-
1
-
-
0015456905
-
Genetics of hyperlipidemia in coronary heart disease
-
Goldstein JL, Hazzard WR, Schrott HG, Bierman EL, Motulsky AG. Genetics of hyperlipidemia in coronary heart disease. Trans Assoc Am Physicians. 1972;85:120-138.
-
(1972)
Trans Assoc Am Physicians
, vol.85
, pp. 120-138
-
-
Goldstein, J.L.1
Hazzard, W.R.2
Schrott, H.G.3
Bierman, E.L.4
Motulsky, A.G.5
-
2
-
-
0018843763
-
Very low density lipoprotein overproduction in genetic forms of hypertriglyceridaemia
-
Chait A, Albers JJ, Brunzell JD. Very low density lipoprotein overproduction in genetic forms of hypertriglyceridaemia. Eur J Clin Invest. 1980;10:17-22.
-
(1980)
Eur J Clin Invest
, vol.10
, pp. 17-22
-
-
Chait, A.1
Albers, J.J.2
Brunzell, J.D.3
-
3
-
-
16644384064
-
Apolipoprotein B as a marker of familial hyper-lipoproteinemia
-
Sveger T, Nordborg K. Apolipoprotein B as a marker of familial hyper-lipoproteinemia. J Atheroscler Thromb. 2004;11:286-292.
-
(2004)
J Atheroscler Thromb
, vol.11
, pp. 286-292
-
-
Sveger, T.1
Nordborg, K.2
-
4
-
-
0031918837
-
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
-
DOI 10.1038/ng0498-369
-
Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamaki J, Suomalainen AJ, Syvanen AC, Lehtimaki T, Viikari JS, Laakso M, Taskinen MR, Ehnholm C, Peltonen L. Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23. Nat Genet. 1998;18: 369-373. (Pubitemid 28158167)
-
(1998)
Nature Genetics
, vol.18
, Issue.4
, pp. 369-373
-
-
Pajukanta, P.1
Nuotio, I.2
Terwilliger, J.D.3
Porkka, K.V.K.4
Ylitalo, K.5
Pihlajamaki, J.6
Suomalainen, A.J.7
Syvanen, A.-C.8
Lehtimaki, T.9
Viikari, J.S.A.10
Laakso, M.11
Taskinen, M.-R.12
Ehnholm, C.13
Peltonen, L.14
-
5
-
-
10744231819
-
Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia
-
Naoumova RP, Bonney SA, Eichenbaum-Voline S, Patel HN, Jones B, Jones EL, Amey J, Colilla S, Neuwirth CK, Allotey R, Seed M, Bet-teridge DJ, Galton DJ, Cox NJ, Bell GI, Scott J, Shoulders CC. Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia. Arte-rioscler Thromb Vasc Biol. 2003;23:2070-2077.
-
(2003)
Arte-rioscler Thromb Vasc Biol
, vol.23
, pp. 2070-2077
-
-
Naoumova, R.P.1
Bonney, S.A.2
Eichenbaum-Voline, S.3
Patel, H.N.4
Jones, B.5
Jones, E.L.6
Amey, J.7
Colilla, S.8
Neuwirth, C.K.9
Allotey, R.10
Seed, M.11
Bet-Teridge, D.J.12
Galton, D.J.13
Cox, N.J.14
Bell, G.I.15
Scott, J.16
Shoulders, C.C.17
-
6
-
-
0037385395
-
Combined analysis of genome scans of Dutch and Finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q
-
Pajukanta P, Allayee H, Krass KL, Kuraishy A, Soro A, Lilja HE, Mar R, Taskinen MR, Nuotio I, Laakso M, Rotter JI, de Bruin TW, Cantor RM, Lusis AJ, Peltonen L. Combined analysis of genome scans of Dutch and Finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q. Am J Hum Genet. 2003;72:903-917.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 903-917
-
-
Pajukanta, P.1
Allayee, H.2
Krass, K.L.3
Kuraishy, A.4
Soro, A.5
Lilja, H.E.6
Mar, R.7
Taskinen, M.R.8
Nuotio, I.9
Laakso, M.10
Rotter, J.I.11
De Bruin, T.W.12
Cantor, R.M.13
Lusis, A.J.14
Peltonen, L.15
-
7
-
-
12144287541
-
Familial combined hyperlipid-emia is associated with upstream transcription factor 1 (USF1)
-
Pajukanta P, Lilja HE, Sinsheimer JS, Cantor RM, Lusis AJ, Gentile M, Duan XJ, Soro-Paavonen A, Naukkarinen J, Saarela J, Laakso M, Ehnholm C, Taskinen MR, Peltonen L. Familial combined hyperlipid-emia is associated with upstream transcription factor 1 (USF1). Nat Genet. 2004;36:371-376.
