-
1
-
-
20344393370
-
Variability in organ-specific EGFR mutational spectra in tumour epithelium and stroma may be the biological basis for differential responses to tyrosine kinase inhibitors
-
Weber F, Fukino K, Sawada T, Williams N, Sweet K, Brena RM, et al. Variability in organ-specific EGFR mutational spectra in tumour epithelium and stroma may be the biological basis for differential responses to tyrosine kinase inhibitors. Br J Cancer. 2005;92(10):1922-6, http://dx.doi.org/10.1038/sj.bjc.6602557.
-
(2005)
Br J Cancer
, vol.92
, Issue.10
, pp. 1922-1926
-
-
Weber, F.1
Fukino, K.2
Sawada, T.3
Williams, N.4
Sweet, K.5
Brena, R.M.6
-
2
-
-
70349432408
-
Impact of KIT and PDGFRA gene mutations on prognosis of patients with gastrointestinal stromal tumors after complete primary tumor resection
-
Hou YY, Grabellus F, Weber F, Zhou Y, Tan YS, Li J, et al. Impact of KIT and PDGFRA gene mutations on prognosis of patients with gastrointestinal stromal tumors after complete primary tumor resection. J Gastrointest Surg. 2009;13(9):1583-92, http://dx.doi.org/10.1007/s11605-009-0842-6.
-
(2009)
J Gastrointest Surg
, vol.13
, Issue.9
, pp. 1583-1592
-
-
Hou, Y.Y.1
Grabellus, F.2
Weber, F.3
Zhou, Y.4
Tan, Y.S.5
Li, J.6
-
3
-
-
77953586698
-
Allelic variant at-79 (C. T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels
-
Landa I, Montero-Conde C, Malanga D, De Gisi S, Pita G, Leandro-Garcia LJ, et al. Allelic variant at-79 (C. T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels. Endocr Relat Cancer. 2010;17(2):317-28.
-
(2010)
Endocr Relat Cancer
, vol.17
, Issue.2
, pp. 317-328
-
-
Landa, I.1
Montero-Conde, C.2
Malanga, D.3
de Gisi, S.4
Pita, G.5
Leandro-Garcia, L.J.6
-
4
-
-
33744485019
-
Gene-expression profiling in differentiated thyroid cancer: A viable strategy for the practice of genomic medicine?
-
Weber F, Eng C. Gene-expression profiling in differentiated thyroid cancer: a viable strategy for the practice of genomic medicine? Future Oncol. 2005;1(4):497-510.
-
(2005)
Future Oncol
, vol.1
, Issue.4
, pp. 497-510
-
-
Weber, F.1
Eng, C.2
-
5
-
-
84859994910
-
A combined molecular-pathologic score improves risk stratification of thyroid papillary microcarcinoma
-
Aug 31 [epub ahead of print]
-
Niemeier LA, Kuffner Akatsu H, Song C, Carty SE, Hodak SP, Yip L, et al. A combined molecular-pathologic score improves risk stratification of thyroid papillary microcarcinoma. Cancer. Aug 31 [epub ahead of print].
-
Cancer
-
-
Niemeier, L.A.1
Kuffner Akatsu, H.2
Song, C.3
Carty, S.E.4
Hodak, S.P.5
Yip, L.6
-
6
-
-
77954407332
-
Genomewide association studies and assessment of the risk of disease
-
Manolio TA. Genomewide association studies and assessment of the risk of disease. N Engl J Med. 2010;363(2):166-76.
-
(2010)
N Engl J Med
, vol.363
, Issue.2
, pp. 166-176
-
-
Manolio, T.A.1
-
7
-
-
79953183422
-
Aquaporin 5 gene promoter: 1364A/C polymorphism associated with 30-day survival in severe sepsis
-
Adamzik M, Frey UH, Mohlenkamp S, Scherag A, Waydhas C, Marggraf G, et al. Aquaporin 5 gene promoter: 1364A/C polymorphism associated with 30-day survival in severe sepsis. Anesthesiology. 2011;114(4):912-17.
