-
1
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, et al. (2010) Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466: 707-713.
-
(2010)
Nature
, vol.466
, pp. 707-713
-
-
Teslovich, T.M.1
Musunuru, K.2
Smith, A.V.3
Edmondson, A.C.4
Stylianou, I.M.5
-
2
-
-
77952147434
-
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration
-
Chen W, Stambolian D, Edwards AO, Branham KE, Othman M, et al. (2010) Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Proc Natl Acad Sci U S A 07 (16): 7401-6.
-
(2010)
Proc Natl Acad Sci U S A
, vol.7
, Issue.16
, pp. 7401-7406
-
-
Chen, W.1
Stambolian, D.2
Edwards, A.O.3
Branham, K.E.4
Othman, M.5
-
3
-
-
67349199566
-
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
-
Barrett JC, Clayton DG, Concannon P, Akolkar B, Cooper JD, et al. (2009) Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. Nat Genet 41 (6): 703-7.
-
(2009)
Nat Genet
, vol.41
, Issue.6
, pp. 703-707
-
-
Barrett, J.C.1
Clayton, D.G.2
Concannon, P.3
Akolkar, B.4
Cooper, J.D.5
-
4
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, et al. (2009) Finding the missing heritability of complex diseases. Nature 461 (7265): 747-53.
-
(2009)
Nature
, vol.461
, Issue.7265
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
-
5
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, et al. (2008) Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet 40 (2): 161-169.
-
(2008)
Nat Genet
, vol.40
, Issue.2
, pp. 161-169
-
-
Willer, C.J.1
Sanna, S.2
Jackson, A.U.3
Scuteri, A.4
Bonnycastle, L.L.5
-
6
-
-
58149163149
-
Common variants at 30 loci contribute to polygenic dyslipidemia
-
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, et al. (2009) Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet 41 (1): 56-65.
-
(2009)
Nat Genet
, vol.41
, Issue.1
, pp. 56-65
-
-
Kathiresan, S.1
Willer, C.J.2
Peloso, G.M.3
Demissie, S.4
Musunuru, K.5
-
7
-
-
77952574849
-
Uncovering the roles of rare variants in common disease through whole-genome sequencing
-
Cirulli ET, Goldstein DB, (2010) Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat Rev Genet 11 (6): 415-25.
-
(2010)
Nat Rev Genet
, vol.11
, Issue.6
, pp. 415-425
-
-
Cirulli, E.T.1
Goldstein, D.B.2
-
8
-
-
33748039452
-
Heritability of cardiovascular and personality traits in 6,148 Sardinians
-
doi:10.1371/journal.pgen.0020132
-
Pilia G, Chen WM, Scuteri A, Orrú M, Albai G, et al. (2006) Heritability of cardiovascular and personality traits in 6,148 Sardinians. PLoS Genet 2: e132 doi:10.1371/journal.pgen.0020132.
-
(2006)
PLoS Genet
, vol.2
-
-
Pilia, G.1
Chen, W.M.2
Scuteri, A.3
Orrú, M.4
Albai, G.5
-
9
-
-
77955070766
-
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
-
Johansen CT, Wang J, Lanktree MB, Cao H, McIntyre AD, et al. (2010) Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. Nat Genet 42 (8): 684-7.
-
(2010)
Nat Genet
, vol.42
, Issue.8
, pp. 684-687
-
-
Johansen, C.T.1
Wang, J.2
Lanktree, M.B.3
Cao, H.4
McIntyre, A.D.5
-
10
-
-
70350231628
-
Genotype Imputation
-
Li Y, Willer C, Sanna S, Abecasis GR, (2009) Genotype Imputation. Annu Rev Genomics Hum Genet 10: 387-406.
-
(2009)
Annu Rev Genomics Hum Genet
, vol.10
, pp. 387-406
-
-
Li, Y.1
Willer, C.2
Sanna, S.3
Abecasis, G.R.4
-
11
-
-
77955499945
-
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus
-
Musunuru K, Strong A, Frank-Kamenetsky M, Lee NE, Ahfeldt T, et al. (2010) From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus. Nature 466 (7307): 714-9.
