-
1
-
-
84865429505
-
A personal view on systems medicine and the emergence of proactive P4 medicine: Predictive, preventive, personalized and participatory
-
Hood, L. & Flores, M. A personal view on systems medicine and the emergence of proactive P4 medicine: predictive, preventive, personalized and participatory. New Biotechnol. 29, 613-624 (2012).
-
(2012)
New Biotechnol.
, vol.29
, pp. 613-624
-
-
Hood, L.1
Flores, M.2
-
3
-
-
33947712686
-
Stratified medicine: Strategic and economic implications of combining drugs and clinical biomarkers
-
Trusheim, M.R., Berndt, E.R. & Douglas, F.L. Stratified medicine: strategic and economic implications of combining drugs and clinical biomarkers. Nat. Rev. Drug Discov. 6, 287-293 (2007).
-
(2007)
Nat. Rev. Drug Discov.
, vol.6
, pp. 287-293
-
-
Trusheim, M.R.1
Berndt, E.R.2
Douglas, F.L.3
-
4
-
-
84893785215
-
Therapeutic drug monitoring as a component of personalized medicine: Applications in pediatric drug development
-
Momper, J.D. & Wagner, J.A. Therapeutic Drug Monitoring as a Component of Personalized Medicine: Applications in Pediatric Drug Development. Clin. Pharmacol. Ther. 95, 138-140 (2014).
-
(2014)
Clin. Pharmacol. Ther.
, vol.95
, pp. 138-140
-
-
Momper, J.D.1
Wagner, J.A.2
-
5
-
-
84867027478
-
The determination and interpretation of the therapeutic index in drug development
-
Muller, P.Y. & Milton, M.N. The determination and interpretation of the therapeutic index in drug development. Nat. Rev. Drug Discov. 11, 751-761 (2012).
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 751-761
-
-
Muller, P.Y.1
Milton, M.N.2
-
6
-
-
58149186582
-
Do molecularly targeted agents in oncology have reduced attrition rates?
-
Walker, I. & Newell, H. Do molecularly targeted agents in oncology have reduced attrition rates? Nat. Rev. Drug Discov. 8, 15-16 (2009).
-
(2009)
Nat. Rev. Drug Discov.
, vol.8
, pp. 15-16
-
-
Walker, I.1
Newell, H.2
-
7
-
-
80455162465
-
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation
-
Ramsey, B.W. et al. A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. N. Engl. J. Med. 365, 1663-1672 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 1663-1672
-
-
Ramsey, B.W.1
-
8
-
-
84892485096
-
Precision medicine: An approach to R&D for delivering superior medicines to patients
-
Dolsten, M. & Sogaard, M. Precision medicine: an approach to R&D for delivering superior medicines to patients. Clin. Transl. Med. 1, 7 (2012).
-
(2012)
Clin. Transl. Med.
, vol.1
, pp. 7
-
-
Dolsten, M.1
Sogaard, M.2
-
9
-
-
84857743319
-
Diagnosing the decline in pharmaceutical R&D efficiency
-
Scannell, J.W., Blanckley, A., Boldon, H. & Warrington, B. Diagnosing the decline in pharmaceutical R&D efficiency. Nat. Rev. Drug Discov. 11, 191-200 (2012).
-
(2012)
Nat. Rev. Drug Discov.
, vol.11
, pp. 191-200
-
-
Scannell, J.W.1
Blanckley, A.2
Boldon, H.3
Warrington, B.4
-
10
-
-
84872011999
-
Evidence-based laboratory medicine in oncology drug development: From biomarkers to diagnostics
-
Modur, V., Hailman, E. & Barrett, J.C. Evidence-based laboratory medicine in oncology drug development: from biomarkers to diagnostics. Clin. Chem. 59, 102-109 (2013).
-
(2013)
Clin. Chem.
, vol.59
, pp. 102-109
-
-
Modur, V.1
Hailman, E.2
Barrett, J.C.3
-
11
-
-
84862286182
-
Inhibitors of the anaplastic lymphoma kinase
-
Mologni, L. Inhibitors of the anaplastic lymphoma kinase. Expert Opin. Investig. Drugs 21, 985-994 (2012).
-
(2012)
Expert Opin. Investig. Drugs
, vol.21
, pp. 985-994
-
-
Mologni, L.1
-
12
-
-
80155151884
-
Vemurafenib
-
Flaherty, K.T., Yasothan, U. & Kirkpatrick, P. Vemurafenib. Nat. Rev. Drug Discov. 10, 811-812 (2011).