-
(2011)
Anesthesiology
, vol.114
, Issue.4
, pp. 912-917
-
-
Adamzik, M.1
Frey, U.H.2
Mohlenkamp, S.3
Scherag, A.4
Waydhas, C.5
Marggraf, G.6
-
8
-
-
77957735529
-
A genome-wide scan for common alleles affecting risk for autism
-
Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, et al. A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet. 2010;19(20):4072-82.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.20
, pp. 4072-4082
-
-
Anney, R.1
Klei, L.2
Pinto, D.3
Regan, R.4
Conroy, J.5
Magalhaes, T.R.6
-
9
-
-
58149347486
-
Genome-wide association studies: Potential next steps on a genetic journey
-
McCarthy MI, Hirschhorn JN. Genome-wide association studies: potential next steps on a genetic journey. Hum Mol Genet. 2008;17(R2):R156-65, http://dx.doi.org/10.1093/hmg/ddn289.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.R2
-
-
McCarthy, M.I.1
Hirschhorn, J.N.2
-
10
-
-
79957523471
-
The genomic architecture of sporadic heart failure
-
Dorn GW, 2nd. The genomic architecture of sporadic heart failure. Circ Res. 2011;108(10):1270-83.
-
(2011)
Circ Res
, vol.108
, Issue.10
, pp. 1270-1283
-
-
Dorn II, G.W.1
-
11
-
-
79955683789
-
Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases
-
Park SJ, Jung EH, Ryu RS, Kang HW, Ko JM, Kim HJ, et al. Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases. Mol Cytogenet. 2011;4:12.
-
(2011)
Mol Cytogenet
, vol.4
, pp. 12
-
-
Park, S.J.1
Jung, E.H.2
Ryu, R.S.3
Kang, H.W.4
Ko, J.M.5
Kim, H.J.6
-
12
-
-
75549084134
-
Personalized genomic information: Preparing for the future of genetic medicine
-
Guttmacher AE, McGuire AL, Ponder B, Stefansson K. Personalized genomic information: preparing for the future of genetic medicine. Nat Rev Genet. 2010;11(2):161-5.
-
(2010)
Nat Rev Genet
, vol.11
, Issue.2
, pp. 161-165
-
-
Guttmacher, A.E.1
McGuire, A.L.2
Ponder, B.3
Stefansson, K.4
-
13
-
-
78149392286
-
Being more realistic about the public health impact of genomic medicine
-
Hall WD, Mathews R, Morley KI. Being more realistic about the public health impact of genomic medicine. PLoS Med. 2010;7(10):e1000347, http://dx.doi.org/10.1371/journal.pmed.1000347
-
(2010)
PLoS Med
, vol.7
, Issue.10
-
-
Hall, W.D.1
Mathews, R.2
Morley, K.I.3
-
14
-
-
77952786822
-
Genomic medicine: An updated primer
-
Feero WG, Guttmacher AE, Collins FS. Genomic medicine: an updated primer. N Engl J Med. 2010;362(21):2001-11, http://dx.doi.org/10.1056/NEJMra0907175.
-
(2010)
N Engl J Med
, vol.362
, Issue.21
, pp. 2001-2011
-
-
Feero, W.G.1
Guttmacher, A.E.2
Collins, F.S.3
-
15
-
-
58749087343
-
Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3
-
Paynter NP, Chasman DI, Buring JE, Shiffman D, Cook NR, Ridker PM. Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3. Ann Intern Med. 2009;150(2):65-72.
-
(2009)
Ann Intern Med
, vol.150
, Issue.2
, pp. 65-72
-
-
Paynter, N.P.1
Chasman, D.I.2
Buring, J.E.3
Shiffman, D.4
Cook, N.R.5
Ridker, P.M.6
-
16
-
-
51749105925
-
The HCP5 single-nucleotide polymorphism: A simple screening tool for prediction of hypersensitivity reaction to abacavir
-
Colombo S, Rauch A, Rotger M, Fellay J, Martinez R, Fux C, et al. The HCP5 single-nucleotide polymorphism: a simple screening tool for prediction of hypersensitivity reaction to abacavir. J Infect Dis. 2008;198(6):864-7, http://dx.doi.org/10.1086/591184.
