Marc Greenblatt
Marc Greenblatt
Associate Professor of Medicine, University of Vermont
Verified email at
Cited by
Cited by
Mutations in the p53 tumor suppressor gene: clues to cancer etiology and molecular pathogenesis
MS Greenblatt, WP Bennett, M Hollstein, CC Harris
Cancer research 54 (18), 4855-4878, 1994
Database of p53 gene somatic mutations in human tumors and cell lines.
M Hollstein, K Rice, MS Greenblatt, T Soussi, R Fuchs, T Sřrlie, E Hovig, ...
Nucleic acids research 22 (17), 3551, 1994
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results
SE Plon, DM Eccles, D Easton, WD Foulkes, M Genuardi, MS Greenblatt, ...
Human mutation 29 (11), 1282-1291, 2008
Somatic point mutations in the p53 gene of human tumors and cell lines: updated compilation
M Hollstein, B Shomer, M Greenblatt, T Soussi, E Hovig, R Montesano, ...
Nucleic acids research 24 (1), 141-146, 1996
HGVS recommendations for the description of sequence variants: 2016 update
JT den Dunnen, R Dalgleish, DR Maglott, RK Hart, MS Greenblatt, ...
Human mutation 37 (6), 564-569, 2016
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer
P Kaurah, A MacMillan, N Boyd, J Senz, A De Luca, N Chun, G Suriano, ...
Jama 297 (21), 2360-2372, 2007
Database of p53 gene somatic mutations in human tumors and cell lines: updated compilation and future prospects
P Hainaut, T Soussi, B Shomer, M Hollstein, M Greenblatt, E Hovig, ...
Nucleic acids research 25 (1), 151-157, 1997
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database
BA Thompson, AB Spurdle, JP Plazzer, MS Greenblatt, K Akagi, ...
Nature genetics 46 (2), 107, 2014
TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations: distinctive spectrum and structural distribution
MS Greenblatt, PO Chappuis, JP Bond, N Hamel, WD Foulkes
Cancer research 61 (10), 4092-4097, 2001
Evolutionary conservation and somatic mutation hotspot maps of p53: correlation with p53 protein structural and functional features
DR Walker, JP Bond, RE Tarone, CC Harris, W Makalowski, MS Boguski, ...
Oncogene 18 (1), 211-218, 1999
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1
TE Raevaara, MK Korhonen, H Lohi, H Hampel, E Lynch, KE Lönnqvist, ...
Gastroenterology 129 (2), 537-549, 2005
In silico analysis of missense substitutions using sequence‐alignment based methods
SV Tavtigian, MS Greenblatt, F Lesueur, GB Byrnes, ...
Human mutation 29 (11), 1327-1336, 2008
Genetic evidence and integration of various data sources for classifying uncertain variants into a single model
DE Goldgar, DF Easton, GB Byrnes, AB Spurdle, ES Iversen, ...
Human mutation 29 (11), 1265-1272, 2008
Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR)
PA Chan, S Duraisamy, PJ Miller, JA Newell, C McBride, JP Bond, ...
Human mutation 28 (7), 683-693, 2007
Deletions and insertions in the p53 tumor suppressor gene in human cancers: confirmation of the DNA polymerase slippage/misalignment model
MS Greenblatt, AP Grollman, CC Harris
Cancer Research 56 (9), 2130-2136, 1996
Assessment of functional effects of unclassified genetic variants
FJ Couch, LJ Rasmussen, R Hofstra, ANA Monteiro, MS Greenblatt, ...
Human mutation 29 (11), 1314-1326, 2008
Defective nucleotide excision repair in xpc mutant mice and its association with cancer predisposition
EC Friedberg, JP Bond, DK Burns, DL Cheo, MS Greenblatt, LB Meira, ...
Mutation Research/DNA Repair 459 (2), 99-108, 2000
Detailed computational study of p53 and p16: using evolutionary sequence analysis and disease-associated mutations to predict the functional consequences of allelic variants
MS Greenblatt, JG Beaudet, JR Gump, KS Godin, L Trombley, J Koh, ...
Oncogene 22 (8), 1150-1163, 2003
The human variome project
RGH Cotton, AD Auerbach, M Axton, CI Barash, SF Berkovic, AJ Brookes, ...
Science 322 (5903), 861-862, 2008
Calibration of multiple in silico tools for predicting pathogenicity of mismatch repair gene missense substitutions
BA Thompson, MS Greenblatt, MP Vallee, JC Herkert, C Tessereau, ...
Human mutation 34 (1), 255-265, 2013
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