-
1
-
-
40849097776
-
Heritability in the genomics era—concepts and misconceptions
-
18319743
-
Visscher P. M., Hill W. G., Wray N. R., (2008). Heritability in the genomics era—concepts and misconceptions. Nature Reviews Genetics, 9(4), 255–266. doi: 10.1038/nrg2322 18319743
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.4
, pp. 255-266
-
-
Visscher, P.M.1
Hill, W.G.2
Wray, N.R.3
-
2
-
-
84933279742
-
Meta-analysis of the heritability of human traits based on fifty years of twin studies
-
25985137
-
Polderman T. J., Benyamin B., De Leeuw C. A., Sullivan P. F., Van Bochoven A., Visscher P. M., et al. (2015). Meta-analysis of the heritability of human traits based on fifty years of twin studies. Nature Genetics, 47(7), 702–709. doi: 10.1038/ng.3285 25985137
-
(2015)
Nature Genetics
, vol.47
, Issue.7
, pp. 702-709
-
-
Polderman, T.J.1
Benyamin, B.2
De Leeuw, C.A.3
Sullivan, P.F.4
Van Bochoven, A.5
Visscher, P.M.6
-
3
-
-
79952489475
-
Estimating missing heritability for disease from genome-wide association studies
-
21376301
-
Lee S. H., Wray N. R., Goddard M. E., Visscher P. M., (2011). Estimating missing heritability for disease from genome-wide association studies. The American Journal of Human Genetics, 88(3), 294–305. doi: 10.1016/j.ajhg.2011.02.002 21376301
-
(2011)
The American Journal of Human Genetics
, vol.88
, Issue.3
, pp. 294-305
-
-
Lee, S.H.1
Wray, N.R.2
Goddard, M.E.3
Visscher, P.M.4
-
4
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
20562875
-
Yang J., Benyamin B., McEvoy B. P., Gordon S., Henders A. K., Nyholt D. R., et al. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature Genetics, 42(7), 565–569. doi: 10.1038/ng.608 20562875
-
(2010)
Nature Genetics
, vol.42
, Issue.7
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
Nyholt, D.R.6
-
5
-
-
78650856517
-
GCTA: a tool for genome-wide complex trait analysis
-
21167468
-
Yang J., Lee S. H., Goddard M. E., Visscher P. M., (2011). GCTA: a tool for genome-wide complex trait analysis. The American Journal of Human Genetics, 88(1), 76–82. doi: 10.1016/j.ajhg.2010.11.011 21167468
-
(2011)
The American Journal of Human Genetics
, vol.88
, Issue.1
, pp. 76-82
-
-
Yang, J.1
Lee, S.H.2
Goddard, M.E.3
Visscher, P.M.4
-
6
-
-
0346361698
-
Socioeconomic status modifies heritability of IQ in young children
-
14629696
-
Turkheimer E., Haley A., Waldron M., D'Onofrio B., Gottesman I. I., (2003). Socioeconomic status modifies heritability of IQ in young children. Psychological Science, 14(6), 623–628. doi: 10.1046/j.0956-7976.2003.psci_1475.x 14629696
-
(2003)
Psychological Science
, vol.14
, Issue.6
, pp. 623-628
-
-
Turkheimer, E.1
Haley, A.2
Waldron, M.3
D'Onofrio, B.4
Gottesman, I.I.5
-
7
-
-
84926430250
-
UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age
-
25826379
-
Sudlow C., Gallacher J., Allen N., Beral V., Burton P., Danesh J., et al. (2015). UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age. PLoS Medicine, 12(3), e1001779. doi: 10.1371/journal.pmed.1001779 25826379
-
(2015)
PLoS Medicine
, vol.12
, Issue.3
, pp. e1001779
-
-
Sudlow, C.1
Gallacher, J.2
Allen, N.3
Beral, V.4
Burton, P.5
Danesh, J.6
-
8
-
-
84923946495
-
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
-
25642630
-
Bulik-Sullivan B. K., Loh P. R., Finucane H. K., Ripke S., Yang J., Patterson N., et al. (2015). LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nature Genetics, 47(3), 291–295. doi: 10.1038/ng.3211 25642630
-
(2015)
Nature Genetics
, vol.47
, Issue.3
, pp. 291-295
-
-
Bulik-Sullivan, B.K.1
Loh, P.R.2
Finucane, H.K.3
Ripke, S.4
Yang, J.5
Patterson, N.6
-
9
-
-
84965076156
-
Developing and evaluating polygenic risk prediction models for stratified disease prevention
-
27140283
-
Chatterjee N., Shi J., García-Closas M., (2016). Developing and evaluating polygenic risk prediction models for stratified disease prevention. Nature Reviews Genetics, 17(7), 392–406. doi: 10.1038/nrg.2016.27 27140283
-
(2016)
Nature Reviews Genetics
, vol.17
, Issue.7
, pp. 392-406
-
-
Chatterjee, N.1
Shi, J.2
García-Closas, M.3
-
10
-
-
84916623158
-
Measuring missing heritability: inferring the contribution of common variants
-
Golan D., Lander E. S., Rosset S., (2014). Measuring missing heritability: inferring the contribution of common variants. Proceedings of the National Academy of Sciences, 111(49), E5272–E5281.