-
(2010)
Nature
, vol.466
, Issue.7307
, pp. 714-719
-
-
Musunuru, K.1
Strong, A.2
Frank-Kamenetsky, M.3
Lee, N.E.4
Ahfeldt, T.5
-
12
-
-
33645103550
-
Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
-
Cohen JC, Boerwinkle E, Mosley TH Jr, Hobbs HH, (2006) Sequence variations in PCSK9, low LDL, and protection against coronary heart disease. N Engl J Med 354 (12): 1264-72.
-
(2006)
N Engl J Med
, vol.354
, Issue.12
, pp. 1264-1272
-
-
Cohen, J.C.1
Boerwinkle, E.2
Mosley Jr., T.H.3
Hobbs, H.H.4
-
13
-
-
77953309816
-
PCSK9 R46L, low-density lipoprotein cholesterol levels, and risk of ischemic heart disease: 3 independent studies and meta-analyses
-
Benn MJ, Nordestgaard BG, Grande P, Schnohr P, Tybjaerg-Hansen A, (2010) PCSK9 R46L, low-density lipoprotein cholesterol levels, and risk of ischemic heart disease: 3 independent studies and meta-analyses. J Am Coll Cardiol 55 (25): 2833-42.
-
(2010)
J Am Coll Cardiol
, vol.55
, Issue.25
, pp. 2833-2842
-
-
Benn, M.J.1
Nordestgaard, B.G.2
Grande, P.3
Schnohr, P.4
Tybjaerg-Hansen, A.5
-
14
-
-
0028278865
-
Genotyping compared with protein phenotyping of the common apolipoprotein E polymorphism
-
Hansena PS, Gerdesa LU, Klausena IC, Gregersenb N, Faergeman O, (1994) Genotyping compared with protein phenotyping of the common apolipoprotein E polymorphism. Clin Chim Acta 224 (2): 131-7.
-
(1994)
Clin Chim Acta
, vol.224
, Issue.2
, pp. 131-137
-
-
Hansena, P.S.1
Gerdesa, L.U.2
Klausena, I.C.3
Gregersenb, N.4
Faergeman, O.5
-
15
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
-
Scott LJ, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, Duren WL, et al. (2007) A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 316: 1341-5.
-
(2007)
Science
, vol.316
, pp. 1341-1345
-
-
Scott, L.J.1
Mohlke, K.L.2
Bonnycastle, L.L.3
Willer, C.J.4
Li, Y.5
Duren, W.L.6
-
16
-
-
70349147046
-
Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men
-
Stancáková A, Kuulasmaa T, Paananen J, Jackson AU, Bonnycastle LL, et al. (2009) Association of 18 confirmed susceptibility loci for type 2 diabetes with indices of insulin release, proinsulin conversion, and insulin sensitivity in 5,327 nondiabetic Finnish men. Diabetes 58: 1212-21.
-
(2009)
Diabetes
, vol.58
, pp. 1212-1221
-
-
Stancáková, A.1
Kuulasmaa, T.2
Paananen, J.3
Jackson, A.U.4
Bonnycastle, L.L.5
-
17
-
-
0345713141
-
Rapid changes in the prevalence of obesity and known diabetes in an adult Norwegian population. The Nord-Trøndelag Health Surveys: 1984-1986 and 1995-1997
-
Midthjell K, Krüger O, Holmen J, Tverdal A, Claudi T, et al. (1999) Rapid changes in the prevalence of obesity and known diabetes in an adult Norwegian population. The Nord-Trøndelag Health Surveys: 1984-1986 and 1995-1997. Diabetes Care 22: 1813-20.
-
(1999)
Diabetes Care
, vol.22
, pp. 1813-1820
-
-
Midthjell, K.1
Krüger, O.2
Holmen, J.3
Tverdal, A.4
Claudi, T.5
-
18
-
-
1542327893
-
The Nord-Trondelag Health Study 1995-97 (HUNT 2): Objectives, contents, methods and participation
-
Holmen J, Midthjell K, Kruger O, Langhammer A, Lingaas Holmen T, et al. (2003) The Nord-Trondelag Health Study 1995-97 (HUNT 2): Objectives, contents, methods and participation. Norsk Epidemiol 13: 19-32.