-
(2011)
Nat. Rev. Drug Discov.
, vol.10
, pp. 811-812
-
-
Flaherty, K.T.1
Yasothan, U.2
Kirkpatrick, P.3
-
13
-
-
69949126786
-
Personalized medicine and inhibition of EGFR signaling in lung cancer
-
Gazdar, A.F. Personalized medicine and inhibition of EGFR signaling in lung cancer. N. Engl. J. Med. 361, 1018-1020 (2009).
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 1018-1020
-
-
Gazdar, A.F.1
-
14
-
-
84866595897
-
The 1200 Patients Project: Creating a new medical model system for clinical implementation of pharmacogenomics
-
O'Donnell, P.H. et al. The 1200 Patients Project: creating a new medical model system for clinical implementation of pharmacogenomics. Clin. Pharmacol. Ther. 92, 446-449 (2012).
-
(2012)
Clin. Pharmacol. Ther.
, vol.92
, pp. 446-449
-
-
O'Donnell, P.H.1
-
15
-
-
84862620703
-
Operational implementation of prospective genotyping for personalized medicine: The design of the Vanderbilt PREDICT Project
-
Pulley, J.M. et al. Operational implementation of prospective genotyping for personalized medicine: the design of the Vanderbilt PREDICT Project. Clin. Pharmacol. Ther. 92, 87-95 (2012).
-
(2012)
Clin. Pharmacol. Ther.
, vol.92
, pp. 87-95
-
-
Pulley, J.M.1
-
16
-
-
84892728434
-
Sequencing depth and coverage: Key considerations in genomic analyses
-
Sims, D., Sudbery, I., Ilott, N.E., Heger, A. & Ponting, C.P. Sequencing depth and coverage: key considerations in genomic analyses. Nat. Rev. Genet. 15, 121-132 (2014).
-
(2014)
Nat. Rev. Genet.
, vol.15
, pp. 121-132
-
-
Sims, D.1
Sudbery, I.2
Ilott, N.E.3
Heger, A.4
Ponting, C.P.5
-
17
-
-
84884994218
-
The cancer genome atlas pan-cancer analysis project
-
The Cancer Genome Atlas Research Network. The Cancer Genome Atlas Pan-Cancer analysis project. Nat. Genet. 45, 1113-1120 (2013).
-
(2013)
Nat. Genet.
, vol.45
, pp. 1113-1120
-
-
The Cancer Genome Atlas Research Network1
-
18
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
The 1000 Genomes Project Consortium. An integrated map of genetic variation from 1,092 human genomes. Nature 491, 56-65 (2012).
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
The 1000 Genomes Project Consortium1
-
19
-
-
84886548344
-
100k Genome Project: Sequencing and much more
-
Haga, S.B. 100k Genome Project: sequencing and much more. Personal. Med. 10, 761-764 (2013).
-
(2013)
Personal. Med.
, vol.10
, pp. 761-764
-
-
Haga, S.B.1
-
20
-
-
84904804929
-
Biological insights from 108 schizophrenia-associated genetic loci
-
Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511, 421-427 (2014).
-
(2014)
Nature
, vol.511
, pp. 421-427
-
-
-
21
-
-
84863116742
-
A systematic survey of loss-of-function variants in human protein-coding genes
-
MacArthur, D.G. et al. A systematic survey of loss-of-function variants in human protein-coding genes. Science 335, 823-828 (2012).
-
(2012)
Science
, vol.335
, pp. 823-828
-
-
MacArthur, D.G.1
-
22
-
-
69249147045
-
Expression profiling of microRNAs by deep sequencing
-
Creighton, C.J., Reid, J.G. & Gunaratne, P.H. Expression profiling of microRNAs by deep sequencing. Brief. Bioinform. 10, 490-497 (2009).
-
(2009)
Brief. Bioinform.
, vol.10
, pp. 490-497
-
-
Creighton, C.J.1
Reid, J.G.2
Gunaratne, P.H.3
-
23
-
-
84902148239
-
Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine
-
Van Allen, E.M. et al. Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. Nat. Med. 20, 682-688 (2014).
-
(2014)
Nat. Med.
, vol.20
, pp. 682-688
-
-
Van Allen, E.M.1
-
24
-
-
79955038968
-
Use of whole-genome sequencing to diagnose a cryptic fusion oncogene
-
Welch, J.S. et al. Use of whole-genome sequencing to diagnose a cryptic fusion oncogene. JAMA 305, 1577-1584 (2011).
