-
1
-
-
84855353573
-
Heart disease and stroke statistics--2012 update: a report from the American Heart Association
-
10.1161/CIR.0b013e31823ac046
-
Roger VL, Go AS, Lloyd-Jones DM, Benjamin EJ, Berry JD, et al. (2012) Heart disease and stroke statistics--2012 update: a report from the American Heart Association. Circulation 125: e2-e220. doi:10.1161/CIR.0b013e31823ac046. PubMed: 22179539.
-
(2012)
Circulation
, vol.125
-
-
Roger, V.L.1
Go, A.S.2
Lloyd-Jones, D.M.3
Benjamin, E.J.4
Berry, J.D.5
-
2
-
-
77649149361
-
Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family
-
10.1002/art.27288
-
Chen HC, Kraus VB, Li YJ, Nelson S, Haynes C, et al. (2010) Genome-wide linkage analysis of quantitative biomarker traits of osteoarthritis in a large, multigenerational extended family. Arthritis Rheum 62: 781-790. doi:10.1002/art.27288. PubMed: 20187133.
-
(2010)
Arthritis Rheum
, vol.62
, pp. 781-790
-
-
Chen, H.C.1
Kraus, V.B.2
Li, Y.J.3
Nelson, S.4
Haynes, C.5
-
3
-
-
0034753277
-
The genetic dissection of complex traits in a founder population
-
10.1086/324025
-
Ober C, Abney M, McPeek MS, (2001) The genetic dissection of complex traits in a founder population. Am J Hum Genet 69: 1068-1079. doi:10.1086/324025. PubMed: 11590547.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1068-1079
-
-
Ober, C.1
Abney, M.2
McPeek, M.S.3
-
4
-
-
0033759689
-
Improved inference of relationship for pairs of individuals
-
10.1086/321195
-
Epstein MP, Duren WL, Boehnke M, (2000) Improved inference of relationship for pairs of individuals. Am J Hum Genet 67: 1219-1231. doi:10.1086/321195. PubMed: 11032786.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1219-1231
-
-
Epstein, M.P.1
Duren, W.L.2
Boehnke, M.3
-
5
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
10.1086/519795
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559-575. doi:10.1086/519795. PubMed: 17701901.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
-
6
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
10.1038/ng1295-402
-
O'Connell JR, Weeks DE, (1995) The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 11: 402-408. doi:10.1038/ng1295-402. PubMed: 7493020.
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
7
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
10.1086/301844
-
Almasy L, Blangero J, (1998) Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet 62: 1198-1211. doi:10.1086/301844. PubMed: 9545414.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
8
-
-
0035220056
-
Variance component methods for detecting complex trait loci
-
10.1016/S0065-2660(01)42021-9
-
Blangero J, Williams JT, Almasy L, (2001) Variance component methods for detecting complex trait loci. Adv Genet 42: 151-181. doi:10.1016/S0065-2660(01)42021-9. PubMed: 11037320.
-
(2001)
Adv Genet
, vol.42
, pp. 151-181
-
-
Blangero, J.1
Williams, J.T.2
Almasy, L.3
-
9
-
-
0028058128
-
Robust variance-components approach for assessing genetic linkage in pedigrees
-
8116623
-
Amos CI, (1994) Robust variance-components approach for assessing genetic linkage in pedigrees. Am J Hum Genet 54: 535-543. PubMed: 8116623.
-
(1994)
Am J Hum Genet
, vol.54
, pp. 535-543
-
-
Amos, C.I.1
-
10
-
-
0030671145
-
Markov chain Monte Carlo methods for radiation hybrid mapping
-
10.1089/cmb.1997.4.505
-
Heath SC, (1997) Markov chain Monte Carlo methods for radiation hybrid mapping. J Comput Biol 4: 505-515. doi:10.1089/cmb.1997.4.505. PubMed: 9385542.
-
(1997)
J Comput Biol
, vol.4
, pp. 505-515
-
-
Heath, S.C.1
-
11
-
-
36948999005
-
Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI family heart study follow-up examination
-
10.1038/sj.gene.6364434
-
Bielinski SJ, Pankow JS, Miller MB, Hopkins PN, Eckfeldt JH, et al. (2007) Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI family heart study follow-up examination. Genes Immun 8: 684-690. doi:10.1038/sj.gene.6364434. PubMed: 17917677.
