-
1
-
-
84871969762
-
Large-scale association analysis identifies new risk loci for coronary artery disease
-
Consortium, C.A.D., Deloukas, P., Kanoni, S., Willenborg, C., Farrall, M., Assimes, T.L., Thompson, J.R., Ingelsson, E., Saleheen, D., Erdmann, J. et al. (2013) Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet., 45, 25-33.
-
(2013)
Nat. Genet
, vol.45
, pp. 25-33
-
-
Consortium, C.A.D.1
Deloukas, P.2
Kanoni, S.3
Willenborg, C.4
Farrall, M.5
Assimes, T.L.6
Thompson, J.R.7
Ingelsson, E.8
Saleheen, D.9
Erdmann, J.10
-
2
-
-
84887099827
-
Discovery and refinement of loci associated with lipid levels
-
Global Lipids Genetics, C., Willer, C.J., Schmidt, E.M., Sengupta, S., Peloso, G.M., Gustafsson, S., Kanoni, S., Ganna, A., Chen, J., Buchkovich, M.L. et al. (2013) Discovery and refinement of loci associated with lipid levels. Nat. Genet., 45, 1274-1283.
-
(2013)
Nat. Genet
, vol.45
, pp. 1274-1283
-
-
Global Lipids Genetics, C.1
Willer, C.J.2
Schmidt, E.M.3
Sengupta, S.4
Peloso, G.M.5
Gustafsson, S.6
Kanoni, S.7
Ganna, A.8
Chen, J.9
Buchkovich, M.L.10
-
3
-
-
77955505564
-
Biological, clinical and population relevance of 95 loci for blood lipids
-
Teslovich, T.M., Musunuru, K., Smith, A.V., Edmondson, A.C., Stylianou, I.M., Koseki, M., Pirruccello, J.P., Ripatti, S., Chasman, D.I., Willer, C.J. 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
Koseki, M.6
Pirruccello, J.P.7
Ripatti, S.8
Chasman, D.I.9
Willer, C.J.10
-
4
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio, T.A., Collins, F.S., Cox, N.J., Goldstein, D.B., Hindorff, L.A., Hunter, D.J., McCarthy, M.I., Ramos, E.M., Cardon, L.R., Chakravarti, A. et al. (2009) Finding the missing heritability of complex diseases. Nature, 461, 747-753.
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
Collins, F.S.2
Cox, N.J.3
Goldstein, D.B.4
Hindorff, L.A.5
Hunter, D.J.6
McCarthy, M.I.7
Ramos, E.M.8
Cardon, L.R.9
Chakravarti, A.10
-
5
-
-
73649103089
-
Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis
-
Chasman, D.I., Pare, G., Mora, S., Hopewell, J.C., Peloso, G., Clarke, R., Cupples, L.A., Hamsten, A., Kathiresan, S., Malarstig, A. et al. (2009) Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis. PLoS Genet., 5, e1000730.
-
(2009)
PLoS Genet
, vol.5
-
-
Chasman, D.I.1
Pare, G.2
Mora, S.3
Hopewell, J.C.4
Peloso, G.5
Clarke, R.6
Cupples, L.A.7
Hamsten, A.8
Kathiresan, S.9
Malarstig, A.10
-
6
-
-
58149163149
-
Common variants at 30 loci contribute to polygenic dyslipidemia
-
Kathiresan, S., Willer, C.J., Peloso, G.M., Demissie, S., Musunuru, K., Schadt, E.E., Kaplan, L., Bennett, D., Li, Y., Tanaka, T. et al. (2009) Common variants at 30 loci contribute to polygenic dyslipidemia. Nat. Genet., 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
-
7
-
-
38849166666
-
LDL-cholesterol concentrations: a genome-wide association study
-
Sandhu, M.S., Waterworth, D.M., Debenham, S.L., Wheeler, E., Papadakis, K., Zhao, J.H., Song, K., Yuan, X., Johnson, T., Ashford, S. et al. (2008) LDL-cholesterol concentrations: a genome-wide association study. Lancet, 371, 483-491.
