-
1
-
-
70350221648
-
Next generation disparities in human genomics: concerns and remedies
-
1 Need, A.C., Goldstein, D.B., Next generation disparities in human genomics: concerns and remedies. Trends Genet. 25 (2009), 489–494.
-
(2009)
Trends Genet.
, vol.25
, pp. 489-494
-
-
Need, A.C.1
Goldstein, D.B.2
-
2
-
-
79960429419
-
Genomics for the world
-
2 Bustamante, C.D., Burchard, E.G., De la Vega, F.M., Genomics for the world. Nature 475 (2011), 163–165.
-
(2011)
Nature
, vol.475
, pp. 163-165
-
-
Bustamante, C.D.1
Burchard, E.G.2
De la Vega, F.M.3
-
3
-
-
84979523711
-
Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine
-
3 Petrovski, S., Goldstein, D.B., Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine. Genome Biol., 17, 2016, 157.
-
(2016)
Genome Biol.
, vol.17
, pp. 157
-
-
Petrovski, S.1
Goldstein, D.B.2
-
4
-
-
84991669666
-
Genomics is failing on diversity
-
4 Popejoy, A.B., Fullerton, S.M., Genomics is failing on diversity. Nature 538 (2016), 161–164.
-
(2016)
Nature
, vol.538
, pp. 161-164
-
-
Popejoy, A.B.1
Fullerton, S.M.2
-
5
-
-
84884546005
-
Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study
-
5 Carlson, C.S., Matise, T.C., North, K.E., Haiman, C.A., Fesinmeyer, M.D., Buyske, S., Schumacher, F.R., Peters, U., Franceschini, N., Ritchie, M.D., et al., PAGE Consortium. Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study. PLoS Biol., 11, 2013, e1001661.
-
(2013)
PLoS Biol.
, vol.11
, pp. e1001661
-
-
Carlson, C.S.1
Matise, T.C.2
North, K.E.3
Haiman, C.A.4
Fesinmeyer, M.D.5
Buyske, S.6
Schumacher, F.R.7
Peters, U.8
Franceschini, N.9
Ritchie, M.D.10
-
6
-
-
77957370404
-
Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups
-
6 Waters, K.M., Stram, D.O., Hassanein, M.T., Le Marchand, L., Wilkens, L.R., Maskarinec, G., Monroe, K.R., Kolonel, L.N., Altshuler, D., Henderson, B.E., Haiman, C.A., Consistent association of type 2 diabetes risk variants found in europeans in diverse racial and ethnic groups. PLoS Genet., 6, 2010, 6.
-
(2010)
PLoS Genet.
, vol.6
, pp. 6
-
-
Waters, K.M.1
Stram, D.O.2
Hassanein, M.T.3
Le Marchand, L.4
Wilkens, L.R.5
Maskarinec, G.6
Monroe, K.R.7
Kolonel, L.N.8
Altshuler, D.9
Henderson, B.E.10
Haiman, C.A.11
-
7
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
7 Hindorff, L.A., Sethupathy, P., Junkins, H.A., Ramos, E.M., Mehta, J.P., Collins, F.S., Manolio, T.A., Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl. Acad. Sci. USA 106 (2009), 9362–9367.
-
(2009)
Proc. Natl. Acad. Sci. USA
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
Sethupathy, P.2
Junkins, H.A.3
Ramos, E.M.4
Mehta, J.P.5
Collins, F.S.6
Manolio, T.A.7
-
8
-
-
84990250458
-
Using genetic distance to infer the accuracy of genomic prediction
-
8 Scutari, M., Mackay, I., Balding, D., Using genetic distance to infer the accuracy of genomic prediction. PLoS Genet., 12, 2016, e1006288.
-
(2016)
PLoS Genet.
, vol.12
, pp. e1006288
-
-
Scutari, M.1
Mackay, I.2
Balding, D.3
-
9
-
-
84982187833
-
Genetic misdiagnoses and the potential for health disparities
-
9 Manrai, A.K., Funke, B.H., Rehm, H.L., Olesen, M.S., Maron, B.A., Szolovits, P., Margulies, D.M., Loscalzo, J., Kohane, I.S., Genetic misdiagnoses and the potential for health disparities. N. Engl. J. Med. 375 (2016), 655–665.
-
(2016)
N. Engl. J. Med.
, vol.375
, pp. 655-665
-
-
Manrai, A.K.1
Funke, B.H.2
Rehm, H.L.3
Olesen, M.S.4
Maron, B.A.5
Szolovits, P.6
Margulies, D.M.7
Loscalzo, J.8
Kohane, I.S.9
-
10
-
-
84908890496
-
Defining the role of common variation in the genomic and biological architecture of adult human height
-
10 Wood, A.R., Esko, T., Yang, J., Vedantam, S., Pers, T.H., Gustafsson, S., Chu, A.Y., Estrada, K., Luan, J., Kutalik, Z., et al. Electronic Medical Records and Genomics (eMEMERGEGE) Consortium MIGen Consortium PAGEGE Consortium, LifeLines Cohort Study. Defining the role of common variation in the genomic and biological architecture of adult human height. Nat. Genet. 46 (2014), 1173–1186.
-
(2014)
Nat. Genet.
, vol.46
, pp. 1173-1186
-
-
Wood, A.R.1
Esko, T.2
Yang, J.3
Vedantam, S.4
Pers, T.H.5
Gustafsson, S.6
Chu, A.Y.7
Estrada, K.8
Luan, J.9
Kutalik, Z.10
-
11
-
-
84904804929
-
Biological insights from 108 schizophrenia-associated genetic loci
-
11 Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511 (2014), 421–427.
-
(2014)
Nature
, vol.511
, pp. 421-427
-
-
-
12
-
-
84978682985
-
Evaluating the contribution of genetics and familial shared environment to common disease using the UK Biobank
-
12 Muñoz, M., Pong-Wong, R., Canela-Xandri, O., Rawlik, K., Haley, C.S., Tenesa, A., Evaluating the contribution of genetics and familial shared environment to common disease using the UK Biobank. Nat. Genet. 48 (2016), 980–983.
-
(2016)
Nat. Genet.
, vol.48
, pp. 980-983
-
-
Muñoz, M.1
Pong-Wong, R.2
Canela-Xandri, O.3
Rawlik, K.4
Haley, C.S.5
Tenesa, A.6
-
13
-
-
84857641821
-
Differential confounding of rare and common variants in spatially structured populations
-
13 Mathieson, I., McVean, G., Differential confounding of rare and common variants in spatially structured populations. Nat. Genet. 44 (2012), 243–246.
-
(2012)
Nat. Genet.
, vol.44
, pp. 243-246
-
-
Mathieson, I.1
McVean, G.2
-
14
-
-
79961091828
-
Demographic history and rare allele sharing among human populations
-
14 Gravel, S., Henn, B.M., Gutenkunst, R.N., Indap, A.R., Marth, G.T., Clark, A.G., Yu, F., Gibbs, R.A., Bustamante, C.D., 1000 Genomes Project. Demographic history and rare allele sharing among human populations. Proc. Natl. Acad. Sci. USA 108 (2011), 11983–11988.