-
(2004)
Nat Genet
, vol.36
, pp. 371-376
-
-
Pajukanta, P.1
Lilja, H.E.2
Sinsheimer, J.S.3
Cantor, R.M.4
Lusis, A.J.5
Gentile, M.6
Duan, X.J.7
Soro-Paavonen, A.8
Naukkarinen, J.9
Saarela, J.10
Laakso, M.11
Ehnholm, C.12
Taskinen, M.R.13
Peltonen, L.14
-
8
-
-
33748674433
-
Unraveling the complex genetics of familial combined hyperlipidemia
-
Suviolahti E, Lilja HE, Pajukanta P. Unraveling the complex genetics of familial combined hyperlipidemia. Ann Med. 2006;38:337-351.
-
(2006)
Ann Med
, vol.38
, pp. 337-351
-
-
Suviolahti, E.1
Lilja, H.E.2
Pajukanta, P.3
-
9
-
-
33947641542
-
Cardiovascular risk factors in the urban Mexican population: The FRIMEX study
-
Meaney E, Lara-Esqueda A, Ceballos-Reyes GM, Asbun J, Vela A, Martinez-Marroquin Y, Lopez V, Meaney A, de la Cabada-Tamez E, Velazquez-Monroy O, Tapia-Conyer R. Cardiovascular risk factors in the urban Mexican population: the FRIMEX study. Public Health. 2007;121: 378-384.
-
(2007)
Public Health
, vol.121
, pp. 378-384
-
-
Meaney, E.1
Lara-Esqueda, A.2
Ceballos-Reyes, G.M.3
Asbun, J.4
Vela, A.5
Martinez-Marroquin, Y.6
Lopez, V.7
Meaney, A.8
De La Cabada-Tamez, E.9
Velazquez-Monroy, O.10
Tapia-Conyer, R.11
-
10
-
-
58249093876
-
Combined hyperlipidemia in relation to race/ethnicity, obesity, and insulin resistance in the Multi-Ethnic Study of Atherosclerosis
-
Paramsothy P, Knopp R, Bertoni AG, Tsai MY, Rue T, Heckbert SR. Combined hyperlipidemia in relation to race/ethnicity, obesity, and insulin resistance in the Multi-Ethnic Study of Atherosclerosis. Metabolism. 2009;58:212-219.
-
(2009)
Metabolism
, vol.58
, pp. 212-219
-
-
Paramsothy, P.1
Knopp, R.2
Bertoni, A.G.3
Tsai, M.Y.4
Rue, T.5
Heckbert, S.R.6
-
11
-
-
58149163149
-
Common variants at 30 loci contribute to polygenic dyslipidemia
-
Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt NP, Parish S, Clarke R, Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN, Sundvall J, Laakso M, Ferrucci L, Scheet P, Sanna S, Uda M, Yang Q, Lunetta KL, Dupuis J, de Bakker PI, O'Donnell CJ, Chambers JC, Kooner JS, Hercberg S, Meneton P, Lakatta EG, Scuteri A, Schlessinger D, Tuomilehto J, Collins FS, Groop L, Altshuler D, Collins R, Lathrop GM, Melander O, Salomaa V, Peltonen L, Orho-Melander M, Ordovas JM, Boehnke M, Abecasis GR, Mohlke KL, Cupples LA. Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet. 2009;41:56-65.