-
(2008)
J Infect Dis
, vol.198
, Issue.6
, pp. 864-867
-
-
Colombo, S.1
Rauch, A.2
Rotger, M.3
Fellay, J.4
Martinez, R.5
Fux, C.6
-
17
-
-
80053464779
-
Evaluation of a Microarray-Based Genotyping Assay for the Rapid Detection of Cytochrome P450 2C19 *2 and *3 Polymorphisms From Whole Blood Using Nanoparticle Probes
-
Buchan BW, Peterson JF, Cogbill CH, Anderson DK, Ledford JS, White MN, et al. Evaluation of a Microarray-Based Genotyping Assay for the Rapid Detection of Cytochrome P450 2C19 *2 and *3 Polymorphisms From Whole Blood Using Nanoparticle Probes. Am J Clin Pathol. 2011;136(4):604-8.
-
(2011)
Am J Clin Pathol
, vol.136
, Issue.4
, pp. 604-608
-
-
Buchan, B.W.1
Peterson, J.F.2
Cogbill, C.H.3
Anderson, D.K.4
Ledford, J.S.5
White, M.N.6
-
18
-
-
0043029208
-
Prophylactic thyroidectomy in multiple endocrine neoplasia: The impact of molecular mechanisms of RET proto-oncogene
-
Frilling A, Weber F, Tecklenborg C, Broelsch CE. Prophylactic thyroidectomy in multiple endocrine neoplasia: the impact of molecular mechanisms of RET proto-oncogene. Langenbecks Arch Surg. 2003;388(1):17-26.
-
(2003)
Langenbecks Arch Surg
, vol.388
, Issue.1
, pp. 17-26
-
-
Frilling, A.1
Weber, F.2
Tecklenborg, C.3
Broelsch, C.E.4
-
19
-
-
31144443745
-
Prophylactic thyroid surgery
-
Frilling A, Weber F. Prophylactic thyroid surgery. Chirurg. 2006;77(1):6-14, http://dx.doi.org/10.1007/s00104-005-1118-7.
-
(2006)
Chirurg
, vol.77
, Issue.1
, pp. 6-14
-
-
Frilling, A.1
Weber, F.2
-
20
-
-
42049121908
-
Update on the molecular diagnosis of endocrine tumors: Toward-omics-based personalized healthcare?
-
Weber F, Eng C. Update on the molecular diagnosis of endocrine tumors: toward-omics-based personalized healthcare? J Clin Endocrinol Metab. 2008;93(4):1097-104, http://dx.doi.org/10.1210/jc.2008-0212.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, Issue.4
, pp. 1097-1104
-
-
Weber, F.1
Eng, C.2
-
21
-
-
0032894774
-
RET proto-oncogene in the development of human cancer
-
Eng C. RET proto-oncogene in the development of human cancer. J Clin Oncol. 1999;17(1):380-93.
-
(1999)
J Clin Oncol
, vol.17
, Issue.1
, pp. 380-393
-
-
Eng, C.1
-
22
-
-
0028807798
-
Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma
-
discussion 1103-4
-
Frilling A, Dralle H, Eng C, Raue F, Broelsch CE. Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma. Surgery. 1995;118(6):1099-103; discussion 1103-4, http://dx.doi.org/10.1016/S0039-6060(05)80120-5
-
(1995)
Surgery
, vol.118
, Issue.6
, pp. 1099-1103
-
-
Frilling, A.1
Dralle, H.2
Eng, C.3
Raue, F.4
Broelsch, C.E.5
-
23
-
-
4644256817
-
The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis
-
Eng C, Clayton D, Schuffenecker I, Lenoir G, Cote G, Gagel RF, et al. The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. JAMA. 1996;276(19):1575-9.