-
(2014)
Proceedings of the National Academy of Sciences
, vol.111
, Issue.49
, pp. E5272-E5281
-
-
Golan, D.1
Lander, E.S.2
Rosset, S.3
-
11
-
-
85000443086
-
Partitioning heritability by functional annotation using genome-wide association summary statistics
-
26414678
-
Finucane H. K., Bulik-Sullivan B., Gusev A., Trynka G., Reshef Y., Loh P. R., et al. (2015). Partitioning heritability by functional annotation using genome-wide association summary statistics. Nature Genetics, 47(11), 1228–1235. doi: 10.1038/ng.3404 26414678
-
(2015)
Nature Genetics
, vol.47
, Issue.11
, pp. 1228-1235
-
-
Finucane, H.K.1
Bulik-Sullivan, B.2
Gusev, A.3
Trynka, G.4
Reshef, Y.5
Loh, P.R.6
-
12
-
-
85000692305
-
An atlas of genetic correlations across human diseases and traits
-
Bulik-Sullivan B., Finucane H. K., Anttila V., Gusev A., Day F. R., Loh P. R., et al. (2015a). An atlas of genetic correlations across human diseases and traits. Nature Genetics, 47(11), 1236–1241.
-
(2015)
Nature Genetics
, vol.47
, Issue.11
, pp. 1236-1241
-
-
Bulik-Sullivan, B.1
Finucane, H.K.2
Anttila, V.3
Gusev, A.4
Day, F.R.5
Loh, P.R.6
-
13
-
-
85009844693
-
LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis
-
. ., btw613
-
Zheng J., Erzurumluoglu A. M., Elsworth B. L., Kemp J. P., Howe L., Haycock P. C., et al. (2016). LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. Bioinformatics, btw613.
-
(2016)
Bioinformatics
-
-
Zheng, J.1
Erzurumluoglu, A.M.2
Elsworth, B.L.3
Kemp, J.P.4
Howe, L.5
Haycock, P.C.6
-
14
-
-
0033949377
-
Haseman and Elston revisited
-
10861893
-
Elston R. C., Buxbaum S., Jacobs K. B., Olson J. M., (2000). Haseman and Elston revisited. Genetic Epidemiology, 19(1), 1–17. doi: 10.1002/1098-2272(200007)19:1<1::AID-GEPI1>3.0.CO;2-E 10861893
-
(2000)
Genetic Epidemiology
, vol.19
, Issue.1
, pp. 1-17
-
-
Elston, R.C.1
Buxbaum, S.2
Jacobs, K.B.3
Olson, J.M.4
-
15
-
-
0015309467
-
The investigation of linkage between a quantitative trait and a marker locus
-
4157472
-
Haseman J. K., Elston R. C., (1972). The investigation of linkage between a quantitative trait and a marker locus. Behavior Genetics, 2(1), 3–19. 4157472
-
(1972)
Behavior Genetics
, vol.2
, Issue.1
, pp. 3-19
-
-
Haseman, J.K.1
Elston, R.C.2
-
16
-
-
0034987802
-
Equivalence between Haseman-Elston and variance-components linkage analyses for sib pairs
-
11353401
-
Sham P. C., Purcell S., (2001). Equivalence between Haseman-Elston and variance-components linkage analyses for sib pairs. The American Journal of Human Genetics, 68(6), 1527–1532. doi: 10.1086/320593 11353401
-
(2001)
The American Journal of Human Genetics
, vol.68
, Issue.6
, pp. 1527-1532
-
-
Sham, P.C.1
Purcell, S.2
-
17
-
-
84901380413
-
Statistical power to detect genetic (co) variance of complex traits using SNP data in unrelated samples
-
24721987
-
Visscher P. M., Hemani G., Vinkhuyzen A. A., Chen G. B., Lee S. H., Wray N. R., et al. (2014). Statistical power to detect genetic (co) variance of complex traits using SNP data in unrelated samples. PLoS Genetics, 10(4), e1004269. doi: 10.1371/journal.pgen.1004269 24721987
-
(2014)
PLoS Genetics
, vol.10
, Issue.4
, pp. e1004269
-
-
Visscher, P.M.1
Hemani, G.2
Vinkhuyzen, A.A.3
Chen, G.B.4
Lee, S.H.5
Wray, N.R.6
-
19
-
-
33750544922
-
Bias, precision and heritability of self-reported and clinically measured height in Australian twins
-
16933140
-
MacGregor S., Cornes B. K., Martin N. G., Visscher P. M., (2006). Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Human Genetics, 120(4), 571–580. doi: 10.1007/s00439-006-0240-z 16933140
-
(2006)
Human Genetics
, vol.120
, Issue.4
, pp. 571-580
-
-
MacGregor, S.1
Cornes, B.K.2
Martin, N.G.3
Visscher, P.M.4
-
20
-
-
43249106445
-
Heritability of body size and muscle strength in young adulthood: a study of one million Swedish men
-
18271028
-
Silventoinen K., Magnusson P. K., Tynelius P., Kaprio J., Rasmussen F., (2008). Heritability of body size and muscle strength in young adulthood: a study of one million Swedish men. Genetic Epidemiology, 32(4), 341–349. doi: 10.1002/gepi.20308 18271028
-
(2008)
Genetic Epidemiology
, vol.32
, Issue.4
, pp. 341-349
-
-
Silventoinen, K.1
Magnusson, P.K.2
Tynelius, P.3
Kaprio, J.4
Rasmussen, F.5
-
21
-
-
9144254700
-
Heritability of adult body height: a comparative study of twin cohorts in eight countries
-
Silventoinen K., Sammalisto S., Perola M., Boomsma D. I., Cornes B. K., Davis C., et al. (2003). Heritability of adult body height: a comparative study of twin cohorts in eight countries. Twin Research, 6(05), 399–408.
