-
1
-
-
77953661116
-
Common variants in HSPB7 and FRMD4B associated with advanced heart failure
-
Cappola TP, Li M, He J, Ky B, Gilmore J, Qu L, Keating B, Reilly M, Kim CE, Glessner J, Frackelton E, Hakonarson H, Syed F, Hindes A, Matkovich SJ, Cresci S, Dorn II GW. 2010. Common variants in HSPB7 and FRMD4B associated with advanced heart failure. Circ Cardiovasc Genet 3:147-54.
-
(2010)
Circ Cardiovasc Genet
, vol.3
, pp. 147-154
-
-
Cappola, T.P.1
Li, M.2
He, J.3
Ky, B.4
Gilmore, J.5
Qu, L.6
Keating, B.7
Reilly, M.8
Kim, C.E.9
Glessner, J.10
Frackelton, E.11
Hakonarson, H.12
Syed, F.13
Hindes, A.14
Matkovich, S.J.15
Cresci, S.16
Dorn II, G.W.17
-
2
-
-
79952309013
-
Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation
-
Cappola TP, Matkovich SJ, Wang W, van Booven D, Li M, Wang X, Qu L, Sweitzer NK, Fang JC, Reilly MP, Hakonarson H, Nerbonne JM, Dorn II GW. 2011. Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation. Proc Natl Acad Sci U S A 108:2456-61.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 2456-2461
-
-
Cappola, T.P.1
Matkovich, S.J.2
Wang, W.3
Van Booven, D.4
Li, M.5
Wang, X.6
Qu, L.7
Sweitzer, N.K.8
Fang, J.C.9
Reilly, M.P.10
Hakonarson, H.11
Nerbonne, J.M.12
Dorn II, G.W.13
-
3
-
-
33645090921
-
Haplotype-based association analysis in cohort and nested case-control studies
-
Chen J, Chatterjee N. 2006. Haplotype-based association analysis in cohort and nested case-control studies. Biometrics 62:28-35.
-
(2006)
Biometrics
, vol.62
, pp. 28-35
-
-
Chen, J.1
Chatterjee, N.2
-
4
-
-
10844247038
-
A haplotype-based test of association using data from cohort and nested case-control epidemiologic studies
-
DOI 10.1159/000081453
-
Chen J, Peters U, Foster C, Chatterjee N. 2004. A haplotype-based test of association using data from cohort and nested case-control epidemiologic studies. Hum Hered 58:18-29. (Pubitemid 39664273)
-
(2004)
Human Heredity
, vol.58
, Issue.1
, pp. 18-29
-
-
Chen, J.1
Peters, U.2
Foster, C.3
Chatterjee, N.4
-
5
-
-
0000336139
-
Regression models and life tables (with discussion)
-
Cox D. 1972. Regression models and life tables (with discussion). J R Stat Soc Series B 34:187-220.
-
(1972)
J R Stat Soc Series B
, vol.34
, pp. 187-220
-
-
Cox, D.1
-
6
-
-
0002629270
-
Maximum likelihood from incomplete data via the EM algorithm
-
Dempster AP, Laird NM, Rubin D. 1977. Maximum likelihood from incomplete data via the EM algorithm. J R Stat Soc Series B 39:1-38.
-
(1977)
J R Stat Soc Series B
, vol.39
, pp. 1-38
-
-
Dempster, A.P.1
Laird, N.M.2
Rubin, D.3
-
7
-
-
33747601415
-
Simple estimates of haplotype relative risks in case-control data
-
DOI 10.1002/gepi.20161
-
French B, Lumley T, Monks SA, Rice KM, Hindorff LA, Reiner AP, Psaty BM. 2006. Simple estimates of haplotype relative risks in case-control data. Genet Epidemiol 30:485-94. (Pubitemid 44267165)
-
(2006)
Genetic Epidemiology
, vol.30
, Issue.6
, pp. 485-494
-
-
French, B.1
Lumley, T.2
Monks, S.A.3
Rice, K.M.4
Hindorff, L.A.5
Reiner, A.P.6
Psaty, B.M.7
-
8
-
-
84857773657
-
Haplo.ccs: Estimate haplotype relative risks in case-control data
-
French B, Lumley T. 2007. haplo.ccs: Estimate haplotype relative risks in case-control data. R package version 1.3. http://CRAN. R-project.org/package= haplo.ccs
-
(2007)
R Package Version 1.3
-
-
French, B.1
Lumley, T.2
-
9
-
-
56349155783
-
Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies
-
Keating BJ, Tischfield S, Murray SS, Bhangale T, Price TS, Glessner JT, Galver L, Barrett JC, Grant SF, Farlow DN, Chandrupatla HR, Hansen M, Ajmal S, Papanicolaou GJ, Guo Y, Li M, Derohannessian S, de Bakker PI, Bailey SD, Montpetit A, Edmondson AC, Taylor K, Gai X, Wang SS, Fornage M, Shaikh T, Groop L, Boehnke M, Hall AS, Hattersley AT, Frackelton E, Patterson N, Chiang CW, Kim CE, Fabsitz RR, Ouwehand W, Price AL, Munroe P, Caulfield M, Drake T, Boerwinkle E, Reich D, Whitehead AS, Cappola TP, Samani NJ, Lusis AJ, Schadt E, Wilson JG, Koenig W, McCarthy MI, Kathiresan S, Gabriel SB, Hakonarson H, Anand SS, Reilly M, Engert JC, Nickerson DA, Rader DJ, Hirschhorn JN, Fitzgerald GA. 2008. Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies. PLoS One 3:e3583.