-
(2011)
JAMA
, vol.305
, pp. 1577-1584
-
-
Welch, J.S.1
-
25
-
-
79251645624
-
Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease
-
Worthey, E.A. et al. Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease. Genet. Med. 13, 255-262 (2011).
-
(2011)
Genet. Med.
, vol.13
, pp. 255-262
-
-
Worthey, E.A.1
-
26
-
-
79959316645
-
Whole-genome sequencing for optimized patient management
-
Bainbridge, M.N. et al. Whole-genome sequencing for optimized patient management. Sci. Transl. Med. 3, 87re3 (2011).
-
(2011)
Sci. Transl. Med.
, vol.3
, pp. 87re3
-
-
Bainbridge, M.N.1
-
27
-
-
73149123343
-
Genetic diagnosis by whole exome capture and massively parallel DNA sequencing
-
Choi, M. et al. Genetic diagnosis by whole exome capture and massively parallel DNA sequencing. Proc. Natl. Acad. Sci. U. S. A. 106, 19096-19101 (2009).
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 19096-19101
-
-
Choi, M.1
-
28
-
-
84908671756
-
Translation of genomics-guided RNA-based personalised cancer vaccines: Towards the bedside
-
Boisguerin, V. et al. Translation of genomics-guided RNA-based personalised cancer vaccines: towards the bedside. Br. J. Cancer 111, 1469-1475 (2014).
-
(2014)
Br. J. Cancer
, vol.111
, pp. 1469-1475
-
-
Boisguerin, V.1
-
29
-
-
84902602767
-
Actionable diagnosis of neuroleptospirosis by next-generation sequencing
-
Wilson, M.R. et al. Actionable diagnosis of neuroleptospirosis by next-generation sequencing. N. Engl. J. Med. 370, 2408-2417 (2014).
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 2408-2417
-
-
Wilson, M.R.1
-
30
-
-
84867214350
-
Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units
-
Saunders, C.J. et al. Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. Sci. Transl. Med. 4, 154ra135 (2012).
-
(2012)
Sci. Transl. Med.
, vol.4
, pp. 154ra135
-
-
Saunders, C.J.1
-
31
-
-
70350448214
-
Early treatment with alglucosidase alfa prolongs long-term survival of infants with Pompe disease
-
Kishnani, P.S. et al. Early treatment with alglucosidase alfa prolongs long-term survival of infants with Pompe disease. Pediatr. Res. 66, 329-335 (2009).
-
(2009)
Pediatr. Res.
, vol.66
, pp. 329-335
-
-
Kishnani, P.S.1
-
32
-
-
84866412139
-
Whole genomes, small children, big questions
-
Lunshof, J.E. Whole genomes, small children, big questions. Personal. Med. 9, 667-669 (2012).
-
(2012)
Personal. Med.
, vol.9
, pp. 667-669
-
-
Lunshof, J.E.1
-
33
-
-
84896769549
-
Clinical interpretation and implications of wholegenome sequencing
-
Dewey, F.E. et al. Clinical interpretation and implications of wholegenome sequencing. JAMA 311, 1035-1045 (2014).
-
(2014)
JAMA
, vol.311
, pp. 1035-1045
-
-
Dewey, F.E.1
-
34
-
-
84924725169
-
Obstacles and opportunities for the future of genomic medicine
-
Solomon, B.D. Obstacles and opportunities for the future of genomic medicine. Mol. Genet. Genomic Med. 2, 205-209 (2014).
-
(2014)
Mol. Genet. Genomic Med.
, vol.2
, pp. 205-209
-
-
Solomon, B.D.1
-
35
-
-
84899618905
-
Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: Implications for individual genome sequencing
-
Bodian, D.L. et al. Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. PLoS ONE 9, e94554 (2014).
-
(2014)
PLoS ONE
, vol.9
-
-
Bodian, D.L.1
-
36
-
-
33750211858
-
A gene-centric approach to genome-wide association studies
-
Jorgenson, E. & Witte, J.S. A gene-centric approach to genome-wide association studies. Nat. Rev. Genet. 7, 885-891 (2006).
-
(2006)
Nat. Rev. Genet.
, vol.7
, pp. 885-891
-
-
Jorgenson, E.1
Witte, J.S.2
-
37
-
-
3042561451
-
Evaluation of five different cDNA labeling methods for microarrays using spike controls
-
Badiee, A., Eiken, H., Steen, V. & Lovlie, R. Evaluation of five different cDNA labeling methods for microarrays using spike controls. BMC Biotechnol. 3, 23 (2003).