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 11983-11988
-
-
Gravel, S.1
Henn, B.M.2
Gutenkunst, R.N.3
Indap, A.R.4
Marth, G.T.5
Clark, A.G.6
Yu, F.7
Gibbs, R.A.8
Bustamante, C.D.9
-
15
-
-
84943182742
-
The UK10K project identifies rare variants in health and disease
-
15 Walter, K., Min, J.L., Huang, J., Crooks, L., Memari, Y., McCarthy, S., Perry, J.R., Xu, C., Futema, M., Lawson, D., et al., UK10K Consortium. The UK10K project identifies rare variants in health and disease. Nature 526 (2015), 82–90.
-
(2015)
Nature
, vol.526
, pp. 82-90
-
-
Walter, K.1
Min, J.L.2
Huang, J.3
Crooks, L.4
Memari, Y.5
McCarthy, S.6
Perry, J.R.7
Xu, C.8
Futema, M.9
Lawson, D.10
-
16
-
-
55549115654
-
Genes mirror geography within Europe
-
16 Novembre, J., Johnson, T., Bryc, K., Kutalik, Z., Boyko, A.R., Auton, A., Indap, A., King, K.S., Bergmann, S., Nelson, M.R., et al. Genes mirror geography within Europe. Nature 456 (2008), 98–101.
-
(2008)
Nature
, vol.456
, pp. 98-101
-
-
Novembre, J.1
Johnson, T.2
Bryc, K.3
Kutalik, Z.4
Boyko, A.R.5
Auton, A.6
Indap, A.7
King, K.S.8
Bergmann, S.9
Nelson, M.R.10
-
17
-
-
84867130076
-
Exome sequencing and complex disease: practical aspects of rare variant association studies
-
17 Do, R., Kathiresan, S., Abecasis, G.R., Exome sequencing and complex disease: practical aspects of rare variant association studies. Hum. Mol. Genet. 21:R1 (2012), R1–R9.
-
(2012)
Hum. Mol. Genet.
, vol.21
, Issue.R1
, pp. R1-R9
-
-
Do, R.1
Kathiresan, S.2
Abecasis, G.R.3
-
18
-
-
84982253941
-
Analysis of protein-coding genetic variation in 60,706 humans
-
18 Lek, M., Karczewski, K.J., Minikel, E.V., Samocha, K.E., Banks, E., Fennell, T., O'Donnell-Luria, A.H., Ware, J.S., Hill, A.J., Cummings, B.B., et al., Exome Aggregation Consortium. Analysis of protein-coding genetic variation in 60,706 humans. Nature 536 (2016), 285–291.
-
(2016)
Nature
, vol.536
, pp. 285-291
-
-
Lek, M.1
Karczewski, K.J.2
Minikel, E.V.3
Samocha, K.E.4
Banks, E.5
Fennell, T.6
O'Donnell-Luria, A.H.7
Ware, J.S.8
Hill, A.J.9
Cummings, B.B.10
-
19
-
-
84943171338
-
A global reference for human genetic variation
-
19 Auton, A., Brooks, L.D., Durbin, R.M., Garrison, E.P., Kang, H.M., Korbel, J.O., Marchini, J.L., McCarthy, S., McVean, G.A., Abecasis, G.R., 1000 Genomes Project Consortium. A global reference for human genetic variation. Nature 526 (2015), 68–74.
-
(2015)
Nature
, vol.526
, pp. 68-74
-
-
Auton, A.1
Brooks, L.D.2
Durbin, R.M.3
Garrison, E.P.4
Kang, H.M.5
Korbel, J.O.6
Marchini, J.L.7
McCarthy, S.8
McVean, G.A.9
Abecasis, G.R.10
-
20
-
-
84863556835
-
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
-
20 Tennessen, J.A., Bigham, A.W., O'Connor, T.D., Fu, W., Kenny, E.E., Gravel, S., McGee, S., Do, R., Liu, X., Jun, G., et al. Broad GO Seattle GO, NHLBI Exome Sequencing Project. Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science 337 (2012), 64–69.
-
(2012)
Science
, vol.337
, pp. 64-69
-
-
Tennessen, J.A.1
Bigham, A.W.2
O'Connor, T.D.3
Fu, W.4
Kenny, E.E.5
Gravel, S.6
McGee, S.7
Do, R.8
Liu, X.9
Jun, G.10
-
21
-
-
76749155514
-
A composite of multiple signals distinguishes causal variants in regions of positive selection
-
21 Grossman, S.R., Shlyakhter, I., Karlsson, E.K., Byrne, E.H., Morales, S., Frieden, G., Hostetter, E., Angelino, E., Garber, M., Zuk, O., et al. A composite of multiple signals distinguishes causal variants in regions of positive selection. Science 327 (2010), 883–886.
-
(2010)
Science
, vol.327
, pp. 883-886
-
-
Grossman, S.R.1
Shlyakhter, I.2
Karlsson, E.K.3
Byrne, E.H.4
Morales, S.5
Frieden, G.6
Hostetter, E.7
Angelino, E.8
Garber, M.9
Zuk, O.10
-
22
-
-
84863116742
-
A systematic survey of loss-of-function variants in human protein-coding genes
-
22 MacArthur, D.G., Balasubramanian, S., Frankish, A., Huang, N., Morris, J., Walter, K., Jostins, L., Habegger, L., Pickrell, J.K., Montgomery, S.B., et al., 1000 Genomes Project Consortium. A systematic survey of loss-of-function variants in human protein-coding genes. Science 335 (2012), 823–828.
-
(2012)
Science
, vol.335
, pp. 823-828
-
-
MacArthur, D.G.1
Balasubramanian, S.2
Frankish, A.3
Huang, N.4
Morris, J.5
Walter, K.6
Jostins, L.7
Habegger, L.8
Pickrell, J.K.9
Montgomery, S.B.10
-
23
-
-
39749139577
-
Proportionally more deleterious genetic variation in European than in African populations
-
23 Lohmueller, K.E., Indap, A.R., Schmidt, S., Boyko, A.R., Hernandez, R.D., Hubisz, M.J., Sninsky, J.J., White, T.J., Sunyaev, S.R., Nielsen, R., et al. Proportionally more deleterious genetic variation in European than in African populations. Nature 451 (2008), 994–997.
-
(2008)
Nature
, vol.451
, pp. 994-997
-
-
Lohmueller, K.E.1
Indap, A.R.2
Schmidt, S.3
Boyko, A.R.4
Hernandez, R.D.5
Hubisz, M.J.6
Sninsky, J.J.7
White, T.J.8
Sunyaev, S.R.9
Nielsen, R.10
-
24
-
-
84921818763
-
Characteristics of neutral and deleterious protein-coding variation among individuals and populations
-
24 Fu, W., Gittelman, R.M., Bamshad, M.J., Akey, J.M., Characteristics of neutral and deleterious protein-coding variation among individuals and populations. Am. J. Hum. Genet. 95 (2014), 421–436.
-
(2014)
Am. J. Hum. Genet.
, vol.95
, pp. 421-436
-
-
Fu, W.1
Gittelman, R.M.2
Bamshad, M.J.3
Akey, J.M.4
-
25
-
-
84895867277
-
The deleterious mutation load is insensitive to recent population history
-
25 Simons, Y.B., Turchin, M.C., Pritchard, J.K., Sella, G., The deleterious mutation load is insensitive to recent population history. Nat. Genet. 46 (2014), 220–224.
-
(2014)
Nat. Genet.
