-
1
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA. 2010. A map of human genome variation from population-scale sequencing. Nature 467:1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Abecasis, G.R.1
Altshuler, D.2
Auton, A.3
Brooks, L.D.4
Durbin, R.M.5
Gibbs, R.A.6
Hurles, M.E.7
McVean, G.A.8
-
2
-
-
77956331627
-
Integrating common and rare genetic variation in diverse human populations
-
Altshuler DM, Gibbs RA, Peltonen L, Dermitzakis E, Schaffner SF, Yu F, Bonnen PE, de Bakker PI, Deloukas P, Gabriel SB, Gwilliam R, Hunt S, Inouye M, Jia X, Palotie A, Parkin M, Whittaker P, Chang K, Hawes A, Lewis LR, Ren Y, Wheeler D, Muzny DM, Barnes C, Darvishi K, Hurles M, Korn JM, Kristiansson K, Lee C, McCarrol SA, Nemesh J, Keinan A, Montgomery SB, Pollack S, Price AL, Soranzo N, Gonzaga-Jauregui C, Anttila V, Brodeur W, Daly MJ, Leslie S, McVean G, Moutsianas L, Nguyen H, Zhang Q, Ghori MJ, McGinnis R, McLaren W, Takeuchi F, Grossman SR, Shlyakhter I, Hostetter EB, Sabeti PC, Adebamowo CA, Foster MW, Gordon DR, Licinio J, Manca MC, Marshall PA, Matsuda I, Ngare D, Wang VO, Reddy D, Rotimi CN, Royal CD, Sharp RR, Zeng C, Brooks LD, McEwen JE. 2010. Integrating common and rare genetic variation in diverse human populations. Nature 467:52-58.
-
(2010)
Nature
, vol.467
, pp. 52-58
-
-
Altshuler, D.M.1
Gibbs, R.A.2
Peltonen, L.3
Dermitzakis, E.4
Schaffner, S.F.5
Yu, F.6
Bonnen, P.E.7
de Bakker, P.I.8
Deloukas, P.9
Gabriel, S.B.10
Gwilliam, R.11
Hunt, S.12
Inouye, M.13
Jia, X.14
Palotie, A.15
Parkin, M.16
Whittaker, P.17
Chang, K.18
Hawes, A.19
Lewis, L.R.20
Ren, Y.21
Wheeler, D.22
Muzny, D.M.23
Barnes, C.24
Darvishi, K.25
Hurles, M.26
Korn, J.M.27
Kristiansson, K.28
Lee, C.29
McCarrol, S.A.30
Nemesh, J.31
Keinan, A.32
Montgomery, S.B.33
Pollack, S.34
Price, A.L.35
Soranzo, N.36
Gonzaga-Jauregui, C.37
Anttila, V.38
Brodeur, W.39
Daly, M.J.40
Leslie, S.41
McVean, G.42
Moutsianas, L.43
Nguyen, H.44
Zhang, Q.45
Ghori, M.J.46
McGinnis, R.47
McLaren, W.48
Takeuchi, F.49
Grossman, S.R.50
Shlyakhter, I.51
Hostetter, E.B.52
Sabeti, P.C.53
Adebamowo, C.A.54
Foster, M.W.55
Gordon, D.R.56
Licinio, J.57
Manca, M.C.58
Marshall, P.A.59
Matsuda, I.60
Ngare, D.61
Wang, V.O.62
Reddy, D.63
Rotimi, C.N.64
Royal, C.D.65
Sharp, R.R.66
Zeng, C.67
Brooks, L.D.68
McEwen, J.E.69
more..
-
3
-
-
84864656289
-
Communicating new knowledge on previously reported genetic variants
-
Aronson SJ, Clark EH, Varugheese M, Baxter S, Babb LJ, Rehm HL. 2012. Communicating new knowledge on previously reported genetic variants. Genet Med 14:713-719.
-
(2012)
Genet Med
, vol.14
, pp. 713-719
-
-
Aronson, S.J.1
Clark, E.H.2
Varugheese, M.3
Baxter, S.4
Babb, L.J.5
Rehm, H.L.6
-
4
-
-
79959276553
-
Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time
-
Berg JS, Khoury MJ, Evans JP. 2011. Deploying whole genome sequencing in clinical practice and public health: Meeting the challenge one bin at a time. Genet Med 13:499-504.
-
(2011)
Genet Med
, vol.13
, pp. 499-504
-
-
Berg, J.S.1
Khoury, M.J.2
Evans, J.P.3
-
5
-
-
77953304931
-
Warfarin genotyping reduces hospitalization rates results from the MM-WES (Medco-Mayo Warfarin Effectiveness study)
-
Epstein RS, Moyer TP, Aubert RE, Kane O, Xia DJ, Verbrugge F, Gage RR, Teagarden BF Jr. 2010. Warfarin genotyping reduces hospitalization rates results from the MM-WES (Medco-Mayo Warfarin Effectiveness study). J Am Coll Cardiol 55:2804-2812.