-
(2003)
Twin Research
, vol.6
, Issue.5
, pp. 399-408
-
-
Silventoinen, K.1
Sammalisto, S.2
Perola, M.3
Boomsma, D.I.4
Cornes, B.K.5
Davis, C.6
-
22
-
-
79957456397
-
From Galton to GWAS: quantitative genetics of human height
-
21429269
-
Visscher P. M., McEvoy B., Yang J., (2010). From Galton to GWAS: quantitative genetics of human height. Genetics Research, 92, 371–379. doi: 10.1017/S0016672310000571 21429269
-
(2010)
Genetics Research
, vol.92
, pp. 371-379
-
-
Visscher, P.M.1
McEvoy, B.2
Yang, J.3
-
23
-
-
84878502589
-
Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits
-
23737753
-
Zaitlen N., Kraft P., Patterson N., Pasaniuc B., Bhatia G., Pollack S., et al. (2013). Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits. PLoS Genetics, 9(5), e1003520. doi: 10.1371/journal.pgen.1003520 23737753
-
(2013)
PLoS Genetics
, vol.9
, Issue.5
, pp. e1003520
-
-
Zaitlen, N.1
Kraft, P.2
Patterson, N.3
Pasaniuc, B.4
Bhatia, G.5
Pollack, S.6
-
24
-
-
84922537760
-
Leveraging population admixture to characterize the heritability of complex traits
-
25383972
-
Zaitlen N., Pasaniuc B., Sankararaman S., Bhatia G., Zhang J., Gusev A., et al. (2014). Leveraging population admixture to characterize the heritability of complex traits. Nature Genetics, 46(12), 1356–1362. doi: 10.1038/ng.3139 25383972
-
(2014)
Nature Genetics
, vol.46
, Issue.12
, pp. 1356-1362
-
-
Zaitlen, N.1
Pasaniuc, B.2
Sankararaman, S.3
Bhatia, G.4
Zhang, J.5
Gusev, A.6
-
25
-
-
84856405512
-
The mystery of missing heritability: Genetic interactions create phantom heritability
-
Zuk O., Hechter E., Sunyaev S. R., Lander E. S., (2012). The mystery of missing heritability: Genetic interactions create phantom heritability. Proceedings of the National Academy of Sciences, 109(4), 1193–1198.
-
(2012)
Proceedings of the National Academy of Sciences
, vol.109
, Issue.4
, pp. 1193-1198
-
-
Zuk, O.1
Hechter, E.2
Sunyaev, S.R.3
Lander, E.S.4
-
26
-
-
84859261092
-
Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits
-
22479213
-
Vattikuti S., Guo J., Chow C. C., (2012). Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits. PLoS Genetics, 8(3), e1002637. doi: 10.1371/journal.pgen.1002637 22479213
-
(2012)
PLoS Genetics
, vol.8
, Issue.3
, pp. e1002637
-
-
Vattikuti, S.1
Guo, J.2
Chow, C.C.3
-
27
-
-
84944358132
-
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
-
26323059
-
Yang J., Bakshi A., Zhu Z., Hemani G., Vinkhuyzen A. A., Lee S. H., et al. (2015). Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index. Nature Genetics, 47(10), 1114–1120. doi: 10.1038/ng.3390 26323059
-
(2015)
Nature Genetics
, vol.47
, Issue.10
, pp. 1114-1120
-
-
Yang, J.1
Bakshi, A.2
Zhu, Z.3
Hemani, G.4
Vinkhuyzen, A.A.5
Lee, S.H.6
-
28
-
-
84885360262
-
Childhood socioeconomic status amplifies genetic effects on adult intelligence
-
24002887
-
Bates T. C., Lewis G. J., Weiss A., (2013). Childhood socioeconomic status amplifies genetic effects on adult intelligence. Psychological Science, 24(10), 2111–2116. doi: 10.1177/0956797613488394 24002887
-
(2013)
Psychological Science
, vol.24
, Issue.10
, pp. 2111-2116
-
-
Bates, T.C.1
Lewis, G.J.2
Weiss, A.3
-
29
-
-
84856480950
-
Socioeconomic status (SES) and children's intelligence (IQ): In a UK-representative sample SES moderates the environmental, not genetic, effect on IQ
-
22312423
-
Hanscombe K. B., Trzaskowski M., Haworth C. M., Davis O. S., Dale P. S., Plomin R., (2012). Socioeconomic status (SES) and children's intelligence (IQ): In a UK-representative sample SES moderates the environmental, not genetic, effect on IQ. PLoS One, 7(2), e30320. doi: 10.1371/journal.pone.0030320 22312423
-
(2012)
PLoS One
, vol.7
, Issue.2
, pp. e30320
-
-
Hanscombe, K.B.1
Trzaskowski, M.2
Haworth, C.M.3
Davis, O.S.4
Dale, P.S.5
Plomin, R.6
-
30
-
-
85017330967
-
Replication of a gene–environment interaction via multimodel inference: additive-genetic variance in Adolescents’ General Cognitive Ability Increases with Family-of-Origin Socioeconomic Status
-
25539975
-
Kirkpatrick R. M., McGue M., Iacono W. G., (2015). Replication of a gene–environment interaction via multimodel inference: additive-genetic variance in Adolescents’ General Cognitive Ability Increases with Family-of-Origin Socioeconomic Status. Behavior Genetics, 45(2), 200–214. doi: 10.1007/s10519-014-9698-y 25539975
