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Reece Hart
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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
11262016
Analysis and application of potential energy smoothing and search methods for global optimization
RV Pappu, RK Hart, JW Ponder
The Journal of Physical Chemistry B 102 (48), 9725-9742, 1998
3051998
Functional characterization of the Bcl-2 gene family in the zebrafish
E Kratz, PM Eimon, K Mukhyala, H Stern, J Zha, A Strasser, R Hart, ...
Cell Death & Differentiation 13 (10), 1631-1640, 2006
1432006
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
CA Brownstein, AH Beggs, N Homer, B Merriman, TW Yu, KC Flannery, ...
Genome biology 15 (3), 1-18, 2014
1082014
VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions
PJ Freeman, RK Hart, LJ Gretton, AJ Brookes, R Dalgleish
Human mutation 39 (1), 61-68, 2018
702018
Somatic cancer variant curation and harmonization through consensus minimum variant level data
DI Ritter, S Roychowdhury, A Roy, S Rao, MJ Landrum, D Sonkin, ...
Genome Medicine 8 (1), 1-9, 2016
542016
Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13
JH Eubanks, L Selleri, R Hart, C Rosette, GA Evans
Genomics 11 (3), 720-729, 1991
411991
Exploring the similarities between potential smoothing and simulated annealing
RK Hart, RV Pappu, JW Ponder
Journal of Computational Chemistry 21 (7), 531-552, 2000
402000
GA4GH: International policies and standards for data sharing across genomic research and healthcare
HL Rehm, AJH Page, L Smith, JB Adams, G Alterovitz, LJ Babb, ...
Cell genomics 1 (2), 100029, 2021
372021
Systematic and fully automated identification of protein sequence patterns
RK Hart, AK Royyuru, G Stolovitzky, A Califano
Journal of Computational Biology 7 (3-4), 585-600, 2000
332000
TINKER-Software Tools for Molecular Design, Washington University, St
JW Ponder, S Rubenstein, C Kundrot, S Huston, M Dudek, Y Kong, R Hart, ...
Louis http://dasher. wustl. edu, 1999
331999
A Python package for parsing, validating, mapping and formatting sequence variants using HGVS nomenclature
RK Hart, R Rico, E Hare, J Garcia, J Westbrook, VA Fusaro
Bioinformatics 31 (2), 268-270, 2015
302015
Systematic and automated discovery of patterns in PROSITE families
R Hart, AK Royyuru, G Stolovitzky, A Califano
Proceedings of the fourth annual international conference on Computational …, 2000
202000
hgvs: a Python package for manipulating sequence variants using HGVS nomenclature: 2018 update
M Wang, KM Callenberg, R Dalgleish, A Fedtsov, NK Fox, PJ Freeman, ...
Human mutation 39 (12), 1803-1813, 2018
152018
The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification
AH Wagner, L Babb, G Alterovitz, M Baudis, M Brush, DL Cameron, ...
Cell genomics 1 (2), 100027, 2021
102021
The GA4GH variation representation specification (VRS): a computational framework for the precise representation and federated identification of molecular variation
AH Wagner, L Babb, G Alterovitz, M Baudis, M Brush, DL Cameron, ...
BioRxiv, 2021
72021
Unison: an integrated platform for computational biology discovery
RK Hart, K Mukhyala
Biocomputing 2009, 403-414, 2009
72009
SeqRepo: A system for managing local collections of biological sequences
RK Hart, A Prlić
PloS one 15 (12), e0239883, 2020
52020
Pathogenicity interpretation in the Age of precision medicine: the 2015 annual scientific meeting of the human genome variation society
WS Oetting, SE Brenner, AJ Brookes, MS Greenblatt, RK Hart, R Karchin, ...
Human mutation 37 (4), 406, 2016
52016
Methods and compositions relating to zpa polypeptides
AJ Ashkenazi, R Hart, E Kratz, K Mukhyala
US Patent App. 12/299,449, 2010
52010
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Articles 1–20