, vol.46
, pp. 220-224
-
-
Simons, Y.B.1
Turchin, M.C.2
Pritchard, J.K.3
Sella, G.4
-
26
-
-
67651225410
-
Sensitive detection of chromosomal segments of distinct ancestry in admixed populations
-
26 Price, A.L., Tandon, A., Patterson, N., Barnes, K.C., Rafaels, N., Ruczinski, I., Beaty, T.H., Mathias, R., Reich, D., Myers, S., Sensitive detection of chromosomal segments of distinct ancestry in admixed populations. PLoS Genet., 5, 2009, e1000519.
-
(2009)
PLoS Genet.
, vol.5
, pp. e1000519
-
-
Price, A.L.1
Tandon, A.2
Patterson, N.3
Barnes, K.C.4
Rafaels, N.5
Ruczinski, I.6
Beaty, T.H.7
Mathias, R.8
Reich, D.9
Myers, S.10
-
27
-
-
79955578094
-
Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium
-
27 Pasaniuc, B., Zaitlen, N., Lettre, G., Chen, G.K., Tandon, A., Kao, W.H.L., Ruczinski, I., Fornage, M., Siscovick, D.S., Zhu, X., et al. Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium. PLoS Genet., 7, 2011, e1001371.
-
(2011)
PLoS Genet.
, vol.7
, pp. e1001371
-
-
Pasaniuc, B.1
Zaitlen, N.2
Lettre, G.3
Chen, G.K.4
Tandon, A.5
Kao, W.H.L.6
Ruczinski, I.7
Fornage, M.8
Siscovick, D.S.9
Zhu, X.10
-
28
-
-
84859235751
-
Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas
-
28 Fejerman, L., Chen, G.K., Eng, C., Huntsman, S., Hu, D., Williams, A., Pasaniuc, B., John, E.M., Via, M., Gignoux, C., et al. Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas. Hum. Mol. Genet. 21 (2012), 1907–1917.
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 1907-1917
-
-
Fejerman, L.1
Chen, G.K.2
Eng, C.3
Huntsman, S.4
Hu, D.5
Williams, A.6
Pasaniuc, B.7
John, E.M.8
Via, M.9
Gignoux, C.10
-
29
-
-
84923773863
-
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25
-
29 Fejerman, L., Ahmadiyeh, N., Hu, D., Huntsman, S., Beckman, K.B., Caswell, J.L., Tsung, K., John, E.M., Torres-Mejia, G., Carvajal-Carmona, L., et al., COLUMBUS Consortium. Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. Nat. Commun., 5, 2014, 5260.
-
(2014)
Nat. Commun.
, vol.5
, pp. 5260
-
-
Fejerman, L.1
Ahmadiyeh, N.2
Hu, D.3
Huntsman, S.4
Beckman, K.B.5
Caswell, J.L.6
Tsung, K.7
John, E.M.8
Torres-Mejia, G.9
Carvajal-Carmona, L.10
-
30
-
-
33749003979
-
Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men
-
30 Freedman, M.L., Haiman, C.A., Patterson, N., McDonald, G.J., Tandon, A., Waliszewska, A., Penney, K., Steen, R.G., Ardlie, K., John, E.M., et al. Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men. Proc. Natl. Acad. Sci. USA 103 (2006), 14068–14073.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 14068-14073
-
-
Freedman, M.L.1
Haiman, C.A.2
Patterson, N.3
McDonald, G.J.4
Tandon, A.5
Waliszewska, A.6
Penney, K.7
Steen, R.G.8
Ardlie, K.9
John, E.M.10
-
31
-
-
80052749307
-
Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection
-
31 Bhatia, G., Patterson, N., Pasaniuc, B., Zaitlen, N., Genovese, G., Pollack, S., Mallick, S., Myers, S., Tandon, A., Spencer, C., et al. Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection. Am. J. Hum. Genet. 89 (2011), 368–381.
-
(2011)
Am. J. Hum. Genet.
, vol.89
, pp. 368-381
-
-
Bhatia, G.1
Patterson, N.2
Pasaniuc, B.3
Zaitlen, N.4
Genovese, G.5
Pollack, S.6
Mallick, S.7
Myers, S.8
Tandon, A.9
Spencer, C.10
-
32
-
-
84888230853
-
Reconstructing the population genetic history of the Caribbean
-
32 Moreno-Estrada, A., Gravel, S., Zakharia, F., McCauley, J.L., Byrnes, J.K., Gignoux, C.R., Ortiz-Tello, P.A., Martínez, R.J., Hedges, D.J., Morris, R.W., et al. Reconstructing the population genetic history of the Caribbean. PLoS Genet., 9, 2013, e1003925.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003925
-
-
Moreno-Estrada, A.1
Gravel, S.2
Zakharia, F.3
McCauley, J.L.4
Byrnes, J.K.5
Gignoux, C.R.6
Ortiz-Tello, P.A.7
Martínez, R.J.8
Hedges, D.J.9
Morris, R.W.10
-
33
-
-
77952324523
-
Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations
-
33 Bryc, K., Velez, C., Karafet, T., Moreno-Estrada, A., Reynolds, A., Auton, A., Hammer, M., Bustamante, C.D., Ostrer, H., Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations. Proc. Natl. Acad. Sci. USA 107:Suppl 2 (2010), 8954–8961.
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 8954-8961
-
-
Bryc, K.1
Velez, C.2
Karafet, T.3
Moreno-Estrada, A.4
Reynolds, A.5
Auton, A.6
Hammer, M.7
Bustamante, C.D.8
Ostrer, H.9
-
34
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
34 Pritchard, J.K., Stephens, M., Donnelly, P., Inference of population structure using multilocus genotype data. Genetics 155 (2000), 945–959.
-
(2000)
Genetics
, vol.155
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
35
-
-
17644402806
-
Estimation of individual admixture: analytical and study design considerations
-
35 Tang, H., Peng, J., Wang, P., Risch, N.J., Estimation of individual admixture: analytical and study design considerations. Genet. Epidemiol. 28 (2005), 289–301.
-
(2005)
Genet. Epidemiol.
, vol.28
, pp. 289-301
-
-
Tang, H.1
Peng, J.2
Wang, P.3
Risch, N.J.4
-
36
-
-
69749099417
-
Fast model-based estimation of ancestry in unrelated individuals
-
36 Alexander, D.H., Novembre, J., Lange, K., Fast model-based estimation of ancestry in unrelated individuals. Genome Res. 19 (2009), 1655–1664.
-
(2009)
Genome Res.
, vol.19
, pp. 1655-1664
-
-
Alexander, D.H.1
Novembre, J.2
Lange, K.3
-
37
-
-
77953811255
-
New approaches to population stratification in genome-wide association studies
-
37 Price, A.L., Zaitlen, N.A., Reich, D., Patterson, N., New approaches to population stratification in genome-wide association studies. Nat. Rev. Genet. 11 (2010), 459–463.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 459-463
-
-
Price, A.L.1
Zaitlen, N.A.2
Reich, D.3
Patterson, N.4
-
38
-
-
84926320923
-
Demography and the age of rare variants
-
38 Mathieson, I., McVean, G., Demography and the age of rare variants. PLoS Genet., 10, 2014, e1004528.
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004528
-
-
Mathieson, I.1
McVean, G.2
-
39
-
-
84982128306
-
Rare variation facilitates inferences of fine-scale population structure in humans
-
39 O'Connor, T.D., Fu, W., Mychaleckyj, J.C., Logsdon, B., Auer, P., Carlson, C.S., Leal, S.M., Smith, J.D., Rieder, M.J., Bamshad, M.J., et al. NHLBI GO Exome Sequencing Project, ESP Population Genetics and Statistical Analysis Working Group, Emily Turner. Rare variation facilitates inferences of fine-scale population structure in humans. Mol. Biol. Evol. 32 (2015), 653–660.
