Deborah G. Phillips

1.4k total citations · 1 hit paper
9 papers, 1.1k citations indexed

About

Deborah G. Phillips is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Deborah G. Phillips has authored 9 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Hematology, 6 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Deborah G. Phillips's work include Hemophilia Treatment and Research (6 papers), Cancer-related gene regulation (6 papers) and Blood Coagulation and Thrombosis Mechanisms (4 papers). Deborah G. Phillips is often cited by papers focused on Hemophilia Treatment and Research (6 papers), Cancer-related gene regulation (6 papers) and Blood Coagulation and Thrombosis Mechanisms (4 papers). Deborah G. Phillips collaborates with scholars based in United States. Deborah G. Phillips's co-authors include Hagop Youssoufian, Stylianos E. Antonarakis, Haig H. Kazazian, Alan F. Scott, Corinne Wong, S Aronis, Valerie A. Brown, H H Kazazian, Michael Dean and Mark Leppert and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Deborah G. Phillips

8 papers receiving 1.0k citations

Hit Papers

Haemophilia A resulting from de novo insertion of L1 sequ... 1988 2026 2000 2013 1988 200 400 600

Peers

Deborah G. Phillips
L.L. Deaven United States
Jurgen Kooren Netherlands
Anne Fertitta United States
P. Wong United States
Peter M. Green United Kingdom
Roy Drissen United Kingdom
Bonnie Burgess-Beusse United States
Deborah G. Phillips
Citations per year, relative to Deborah G. Phillips Deborah G. Phillips (= 1×) peers Ángel Martínez‐Ramírez

Countries citing papers authored by Deborah G. Phillips

Since Specialization
Citations

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

Fields of papers citing papers by Deborah G. Phillips

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah G. Phillips. 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 Deborah G. Phillips. The network helps show where Deborah G. Phillips may publish in the future.

Co-authorship network of co-authors of Deborah G. Phillips

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

All Works

9 of 9 papers shown
1.
Kazazian, Haig H., Deborah G. Phillips, Carol E. Dowling, & Corinne D. Boehm. (1989). Prenatal Diagnosis of Sickle Cell Anemia—1988. Annals of the New York Academy of Sciences. 565(1). 44–47. 5 indexed citations
2.
Youssoufian, Hagop, Carol K. Kasper, Deborah G. Phillips, Haig H. Kazazian, & Stylianos E. Antonarakis. (1988). Restriction endonuclease mapping of six novel deletions of the factor VIII gene in hemophilia A. Human Genetics. 80(2). 143–148. 13 indexed citations
3.
Kazazian, Haig H., Corinne Wong, Hagop Youssoufian, et al.. (1988). Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. Nature. 332(6160). 164–166. 690 indexed citations breakdown →
4.
Dean, Michael, P. O’Connell, Mark Leppert, et al.. (1987). Three additional DNA polymorphisms in the met gene and D7S8 locus: Use in prenatal diagnosis of cystic fibrosis. The Journal of Pediatrics. 111(4). 490–495. 29 indexed citations
5.
Youssoufian, Hagop, Deborah G. Phillips, Haig H. Kazazian, & Stylianos E. Antonarakis. (1987). Mspl polymorphism in the 3′ flanking region of the human factor VIII gene. Nucleic Acids Research. 15(15). 6312–6312. 26 indexed citations
6.
Youssoufian, Hagop, et al.. (1987). Characterization of five partial deletions of the factor VIII gene.. Proceedings of the National Academy of Sciences. 84(11). 3772–3776. 79 indexed citations
7.
Youssoufian, Hagop, Achyut S. Patel, Deborah G. Phillips, H H Kazazian, & Stylianos E. Antonarakis. (1987). HEMOPHILIA A: RECURRENT MUTATIONS AND AN UNUSUAL DELETION. Pediatric Research. 21(4). 296A–296A. 1 indexed citations
8.
Youssoufian, Hagop, Haig H. Kazazian, Deborah G. Phillips, et al.. (1986). Recurrent mutations in haemophilia A give evidence for CpG mutation hotspots. Nature. 324(6095). 380–382. 226 indexed citations
9.
Antonarakis, Stylianos E., Hagop Youssoufian, Carol E. Dowling, et al.. (1986). Comparison of Deficiency Alleles of the  -Globin and Factor VIII:C Genes: New Lessons from a Giant Gene. Cold Spring Harbor Symposia on Quantitative Biology. 51(0). 371–379. 3 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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