David I. Hoar

1.6k total citations
57 papers, 1.3k citations indexed

About

David I. Hoar is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, David I. Hoar has authored 57 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Immunology. Recurrent topics in David I. Hoar's work include DNA Repair Mechanisms (8 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Immune Cell Function and Interaction (7 papers). David I. Hoar is often cited by papers focused on DNA Repair Mechanisms (8 papers), Carcinogens and Genotoxicity Assessment (7 papers) and Immune Cell Function and Interaction (7 papers). David I. Hoar collaborates with scholars based in Canada and United States. David I. Hoar's co-authors include Noreen L. Rudd, Ursula Hennig, Linda Madisen, Margaret Crisp, James F. Reynolds, M. E. Hodes, Paul Keown, P. A. Sargent, Robert Balshaw and Carol Waghorne and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

David I. Hoar

57 papers receiving 1.3k citations

Peers

David I. Hoar

GENET

IMMUN

K L Blanchard United States

R.T. Taggart United States

Hidenobu Takahashi Japan

Claude Besmond France

FS Collins United States

Alain Kitzis France

Þórunn Rafnar Iceland

Renate Hellmiss United States

Massimo P. Crippa Italy

Jiehong Pan United States

K L Blanchard United States

David I. Hoar

988 ×1.5

265 ×0.8

GENET

243 ×1.3

214 ×1.3

IMMUN

74 ×0.5

Citations per year, relative to David I. Hoar David I. Hoar (= 1×) peers K L Blanchard

Countries citing papers authored by David I. Hoar

Since Specialization

Citations

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

Fields of papers citing papers by David I. Hoar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David I. Hoar. 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 David I. Hoar. The network helps show where David I. Hoar may publish in the future.

Co-authorship network of co-authors of David I. Hoar

This figure shows the co-authorship network connecting the top 25 collaborators of David I. Hoar. A scholar is included among the top collaborators of David I. Hoar 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 David I. Hoar. David I. Hoar 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

Hoar, David I., et al.. (2001). Identification of four novel dinucleotide repeat polymorphisms in the IL-2 and IL-2β receptor genes. Human Immunology. 62(4). 368–370. 3 indexed citations

Hoar, David I., et al.. (1996). A novel DRβ1∗03 allele identified by polymerase chain reaction—Restriction fragment length polymorphism. Human Immunology. 46(1). 55–57. 5 indexed citations

Goodfellow, Paul J., et al.. (1993). A new HLA‐DRB1 allele formed by an intra‐exonic interallelic crossover. Tissue Antigens. 42(1). 141–143. 10 indexed citations

Chitayat, David, Kathleen Meagher‐Villemure, Orval Mamer, et al.. (1992). Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria. The Journal of Pediatrics. 121(1). 86–89. 31 indexed citations

Poon, Man‐Chiu, et al.. (1992). Identification of factor IX mutations in haemophilia B: application of polymerase chain reaction and single strand conformation analysis. Human Genetics. 88(4). 426–430. 11 indexed citations

Hoar, David I., et al.. (1992). Tentative assignment of gene for oto‐palato‐digital syndrome to distal Xq (Xq26–q28). American Journal of Medical Genetics. 42(2). 170–172. 12 indexed citations

Parslow, Malcolm, et al.. (1991). Genetic stability of the D1Z2 region: implications for DNA genotyping and paternity testing. Genome. 34(5). 733–738. 1 indexed citations

Hoar, David I., et al.. (1990). Ethnic-Specific Allelic Variation within the D1Z2 Locus. Human Heredity. 40(1). 1–14. 1 indexed citations

Rudd, Noreen L., David I. Hoar, Susan Williams, & Ursula Hennig. (1989). Genotype and the cryopreservation process affect the levels of aneuploidy and chromosome breakage in cultured human fibroblasts. Genome. 32(2). 196–202. 9 indexed citations

10.

Clark, Arthur W., Craig A. Krekoski, Irma M. Parhad, et al.. (1989). Altered expression of genes for amyloid and cytoskeletal proteins in alzheimer cortex. Annals of Neurology. 25(4). 331–339. 61 indexed citations

11.

Hoar, David I., et al.. (1989). Primate evolution of a human chromosome 1 hypervariable repetitive element. Journal of Molecular Evolution. 28(3). 212–219. 11 indexed citations

12.

Martin, Renée H., et al.. (1989). Assessment of the sephadex technique for selection of X-bearing human sperm by analysis of sperm chromosomes, deoxyribonucleic acid and Y-bodies. Fertility and Sterility. 52(5). 829–835. 27 indexed citations

13.

Hennig, Ursula, Noreen L. Rudd, & David I. Hoar. (1988). Kinetochore immunofluorescence in micronuclei: A rapid method for the in situ detection of aneuploidy and chromosome breakage in human fibroblasts. Mutation Research/Environmental Mutagenesis and Related Subjects. 203(6). 405–414. 78 indexed citations

14.

Matheson, David S., et al.. (1988). Studies on the mechanism of activation of human natural killer function by interferon and inhibitors of thymidylate synthesis. Cellular Immunology. 111(1). 118–125. 8 indexed citations

15.

Rudd, Noreen L., et al.. (1988). The use of DNA probes to establish parental origin in Down syndrome. Human Genetics. 78(2). 175–178. 16 indexed citations

16.

Rudd, Noreen L., et al.. (1988). Micronucleus assay in human fibroblasts: A measure of spontaneous chromosomal instability and mutagen hypersensitivity. Environmental Mutagenesis. 12(1). 3–13. 24 indexed citations

17.

Lowry, R. Brian, et al.. (1988). Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: A new X‐linked mental retardation syndrome. American Journal of Medical Genetics. 31(4). 741–751. 28 indexed citations

18.

Bickel, William S., et al.. (1987). Light scattering from fibers: An extension of a single-slit diffraction experiment. American Journal of Physics. 55(6). 555–559. 8 indexed citations

19.

Hoar, David I., et al.. (1979). Host-cell reactivation of UV-irradiated adenovirus in cockayne syndrome. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 62(3). 401–405. 12 indexed citations

20.

Hoar, David I.. (1970). Fertility Regulation in F-Like Resistance Transfer Factors. Journal of Bacteriology. 101(3). 916–920. 26 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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