-
(2009)
Nat Genet
, vol.41
, pp. 56-65
-
-
Kathiresan, S.1
Willer, C.J.2
Peloso, G.M.3
Demissie, S.4
Musunuru, K.5
Schadt, E.E.6
Kaplan, L.7
Bennett, D.8
Li, Y.9
Tanaka, T.10
Voight, B.F.11
Bonnycastle, L.L.12
Jackson, A.U.13
Crawford, G.14
Surti, A.15
Guiducci, C.16
Burtt, N.P.17
Parish, S.18
Clarke, R.19
Zelenika, D.20
Kubalanza, K.A.21
Morken, M.A.22
Scott, L.J.23
Stringham, H.M.24
Galan, P.25
Swift, A.J.26
Kuusisto, J.27
Bergman, R.N.28
Sundvall, J.29
Laakso, M.30
Ferrucci, L.31
Scheet, P.32
Sanna, S.33
Uda, M.34
Yang, Q.35
Lunetta, K.L.36
Dupuis, J.37
De Bakker, P.I.38
O'Donnell, C.J.39
Chambers, J.C.40
Kooner, J.S.41
Hercberg, S.42
Meneton, P.43
Lakatta, E.G.44
Scuteri, A.45
Schlessinger, D.46
Tuomilehto, J.47
Collins, F.S.48
Groop, L.49
Altshuler, D.50
Collins, R.51
Lathrop, G.M.52
Melander, O.53
Salomaa, V.54
Peltonen, L.55
Orho-Melander, M.56
Ordovas, J.M.57
Boehnke, M.58
Abecasis, G.R.59
Mohlke, K.L.60
Cupples, L.A.61
more..
-
12
-
-
58549109632
-
Plasma lipoproteins: Genetic influences and clinical implications
-
Hegele RA. Plasma lipoproteins: genetic influences and clinical implications. Nat Rev Genet. 2009;10:109-121.
-
(2009)
Nat Rev Genet
, vol.10
, pp. 109-121
-
-
Hegele, R.A.1
-
13
-
-
30344463185
-
The quantitative trait linkage disequilibrium test: A more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification
-
Havill LM, Dyer TD, Richardson DK, Mahaney MC, Blangero J. The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification. BMC Genet. 2005;6(suppl 1):S91.
-
(2005)
BMC Genet
, vol.6
, Issue.SUPPL. 1
-
-
Havill, L.M.1
Dyer, T.D.2
Richardson, D.K.3
Mahaney, M.C.4
Blangero, J.5
-
14
-
-
33747039577
-
Common hepatic nuclear factor-4a variants are associated with high serum lipid levels and the metabolic syndrome
-
Weissglas-Volkov D, Huertas-Vazquez A, Suviolahti E, Lee J, Plaisier C, Canizales-Quinteros S, Tusie-Luna T, Aguilar-Salinas C, Taskinen MR, Pajukanta P. Common hepatic nuclear factor-4a variants are associated with high serum lipid levels and the metabolic syndrome. Diabetes. 2006;55:1970-1977.