-
(2008)
Lancet
, vol.371
, pp. 483-491
-
-
Sandhu, M.S.1
Waterworth, D.M.2
Debenham, S.L.3
Wheeler, E.4
Papadakis, K.5
Zhao, J.H.6
Song, K.7
Yuan, X.8
Johnson, T.9
Ashford, S.10
-
8
-
-
38649125868
-
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
-
Willer, C.J., Sanna, S., Jackson, A.U., Scuteri, A., Bonnycastle, L.L., Clarke, R., Heath, S.C., Timpson, N.J., Najjar, S.S., Stringham, H.M. et al. (2008) Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat. Genet., 40, 161-169.
-
(2008)
Nat. Genet
, vol.40
, pp. 161-169
-
-
Willer, C.J.1
Sanna, S.2
Jackson, A.U.3
Scuteri, A.4
Bonnycastle, L.L.5
Clarke, R.6
Heath, S.C.7
Timpson, N.J.8
Najjar, S.S.9
Stringham, H.M.10
-
9
-
-
44949140832
-
The lipoprotein subfraction profile: heritability and identification of quantitative trait loci
-
Kaess, B., Fischer, M., Baessler, A., Stark, K., Huber, F., Kremer, W., Kalbitzer, H.R., Schunkert, H., Riegger, G. and Hengstenberg, C. (2008) The lipoprotein subfraction profile: heritability and identification of quantitative trait loci. J. Lipid Res., 49, 715-723.
-
(2008)
J. Lipid Res
, vol.49
, pp. 715-723
-
-
Kaess, B.1
Fischer, M.2
Baessler, A.3
Stark, K.4
Huber, F.5
Kremer, W.6
Kalbitzer, H.R.7
Schunkert, H.8
Riegger, G.9
Hengstenberg, C.10
-
10
-
-
80053549439
-
Clan genomics and the complex architecture of human disease
-
Lupski, J.R., Belmont, J.W., Boerwinkle, E. and Gibbs, R.A. (2011) Clan genomics and the complex architecture of human disease. Cell, 147, 32-43.
-
(2011)
Cell
, vol.147
, pp. 32-43
-
-
Lupski, J.R.1
Belmont, J.W.2
Boerwinkle, E.3
Gibbs, R.A.4
-
11
-
-
68649101805
-
Common vs. rare allele hypotheses for complex diseases
-
Schork, N.J., Murray, S.S., Frazer, K.A. and Topol, E.J. (2009) Common vs. rare allele hypotheses for complex diseases. Curr. Opin. Genet. Dev., 19, 212-219.
-
(2009)
Curr. Opin. Genet. Dev
, vol.19
, pp. 212-219
-
-
Schork, N.J.1
Murray, S.S.2
Frazer, K.A.3
Topol, E.J.4
-
12
-
-
84887099827
-
Discovery and refinement of loci associated with lipid levels
-
Willer, C.J., Schmidt, E.M., Sengupta, S., Peloso, G.M., Gustafsson, S., Kanoni, S., Ganna, A., Chen, J., Buchkovich, M.L., Mora, S. et al. (2013) Discovery and refinement of loci associated with lipid levels. Nat. Genet., 45, 1274-1283.
-
(2013)
Nat. Genet
, vol.45
, pp. 1274-1283
-
-
Willer, C.J.1
Schmidt, E.M.2
Sengupta, S.3
Peloso, G.M.4
Gustafsson, S.5
Kanoni, S.6
Ganna, A.7
Chen, J.8
Buchkovich, M.L.9
Mora, S.10
-
13
-
-
77954143522
-
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
-
Voight, B.F., Scott, L.J., Steinthorsdottir, V., Morris, A.P., Dina, C., Welch, R.P., Zeggini, E., Huth, C., Aulchenko, Y.S., Thorleifsson, G. et al. (2010) Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat. Genet., 42, 579-589.
