-
-
0019152816
-
Nonalcoholic steatohepatitis: Mayo Clinic experiences with a hitherto unnamed disease
-
Ludwig, J., Viggiano, T.R., McGill, D.B. & Oh, B.J. Nonalcoholic steatohepatitis: Mayo Clinic experiences with a hitherto unnamed disease. Mayo Clin. Proc. 55, 434-438 (1980).
-
(1980)
Mayo Clin. Proc.
, vol.55
, pp. 434-438
-
-
Ludwig, J.1
Viggiano, T.R.2
McGill, D.B.3
Oh, B.J.4
-
27
-
-
56749096610
-
Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease
-
Romeo, S. et al. Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nat. Genet. 40, 1461-1465 (2008).
-
(2008)
Nat. Genet.
, vol.40
, pp. 1461-1465
-
-
Romeo, S.1
-
28
-
-
84898058711
-
Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease
-
Kozlitina, J. et al. Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease. Nat. Genet. 46, 352-356 (2014).
-
(2014)
Nat. Genet.
, vol.46
, pp. 352-356
-
-
Kozlitina, J.1
-
29
-
-
84939168174
-
Hepatic de novo lipogenesis in obese youth is modulated by a common variant in the GCKR gene
-
Santoro, N. et al. Hepatic de novo lipogenesis in obese youth is modulated by a common variant in the GCKR gene. J. Clin. Endocrinol. Metab. 100, E1125-E1132 (2015).
-
(2015)
J. Clin. Endocrinol. Metab.
, vol.100
, pp. E1125-E1132
-
-
Santoro, N.1
-
30
-
-
79953745343
-
Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits
-
Speliotes, E.K. et al. Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genet. 7, e1001324 (2011).
-
(2011)
PLoS Genet.
, vol.7
, pp. e1001324
-
-
Speliotes, E.K.1
-
31
-
-
10644220306
-
Prevalence of hepatic steatosis in an urban population in the United States: Impact of ethnicity
-
Browning, J.D. et al. Prevalence of hepatic steatosis in an urban population in the United States: impact of ethnicity. Hepatology 40, 1387-1395 (2004).
-
(2004)
Hepatology
, vol.40
, pp. 1387-1395
-
-
Browning, J.D.1
-
33
-
-
0025959790
-
Effect modification and the limits of biological inference from epidemiologic data
-
Thompson, W.D. Effect modification and the limits of biological inference from epidemiologic data. J. Clin. Epidemiol. 44, 221-232 (1991).
-
(1991)
J. Clin. Epidemiol.
, vol.44
, pp. 221-232
-
-
Thompson, W.D.1
-
34
-
-
79955936872
-
Behavior of QQ-plots and genomic control in studies of gene-environment interaction
-
Voorman, A., Lumley, T., McKnight, B. & Rice, K. Behavior of QQ-plots and genomic control in studies of gene-environment interaction. PLoS One 6, e19416 (2011).
-
(2011)
PLoS One
, vol.6
, pp. e19416
-
-
Voorman, A.1
Lumley, T.2
McKnight, B.3
Rice, K.4
-
35
-
-
84856957313
-
Pathophysiology guided treatment of nonalcoholic steatohepatitis
-
Nguyen, T.A. & Sanyal, A.J. Pathophysiology guided treatment of nonalcoholic steatohepatitis. J. Gastroenterol. Hepatol. 27 (suppl. 2), 58-64 (2012).
-
(2012)
J. Gastroenterol. Hepatol.
, vol.27
, pp. 58-64
-
-
Nguyen, T.A.1
Sanyal, A.J.2
-
36
-
-
79959517565
-
Human fatty liver disease: Old questions and new insights
-
Cohen, J.C., Horton, J.D. & Hobbs, H.H. Human fatty liver disease: old questions and new insights. Science 332, 1519-1523 (2011).