-
(2003)
Norsk Epidemiol
, vol.13
, pp. 19-32
-
-
Holmen, J.1
Midthjell, K.2
Kruger, O.3
Langhammer, A.4
Lingaas Holmen, T.5
-
19
-
-
78649303807
-
Incidence of and risk factors for type-2 diabetes in a general population
-
Joseph J, Svartberg J, Njolstad I, Schirmer H, (2010) Incidence of and risk factors for type-2 diabetes in a general population. Scand j Public Health 38: 768-75.
-
(2010)
Scand J Public Health
, vol.38
, pp. 768-775
-
-
Joseph, J.1
Svartberg, J.2
Njolstad, I.3
Schirmer, H.4
-
20
-
-
78650969559
-
Analysis of 12,517 inhabitants of a Sardinian geographic isolate reveals that predispositions to thrombocytopenia and thrombocytosis are inherited traits
-
Biino G, Balduini CL, Casula L, Cavallo P, et al. (2011) Analysis of 12,517 inhabitants of a Sardinian geographic isolate reveals that predispositions to thrombocytopenia and thrombocytosis are inherited traits. Haematologica 96 (1): 96-101.
-
(2011)
Haematologica
, vol.96
, Issue.1
, pp. 96-101
-
-
Biino, G.1
Balduini, C.L.2
Casula, L.3
Cavallo, P.4
-
21
-
-
0019783892
-
Human E apoprotein heterogeneity. Cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms
-
Weisgraber KH, Rall SC Jr, Mahley RW, (1981) Human E apoprotein heterogeneity. Cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms. J Biol Chem 256 (17): 9077-83.
-
(1981)
J Biol Chem
, vol.256
, Issue.17
, pp. 9077-9083
-
-
Weisgraber, K.H.1
Rall Jr., S.C.2
Mahley, R.W.3
-
22
-
-
0021824223
-
J. Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variation
-
Sing CF, Davignon, (1985) J. Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variation. Am J Hum Genet 37: 268-85.
-
(1985)
Am J Hum Genet
, vol.37
, pp. 268-285
-
-
Sing, C.F.1
Davignon2
-
23
-
-
0033787023
-
Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene
-
Nickerson DA, Taylor SL, Fullerton SM, Weiss KM, Clark AG, et al. (2000) Sequence diversity and large-scale typing of SNPs in the human apolipoprotein E gene. Genome Res 10 (10): 1532-45.
-
(2000)
Genome Res
, vol.10
, Issue.10
, pp. 1532-1545
-
-
Nickerson, D.A.1
Taylor, S.L.2
Fullerton, S.M.3
Weiss, K.M.4
Clark, A.G.5
-
24
-
-
0036724353
-
Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism
-
Stengård JH, Clark AG, Weiss KM, Kardia S, Nickerson DA, et al. (2002) Contributions of 18 additional DNA sequence variations in the gene encoding apolipoprotein E to explaining variation in quantitative measures of lipid metabolism. Am J Hum Genet 71 (3): 501-517.
-
(2002)
Am J Hum Genet
, vol.71
, Issue.3
, pp. 501-517
-
-
Stengård, J.H.1
Clark, A.G.2
Weiss, K.M.3
Kardia, S.4
Nickerson, D.A.5
-
25
-
-
78649469071
-
Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation
-
Galarneau G, Palmer CD, Sankaran VG, Orkin SH, Hirschhorn JN, et al. (2011) Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation. Nat Genet 42: 1049-51.
-
(2011)
Nat Genet
, vol.42
, pp. 1049-1051
-
-
Galarneau, G.1
Palmer, C.D.2
Sankaran, V.G.3
Orkin, S.H.4
Hirschhorn, J.N.5
-
26
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
doi:10.1371/journal.pbio.1000294
-
Dickson SP, Wang K, Krantz I, Hakonarson H, Goldstein DB, (2010) Rare variants create synthetic genome-wide associations. PLoS Biol 8: e1000294 doi:10.1371/journal.pbio.1000294.
-
(2010)
PLoS Biol
, vol.8
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
27
-
-
79851468862
-
Synthetic associations are unlikely to account for many common disease genome-wide association signals
-
doi:10.1371/journal.pbio.1000580
-
Anderson CA, Soranzo N, Zeggini E, Barrett JC, (2011) Synthetic associations are unlikely to account for many common disease genome-wide association signals. PLoS Biol 9: e1000580 doi:10.1371/journal.pbio.1000580.
