-
2
-
-
84880452562
-
Genomics-driven oncology: Framework for an emerging paradigm
-
Garraway, L.A. Genomics-driven oncology: Framework for an emerging paradigm. J. Clin. Oncol., 2013, 3, 1806-1814.
-
(2013)
J. Clin. Oncol
, vol.3
, pp. 1806-1814
-
-
Garraway, L.A.1
-
3
-
-
54949085398
-
K-ras mutations and benefit from cetuximab in advanced colorectal cancer
-
Karapetis, C.S.; Khambata-Ford, S.; Jonker D.J.; O'Callaghan, C.J.; Tu D.; Tebbutt, N.C.; Simes, R.J.; Chalchal, H.; Shapiro, J.D.; Robitaille, S.; Price, T.J.; Shepherd, L.; Au, H.J.; Langer, C.; Moore, M.J.; Zalcberg, J.R. K-ras mutations and benefit from cetuximab in advanced colorectal cancer. N. Engl. J. Med., 2008, 359, 1757-1765
-
(2008)
N. Engl. J. Med
, vol.359
, pp. 1757-1765
-
-
Karapetis, C.S.1
Khambata-Ford, S.2
Jonker, D.J.3
O'callaghan, C.J.4
Tu, D.5
Tebbutt, N.C.6
Simes, R.J.7
Chalchal, H.8
Shapiro, J.D.9
Robitaille, S.10
Price, T.J.11
Shepherd, L.12
Au, H.J.13
Langer, C.14
Moore, M.J.15
Zalcberg, J.R.16
-
4
-
-
84875217898
-
Disease-targeted sequencing: A cornerstone in the clinic. Nat
-
Rehm, H.L. Disease-targeted sequencing: a cornerstone in the clinic. Nat. Rev. Genet., 2013, 14(4), 295-300.
-
(2013)
Rev. Genet
, vol.14
, Issue.4
, pp. 295-300
-
-
Rehm, H.L.1
-
5
-
-
2342471392
-
Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-
-
Lynch, T.J.; Bell, D.W.; Sordella, R.; Sordella, R.; Gurubhagavatula, S.; Okimoto, R.A.; Brannigan, B.W.; Harris, P.L.; Haserlat, S.M.; Supko, J.G.; Haluska, F.G.; Louis, D.N.; Christiani, D.C.; Settleman, J.; Haber, D.A. Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib. N. Engl. J. Med., 2004, 350, 2129-2139
-
(2004)
N. Engl. J. Med
, vol.350
, pp. 2129-2139
-
-
Lynch, T.J.1
Bell, D.W.2
Sordella, R.3
Sordella, R.4
Gurubhagavatula, S.5
Okimoto, R.A.6
Brannigan, B.W.7
Harris, P.L.8
Haserlat, S.M.9
Supko, J.G.10
Haluska, F.G.11
Louis, D.N.12
Christiani, D.C.13
Settleman, J.14
Haber, D.A.15
-
6
-
-
34547638047
-
Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer
-
Soda, M.; Choi, Y.L.; Enomoto, M.; Takada, S.; Yamashita, Y.; Ishikawa, S.; Fujiwara, S.; Watanabe, H.; Kurashina, K.; Hatanaka, H.; Bando, M.; Ohno, S.; Ishikawa, Y.; Aburatani, H.; Niki, T.; Sohara, Y.; Sugiyama, Y.; Mano, H. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature, 2007, 448, 561-566.
-
(2007)
Nature
, vol.448
, pp. 561-566
-
-
Soda, M.1
Choi, Y.L.2
Enomoto, M.3
Takada, S.4
Yamashita, Y.5
Ishikawa, S.6
Fujiwara, S.7
Watanabe, H.8
Kurashina, K.9
Hatanaka, H.10
Bando, M.11
Ohno, S.12
Ishikawa, Y.13
Aburatani, H.14
Niki, T.15
Sohara, Y.16
Sugiyama, Y.17
Mano, H.18
-
7
-
-
78049425319
-
Anaplastic lymphoma kinase inhibition in non-small-cell lung cancer
-
Kwak, E.L.; Bang, Y.J.; Camidge, D.R.; Shaw, A.T.; Solomon, B.; Maki, R.G.; Ou, S.H.; Dezube, B.J.; Jänne, P.A.; Costa, D.B.; Varella-Garcia, M.; Kim, W.H.; Lynch, T.J.; Fidias, P.; Stubbs, H.; Engelman, J.A.; Sequist, L.V.; Tan, W.; Gandhi, L.; Mino-Kenudson, M.; Wei, G.C.; Shreeve, S.M.; Ratain, M.J.; Settleman, J.; Christensen, J.G.; Haber, D.A.; Wilner, K.; Salgia, R.; Shapiro, G.I.; Clark, J.W.; Iafrate, A.J. Anaplastic lymphoma kinase inhibition in non-small-cell lung cancer. N. Engl. J. Med., 2010, 363, 1693-1703.
