David Housman

1.7k total citations
20 papers, 1.1k citations indexed

About

David Housman is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, David Housman has authored 20 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in David Housman's work include Genomics and Chromatin Dynamics (4 papers), Genetic Neurodegenerative Diseases (3 papers) and Animal Genetics and Reproduction (3 papers). David Housman is often cited by papers focused on Genomics and Chromatin Dynamics (4 papers), Genetic Neurodegenerative Diseases (3 papers) and Animal Genetics and Reproduction (3 papers). David Housman collaborates with scholars based in United States, United Kingdom and Italy. David Housman's co-authors include Scott W. Lowe, H. Earl Ruley, Tyler Jacks, John M. Essigmann, S. L. BRUHN, Stephen J. Lippard, Vincent P. Stanton, E N Geissler, Robert Levenson and Hiroyuki Aburatani and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and Cellular and Molecular Life Sciences.

In The Last Decade

David Housman

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
David Housman United States 15 837 290 211 109 86 20 1.1k
Suresh Shenoy United States 17 948 1.1× 271 0.9× 179 0.8× 73 0.7× 124 1.4× 27 1.4k
Miriam Fuchs United States 10 1.7k 2.1× 419 1.4× 339 1.6× 72 0.7× 208 2.4× 10 2.0k
G. J. Todaro United States 9 565 0.7× 217 0.7× 114 0.5× 125 1.1× 110 1.3× 10 958
L J Cisek United States 8 756 0.9× 181 0.6× 139 0.7× 39 0.4× 64 0.7× 9 1.0k
Nathalie Scamuffa France 16 864 1.0× 176 0.6× 396 1.9× 67 0.6× 132 1.5× 21 1.4k
Yvonne Franke United States 16 807 1.0× 304 1.0× 160 0.8× 124 1.1× 243 2.8× 30 1.2k
Sharon Biton Israel 12 1.3k 1.5× 385 1.3× 123 0.6× 81 0.7× 192 2.2× 13 1.5k
Kevin A. W. Lee Hong Kong 19 1.1k 1.4× 193 0.7× 254 1.2× 82 0.8× 172 2.0× 33 1.5k
Valtteri Wirta Sweden 13 568 0.7× 321 1.1× 153 0.7× 54 0.5× 84 1.0× 40 1.1k
Yoshikazu Kurosawa Japan 20 540 0.6× 143 0.5× 131 0.6× 83 0.8× 152 1.8× 39 882

Countries citing papers authored by David Housman

Since Specialization
Citations

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

Fields of papers citing papers by David Housman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Housman