-
(1996)
JAMA
, vol.276
, Issue.19
, pp. 1575-1579
-
-
Eng, C.1
Clayton, D.2
Schuffenecker, I.3
Lenoir, G.4
Cote, G.5
Gagel, R.F.6
-
24
-
-
58249114021
-
Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC. TGG) mutation
-
Milos IN, Frank-Raue K, Wohllk N, Maia AL, Pusiol E, Patocs A, et al. Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC. TGG) mutation. Endocr Relat Cancer. 2008;15(4):1035-41, http://dx.doi.org/10.1677/ERC-08-0105.
-
(2008)
Endocr Relat Cancer
, vol.15
, Issue.4
, pp. 1035-1041
-
-
Milos, I.N.1
Frank-Raue, K.2
Wohllk, N.3
Maia, A.L.4
Pusiol, E.5
Patocs, A.6
-
25
-
-
27744515971
-
Editorial: Germline variants within RET: Clinical utility or scientific playtoy?
-
Weber F, Eng C. Editorial: germline variants within RET: clinical utility or scientific playtoy? J Clin Endocrinol Metab. 2005;90(11):6334-6, http://dx.doi.org/10.1210/jc.2005-2030.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, Issue.11
, pp. 6334-6336
-
-
Weber, F.1
Eng, C.2
-
26
-
-
66949149437
-
Evaluation of RET polymorphisms in a six-generation family with G533C RET mutation: Specific RET variants may modulate age at onset and clinical presentation
-
Tamanaha R, Camacho CP, Pereira AC, da Silva AM, Maciel RM, Cerutti JM. Evaluation of RET polymorphisms in a six-generation family with G533C RET mutation: specific RET variants may modulate age at onset and clinical presentation. Clin Endocrinol (Oxf). 2009;71(1):56-64, http://dx.doi.org/10.1111/j.1365-2265.2008.03491.x.
-
(2009)
Clin Endocrinol (Oxf)
, vol.71
, Issue.1
, pp. 56-64
-
-
Tamanaha, R.1
Camacho, C.P.2
Pereira, A.C.3
da Silva, A.M.4
Maciel, R.M.5
Cerutti, J.M.6
-
27
-
-
79959355075
-
Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease
-
Jiang Q, Ho YY, Hao L, Nichols Berrios C, Chakravarti A. Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease. PLoS One. 2011;6(6):e21219.
-
(2011)
PLoS One
, vol.6
, Issue.6
-
-
Jiang, Q.1
Ho, Y.Y.2
Hao, L.3
Nichols Berrios, C.4
Chakravarti, A.5
-
28
-
-
70350217774
-
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients
-
Erlic Z, Rybicki L, Peczkowska M, Golcher H, Kann PH, Brauckhoff M, et al. Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. Clin Cancer Res. 2009;15(20):6378-85, http://dx.doi.org/10.1158/1078-0432.CCR-09-1237.
-
(2009)
Clin Cancer Res
, vol.15
, Issue.20
, pp. 6378-6385
-
-
Erlic, Z.1
Rybicki, L.2
Peczkowska, M.3
Golcher, H.4
Kann, P.H.5
Brauckhoff, M.6
-
29
-
-
4944220064
-
Malignant pheochromocytoma: Current status and initiatives for future progress
-
Eisenhofer G, Bornstein SR, Brouwers FM, Cheung NK, Dahia PL, de Krijger RR, et al. Malignant pheochromocytoma: current status and initiatives for future progress. Endocr Relat Cancer. 2004;11(3):423-36, http://dx.doi.org/10.1677/erc.1.00829.
-
(2004)
Endocr Relat Cancer
, vol.11
, Issue.3
, pp. 423-436
-
-
Eisenhofer, G.1
Bornstein, S.R.2
Brouwers, F.M.3
Cheung, N.K.4
Dahia, P.L.5
de Krijger, R.R.6
-
30
-
-
0034183813
-
Familial papillary thyroid cancer: Many syndromes, too many genes?