-
(2010)
Nat. Genet
, vol.42
, pp. 579-589
-
-
Voight, B.F.1
Scott, L.J.2
Steinthorsdottir, V.3
Morris, A.P.4
Dina, C.5
Welch, R.P.6
Zeggini, E.7
Huth, C.8
Aulchenko, Y.S.9
Thorleifsson, G.10
-
14
-
-
73549097512
-
Genetic variants associated with Lp(a) lipoprotein level and coronary disease
-
Clarke, R., Peden, J.F., Hopewell, J.C., Kyriakou, T., Goel, A., Heath, S.C., Parish, S., Barlera, S., Franzosi, M.G., Rust, S. et al. (2009) Genetic variants associated with Lp(a) lipoprotein level and coronary disease. N. Engl. J. Med., 361, 2518-2528.
-
(2009)
N. Engl. J. Med
, vol.361
, pp. 2518-2528
-
-
Clarke, R.1
Peden, J.F.2
Hopewell, J.C.3
Kyriakou, T.4
Goel, A.5
Heath, S.C.6
Parish, S.7
Barlera, S.8
Franzosi, M.G.9
Rust, S.10
-
15
-
-
0034801632
-
ABCA6, a novel a subclass ABC transporter
-
Kaminski, W.E., Wenzel, J.J., Piehler, A., Langmann, T. and Schmitz, G. (2001) ABCA6, a novel a subclass ABC transporter. Biochem. Biophys. Res. Commun., 285, 1295-1301.
-
(2001)
Biochem. Biophys. Res. Commun
, vol.285
, pp. 1295-1301
-
-
Kaminski, W.E.1
Wenzel, J.J.2
Piehler, A.3
Langmann, T.4
Schmitz, G.5
-
16
-
-
84884406184
-
FoxO regulates expression of ABCA6, an intracellular ATPbinding-cassette transporter responsive to cholesterol
-
Gai, J., Ji, M., Shi, C., Li, W., Chen, S., Wang, Y. and Li, H. (2013) FoxO regulates expression of ABCA6, an intracellular ATPbinding-cassette transporter responsive to cholesterol. Int. J. Biochem. Cell Biol., 45, 2651-2659.
-
(2013)
Int. J. Biochem. Cell Biol
, vol.45
, pp. 2651-2659
-
-
Gai, J.1
Ji, M.2
Shi, C.3
Li, W.4
Chen, S.5
Wang, Y.6
Li, H.7
-
17
-
-
84862832570
-
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits
-
Yang, J., Ferreira, T., Morris, A.P., Medland, S.E., Genetic Investigation of, A.T.C., Replication, D.I.G., Meta-analysis, C., Madden, P.A., Heath, A.C., Martin, N.G. et al. (2012) Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nat. Genet., 44, 369-375.
-
(2012)
Nat. Genet
, vol.44
, pp. 369-375
-
-
Yang, J.1
Ferreira, T.2
Morris, A.P.3
Medland, S.E.4
Replication, D.I.G.5
Meta-Analysis, C.6
Madden, P.A.7
Heath, A.C.8
Martin, N.G.9
-
18
-
-
79953178222
-
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium
-
Kraja, A.T., Vaidya, D., Pankow, J.S., Goodarzi, M.O., Assimes, T.L., Kullo, I.J., Sovio, U., Mathias, R.A., Sun, Y.V., Franceschini, N. et al. (2011) A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Diabetes, 60, 1329-1339.
-
(2011)
Diabetes
, vol.60
, pp. 1329-1339
-
-
Kraja, A.T.1
Vaidya, D.2
Pankow, J.S.3
Goodarzi, M.O.4
Assimes, T.L.5
Kullo, I.J.6
Sovio, U.7
Mathias, R.A.8
Sun, Y.V.9
Franceschini, N.10
-
19
-
-
84896331788
-
Systemic lupus erythematosus: old and new susceptibility genes versus clinical manifestations
-
de Azevêdo Silva J., Addobbati C., Sandrin-Garcia P., Crovella S. (2014) Systemic lupus erythematosus: old and new susceptibility genes versus clinical manifestations. Curr. Genomics, 15, 52-65.