-
(2007)
Genes Immun
, vol.8
, pp. 684-690
-
-
Bielinski, S.J.1
Pankow, J.S.2
Miller, M.B.3
Hopkins, P.N.4
Eckfeldt, J.H.5
-
12
-
-
58549117464
-
Determinants of variation in human serum paraoxonase activity
-
10.1038/hdy.2008.110
-
Rainwater DL, Rutherford S, Dyer TD, Rainwater ED, Cole SA, et al. (2009) Determinants of variation in human serum paraoxonase activity. Heredity (Edinb) 102: 147-154. doi:10.1038/hdy.2008.110. PubMed: 18971955.
-
(2009)
Heredity (Edinb)
, vol.102
, pp. 147-154
-
-
Rainwater, D.L.1
Rutherford, S.2
Dyer, T.D.3
Rainwater, E.D.4
Cole, S.A.5
-
13
-
-
24044536902
-
Genome scan of systemic biomarkers of vascular inflammation in the Framingham Heart Study: evidence for susceptibility loci on 1q
-
10.1016/j.atherosclerosis.2005.02.015
-
Dupuis J, Larson MG, Vasan RS, Massaro JM, Wilson PW, et al. (2005) Genome scan of systemic biomarkers of vascular inflammation in the Framingham Heart Study: evidence for susceptibility loci on 1q. Atherosclerosis 182: 307-314. doi:10.1016/j.atherosclerosis.2005.02.015. PubMed: 16159603.
-
(2005)
Atherosclerosis
, vol.182
, pp. 307-314
-
-
Dupuis, J.1
Larson, M.G.2
Vasan, R.S.3
Massaro, J.M.4
Wilson, P.W.5
-
14
-
-
8944258922
-
The Yin and Yang of oxidation in the development of the fatty streak. A review based on the 1994 George Lyman Duff Memorial Lecture
-
10.1161/01.ATV.16.7.831
-
Navab M, Berliner JA, Watson AD, Hama SY, Territo MC, et al. (1996) The Yin and Yang of oxidation in the development of the fatty streak. A review based on the 1994 George Lyman Duff Memorial Lecture. Arterioscler Thromb Vasc Biol 16: 831-842. doi:10.1161/01.ATV.16.7.831. PubMed: 8673557.
-
(1996)
Arterioscler Thromb Vasc Biol
, vol.16
, pp. 831-842
-
-
Navab, M.1
Berliner, J.A.2
Watson, A.D.3
Hama, S.Y.4
Territo, M.C.5
-
15
-
-
0022904803
-
Distribution of paraoxon hydrolytic activity in the serum of patients after myocardial infarction
-
3006944
-
McElveen J, Mackness MI, Colley CM, Peard T, Warner S, et al. (1986) Distribution of paraoxon hydrolytic activity in the serum of patients after myocardial infarction. Clin Chem 32: 671-673. PubMed: 3006944.
-
(1986)
Clin Chem
, vol.32
, pp. 671-673
-
-
McElveen, J.1
Mackness, M.I.2
Colley, C.M.3
Peard, T.4
Warner, S.5
-
16
-
-
33845567031
-
Multiple QTLs influence variation in paraoxonase 1 activity in Mexican Americans
-
10.1353/hub.2006.0050
-
Winnier DA, Rainwater DL, Cole SA, Dyer TD, Blangero J, et al. (2006) Multiple QTLs influence variation in paraoxonase 1 activity in Mexican Americans. Hum Biol 78: 341-352. doi:10.1353/hub.2006.0050. PubMed: 17216806.
-
(2006)
Hum Biol
, vol.78
, pp. 341-352
-
-
Winnier, D.A.1
Rainwater, D.L.2
Cole, S.A.3
Dyer, T.D.4
Blangero, J.5
-
17
-
-
40949127806
-
Relationship of paraoxonase 1 (PON1) gene polymorphisms and functional activity with systemic oxidative stress and cardiovascular risk
-
10.1001/jama.299.11.1265
-
Bhattacharyya T, Nicholls SJ, Topol EJ, Zhang R, Yang X, et al. (2008) Relationship of paraoxonase 1 (PON1) gene polymorphisms and functional activity with systemic oxidative stress and cardiovascular risk. JAMA 299: 1265-1276. doi:10.1001/jama.299.11.1265. PubMed: 18349088.