-
(2008)
PLoS One
, vol.3
-
-
Keating, B.J.1
Tischfield, S.2
Murray, S.S.3
Bhangale, T.4
Price, T.S.5
Glessner, J.T.6
Galver, L.7
Barrett, J.C.8
Grant, S.F.9
Farlow, D.N.10
Chandrupatla, H.R.11
Hansen, M.12
Ajmal, S.13
Papanicolaou, G.J.14
Guo, Y.15
Li, M.16
Derohannessian, S.17
De Bakker, P.I.18
Bailey, S.D.19
Montpetit, A.20
Edmondson, A.C.21
Taylor, K.22
Gai, X.23
Wang, S.S.24
Fornage, M.25
Shaikh, T.26
Groop, L.27
Boehnke, M.28
Hall, A.S.29
Hattersley, A.T.30
Frackelton, E.31
Patterson, N.32
Chiang, C.W.33
Kim, C.E.34
Fabsitz, R.R.35
Ouwehand, W.36
Price, A.L.37
Munroe, P.38
Caulfield, M.39
Drake, T.40
Boerwinkle, E.41
Reich, D.42
Whitehead, A.S.43
Cappola, T.P.44
Samani, N.J.45
Lusis, A.J.46
Schadt, E.47
Wilson, J.G.48
Koenig, W.49
McCarthy, M.I.50
Kathiresan, S.51
Gabriel, S.B.52
Hakonarson, H.53
Anand, S.S.54
Reilly, M.55
Engert, J.C.56
Nickerson, D.A.57
Rader, D.J.58
Hirschhorn, J.N.59
Fitzgerald, G.A.60
more..
-
10
-
-
68249087127
-
Neuregulin-1 beta is associated with disease severity and adverse outcomes in chronic heart failure
-
Ky B, Kimmel SE, Safa RN, Putt ME, Sweitzer NK, Fang JC, Sawyer DB, Cappola TP. 2009. Neuregulin-1 beta is associated with disease severity and adverse outcomes in chronic heart failure. Circulation 120:310-7.
-
(2009)
Circulation
, vol.120
, pp. 310-317
-
-
Ky, B.1
Kimmel, S.E.2
Safa, R.N.3
Putt, M.E.4
Sweitzer, N.K.5
Fang, J.C.6
Sawyer, D.B.7
Cappola, T.P.8
-
11
-
-
0033814928
-
Implementing a unified approach to family based tests of association
-
Laird N, Horvath S, Xu X. Implementing a unified approach to family based tests of association. Genet Epidemiol 19:S36-S42.