-
(2011)
PLoS Biol
, vol.9
-
-
Anderson, C.A.1
Soranzo, N.2
Zeggini, E.3
Barrett, J.C.4
-
28
-
-
79953738130
-
Quantifying the underestimation of relative risks from genome-wide association studies
-
doi:10.1371/journal.pgen.1001337
-
Spencer C, Hechter E, Vukcevic D, Donnelly P, (2011) Quantifying the underestimation of relative risks from genome-wide association studies. PLoS Genet 7: e1001337 doi:10.1371/journal.pgen.1001337.
-
(2011)
PLoS Genet
, vol.7
-
-
Spencer, C.1
Hechter, E.2
Vukcevic, D.3
Donnelly, P.4
-
29
-
-
0037603589
-
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
-
Abifadel M, Varret M, Rabès JP, Allard D, Ouguerram K, et al. (2003) Mutations in PCSK9 cause autosomal dominant hypercholesterolemia. Nat Genet 34 (2): 154-6.
-
(2003)
Nat Genet
, vol.34
, Issue.2
, pp. 154-156
-
-
Abifadel, M.1
Varret, M.2
Rabès, J.P.3
Allard, D.4
Ouguerram, K.5
-
30
-
-
34547625955
-
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits
-
doi:10.1371/journal.pgen.0030115
-
Scuteri A, Sanna S, Chen WM, Uda M, Albai G, et al. (2007) Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS Genet 3: e115 doi:10.1371/journal.pgen.0030115.
-
(2007)
PLoS Genet
, vol.3
-
-
Scuteri, A.1
Sanna, S.2
Chen, W.M.3
Uda, M.4
Albai, G.5
-
31
-
-
79957951017
-
Low-coverage sequencing: Implications for design of complex trait association studies
-
May 4 [Epub ahead of print]
-
Li Y, Sidore C, Kang HM, Boehnke M, Abecasis GR, (2011) Low-coverage sequencing: Implications for design of complex trait association studies. Genome Res May 4 [Epub ahead of print].
-
(2011)
Genome Res
-
-
Li, Y.1
Sidore, C.2
Kang, H.M.3
Boehnke, M.4
Abecasis, G.R.5
-
32
-
-
58149156287
-
Variants in MTNR1B influence fasting glucose levels
-
Prokopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, et al. (2009) Variants in MTNR1B influence fasting glucose levels. Nat Genet 41 (1): 77-81.
-
(2009)
Nat Genet
, vol.41
, Issue.1
, pp. 77-81
-
-
Prokopenko, I.1
Langenberg, C.2
Florez, J.C.3
Saxena, R.4
Soranzo, N.5
-
33
-
-
78649374846
-
Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls
-
Preuss M, König IR, Thompson JR, Erdmann J, Absher D, et al. (2010) Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls. Circ Cardiovasc Genet 3 (5): 475-83.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, Issue.5
, pp. 475-483
-
-
Preuss, M.1
König, I.R.2
Thompson, J.R.3
Erdmann, J.4
Absher, D.5
-
34
-
-
0033759689
-
Improved inference of relationship for pairs of individuals
-
Epstein MP, Duren WL, Boehnke M, (2000) Improved inference of relationship for pairs of individuals. Am J Hum Genet 67: 1219-1231.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1219-1231
-
-
Epstein, M.P.1
Duren, W.L.2
Boehnke, M.3
-
35
-
-
34547628858
-
Family-based association tests for genome-wide association scans
-
Chen W, Abecasis GR, (2007) Family-based association tests for genome-wide association scans. Am J Hum Genet 81: 913-926.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 913-926
-
-
Chen, W.1
Abecasis, G.R.2
-
36
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR, (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
37
-
-
77956586071
-
LocusZoom: regional visualization of genome-wide association scan results
-
Pruim RJ, Welch RP, Sanna S, Teslovich TM, Chines PS, et al. (2010) LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 26 (18): 2336-7.
-
(2010)
Bioinformatics
, vol.26
, Issue.18
, pp. 2336-2337
-
-
Pruim, R.J.1
Welch, R.P.2
Sanna, S.3
Teslovich, T.M.4
Chines, P.S.5
|