-
(2008)
JAMA
, vol.299
, pp. 1265-1276
-
-
Bhattacharyya, T.1
Nicholls, S.J.2
Topol, E.J.3
Zhang, R.4
Yang, X.5
-
18
-
-
0031915397
-
DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease
-
10.1086/301669
-
Sanghera DK, Aston CE, Saha N, Kamboh MI, (1998) DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease. Am J Hum Genet 62: 36-44. doi:10.1086/301669. PubMed: 9443862.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 36-44
-
-
Sanghera, D.K.1
Aston, C.E.2
Saha, N.3
Kamboh, M.I.4
-
19
-
-
78751703383
-
Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22
-
10.1136/ard.2010.132787
-
Evangelou E, Valdes AM, Kerkhof HJ, Styrkarsdottir U, Zhu Y, et al. (2011) Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22. Ann Rheum Dis 70: 349-355. doi:10.1136/ard.2010.132787. PubMed: 21068099.
-
(2011)
Ann Rheum Dis
, vol.70
, pp. 349-355
-
-
Evangelou, E.1
Valdes, A.M.2
Kerkhof, H.J.3
Styrkarsdottir, U.4
Zhu, Y.5
-
20
-
-
71649092224
-
Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility
-
10.1002/aur.96
-
Cukier HN, Skaar DA, Rayner-Evans MY, Konidari I, Whitehead PL, et al. (2009) Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility. Autism Res 2: 258-266. doi:10.1002/aur.96. PubMed: 19877165.
-
(2009)
Autism Res
, vol.2
, pp. 258-266
-
-
Cukier, H.N.1
Skaar, D.A.2
Rayner-Evans, M.Y.3
Konidari, I.4
Whitehead, P.L.5
-
21
-
-
3242725813
-
Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study
-
10.1086/422699
-
Jiang Y, Wilk JB, Borecki I, Williamson S, DeStefano AL, et al. (2004) Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study. Am J Hum Genet 75: 220-230. doi:10.1086/422699. PubMed: 15197684.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 220-230
-
-
Jiang, Y.1
Wilk, J.B.2
Borecki, I.3
Williamson, S.4
DeStefano, A.L.5
-
22
-
-
0036234398
-
A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program
-
10.1086/340362
-
Wu X, Cooper RS, Borecki I, Hanis C, Bray M, et al. (2002) A combined analysis of genomewide linkage scans for body mass index from the National Heart, Lung, and Blood Institute Family Blood Pressure Program. Am J Hum Genet 70: 1247-1256. doi:10.1086/340362. PubMed: 11923912.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1247-1256
-
-
Wu, X.1
Cooper, R.S.2
Borecki, I.3
Hanis, C.4
Bray, M.5
-
23
-
-
30844439870
-
A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1
-
10.1007/s00439-005-0064-2
-
Schönberger J, Kühler L, Martins E, Lindner TH, Silva-Cardoso J, et al. (2005) A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1. Hum Genet 118: 451-457. doi:10.1007/s00439-005-0064-2. PubMed: 16228230.
-
(2005)
Hum Genet
, vol.118
, pp. 451-457
-
-
Schönberger, J.1
Kühler, L.2
Martins, E.3
Lindner, T.H.4
Silva-Cardoso, J.5
-
24
-
-
0025176813
-
Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia
-
10.1038/343559a0
-
MacLennan DH, Duff C, Zorzato F, Fujii J, Phillips M, et al. (1990) Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia. Nature 343: 559-561. doi:10.1038/343559a0. PubMed: 1967823.