-
(2015)
Behavior Genetics
, vol.45
, Issue.2
, pp. 200-214
-
-
Kirkpatrick, R.M.1
McGue, M.2
Iacono, W.G.3
-
31
-
-
84957951489
-
The Scarr-Rowe interaction in complete seven-year WISC data from the Louisville twin study: Preliminary report
-
26497158
-
Turkheimer E., Beam C. E., Davis D. W., (2015). The Scarr-Rowe interaction in complete seven-year WISC data from the Louisville twin study: Preliminary report. Behavior Genetics, 45(6), 635–639. doi: 10.1007/s10519-015-9760-4 26497158
-
(2015)
Behavior Genetics
, vol.45
, Issue.6
, pp. 635-639
-
-
Turkheimer, E.1
Beam, C.E.2
Davis, D.W.3
-
32
-
-
77958499255
-
The heritability of general cognitive ability increases linearly from childhood to young adulthood
-
19488046
-
Haworth C. M., Wright M. J., Luciano M., Martin N. G., De Geus E. J. C., Van Beijsterveldt C. E. M., et al. (2010). The heritability of general cognitive ability increases linearly from childhood to young adulthood. Molecular psychiatry, 15(11), 1112–1120. doi: 10.1038/mp.2009.55 19488046
-
(2010)
Molecular psychiatry
, vol.15
, Issue.11
, pp. 1112-1120
-
-
Haworth, C.M.1
Wright, M.J.2
Luciano, M.3
Martin, N.G.4
De Geus, E.J.C.5
Van Beijsterveldt, C.E.M.6
-
33
-
-
70350585040
-
Dramatic increase in heritability of cognitive development from early to middle childhood: An 8-year longitudinal study of 8,700 pairs of twins
-
19732386
-
Davis O. S., Haworth C. M., Plomin R., (2009). Dramatic increase in heritability of cognitive development from early to middle childhood: An 8-year longitudinal study of 8,700 pairs of twins. Psychological Science, 20(10), 1301–1308. doi: 10.1111/j.1467-9280.2009.02433.x 19732386
-
(2009)
Psychological Science
, vol.20
, Issue.10
, pp. 1301-1308
-
-
Davis, O.S.1
Haworth, C.M.2
Plomin, R.3
-
34
-
-
84958056096
-
Large cross-national differences in gene × socioeconomic status interaction on intelligence
-
., 0956797615612727
-
Tucker-Drob E. M., Bates T. C., (2015). Large cross-national differences in gene × socioeconomic status interaction on intelligence. Psychological science, 0956797615612727.
-
(2015)
Psychological science
-
-
Tucker-Drob, E.M.1
Bates, T.C.2
-
35
-
-
84907285601
-
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method
-
Rietveld C. A., Esko T., Davies G., Pers T. H., Turley P., Benyamin B., et al. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences, 111(38), 13790–13794.
-
(2014)
Proceedings of the National Academy of Sciences
, vol.111
, Issue.38
, pp. 13790-13794
-
-
Rietveld, C.A.1
Esko, T.2
Davies, G.3
Pers, T.H.4
Turley, P.5
Benyamin, B.6
-
36
-
-
55649114631
-
Sex-specific genetic effects influence variation in body composition
-
18839131
-
Zillikens M. C., Yazdanpanah M., Pardo L. M., Rivadeneira F., Aulchenko Y. S., Oostra B. A., et al. (2008). Sex-specific genetic effects influence variation in body composition. Diabetologia, 51(12), 2233–2241. doi: 10.1007/s00125-008-1163-0 18839131
-
(2008)
Diabetologia
, vol.51
, Issue.12
, pp. 2233-2241
-
-
Zillikens, M.C.1
Yazdanpanah, M.2
Pardo, L.M.3
Rivadeneira, F.4
Aulchenko, Y.S.5
Oostra, B.A.6
-
37
-
-
27144534519
-
Heritability and stability of resting blood pressure
-
Hottenga J. J., Boomsma D. I., Kupper N., Posthuma D., Snieder H., Willemsen G., et al. (2005). Heritability and stability of resting blood pressure. Twin Research and Human Genetics, 8(05), 499–508.
-
(2005)
Twin Research and Human Genetics
, vol.8
, Issue.5
, pp. 499-508
-
-
Hottenga, J.J.1
Boomsma, D.I.2
Kupper, N.3
Posthuma, D.4
Snieder, H.5
Willemsen, G.6
-
38
-
-
0034121235
-
Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins
-
MacGregor A. J., Snieder H., Rigby A. S., Koskenvuo M., Kaprio J., Aho K., et al. (2000). Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins. Arthritis & Rheumatism, 43(1), 30.
-
(2000)
Arthritis & Rheumatism
, vol.43
, Issue.1
, pp. 30
-
-
MacGregor, A.J.1
Snieder, H.2
Rigby, A.S.3
Koskenvuo, M.4
Kaprio, J.5
Aho, K.6
-
39
-
-
84872239752
-
Age-stratified heritability estimation in the Framingham Heart Study families
-
Brown W. M., Beck S. R., Lange E. M., Davis C. C., Kay C. M., Langefeld C. D., et al. (2003). Age-stratified heritability estimation in the Framingham Heart Study families. BMC Genetics, 4(1), 1.