-
(2003)
BMC Biotechnol.
, vol.3
, pp. 23
-
-
Badiee, A.1
Eiken, H.2
Steen, V.3
Lovlie, R.4
-
38
-
-
84855566198
-
Performance comparison of whole-genome sequencing platforms
-
Lam, H.Y.K. et al. Performance comparison of whole-genome sequencing platforms. Nat. Biotech. 30, 78-82 (2012).
-
(2012)
Nat. Biotech.
, vol.30
, pp. 78-82
-
-
Lam, H.Y.K.1
-
39
-
-
84897387657
-
Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls
-
Zook, J.M. et al. Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls. Nat. Biotech. 32, 246-251 (2014).
-
(2014)
Nat. Biotech.
, vol.32
, pp. 246-251
-
-
Zook, J.M.1
-
40
-
-
84883897500
-
ACMG clinical laboratory standards for nextgeneration sequencing
-
Rehm, H.L. et al. ACMG clinical laboratory standards for nextgeneration sequencing. Genet. Med. 15, 733-747 (2013).
-
(2013)
Genet. Med.
, vol.15
, pp. 733-747
-
-
Rehm, H.L.1
-
41
-
-
84876783779
-
Next generation sequencing in clinical medicine: Challenges and lessons for pathology and biomedical informatics
-
Gullapalli, R.R., Desai, K.V., Santana-Santos, L., Kant, J.A. & Becich, M.J. Next generation sequencing in clinical medicine: challenges and lessons for pathology and biomedical informatics. J. Pathol. Inform. 3, 40 (2012).
-
(2012)
J. Pathol. Inform.
, vol.3
, pp. 40
-
-
Gullapalli, R.R.1
Desai, K.V.2
Santana-Santos, L.3
Kant, J.A.4
Becich, M.J.5
-
42
-
-
77952886150
-
Assembly algorithms for nextgeneration sequencing data
-
Miller, J.R., Koren, S. & Sutton, G. Assembly algorithms for nextgeneration sequencing data. Genomics 95, 315-327 (2010).
-
(2010)
Genomics
, vol.95
, pp. 315-327
-
-
Miller, J.R.1
Koren, S.2
Sutton, G.3
-
43
-
-
84907067643
-
Expanding the computational toolbox for mining cancer genomes
-
Ding, L., Wendl, M.C., McMichael, J.F. & Raphael, B.J. Expanding the computational toolbox for mining cancer genomes. Nat. Rev. Genet. 15, 556-570 (2014).
-
(2014)
Nat. Rev. Genet.
, vol.15
, pp. 556-570
-
-
Ding, L.1
Wendl, M.C.2
McMichael, J.F.3
Raphael, B.J.4
-
44
-
-
84875312984
-
Low concordance of multiple variant-calling pipelines: Practical implications for exome and genome sequencing
-
O'Rawe, J. et al. Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing. Genome Med. 5, 1-18 (2013).
-
(2013)
Genome Med.
, vol.5
, pp. 1-18
-
-
O'Rawe, J.1
-
45
-
-
84927912895
-
Diagnosis of an imprinted-gene syndrome by a novel bioinformatics analysis of whole-genome sequences from a family trio
-
Bodian, D.L. et al. Diagnosis of an imprinted-gene syndrome by a novel bioinformatics analysis of whole-genome sequences from a family trio. Mol. Genet. Genomic Med. 2, 530-538 (2014).
-
(2014)
Mol. Genet. Genomic Med.
, vol.2
, pp. 530-538
-
-
Bodian, D.L.1
-
46
-
-
84902578876
-
Diagnostic clinical genome and exome sequencing
-
Biesecker, L.G. & Green, R.C. Diagnostic clinical genome and exome sequencing. N. Engl. J. Med. 370, 2418-2425 (2014).
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 2418-2425
-
-
Biesecker, L.G.1
Green, R.C.2
-
47
-
-
84863825848
-
Limitations of the Human Reference Genome for personalized genomics
-
Rosenfeld, J.A., Mason, C.E. & Smith, T.M. Limitations of the Human Reference Genome for personalized genomics. PLoS ONE 7, e40294 (2012).
-
(2012)
PLoS ONE
, vol.7
-
-
Rosenfeld, J.A.1
Mason, C.E.2
Smith, T.M.3
-
48
-
-
84930526399
-
ClinGen - The clinical genome resource
-
Rehm, H.L. et al. ClinGen - the clinical genome resource. N. Engl. J. Med. 372, 2235-2242 (2015).