-
(2015)
Mol. Biol. Evol.
, vol.32
, pp. 653-660
-
-
O'Connor, T.D.1
Fu, W.2
Mychaleckyj, J.C.3
Logsdon, B.4
Auer, P.5
Carlson, C.S.6
Leal, S.M.7
Smith, J.D.8
Rieder, M.J.9
Bamshad, M.J.10
-
40
-
-
85016903046
-
Joint genotype- and ancestry-based genome-wide association studies in admixed populations
-
40 Szulc, P., Bogdan, M., Frommlet, F., Tang, H., Joint genotype- and ancestry-based genome-wide association studies in admixed populations. bioRxiv, 2016, 10.1101/062554.
-
(2016)
bioRxiv
-
-
Szulc, P.1
Bogdan, M.2
Frommlet, F.3
Tang, H.4
-
41
-
-
84954289735
-
Model-free estimation of recent genetic relatedness
-
41 Conomos, M.P., Reiner, A.P., Weir, B.S., Thornton, T.A., Model-free estimation of recent genetic relatedness. Am. J. Hum. Genet. 98 (2016), 127–148.
-
(2016)
Am. J. Hum. Genet.
, vol.98
, pp. 127-148
-
-
Conomos, M.P.1
Reiner, A.P.2
Weir, B.S.3
Thornton, T.A.4
-
42
-
-
73149100820
-
Leveraging genetic variability across populations for the identification of causal variants
-
42 Zaitlen, N., Paşaniuc, B., Gur, T., Ziv, E., Halperin, E., Leveraging genetic variability across populations for the identification of causal variants. Am. J. Hum. Genet. 86 (2010), 23–33.
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 23-33
-
-
Zaitlen, N.1
Paşaniuc, B.2
Gur, T.3
Ziv, E.4
Halperin, E.5
-
43
-
-
84883786102
-
Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes
-
43 Genovese, G., Handsaker, R.E., Li, H., Kenny, E.E., McCarroll, S.A., Mapping the human reference genome's missing sequence by three-way admixture in Latino genomes. Am. J. Hum. Genet. 93 (2013), 411–421.
-
(2013)
Am. J. Hum. Genet.
, vol.93
, pp. 411-421
-
-
Genovese, G.1
Handsaker, R.E.2
Li, H.3
Kenny, E.E.4
McCarroll, S.A.5
-
44
-
-
84974530800
-
The great migration and African-American genomic diversity
-
44 Baharian, S., Barakatt, M., Gignoux, C.R., Shringarpure, S., Errington, J., Blot, W.J., Bustamante, C.D., Kenny, E.E., Williams, S.M., Aldrich, M.C., Gravel, S., The great migration and African-American genomic diversity. PLoS Genet., 12, 2016, e1006059.
-
(2016)
PLoS Genet.
, vol.12
, pp. e1006059
-
-
Baharian, S.1
Barakatt, M.2
Gignoux, C.R.3
Shringarpure, S.4
Errington, J.5
Blot, W.J.6
Bustamante, C.D.7
Kenny, E.E.8
Williams, S.M.9
Aldrich, M.C.10
Gravel, S.11
-
45
-
-
84865120805
-
Reconstructing Native American population history
-
45 Reich, D., Patterson, N., Campbell, D., Tandon, A., Mazieres, S., Ray, N., Parra, M.V., Rojas, W., Duque, C., Mesa, N., et al. Reconstructing Native American population history. Nature 488 (2012), 370–374.
-
(2012)
Nature
, vol.488
, pp. 370-374
-
-
Reich, D.1
Patterson, N.2
Campbell, D.3
Tandon, A.4
Mazieres, S.5
Ray, N.6
Parra, M.V.7
Rojas, W.8
Duque, C.9
Mesa, N.10
-
46
-
-
84901487813
-
Admixture in Latin America: geographic structure, phenotypic diversity and self-perception of ancestry based on 7,342 individuals
-
46 Ruiz-Linares, A., Adhikari, K., Acuña-Alonzo, V., Quinto-Sanchez, M., Jaramillo, C., Arias, W., Fuentes, M., Pizarro, M., Everardo, P., de Avila, F., et al. Admixture in Latin America: geographic structure, phenotypic diversity and self-perception of ancestry based on 7,342 individuals. PLoS Genet., 10, 2014, e1004572.
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004572
-
-
Ruiz-Linares, A.1
Adhikari, K.2
Acuña-Alonzo, V.3
Quinto-Sanchez, M.4
Jaramillo, C.5
Arias, W.6
Fuentes, M.7
Pizarro, M.8
Everardo, P.9
de Avila, F.10
-
47
-
-
84902603117
-
Human genetics. The genetics of Mexico recapitulates Native American substructure and affects biomedical traits
-
47 Moreno-Estrada, A., Gignoux, C.R., Fernández-López, J.C., Zakharia, F., Sikora, M., Contreras, A.V., Acuña-Alonzo, V., Sandoval, K., Eng, C., Romero-Hidalgo, S., et al. Human genetics. The genetics of Mexico recapitulates Native American substructure and affects biomedical traits. Science 344 (2014), 1280–1285.
-
(2014)
Science
, vol.344
, pp. 1280-1285
-
-
Moreno-Estrada, A.1
Gignoux, C.R.2
Fernández-López, J.C.3
Zakharia, F.4
Sikora, M.5
Contreras, A.V.6
Acuña-Alonzo, V.7
Sandoval, K.8
Eng, C.9
Romero-Hidalgo, S.10
-
48
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
48 Purcell, S.M., Wray, N.R., Stone, J.L., Visscher, P.M., O'Donovan, M.C., Sullivan, P.F., Sklar, P., International Schizophrenia Consortium. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460 (2009), 748–752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
Purcell, S.M.1
Wray, N.R.2
Stone, J.L.3
Visscher, P.M.4
O'Donovan, M.C.5
Sullivan, P.F.6
Sklar, P.7
-
49
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
49 Yang, J., Benyamin, B., McEvoy, B.P., Gordon, S., Henders, A.K., Nyholt, D.R., Madden, P.A., Heath, A.C., Martin, N.G., Montgomery, G.W., et al. Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42 (2010), 565–569.
-
(2010)
Nat. Genet.
, vol.42
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
Gordon, S.4
Henders, A.K.5
Nyholt, D.R.6
Madden, P.A.7
Heath, A.C.8
Martin, N.G.9
Montgomery, G.W.10
-
50
-
-
79959241413
-
Genomic inflation factors under polygenic inheritance
-
50 Yang, J., Weedon, M.N., Purcell, S., Lettre, G., Estrada, K., Willer, C.J., Smith, A.V., Ingelsson, E., O'Connell, J.R., Mangino, M., et al., GIANT Consortium. Genomic inflation factors under polygenic inheritance. Eur. J. Hum. Genet. 19 (2011), 807–812.
-
(2011)
Eur. J. Hum. Genet.