-
(1990)
Nature
, vol.343
, pp. 559-561
-
-
MacLennan, D.H.1
Duff, C.2
Zorzato, F.3
Fujii, J.4
Phillips, M.5
-
25
-
-
84881010311
-
A QTL for Genotype by Sex Interaction for Anthropometric Measurements in Alaskan Eskimos (GOCADAN Study) on Chromosome 19q12-13
-
22016090
-
Voruganti VS, Diego VP, Haack K, Cole SA, Blangero J, et al. (2011) A QTL for Genotype by Sex Interaction for Anthropometric Measurements in Alaskan Eskimos (GOCADAN Study) on Chromosome 19q12-13. Obesity (Silver Spring), 20: 1122-6. PubMed: 22016090.
-
(2011)
Obesity (Silver Spring)
, vol.20
, pp. 1122-1126
-
-
Voruganti, V.S.1
Diego, V.P.2
Haack, K.3
Cole, S.A.4
Blangero, J.5
-
26
-
-
54049098441
-
A whole genome linkage scan identifies multiple chromosomal regions influencing adiposity-related traits among Samoans
-
10.1111/j.1469-1809.2008.00462.x
-
Dai F, Sun G, Aberg K, Keighley ED, Indugula SR, et al. (2008) A whole genome linkage scan identifies multiple chromosomal regions influencing adiposity-related traits among Samoans. Ann Hum Genet 72: 780-792. doi:10.1111/j.1469-1809.2008.00462.x. PubMed: 18616661.
-
(2008)
Ann Hum Genet
, vol.72
, pp. 780-792
-
-
Dai, F.1
Sun, G.2
Aberg, K.3
Keighley, E.D.4
Indugula, S.R.5
-
27
-
-
78651394995
-
Genome-wide linkage scan for resistance to muscle fatigue
-
20459472
-
Thomis MA, De Mars G, Windelinckx A, Peeters MW, Huygens W, et al. (2010) Genome-wide linkage scan for resistance to muscle fatigue. Scand J Med Sci Sports, 21: 580-8. PubMed: 20459472.
-
(2010)
Scand J Med Sci Sports
, vol.21
, pp. 580-588
-
-
Thomis, M.A.1
De Mars, G.2
Windelinckx, A.3
Peeters, M.W.4
Huygens, W.5
-
28
-
-
33645810172
-
Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension
-
10.1093/hmg/ddl058
-
Bell JT, Wallace C, Dobson R, Wiltshire S, Mein C, et al. (2006) Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension. Hum Mol Genet 15: 1365-1374. doi:10.1093/hmg/ddl058. PubMed: 16543358.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1365-1374
-
-
Bell, J.T.1
Wallace, C.2
Dobson, R.3
Wiltshire, S.4
Mein, C.5
-
29
-
-
79953687954
-
Fine-mapping of prostate cancer aggressiveness loci on chromosome 7q22-35
-
20945404
-
Liu X, Cheng I, Plummer SJ, Suarez BK, Casey G, et al. (2010) Fine-mapping of prostate cancer aggressiveness loci on chromosome 7q22-35. Prostate, 71: 682-9. PubMed: 20945404.
-
(2010)
Prostate
, vol.71
, pp. 682-689
-
-
Liu, X.1
Cheng, I.2
Plummer, S.J.3
Suarez, B.K.4
Casey, G.5
-
30
-
-
2342539735
-
Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23
-
10.2337/diabetes.53.5.1375
-
Kim SH, Ma X, Weremowicz S, Ercolino T, Powers C, et al. (2004) Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23. Diabetes 53: 1375-1384. doi:10.2337/diabetes.53.5.1375. PubMed: 15111509.
-
(2004)
Diabetes
, vol.53
, pp. 1375-1384
-
-
Kim, S.H.1
Ma, X.2
Weremowicz, S.3
Ercolino, T.4
Powers, C.5
-
31
-
-
0025186845
-
Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2
-
10.1038/343562a0
-
McCarthy TV, Healy JM, Heffron JJ, Lehane M, Deufel T, et al. (1990) Localization of the malignant hyperthermia susceptibility locus to human chromosome 19q12-13.2. Nature 343: 562-564. doi:10.1038/343562a0. PubMed: 2300206.