-
(2015)
N. Engl. J. Med.
, vol.372
, pp. 2235-2242
-
-
Rehm, H.L.1
-
49
-
-
84930532210
-
The FDA and genomic tests - Getting regulation right
-
Evans, B.J., Burke, W. & Jarvik, G.P. The FDA and genomic tests - getting regulation right. N. Engl. J. Med. 372, 2258-2264 (2015).
-
(2015)
N. Engl. J. Med.
, vol.372
, pp. 2258-2264
-
-
Evans, B.J.1
Burke, W.2
Jarvik, G.P.3
-
50
-
-
84856529558
-
Making personalized cancer medicine a reality: Challenges and opportunities in the development of biomarkers and companion diagnostics
-
Parkinson, D.R., Johnson, B.E. & Sledge, G.W. Making personalized cancer medicine a reality: challenges and opportunities in the development of biomarkers and companion diagnostics. Clin. Cancer Res. 18, 619-624 (2012).
-
(2012)
Clin. Cancer Res.
, vol.18
, pp. 619-624
-
-
Parkinson, D.R.1
Johnson, B.E.2
Sledge, G.W.3
-
52
-
-
84896512336
-
Cancer drug development and the evolving regulatory framework for companion diagnostics in the European Union
-
Pignatti, F. et al. Cancer drug development and the evolving regulatory framework for companion diagnostics in the European Union. Clin. Cancer Res. 20, 1458-1468 (2014).
-
(2014)
Clin. Cancer Res.
, vol.20
, pp. 1458-1468
-
-
Pignatti, F.1
-
53
-
-
84897869777
-
European Medicines Agency initiatives and perspectives on pharmacogenomics
-
Ehmann, F., Caneva, L. & Papaluca, M. European Medicines Agency initiatives and perspectives on pharmacogenomics. Br. J. Clin. Pharmacol. 77, 612-617 (2014).
-
(2014)
Br. J. Clin. Pharmacol.
, vol.77
, pp. 612-617
-
-
Ehmann, F.1
Caneva, L.2
Papaluca, M.3
-
56
-
-
44949211505
-
Managing incidental findings in human subjects research: Analysis and recommendations
-
Wolf, S.M. et al. Managing incidental findings in human subjects research: analysis and recommendations. J. Law Med. Ethics 36, 219-248 (2008).
-
(2008)
J. Law Med. Ethics
, vol.36
, pp. 219-248
-
-
Wolf, S.M.1
-
57
-
-
84885785987
-
Clinical whole-exome sequencing for the diagnosis of Mendelian disorders
-
Yang, Y. et al. Clinical whole-exome sequencing for the diagnosis of Mendelian disorders. N. Engl. J. Med. 369, 1502-1511 (2013).
-
(2013)
N. Engl. J. Med.
, vol.369
, pp. 1502-1511
-
-
Yang, Y.1
-
58
-
-
84887439425
-
Recommendations for returning genomic incidental findings? We need to talk!
-
Burke, W. et al. Recommendations for returning genomic incidental findings? We need to talk! Genet. Med. 15, 854-859 (2013).
-
(2013)
Genet. Med.
, vol.15
, pp. 854-859
-
-
Burke, W.1
-
59
-
-
33750388916
-
The emergence of an ethical duty to disclose genetic research results: International perspectives
-
Knoppers, B.M., Joly, Y., Simard, J. & Durocher, F. The emergence of an ethical duty to disclose genetic research results: international perspectives. Eur. J. Hum. Genet. 14, 1170-1178 (2006).
-
(2006)
Eur. J. Hum. Genet.
, vol.14
, pp. 1170-1178
-
-
Knoppers, B.M.1
Joly, Y.2
Simard, J.3
Durocher, F.4
-
60
-
-
84880535720
-
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
-
Green, R.C. et al. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet. Med. 15, 565-574 (2013).
-
(2013)
Genet. Med.
, vol.15
, pp. 565-574
-
-
Green, R.C.1
-
61
-
-
84939963789
-
Public awareness of genetic nondiscrimination laws in four states and perceived importance of life insurance protections
-
Parkman, A. et al. Public awareness of genetic nondiscrimination laws in four states and perceived importance of life insurance protections. J. Genet. Counsel. 1-10 (2014).