-
(2011)
Science
, vol.332
, pp. 1519-1523
-
-
Cohen, J.C.1
Horton, J.D.2
Hobbs, H.H.3
-
37
-
-
78049337953
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
-
Speliotes, E.K. et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat. Genet. 42, 937-948 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 937-948
-
-
Speliotes, E.K.1
-
38
-
-
84964334172
-
The MBOAT7-TMC4 variant rs641738 increases risk of nonalcoholic fatty liver disease in individuals of European descent
-
Mancina, R.M. et al. The MBOAT7-TMC4 variant rs641738 increases risk of nonalcoholic fatty liver disease in individuals of European descent. Gastroenterology 150, 1219-1230 (2016).
-
(2016)
Gastroenterology
, vol.150
, pp. 1219-1230
-
-
Mancina, R.M.1
-
39
-
-
84920955177
-
Pnpla3I148M knockin mice accumulate PNPLA3 on lipid droplets and develop hepatic steatosis
-
Smagris, E. et al. Pnpla3I148M knockin mice accumulate PNPLA3 on lipid droplets and develop hepatic steatosis. Hepatology 61, 108-118 (2015).
-
(2015)
Hepatology
, vol.61
, pp. 108-118
-
-
Smagris, E.1
-
40
-
-
84856733126
-
Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk
-
Rees, M.G. et al. Cellular characterisation of the GCKR P446L variant associated with type 2 diabetes risk. Diabetologia 55, 114-122 (2012).
-
(2012)
Diabetologia
, vol.55
, pp. 114-122
-
-
Rees, M.G.1
-
41
-
-
77952409634
-
A feed-forward loop amplifies nutritional regulation of PNPLA3
-
Huang, Y. et al. A feed-forward loop amplifies nutritional regulation of PNPLA3. Proc. Natl. Acad. Sci. USA 107, 7892-7897 (2010).
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 7892-7897
-
-
Huang, Y.1
-
42
-
-
82255185907
-
Elevated glucose represses liver glucokinase and induces its regulatory protein to safeguard hepatic phosphate homeostasis
-
Arden, C. et al. Elevated glucose represses liver glucokinase and induces its regulatory protein to safeguard hepatic phosphate homeostasis. Diabetes 60, 3110-3120 (2011).
-
(2011)
Diabetes
, vol.60
, pp. 3110-3120
-
-
Arden, C.1
-
43
-
-
84969277864
-
Inactivation of Tm6sf2, a gene defective in fatty liver disease, impairs lipidation but not secretion of very low density lipoproteins
-
Smagris, E., Gilyard, S., BasuRay, S., Cohen, J.C. & Hobbs, H.H. Inactivation of Tm6sf2, a gene defective in fatty liver disease, impairs lipidation but not secretion of very low density lipoproteins. J. Biol. Chem. 291, 10659-10676 (2016).
-
(2016)
J. Biol. Chem.
, vol.291
, pp. 10659-10676
-
-
Smagris, E.1
Gilyard, S.2
BasuRay, S.3
Cohen, J.C.4
Hobbs, H.H.5
-
44
-
-
84875216097
-
PNPLA3 gene-by-visceral adipose tissue volume interaction and the pathogenesis of fatty liver disease: The NHLBI family heart study
-
Graff, M. et al. PNPLA3 gene-by-visceral adipose tissue volume interaction and the pathogenesis of fatty liver disease: the NHLBI family heart study. Int. J. Obes. (Lond.) 37, 432-438 (2013).
-
(2013)
Int. J. Obes. (Lond.)
, vol.37
, pp. 432-438
-
-
Graff, M.1
-
45
-
-
67749116239
-
Nonalcoholic fatty liver disease and low-carbohydrate diets
-
York, L.W., Puthalapattu, S. & Wu, G.Y. Nonalcoholic fatty liver disease and low-carbohydrate diets. Annu. Rev. Nutr. 29, 365-379 (2009).
-
(2009)
Annu. Rev. Nutr.
