Marc Greenblatt
Marc Greenblatt
Associate Professor of Medicine, University of Vermont
Verified email at vtmednet.org
Title
Cited by
Cited by
Year
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
46641994
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
11801994
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
6102008
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
6061996
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
5022016
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
3882007
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
3721997
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
3232014
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
2252001
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
2041999
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
1962005
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
1912008
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
1782008
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
1502007
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
1351996
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
1052008
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
982000
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
932003
The human variome project
RGH Cotton, AD Auerbach, M Axton, CI Barash, SF Berkovic, AJ Brookes, ...
Science 322 (5903), 861-862, 2008
852008
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
842013
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