Danielle V. Irvine

1.7k total citations
20 papers, 1.3k citations indexed

About

Danielle V. Irvine is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Danielle V. Irvine has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 15 papers in Plant Science and 7 papers in Genetics. Recurrent topics in Danielle V. Irvine's work include Chromosomal and Genetic Variations (14 papers), Genomics and Chromatin Dynamics (10 papers) and Genomic variations and chromosomal abnormalities (5 papers). Danielle V. Irvine is often cited by papers focused on Chromosomal and Genetic Variations (14 papers), Genomics and Chromatin Dynamics (10 papers) and Genomic variations and chromosomal abnormalities (5 papers). Danielle V. Irvine collaborates with scholars based in Australia, United States and France. Danielle V. Irvine's co-authors include Mikel Zaratiegui, Robert A. Martienssen, Richard Saffery, Derek B. Goto, K. H. Andy Choo, Matthew Vaughn, Paul Kalitsis, Elizabeth D. Earle, Michael Cancilla and Suzanne M. Cutts and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Danielle V. Irvine

20 papers receiving 1.3k citations

Peers

Danielle V. Irvine

MB

PS

GENET

CB

CR

Heather C. Gregson United States

Christian Valdes‐Quezada Netherlands

Masashi Ikeno Japan

Eric F. Joyce United States

Craig M. Hart United States

Brenda R. Grimes United States

G. Valentin Börner United States

Jun‐ichirou Ohzeki Japan

Brian R. Calvi United States

Martin Radolf Austria

Heather C. Gregson United States

Danielle V. Irvine

1.4k ×1.3

MB

457 ×0.7

PS

215 ×0.8

GENET

257 ×1.3

CB

66 ×0.6

CR

Citations per year, relative to Danielle V. Irvine Danielle V. Irvine (= 1×) peers Heather C. Gregson

Countries citing papers authored by Danielle V. Irvine

Since Specialization

Citations

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

Fields of papers citing papers by Danielle V. Irvine

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Danielle V. Irvine. 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 Danielle V. Irvine. The network helps show where Danielle V. Irvine may publish in the future.

Co-authorship network of co-authors of Danielle V. Irvine

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

All Works

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20 of 20 papers shown

1.

Zaratiegui, Mikel, Stephane E. Castel, Danielle V. Irvine, et al.. (2011). RNAi promotes heterochromatic silencing through replication-coupled release of RNA Pol II. Nature. 479(7371). 135–138. 129 indexed citations

2.

Zaratiegui, Mikel, Matthew Vaughn, Danielle V. Irvine, et al.. (2010). CENP-B preserves genome integrity at replication forks paused by retrotransposon LTR. Nature. 469(7328). 112–115. 73 indexed citations

3.

Irvine, Danielle V., Derek B. Goto, Matthew Vaughn, et al.. (2009). Mapping epigenetic mutations in fission yeast using whole-genome next-generation sequencing. Genome Research. 19(6). 1077–1083. 44 indexed citations

4.

Zaratiegui, Mikel, Danielle V. Irvine, & Robert A. Martienssen. (2007). Noncoding RNAs and Gene Silencing. Cell. 128(4). 763–776. 322 indexed citations

5.

Irvine, Danielle V., Mikel Zaratiegui, Niraj H. Tolia, et al.. (2006). Argonaute Slicing Is Required for Heterochromatic Silencing and Spreading. Science. 313(5790). 1134–1137. 152 indexed citations

6.

Irvine, Danielle V., Margaret Shaw, K. H. Andy Choo, & Richard Saffery. (2005). Engineering chromosomes for delivery of therapeutic genes. Trends in biotechnology. 23(12). 575–583. 22 indexed citations

7.

Irvine, Danielle V., David J. Amor, Jo K. Perry, et al.. (2004). Chromosome size and origin as determinants of the level of CENP-A incorporation into human centromeres. Chromosome Research. 12(8). 805–815. 47 indexed citations

8.

Voullaire, Lucille, Richard Saffery, Elizabeth D. Earle, et al.. (2001). Mosaic inv dup(8p) marker chromosome with stable neocentromere suggests neocentromerization is a post-zygotic event. American Journal of Medical Genetics. 102(1). 86–94. 26 indexed citations

9.

Saffery, Richard, Lee H. Wong, Danielle V. Irvine, et al.. (2001). Construction of neocentromere-based human minichromosomes by telomere-associated chromosomal truncation. Proceedings of the National Academy of Sciences. 98(10). 5705–5710. 63 indexed citations

10.

Barry, Alyssa E., Emily V. Howman, Michael Cancilla, et al.. (2000). The 10q25 Neocentromere and its Inactive Progenitor Have Identical Primary Nucleotide Sequence: Further Evidence for Epigenetic Modification. Genome Research. 10(6). 832–838. 35 indexed citations

11.

Saffery, Richard, et al.. (2000). Components of the human spindle checkpoint control mechanism localize specifically to the active centromere on dicentric chromosomes. Human Genetics. 107(4). 376–384. 18 indexed citations

12.

Saffery, Richard, Danielle V. Irvine, Benjamin T. Kile, et al.. (1999). Cloning, expression, and promoter structure of a mammalian Inner Centromere Protein (INCENP). Mammalian Genome. 10(4). 415–418. 8 indexed citations

13.

Saffery, Richard, Elizabeth D. Earle, Danielle V. Irvine, Paul Kalitsis, & K. H. Andy Choo. (1999). Conservation of Centromere Proteins in Vertebrates. Chromosome Research. 7(4). 261–265. 39 indexed citations

14.

Voullaire, Lucille, Richard Saffery, Elizabeth D. Earle, et al.. (1999). Trisomy 20p resulting from inverted duplication and neocentromere formation. American Journal of Medical Genetics. 85(4). 403–408. 31 indexed citations

15.

Voullaire, Lucille, Richard Saffery, Elizabeth D. Earle, et al.. (1999). Trisomy 20p resulting from inverted duplication and neocentromere formation. American Journal of Medical Genetics. 85(4). 403–408. 3 indexed citations

16.

Oates, Andrew C., Alison Brownlie, Stephen J. P. Pratt, et al.. (1999). Gene Duplication of Zebrafish JAK2 Homologs Is Accompanied by Divergent Embryonic Expression Patterns: Only jak2a Is Expressed During Erythropoiesis. Blood. 94(8). 2622–2636. 73 indexed citations

17.

Oates, Andrew C., et al.. (1998). Embryonic expression and activity of doughnut, a second RYK homolog in Drosophila. Mechanisms of Development. 78(1-2). 165–169. 16 indexed citations

18.

Fowler, Kerry J., Richard Saffery, Danielle V. Irvine, H.E. Trowell, & K.H. Andy Choo. (1998). Mouse centromere protein F (Cenpf) gene maps to the distal region of Chromosome 1 by interspecific backcross analysis. Cytogenetic and Genome Research. 82(3-4). 180–181. 2 indexed citations

19.

Fowler, Kerry J., Richard Saffery, Benjamin T. Kile, et al.. (1998). Genetic mapping of mouse centromere protein (Incenp and Cenpe) genes. Cytogenetic and Genome Research. 82(1-2). 67–70. 7 indexed citations

20.

Hudson, Damien F., Kerry J. Fowler, Elizabeth D. Earle, et al.. (1998). Centromere Protein B Null Mice are Mitotically and Meiotically Normal but Have Lower Body and Testis Weights. The Journal of Cell Biology. 141(2). 309–319. 202 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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