-
(2006)
Diabetes
, vol.55
, pp. 1970-1977
-
-
Weissglas-Volkov, D.1
Huertas-Vazquez, A.2
Suviolahti, E.3
Lee, J.4
Plaisier, C.5
Canizales-Quinteros, S.6
Tusie-Luna, T.7
Aguilar-Salinas, C.8
Taskinen, M.R.9
Pajukanta, P.10
-
15
-
-
0033362160
-
Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
-
Pajukanta P, Terwilliger JD, Perola M, Hiekkalinna T, Nuotio I, Ellonen P, Parkkonen M, Hartiala J, Ylitalo K, Pihlajamaki J, Porkka K, Laakso M, Viikari J, Ehnholm C, Taskinen MR, Peltonen L. Genomewide scan for familial combined hyperlipidemia genes in Finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels. Am J Hum Genet. 1999;64:1453-1463.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1453-1463
-
-
Pajukanta, P.1
Terwilliger, J.D.2
Perola, M.3
Hiekkalinna, T.4
Nuotio, I.5
Ellonen, P.6
Parkkonen, M.7
Hartiala, J.8
Ylitalo, K.9
Pihlajamaki, J.10
Porkka, K.11
Laakso, M.12
Viikari, J.13
Ehnholm, C.14
Taskinen, M.R.15
Peltonen, L.16
-
16
-
-
33745597381
-
Variance component models for X-linked QTLs
-
Lange K, Sobel E. Variance component models for X-linked QTLs. Genet Epidemiol. 2006;30:380-383.
-
(2006)
Genet Epidemiol
, vol.30
, pp. 380-383
-
-
Lange, K.1
Sobel, E.2
-
17
-
-
0031966959
-
Multipoint quantitative-trait linkage analysis in general pedigrees
-
Almasy L, Blangero J. Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet. 1998;62:1198-1211.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1198-1211
-
-
Almasy, L.1
Blangero, J.2
-
18
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995;11: 241-247.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
19
-
-
0033652887
-
Family-based tests of association in the presence of linkage
-
Lake SL, Blacker D, Laird NM. Family-based tests of association in the presence of linkage. Am J Hum Genet. 2000;67:1515-1525.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1515-1525
-
-
Lake, S.L.1
Blacker, D.2
Laird, N.M.3
-
20
-
-
5344249336
-
Quantitative trait loci for apolipoprotein B, cholesterol, and triglyc-erides in familial combined hyperlipidemia pedigrees
-
Cantor RM, de Bruin T, Kono N, Napier S, van Nas A, Allayee H, Lusis AJ. Quantitative trait loci for apolipoprotein B, cholesterol, and triglyc-erides in familial combined hyperlipidemia pedigrees. Arterioscler Thromb Vasc Biol. 2004;24:1935-1941.
-
(2004)
Arterioscler Thromb Vasc Biol
, vol.24
, pp. 1935-1941
-
-
Cantor, R.M.1
De Bruin, T.2
Kono, N.3
Napier, S.4
Van Nas, A.5
Allayee, H.6
Lusis, A.J.7
-
21
-
-
34250894969
-
A genomewide admixture map for Latino populations
-
Price AL, Patterson N, Yu F, Cox DR, Waliszewska A, McDonald GJ, Tandon A, Schirmer C, Neubauer J, Bedoya G, Duque C, Villegas A, Bortolini MC, Salzano FM, Gallo C, Mazzotti G, Tello-Ruiz M, Riba L, Aguilar-Salinas CA, Canizales-Quinteros S, Menjivar M, Klitz W, Henderson B, Haiman CA, Winkler C, Tusie-Luna T, Ruiz-Linares A, Reich D. A genomewide admixture map for Latino populations. Am J Hum Genet. 2007;80:1024-1036.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 1024-1036
-
-
Price, A.L.1
Patterson, N.2
Yu, F.3
Cox, D.R.4
Waliszewska, A.5
McDonald, G.J.6
Tandon, A.7
Schirmer, C.8
Neubauer, J.9
Bedoya, G.10
Duque, C.11
Villegas, A.12
Bortolini, M.C.13
Salzano, F.M.14
Gallo, C.15
Mazzotti, G.16
Tello-Ruiz, M.17
Riba, L.18
Aguilar-Salinas, C.A.19
Canizales-Quinteros, S.20
Menjivar, M.21
Klitz, W.22
Henderson, B.23
Haiman, C.A.24
Winkler, C.25
Tusie-Luna, T.26
Ruiz-Linares, A.27
Reich, D.28
more..