-
(2010)
J Am Coll Cardiol
, vol.55
, pp. 2804-2812
-
-
Epstein, R.S.1
Moyer, T.P.2
Aubert, R.E.3
Kane, O.4
Xia, D.J.5
Verbrugge, F.6
Gage, R.R.7
Teagarden Jr, B.F.8
-
7
-
-
69549083158
-
Evaluating the utility of personal genomic information
-
Foster MW, Mulvihill JJ, Sharp RR. 2009. Evaluating the utility of personal genomic information. Genet Med 11:570-574.
-
(2009)
Genet Med
, vol.11
, pp. 570-574
-
-
Foster, M.W.1
Mulvihill, J.J.2
Sharp, R.R.3
-
8
-
-
84859619831
-
Return of individual research results from genome-wide association studies: Experience of the Electronic Medical Records and Genomics (eMERGE) Network
-
Fullerton SM, Wolf WA, Brothers KB, Clayton EW, Crawford DC, Denny JC, Greenland P, Koenig BA, Leppig KA, Lindor NM, McCarty CA, McGuire AL, McPeek Hinz ER, Mirel DB, Ramos EM, Ritchie MD, Smith ME, Waudby CJ, Burke W, Jarvik GP. 2012. Return of individual research results from genome-wide association studies: Experience of the Electronic Medical Records and Genomics (eMERGE) Network. Genet Med 14:424-431.
-
(2012)
Genet Med
, vol.14
, pp. 424-431
-
-
Fullerton, S.M.1
Wolf, W.A.2
Brothers, K.B.3
Clayton, E.W.4
Crawford, D.C.5
Denny, J.C.6
Greenland, P.7
Koenig, B.A.8
Leppig, K.A.9
Lindor, N.M.10
McCarty, C.A.11
McGuire, A.L.12
McPeek Hinz, E.R.13
Mirel, D.B.14
Ramos, E.M.15
Ritchie, M.D.16
Smith, M.E.17
Waudby, C.J.18
Burke, W.19
Jarvik, G.P.20
more..
-
9
-
-
80855148238
-
Motivations and perceptions of early adopters of personalized genomics: Perspectives from research participants
-
Gollust SE, Gordon ES, Zayac C, Griffin G, Christman MF, Pyeritz RE, Wawak L, Bernhardt BA. 2012. Motivations and perceptions of early adopters of personalized genomics: Perspectives from research participants. Public Health Genomics 15:22-30.
-
(2012)
Public Health Genomics
, vol.15
, pp. 22-30
-
-
Gollust, S.E.1
Gordon, E.S.2
Zayac, C.3
Griffin, G.4
Christman, M.F.5
Pyeritz, R.E.6
Wawak, L.7
Bernhardt, B.A.8
-
10
-
-
84880059657
-
The Electronic Medical Records and Genomics (eMERGE) Network: Past, present and future
-
Gottesman O, Kuivaniemi H, Tromp G, Faucett WA, Li R, Manolio TA, Sanderson SC, Kannry J, Zinberg R, Basford MA, Brilliant M, Carey DJ, Chisolm RL, Chute CG, Connolly JJ, Crosslin D, Denny JC, Gallego CJ, Haines JL, Hakonarson H, Harley J, Jarvik GP, Kohane I, Kullo IJ, Larson EB, McCarty C, Ritchie MD, Roden D, Smith ME, Bottinger EP, Williams MS. 2013. The Electronic Medical Records and Genomics (eMERGE) Network: Past, present and future. Genet Med 15:761-771.
-
(2013)
Genet Med
, vol.15
, pp. 761-771
-
-
Gottesman, O.1
Kuivaniemi, H.2
Tromp, G.3
Faucett, W.A.4
Li, R.5
Manolio, T.A.6
Sanderson, S.C.7
Kannry, J.8
Zinberg, R.9
Basford, M.A.10
Brilliant, M.11
Carey, D.J.12
Chisolm, R.L.13
Chute, C.G.14
Connolly, J.J.15
Crosslin, D.16
Denny, J.C.17
Gallego, C.J.18
Haines, J.L.19
Hakonarson, H.20
Harley, J.21
Jarvik, G.P.22
Kohane, I.23
Kullo, I.J.24
Larson, E.B.25
McCarty, C.26
Ritchie, M.D.27
Roden, D.28
Smith, M.E.29
Bottinger, E.P.30
Williams, M.S.31
more..