-
(2010)
N. Engl. J. Med
, vol.363
, pp. 1693-1703
-
-
Kwak, E.L.1
Bang, Y.J.2
Camidge, D.R.3
Shaw, A.T.4
Solomon, B.5
Maki, R.G.6
Ou, S.H.7
Dezube, B.J.8
Jänne, P.A.9
Costa, D.B.10
Varella-Garcia, M.11
Kim, W.H.12
Lynch, T.J.13
Fidias, P.14
Stubbs, H.15
Engelman, J.A.16
Sequist, L.V.17
Tan, W.18
Gandhi, L.19
Mino-Kenudson, M.20
Wei, G.C.21
Shreeve, S.M.22
Ratain, M.J.23
Settleman, J.24
Christensen, J.G.25
Haber, D.A.26
Wilner, K.27
Salgia, R.28
Shapiro, G.I.29
Clark, J.W.30
Iafrate, A.J.31
more..
-
8
-
-
79951976403
-
Crizotinib in anaplastic large-cell lymphoma
-
Gambacorti-Passerini, C.; Messa, C.; Pogliani, E.M. Crizotinib in anaplastic large-cell lymphoma. N. Engl. J. Med., 2011, 364, 775-776
-
(2011)
N. Engl. J. Med
, vol.364
, pp. 775-776
-
-
Gambacorti-Passerini, C.1
Messa, C.2
Pogliani, E.M.3
-
9
-
-
84879290901
-
Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: Guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular Pathology
-
Lindeman, N.I.; Cagle, P.T.; Beasley, M.B.; Chitale, D.A.; Dacic, S.; Giaccone, G.; Jenkins, R.B.; Kwiatkowski, D.J.; Saldivar, J.S.; Squire, J.; Thunnissen, E.; Ladanyi, M. Molecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular Pathology. J. Mol. Diagn., 2013, 15(4), 415-453
-
(2013)
J. Mol. Diagn
, vol.15
, Issue.4
, pp. 415-453
-
-
Lindeman, N.I.1
Cagle, P.T.2
Beasley, M.B.3
Chitale, D.A.4
Dacic, S.5
Giaccone, G.6
Jenkins, R.B.7
Kwiatkowski, D.J.8
Saldivar, J.S.9
Squire, J.10
Thunnissen, E.11
Ladanyi, M.12
-
10
-
-
84928215463
-
Assessing the clinical value of targeted, massively parallel sequencing in a longitudinal, prospective population-based study of cancer patients
-
Wong, S.Q.; Fellowes, A.; Doig, K.; Ellul, J.; Bosma, T.J.; Irwin, D.; Vedururu, R.; Tan, A.Y.; Weiss, J.; Chan, K.S.; Lucas, M.; Thomas, D.M.; Dobrovic, A.; Parisot, J.P.; Fox, S.B. Assessing the clinical value of targeted, massively parallel sequencing in a longitudinal, prospective population-based study of cancer patients. Br. J. Cancer, 2015, 112, 1411-1420.
-
(2015)
Br. J. Cancer
, vol.112
, pp. 1411-1420
-
-
Wong, S.Q.1
Fellowes, A.2
Doig, K.3
Ellul, J.4
Bosma, T.J.5
Irwin, D.6
Vedururu, R.7
Tan, A.Y.8
Weiss, J.9
Chan, K.S.10
Lucas, M.11
Thomas, D.M.12
Dobrovic, A.13
Parisot, J.P.14
Fox, S.B.15
-
11
-
-
0142178215
-
New York Breast Cancer Study Group. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
King, M.C.; Marks, J.H.; Mandell, J.B. New York Breast Cancer Study Group. Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science, 2003, 302(5645), 643-646.
-
(2003)
Science
, vol.302
, Issue.5645
, pp. 643-646
-
-
King, M.C.1
Marks, J.H.2
Mandell, J.B.3
-
12
-
-
64849092309
-
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene
-
Jones, S.; Hruban, R.H.; Kamiyama, M.; Borges, M.; Zhang, X.; Parsons, D.W.; Lin, J.C.; Palmisano, E.; Brune, K.; Jaffee, E.M.; Iacobuzio-Donahue, C.A.; Maitra, A.; Parmigiani, G.; Kern, S.E.; Velculescu, V.E.; Kinzler, K.W.; Vogelstein, B.; Eshleman, J.R.; Goggins, M.; Klein, A.P. Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. Science, 2009, 324 (5924), 217
-
(2009)
Science
, vol.324
, Issue.5924
-
-
Jones, S.1
Hruban, R.H.2
Kamiyama, M.3
Borges, M.4
Zhang, X.5
Parsons, D.W.6
Lin, J.C.7
Palmisano, E.8
Brune, K.9
Jaffee, E.M.10
Iacobuzio-Donahue, C.A.11
Maitra, A.12
Parmigiani, G.13
Kern, S.E.14
Velculescu, V.E.15
Kinzler, K.W.16
Vogelstein, B.17
Eshleman, J.R.18
Goggins, M.19
Klein, A.P.20
more..