, vol.29
, pp. 365-379
-
-
York, L.W.1
Puthalapattu, S.2
Wu, G.Y.3
-
46
-
-
78651328101
-
Increased hepatic fat in overweight Hispanic youth influenced by interaction between genetic variation in PNPLA3 and high dietary carbohydrate and sugar consumption
-
Davis, J.N. et al. Increased hepatic fat in overweight Hispanic youth influenced by interaction between genetic variation in PNPLA3 and high dietary carbohydrate and sugar consumption. Am. J. Clin. Nutr. 92, 1522-1527 (2010).
-
(2010)
Am. J. Clin. Nutr.
, vol.92
, pp. 1522-1527
-
-
Davis, J.N.1
-
47
-
-
78650486196
-
Prevalence of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis among a largely middle-aged population utilizing ultrasound and liver biopsy: A prospective study
-
Williams, C.D. et al. Prevalence of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis among a largely middle-aged population utilizing ultrasound and liver biopsy: a prospective study. Gastroenterology 140, 124-131 (2011).
-
(2011)
Gastroenterology
, vol.140
, pp. 124-131
-
-
Williams, C.D.1
-
48
-
-
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
-
49
-
-
80055024880
-
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
-
Chambers, J.C. et al. Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Nat. Genet. 43, 1131-1138 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 1131-1138
-
-
Chambers, J.C.1
-
50
-
-
84876320981
-
Association of the I148M/PNPLA3 variant with elevated alanine transaminase levels in normal-weight and overweight/obese Mexican children
-
Larrieta-Carrasco, E. et al. Association of the I148M/PNPLA3 variant with elevated alanine transaminase levels in normal-weight and overweight/obese Mexican children. Gene 520, 185-188 (2013).
-
(2013)
Gene
, vol.520
, pp. 185-188
-
-
Larrieta-Carrasco, E.1
-
51
-
-
82155164171
-
The association of PNPLA3 variants with liver enzymes in childhood obesity is driven by the interaction with abdominal fat
-
Giudice, E.M. et al. The association of PNPLA3 variants with liver enzymes in childhood obesity is driven by the interaction with abdominal fat. PLoS One 6, e27933 (2011).
-
(2011)
PLoS One
, vol.6
, pp. e27933
-
-
Giudice, E.M.1
-
52
-
-
77949751643
-
Effect of body mass index and alcohol consumption on liver disease: Analysis of data from two prospective cohort studies
-
Hart, C.L., Morrison, D.S., Batty, G.D., Mitchell, R.J. & Davey Smith, G. Effect of body mass index and alcohol consumption on liver disease: analysis of data from two prospective cohort studies. Br. Med. J. 340, c1240 (2010).
-
(2010)
Br. Med. J.
, vol.340
, pp. c1240
-
-
Hart, C.L.1
Morrison, D.S.2
Batty, G.D.3
Mitchell, R.J.4
Davey Smith, G.5
-
53
-
-
73349111259
-
Variant in PNPLA3 is associated with alcoholic liver disease
-
Tian, C., Stokowski, R.P., Kershenobich, D., Ballinger, D.G. & Hinds, D.A. Variant in PNPLA3 is associated with alcoholic liver disease. Nat. Genet. 42, 21-23 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 21-23
-
-
Tian, C.1
Stokowski, R.P.2
Kershenobich, D.3
Ballinger, D.G.4
Hinds, D.A.5
-
54
-
-
84923171580
-
Genetic studies of body mass index yield new insights for obesity biology
-
Locke, A.E. et al. Genetic studies of body mass index yield new insights for obesity biology. Nature 518, 197-206 (2015).
-
(2015)
Nature
, vol.518
, pp. 197-206
-
-
Locke, A.E.1
-
55
-
-
80053907554
-
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
-
Ehret, G.B. et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 478, 103-109 (2011).
-
(2011)
Nature
, vol.478
, pp. 103-109
-
-
Ehret, G.B.1
-
56
-
-
75749086085
-
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
-
Dupuis, J. et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat. Genet. 42, 105-116 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 105-116
-
-
Dupuis, J.1
-
57
-
-
70349566593
-
Diabetes mellitus: A "thrifty" genotype rendered detrimental by "progress"?