, vol.19
, pp. 807-812
-
-
Yang, J.1
Weedon, M.N.2
Purcell, S.3
Lettre, G.4
Estrada, K.5
Willer, C.J.6
Smith, A.V.7
Ingelsson, E.8
O'Connell, J.R.9
Mangino, M.10
-
51
-
-
34948877698
-
Prediction of individual genetic risk to disease from genome-wide association studies
-
51 Wray, N.R., Goddard, M.E., Visscher, P.M., Prediction of individual genetic risk to disease from genome-wide association studies. Genome Res. 17 (2007), 1520–1528.
-
(2007)
Genome Res.
, vol.17
, pp. 1520-1528
-
-
Wray, N.R.1
Goddard, M.E.2
Visscher, P.M.3
-
52
-
-
84879324656
-
Pitfalls of predicting complex traits from SNPs
-
52 Wray, N.R., Yang, J., Hayes, B.J., Price, A.L., Goddard, M.E., Visscher, P.M., Pitfalls of predicting complex traits from SNPs. Nat. Rev. Genet. 14 (2013), 507–515.
-
(2013)
Nat. Rev. Genet.
, vol.14
, pp. 507-515
-
-
Wray, N.R.1
Yang, J.2
Hayes, B.J.3
Price, A.L.4
Goddard, M.E.5
Visscher, P.M.6
-
53
-
-
84908121749
-
Research review: polygenic methods and their application to psychiatric traits
-
53 Wray, N.R., Lee, S.H., Mehta, D., Vinkhuyzen, A.A., Dudbridge, F., Middeldorp, C.M., Research review: polygenic methods and their application to psychiatric traits. J. Child Psychol. Psychiatry 55 (2014), 1068–1087.
-
(2014)
J. Child Psychol. Psychiatry
, vol.55
, pp. 1068-1087
-
-
Wray, N.R.1
Lee, S.H.2
Mehta, D.3
Vinkhuyzen, A.A.4
Dudbridge, F.5
Middeldorp, C.M.6
-
54
-
-
84965076156
-
Developing and evaluating polygenic risk prediction models for stratified disease prevention
-
54 Chatterjee, N., Shi, J., García-Closas, M., Developing and evaluating polygenic risk prediction models for stratified disease prevention. Nat. Rev. Genet. 17 (2016), 392–406.
-
(2016)
Nat. Rev. Genet.
, vol.17
, pp. 392-406
-
-
Chatterjee, N.1
Shi, J.2
García-Closas, M.3
-
55
-
-
84963653782
-
Polygenic epidemiology
-
55 Dudbridge, F., Polygenic epidemiology. Genet. Epidemiol. 40 (2016), 268–272.
-
(2016)
Genet. Epidemiol.
, vol.40
, pp. 268-272
-
-
Dudbridge, F.1
-
56
-
-
85016902841
-
Exploring the predictive power of polygenic scores derived from genome-wide association studies: a study of 10 complex traits
-
56 So, H.C., Sham, P.C., Exploring the predictive power of polygenic scores derived from genome-wide association studies: a study of 10 complex traits. Bioinformatics 33 (2017), 886–892.
-
(2017)
Bioinformatics
, vol.33
, pp. 886-892
-
-
So, H.C.1
Sham, P.C.2
-
57
-
-
84946158905
-
PRSice: polygenic risk score software
-
57 Euesden, J., Lewis, C.M., O'Reilly, P.F., PRSice: polygenic risk score software. Bioinformatics 31 (2015), 1466–1468.
-
(2015)
Bioinformatics
, vol.31
, pp. 1466-1468
-
-
Euesden, J.1
Lewis, C.M.2
O'Reilly, P.F.3
-
58
-
-
85007574079
-
Winner's curse correction and variable thresholding improve performance of polygenic risk modeling based on genome-wide association study summary-level data
-
58 Shi, J., Park, J.H., Duan, J., Berndt, S.T., Moy, W., Yu, K., Song, L., Wheeler, W., Hua, X., Silverman, D., et al. MGS (Molecular Genetics of Schizophrenia) GWAS Consortium GECCO (The Genetics and Epidemiology of Colorectal Cancer Consortium) GAME-ON/TRICL (Transdisciplinary Research in Cancer of the Lung) GWAS Consortium PRACTICAL (PRostate cancer AssoCiation group To Investigate Cancer Associated aLterations) Consortium PanScan Consortium, GAME-ON/ELLIPSE Consortium. Winner's curse correction and variable thresholding improve performance of polygenic risk modeling based on genome-wide association study summary-level data. PLoS Genet., 12, 2016, e1006493.
-
(2016)
PLoS Genet.
, vol.12
, pp. e1006493
-
-
Shi, J.1
Park, J.H.2
Duan, J.3
Berndt, S.T.4
Moy, W.5
Yu, K.6
Song, L.7
Wheeler, W.8
Hua, X.9
Silverman, D.10
-
59
-
-
84876007072
-
Power and predictive accuracy of polygenic risk scores
-
59 Dudbridge, F., Power and predictive accuracy of polygenic risk scores. PLoS Genet., 9, 2013, e1003348.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1003348
-
-
Dudbridge, F.1
-
60
-
-
45949085378
-
Polygenes, risk prediction, and targeted prevention of breast cancer
-
60 Pharoah, P.D., Antoniou, A.C., Easton, D.F., Ponder, B.A., Polygenes, risk prediction, and targeted prevention of breast cancer. N. Engl. J. Med. 358 (2008), 2796–2803.
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 2796-2803
-
-
Pharoah, P.D.1
Antoniou, A.C.2
Easton, D.F.3
Ponder, B.A.4
-
61
-
-
69449102525
-
Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk
-
61 Evans, D.M., Visscher, P.M., Wray, N.R., Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. Hum. Mol. Genet. 18 (2009), 3525–3531.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3525-3531
-
-
Evans, D.M.1
Visscher, P.M.2
Wray, N.R.3
-
62
-
-
84969760786
-
Genome-wide association study identifies 74 loci associated with educational attainment
-
62 Okbay, A., Beauchamp, J.P., Fontana, M.A., Lee, J.J., Pers, T.H., Rietveld, C.A., Turley, P., Chen, G.B., Emilsson, V., Meddens, S.F., et al., LifeLines Cohort Study. Genome-wide association study identifies 74 loci associated with educational attainment. Nature 533 (2016), 539–542.
-
(2016)
Nature
, vol.533
, pp. 539-542
-
-
Okbay, A.1
Beauchamp, J.P.2
Fontana, M.A.3
Lee, J.J.4
Pers, T.H.5
Rietveld, C.A.6
Turley, P.7
Chen, G.B.8
Emilsson, V.9
Meddens, S.F.10
-
63
-
-
77957947562
-
Hundreds of variants clustered in genomic loci and biological pathways affect human height
-
63 Lango Allen, H., Estrada, K., Lettre, G., Berndt, S.I., Weedon, M.N., Rivadeneira, F., Willer, C.J., Jackson, A.U., Vedantam, S., Raychaudhuri, S., et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467 (2010), 832–838.
-
(2010)
Nature
, vol.467
, pp. 832-838
-
-
Lango Allen, H.1
Estrada, K.2
Lettre, G.3
Berndt, S.I.4
Weedon, M.N.5
Rivadeneira, F.6
Willer, C.J.7
Jackson, A.U.8
Vedantam, S.9
Raychaudhuri, S.10
-
64
-
-
77950329947
-
Evidence for polygenic susceptibility to multiple sclerosis–the shape of things to come
-
64 Bush, W.S., Sawcer, S.J., de Jager, P.L., Oksenberg, J.R., McCauley, J.L., Pericak-Vance, M.A., Haines, J.L., International Multiple Sclerosis Genetics Consortium (IMSGC). Evidence for polygenic susceptibility to multiple sclerosis–the shape of things to come. Am. J. Hum. Genet. 86 (2010), 621–625.