-
13
-
-
66149098136
-
Italian Pheochromocytoma/Paraganglioma Network. Clinically guided genetic screening in a large cohort of Italian patients with pheo-chromocytomas and/or functional or nonfunctional paraganglio-mas
-
Mannelli, M.; Castellano, M.; Schiavi, F.; Filetti, S.; Giacchè, M.; Mori, L.; Pignataro, V.; Bernini, G.; Giachè, V.; Bacca, A.; Biondi, B.; Corona, G.; Di Trapani, G.; Grossrubatscher, E.; Reimondo, G.; Arnaldi, G.; Giacchetti, G.; Veglio, F.; Loli, P.; Colao, A; Ambrosio, M.R.; Terzolo, M.; Letizia, C.; Ercolino, T.; Opocher, G.; Italian Pheochromocytoma/Paraganglioma Network. Clinically guided genetic screening in a large cohort of Italian patients with pheo-chromocytomas and/or functional or nonfunctional paraganglio-mas. J. Clin. Endocrinol. Metab., 2009, 94, 1541-1547.
-
(2009)
J. Clin. Endocrinol. Metab
, vol.94
, pp. 1541-1547
-
-
Mannelli, M.1
Castellano, M.2
Schiavi, F.3
Filetti, S.4
Giacchè, M.5
Mori, L.6
Pignataro, V.7
Bernini, G.8
Giachè, V.9
Bacca, A.10
Biondi, B.11
Corona, G.12
Di Trapani, G.13
Grossrubatscher, E.14
Reimondo, G.15
Arnaldi, G.16
Giacchetti, G.17
Veglio, F.18
Loli, P.19
Colao, A.20
Ambrosio, M.R.21
Terzolo, M.22
Letizia, C.23
Ercolino, T.24
Opocher, G.25
more..
-
14
-
-
84885785987
-
Clinical whole-exome sequencing for the diagnosis of mendelian disorders
-
Yang, Y.; Muzny, D.M.; Reid, J.G.; Bainbridge, M.N.; Willis, A.; Ward, P.A.; Braxton, A.; Beuten, J.; Xia, F.; Niu, Z.; Hardison, M.; Person, R.; Bekheirnia, M.R.; Leduc, M.S.; Kirby, A.; Pham, P.; Scull, J.; Wang, M.; Ding, Y.; Plon, S.E.; Lupski, J.R.; Beaudet, A.L.; Gibbs, R.A.; Eng, CM. Clinical whole-exome sequencing for the diagnosis of mendelian disorders. N. Engl. J. Med., 2013, 369(16), 1502-1511.
-
(2013)
N. Engl. J. Med
, vol.369
, Issue.16
, pp. 1502-1511
-
-
Yang, Y.1
Muzny, D.M.2
Reid, J.G.3
Bainbridge, M.N.4
Willis, A.5
Ward, P.A.6
Braxton, A.7
Beuten, J.8
Xia, F.9
Niu, Z.10
Hardison, M.11
Person, R.12
Bekheirnia, M.R.13
Leduc, M.S.14
Kirby, A.15
Pham, P.16
Scull, J.17
Wang, M.18
Ding, Y.19
Plon, S.E.20
Lupski, J.R.21
Beaudet, A.L.22
Gibbs, R.A.23
Eng, C.M.24
more..
-
15
-
-
84896769549
-
Clinical Interpretation and Implications of Whole-Genome Sequencing
-
Dewey, F.E.; Grove, M.E.; Pan, C.; Goldstein, B.A.; Bernstein, J.A.; Chaib, H.; Merker, J.D.; Goldfeder, R.L.; Enns, G.M.; David, S.P.; Pakdaman, N.; Ormond, K.E.; Caleshu, C.; Kingham, K.; Klein, T.E.; Whirl-Carrillo, M.; Sakamoto, K.; Wheeler, M.T.; Butte, A.J.; Ford, J.M.; Boxer, L.; Ioannidis, J.P.; Yeung, A.C.; Altman, R.B.; Assimes, T.L.; Snyder, M.; Ashley, E.A.; Quertermous, T. Clinical Interpretation and Implications of Whole-Genome Sequencing. JAMA, 2014, 311(10), 1035-1044.