-
(1990)
Nature
, vol.343
, pp. 562-564
-
-
McCarthy, T.V.1
Healy, J.M.2
Heffron, J.J.3
Lehane, M.4
Deufel, T.5
-
32
-
-
77950296637
-
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL)
-
10.1038/ng.553
-
Franke A, Balschun T, Sina C, Ellinghaus D, Häsler R, et al. (2010) Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). Nat Genet 42: 292-294. doi:10.1038/ng.553. PubMed: 20228798.
-
(2010)
Nat Genet
, vol.42
, pp. 292-294
-
-
Franke, A.1
Balschun, T.2
Sina, C.3
Ellinghaus, D.4
Häsler, R.5
-
33
-
-
70350502096
-
Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands
-
10.1186/1471-2350-10-107
-
Aberg K, Dai F, Viali S, Tuitele J, Sun G, et al. (2009) Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands. BMC Med Genet 10: 107. doi:10.1186/1471-2350-10-107. PubMed: 19852796.
-
(2009)
BMC Med Genet
, vol.10
, pp. 107
-
-
Aberg, K.1
Dai, F.2
Viali, S.3
Tuitele, J.4
Sun, G.5
-
34
-
-
67949121858
-
Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci
-
10.1016/j.bone.2009.05.002
-
Peacock M, Koller DL, Lai D, Hui S, Foroud T, et al. (2009) Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci. Bone 45: 443-448. doi:10.1016/j.bone.2009.05.002. PubMed: 19427925.
-
(2009)
Bone
, vol.45
, pp. 443-448
-
-
Peacock, M.1
Koller, D.L.2
Lai, D.3
Hui, S.4
Foroud, T.5
-
35
-
-
67651122988
-
Genome-wide linkage analysis of serum creatinine in three isolated European populations
-
10.1038/ki.2009.135
-
Pattaro C, Aulchenko YS, Isaacs A, Vitart V, Hayward C, et al. (2009) Genome-wide linkage analysis of serum creatinine in three isolated European populations. Kidney Int 76: 297-306. doi:10.1038/ki.2009.135. PubMed: 19387472.
-
(2009)
Kidney Int
, vol.76
, pp. 297-306
-
-
Pattaro, C.1
Aulchenko, Y.S.2
Isaacs, A.3
Vitart, V.4
Hayward, C.5
-
36
-
-
52949131340
-
Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13
-
10.1038/ng.218
-
Barton A, Thomson W, Ke X, Eyre S, Hinks A, et al. (2008) Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13. Nat Genet 40: 1156-1159. doi:10.1038/ng.218. PubMed: 18794857.
-
(2008)
Nat Genet
, vol.40
, pp. 1156-1159
-
-
Barton, A.1
Thomson, W.2
Ke, X.3
Eyre, S.4
Hinks, A.5
-
37
-
-
34548303945
-
Evidence for two schizophrenia susceptibility genes on chromosome 22q13
-
10.1097/YPG.0b013e3281ac2345
-
Condra JA, Neibergs H, Wei W, Brennan MD, (2007) Evidence for two schizophrenia susceptibility genes on chromosome 22q13. Psychiatr Genet 17: 292-298. doi:10.1097/YPG.0b013e3281ac2345. PubMed: 17728668.
-
(2007)
Psychiatr Genet
, vol.17
, pp. 292-298
-
-
Condra, J.A.1
Neibergs, H.2
Wei, W.3
Brennan, M.D.4
-
38
-
-
29144432196
-
A male-specific quantitative trait locus on 1p21 controlling human stature
-
10.1136/jmg.2005.031278
-
Sammalisto S, Hiekkalinna T, Suviolahti E, Sood K, Metzidis A, et al. (2005) A male-specific quantitative trait locus on 1p21 controlling human stature. J Med Genet 42: 932-939. doi:10.1136/jmg.2005.031278. PubMed: 15827092.
-
(2005)
J Med Genet
, vol.42
, pp. 932-939
-
-
Sammalisto, S.1
Hiekkalinna, T.2
Suviolahti, E.3
Sood, K.4
Metzidis, A.5
-
39
-
-
19944434383
-
An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found
-
15668479
-
Hartikainen JM, Tuhkanen H, Kataja V, Dunning AM, Antoniou A, et al. (2005) An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found. Cancer Epidemiol Biomarkers Prev 14: 75-80. PubMed: 15668479.