-
(2014)
Curr. Genomics
, vol.15
, pp. 52-65
-
-
de Azevêdo Silva, J.1
Addobbati, C.2
Sandrin-Garcia, P.3
Crovella, S.4
-
20
-
-
84862909349
-
Five years of GWAS discovery
-
Visscher, P.M., Brown, M.A., McCarthy, M.I. and Yang, J. (2012) Five years of GWAS discovery. Am. J. Hum. Genet., 90, 7-24.
-
(2012)
Am. J. Hum. Genet
, vol.90
, pp. 7-24
-
-
Visscher, P.M.1
Brown, M.A.2
McCarthy, M.I.3
Yang, J.4
-
21
-
-
84893720400
-
Whole-exome sequencing identifies rare and lowfrequency coding variants associated with LDL cholesterol
-
Lange, L.A., Hu, Y., Zhang, H., Xue, C., Schmidt, E.M., Tang, Z.Z., Bizon, C., Lange, E.M., Smith, J.D., Turner, E.H. et al. (2014) Whole-exome sequencing identifies rare and lowfrequency coding variants associated with LDL cholesterol. Am. J. Hum. Genet., 94, 233-245.
-
(2014)
Am. J. Hum. Genet
, vol.94
, pp. 233-245
-
-
Lange, L.A.1
Hu, Y.2
Zhang, H.3
Xue, C.4
Schmidt, E.M.5
Tang, Z.Z.6
Bizon, C.7
Lange, E.M.8
Smith, J.D.9
Turner, E.H.10
-
22
-
-
84893756641
-
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56, 000 whites and blacks
-
Peloso, G.M., Auer, P.L., Bis, J.C., Voorman, A., Morrison, A.C., Stitziel, N.O., Brody, J.A., Khetarpal, S.A., Crosby, J.R., Fornage, M. et al. (2014) Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56, 000 whites and blacks. Am. J. Hum. Genet., 94, 223-232.
-
(2014)
Am. J. Hum. Genet
, vol.94
, pp. 223-232
-
-
Peloso, G.M.1
Auer, P.L.2
Bis, J.C.3
Voorman, A.4
Morrison, A.C.5
Stitziel, N.O.6
Brody, J.A.7
Khetarpal, S.A.8
Crosby, J.R.9
Fornage, M.10
-
23
-
-
84890308141
-
Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia
-
Rosenthal, E.A., Ranchalis, J., Crosslin, D.R., Burt, A., Brunzell, J.D., Motulsky, A.G., Nickerson, D.A., Project, N.G.E.S., Wijsman, E.M. and Jarvik, G.P. (2013) Joint linkage and association analysis with exome sequence data implicates SLC25A40 in hypertriglyceridemia. Am. J. Hum. Genet., 93, 1035-1045.
-
(2013)
Am. J. Hum. Genet
, vol.93
, pp. 1035-1045
-
-
Rosenthal, E.A.1
Ranchalis, J.2
Crosslin, D.R.3
Burt, A.4
Brunzell, J.D.5
Motulsky, A.G.6
Nickerson, D.A.7
Project, N.G.E.S.8
Wijsman, E.M.9
Jarvik, G.P.10
-
24
-
-
84930090376
-
The impact of low-frequency and rare variants on lipid levels
-
Surakka, I., Horikoshi, M., Mägi, R., Sarin, A.P., Mahajan, A., Lagou, V., Marullo, L., Ferreira, T., Miraglio, B., Timonen, S. et al. (2015) The impact of low-frequency and rare variants on lipid levels. Nat. Genet., 47, 589-597.
