Paul J Goodfellow
Paul J Goodfellow
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Cited by
Cited by
Integrated genomic characterization of endometrial carcinoma.
LDA Cancer Genome Atlas Research Network., Kandoth C, Schultz N, Cherniack ...
Nature 497, 67-73, 201
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
H Donis-Keller, S Dou, D Chi, KM Carlson, K Toshima, TC Lairmore, ...
Human molecular genetics 2 (7), 851-856, 1993
Genome remodelling in a basal-like breast cancer metastasis and xenograft
LI Ding, MJ Ellis, S Li, DE Larson, K Chen, JW Wallis, CC Harris, ...
Nature 464 (7291), 999-1005, 2010
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.
KM Carlson, S Dou, D Chi, N Scavarda, K Toshima, CE Jackson, ...
Proceedings of the National Academy of Sciences 91 (4), 1579-1583, 1994
DICER1 mutations in familial pleuropulmonary blastoma
DA Hill, J Ivanovich, JR Priest, CA Gurnett, LP Dehner, D Desruisseau, ...
Science 325 (5943), 965-965, 2009
Prevalence and spectrum of germline cancer susceptibility gene mutations among patients with early-onset colorectal cancer
R Pearlman, WL Frankel, B Swanson, W Zhao, A Yilmaz, K Miller, ...
JAMA oncology 3 (4), 464-471, 2017
Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage
NE Simpson, KK Kidd, PJ Goodfellow, H McDermid, S Myers, JR Kidd, ...
Nature 328 (6130), 528-530, 1987
MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic endometrial cancers
SB Simpkins, T Bocker, EM Swisher, DG Mutch, DJ Gersell, AJ Kovatich, ...
Human molecular genetics 8 (4), 661-666, 1999
Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
PM Pollock, MG Gartside, LC Dejeza, MA Powell, MA Mallon, H Davies, ...
Oncogene 26 (50), 7158-7162, 2007
A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene
AJ Whelan, D Bartsch, PJ Goodfellow
New England Journal of Medicine 333 (15), 975-977, 1995
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
RL Milne, KB Kuchenbaecker, K Michailidou, J Beesley, S Kar, ...
Nature genetics 49 (12), 1767-1778, 2017
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer
CA Haiman, GK Chen, CM Vachon, F Canzian, A Dunning, RC Millikan, ...
Nature genetics 43 (12), 1210-1214, 2011
The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia
C Braybrook, K Doudney, ACB Marçano, A Arnason, A Bjornsson, ...
Nature genetics 29 (2), 179-183, 2001
Epigenetic Repression of microRNA-129-2 Leads to Overexpression of SOX4 Oncogene in Endometrial Cancer
YW Huang, JC Liu, DE Deatherage, J Luo, DG Mutch, PJ Goodfellow, ...
Cancer research 69 (23), 9038-9046, 2009
Use of mutation profiles to refine the classification of endometrial carcinomas
MK McConechy, J Ding, MCU Cheang, KC Wiegand, J Senz, AA Tone, ...
The Journal of pathology 228 (1), 20-30, 2012
Integrated analysis of germline and somatic variants in ovarian cancer
KL Kanchi, KJ Johnson, C Lu, MD McLellan, MDM Leiserson, MC Wendl, ...
Nature communications 5 (1), 3156, 2014
Germline and somatic tumor testing in epithelial ovarian cancer: ASCO guideline
PA Konstantinopoulos, B Norquist, C Lacchetti, D Armstrong, RN Grisham, ...
Journal of clinical oncology: official journal of the American Society of …, 2020
Patterns and functional implications of rare germline variants across 12 cancer types.
Nature Communications 6 (10086), 2015
Parent-of-origin effects in multiple endocrine neoplasia type 2B.
KM Carlson, J Bracamontes, CE Jackson, R Clark, A Lacroix, SA Wells Jr, ...
American journal of human genetics 55 (6), 1076, 1994
Ovarian and endometrial endometrioid carcinomas have distinct CTNNB1 and PTEN mutation profiles
MK McConechy, J Ding, J Senz, W Yang, N Melnyk, AA Tone, LM Prentice, ...
Modern pathology 27 (1), 128-134, 2014
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