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 621-625
-
-
Bush, W.S.1
Sawcer, S.J.2
de Jager, P.L.3
Oksenberg, J.R.4
McCauley, J.L.5
Pericak-Vance, M.A.6
Haines, J.L.7
-
65
-
-
84860333083
-
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
-
65 Stahl, E.A., Wegmann, D., Trynka, G., Gutierrez-Achury, J., Do, R., Voight, B.F., Kraft, P., Chen, R., Kallberg, H.J., Kurreeman, F.A., et al. Diabetes Genetics Replication and Meta-analysis Consortium, Myocardial Infarction Genetics Consortium. Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis. Nat. Genet. 44 (2012), 483–489.
-
(2012)
Nat. Genet.
, vol.44
, pp. 483-489
-
-
Stahl, E.A.1
Wegmann, D.2
Trynka, G.3
Gutierrez-Achury, J.4
Do, R.5
Voight, B.F.6
Kraft, P.7
Chen, R.8
Kallberg, H.J.9
Kurreeman, F.A.10
-
66
-
-
84925130699
-
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder
-
66 Maier, R., Moser, G., Chen, G.B., Ripke, S., Coryell, W., Potash, J.B., Scheftner, W.A., Shi, J., Weissman, M.M., Hultman, C.M., et al., Cross-Disorder Working Group of the Psychiatric Genomics Consortium. Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. Am. J. Hum. Genet. 96 (2015), 283–294.
-
(2015)
Am. J. Hum. Genet.
, vol.96
, pp. 283-294
-
-
Maier, R.1
Moser, G.2
Chen, G.B.3
Ripke, S.4
Coryell, W.5
Potash, J.B.6
Scheftner, W.A.7
Shi, J.8
Weissman, M.M.9
Hultman, C.M.10
-
67
-
-
84952665106
-
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
-
67 Vilhjálmsson, B.J., Yang, J., Finucane, H.K., Gusev, A., Lindström, S., Ripke, S., Genovese, G., Loh, P.R., Bhatia, G., Do, R., et al., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) study. Modeling linkage disequilibrium increases accuracy of polygenic risk scores. Am. J. Hum. Genet. 97 (2015), 576–592.
-
(2015)
Am. J. Hum. Genet.
, vol.97
, pp. 576-592
-
-
Vilhjálmsson, B.J.1
Yang, J.2
Finucane, H.K.3
Gusev, A.4
Lindström, S.5
Ripke, S.6
Genovese, G.7
Loh, P.R.8
Bhatia, G.9
Do, R.10
-
68
-
-
84911893507
-
A hidden Markov model for investigating recent positive selection through haplotype structure
-
68 Chen, H., Hey, J., Slatkin, M., A hidden Markov model for investigating recent positive selection through haplotype structure. Theor. Popul. Biol. 99 (2015), 18–30.
-
(2015)
Theor. Popul. Biol.
, vol.99
, pp. 18-30
-
-
Chen, H.1
Hey, J.2
Slatkin, M.3
-
69
-
-
34250882721
-
A genomewide admixture mapping panel for Hispanic/Latino populations
-
69 Mao, X., Bigham, A.W., Mei, R., Gutierrez, G., Weiss, K.M., Brutsaert, T.D., Leon-Velarde, F., Moore, L.G., Vargas, E., McKeigue, P.M., et al. A genomewide admixture mapping panel for Hispanic/Latino populations. Am. J. Hum. Genet. 80 (2007), 1171–1178.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 1171-1178
-
-
Mao, X.1
Bigham, A.W.2
Mei, R.3
Gutierrez, G.4
Weiss, K.M.5
Brutsaert, T.D.6
Leon-Velarde, F.7
Moore, L.G.8
Vargas, E.9
McKeigue, P.M.10
-
70
-
-
84901370399
-
A general approach for haplotype phasing across the full spectrum of relatedness
-
70 O'Connell, J., Gurdasani, D., Delaneau, O., Pirastu, N., Ulivi, S., Cocca, M., Traglia, M., Huang, J., Huffman, J.E., Rudan, I., et al. A general approach for haplotype phasing across the full spectrum of relatedness. PLoS Genet., 10, 2014, e1004234.
-
(2014)
PLoS Genet.
, vol.10
, pp. e1004234
-
-
O'Connell, J.1
Gurdasani, D.2
Delaneau, O.3
Pirastu, N.4
Ulivi, S.5
Cocca, M.6
Traglia, M.7
Huang, J.8
Huffman, J.E.9
Rudan, I.10
-
71
-
-
84881665614
-
RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference
-
71 Maples, B.K., Gravel, S., Kenny, E.E., Bustamante, C.D., RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference. Am. J. Hum. Genet. 93 (2013), 278–288.
-
(2013)
Am. J. Hum. Genet.
, vol.93
, pp. 278-288
-
-
Maples, B.K.1
Gravel, S.2
Kenny, E.E.3
Bustamante, C.D.4
-
72
-
-
84862587557
-
Population genetics models of local ancestry
-
72 Gravel, S., Population genetics models of local ancestry. Genetics 191 (2012), 607–619.
-
(2012)
Genetics
, vol.191
, pp. 607-619
-
-
Gravel, S.1
-
73
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
73 Abecasis, G.R., Auton, A., Brooks, L.D., DePristo, M.A., Durbin, R.M., Handsaker, R.E., Kang, H.M., Marth, G.T., McVean, G.A., 1000 Genomes Project Consortium. An integrated map of genetic variation from 1,092 human genomes. Nature 491 (2012), 56–65.
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
Abecasis, G.R.1
Auton, A.2
Brooks, L.D.3
DePristo, M.A.4
Durbin, R.M.5
Handsaker, R.E.6
Kang, H.M.7
Marth, G.T.8
McVean, G.A.9
-
74
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
74 Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M.A., Bender, D., Maller, J., Sklar, P., de Bakker, P.I., Daly, M.J., Sham, P.C., PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81 (2007), 559–575.
-
(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
Bender, D.6
Maller, J.7
Sklar, P.8
de Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
75
-
-
84975828278
-
Efficient coalescent simulation and genealogical analysis for large sample sizes
-
75 Kelleher, J., Etheridge, A.M., McVean, G., Efficient coalescent simulation and genealogical analysis for large sample sizes. PLoS Comput. Biol., 12, 2016, e1004842.
-
(2016)
PLoS Comput. Biol.
, vol.12
, pp. e1004842
-
-
Kelleher, J.1
Etheridge, A.M.2
McVean, G.3
-
76
-
-
84991369066
-
A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome
-
76 Mathias, R.A., Taub, M.A., Gignoux, C.R., Fu, W., Musharoff, S., O'Connor, T.D., Vergara, C., Torgerson, D.G., Pino-Yanes, M., Shringarpure, S.S., et al., CAAPA. A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome. Nat. Commun., 7, 2016, 12522.
-
(2016)
Nat. Commun.
