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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
52411994
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
14412016
Database of p53 gene somatic mutations in human tumors and cell lines.
M Hollstein, K Rice, MS Greenblatt, T Soussi, R Fuchs, T Sørlie, E Hovig, ...
Nucleic acids research 22 (17), 3551, 1994
13551994
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
9932008
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
6941996
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
5212007
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), 107-115, 2014
4842014
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database
M Dominguez-Valentin, JR Sampson, TT Seppälä, SW Ten Broeke, ...
Genetics in Medicine 22 (1), 15-25, 2020
4832020
Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework
SV Tavtigian, MS Greenblatt, SM Harrison, RL Nussbaum, SA Prabhu, ...
Genetics in medicine 20 (9), 1054-1060, 2018
4012018
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
3991997
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework
SE Brnich, AN Abou Tayoun, FJ Couch, GR Cutting, MS Greenblatt, ...
Genome medicine 12, 1-12, 2020
3632020
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
2732001
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
2302008
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
2301999
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
2262008
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
2232005
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
1572007
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
1561996
Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria
V Pejaver, AB Byrne, BJ Feng, KA Pagel, SD Mooney, R Karchin, ...
The American Journal of Human Genetics 109 (12), 2163-2177, 2022
1262022
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
1252008
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