-
Genet Epidemiol
, vol.19
-
-
Laird, N.1
Horvath, S.2
Xu, X.3
-
12
-
-
2342452445
-
Haplotype-based association analysis in cohort studies of unrelated individuals
-
DOI 10.1002/gepi.10317
-
Lin DY. 2004. Haplotype-based association analysis in cohort studies of unrelated individuals. Genet Epidemiol 26:255-64. (Pubitemid 38580377)
-
(2004)
Genetic Epidemiology
, vol.26
, Issue.4
, pp. 255-264
-
-
Lin, D.Y.1
-
13
-
-
33645517140
-
Likelihood-based inference on haplotype effects in genetic association studies
-
DOI 10.1198/016214505000000808
-
Lin DY, Zeng D. 2006. Likelihood-based inference on haplotype effects in genetic association studies. J Am Stat Assoc 101:89-104. (Pubitemid 43500028)
-
(2006)
Journal of the American Statistical Association
, vol.101
, Issue.473
, pp. 89-104
-
-
Lin, D.Y.1
Zeng, D.2
-
14
-
-
34547610243
-
Renin-angiotensin system haplotypes and the risk of myocardial infarction and stroke in pharmacologically treated hypertensive patients
-
DOI 10.1093/aje/kwm059
-
Marciante KD, Bis JC, Rieder MJ, Reiner AP, Lumley T, Monks SA, Kooperberg C, Carlson C, Heckbert SR, Psaty BM. 2007. Renin-angiotensin system haplotypes and the risk of myocardial infarction and stroke in pharmacologically treated hypertensive patients. Am J Epidemiol 166:19-27. (Pubitemid 47234299)
-
(2007)
American Journal of Epidemiology
, vol.166
, Issue.1
, pp. 19-27
-
-
Marciante, K.D.1
Bis, J.C.2
Rieder, M.J.3
Reiner, A.P.4
Lumley, T.5
Monks, S.A.6
Kooperberg, C.7
Carlson, C.8
Heckbert, S.R.9
Psaty, B.M.10
-
15
-
-
76249100400
-
Genetic variation in insulinlike growth factor signaling genes and breast cancer risk among BRCA1 and BRCA2 carriers
-
Neuhausen SL, Brummel S, Ding YC, Singer CF, Pfeiler G, Lynch HT, Nathanson KL, Rebbeck TR, Garber JE, Couch F, Weitzel J, Narod SA, Ganz PA, Daly MB, Godwin AK, Isaacs C, Olopade OI, Tomlinson G, Rubinstein WS, Tung N, Blum JL, Gillen DL. 2009. Genetic variation in insulinlike growth factor signaling genes and breast cancer risk among BRCA1 and BRCA2 carriers. Breast Cancer Res 11:R76.
-
(2009)
Breast Cancer Res
, vol.11
-
-
Neuhausen, S.L.1
Brummel, S.2
Ding, Y.C.3
Singer, C.F.4
Pfeiler, G.5
Lynch, H.T.6
Nathanson, K.L.7
Rebbeck, T.R.8
Garber, J.E.9
Couch, F.10
Weitzel, J.11
Narod, S.A.12
Ganz, P.A.13
Daly, M.B.14
Godwin, A.K.15
Isaacs, C.16
Olopade, O.I.17
Tomlinson, G.18
Rubinstein, W.S.19
Tung, N.20
Blum, J.L.21
Gillen, D.L.22
more..
-
16
-
-
67651000083
-
Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers
-
kConFab
-
Rebbeck TR, Mitra N, Domchek SM, Wan F, Chuai S, Friebel TM, Panossian S, Spurdle A, Chenevix-Trench G, kConFab, Singer CF, Pfeiler G, Neuhausen SL, Lynch HT, Garber JE, Weitzel JN, Isaacs C, Couch F, Narod SA, Rubinstein WS, Tomlinson GE, Ganz PA, Olopade OI, Tung N, Blum JL, Greenberg R, Nathanson KL, Daly MB. 2009. Modification of ovarian cancer risk by BRCA1/2-interacting genes in a multicenter cohort of BRCA1/2 mutation carriers. Cancer Res 69:5801-10.
-
(2009)
Cancer Res
, vol.69
, pp. 5801-5810
-
-
Rebbeck, T.R.1
Mitra, N.2
Domchek, S.M.3
Wan, F.4
Chuai, S.5
Friebel, T.M.6
Panossian, S.7
Spurdle, A.8
Chenevix-Trench, G.9
Singer, C.F.10
Pfeiler, G.11
Neuhausen, S.L.12
Lynch, H.T.13
Garber, J.E.14
Weitzel, J.N.15
Isaacs, C.16
Couch, F.17
Narod, S.A.18
Rubinstein, W.S.19
Tomlinson, G.E.20
Ganz, P.A.21
Olopade, O.I.22
Tung, N.23
Blum, J.L.24
Greenberg, R.25
Nathanson, K.L.26
Daly, M.B.27
more..