This figure shows the co-authorship network connecting the top 25 collaborators of David Housman. A scholar is included among the top collaborators of David Housman 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 Housman. David Housman 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.
Gayán, Javier, Denise Brocklebank, J. Michael Andresen, et al.. (2008). Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds. Genetic Epidemiology. 32(5). 445–453. 51 indexed citations
2.
Fluiter, Kees, David Housman, Anneloor L.M.A. ten Asbroek, & Frank Baas. (2003). Killing cancer by targeting genes that cancer cells have lost: Allele-specific inhibition, a novel approach to the treatment of genetic disorders. Cellular and Molecular Life Sciences. 60(5). 834–843. 11 indexed citations
3.
Chattopadhyay, Samit, et al.. (2000). SMAR1, a Novel, Alternatively Spliced Gene Product, Binds the Scaffold/Matrix-Associated Region at the T Cell Receptor β Locus. Genomics. 68(1). 93–96. 50 indexed citations
4.
Lloyd, S. J., Jeremy Brown, Susanne Gydesen, et al.. (1999). Molecular Genetic Characterisation of Frontotemporal Dementia on Chromosome 3. Dementia and Geriatric Cognitive Disorders. 10(Suppl. 1). 93–101. 44 indexed citations
5.
Antonarakis, Stylianos E., Jean‐Louis Blouin, Virginia K. Lasseter, et al.. (1999). Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21. American Journal of Medical Genetics. 88(4). 348–351. 30 indexed citations
6.
Beckers, Marie‐Claire, Eduardo Diez, Céline Morissette, et al.. (1997). High-Resolution Linkage Map of Mouse Chromosome 13 in the Vicinity of the Host Resistance LocusLgn1. Genomics. 39(3). 254–263. 19 indexed citations
7.
Aburatani, Hiroyuki, Vincent P. Stanton, & David Housman. (1996). High-resolution physical mapping by combined Alu-hybridization/PCR screening: construction of a yeast artificial chromosome map covering 31 centimorgans in 3p21-p14.. Proceedings of the National Academy of Sciences. 93(9). 4474–4479. 11 indexed citations
8.
Cai, Wei, et al.. (1995). Ordered restriction endonuclease maps of yeast artificial chromosomes created by optical mapping on surfaces.. Proceedings of the National Academy of Sciences. 92(11). 5164–5168. 94 indexed citations
9.
Lowe, Scott W., Tyler Jacks, David Housman, & H. Earl Ruley. (1994). Abrogation of oncogene-associated apoptosis allows transformation of p53-deficient cells.. Proceedings of the National Academy of Sciences. 91(6). 2026–2030. 252 indexed citations
10.
Snell, Russell G., Lynn Doucette‐Stamm, Stacy Taylor, et al.. (1993). The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library. Human Molecular Genetics. 2(3). 305–309. 14 indexed citations
11.
Haas, Melanie, et al.. (1993). Isolation and FISH Mapping of 80 Cosmid Clones on the Short Arm of Human Chromosome 3. Genomics. 16(1). 90–96. 6 indexed citations
12.
Królewski, Andrzej S., Bozena Krolewski, Mark R. Gray, et al.. (1992). High-frequency DNA sequence polymorphisms in the insulin receptor gene detected by denaturing gradient gel blots. Genomics. 12(4). 705–709. 10 indexed citations
13.
14.
Geissler, E N, J. David Brook, Francis H. Martin, et al.. (1991). Stem cell factor (SCF), a novel hematopoietic growth factor and ligand for c-kit tyrosine kinase receptor, maps on human chromosome 12 between 12q14.3 and 12qter. Somatic Cell and Molecular Genetics. 17(2). 207–214. 67 indexed citations
15.
Brilliant, Murray H., Gábor Szabó, Zoya Katarova, et al.. (1990). Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10. Genomics. 6(1). 115–122. 35 indexed citations
16.
Morse, Helvise G., et al.. (1987). Analysis of human chromosome 11 by somatic cell genetics: Reexamination of derivatives of human-hamster cell line J1. Somatic Cell and Molecular Genetics. 13(4). 293–304. 18 indexed citations
17.
Kent, Rachel B., Dorothy Fallows, E N Geissler, et al.. (1987). Genes encoding alpha and beta subunits of Na,K-ATPase are located on three different chromosomes in the mouse.. Proceedings of the National Academy of Sciences. 84(15). 5369–5373. 107 indexed citations
18.
Levenson, Robert, Vincent R. Racaniello, Lorraine M. Albritton, & David Housman. (1984). Molecular cloning of the mouse ouabain-resistance gene.. Proceedings of the National Academy of Sciences. 81(5). 1489–1493. 39 indexed citations
19.
Gusella, J.F., Carol Jones, Fa‐Ten Kao, David Housman, & Theodore T. Puck. (1982). Genetic fine-structure mapping in human chromosome 11 by use of repetitive DNA sequences.. Proceedings of the National Academy of Sciences. 79(24). 7804–7808. 49 indexed citations
20.
Nathan, D G, et al.. (1978). 637 TWO CLASSES OF HUMAN EKYTHROID BURST FORMING UNITS WITH DIFFERENT RESPONSES TO ERYTHROPOIETIN (EPO): BFU-EA AND BFU-Ef. Pediatric Research. 12. 470–470. 1 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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