-
(2003)
BMC Genetics
, vol.4
, Issue.1
, pp. 1
-
-
Brown, W.M.1
Beck, S.R.2
Lange, E.M.3
Davis, C.C.4
Kay, C.M.5
Langefeld, C.D.6
-
40
-
-
60049101443
-
Genetic influences on change in BMI from middle to old age: a 29-year follow-up study of twin sisters
-
19067155
-
Ortega-Alonso A., Sipilä S., Kujala U. M., Kaprio J., Rantanen T., (2009). Genetic influences on change in BMI from middle to old age: a 29-year follow-up study of twin sisters. Behavior Genetics, 39(2), 154–164. doi: 10.1007/s10519-008-9245-9 19067155
-
(2009)
Behavior Genetics
, vol.39
, Issue.2
, pp. 154-164
-
-
Ortega-Alonso, A.1
Sipilä, S.2
Kujala, U.M.3
Kaprio, J.4
Rantanen, T.5
-
41
-
-
0942290488
-
Twin study of genetic and environmental influences on adult body size, shape, and composition
-
14610529
-
Schousboe K., Visscher P. M., Erbas B., Kyvik K. O., Hopper J. L., Henriksen J. E., et al. (2004). Twin study of genetic and environmental influences on adult body size, shape, and composition. International Journal of Obesity, 28(1), 39–48. doi: 10.1038/sj.ijo.0802524 14610529
-
(2004)
International Journal of Obesity
, vol.28
, Issue.1
, pp. 39-48
-
-
Schousboe, K.1
Visscher, P.M.2
Erbas, B.3
Kyvik, K.O.4
Hopper, J.L.5
Henriksen, J.E.6
-
42
-
-
58149303021
-
Increasing heritability of BMI and stronger associations with the FTO gene over childhood
-
18846049
-
Haworth C., Carnell S., Meaburn E. L., Davis O. S., Plomin R., Wardle J., (2008). Increasing heritability of BMI and stronger associations with the FTO gene over childhood. Obesity, 16(12), 2663–2668. doi: 10.1038/oby.2008.434 18846049
-
(2008)
Obesity
, vol.16
, Issue.12
, pp. 2663-2668
-
-
Haworth, C.1
Carnell, S.2
Meaburn, E.L.3
Davis, O.S.4
Plomin, R.5
Wardle, J.6
-
43
-
-
84885861142
-
Variation in the heritability of body mass index based on diverse twin studies: a systematic review
-
23980914
-
Min J., Chiu D. T., Wang Y., (2013). Variation in the heritability of body mass index based on diverse twin studies: a systematic review. Obesity Reviews, 14(11), 871–882. doi: 10.1111/obr.12065 23980914
-
(2013)
Obesity Reviews
, vol.14
, Issue.11
, pp. 871-882
-
-
Min, J.1
Chiu, D.T.2
Wang, Y.3
-
44
-
-
0025953819
-
Heritability of ventilatory function in smoking and nonsmoking New Mexico Hispanics
-
1928947
-
Coultas D. B., Hanis C. L., Howard C. A., Skipper B. J., Samet J. M., (1991). Heritability of ventilatory function in smoking and nonsmoking New Mexico Hispanics. American Review of Respiratory Disease, 144(4), 770–775. doi: 10.1164/ajrccm/144.4.770 1928947
-
(1991)
American Review of Respiratory Disease
, vol.144
, Issue.4
, pp. 770-775
-
-
Coultas, D.B.1
Hanis, C.L.2
Howard, C.A.3
Skipper, B.J.4
Samet, J.M.5
-
45
-
-
33645738758
-
Heritability and stability of resting blood pressure in Australian twins
-
Hottenga J. J., Whitfield J. B., De Geus E. J., Boomsma D. I., Martin N. G., (2006). Heritability and stability of resting blood pressure in Australian twins. Twin Research and Human Genetics, 9(02), 205–209.
-
(2006)
Twin Research and Human Genetics
, vol.9
, Issue.2
, pp. 205-209
-
-
Hottenga, J.J.1
Whitfield, J.B.2
De Geus, E.J.3
Boomsma, D.I.4
Martin, N.G.5
-
46
-
-
0027938319
-
Genetic and environmental influences on pulmonary function in aging Swedish twins
-
McClearn G. E., Svartengren M., Pedersen N. L., Heller D. A., Plomin R., (1994). Genetic and environmental influences on pulmonary function in aging Swedish twins. Journal of Gerontology, 49(6), M264–M268.