-
17
-
-
80052225995
-
Modification of BRCA1-associated breast and ovarian cancer risk by BRCA1-interacting genes
-
for the Epidemiological Study of BRCA1 and BRCA2 Mutation Carriers EMBRACE
-
Rebbeck TR, Mitra N, Domchek SM, Wan F, Friebel TM, Tran TV, Singer CF, Tea MK, Blum JL, Tung N, Olopade OI, Weitzel JN, Lynch HT, Snyder CL, Garber JE, Antoniou AC, Peock S, Evans DG, Paterson J, Kennedy MJ, Donaldson A, Dorkins H, Easton DF; for the Epidemiological Study of BRCA1 and BRCA2 Mutation Carriers (EMBRACE), Rubinstein WS, Daly MB, Isaacs C, Nevanlinna H, Couch FJ, Andrulis IL, Freidman E, Laitman Y, Ganz PA, Tomlinson GE, Neuhausen SL, Narod SA, Phelan CM, Greenberg R, Nathanson KL. 2011. Modification of BRCA1-associated breast and ovarian cancer risk by BRCA1-interacting genes. Cancer Res 71:5792-805.
-
(2011)
Cancer Res
, vol.71
, pp. 5792-5805
-
-
Rebbeck, T.R.1
Mitra, N.2
Domchek, S.M.3
Wan, F.4
Friebel, T.M.5
Tran, T.V.6
Singer, C.F.7
Tea, M.K.8
Blum, J.L.9
Tung, N.10
Olopade, O.I.11
Weitzel, J.N.12
Lynch, H.T.13
Snyder, C.L.14
Garber, J.E.15
Antoniou, A.C.16
Peock, S.17
Evans, D.G.18
Paterson, J.19
Kennedy, M.J.20
Donaldson, A.21
Dorkins, H.22
Easton, D.F.23
Rubinstein, W.S.24
Daly, M.B.25
Isaacs, C.26
Nevanlinna, H.27
Couch, F.J.28
Andrulis, I.L.29
Freidman, E.30
Laitman, Y.31
Ganz, P.A.32
Tomlinson, G.E.33
Neuhausen, S.L.34
Narod, S.A.35
Phelan, C.M.36
Greenberg, R.37
Nathanson, K.L.38
more..
-
18
-
-
0036155283
-
Score tests for association between traits and haplotypes when linkage phase is ambiguous
-
DOI 10.1086/338688
-
Schaid DJ, Rowland CM, Tines DE, Jacobson RM, Poland GA. 2002. Score tests for association of traits with haplotypes when linkage phase is ambiguous. Am J Hum Genet 70:425-34. (Pubitemid 34112296)
-
(2002)
American Journal of Human Genetics
, vol.70
, Issue.2
, pp. 425-434
-
-
Schaid, D.J.1
Rowland, C.M.2
Tines, D.E.3
Jacobson, R.M.4
Poland, G.A.5
-
19
-
-
10044294770
-
Evaluating associations of haplotypes with traits
-
DOI 10.1002/gepi.20037
-
Schaid DJ. 2004. Evaluating associations of haplotypes with traits. Genet Epidemiol 27:348-64. (Pubitemid 39602319)
-
(2004)
Genetic Epidemiology
, vol.27
, Issue.4
, pp. 348-364
-
-
Schaid, D.J.1
-
21
-
-
84857771818
-
Haplo.stats: Statistical analysis of haplotypes with traits and covariates when linkage phase is ambiguous
-
Sinnwell JP, Schaid DJ. 2009. haplo.stats: Statistical analysis of haplotypes with traits and covariates when linkage phase is ambiguous. R package version 1.4.4. http://CRAN. R-project.org/package=haplo.stats
-
(2009)
R Package Version 1.4.4
-
-
Sinnwell, J.P.1
Schaid, D.J.2
-
22
-
-
39849100397
-
Estimating effects of rare haplotypes on failure time using a penalized Cox proportional hazards regression model
-
Souverein OW, Zwinderman AH, Jukema JW, Tanck MW. 2008. Estimating effects of rare haplotypes on failure time using a penalized Cox proportional hazards regression model. BMC Genet 9:9.