-
(2014)
J. Genet. Counsel.
, pp. 1-10
-
-
Parkman, A.1
-
65
-
-
84902553652
-
Cloud-based bioinformatics workflow platform for largescale next-generation sequencing analyses
-
Liu, B. et al. Cloud-based bioinformatics workflow platform for largescale next-generation sequencing analyses. J. Biomed. Inform. 49, 119-133 (2014).
-
(2014)
J. Biomed. Inform.
, vol.49
, pp. 119-133
-
-
Liu, B.1
-
66
-
-
84883426914
-
Analysis of the security and privacy requirements of cloud-based electronic health records systems
-
Rodrigues, J.J., de la Torre, I., Fernández, G. & López-Coronado, M. Analysis of the security and privacy requirements of cloud-based electronic health records systems. J. Med. Internet Res. 15, e186 (2013).
-
(2013)
J. Med. Internet Res.
, vol.15
, pp. e186
-
-
Rodrigues, J.J.1
De La Torre, I.2
Fernández, G.3
López-Coronado, M.4
-
67
-
-
84862726370
-
Economic challenges and possible policy actions to advance stratified medicine
-
Trusheim, M.R. & Berndt, E.R. Economic challenges and possible policy actions to advance stratified medicine. Person. Med. 9, 413-427 (2012).
-
(2012)
Person. Med.
, vol.9
, pp. 413-427
-
-
Trusheim, M.R.1
Berndt, E.R.2
-
68
-
-
84899585223
-
Whole genome sequencing as a diagnostic test: Challenges and opportunities
-
Chrystoja, C.C. & Diamandis, E.P. Whole genome sequencing as a diagnostic test: challenges and opportunities. Clin. Chem. 60, 724-733 (2014).
-
(2014)
Clin. Chem.
, vol.60
, pp. 724-733
-
-
Chrystoja, C.C.1
Diamandis, E.P.2
-
69
-
-
80155150460
-
Quantifying factors for the success of stratified medicine
-
Trusheim, M.R. et al. Quantifying factors for the success of stratified medicine. Nat. Rev. Drug Discov. 10, 817-833 (2011).
-
(2011)
Nat. Rev. Drug Discov.
, vol.10
, pp. 817-833
-
-
Trusheim, M.R.1
-
70
-
-
84898405421
-
The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders
-
Shashi, V. et al. The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders. Genet. Med. 16, 176-182 (2014).
-
(2014)
Genet. Med.
, vol.16
, pp. 176-182
-
-
Shashi, V.1
-
71
-
-
84860570409
-
Next-generation sequencing: Ready for the clinics?
-
Desai, A.N. & Jere, A. Next-generation sequencing: ready for the clinics? Clin. Genet. 81, 503-510 (2012).
-
(2012)
Clin. Genet.
, vol.81
, pp. 503-510
-
-
Desai, A.N.1
Jere, A.2
-
72
-
-
84925400314
-
Cutting the Gordian helix - Regulating genomic testing in the era of precision medicine
-
Lander, E.S. Cutting the Gordian helix - regulating genomic testing in the era of precision medicine. N. Engl. J. Med. 372, 1185-1186 (2015).
-
(2015)
N. Engl. J. Med.
, vol.372
, pp. 1185-1186
-
-
Lander, E.S.1
-
73
-
-
84903137437
-
Next-generation sequencing in precision oncology: Challenges and opportunities
-
Kruglyak, K.M., Lin, E. & Ong, F.S. Next-generation sequencing in precision oncology: challenges and opportunities. Expert Rev. Mol. Diagn. 14, 635-637 (2014).
-
(2014)
Expert Rev. Mol. Diagn.
, vol.14
, pp. 635-637
-
-
Kruglyak, K.M.1
Lin, E.2
Ong, F.S.3
-
74
-
-
84887462642
-
"N of 1" case reports in the era of whole-genome sequencing
-
Brannon, A.R. & Sawyers, C.L. "N of 1" case reports in the era of whole-genome sequencing. J. Clin. Investig. 123, 4568-4570 (2013).
-
(2013)
J. Clin. Investig.
, vol.123
, pp. 4568-4570
-
-
Brannon, A.R.1
Sawyers, C.L.2
-
75
-
-
84896797913
-
Clinical application of whole-genome sequencing: Proceed with care
-
Feero, W. Clinical application of whole-genome sequencing: proceed with care. JAMA 311, 1017-1019 (2014).
-
(2014)
JAMA
, vol.311
, pp. 1017-1019
-
-
Feero, W.1
|