-
(2014)
JAMA
, vol.311
, Issue.10
, pp. 1035-1044
-
-
Dewey, F.E.1
Grove, M.E.2
Pan, C.3
Goldstein, B.A.4
Bernstein, J.A.5
Chaib, H.6
Merker, J.D.7
Goldfeder, R.L.8
Enns, G.M.9
David, S.P.10
Pakdaman, N.11
Ormond, K.E.12
Caleshu, C.13
Kingham, K.14
Klein, T.E.15
Whirl-Carrillo, M.16
Sakamoto, K.17
Wheeler, M.T.18
Butte, A.J.19
Ford, J.M.20
Boxer, L.21
Ioannidis, J.P.22
Yeung, A.C.23
Altman, R.B.24
Assimes, T.L.25
Snyder, M.26
Ashley, E.A.27
Quertermous, T.28
more..
-
16
-
-
84864744400
-
Improvement of cellularity on cell block preparations using the socalled tissue coagulum clot method during endobronchial ultrasound-guided trans-bronchial fine-needle aspiration
-
Yung, R.C.; Otell, S.; Illei, P.; Clark, D.P.; Feller-Kopman, D.; Yarmus, L.; Askin, F.; Gabrielson, E.; Li, Q.K. Improvement of cellularity on cell block preparations using the socalled tissue coagulum clot method during endobronchial ultrasound-guided trans-bronchial fine-needle aspiration. Cancer Cytopathol., 2012, 120, 185-195.
-
(2012)
Cancer Cytopathol
, vol.120
, pp. 185-195
-
-
Yung, R.C.1
Otell, S.2
Illei, P.3
Clark, D.P.4
Feller-Kopman, D.5
Yarmus, L.6
Askin, F.7
Gabrielson, E.8
Li, Q.K.9
-
17
-
-
84893750117
-
Next-generation sequencing-based multi-gene mutation profiling of solid tumors using fine needle aspiration samples: Promises and challenges for routine clinical diagnostics. Mod
-
Kanagal-Shamanna, R.; Portier, B.P.; Singh, R.R.; Routbort, M.J.; Aldape, K.D.; Handal, B.A.; Rahimi, H.; Reddy, N.G.; Barkoh, B.A.; Mishra, B.M.; Paladugu, A.V.; Manekia, J.H.; Kalhor, N.; Chowdhuri, S.R.; Staerkel, G.A.; Medeiros, L.J.; Luthra, R.; Patel, K.P. Next-generation sequencing-based multi-gene mutation profiling of solid tumors using fine needle aspiration samples: promises and challenges for routine clinical diagnostics. Mod. Pathol., 2014, 27(2), 314-327.
-
(2014)
Pathol
, vol.27
, Issue.2
, pp. 314-327
-
-
Kanagal-Shamanna, R.1
Portier, B.P.2
Singh, R.R.3
Routbort, M.J.4
Aldape, K.D.5
Handal, B.A.6
Rahimi, H.7
Reddy, N.G.8
Barkoh, B.A.9
Mishra, B.M.10
Paladugu, A.V.11
Manekia, J.H.12
Kalhor, N.13
Chowdhuri, S.R.14
Staerkel, G.A.15
Medeiros, L.J.16
Luthra, R.17
Patel, K.P.18
-
18
-
-
80155150303
-
Personalized medicine in lung cancer: What we need to know. Nature
-
Mok, T. S. Personalized medicine in lung cancer: what we need to know. Nature Rev. Clin. Oncol., 2011, 8, 661-668.
-
(2011)
Rev. Clin. Oncol
, vol.8
, pp. 661-668
-
-
Mok, T.S.1
-
19
-
-
84857969863
-
Chipping away at the lung cancer genome. Nat
-
Pao, W.; Hutchinson, K.E. Chipping away at the lung cancer genome. Nat. Med., 2012, 18, 349-351.
-
(2012)
Med
, vol.18
, pp. 349-351
-
-
Pao, W.1
Hutchinson, K.E.2
-
20
-
-
84893411121
-
Molecular Typing of Lung Adenocarcinoma on Cytology Samples Using a Multigene Next Generation Sequencing Panel
-
Scarpa, A.; Sikora, K.; Fassan, M.; Rachiglio, A.M.; Cappellesso, R.; Antonello, D.; Amato, E.; Mafficini, A.; Lambiase, M.; Esposito, C.; Bria, E.; Simonato, F.; Scardoni, M.; Turri, G.; Chilosi, M.; Tortora, G.; Fassina, A.; Normanno, N. Molecular Typing of Lung Adenocarcinoma on Cytology Samples Using a Multigene Next Generation Sequencing Panel. PLoS ONE, 2013, 8(11), e80478
-
(2013)
Plos ONE
, vol.8
, Issue.11
-
-
Scarpa, A.1
Sikora, K.2
Fassan, M.3
Rachiglio, A.M.4
Cappellesso, R.5
Antonello, D.6
Amato, E.7
Mafficini, A.8
Lambiase, M.9
Esposito, C.10
Bria, E.11
Simonato, F.12
Scardoni, M.13
Turri, G.14
Chilosi, M.15
Tortora, G.16
Fassina, A.17
Normanno, N.18
-
21
-
-
84916938168
-
The changing epidemiology of thyroid cancer: Why is incidence increasing?