, vol.7
, pp. 12522
-
-
Mathias, R.A.1
Taub, M.A.2
Gignoux, C.R.3
Fu, W.4
Musharoff, S.5
O'Connor, T.D.6
Vergara, C.7
Torgerson, D.G.8
Pino-Yanes, M.9
Shringarpure, S.S.10
-
77
-
-
85016864993
-
Efficient analysis of large datasets and sex bias with ADMIXTURE
-
77 Shringarpure, S.S., Bustamante, C.D., Lange, K.L., Alexander, D.H., Efficient analysis of large datasets and sex bias with ADMIXTURE. bioRxiv, 2016, 10.1101/039347.
-
(2016)
bioRxiv
-
-
Shringarpure, S.S.1
Bustamante, C.D.2
Lange, K.L.3
Alexander, D.H.4
-
78
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
78 Price, A.L., Patterson, N.J., Plenge, R.M., Weinblatt, M.E., Shadick, N.A., Reich, D., Principal components analysis corrects for stratification in genome-wide association studies. Nat. Genet. 38 (2006), 904–909.
-
(2006)
Nat. Genet.
, vol.38
, pp. 904-909
-
-
Price, A.L.1
Patterson, N.J.2
Plenge, R.M.3
Weinblatt, M.E.4
Shadick, N.A.5
Reich, D.6
-
79
-
-
84861127863
-
Fast and accurate inference of local ancestry in Latino populations
-
79 Baran, Y., Pasaniuc, B., Sankararaman, S., Torgerson, D.G., Gignoux, C., Eng, C., Rodriguez-Cintron, W., Chapela, R., Ford, J.G., Avila, P.C., et al. Fast and accurate inference of local ancestry in Latino populations. Bioinformatics 28 (2012), 1359–1367.
-
(2012)
Bioinformatics
, vol.28
, pp. 1359-1367
-
-
Baran, Y.1
Pasaniuc, B.2
Sankararaman, S.3
Torgerson, D.G.4
Gignoux, C.5
Eng, C.6
Rodriguez-Cintron, W.7
Chapela, R.8
Ford, J.G.9
Avila, P.C.10
-
80
-
-
66249116333
-
The genetic structure and history of Africans and African Americans
-
80 Tishkoff, S.A., Reed, F.A., Friedlaender, F.R., Ehret, C., Ranciaro, A., Froment, A., Hirbo, J.B., Awomoyi, A.A., Bodo, J.M., Doumbo, O., et al. The genetic structure and history of Africans and African Americans. Science 324 (2009), 1035–1044.
-
(2009)
Science
, vol.324
, pp. 1035-1044
-
-
Tishkoff, S.A.1
Reed, F.A.2
Friedlaender, F.R.3
Ehret, C.4
Ranciaro, A.5
Froment, A.6
Hirbo, J.B.7
Awomoyi, A.A.8
Bodo, J.M.9
Doumbo, O.10
-
81
-
-
76249114566
-
Characterizing the admixed African ancestry of African Americans
-
81 Zakharia, F., Basu, A., Absher, D., Assimes, T.L., Go, A.S., Hlatky, M.A., Iribarren, C., Knowles, J.W., Li, J., Narasimhan, B., et al. Characterizing the admixed African ancestry of African Americans. Genome Biol., 10, 2009, R141.
-
(2009)
Genome Biol.
, vol.10
, pp. R141
-
-
Zakharia, F.1
Basu, A.2
Absher, D.3
Assimes, T.L.4
Go, A.S.5
Hlatky, M.A.6
Iribarren, C.7
Knowles, J.W.8
Li, J.9
Narasimhan, B.10
-
82
-
-
84925432613
-
Genome-wide ancestry of 17th-century enslaved Africans from the Caribbean
-
82 Schroeder, H., Ávila-Arcos, M.C., Malaspinas, A.S., Poznik, G.D., Sandoval-Velasco, M., Carpenter, M.L., Moreno-Mayar, J.V., Sikora, M., Johnson, P.L., Allentoft, M.E., et al. Genome-wide ancestry of 17th-century enslaved Africans from the Caribbean. Proc. Natl. Acad. Sci. USA 112 (2015), 3669–3673.
-
(2015)
Proc. Natl. Acad. Sci. USA
, vol.112
, pp. 3669-3673
-
-
Schroeder, H.1
Ávila-Arcos, M.C.2
Malaspinas, A.S.3
Poznik, G.D.4
Sandoval-Velasco, M.5
Carpenter, M.L.6
Moreno-Mayar, J.V.7
Sikora, M.8
Johnson, P.L.9
Allentoft, M.E.10
-
83
-
-
84892684329
-
Reconstructing Native American migrations from whole-genome and whole-exome data
-
83 Gravel, S., Zakharia, F., Moreno-Estrada, A., Byrnes, J.K., Muzzio, M., Rodriguez-Flores, J.L., Kenny, E.E., Gignoux, C.R., Maples, B.K., Guiblet, W., et al., 1000 Genomes Project. Reconstructing Native American migrations from whole-genome and whole-exome data. PLoS Genet., 9, 2013, e1004023.
-
(2013)
PLoS Genet.
, vol.9
, pp. e1004023
-
-
Gravel, S.1
Zakharia, F.2
Moreno-Estrada, A.3
Byrnes, J.K.4
Muzzio, M.5
Rodriguez-Flores, J.L.6
Kenny, E.E.7
Gignoux, C.R.8
Maples, B.K.9
Guiblet, W.10
-
84
-
-
84991409036
-
Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry
-
84 Kessler, M.D., Yerges-Armstrong, L., Taub, M.A., Shetty, A.C., Maloney, K., Jeng, L.J.B., Ruczinski, I., Levin, A.M., Williams, L.K., Beaty, T.H., et al., Consortium on Asthma among African-ancestry Populations in the Americas (CAAPA). Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry. Nat. Commun., 7, 2016, 12521.
-
(2016)
Nat. Commun.
, vol.7
, pp. 12521
-
-
Kessler, M.D.1
Yerges-Armstrong, L.2
Taub, M.A.3
Shetty, A.C.4
Maloney, K.5
Jeng, L.J.B.6
Ruczinski, I.7
Levin, A.M.8
Williams, L.K.9
Beaty, T.H.10
-
85
-
-
84923169934
-
New genetic loci link adipose and insulin biology to body fat distribution
-
85 Shungin, D., Winkler, T.W., Croteau-Chonka, D.C., Ferreira, T., Locke, A.E., Mägi, R., Strawbridge, R.J., Pers, T.H., Fischer, K., Justice, A.E., et al. ADIPOGen Consortium CARDIOGRAMplusC4D Consortium CKDGen Consortium GEFOS Consortium GENIE Consortium GLGC ICBP International Endogene Consortium LifeLines Cohort Study MAGIC Investigators MuTHER Consortium PAGE Consortium, ReproGen Consortium. New genetic loci link adipose and insulin biology to body fat distribution. Nature 518 (2015), 187–196.
-
(2015)
Nature
, vol.518
, pp. 187-196
-
-
Shungin, D.1
Winkler, T.W.2
Croteau-Chonka, D.C.3
Ferreira, T.4
Locke, A.E.5
Mägi, R.6
Strawbridge, R.J.7
Pers, T.H.8
Fischer, K.9
Justice, A.E.10
-
86
-
-
84948984088
-
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
-
86 Gaulton, K.J., Ferreira, T., Lee, Y., Raimondo, A., Mägi, R., Reschen, M.E., Mahajan, A., Locke, A., Rayner, N.W., Robertson, N., et al., DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci. Nat. Genet. 47 (2015), 1415–1425.