-
(2008)
BMC Genet
, vol.9
, pp. 9
-
-
Souverein, O.W.1
Zwinderman, A.H.2
Jukema, J.W.3
Tanck, M.W.4
-
23
-
-
78449233578
-
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy
-
Stark K, Esslinger UB, Reinhard W, Petrov G, Winkler T, Komajda M, Isnard R, Charron P, Villard E, Cambien F, Tiret L, Aumont MC, Dubourg O, Trochu JN, Fauchier L, Degroote P, Richter A, Maisch B, Wichter T, Zollbrecht C, Grassl M, Schunkert H, Linsel-Nitschke P, Erdmann J, Baumert J, Illig T, Klopp N, Wichmann HE, Meisinger C, Koenig W, Lichtner P, Meitinger T, Schillert A, König IR, Hetzer R, Heid IM, Regitz-Zagrosek V, Hengstenberg C. 2010. Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. PLoS Genet 6:e1001167.
-
(2010)
PLoS Genet
, vol.6
-
-
Stark, K.1
Esslinger, U.B.2
Reinhard, W.3
Petrov, G.4
Winkler, T.5
Komajda, M.6
Isnard, R.7
Charron, P.8
Villard, E.9
Cambien, F.10
Tiret, L.11
Aumont, M.C.12
Dubourg, O.13
Trochu, J.N.14
Fauchier, L.15
Degroote, P.16
Richter, A.17
Maisch, B.18
Wichter, T.19
Zollbrecht, C.20
Grassl, M.21
Schunkert, H.22
Linsel-Nitschke, P.23
Erdmann, J.24
Baumert, J.25
Illig, T.26
Klopp, N.27
Wichmann, H.E.28
Meisinger, C.29
Koenig, W.30
Lichtner, P.31
Meitinger, T.32
Schillert, A.33
König, I.R.34
Hetzer, R.35
Heid, I.M.36
Regitz-Zagrosek, V.37
Hengstenberg, C.38
more..
-
24
-
-
0242691208
-
A comparison of bayesian methods for haplotype reconstruction from population genotype data
-
DOI 10.1086/379378
-
Stephens M, Donnelly P. 2003. A comparison of Bayesian methods for haplotype reconstruction from population genotype data. Am J Hum Genet 73:1162-69. (Pubitemid 37414228)
-
(2003)
American Journal of Human Genetics
, vol.73
, Issue.5
, pp. 1162-1169
-
-
Stephens, M.1
Donnelly, P.2
-
25
-
-
21044444898
-
Estimating haplotype relative risks on human survival in population-based association studies
-
DOI 10.1159/000085223
-
Tan Q, Christiansen L, Bathum L, Zhao JH, Yashin AI, Vaupel JW, Christensen K, Kruse TA. 2005. Estimating haplotype relative risks on human survival in population-based association studies. Hum Hered 59:88-97. (Pubitemid 40874844)
-
(2005)
Human Heredity
, vol.59
, Issue.2
, pp. 88-97
-
-
Tan, Q.1
Christiansen, L.2
Bathum, L.3
Jing, H.Z.4
Yashin, A.I.5
Vaupel, J.W.6
Christensen, K.7
Kruse, T.A.8
-
26
-
-
7744247432
-
Cox proportional hazards survival regression in haplotype-based association analysis using the Stochastic-EM algorithm
-
DOI 10.1038/sj.ejhg.5201238
-
Tregouet DA, Tiret L. 2004. Cox proportional hazards survival regression in haplotype-based association analysis using the Stochastic-EM algorithm. Eur J Hum Genet 12:971-4. (Pubitemid 39462132)
-
(2004)
European Journal of Human Genetics
, vol.12
, Issue.11
, pp. 971-974
-
-
Tregouet, D.-A.1
Tiret, L.2
-
27
-
-
14644440626
-
A method for evaluating the impact of individual haplotypes on disease incidence in molecular epidemiology studies
-
Venkatraman ES, Mitra N, Begg CB. 2004. A method for evaluating the impact of individual haplotypes on disease incidence in molecular epidemiology studies. Stat Appl Genet Mol Biol 3:27.
-
(2004)
Stat Appl Genet Mol Biol
, vol.3
, pp. 27
-
-
Venkatraman, E.S.1
Mitra, N.2
Begg, C.B.3
-
28
-
-
0036284203
-
Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals
-
DOI 10.1159/000057986
-
Zaykin DV, Westfall PH, Young SS, Karnoub MA, Wagner MJ, Ehm MG. 2002. Testing associations of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals. Hum Hered 53:79-91. (Pubitemid 34621657)
-
(2002)
Human Heredity
, vol.53
, Issue.2
, pp. 79-91
-
-
Zaykin, D.V.1
Westfall, P.H.2
Young, S.S.3
Karnoub, M.A.4
Wagner, M.J.5
Ehm, M.G.6
|