-
Vigneri, R.; Malandrino, P.; Vigneri, P. The changing epidemiology of thyroid cancer: why is incidence increasing? Current Opin. Oncol., 2015, 27, 1-7.
-
(2015)
Current Opin. Oncol
, vol.27
, pp. 1-7
-
-
Vigneri, R.1
Malandrino, P.2
Vigneri, P.3
-
22
-
-
3242879158
-
Changing trends in thyroid practice: Understanding nodular thyroid disease
-
Gharib, H. Changing trends in thyroid practice: understanding nodular thyroid disease. Endocr. Pract., 2004, 10(1), 31-39
-
(2004)
Endocr. Pract
, vol.10
, Issue.1
, pp. 31-39
-
-
Gharib, H.1
-
23
-
-
80053150200
-
Molecular genetics and diagnosis of thyroid cancer
-
Nikiforov, Y.E.; Nikiforova, M.N. Molecular genetics and diagnosis of thyroid cancer. Nat. Rev. Endocrinol., 2011, 7, 569-580.
-
(2011)
Nat. Rev. Endocrinol
, vol.7
, pp. 569-580
-
-
Nikiforov, Y.E.1
Nikiforova, M.N.2
-
24
-
-
84875295216
-
Progress in molecularbased management of differentiated thyroid cancer
-
Xing, M.; Haugen, B.R.; Schlumberger, M. Progress in molecularbased management of differentiated thyroid cancer. Lancet, 2013, 381(9871), 1058-1069.
-
(2013)
Lancet
, vol.381
, Issue.9871
, pp. 1058-1069
-
-
Xing, M.1
Haugen, B.R.2
Schlumberger, M.3
-
25
-
-
80655147350
-
Impact of mutational testing on the diagnosis and management of patients with cytologically indeterminate thyroid nodules: A prospective analysis of 1056 FNA samples
-
Nikiforov, Y.E.; Ohori, N.P.; Hodak, S.P.; Carty, S.E.; LeBeau, S.O.; Ferris, R.L.; Yip, L.; Seethala, R.R.; Tublin, M.E.; Stang, M.T.; Coyne, C.; Johnson, J.T.; Stewart, A.F.; Nikiforova, M.N. Impact of mutational testing on the diagnosis and management of patients with cytologically indeterminate thyroid nodules: a prospective analysis of 1056 FNA samples. J. Clin. Endocrinol. Me-tab., 2011, 96, 3390-3397.
-
(2011)
J. Clin. Endocrinol. Me-Tab
, vol.96
, pp. 3390-3397
-
-
Nikiforov, Y.E.1
Ohori, N.P.2
Hodak, S.P.3
Carty, S.E.4
Lebeau, S.O.5
Ferris, R.L.6
Yip, L.7
Seethala, R.R.8
Tublin, M.E.9
Stang, M.T.10
Coyne, C.11
Johnson, J.T.12
Stewart, A.F.13
Nikiforova, M.N.14
-
26
-
-
84887472968
-
Targeted next-generation sequencing panel (ThyroSeq) for detection of mutations in thyroid cancer
-
Nikiforova, M.N.; Wald, A.I.; Roy, S.; Durso, M.B.; Nikiforov, Y.E. Targeted next-generation sequencing panel (ThyroSeq) for detection of mutations in thyroid cancer. J. Clin. Endocrinol. Metab., 2013, 98(11), E1852-E1860.
-
(2013)
J. Clin. Endocrinol. Metab
, vol.98
, Issue.11
, pp. E1852-E1860
-
-
Nikiforova, M.N.1
Wald, A.I.2
Roy, S.3
Durso, M.B.4
Nikiforov, Y.E.5
-
27
-
-
84913605660
-
Highly accurate diagnosis of cancer in thyroid nodules with follicular neoplasm/suspicious for a follicular neoplasm cytology by ThyroSeq v2 next-generation sequencing assay
-
Nikiforov, Y.E.; Carty, S.E.; Chiosea, S.I.; Coyne, C.; Duvvuri, U.; Ferris, R.L.; Gooding, W.E.; Hodak, S.P.; LeBeau, S.O.; Ohori, N.P.; Seethala, R.R.; Tublin, M.E.; Yip, L.; Nikiforova, M.N. Highly accurate diagnosis of cancer in thyroid nodules with follicular neoplasm/suspicious for a follicular neoplasm cytology by ThyroSeq v2 next-generation sequencing assay. Cancer, 2014, 120(23), 3627-3634.
