Richard Segraves

7.6k total citations · 3 hit papers
30 papers, 5.7k citations indexed

About

Richard Segraves is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Richard Segraves has authored 30 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 18 papers in Molecular Biology and 16 papers in Plant Science. Recurrent topics in Richard Segraves's work include Genomic variations and chromosomal abnormalities (20 papers), Chromosomal and Genetic Variations (16 papers) and Gene expression and cancer classification (7 papers). Richard Segraves is often cited by papers focused on Genomic variations and chromosomal abnormalities (20 papers), Chromosomal and Genetic Variations (16 papers) and Gene expression and cancer classification (7 papers). Richard Segraves collaborates with scholars based in United States, Denmark and United Kingdom. Richard Segraves's co-authors include Joe W. Gray, Colin C. Collins, Daniel Pinkel, Donna G. Albertson, James C. Fuscoe, D. Pinkel, Wen-Lin Kuo, Shanaz H. Dairkee, J. N. Lucas and David Kowbel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Blood.

In The Last Decade

Richard Segraves

28 papers receiving 5.6k 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.

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1998 1.6k citations Richard Segraves, Damir Sudar et al. Nature Genetics profile →
Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1988 1.1k citations D. Pinkel, J. E. Landegent et al. Proceedings of the National Academy of Sciences profile →
Assembly of microarrays for genome-wide measurement of DNA copy number

2001 712 citations Antoine M. Snijders, Richard Segraves et al. Nature Genetics profile →

Peers

Richard Segraves

GENET

PPCH

D. Pinkel United States

Anders Zetterberg Sweden

Dan Pinkel United States

Robert Lucito United States

Bryan D. Young United Kingdom

Jean Feunteun France

Bing Huey United States

Hesed Padilla‐Nash United States

Cynthia Helms United States

Adrian P. Bracken Ireland

D. Pinkel United States

Richard Segraves

1.5k ×0.4

GENET

2.5k ×0.7

960 ×0.5

925 ×0.8

312 ×0.4

PPCH

Citations per year, relative to Richard Segraves Richard Segraves (= 1×) peers D. Pinkel

Countries citing papers authored by Richard Segraves

Since Specialization

Citations

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

Fields of papers citing papers by Richard Segraves

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Richard Segraves

This figure shows the co-authorship network connecting the top 25 collaborators of Richard Segraves. A scholar is included among the top collaborators of Richard Segraves 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 Richard Segraves. Richard Segraves 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

Fridlyand, Jane, Antoine M. Snijders, Bauke Ylstra, et al.. (2006). Breast tumor copy number aberration phenotypes and genomic instability. BMC Cancer. 6(1). 96–96. 206 indexed citations

Zhang, Xiaoxiao, Antoine M. Snijders, Richard Segraves, et al.. (2005). High-Resolution Mapping of Genotype-Phenotype Relationships in Cri du Chat Syndrome Using Array Comparative Genomic Hybridization. The American Journal of Human Genetics. 76(2). 312–326. 95 indexed citations

DeVries, Sandy, Sarah J. Nyante, Richard Segraves, et al.. (2005). Array-Based Comparative Genomic Hybridization from Formalin-Fixed, Paraffin-Embedded Breast Tumors. Journal of Molecular Diagnostics. 7(1). 65–71. 50 indexed citations

Locke, Devin P., Richard Segraves, Robert D. Nicholls, et al.. (2004). BAC microarray analysis of 15q11–q13 rearrangements and the impact of segmental duplications. Journal of Medical Genetics. 41(3). 175–182. 79 indexed citations

Snijders, Antoine M., et al.. (2004). BAC Microarray-Based Comparative Genomic Hybridization. Humana Press eBooks. 256. 39–56. 27 indexed citations

Leamon, John H., Tanja Pejović, Stefan Hamann, et al.. (2003). Whole Genome Analysis of Genetic Alterations in Small DNA Samples Using Hyperbranched Strand Displacement Amplification and Array–CGH. Genome Research. 13(2). 294–307. 212 indexed citations

Locke, Devin P., Richard Segraves, Lucia Carbone, et al.. (2003). Large-Scale Variation Among Human and Great Ape Genomes Determined by Array Comparative Genomic Hybridization. Genome Research. 13(3). 347–357. 105 indexed citations

Snijders, Antoine M., Jane Fridlyand, Dorus A. Mans, et al.. (2003). Shaping of tumor and drug-resistant genomes by instability and selection. Oncogene. 22(28). 4370–4379. 61 indexed citations

Albertson, Donna G., Katherine A. Rauen, Philip D. Cotter, et al.. (2003). High-resolution array CGH A validation study for the detection of submicroscopic deletions in DiGeorge and velo-cardio-facial syndromes. The American Journal of Human Genetics. 73(5). 208. 1 indexed citations

10.

Jain, Ajay N., Taku A. Tokuyasu, Antoine M. Snijders, et al.. (2002). Fully Automatic Quantification of Microarray Image Data. Genome Research. 12(2). 325–332. 269 indexed citations

11.

Albertson, Donna G., Bauke Ylstra, Richard Segraves, et al.. (2000). Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene. Nature Genetics. 25(2). 144–146. 463 indexed citations

12.

Segraves, Richard, Damir Sudar, Steven M. Clark, et al.. (1998). High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Nature Genetics. 20(2). 207–211. 1617 indexed citations breakdown →

13.

Pinkel, Daniel, Richard Segraves, Damir Sudar, et al.. (1997). Comparative Genomic Hybridization to Dna Microarrays. Microscopy and Microanalysis. 3(S2). 205–206.

14.

Robbins, Wendie A., Richard Segraves, Daniel Pinkel, & Andrew J. Wyrobek. (1993). Detection of aneuploid human sperm by fluorescence in situ hybridization: evidence for a donor difference in frequency of sperm disomic for chromosomes 1 and Y.. Europe PMC (PubMed Central). 52(4). 799–807. 132 indexed citations

15.

Collins, Colin C., et al.. (1991). Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes. Genomics. 11(4). 997–1006. 187 indexed citations

16.

Brandriff, Brigitte, Laurie Gordon, Richard Segraves, & D. Pinkel. (1991). The male-derived genome after sperm-egg fusion: Spatial distribution of chromosomal DNA and paternal-maternal genomic association. Chromosoma. 100(4). 262–266. 30 indexed citations

17.

Weier, Heinz-Ulrich G., J. N. Lucas, M. Poggensee, et al.. (1991). Two-color hybridization with high complexity chromosome-specific probes and a degenerate alpha satellite probe DNA allows unambiguous discrimination between symmetrical and asymmetrical translocations. Chromosoma. 100(6). 371–376. 76 indexed citations

18.

Kuo, Wen-Lin, et al.. (1991). Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes.. PubMed. 49(1). 112–9. 100 indexed citations

19.

Weier, Heinz-Ulrich, Richard Segraves, D. Pinkel, & J. W. Gray. (1990). Synthesis of Y chromosome-specific labeled DNA probes by in vitro DNA amplification.. Journal of Histochemistry & Cytochemistry. 38(3). 421–426. 39 indexed citations

20.

Pinkel, D., J. E. Landegent, Colin C. Collins, et al.. (1988). Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.. Proceedings of the National Academy of Sciences. 85(23). 9138–9142. 1089 indexed citations breakdown →

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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