-
Eng C. Familial papillary thyroid cancer: many syndromes, too many genes? J Clin Endocrinol Metab. 2000;85(5):1755-7, http://dx.doi.org/10.1210/jc.85.5.1755.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, Issue.5
, pp. 1755-1757
-
-
Eng, C.1
-
31
-
-
78650412570
-
Mendelian genetics of rare-andnot so rare-cancers
-
Eng C. Mendelian genetics of rare-andnot so rare-cancers. Ann NY Acad Sci. 2010;1214:70-82.
-
(2010)
Ann NY Acad Sci
, vol.1214
, pp. 70-82
-
-
Eng, C.1
-
32
-
-
77953686253
-
Common alleles of predisposition in endocrine neoplasia
-
Eng C. Common alleles of predisposition in endocrine neoplasia. Curr Opin Genet Dev. 2010;20(3):251-6.
-
(2010)
Curr Opin Genet Dev
, vol.20
, Issue.3
, pp. 251-256
-
-
Eng, C.1
-
33
-
-
6344277885
-
Cribriform-morular variant of papillary thyroid carcinoma: Clue to early detection of familial adenomatous polyposis-associated colon cancer
-
Tomoda C, Miyauchi A, Uruno T, Takamura Y, Ito Y, Miya A, et al. Cribriform-morular variant of papillary thyroid carcinoma: clue to early detection of familial adenomatous polyposis-associated colon cancer. World J Surg. 2004;28(9):886-9, http://dx.doi.org/10.1007/s00268-004-7475-4.
-
(2004)
World J Surg
, vol.28
, Issue.9
, pp. 886-889
-
-
Tomoda, C.1
Miyauchi, A.2
Uruno, T.3
Takamura, Y.4
Ito, Y.5
Miya, A.6
-
34
-
-
55749095542
-
The clinical characteristics of Werner syndrome: Molecular and biochemical diagnosis
-
Muftuoglu M, Oshima J, von Kobbe C, Cheng WH, Leistritz DF, Bohr VA. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis. Hum Genet. 2008;124(4):369-77, http://dx.doi.org/10.1007/s00439-008-0562-0.
-
(2008)
Hum Genet
, vol.124
, Issue.4
, pp. 369-377
-
-
Muftuoglu, M.1
Oshima, J.2
von Kobbe, C.3
Cheng, W.H.4
Leistritz, D.F.5
Bohr, V.A.6
-
35
-
-
0030835716
-
Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)
-
Stratakis CA, Courcoutsakis NA, Abati A, Filie A, Doppman JL, Carney JA, et al. Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex). J Clin Endocrinol Metab. 1997;82(7):2037-43, http://dx.doi.org/10.1210/jc.82.7.2037.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, Issue.7
, pp. 2037-2043
-
-
Stratakis, C.A.1
Courcoutsakis, N.A.2
Abati, A.3
Filie, A.4
Doppman, J.L.5
Carney, J.A.6
-
36
-
-
40149103527
-
Two common and three novel PDS mutations in Thai patients with Pendred syndrome
-
Snabboon T, Plengpanich W, Saengpanich S, Sirisalipoch S, Keelawat S, Sunthornyothin S, et al. Two common and three novel PDS mutations in Thai patients with Pendred syndrome. J Endocrinol Invest. 2007;30(11):907-13.
-
(2007)
J Endocrinol Invest
, vol.30
, Issue.11
, pp. 907-913
-
-
Snabboon, T.1
Plengpanich, W.2
Saengpanich, S.3
Sirisalipoch, S.4
Keelawat, S.5
Sunthornyothin, S.6
-
37
-
-
0032930663
-
Familial papillary thyroid carcinoma is genetically distinct from familial adenomatous polyposis coli
-
Malchoff CD, Sarfarazi M, Tendler B, Forouhar F, Whalen G, Malchoff DM. Familial papillary thyroid carcinoma is genetically distinct from familial adenomatous polyposis coli. Thyroid. 1999;9(3):247-52, http://dx.doi.org/10.1089/thy.1999.9.247.