-
(2014)
Cancer
, vol.120
, Issue.23
, pp. 3627-3634
-
-
Nikiforov, Y.E.1
Carty, S.E.2
Chiosea, S.I.3
Coyne, C.4
Duvvuri, U.5
Ferris, R.L.6
Gooding, W.E.7
Hodak, S.P.8
Lebeau, S.O.9
Ohori, N.P.10
Seethala, R.R.11
Tublin, M.E.12
Yip, L.13
Nikiforova, M.N.14
-
28
-
-
84925233233
-
Next-generation sequencing improves the diagnosis of thyroid FNA specimens with indeterminate cytology
-
Le Mercier, M.; D'Haene, N.; De Nève, N.; Blanchard, O.; Degand, C.; Rorive, S.; Salmon, I. Next-generation sequencing improves the diagnosis of thyroid FNA specimens with indeterminate cytology. Histopathology, 2015, 66(2), 215-224.
-
(2015)
Histopathology
, vol.66
, Issue.2
, pp. 215-224
-
-
Le Mercier, M.1
D'haene, N.2
De Nève, N.3
Blanchard, O.4
Degand, C.5
Rorive, S.6
Salmon, I.7
-
29
-
-
84907045086
-
Pancreatic Adenocarcinoma
-
Ryan, D.P.; Hong, T.S.; Bardeesy, N. Pancreatic Adenocarcinoma. N. Engl. J. Med., 2014, 371, 1039-1049.
-
(2014)
N. Engl. J. Med
, vol.371
, pp. 1039-1049
-
-
Ryan, D.P.1
Hong, T.S.2
Bardeesy, N.3
-
30
-
-
84895105113
-
Next Generation sequencing improves the accuracy of KRAS Mutation analysis in endoscopic ultrasound fine needle aspiration pancreatic lesions
-
de Biase, D.; Visani, M.; Baccarini, P.; Polifemo, A.M.; Maimone, A.; Fornelli, A.; Giuliani, A.; Zanini, N.; Fabbri, C.; Pession, A.; Tallini, G. Next Generation sequencing improves the accuracy of KRAS Mutation analysis in endoscopic ultrasound fine needle aspiration pancreatic lesions. PLoS ONE, 2014, 9(2), e87651.
-
(2014)
Plos ONE
, vol.9
, Issue.2
-
-
De Biase, D.1
Visani, M.2
Baccarini, P.3
Polifemo, A.M.4
Maimone, A.5
Fornelli, A.6
Giuliani, A.7
Zanini, N.8
Fabbri, C.9
Pession, A.10
Tallini, G.11
-
31
-
-
84880557325
-
Genomic medicine: A decade of successes, challenges, and opportunity
-
189sr4
-
McCarthy, J.J.; McLeod, H.L.; Ginsburg, G.S. Genomic medicine: a decade of successes, challenges, and opportunity. Sci. Transl. Med., 2013, 5(189), 189sr4
-
(2013)
Sci. Transl. Med
, vol.5
, Issue.189
-
-
McCarthy, J.J.1
McLeod, H.L.2
Ginsburg, G.S.3
-
32
-
-
77952968845
-
Call to action: Training pathology residents in genomics and personalized medicine
-
Haspel, R.L.; Arnaout, R.; Briere, L.; Kantarci, S.; Marchand, K.; Tonellato, P.; Connolly, J.; Boguski, M.S.; Saffitz, J.E. A call to action: Training pathology residents in genomics and personalized medicine. Am. J. Clin. Pathol., 2010, 133, 832-834
-
(2010)
Am. J. Clin. Pathol
, vol.133
, pp. 832-834
-
-
Haspel, R.L.1
Arnaout, R.2
Briere, L.3
Kantarci, S.4
Marchand, K.5
Tonellato, P.6
Connolly, J.7
Boguski, M.S.8
Saffitz, J.9
-
33
-
-
84935042658
-
-
(Accessed 2010)
-
ASCP. Training Residents in Genomics website. www.pathology learning.org/trig (Accessed 2010)
-
Training Residents in Genomics
-
-
-
34
-
-
84874533602
-
Integration of genomic medicine into pathology residency training: The Stanford open curriculum
-
Schrijver, I.; Natkunam, Y.; Galli, S.; Boyd, S.D. Integration of genomic medicine into pathology residency training: The Stanford open curriculum. J. Mol. Diagn., 2013, 15, 141-148.