-
(1994)
Journal of Gerontology
, vol.49
, Issue.6
, pp. M264-M268
-
-
McClearn, G.E.1
Svartengren, M.2
Pedersen, N.L.3
Heller, D.A.4
Plomin, R.5
-
47
-
-
84888137548
-
Heritability analyses show visit-to-visit blood pressure variability reflects different pathological phenotypes in younger and older adults: evidence from UK twins
-
24029873
-
Menni C., Mangino M., Zhang F., Clement G., Snieder H., Padmanabhan S., et al. (2013). Heritability analyses show visit-to-visit blood pressure variability reflects different pathological phenotypes in younger and older adults: evidence from UK twins. Journal of Hypertension, 31(12), 2356–2361. doi: 10.1097/HJH.0b013e32836523c1 24029873
-
(2013)
Journal of Hypertension
, vol.31
, Issue.12
, pp. 2356-2361
-
-
Menni, C.1
Mangino, M.2
Zhang, F.3
Clement, G.4
Snieder, H.5
Padmanabhan, S.6
-
48
-
-
84940437553
-
Genetic influence on age at first birth of female twins born in the UK, 1919–68
-
26234944
-
Tropf F. C., Barban N., Mills M. C., Snieder H., Mandemakers J. J., (2015). Genetic influence on age at first birth of female twins born in the UK, 1919–68. Population studies, 69(2), 129–145. doi: 10.1080/00324728.2015.1056823 26234944
-
(2015)
Population studies
, vol.69
, Issue.2
, pp. 129-145
-
-
Tropf, F.C.1
Barban, N.2
Mills, M.C.3
Snieder, H.4
Mandemakers, J.J.5
-
49
-
-
0035001426
-
The impact of genetic and environmental influences on blood pressure variance across age-groups
-
11403347
-
Vinck W. J., Fagard R. H., Loos R., Vlietinck R., (2001). The impact of genetic and environmental influences on blood pressure variance across age-groups. Journal of Hypertension, 19(6), 1007–1013. 11403347
-
(2001)
Journal of Hypertension
, vol.19
, Issue.6
, pp. 1007-1013
-
-
Vinck, W.J.1
Fagard, R.H.2
Loos, R.3
Vlietinck, R.4
-
50
-
-
84928595221
-
Genetic contribution to the variance of blood pressure and heart rate: A systematic review and meta-regression of twin studies
-
Wang B., Liao C., Zhou B., Cao W., Lv J., Yu C., et al. (2015). Genetic contribution to the variance of blood pressure and heart rate: A systematic review and meta-regression of twin studies. Twin Research and Human Genetics, 18(02), 158–170.
-
(2015)
Twin Research and Human Genetics
, vol.18
, Issue.2
, pp. 158-170
-
-
Wang, B.1
Liao, C.2
Zhou, B.3
Cao, W.4
Lv, J.5
Yu, C.6
-
51
-
-
85018454218
-
-
Domingue, B. W., Belsky, D. W., Harrati, A., Conley, D., Weir, D., Boardman, J
-
Domingue, B. W., Belsky, D. W., Harrati, A., Conley, D., Weir, D., Boardman, J. (2016). Mortality selection in a genetic sample and implications for association studies. bioRxiv, 049635
-
(2016)
Mortality selection in a genetic sample and implications for association studies. bioRxiv
-
-
-
52
-
-
84960984438
-
-
26956984
-
Tyrrell J., Jones S. E., Beaumont R., Astley C. M., Lovell R., Yaghootkar H., et al. (2016). Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank. bmj, 352, i582. doi: 10.1136/bmj.i582 26956984
-
(2016)
Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank bmj
, vol.352
, pp. i582
-
-
Tyrrell, J.1
Jones, S.E.2
Beaumont, R.3
Astley, C.M.4
Lovell, R.5
Yaghootkar, H.6
-
53
-
-
84977660577
-
Cognitive test scores in UK Biobank: data reduction in 480,416 participants and longitudinal stability in 20,346 participants
-
27110937
-
Lyall D. M., Cullen B., Allerhand M., Smith D. J., Mackay D., Evans J., et al. (2016). Cognitive test scores in UK Biobank: data reduction in 480,416 participants and longitudinal stability in 20,346 participants. PloS one, 11(4), e0154222. doi: 10.1371/journal.pone.0154222 27110937
-
(2016)
PloS one
, vol.11
, Issue.4
, pp. e0154222
-
-
Lyall, D.M.1
Cullen, B.2
Allerhand, M.3
Smith, D.J.4
Mackay, D.5
Evans, J.6
-
54
-
-
84988442262
-
Characteristics of rheumatoid arthritis and its association with major comorbid conditions: cross-sectional study of 502 649 UK Biobank participants
-
27403335
-
Siebert S., Lyall D. M., Mackay D. F., Porter D., McInnes I. B., Sattar N., et al. (2016). Characteristics of rheumatoid arthritis and its association with major comorbid conditions: cross-sectional study of 502 649 UK Biobank participants. RMD open, 2(1), e000267. doi: 10.1136/rmdopen-2016-000267 27403335
-
(2016)
RMD open
, vol.2
, Issue.1
, pp. e000267
-
-
Siebert, S.1
Lyall, D.M.2
Mackay, D.F.3
Porter, D.4
McInnes, I.B.5
Sattar, N.6
-
55
-
-
84961290792
-
Validation of electronic health record phenotyping of bipolar disorder cases and controls
-
25827034
-
Castro V. M., Minnier J., Murphy S. N., Kohane I., Churchill S. E., Gainer V., et al. (2015). Validation of electronic health record phenotyping of bipolar disorder cases and controls. American Journal of Psychiatry, 172(4), 363–372. doi: 10.1176/appi.ajp.2014.14030423 25827034
-
(2015)
American Journal of Psychiatry
, vol.172
, Issue.4
, pp. 363-372
-
-
Castro, V.M.1
Minnier, J.2
Murphy, S.N.3
Kohane, I.4
Churchill, S.E.5
Gainer, V.6
-
56
-
-
84995810431
-
Extracting information from the text of electronic medical records to improve case detection: a systematic review
-
., ocv180
-
Ford E., Carroll J. A., Smith H. E., Scott D., Cassell J. A., (2016). Extracting information from the text of electronic medical records to improve case detection: a systematic review. Journal of the American Medical Informatics Association, ocv180.