-
(1999)
Thyroid
, vol.9
, Issue.3
, pp. 247-252
-
-
Malchoff, C.D.1
Sarfarazi, M.2
Tendler, B.3
Forouhar, F.4
Whalen, G.5
Malchoff, D.M.6
-
38
-
-
26244435937
-
Familial risks for nonmedullary thyroid cancer
-
Hemminki K, Eng C, Chen B. Familial risks for nonmedullary thyroid cancer. J Clin Endocrinol Metab. 2005;90(10):5747-53, http://dx.doi.org/10.1210/jc.2005-0935.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, Issue.10
, pp. 5747-5753
-
-
Hemminki, K.1
Eng, C.2
Chen, B.3
-
39
-
-
0028143018
-
Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands
-
Goldgar DE, Easton DF, Cannon-Albright LA, Skolnick MH. Systematic population-based assessment of cancer risk in first-degree relatives of cancer probands. J Natl Cancer Inst. 1994;86(21):1600-8.
-
(1994)
J Natl Cancer Inst
, vol.86
, Issue.21
, pp. 1600-1608
-
-
Goldgar, D.E.1
Easton, D.F.2
Cannon-Albright, L.A.3
Skolnick, M.H.4
-
40
-
-
33645471193
-
On the prevalence of familial nonmedullary thyroid cancer in multiply affected kindreds
-
Charkes ND. On the prevalence of familial nonmedullary thyroid cancer in multiply affected kindreds. Thyroid. 2006;16(2):181-6, http://dx.doi.org/10.1089/thy.2006.16.181.
-
(2006)
Thyroid
, vol.16
, Issue.2
, pp. 181-186
-
-
Charkes, N.D.1
-
41
-
-
8744316712
-
Clinical genetic counselling for familial cancers requires reliable data on familial cancer risks and general action plans
-
Hemminki K, Eng C. Clinical genetic counselling for familial cancers requires reliable data on familial cancer risks and general action plans. J Med Genet. 2004;41(11):801-7, http://dx.doi.org/10.1136/jmg.2004.022731.
-
(2004)
J Med Genet
, vol.41
, Issue.11
, pp. 801-807
-
-
Hemminki, K.1
Eng, C.2
-
42
-
-
78349270927
-
Familial nonmedullary thyroid cancer: A review of the genetics
-
Khan A, Smellie J, Nutting C, Harrington K, Newbold K. Familial nonmedullary thyroid cancer: a review of the genetics. Thyroid. 2010; 20(7):795-801.
-
(2010)
Thyroid
, vol.20
, Issue.7
, pp. 795-801
-
-
Khan, A.1
Smellie, J.2
Nutting, C.3
Harrington, K.4
Newbold, K.5
-
43
-
-
0033305017
-
Genetic heterogeneity in familial nonmedullary thyroid carcinoma: Exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium
-
Lesueur F, Stark M, Tocco T, Ayadi H, Delisle MJ, Goldgar DE, et al. Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium. J Clin Endocrinol Metab. 1999;84(6):2157-62, http://dx.doi.org/10.1210/jc.84.6.2157.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, Issue.6
, pp. 2157-2162
-
-
Lesueur, F.1
Stark, M.2
Tocco, T.3
Ayadi, H.4
Delisle, M.J.5
Goldgar, D.E.6
-
44
-
-
16944363399
-
Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer
-
Bignell GR, Canzian F, Shayeghi M, Stark M, Shugart YY, Biggs P, et al. Familial nontoxic multinodular thyroid goiter locus maps to chromosome 14q but does not account for familial nonmedullary thyroid cancer. Am J Hum Genet. 1997;61(5):1123-30, http://dx.doi.org/10.1086/301610.