-
11
-
-
79951472909
-
Charting a course for genomic medicine from base pairs to bedside
-
Green ED, Guyer MS. 2011. Charting a course for genomic medicine from base pairs to bedside. Nature 470:204-213.
-
(2011)
Nature
, vol.470
, pp. 204-213
-
-
Green, E.D.1
Guyer, M.S.2
-
12
-
-
84859577332
-
Exploring concordance and discordance for return of incidental findings from clinical sequencing
-
Green RC, Berg JS, Berry GT, Biesecker LG, Dimmock DP, Evans JP, Grody WW, Hegde MR, Kalia S, Korf BR, Krantz I, McGuire AL, Miller DT, Murray MF, Nussbaum RL, Plon SE, Rehm HL, Jacob HJ. 2012. Exploring concordance and discordance for return of incidental findings from clinical sequencing. Genet Med 14:405-410.
-
(2012)
Genet Med
, vol.14
, pp. 405-410
-
-
Green, R.C.1
Berg, J.S.2
Berry, G.T.3
Biesecker, L.G.4
Dimmock, D.P.5
Evans, J.P.6
Grody, W.W.7
Hegde, M.R.8
Kalia, S.9
Korf, B.R.10
Krantz, I.11
McGuire, A.L.12
Miller, D.T.13
Murray, M.F.14
Nussbaum, R.L.15
Plon, S.E.16
Rehm, H.L.17
Jacob, H.J.18
-
13
-
-
79952052294
-
Evaluation of the validity and utility of genetic testing for rare diseases
-
Grosse SD, Kalman L, Khoury MJ. 2010. Evaluation of the validity and utility of genetic testing for rare diseases. Adv Exp Med Biol 686:115-131.
-
(2010)
Adv Exp Med Biol
, vol.686
, pp. 115-131
-
-
Grosse, S.D.1
Kalman, L.2
Khoury, M.J.3
-
14
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff LA, Sethupathy P, Junkins HA, Ramos EM, Mehta JP, Collins FS, Manolio TA. 2009. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 106:9362-9367.
-
(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
-
16
-
-
84857267425
-
Beyond base pairs to bedside: A population perspective on how genomics can improve health
-
Khoury MJ, Gwinn M, Bowen MS, Dotson WD. 2012. Beyond base pairs to bedside: A population perspective on how genomics can improve health. Am J Public Health 102:34-37.
-
(2012)
Am J Public Health
, vol.102
, pp. 34-37
-
-
Khoury, M.J.1
Gwinn, M.2
Bowen, M.S.3
Dotson, W.D.4
-
17
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio TA, Collins FS, Cox NJ, Goldstein DB, Hindorff LA, Hunter DJ, McCarthy MI, Ramos EM, Cardon LR, Chakravarti A, Cho JH, Guttmacher AE, Kong A, Kruglyak L, Mardis E, Rotimi CN, Slatkin M, Valle D, Whittemore AS, Boehnke M, Clark AG, Eichler EE, Gibson G, Haines JL, Mackay TF, McCarroll SA, Visscher PM. 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
Cho, J.H.11
Guttmacher, A.E.12
Kong, A.13
Kruglyak, L.14
Mardis, E.15
Rotimi, C.N.16
Slatkin, M.17
Valle, D.18
Whittemore, A.S.19
Boehnke, M.20
Clark, A.G.21
Eichler, E.E.22
Gibson, G.23
Haines, J.L.24
Mackay, T.F.25
McCarroll, S.A.26
Visscher, P.M.27
more..
-
18
-
-
84875939245
-
Implementing genomic medicine in the clinic: The future is here
-
Manolio TA, Chisholm RL, Ozenberger B, Roden DM, Williams MS, Wilson R, Bick D, Bottinger EP, Brilliant MH, Eng C, Frazer KA, Korf B, Ledbetter DH, Lupski JR, Marsh C, Mrazek D, Murray MF, O'Donnell PH, Rader DJ, Relling MV, Shuldiner AR, Valle D, Weinshilboum R, Green ED, Ginsburg GS. 2013. Implementing genomic medicine in the clinic: The future is here. Genet Med 15:258-267.
-
(2013)
Genet Med
, vol.15
, pp. 258-267
-
-
Manolio, T.A.1
Chisholm, R.L.2
Ozenberger, B.3
Roden, D.M.4
Williams, M.S.5
Wilson, R.6
Bick, D.7
Bottinger, E.P.8
Brilliant, M.H.9
Eng, C.10
Frazer, K.A.11
Korf, B.12
Ledbetter, D.H.13
Lupski, J.R.14
Marsh, C.15
Mrazek, D.16
Murray, M.F.17
O'Donnell, P.H.18
Rader, D.J.19
Relling, M.V.20
Shuldiner, A.R.21
Valle, D.22
Weinshilboum, R.23
Green, E.D.24
Ginsburg, G.S.25
more..