-
22
-
-
33645096052
-
Apo B versus cholesterol in estimating cardiovascular risk and in guiding therapy: Report of the thirty-person/ten-country panel
-
Barter PJ, Ballantyne CM, Carmena R, Castro Cabezas M, Chapman MJ, Couture P, de Graaf J, Durrington PN, Faergeman O, Frohlich J, Furberg CD, Gagne C, Haffner SM, Humphries SE, Jungner I, Krauss RM, Kwiterovich P, Marcovina S, Packard CJ, Pearson TA, Reddy KS, Rosenson R, Sarrafzadegan N, Sniderman AD, Stalenhoef AF, Stein E, Talmud PJ, Tonkin AM, Walldius G, Williams KM. Apo B versus cholesterol in estimating cardiovascular risk and in guiding therapy: report of the thirty-person/ten-country panel. J Intern Med. 2006;259: 247-258.
-
(2006)
J Intern Med
, vol.259
, pp. 247-258
-
-
Barter, P.J.1
Ballantyne, C.M.2
Carmena, R.3
Castro Cabezas, M.4
Chapman, M.J.5
Couture, P.6
De Graaf, J.7
Durrington, P.N.8
Faergeman, O.9
Frohlich, J.10
Furberg, C.D.11
Gagne, C.12
Haffner, S.M.13
Humphries, S.E.14
Jungner, I.15
Krauss, R.M.16
Kwiterovich, P.17
Marcovina, S.18
Packard, C.J.19
Pearson, T.A.20
Reddy, K.S.21
Rosenson, R.22
Sarrafzadegan, N.23
Sniderman, A.D.24
Stalenhoef, A.F.25
Stein, E.26
Talmud, P.J.27
Tonkin, A.M.28
Walldius, G.29
Williams, K.M.30
more..
-
23
-
-
0025086368
-
Recent progress in understanding apolipoprotein B
-
Young SG. Recent progress in understanding apolipoprotein B. Circulation. 1990;82:1574-1594.
-
(1990)
Circulation
, vol.82
, pp. 1574-1594
-
-
Young, S.G.1
-
24
-
-
0029900758
-
Apolipoprotein B RNA editing enzyme-deficient mice are viable despite alterations in lipoprotein metabolism
-
Morrison JR, Paszty C, Stevens ME, Hughes SD, Forte T, Scott J, Rubin EM. Apolipoprotein B RNA editing enzyme-deficient mice are viable despite alterations in lipoprotein metabolism. Proc Natl Acad Sci USA. 1996;93:7154-7159.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 7154-7159
-
-
Morrison, J.R.1
Paszty, C.2
Stevens, M.E.3
Hughes, S.D.4
Forte, T.5
Scott, J.6
Rubin, E.M.7
-
25
-
-
0037188510
-
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly
-
Lettice LA, Horikoshi T, Heaney SJ, van Baren MJ, van der Linde HC, Breedveld GJ, Joosse M, Akarsu N, Oostra BA, Endo N, Shibata M, Suzuki M, Takahashi E, Shinka T, Nakahori Y, Ayusawa D, Nakabayashi K, Scherer SW, Heutink P, Hill RE, Noji S. Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly. Proc Natl Acad Sci USA. 2002;99:7548-7553.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 7548-7553
-
-
Lettice, L.A.1
Horikoshi, T.2
Heaney, S.J.3
Van Baren, M.J.4
Van Der Linde, H.C.5
Breedveld, G.J.6
Joosse, M.7
Akarsu, N.8
Oostra, B.A.9
Endo, N.10
Shibata, M.11
Suzuki, M.12
Takahashi, E.13
Shinka, T.14
Nakahori, Y.15
Ayusawa, D.16
Nakabayashi, K.17
Scherer, S.W.18
Heutink, P.19
Hill, R.E.20
Noji, S.21
more..
-
26
-
-
34250305146
-
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
-
ENCODE Project Consortium
-
ENCODE Project Consortium. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature. 2007;447:799-816.
-
(2007)
Nature
, vol.447
, pp. 799-816
-
-
|