-
(2013)
J. Mol. Diagn
, vol.15
, pp. 141-148
-
-
Schrijver, I.1
Natkunam, Y.2
Galli, S.3
Boyd, S.D.4
-
35
-
-
84891809093
-
Clinvar: Public archive of relation-ships among sequence variation and human phenotype
-
Landrum, M.J.; Lee, J.M.; Riley, G.R.; Jang, W.; Rubinstein, W.S.; Church, D.M.; Maglott, D.R. Clinvar: Public archive of relation-ships among sequence variation and human phenotype. Nucleic Acids Res., 2014, 42, D980-D985
-
(2014)
Nucleic Acids Res
, vol.42
, pp. D980-D985
-
-
Landrum, M.J.1
Lee, J.M.2
Riley, G.R.3
Jang, W.4
Rubinstein, W.S.5
Church, D.M.6
Maglott, D.R.7
-
36
-
-
84895840909
-
Points to consider for informed consent for genome/exome sequencing
-
ACMG Board of Directors. Points to consider for informed consent for genome/exome sequencing. Genet. Med., 2013, 15, 748-749
-
(2013)
Genet. Med
, vol.15
, pp. 748-749
-
-
-
37
-
-
84880535720
-
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
-
Green, R.C.; Berg, J.S.; Grody, W.W.; Kalia, S.S.; Korf, B.R.; Martin, C.L. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet. Med., 2013, 15(7), 565-574.
-
(2013)
Genet. Med
, vol.15
, Issue.7
, pp. 565-574
-
-
Green, R.C.1
Berg, J.S.2
Grody, W.W.3
Kalia, S.S.4
Korf, B.R.5
Martin, C.L.6
-
38
-
-
84878612543
-
-
(Accessed 2010)
-
ACMG updates recommendations on “opt-out” for genome sequencing return of results. American College of Medical Genetics and Genomics. www.acmg.net/docs/Release_ACMGUpdates Rec-ommendations_final.pdf (Accessed 2010)
-
American College of Medical Genetics and Genomics
-
-
-
39
-
-
84905815773
-
Clinical Tumor Sequencing: An Incidental Casualty of the American College of Medical Genetics and Genomics Recommendations for Reporting of Incidental Findings
-
Parsons, D.W.; Roy, A.; Plon, S.E.; Roychowdhury, S.; Chinnaiyan, A.M. Clinical Tumor Sequencing: An Incidental Casualty of the American College of Medical Genetics and Genomics Recommendations for Reporting of Incidental Findings. J. Clin. Oncol., 2014, 32, 2203-2205.
-
(2014)
J. Clin. Oncol
, vol.32
, pp. 2203-2205
-
-
Parsons, D.W.1
Roy, A.2
Plon, S.E.3
Roychowdhury, S.4
Chinnaiyan, A.M.5
-
40
-
-
84920528362
-
ACMG policy statement: Updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. Genet
-
ACMG Board of Directors. ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing. Genet. Med., 2015, 17, 68-69.
-
(2015)
Med
, vol.17
, pp. 68-69
-
-
-
41
-
-
84867350321
-
Opportunities and challenges associated with clinical diagnostic genome sequencing: A report of the association for molecular pathology
-
Schrijver, I.; Aziz, N.; Farkas, D.H.; Furtado, M.; Gonzalez, A.F.; Greiner, T.C.; Grody, W.W.; Hambuch, T.; Kalman, L.; Kant, J.A.; Klein, R.D.; Leonard, D.G.; Lubin, I.M.; Mao, R.; Nagan, N.; Pratt, V.M.; Sobel, M.E.; Voelkerding, K.V.; Gibson, J.S. Opportunities and challenges associated with clinical diagnostic genome sequencing: A report of the association for molecular pathology. J. Mol. Diagn., 2012, 14, 525-540.
-
(2012)
J. Mol. Diagn
, vol.14
, pp. 525-540
-
-
Schrijver, I.1
Aziz, N.2
Farkas, D.H.3
Furtado, M.4
Gonzalez, A.F.5
Greiner, T.C.6
Grody, W.W.7
Hambuch, T.8
Kalman, L.9
Kant, J.A.10
Klein, R.D.11
Leonard, D.G.12
Lubin, I.M.13
Mao, R.14
Nagan, N.15
Pratt, V.M.16
Sobel, M.E.17
Voelkerding, K.V.18
Gibson, J.S.19
-
42
-
-
84869429716
-
Assuring the quality of next-generation sequencing in clinical laboratory practice
-
Gargis, A.S.; Kalman, L.; Berry, M.W.; Bick, D.P.; Dimmock, D.P.; Hambuch, T.; Lu, F.; Lyon, E.; Voelkerding, K.V.; Zehnbauer, B.A.; Agarwala, R.; Bennett, S.F.; Chen, B.; Chin, E.L.; Compton, J.G.; Das, S.; Farkas, D.H.; Ferber, M.J.; Funke, B.H.; Furtado, M.R.; Ganova-Raeva, L.M.; Geigenmüller, U.; Gunselman, S.J.; Hegde, M.R.; Johnson, P.L.; Kasarskis, A.; Kul- karni, S.; Lenk, T.; Liu, C.S.; Manion, M.; Manolio, T.A.; Mardis, E.R.; Merker, J.D.; Rajeevan, M.S.; Reese, M.G.; Rehm, H.L.; Simen, B.B.; Yeakley, J.M.; Zook, J.M.; Lubin, I.M. Assuring the quality of next-generation sequencing in clinical laboratory practice. Nat. Biotechnol., 2012, 30, 1033-1036.