-
(2015)
Nat. Genet
, vol.47
, pp. 589-597
-
-
Surakka, I.1
Horikoshi, M.2
Mägi, R.3
Sarin, A.P.4
Mahajan, A.5
Lagou, V.6
Marullo, L.7
Ferreira, T.8
Miraglio, B.9
Timonen, S.10
-
25
-
-
19544391975
-
A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups
-
Capon, F., Allen, M.H., Ameen, M., Burden, A.D., Tillman, D., Barker, J.N. and Trembath, R.C. (2004) A synonymous SNP of the corneodesmosin gene leads to increased mRNA stability and demonstrates association with psoriasis across diverse ethnic groups. Hum. Mol. Genet., 13, 2361-2368.
-
(2004)
Hum. Mol. Genet
, vol.13
, pp. 2361-2368
-
-
Capon, F.1
Allen, M.H.2
Ameen, M.3
Burden, A.D.4
Tillman, D.5
Barker, J.N.6
Trembath, R.C.7
-
26
-
-
85018215032
-
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci
-
Demerath E.W., Guan W., Grove M.L., Aslibekyan S., Mendelson M., Zhou Y.H., HedmanÅ.K., Sandling J.K., Li L.A., Irvin M.R. et al. (2015) Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci. Hum. Mol. Genet., 24, 4464-4479.
-
(2015)
Hum. Mol. Genet
, vol.24
, pp. 4464-4479
-
-
Demerath, E.W.1
Guan, W.2
Grove, M.L.3
Aslibekyan, S.4
Mendelson, M.5
Zhou, Y.H.6
Hedman, Å.K.7
Sandling, J.K.8
Li, L.A.9
Irvin, M.R.10
-
27
-
-
84868470681
-
Large-scale genecentric meta-analysis across 32 studies identifies multiple lipid loci
-
Asselbergs, F.W., Guo, Y., van Iperen, E.P., Sivapalaratnam, S., Tragante, V., Lanktree, M.B., Lange, L.A., Almoguera, B., Appelman, Y.E., Barnard, J. et al. (2012) Large-scale genecentric meta-analysis across 32 studies identifies multiple lipid loci. Am. J. Hum. Genet., 91, 823-838.
-
(2012)
Am. J. Hum. Genet
, vol.91
, pp. 823-838
-
-
Asselbergs, F.W.1
Guo, Y.2
van Iperen, E.P.3
Sivapalaratnam, S.4
Tragante, V.5
Lanktree, M.B.6
Lange, L.A.7
Almoguera, B.8
Appelman, Y.E.9
Barnard, J.10
-
28
-
-
79960943621
-
Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability
-
Sanna, S., Li, B., Mulas, A., Sidore, C., Kang, H.M., Jackson, A.U., Piras, M.G., Usala, G., Maninchedda, G., Sassu, A. et al. (2011) Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability. PLoS Genet., 7, e1002198.
-
(2011)
PLoS Genet
, vol.7
-
-
Sanna, S.1
Li, B.2
Mulas, A.3
Sidore, C.4
Kang, H.M.5
Jackson, A.U.6
Piras, M.G.7
Usala, G.8
Maninchedda, G.9
Sassu, A.10
-
29
-
-
84925860386
-
Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease
-
Tada, H., Won, H.H., Melander, O., Yang, J., Peloso, G.M. and Kathiresan, S. (2014) Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease. Circ. Cardiovasc. Genet., 7, 583-587.
-
(2014)
Circ. Cardiovasc. Genet
, vol.7
, pp. 583-587
-
-
Tada, H.1
Won, H.H.2
Melander, O.3
Yang, J.4
Peloso, G.M.5
Kathiresan, S.6
-
30
-
-
84875996758
-
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained
-
Wu, Y., Waite, L.L., Jackson, A.U., Sheu, W.H., Buyske, S., Absher, D., Arnett, D.K., Boerwinkle, E., Bonnycastle, L.L., Carty, C.L. et al. (2013) Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained. PLoS Genet., 9, e1003379.