-
(2005)
Cancer Epidemiol Biomarkers Prev
, vol.14
, pp. 75-80
-
-
Hartikainen, J.M.1
Tuhkanen, H.2
Kataja, V.3
Dunning, A.M.4
Antoniou, A.5
-
40
-
-
33846123302
-
The role of genetic variants of matrix metalloproteinases in coronary and carotid atherosclerosis
-
10.1136/jmg.2006.040808
-
Abilleira S, Bevan S, Markus HS, (2006) The role of genetic variants of matrix metalloproteinases in coronary and carotid atherosclerosis. J Med Genet 43: 897-901. doi:10.1136/jmg.2006.040808. PubMed: 16905683.
-
(2006)
J Med Genet
, vol.43
, pp. 897-901
-
-
Abilleira, S.1
Bevan, S.2
Markus, H.S.3
-
41
-
-
39349090432
-
Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension
-
10.1093/eurheartj/ehn028
-
Mayosi BM, Avery PJ, Farrall M, Keavney B, Watkins H, (2008) Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension. Eur Heart J 29: 525-530. doi:10.1093/eurheartj/ehn028. PubMed: 18276622.
-
(2008)
Eur Heart J
, vol.29
, pp. 525-530
-
-
Mayosi, B.M.1
Avery, P.J.2
Farrall, M.3
Keavney, B.4
Watkins, H.5
-
42
-
-
1442349990
-
A genome-wide scan for childhood obesity-associated traits in French families shows significant linkage on chromosome 6q22.31-q23.2
-
10.2337/diabetes.53.3.803
-
Meyre D, Lecoeur C, Delplanque J, Francke S, Vatin V, et al. (2004) A genome-wide scan for childhood obesity-associated traits in French families shows significant linkage on chromosome 6q22.31-q23.2. Diabetes 53: 803-811. doi:10.2337/diabetes.53.3.803. PubMed: 14988267.
-
(2004)
Diabetes
, vol.53
, pp. 803-811
-
-
Meyre, D.1
Lecoeur, C.2
Delplanque, J.3
Francke, S.4
Vatin, V.5
-
43
-
-
0037389679
-
Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families
-
10.1002/art.10989
-
Jawaheer D, Seldin MF, Amos CI, Chen WV, Shigeta R, et al. (2003) Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase families. Arthritis Rheum 48: 906-916. doi:10.1002/art.10989. PubMed: 12687532.
-
(2003)
Arthritis Rheum
, vol.48
, pp. 906-916
-
-
Jawaheer, D.1
Seldin, M.F.2
Amos, C.I.3
Chen, W.V.4
Shigeta, R.5
-
44
-
-
79952282953
-
A genome-wide admixture scan for ancestry-linked genes predisposing to sarcoidosis in African-Americans
-
10.1038/gene.2010.56
-
Rybicki BA, Levin AM, McKeigue P, Datta I, Gray-McGuire C, et al. (2011) A genome-wide admixture scan for ancestry-linked genes predisposing to sarcoidosis in African-Americans. Genes Immun 12: 67-77. doi:10.1038/gene.2010.56. PubMed: 21179114.
-
(2011)
Genes Immun
, vol.12
, pp. 67-77
-
-
Rybicki, B.A.1
Levin, A.M.2
McKeigue, P.3
Datta, I.4
Gray-McGuire, C.5
-
45
-
-
68449096727
-
Common variants on chromosome 6p22.1 are associated with schizophrenia
-
19571809
-
Shi J, Levinson DF, Duan J, Sanders AR, Zheng Y, et al. (2009) Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 460: 753-757. PubMed: 19571809.
-
(2009)
Nature
, vol.460
, pp. 753-757
-
-
Shi, J.1
Levinson, D.F.2
Duan, J.3
Sanders, A.R.4
Zheng, Y.5
-
46
-
-
34548187288
-
Genome-wide scans meta-analysis for pulse pressure
-
10.1161/HYPERTENSIONAHA.107.090316
-
Zintzaras E, Kitsios G, Kent D, Camp NJ, Atwood L, et al. (2007) Genome-wide scans meta-analysis for pulse pressure. Hypertension 50: 557-564. doi:10.1161/HYPERTENSIONAHA.107.090316. PubMed: 17635856.