-
(2015)
Nat. Genet.
, vol.47
, pp. 1415-1425
-
-
Gaulton, K.J.1
Ferreira, T.2
Lee, Y.3
Raimondo, A.4
Mägi, R.5
Reschen, M.E.6
Mahajan, A.7
Locke, A.8
Rayner, N.W.9
Robertson, N.10
-
87
-
-
84895868553
-
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
-
87 Mahajan, A., Go, M.J., Zhang, W., Below, J.E., Gaulton, K.J., Ferreira, T., Horikoshi, M., Johnson, A.D., Ng, M.C., Prokopenko, I., et al. DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium South Asian Type 2 Diabetes (SAT2D) Consortium Mexican American Type 2 Diabetes (MAT2D) Consortium, Type 2 Diabetes Genetic Exploration by Nex-generation sequencing in muylti-Ethnic Samples (T2D-GENES) Consortium. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat. Genet. 46 (2014), 234–244.
-
(2014)
Nat. Genet.
, vol.46
, pp. 234-244
-
-
Mahajan, A.1
Go, M.J.2
Zhang, W.3
Below, J.E.4
Gaulton, K.J.5
Ferreira, T.6
Horikoshi, M.7
Johnson, A.D.8
Ng, M.C.9
Prokopenko, I.10
-
88
-
-
77957113600
-
A large-scale, consortium-based genomewide association study of asthma
-
88 Moffatt, M.F., Gut, I.G., Demenais, F., Strachan, D.P., Bouzigon, E., Heath, S., von Mutius, E., Farrall, M., Lathrop, M., Cookson, W.O., GABRIEL Consortium. A large-scale, consortium-based genomewide association study of asthma. N. Engl. J. Med. 363 (2010), 1211–1221.
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 1211-1221
-
-
Moffatt, M.F.1
Gut, I.G.2
Demenais, F.3
Strachan, D.P.4
Bouzigon, E.5
Heath, S.6
von Mutius, E.7
Farrall, M.8
Lathrop, M.9
Cookson, W.O.10
-
89
-
-
80055080761
-
Identification, replication, and fine-mapping of loci associated with adult height in individuals of african ancestry
-
89 N'Diaye, A., Chen, G.K., Palmer, C.D., Ge, B., Tayo, B., Mathias, R.A., Ding, J., Nalls, M.A., Adeyemo, A., Adoue, V., et al. Identification, replication, and fine-mapping of loci associated with adult height in individuals of african ancestry. PLoS Genet., 7, 2011, e1002298.
-
(2011)
PLoS Genet.
, vol.7
, pp. e1002298
-
-
N'Diaye, A.1
Chen, G.K.2
Palmer, C.D.3
Ge, B.4
Tayo, B.5
Mathias, R.A.6
Ding, J.7
Nalls, M.A.8
Adeyemo, A.9
Adoue, V.10
-
90
-
-
8844232807
-
Human size evolution: no evolutionary allometric relationship between male and female stature
-
90 Gustafsson, A., Lindenfors, P., Human size evolution: no evolutionary allometric relationship between male and female stature. J. Hum. Evol. 47 (2004), 253–266.
-
(2004)
J. Hum. Evol.
, vol.47
, pp. 253-266
-
-
Gustafsson, A.1
Lindenfors, P.2
-
91
-
-
84887259083
-
Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010
-
91 Whiteford, H.A., Degenhardt, L., Rehm, J., Baxter, A.J., Ferrari, A.J., Erskine, H.E., Charlson, F.J., Norman, R.E., Flaxman, A.D., Johns, N., et al. Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. Lancet 382 (2013), 1575–1586.
-
(2013)
Lancet
, vol.382
, pp. 1575-1586
-
-
Whiteford, H.A.1
Degenhardt, L.2
Rehm, J.3
Baxter, A.J.4
Ferrari, A.J.5
Erskine, H.E.6
Charlson, F.J.7
Norman, R.E.8
Flaxman, A.D.9
Johns, N.10
-
92
-
-
84883778249
-
Additive genetic variation in schizophrenia risk is shared by populations of African and European descent
-
92 de Candia, T.R., Lee, S.H., Yang, J., Browning, B.L., Gejman, P.V., Levinson, D.F., Mowry, B.J., Hewitt, J.K., Goddard, M.E., O'Donovan, M.C., et al. International Schizophrenia Consortium, Molecular Genetics of Schizophrenia Collaboration. Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. Am. J. Hum. Genet. 93 (2013), 463–470.
-
(2013)
Am. J. Hum. Genet.
, vol.93
, pp. 463-470
-
-
de Candia, T.R.1
Lee, S.H.2
Yang, J.3
Browning, B.L.4
Gejman, P.V.5
Levinson, D.F.6
Mowry, B.J.7
Hewitt, J.K.8
Goddard, M.E.9
O'Donovan, M.C.10
-
93
-
-
84896780157
-
An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases
-
93 Chan, Y., Lim, E.T., Sandholm, N., Wang, S.R., McKnight, A.J., Ripke, S., Daly, M.J., Neale, B.M., Salem, R.M., Hirschhorn, J.N. DIAGRAM Consortium GENIE Consortium GIANT Consortium IIBDGC Consortium, PGC Consortium. An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases. Am. J. Hum. Genet. 94 (2014), 437–452.
-
(2014)
Am. J. Hum. Genet.
, vol.94
, pp. 437-452
-
-
Chan, Y.1
Lim, E.T.2
Sandholm, N.3
Wang, S.R.4
McKnight, A.J.5
Ripke, S.6
Daly, M.J.7
Neale, B.M.8
Salem, R.M.9
Hirschhorn, J.N.10
-
94
-
-
84955582450
-
Quantifying prion disease penetrance using large population control cohorts
-
94 Minikel, E.V., Vallabh, S.M., Lek, M., Estrada, K., Samocha, K.E., Sathirapongsasuti, J.F., McLean, C.Y., Tung, J.Y., Yu, L.P., Gambetti, P., et al., Exome Aggregation Consortium (ExAC). Quantifying prion disease penetrance using large population control cohorts. Sci. Transl. Med., 8, 2016, 322ra9.
-
(2016)
Sci. Transl. Med.
, vol.8
, pp. 322ra9
-
-
Minikel, E.V.1
Vallabh, S.M.2
Lek, M.3
Estrada, K.4
Samocha, K.E.5
Sathirapongsasuti, J.F.6
McLean, C.Y.7
Tung, J.Y.8
Yu, L.P.9
Gambetti, P.10
-
95
-
-
84920807370
-
Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations
-
95 Li, Y.R., Keating, B.J., Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations. Genome Med., 6, 2014, 91.
-
(2014)
Genome Med.
, vol.6
, pp. 91
-
-
Li, Y.R.1
Keating, B.J.2
-
96
-
-
77951133654
-
Genome-wide association studies in diverse populations
-
96 Rosenberg, N.A., Huang, L., Jewett, E.M., Szpiech, Z.A., Jankovic, I., Boehnke, M., Genome-wide association studies in diverse populations. Nat. Rev. Genet. 11 (2010), 356–366.
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 356-366
-
-
Rosenberg, N.A.1
Huang, L.2
Jewett, E.M.3
Szpiech, Z.A.4
Jankovic, I.5
Boehnke, M.6
|