-
(2016)
Journal of the American Medical Informatics Association
-
-
Ford, E.1
Carroll, J.A.2
Smith, H.E.3
Scott, D.4
Cassell, J.A.5
-
57
-
-
84930651751
-
Development of phenotype algorithms using electronic medical records and incorporating natural language processing
-
25911572
-
Liao K. P., Cai T., Savova G. K., Murphy S. N., Karlson E. W., Ananthakrishnan A. N., et al. (2015). Development of phenotype algorithms using electronic medical records and incorporating natural language processing. BMJ, 350, h1885. doi: 10.1136/bmj.h1885 25911572
-
(2015)
BMJ
, vol.350
, pp. h1885
-
-
Liao, K.P.1
Cai, T.2
Savova, G.K.3
Murphy, S.N.4
Karlson, E.W.5
Ananthakrishnan, A.N.6
-
58
-
-
82655165845
-
Using electronic medical records to enable large-scale studies in psychiatry: treatment resistant depression as a model
-
21682950
-
Perlis R. H., Iosifescu D. V., Castro V. M., Murphy S. N., Gainer V. S., Minnier J., et al. (2012). Using electronic medical records to enable large-scale studies in psychiatry: treatment resistant depression as a model. Psychological Medicine, 42(1), 41–50. doi: 10.1017/S0033291711000997 21682950
-
(2012)
Psychological Medicine
, vol.42
, Issue.1
, pp. 41-50
-
-
Perlis, R.H.1
Iosifescu, D.V.2
Castro, V.M.3
Murphy, S.N.4
Gainer, V.S.5
Minnier, J.6
-
59
-
-
84870919039
-
Improved heritability estimation from genome-wide SNPs
-
23217325
-
Speed D., Hemani G., Johnson M. R., Balding D. J., (2012). Improved heritability estimation from genome-wide SNPs. The American Journal of Human Genetics, 91(6), 1011–1021. doi: 10.1016/j.ajhg.2012.10.010 23217325
-
(2012)
The American Journal of Human Genetics
, vol.91
, Issue.6
, pp. 1011-1021
-
-
Speed, D.1
Hemani, G.2
Johnson, M.R.3
Balding, D.J.4
-
60
-
-
84890259689
-
Estimation of SNP heritability from dense genotype data
-
24314550
-
Lee S. H., Yang J., Chen G. B., Ripke S., Stahl E. A., Hultman C. M., et al. (2013). Estimation of SNP heritability from dense genotype data. The American Journal of Human Genetics, 93(6), 1151–1155. doi: 10.1016/j.ajhg.2013.10.015 24314550
-
(2013)
The American Journal of Human Genetics
, vol.93
, Issue.6
, pp. 1151-1155
-
-
Lee, S.H.1
Yang, J.2
Chen, G.B.3
Ripke, S.4
Stahl, E.A.5
Hultman, C.M.6
-
61
-
-
79957588287
-
Genome partitioning of genetic variation for complex traits using common SNPs
-
21552263
-
Yang J., Manolio T. A., Pasquale L. R., Boerwinkle E., Caporaso N., Cunningham J. M., et al. (2011). Genome partitioning of genetic variation for complex traits using common SNPs. Nature genetics, 43(6), 519–525. doi: 10.1038/ng.823 21552263
-
(2011)
Nature genetics
, vol.43
, Issue.6
, pp. 519-525
-
-
Yang, J.1
Manolio, T.A.2
Pasquale, L.R.3
Boerwinkle, E.4
Caporaso, N.5
Cunningham, J.M.6
-
62
-
-
84997409303
-
Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility
-
049163
-
Tropf, F. C., Verweij, R. M., van der Most, P. J., Stulp, G., Bakshi, A., Briley, D. A., et al. (2016). Mega-analysis of 31,396 individuals from 6 countries uncovers strong gene-environment interaction for human fertility. BioRxiv, 049163.
-
(2016)
BioRxiv
-
-
Tropf, F.C.1
Verweij, R.M.2
van der Most, P.J.3
Stulp, G.4
Bakshi, A.5
Briley, D.A.6
-
63
-
-
84959227093
-
Genome-wide genetic homogeneity between sexes and populations for human height and body mass index
-
. ., ddv443
-
Yang J., Bakshi A., Zhu Z., Hemani G., Vinkhuyzen A. A., Nolte I. M., et al. (2015). Genome-wide genetic homogeneity between sexes and populations for human height and body mass index. Human molecular genetics, ddv443.
-
(2015)
Human molecular genetics
-
-
Yang, J.1
Bakshi, A.2
Zhu, Z.3
Hemani, G.4
Vinkhuyzen, A.A.5
Nolte, I.M.6
-
64
-
-
84927126442
-
Relatedness in the post-genomic era: is it still useful?
-
25404112
-
Speed D., Balding D. J., (2015). Relatedness in the post-genomic era: is it still useful?Nature Reviews Genetics, 16(1), 33–44. doi: 10.1038/nrg3821 25404112
-
(2015)
Nature Reviews Genetics
, vol.16
, Issue.1
, pp. 33-44
-
-
Speed, D.1
Balding, D.J.2
-
65
-
-
84953286476
-
Limitations of GCTA as a solution to the missing heritability problem
-
Kumar S. K., Feldman M. W., Rehkopf D. H., Tuljapurkar S., (2016). Limitations of GCTA as a solution to the missing heritability problem. Proceedings of the National Academy of Sciences, 113(1), E61–E70.