-
Neel, J.V. Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"? Am. J. Hum. Genet. 14, 353-362 (1962).
-
(1962)
Am. J. Hum. Genet.
, vol.14
, pp. 353-362
-
-
Neel, J.V.1
-
58
-
-
77957941549
-
Patatin-like phospholipase domain-containing 3 and the pathogenesis and progression of pediatric nonalcoholic fatty liver disease
-
Browning, J.D., Cohen, J.C. & Hobbs, H.H. Patatin-like phospholipase domain-containing 3 and the pathogenesis and progression of pediatric nonalcoholic fatty liver disease. Hepatology 52, 1189-1192 (2010).
-
(2010)
Hepatology
, vol.52
, pp. 1189-1192
-
-
Browning, J.D.1
Cohen, J.C.2
Hobbs, H.H.3
-
59
-
-
12144259379
-
Magnetic resonance spectroscopy to measure hepatic triglyceride content: Prevalence of hepatic steatosis in the general population
-
Szczepaniak, L.S. et al. Magnetic resonance spectroscopy to measure hepatic triglyceride content: prevalence of hepatic steatosis in the general population. Am. J. Physiol. Endocrinol. Metab. 288, E462-E468 (2005).
-
(2005)
Am. J. Physiol. Endocrinol. Metab.
, vol.288
, pp. E462-E468
-
-
Szczepaniak, L.S.1
-
60
-
-
84901044369
-
The ABCG5/8 cholesterol transporter and myocardial infarction versus gallstone disease
-
Stender, S., Frikke-Schmidt, R., Nordestgaard, B.G. & Tybjaerg-Hansen, A. The ABCG5/8 cholesterol transporter and myocardial infarction versus gallstone disease. J. Am. Coll. Cardiol. 63, 2121-2128 (2014).
-
(2014)
J. Am. Coll. Cardiol.
, vol.63
, pp. 2121-2128
-
-
Stender, S.1
Frikke-Schmidt, R.2
Nordestgaard, B.G.3
Tybjaerg-Hansen, A.4
-
61
-
-
2942548997
-
The Dallas Heart Study: A population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health
-
Victor, R.G. et al. The Dallas Heart Study: a population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health. Am. J. Cardiol. 93, 1473-1480 (2004).
-
(2004)
Am. J. Cardiol.
, vol.93
, pp. 1473-1480
-
-
Victor, R.G.1
-
62
-
-
0030964350
-
Data quality of administratively collected hospital discharge data for liver cirrhosis epidemiology
-
Vestberg, K. et al. Data quality of administratively collected hospital discharge data for liver cirrhosis epidemiology. J. Med. Syst. 21, 11-20 (1997).
-
(1997)
J. Med. Syst.
, vol.21
, pp. 11-20
-
-
Vestberg, K.1
-
63
-
-
84957804874
-
A robust example of collider bias in a genetic association study
-
Day, F.R., Loh, P.R., Scott, R.A., Ong, K.K. & Perry, J.R. A robust example of collider bias in a genetic association study. Am. J. Hum. Genet. 98, 392-393 (2016).
-
(2016)
Am. J. Hum. Genet.
, vol.98
, pp. 392-393
-
-
Day, F.R.1
Loh, P.R.2
Scott, R.A.3
Ong, K.K.4
Perry, J.R.5
-
64
-
-
85031678782
-
A review of instrumental variable estimators for Mendelian randomization
-
Burgess, S., Small, D.S. & Thompson, S.G. A review of instrumental variable estimators for Mendelian randomization. Stat. Methods Med. Res. http://dx.doi.org/10.1177/0962280215597579 (2015).
-
(2015)
Stat. Methods Med. Res.
-
-
Burgess, S.1
Small, D.S.2
Thompson, S.G.3
|