-
(2007)
Hypertension
, vol.50
, pp. 557-564
-
-
Zintzaras, E.1
Kitsios, G.2
Kent, D.3
Camp, N.J.4
Atwood, L.5
-
47
-
-
33751265737
-
Identification of chromosomal regions linked to premature myocardial infarction: a meta-analysis of whole-genome searches
-
10.1007/s10038-006-0053-x
-
Zintzaras E, Kitsios G, (2006) Identification of chromosomal regions linked to premature myocardial infarction: a meta-analysis of whole-genome searches. J Hum Genet 51: 1015-1021. doi:10.1007/s10038-006-0053-x. PubMed: 17024316.
-
(2006)
J Hum Genet
, vol.51
, pp. 1015-1021
-
-
Zintzaras, E.1
Kitsios, G.2
-
48
-
-
0037986588
-
Evidence for a major quantitative trait locus on chromosome 17q21 affecting low-density lipoprotein peak particle diameter
-
10.1161/01.CIR.0000065577.60129.F5
-
Bossé Y, Pérusse L, Després JP, Lamarche B, Chagnon YC, et al. (2003) Evidence for a major quantitative trait locus on chromosome 17q21 affecting low-density lipoprotein peak particle diameter. Circulation 107: 2361-2368. doi:10.1161/01.CIR.0000065577.60129.F5. PubMed: 12732599.
-
(2003)
Circulation
, vol.107
, pp. 2361-2368
-
-
Bossé, Y.1
Pérusse, L.2
Després, J.P.3
Lamarche, B.4
Chagnon, Y.C.5
-
49
-
-
18244401151
-
Localization of a susceptibility gene for common forms of stroke to 5q12
-
10.1086/339252
-
Gretarsdottir S, Sveinbjörnsdottir S, Jonsson HH, Jakobsson F, Einarsdottir E, et al. (2002) Localization of a susceptibility gene for common forms of stroke to 5q12. Am J Hum Genet 70: 593-603. doi:10.1086/339252. PubMed: 11833004.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 593-603
-
-
Gretarsdottir, S.1
Sveinbjörnsdottir, S.2
Jonsson, H.H.3
Jakobsson, F.4
Einarsdottir, E.5
-
50
-
-
84881010903
-
Granulocyte colony-stimulating factor attenuates oxidative stress-induced apoptosis in vascular endothelial cells and exhibits functional and morphological protective effect in oxygen-induced retinopathy
-
Kojima H, Otani A, Oishi A, Makiyama Y, Nakagawa S, et al. (2010) Granulocyte colony-stimulating factor attenuates oxidative stress-induced apoptosis in vascular endothelial cells and exhibits functional and morphological protective effect in oxygen-induced retinopathy. Blood.
-
(2010)
Blood
-
-
Kojima, H.1
Otani, A.2
Oishi, A.3
Makiyama, Y.4
Nakagawa, S.5
-
51
-
-
33745184400
-
New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate
-
10.1093/hmg/ddl097
-
Ciullo M, Bellenguez C, Colonna V, Nutile T, Calabria A, et al. (2006) New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate. Hum Mol Genet 15: 1735-1743. doi:10.1093/hmg/ddl097. PubMed: 16611673.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1735-1743
-
-
Ciullo, M.1
Bellenguez, C.2
Colonna, V.3
Nutile, T.4
Calabria, A.5
-
52
-
-
0036345144
-
A genome-wide linkage scan for steroids and SHBG levels in black and white families: the HERITAGE Family Study
-
10.1210/jc.87.8.3708
-
Ukkola O, Rankinen T, Gagnon J, Leon AS, Skinner JS, et al. (2002) A genome-wide linkage scan for steroids and SHBG levels in black and white families: the HERITAGE Family Study. J Clin Endocrinol Metab 87: 3708-3720. doi:10.1210/jc.87.8.3708. PubMed: 12161500.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 3708-3720
-
-
Ukkola, O.1
Rankinen, T.2
Gagnon, J.3
Leon, A.S.4
Skinner, J.S.5
-
53
-
-
0035825981
-
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners
-
10.1002/ajmg.1192
-
Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, et al. (2001) Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners. Am J Med Genet 105: 163-167. doi:10.1002/ajmg.1192. PubMed: 11304830.
