Reece K. Hart

3.4k total citations · 1 hit paper
18 papers, 1.7k citations indexed

About

Reece K. Hart is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Reece K. Hart has authored 18 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Reece K. Hart's work include Genomics and Rare Diseases (8 papers), Genomics and Phylogenetic Studies (6 papers) and Protein Structure and Dynamics (3 papers). Reece K. Hart is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genomics and Phylogenetic Studies (6 papers) and Protein Structure and Dynamics (3 papers). Reece K. Hart collaborates with scholars based in United States, United Kingdom and Netherlands. Reece K. Hart's co-authors include Raymond Dalgleish, Johan T. den Dunnen, Donna Maglott, Jean McGowan‐Jordan, Anne‐Françoise Roux, Peter E.M. Taschner, Stylianos E. Antonarakis, Marc S. Greenblatt, Tim D. Smith and Rohit V. Pappu and has published in prestigious journals such as Bioinformatics, PLoS ONE and The Journal of Physical Chemistry B.

In The Last Decade

Reece K. Hart

18 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

2016 1.0k citations Johan T. den Dunnen, Raymond Dalgleish et al. Human Mutation profile →

Peers

Countries citing papers authored by Reece K. Hart

Since Specialization

Citations

This map shows the geographic impact of Reece K. Hart's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Reece K. Hart with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Reece K. Hart more than expected).

Fields of papers citing papers by Reece K. Hart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Reece K. Hart. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Reece K. Hart. The network helps show where Reece K. Hart may publish in the future.

Co-authorship network of co-authors of Reece K. Hart

This figure shows the co-authorship network connecting the top 25 collaborators of Reece K. Hart. A scholar is included among the top collaborators of Reece K. Hart based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Reece K. Hart. Reece K. Hart is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	HGVS Nomenclature 2024: improvements to community engagement, usability, and computability 2024 ·Genome Medicine ·Reece K. Hart, Ivo F.A.C. Fokkema, Marina T. DiStefano, Ros Hastings, Jeroen F. J. Laros, Rachel L. Taylor, Alex H. Wagner, Johan T. den Dunnen	7
2	Development and application of a computable genotype model in the GA4GH Variation Representation Specification 2022 ·PubMed ·(unknown), Lawrence Babb, Srikar Chamala, Melissa Cline, Robert R. Freimuth, Reece K. Hart, Kori Kuzma, Jennifer Lee, Tristan Nelson, Andreas Prlić, Kevin Riehle, (unknown), (unknown), Andrew Yates, Heidi L. Rehm, Alex H. Wagner	2
3	SeqRepo: A system for managing local collections of biological sequences 2020 ·PLoS ONE ·Reece K. Hart, Andreas Prlić	4
4	hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update 2018 ·Human Mutation ·Meng Wang, Keith M. Callenberg, Raymond Dalgleish, (unknown), Naomi K. Fox, Peter Freeman, Kevin B. Jacobs, (unknown), Andrew McMurry, Andreas Prlić, (unknown), Reece K. Hart	16
5	VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions 2017 ·Human Mutation ·Peter Freeman, Reece K. Hart, (unknown), Anthony J. Brookes, Raymond Dalgleish	99
6	Somatic cancer variant curation and harmonization through consensus minimum variant level data 2016 ·Genome Medicine ·(unknown), Deborah Ritter, Sameek Roychowdhury, Angshumoy Roy, Shruti Rao, Melissa Landrum, Dmitriy Sonkin, Mamatha Shekar, Caleb Davis, Reece K. Hart, Christine Micheel, Meredith Weaver, Eliezer M. Van Allen, D. Williams Parsons, Howard L. McLeod, Michael S. Watson, Sharon E. Plon, Shashikant Kulkarni, Subha Madhavan	42
7	HGVS Recommendations for the Description of Sequence Variants: 2016 Update breakdown → 2016 ·Human Mutation ·Johan T. den Dunnen, Raymond Dalgleish, Donna Maglott, Reece K. Hart, Marc S. Greenblatt, Jean McGowan‐Jordan, Anne‐Françoise Roux, Tim D. Smith, Stylianos E. Antonarakis, Peter E.M. Taschner	1035
8	HGVS Recommendations for the Description of Sequence Variants 2016 ·Johan T. den Dunnen, Raymond Dalgleish, Donna Maglott, Reece K. Hart, Marc S. Greenblatt, Jean McGowan‐Jordan, Anne‐Françoise Roux, Timothy P. L. Smith, Stylianos E. Antonarakis, Peter E.M. Taschner	20
9	Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation Society 2016 ·Human Mutation ·William S. Oetting, Steven E. Brenner, Anthony J. Brookes, Marc S. Greenblatt, Reece K. Hart, Rachel Karchin, Shamil Sunyaev, Peter E.M. Taschner	5
10	A Python package for parsing, validating, mapping and formatting sequence variants using HGVS nomenclature 2014 ·Bioinformatics ·Reece K. Hart, (unknown), Emily E. Hare, John Garcia, (unknown), Vincent A. Fusaro	24
11	UNISON: AN INTEGRATED PLATFORM FOR COMPUTATIONAL BIOLOGY DISCOVERY 2008 ·PubMed ·Reece K. Hart, Kiran Mukhyala	5
12	Functional characterization of the Bcl-2 gene family in the zebrafish 2006 ·Cell Death and Differentiation ·Erica Kratz, Peter M. Eimon, Kiran Mukhyala, Howard M. Stern, J. Zha, Andreas Strasser, Reece K. Hart, Avi Ashkenazi	118
13	Systematic and automated discovery of patterns in PROSITE families 2000 ·Reece K. Hart, Ajay K. Royyuru, Gustavo Stolovitzky, Andrea Califano	11
14	Exploring the similarities between potential smoothing and simulated annealing 2000 ·Journal of Computational Chemistry ·Reece K. Hart, Rohit V. Pappu, Jay W. Ponder	21
15	Systematic and Fully Automated Identification of Protein Sequence Patterns 2000 ·Journal of Computational Biology ·Reece K. Hart, Ajay K. Royyuru, Gustavo Stolovitzky, Andrea Califano	18
16	Analysis and Application of Potential Energy Smoothing and Search Methods for Global Optimization 1998 ·The Journal of Physical Chemistry B ·Rohit V. Pappu, Reece K. Hart, Jay W. Ponder	221
17	MD-directed critical pathways: it's time. 1992 ·PubMed ·Reece K. Hart, (unknown)	22
18	Isolation, localization, and physical mapping of a highly polymorphic locus on human chromosome 11q13 1991 ·Genomics ·James H. Eubanks, Licia Selleri, Reece K. Hart, Caridad Rosette, Glen A. Evans	29

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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