-
(2016)
Proceedings of the National Academy of Sciences
, vol.113
, Issue.1
, pp. E61-E70
-
-
Kumar, S.K.1
Feldman, M.W.2
Rehkopf, D.H.3
Tuljapurkar, S.4
-
66
-
-
84982976085
-
GCTA-GREML accounts for linkage disequilibrium when estimating genetic variance from genome-wide SNPs
-
Yang J., Lee S. H., Wray N. R., Goddard M. E., Visscher P. M., (2016). GCTA-GREML accounts for linkage disequilibrium when estimating genetic variance from genome-wide SNPs. Proceedings of the National Academy of Sciences, 113(32), E4579–E4580.
-
(2016)
Proceedings of the National Academy of Sciences
, vol.113
, Issue.32
, pp. E4579-E4580
-
-
Yang, J.1
Lee, S.H.2
Wray, N.R.3
Goddard, M.E.4
Visscher, P.M.5
-
67
-
-
84982893680
-
Reply to Yang et al.: GCTA produces unreliable heritability estimates
-
., 201608425
-
Kumar S. K., Feldman M. W., Rehkopf D. H., Tuljapurkar S., (2016). Reply to Yang et al.: GCTA produces unreliable heritability estimates. Proceedings of the National Academy of Sciences, 201608425.
-
(2016)
Proceedings of the National Academy of Sciences
-
-
Kumar, S.K.1
Feldman, M.W.2
Rehkopf, D.H.3
Tuljapurkar, S.4
-
68
-
-
84930213392
-
Second-generation PLINK: rising to the challenge of larger and richer datasets
-
Chang C. C., Chow C. C., Tellier L. C., Vattikuti S., Purcell S. M., Lee J. J., (2015). Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience, 4(1), 1.
-
(2015)
Gigascience
, vol.4
, Issue.1
, pp. 1
-
-
Chang, C.C.1
Chow, C.C.2
Tellier, L.C.3
Vattikuti, S.4
Purcell, S.M.5
Lee, J.J.6
-
69
-
-
84923668372
-
Massively expedited genome-wide heritability analysis (MEGHA)
-
Ge T., Nichols T. E., Lee P. H., Holmes A. J., Roffman J. L., Buckner R. L., et al. (2015). Massively expedited genome-wide heritability analysis (MEGHA). Proceedings of the National Academy of Sciences, 112(8), 2479–2484.
-
(2015)
Proceedings of the National Academy of Sciences
, vol.112
, Issue.8
, pp. 2479-2484
-
-
Ge, T.1
Nichols, T.E.2
Lee, P.H.3
Holmes, A.J.4
Roffman, J.L.5
Buckner, R.L.6
-
70
-
-
84995478515
-
Multidimensional heritability analysis of neuroanatomical shape
-
27845344
-
Ge T., Reuter M., Winkler A. M., Holmes A. J., Lee P. H., Tirrell L. S., et al. (2016). Multidimensional heritability analysis of neuroanatomical shape. Nature Communications, 7, 13291. doi: 10.1038/ncomms13291 27845344
-
(2016)
Nature Communications
, vol.7
, pp. 13291
-
-
Ge, T.1
Reuter, M.2
Winkler, A.M.3
Holmes, A.J.4
Lee, P.H.5
Tirrell, L.S.6
-
72
-
-
77955058518
-
The inheritance of liability to certain diseases, estimated from the incidence among relatives
-
Falconer D. S., (1965). The inheritance of liability to certain diseases, estimated from the incidence among relatives. Annals of Human Genetics, 29(1), 51–76.
-
(1965)
Annals of Human Genetics
, vol.29
, Issue.1
, pp. 51-76
-
-
Falconer, D.S.1
-
73
-
-
84885837543
-
Mathematical contributions to the theory of evolution VII—On the application of certain formulae in the theory of correlation to the inheritance of characters not capable of quantitative measurement
-
Pearson K., Lee A., (1901). Mathematical contributions to the theory of evolution VII—On the application of certain formulae in the theory of correlation to the inheritance of characters not capable of quantitative measurement. Proceedings of the Royal Society of London, 66(424–433), 324–327.
-
(1901)
Proceedings of the Royal Society of London
, vol.66
, Issue.424-433
, pp. 324-327
-
-
Pearson, K.1
Lee, A.2
-
74
-
-
0001118328
-
Heritability of threshold characters
-
17247344
-
Dempster E. R., Lerner I. M., (1950). Heritability of threshold characters. Genetics, 35(2), 212. 17247344
-
(1950)
Genetics
, vol.35
, Issue.2
, pp. 212
-
-
Dempster, E.R.1
Lerner, I.M.2
-
75
-
-
84899513456
-
Fast principal component analysis of large-scale genome-wide data
-
24718290
-
Abraham G., Inouye M., (2014). Fast principal component analysis of large-scale genome-wide data. PLoS One, 9(4), e93766. doi: 10.1371/journal.pone.0093766 24718290
-
(2014)
PLoS One
, vol.9
, Issue.4
, pp. e93766
-
-
Abraham, G.1
Inouye, M.2
|