-
19
-
-
84855853297
-
Molecular genetic studies of complex phenotypes
-
Marian AJ. 2012. Molecular genetic studies of complex phenotypes. Transl Res 159:64-79.
-
(2012)
Transl Res
, vol.159
, pp. 64-79
-
-
Marian, A.J.1
-
20
-
-
84861868693
-
Technical desiderata for the integration of genomic data into Electronic Health Records
-
Masys DR, Jarvik GP, Abernethy NF, Anderson NR, Papanicolaou GJ, Paltoo DN, Hoffman MA, Kohane IS, Levy HP. 2012. Technical desiderata for the integration of genomic data into Electronic Health Records. J Biomed Inform 45:419-422.
-
(2012)
J Biomed Inform
, vol.45
, pp. 419-422
-
-
Masys, D.R.1
Jarvik, G.P.2
Abernethy, N.F.3
Anderson, N.R.4
Papanicolaou, G.J.5
Paltoo, D.N.6
Hoffman, M.A.7
Kohane, I.S.8
Levy, H.P.9
-
21
-
-
84875485693
-
Cancer pharmacogenomics: Early promise, but concerted effort needed
-
McLeod HL. 2013. Cancer pharmacogenomics: Early promise, but concerted effort needed. Science 339:1563-1566.
-
(2013)
Science
, vol.339
, pp. 1563-1566
-
-
McLeod, H.L.1
-
22
-
-
67650766641
-
The A's, G's, C's, and T's of health disparities
-
Ramos E, Rotimi C. 2009. The A's, G's, C's, and T's of health disparities. BMC Med Genomics 2:29.
-
(2009)
BMC Med Genomics
, vol.2
, pp. 29
-
-
Ramos, E.1
Rotimi, C.2
-
23
-
-
79951809825
-
CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network
-
Relling MV, Klein TE. 2011. CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network. Clin Pharmacol Ther 89:464-467.
-
(2011)
Clin Pharmacol Ther
, vol.89
, pp. 464-467
-
-
Relling, M.V.1
Klein, T.E.2
-
24
-
-
80053563231
-
Using Alzheimer's disease as a model for genetic risk disclosure: Implications for personal genomics
-
Roberts JS, Christensen KD, Green RC. 2011. Using Alzheimer's disease as a model for genetic risk disclosure: Implications for personal genomics. Clin Genet 80:407-414.
-
(2011)
Clin Genet
, vol.80
, pp. 407-414
-
-
Roberts, J.S.1
Christensen, K.D.2
Green, R.C.3
-
25
-
-
60349121445
-
Results of a survey of an online physician community regarding use of electronic medical records in office practices
-
Ross S. 2009. Results of a survey of an online physician community regarding use of electronic medical records in office practices. J Med Pract Manage 24:254-256.
-
(2009)
J Med Pract Manage
, vol.24
, pp. 254-256
-
-
Ross, S.1
-
26
-
-
79951581464
-
Genetic risk estimation in the Coriell Personalized Medicine Collaborative
-
Stack CB, Gharani N, Gordon ES, Schmidlen T, Christman MF, Keller MA. 2011. Genetic risk estimation in the Coriell Personalized Medicine Collaborative. Genet Med 13:131-139.
-
(2011)
Genet Med
, vol.13
, pp. 131-139
-
-
Stack, C.B.1
Gharani, N.2
Gordon, E.S.3
Schmidlen, T.4
Christman, M.F.5
Keller, M.A.6
-
27
-
-
84875540793
-
Crossing the omic chasm: A time for omic ancillary systems
-
Starren J, Williams MS, Bottinger EP. 2013. Crossing the omic chasm: A time for omic ancillary systems. JAMA 309:1237-1238.
-
(2013)
JAMA
, vol.309
, pp. 1237-1238
-
-
Starren, J.1
Williams, M.S.2
Bottinger, E.P.3
-
28
-
-
59849108152
-
The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: Methods of the EGAPP Working Group
-
Teutsch SM, Bradley LA, Palomaki GE, Haddow JE, Piper M, Calonge N, Dotson WD, Douglas MP, Berg AO. 2009. The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: Methods of the EGAPP Working Group. Genet Med 11:3-14.
-
(2009)
Genet Med
, vol.11
, pp. 3-14
-
-
Teutsch, S.M.1
Bradley, L.A.2
Palomaki, G.E.3
Haddow, J.E.4
Piper, M.5
Calonge, N.6
Dotson, W.D.7
Douglas, M.P.8
Berg, A.O.9
-
29
-
-
79959524146
-
A haplotype map of the human genome
-
The International HapMap Consortium
-
The International HapMap Consortium. 2005. A haplotype map of the human genome. Nature 437:1299-1320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
|