Barbara Hill

4.3k total citations · 1 hit paper
16 papers, 2.4k citations indexed

About

Barbara Hill is a scholar working on Molecular Biology, Biochemistry and Organic Chemistry. According to data from OpenAlex, Barbara Hill has authored 16 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Biochemistry and 4 papers in Organic Chemistry. Recurrent topics in Barbara Hill's work include Sulfur Compounds in Biology (5 papers), Drug Transport and Resistance Mechanisms (4 papers) and Synthesis and Characterization of Heterocyclic Compounds (2 papers). Barbara Hill is often cited by papers focused on Sulfur Compounds in Biology (5 papers), Drug Transport and Resistance Mechanisms (4 papers) and Synthesis and Characterization of Heterocyclic Compounds (2 papers). Barbara Hill collaborates with scholars based in United States, Canada and Netherlands. Barbara Hill's co-authors include Steven E. Schumacher, Rameen Beroukhim, Craig H. Mermel, Matthew Meyerson, Gad Getz, Terrence J. Monks, R. J. Highet, S S Lau, Jeffrey A. Silverman and Serrine S. Lau and has published in prestigious journals such as Bioinformatics, Genome biology and Molecular Pharmacology.

In The Last Decade

Barbara Hill

16 papers receiving 2.4k 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.

GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers

2011 2.0k citations Craig H. Mermel, Steven E. Schumacher et al. Genome biology profile →

Peers

Barbara Hill

PRM

ONCOL

PFM

Laura A. Marlow United States

Shawn Brisbay United States

Elaine Kilgour United Kingdom

K. Shanker India

Huiqin Chen United States

Akiko Kokubu Japan

Ronglai Shen United States

Peter Buechler Germany

Iain D. Miller United Kingdom

Daniel Escuín Spain

Laura A. Marlow United States

Barbara Hill

1.7k ×1.2

773 ×0.7

472 ×0.7

PRM

776 ×1.2

ONCOL

154 ×0.6

PFM

Citations per year, relative to Barbara Hill Barbara Hill (= 1×) peers Laura A. Marlow

Countries citing papers authored by Barbara Hill

Since Specialization

Citations

This map shows the geographic impact of Barbara Hill'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 Barbara Hill with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Hill more than expected).

Fields of papers citing papers by Barbara Hill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara Hill. 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 Barbara Hill. The network helps show where Barbara Hill may publish in the future.

Co-authorship network of co-authors of Barbara Hill

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Hill. A scholar is included among the top collaborators of Barbara Hill 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 Barbara Hill. Barbara Hill is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Gao, Galen F., Coyin Oh, Gordon Saksena, et al.. (2022). Tangent normalization for somatic copy-number inference in cancer genome analysis. Bioinformatics. 38(20). 4677–4686. 4 indexed citations

Reich, Michael, Ted Liefeld, Helga Thorvaldsdóttir, et al.. (2017). The GenePattern Notebook Environment. Cell Systems. 5(2). 149–151.e1. 20 indexed citations

Špidlen, Josef, Karin Breuer, Peter A. Carr, et al.. (2013). GenePattern flow cytometry suite. PubMed. 8(1). 14–14. 13 indexed citations

Reich, Michael, Ted Liefeld, Marco Ocana, et al.. (2013). GenomeSpace: an environment for frictionless bioinformatics. 4. 2 indexed citations

Mermel, Craig H., Steven E. Schumacher, Barbara Hill, et al.. (2011). GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers. Genome biology. 12(4). R41–R41. 2008 indexed citations breakdown →

Hill, Barbara, et al.. (1998). Disorders of genetic origin in dogs. Canine Inherited Disorders Database in progress.. PubMed. 39(11). 686–7. 5 indexed citations

Hill, Barbara, Paul C. Brown, Karl‐Heinz Preisegger, & Jeffrey A. Silverman. (1996). Regulation of mdrlb gene expression in Fischer, Wistar and Sprague-Dawley rats in vivo and in vitro. Carcinogenesis. 17(3). 451–457. 32 indexed citations

Silverman, Jeffrey A. & Barbara Hill. (1995). Characterization of the basal and carcinogen regulatory elements of the rat mdr1b promoter. Molecular Carcinogenesis. 13(1). 50–59. 31 indexed citations

Rivera, María I., et al.. (1994). Metabolism and toxicity of 2-bromo-(diglutathion-S-yl)-hydroquinone and 2-bromo-3-(glutathion-S-yl)hydroquinone in the in situ perfused rat kidney.. Drug Metabolism and Disposition. 22(4). 503–510. 5 indexed citations

10.

Hill, Barbara, et al.. (1993). Identification of multi-S-substituted conjugates of hydroquinone by HPLC-coulometric electrode array analysis and mass spectroscopy. Chemical Research in Toxicology. 6(4). 459–469. 44 indexed citations

11.

Hill, Barbara, et al.. (1992). The effects of 2,3,5-(triglutathion-S-yl)hydroquinone on renal mitochondrial respiratory function in vivo and in vitro: Possible role in cytotoxicity. Toxicology and Applied Pharmacology. 117(2). 165–171. 16 indexed citations

12.

Hill, Barbara, et al.. (1991). The Role of γ-Glutamyl Transpeptidase in Hydroquinone-Glutathione Conjugate Mediated Nephrotoxicity. Advances in experimental medicine and biology. 283. 749–751. 9 indexed citations

13.

Monks, Terrence J., et al.. (1991). Nephrotoxicity of 2-bromo-(cystein-s-yl) hydroquinone and 2-bromo-(N-acetyl-l-cystein-S-yl) hydroquinone thioethers. Toxicology and Applied Pharmacology. 111(2). 279–298. 12 indexed citations

14.

Lau, Serrine S., et al.. (1990). Species differences in renal γ-glutamyl transpeptidase activity do not correlate with susceptibility to 2-bromo-(diglutathion-S-yl)-hydroquinone nephrotoxicity. Toxicology. 64(3). 291–311. 17 indexed citations

15.

Lau, Serrine S., Thomas W. Jones, R. J. Highet, Barbara Hill, & Terrence J. Monks. (1990). Differences in the localization and extent of the renal proximal tubular necrosis caused by mercapturic acid and glutathione conjugates of 1,4-naphthoquinone and menadione. Toxicology and Applied Pharmacology. 104(2). 334–350. 29 indexed citations

16.

Lau, S S, Barbara Hill, R. J. Highet, & Terrence J. Monks. (1988). Sequential oxidation and glutathione addition to 1,4-benzoquinone: correlation of toxicity with increased glutathione substitution.. Molecular Pharmacology. 34(6). 769–778. 146 indexed citations

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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