Mark Hills

1.7k total citations
20 papers, 1.1k citations indexed

About

Mark Hills is a scholar working on Molecular Biology, Physiology and Plant Science. According to data from OpenAlex, Mark Hills has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 9 papers in Physiology and 8 papers in Plant Science. Recurrent topics in Mark Hills's work include Telomeres, Telomerase, and Senescence (9 papers), Chromosomal and Genetic Variations (7 papers) and CRISPR and Genetic Engineering (5 papers). Mark Hills is often cited by papers focused on Telomeres, Telomerase, and Senescence (9 papers), Chromosomal and Genetic Variations (7 papers) and CRISPR and Genetic Engineering (5 papers). Mark Hills collaborates with scholars based in Canada, Netherlands and United Kingdom. Mark Hills's co-authors include Peter M. Lansdorp, Geraldine Aubert, Ester Falconer, Ashley D. Sanders, Hilda A. Pickett, Dimitri Conomos, Michael D. Stutz, Roger R. Reddel, Elizabeth A. Chavez and Diana C.J. Spierings and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Mark Hills

20 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mark Hills Canada 16 772 566 186 169 117 20 1.1k
Ma Wan United States 10 1.3k 1.7× 564 1.0× 93 0.5× 139 0.8× 78 0.7× 12 1.5k
Andrés Canela United States 10 1.1k 1.4× 336 0.6× 197 1.1× 148 0.9× 99 0.8× 11 1.3k
Marta Garcı́a-Cao Spain 9 1.3k 1.7× 829 1.5× 164 0.9× 123 0.7× 176 1.5× 11 1.7k
Serge Bauwens France 18 1.0k 1.3× 697 1.2× 239 1.3× 64 0.4× 38 0.3× 26 1.3k
Hazel A. Cruickshanks United Kingdom 9 810 1.0× 284 0.5× 118 0.6× 89 0.5× 106 0.9× 10 969
Maria L. Naylor United States 11 878 1.1× 407 0.7× 137 0.7× 76 0.4× 154 1.3× 32 1.2k
Deqiang Ding China 12 466 0.6× 214 0.4× 160 0.9× 81 0.5× 81 0.7× 24 682
Fermı́n A. Goytisolo Spain 8 769 1.0× 671 1.2× 125 0.7× 53 0.3× 62 0.5× 8 994
Anwaar Ahmad United States 9 811 1.1× 174 0.3× 154 0.8× 111 0.7× 182 1.6× 13 1.1k
Zhizhuo Zhang Singapore 11 576 0.7× 206 0.4× 61 0.3× 151 0.9× 93 0.8× 12 749

Countries citing papers authored by Mark Hills

Since Specialization
Citations

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

Fields of papers citing papers by Mark Hills

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Hills

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

All Works

20 of 20 papers shown
1.
Hills, Mark, Ester Falconer, Kieran O’Neill, et al.. (2021). Construction of Whole Genomes from Scaffolds Using Single Cell Strand-Seq Data. International Journal of Molecular Sciences. 22(7). 3617–3617. 8 indexed citations
2.
Sanders, Ashley D., Ester Falconer, Mark Hills, Diana C.J. Spierings, & Peter M. Lansdorp. (2017). Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs. Nature Protocols. 12(6). 1151–1176. 65 indexed citations
3.
O’Neill, Kieran, et al.. (2017). Assembling draft genomes using contiBAIT. Bioinformatics. 33(17). 2737–2739. 7 indexed citations
4.
Sanders, Ashley D., Mark Hills, David Porubský, et al.. (2016). Characterizing polymorphic inversions in human genomes by single-cell sequencing. Genome Research. 26(11). 1575–1587. 43 indexed citations
5.
Porubský, David, Ashley D. Sanders, Niek van Wietmarschen, et al.. (2016). Direct chromosome-length haplotyping by single-cell sequencing. Genome Research. 26(11). 1565–1574. 34 indexed citations
6.
Hills, Mark, Hyesook Kim, Hyun‐Seok Oh, et al.. (2015). Telomere maintenance through recruitment of internal genomic regions. Nature Communications. 6(1). 8189–8189. 24 indexed citations
7.
Hills, Mark, Kieran O’Neill, Ester Falconer, Ryan R. Brinkman, & Peter M. Lansdorp. (2013). BAIT: Organizing genomes and mapping rearrangements in single cells. Genome Medicine. 5(9). 82–82. 20 indexed citations
8.
Lee, Michael, Mark Hills, Dimitri Conomos, et al.. (2013). Telomere extension by telomerase and ALT generates variant repeats by mechanistically distinct processes. Nucleic Acids Research. 42(3). 1733–1746. 75 indexed citations
9.
Falconer, Ester, Mark Hills, Ulrike Naumann, et al.. (2012). DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution. Nature Methods. 9(11). 1107–1112. 113 indexed citations
10.
Conomos, Dimitri, Michael D. Stutz, Mark Hills, et al.. (2012). Variant repeats are interspersed throughout the telomeres and recruit nuclear receptors in ALT cells. The Journal of Cell Biology. 199(6). 893–906. 111 indexed citations
11.
Maltby, Vicki E., Benjamín Martín, Julie Brind’Amour, et al.. (2012). Histone H3K4 demethylation is negatively regulated by histone H3 acetylation in Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences. 109(45). 18505–18510. 48 indexed citations
12.
Aubert, Geraldine, Mark Hills, & Peter M. Lansdorp. (2011). Telomere length measurement—Caveats and a critical assessment of the available technologies and tools. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 730(1-2). 59–67. 253 indexed citations
13.
Hills, Mark, et al.. (2009). Probing the mitotic history and developmental stage of hematopoietic cells using single telomere length analysis (STELA). Blood. 113(23). 5765–5775. 32 indexed citations
14.
Calado, Rodrigo T., Joshua A. Regal, Mark Hills, et al.. (2009). Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia. Proceedings of the National Academy of Sciences. 106(4). 1187–1192. 125 indexed citations
15.
Méndez-Bermúdez, Aarón, Mark Hills, Hilda A. Pickett, et al.. (2009). Human telomeres that contain (CTAGGG)n repeats show replication dependent instability in somatic cells and the male germline. Nucleic Acids Research. 37(18). 6225–6238. 33 indexed citations
16.
Hills, Mark & Peter M. Lansdorp. (2009). Short Telomeres Resulting from Heritable Mutations in the Telomerase Reverse Transcriptase Gene Predispose for a Variety of Malignancies. Annals of the New York Academy of Sciences. 1176(1). 178–190. 28 indexed citations
17.
Goldman, Frederick D., Geraldine Aubert, Aloysius J. Klingelhutz, et al.. (2008). Characterization of primitive hematopoietic cells from patients with dyskeratosis congenita. Blood. 111(9). 4523–4531. 42 indexed citations
18.
19.
Maines‐Bandiera, Sarah, Wen‐Lin Kuo, Yinghui Guan, et al.. (2007). Multiple roles of the candidate oncogene ZNF217 in ovarian epithelial neoplastic progression. International Journal of Cancer. 120(9). 1863–1873. 37 indexed citations
20.
Calado, Rodrigo T., Joshua A. Regal, William T. Yewdell, et al.. (2007). Constitutional Loss-of-Function Mutations in Telomerase Are Genetic Risk Factors for Acute Myeloid Leukemia.. Blood. 110(11). 16–16. 4 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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