-
(1997)
Am J Hum Genet
, vol.61
, Issue.5
, pp. 1123-1130
-
-
Bignell, G.R.1
Canzian, F.2
Shayeghi, M.3
Stark, M.4
Shugart, Y.Y.5
Biggs, P.6
-
45
-
-
0034455744
-
Papillary thyroid carcinoma associated with papillary renal neoplasia: Genetic linkage analysis of a distinct heritable tumor syndrome
-
Malchoff CD, Sarfarazi M, Tendler B, Forouhar F, Whalen G, Joshi V, et al. Papillary thyroid carcinoma associated with papillary renal neoplasia: genetic linkage analysis of a distinct heritable tumor syndrome. J Clin Endocrinol Metab. 2000;85(5):1758-64, http://dx.doi.org/10.1210/jc.85.5.1758.
-
(2000)
J Clin Endocrinol Metab
, vol.85
, Issue.5
, pp. 1758-1764
-
-
Malchoff, C.D.1
Sarfarazi, M.2
Tendler, B.3
Forouhar, F.4
Whalen, G.5
Joshi, V.6
-
46
-
-
0034917504
-
Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21
-
McKay JD, Lesueur F, Jonard L, Pastore A, Williamson J, Hoffman L, et al. Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21. Am J Hum Genet. 2001;69(2):440-6, http://dx.doi.org/10.1086/321979.
-
(2001)
Am J Hum Genet
, vol.69
, Issue.2
, pp. 440-446
-
-
McKay, J.D.1
Lesueur, F.2
Jonard, L.3
Pastore, A.4
Williamson, J.5
Hoffman, L.6
-
47
-
-
57349123714
-
Mapping a new familial thyroid epithelial neoplasia susceptibility locus to chromosome 8p23.1-p22 by high-density single-nucleotide polymorphism genome-wide linkage analysis
-
Cavaco BM, Batista PF, Sobrinho LG, Leite V. Mapping a new familial thyroid epithelial neoplasia susceptibility locus to chromosome 8p23.1-p22 by high-density single-nucleotide polymorphism genome-wide linkage analysis. J Clin Endocrinol Metab. 2008;93(11):4426-30, http://dx.doi.org/10.1210/jc.2008-0449.
-
(2008)
J Clin Endocrinol Metab
, vol.93
, Issue.11
, pp. 4426-4430
-
-
Cavaco, B.M.1
Batista, P.F.2
Sobrinho, L.G.3
Leite, V.4
-
48
-
-
41349093968
-
Familial non-medullary thyroid carcinoma (FNMTC): Analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations
-
Cavaco BM, Batista PF, Martins C, Banito A, do Rosario F, Limbert E, et al. Familial non-medullary thyroid carcinoma (FNMTC): analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations. Endocr Relat Cancer. 2008;15(1):207-15, http://dx.doi.org/10.1677/ERC-07-0214.
-
(2008)
Endocr Relat Cancer
, vol.15
, Issue.1
, pp. 207-215
-
-
Cavaco, B.M.1
Batista, P.F.2
Martins, C.3
Banito, A.4
do Rosario, F.5
Limbert, E.6
-
49
-
-
0030896374
-
Familial nonmedullary thyroid carcinoma: A meta-review of case series
-
Loh KC. Familial nonmedullary thyroid carcinoma: a meta-review of case series. Thyroid. 1997;7(1):107-13, http://dx.doi.org/10.1089/thy.1997.7.107.
-
(1997)
Thyroid
, vol.7
, Issue.1
, pp. 107-113
-
-
Loh, K.C.1
-
50
-
-
0031032242
-
Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid
-
Burgess JR, Duffield A, Wilkinson SJ, Ware R, Greenaway TM, Percival J, et al. Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid. J Clin Endocrinol Metab. 1997;82(2):345-8, http://dx.doi.org/10.1210/jc.82.2.345.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, Issue.2
, pp. 345-348
-
-
Burgess, J.R.1
Duffield, A.2
Wilkinson, S.J.3
Ware, R.4
Greenaway, T.M.5
Percival, J.6
-
51
-
-
58249103027
-
Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity
-
Capezzone M, Marchisotta S, Cantara S, Busonero G, Brilli L, Pazaitou-Panayiotou K, et al. Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity. Endocr Relat Cancer. 2008;15(4):1075-81, http://dx.doi.org/10.1677/ERC-08-0080.