-
(2013)
PLoS Genet
, vol.9
-
-
Wu, Y.1
Waite, L.L.2
Jackson, A.U.3
Sheu, W.H.4
Buyske, S.5
Absher, D.6
Arnett, D.K.7
Boerwinkle, E.8
Bonnycastle, L.L.9
Carty, C.L.10
-
31
-
-
84905641946
-
No large-effect low-frequency coding variation found for myocardial infarction
-
Holmen, O.L., Zhang, H., Zhou, W., Schmidt, E., Hovelson, D.H., Langhammer, A., Løchen, M.L., Ganesh, S.K., Mathiesen, E.B., Vatten, L. et al. (2014) No large-effect low-frequency coding variation found for myocardial infarction. Hum. Mol. Genet., 23, 4721-4728.
-
(2014)
Hum. Mol. Genet
, vol.23
, pp. 4721-4728
-
-
Holmen, O.L.1
Zhang, H.2
Zhou, W.3
Schmidt, E.4
Hovelson, D.H.5
Langhammer, A.6
Løchen, M.L.7
Ganesh, S.K.8
Mathiesen, E.B.9
Vatten, L.10
-
32
-
-
84867293769
-
zCall: a rare variant caller for arraybased genotyping: genetics and population analysis
-
Goldstein, J.I., Crenshaw, A., Carey, J., Grant, G.B., Maguire, J., Fromer, M., O'Dushlaine, C., Moran, J.L., Chambert, K., Stevens, C. et al. (2012) zCall: a rare variant caller for arraybased genotyping: genetics and population analysis. Bioinformatics, 28, 2543-2545.
-
(2012)
Bioinformatics
, vol.28
, pp. 2543-2545
-
-
Goldstein, J.I.1
Crenshaw, A.2
Carey, J.3
Grant, G.B.4
Maguire, J.5
Fromer, M.6
O'Dushlaine, C.7
Moran, J.L.8
Chambert, K.9
Stevens, C.10
-
34
-
-
77952714079
-
GWAMA: software for genome-wide association meta-analysis
-
Magi, R. and Morris, A.P. (2010) GWAMA: software for genome-wide association meta-analysis. BMC Bioinformatics, 11, 288.
-
(2010)
BMC Bioinformatics
, vol.11
, pp. 288
-
-
Magi, R.1
Morris, A.P.2
-
35
-
-
77955894071
-
METAL: fast and efficient meta-analysis of genomewide association scans
-
Willer, C.J., Li, Y. and Abecasis, G.R. (2010) METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics, 26, 2190-2191.
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
36
-
-
84890144067
-
Genetic prediction of quantitative lipid traits: comparing shrinkage models to gene scores
-
Warren, H., Casas, J.P., Hingorani, A., Dudbridge, F. and Whittaker, J. (2014) Genetic prediction of quantitative lipid traits: comparing shrinkage models to gene scores. Genet. Epidemiol., 38, 72-83.
-
(2014)
Genet. Epidemiol
, vol.38
, pp. 72-83
-
-
Warren, H.1
Casas, J.P.2
Hingorani, A.3
Dudbridge, F.4
Whittaker, J.5
-
37
-
-
77958110812
-
Conducting meta-analyses in R with the metaphor package
-
Viechtbauer, W. (2010) Conducting meta-analyses in R with the metaphor package. J. Stat. Softw., 36, 1-48.
-
(2010)
J. Stat. Softw
, vol.36
, pp. 1-48
-
-
Viechtbauer, W.1
-
38
-
-
85047690027
-
The inheritance of liability to diseases with variable age of onset, with particular reference to diabetes mellitus
-
Falconer, D.S. (1967) The inheritance of liability to diseases with variable age of onset, with particular reference to diabetes mellitus. Ann. Hum. Genet., 31, 1-20.
-
(1967)
Ann. Hum. Genet
, vol.31
, pp. 1-20
-
-
Falconer, D.S.1
|