-
(2001)
Am J Med Genet
, vol.105
, pp. 163-167
-
-
Simonic, I.1
Nyholt, D.R.2
Gericke, G.S.3
Gordon, D.4
Matsumoto, N.5
-
54
-
-
0036378360
-
Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins
-
10.1046/j.1365-2796.2002.01029.x
-
Zdravkovic S, Wienke A, Pedersen NL, Marenberg ME, Yashin AI, et al. (2002) Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins. J Intern Med 252: 247-254. doi:10.1046/j.1365-2796.2002.01029.x. PubMed: 12270005.
-
(2002)
J Intern Med
, vol.252
, pp. 247-254
-
-
Zdravkovic, S.1
Wienke, A.2
Pedersen, N.L.3
Marenberg, M.E.4
Yashin, A.I.5
-
55
-
-
35748983219
-
Genome-wide association with select biomarker traits in the Framingham Heart Study
-
10.1186/1471-2350-8-S1-S11
-
Benjamin EJ, Dupuis J, Larson MG, Lunetta KL, Booth SL, et al. (2007) Genome-wide association with select biomarker traits in the Framingham Heart Study. BMC Med Genet 8 (Suppl 1):: S11. doi:10.1186/1471-2350-8-S1-S11. PubMed: 17903293.
-
(2007)
BMC Med Genet
, vol.8
, Issue.SUPPL. 1
-
-
Benjamin, E.J.1
Dupuis, J.2
Larson, M.G.3
Lunetta, K.L.4
Booth, S.L.5
-
56
-
-
52349120444
-
Epidemiology, heritability, and genetic linkage of C-reactive protein in African Americans (from the Jackson Heart Study)
-
10.1016/j.amjcard.2008.05.049
-
Fox ER, Benjamin EJ, Sarpong DF, Rotimi CN, Wilson JG, et al. (2008) Epidemiology, heritability, and genetic linkage of C-reactive protein in African Americans (from the Jackson Heart Study). Am J Cardiol 102: 835-841. doi:10.1016/j.amjcard.2008.05.049. PubMed: 18805107.
-
(2008)
Am J Cardiol
, vol.102
, pp. 835-841
-
-
Fox, E.R.1
Benjamin, E.J.2
Sarpong, D.F.3
Rotimi, C.N.4
Wilson, J.G.5
-
57
-
-
46149126872
-
Genome-wide linkage analysis for circulating levels of adipokines and C-reactive protein in the Quebec family study (QFS)
-
10.1007/s10038-008-0291-1
-
Ruchat SM, Després JP, Weisnagel SJ, Chagnon YC, Bouchard C, et al. (2008) Genome-wide linkage analysis for circulating levels of adipokines and C-reactive protein in the Quebec family study (QFS). J Hum Genet 53: 629-636. doi:10.1007/s10038-008-0291-1. PubMed: 18414778.
-
(2008)
J Hum Genet
, vol.53
, pp. 629-636
-
-
Ruchat, S.M.1
Després, J.P.2
Weisnagel, S.J.3
Chagnon, Y.C.4
Bouchard, C.5
-
58
-
-
34247857366
-
Quantitative trait locus on chromosome 20q13 for plasma levels of C-reactive protein in healthy whites: the HERITAGE Family Study
-
10.1152/physiolgenomics.00054.2005
-
Lakka TA, Rankinen T, Rice T, Leon AS, Rao DC, et al. (2006) Quantitative trait locus on chromosome 20q13 for plasma levels of C-reactive protein in healthy whites: the HERITAGE Family Study. Physiol Genomics 27: 103-107. doi:10.1152/physiolgenomics.00054.2005. PubMed: 16822830.
-
(2006)
Physiol Genomics
, vol.27
, pp. 103-107
-
-
Lakka, T.A.1
Rankinen, T.2
Rice, T.3
Leon, A.S.4
Rao, D.C.5
|