-
(2008)
Endocr Relat Cancer
, vol.15
, Issue.4
, pp. 1075-1081
-
-
Capezzone, M.1
Marchisotta, S.2
Cantara, S.3
Busonero, G.4
Brilli, L.5
Pazaitou-Panayiotou, K.6
-
52
-
-
0033675763
-
Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series
-
discussion 50-1
-
Alsanea O, Wada N, Ain K, Wong M, Taylor K, Ituarte PH, et al. Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series. Surgery. 2000;128(6):1043-50; discussion 50-1, http://dx.doi.org/10.1067/msy.2000.110848
-
(2000)
Surgery
, vol.128
, Issue.6
, pp. 1043-1050
-
-
Alsanea, O.1
Wada, N.2
Ain, K.3
Wong, M.4
Taylor, K.5
Ituarte, P.H.6
-
53
-
-
0036691719
-
Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population
-
Uchino S, Noguchi S, Kawamoto H, Yamashita H, Watanabe S, Shuto S. Familial nonmedullary thyroid carcinoma characterized by multifocality and a high recurrence rate in a large study population. World J Surg. 2002;26(8):897-902, http://dx.doi.org/10.1007/s00268-002-6615-y.
-
(2002)
World J Surg
, vol.26
, Issue.8
, pp. 897-902
-
-
Uchino, S.1
Noguchi, S.2
Kawamoto, H.3
Yamashita, H.4
Watanabe, S.5
Shuto, S.6
-
54
-
-
78651284482
-
Clinical characteristics and outcome of familial nonmedullary thyroid cancer: A retrospective controlled study
-
Robenshtok E, Tzvetov G, Grozinsky-Glasberg S, Shraga-Slutzky I, Weinstein R, Lazar L, et al. Clinical characteristics and outcome of familial nonmedullary thyroid cancer: a retrospective controlled study. Thyroid. 2011;21(1):43-8.
-
(2011)
Thyroid
, vol.21
, Issue.1
, pp. 43-48
-
-
Robenshtok, E.1
Tzvetov, G.2
Grozinsky-Glasberg, S.3
Shraga-Slutzky, I.4
Weinstein, R.5
Lazar, L.6
-
55
-
-
57149113140
-
Biological behavior and prognosis of familial papillary thyroid carcinoma
-
Ito Y, Kakudo K, Hirokawa M, Fukushima M, Yabuta T, Tomoda C, et al. Biological behavior and prognosis of familial papillary thyroid carcinoma. Surgery. 2009;145(1):100-5, http://dx.doi.org/10.1016/j.surg.2008.08.004.
-
(2009)
Surgery
, vol.145
, Issue.1
, pp. 100-105
-
-
Ito, Y.1
Kakudo, K.2
Hirokawa, M.3
Fukushima, M.4
Yabuta, T.5
Tomoda, C.6
-
56
-
-
79851493086
-
Effect of direct-to-consumer genomewide profiling to assess disease risk
-
Bloss CS, Schork NJ, Topol EJ. Effect of direct-to-consumer genomewide profiling to assess disease risk. N Engl J Med. 2011;364(6):524-34.
-
(2011)
N Engl J Med
, vol.364
, Issue.6
, pp. 524-534
-
-
Bloss, C.S.1
Schork, N.J.2
Topol, E.J.3
-
57
-
-
33845875992
-
Cancer phenomics: RET and PTEN as illustrative models
-
Zbuk KM, Eng C. Cancer phenomics: RET and PTEN as illustrative models. Nat Rev Cancer. 2007;7(1):35-45, http://dx.doi.org/10.1038/nrc2037.
-
(2007)
Nat Rev Cancer
, vol.7
, Issue.1
, pp. 35-45
-
-
Zbuk, K.M.1
Eng, C.2
|