-
(2012)
Nat. Biotechnol
, vol.30
, pp. 1033-1036
-
-
Gargis, A.S.1
Kalman, L.2
Berry, M.W.3
Bick, D.P.4
Dimmock, D.P.5
Hambuch, T.6
Lu, F.7
Lyon, E.8
Voelkerding, K.V.9
Zehnbauer, B.A.10
Agarwala, R.11
Bennett, S.F.12
Chen, B.13
Chin, E.L.14
Compton, J.G.15
Das, S.16
Farkas, D.H.17
Ferber, M.J.18
Funke, B.H.19
Furtado, M.R.20
Ganova-Raeva, L.M.21
Geigenmüller, U.22
Gunselman, S.J.23
Hegde, M.R.24
Johnson, P.L.25
Kasarskis, A.26
Kul- Karni, S.27
Lenk, T.28
Liu, C.S.29
Manion, M.30
Manolio, T.A.31
Mardis, E.R.32
Merker, J.D.33
Rajeevan, M.S.34
Reese, M.G.35
Rehm, H.L.36
Simen, B.B.37
Yeakley, J.M.38
Zook, J.M.39
Lubin, I.M.40
more..
-
43
-
-
84914162901
-
Next generation diagnostic molecular pathology: Critical appraisal of quality assurance in Europe
-
Dubbink, H.J.; Deans, Z.C.; Tops, B.B.; van Kemenade, F.J.; Koljenovi, S.; van Krieken, H.J.; Blokx, W.A.; Dinjens, W.N.; Groenen, P.J. Next generation diagnostic molecular pathology: Critical appraisal of quality assurance in Europe. Mol. Oncol., 2014, 8, 830-839.
-
(2014)
Mol. Oncol
, vol.8
, pp. 830-839
-
-
Dubbink, H.J.1
Deans, Z.C.2
Tops, B.B.3
Van Kemenade, F.J.4
Koljenovi, S.5
Van Krieken, H.J.6
Blokx, W.A.7
Dinjens, W.N.8
Groenen, P.J.9
-
44
-
-
84864649027
-
Points to consider in the clinical application of genome sequencing
-
ACMG Board of Directors. Points to consider in the clinical application of genome sequencing. Genet. Med., 2012, 14, 759-761.
-
(2012)
Genet. Med
, vol.14
, pp. 759-761
-
-
-
45
-
-
84883897500
-
Working Group of the American College of Medical Genetics and Genomics Laboratory Quality Assurance Commitee. ACMG clinical laboratory standards for next-generation sequencing
-
Rehm, H.L.; Bale, S.J.; Bayrak-Toydemir, P.; Berg, J.S.; Brown, K.K.; Deignan, J.L.; Friez, M.J.; Funke, B.H.; Hegde, M.R.; Lyon, E. Working Group of the American College of Medical Genetics and Genomics Laboratory Quality Assurance Commitee. ACMG clinical laboratory standards for next-generation sequencing. Genet. Med., 2013, 15, 733-747.
-
(2013)
Genet. Med
, vol.15
, pp. 733-747
-
-
Rehm, H.L.1
Bale, S.J.2
Bayrak-Toydemir, P.3
Berg, J.S.4
Brown, K.K.5
Deignan, J.L.6
Friez, M.J.7
Funke, B.H.8
Hegde, M.R.9
Lyon, E.10
-
46
-
-
84928209346
-
-
Genet. Med., (Epub ahead of print, March 5, 2015)
-
Richards, S.; Aziz, N.; Bale, S.; Bick, D.; Das, S.; Gastier-Foster, J.; Grody, W.W.; Hegde, M.; Lyon, E.; Spector, E.; Voelkerding, K.; Rehm, H.L.; on behalf of the ACMG Laboratory Quality Assurance Committee. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet. Med., (Epub ahead of print, March 5, 2015)
-
On Behalf of the ACMG Laboratory Quality Assurance Committee. Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
-
-
Richards, S.1
Aziz, N.2
Bale, S.3
Bick, D.4
Das, S.5
Gastier-Foster, J.6
Grody, W.W.7
Hegde, M.8
Lyon, E.9
Spector, E.10
Voelkerding, K.11
Rehm, H.L.12
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