David E. Housman
Impact in
- Cellular and Molecular Neuroscience top 0.05%
- Genetic Neurodegenerative Diseases
- Oncology top 0.1%
- Drug Transport and Resistance Mechanisms
- Cancer-related Molecular Pathways
Papers in
-
- Genetic Neurodegenerative Diseases 65
- Genetics 98
- Genomic variations and chromosomal abnormalities 43
- Genetic Associations and Epidemiology 36
- Hemoglobinopathies and Related Disorders 22
- Co-authors
- Scott Lowe (5 shared papers)Tyler Jacks (5 shared papers)Philippe Gros (20 shared papers)H. Earl Ruley (3 shared papers)Jerry Pelletier (23 shared papers)James M. Croop (11 shared papers)Tom M. Glaser (18 shared papers)Daniel A. Haber (20 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (67 papers)Genomics (32 papers)Molecular and Cellular Biology (25 papers)Cell (19 papers)Nature Genetics (16 papers)
- Partner nations
- United StatesCanadaUnited Kingdom
In The Last Decade
David E. Housman
400 papers receiving 54.8k citations
David E. Housman's Hit Papers
Peers
Comparison fields: 5 of 184
- Cellular and Molecular Neuroscience 8.9k
- Oncology 8.4k
- Genetics 8.7k
- Molecular Biology 18.4k
- Hematology 3.1k
Countries citing papers authored by David E. Housman
This map shows the geographic impact of David E. 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 E. 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 E. Housman more than expected).
Fields of papers citing papers by David E. Housman
This network shows the impact of papers produced by David E. 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 E. Housman. The network helps show where David E. Housman may publish in the future.
Co-authors
The 25 scholars most cited alongside David E. Housman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 407 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | p53-dependent apoptosis modulates the cytotoxicity of anticancer agents Hit paper breakdown → | 1993 | 2609 |
| 2 | Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member Hit paper breakdown → | 1992 | 2366 |
| 3 | Hypoxia-mediated selection of cells with diminished apoptotic potential in solid tumours Hit paper breakdown → | 1996 | 2023 |
| 4 | Cloning of Human Mineralocorticoid Receptor Complementary DNA: Structural and Functional Kinship with the Glucocorticoid Receptor Hit paper breakdown → | 1987 | 1686 |
| 5 | Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus Hit paper breakdown → | 1990 | 1676 |
| 6 | WT-1 is required for early kidney development Hit paper breakdown → | 1993 | 1674 |
| 7 | p53 Status and the Efficacy of Cancer Therapy in Vivo Hit paper breakdown → | 1994 | 1302 |
| 8 | A Family of cAMP-Binding Proteins That Directly Activate Rap1 Hit paper breakdown → | 1998 | 1184 |
| 9 | High-Resolution Mapping of Human Chromosome 11 by in Situ Hybridization with Cosmid Clones Hit paper breakdown → | 1990 | 1171 |
| 10 | The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene Hit paper breakdown → | 1988 | 1155 |
| 11 | Histone deacetylase inhibitors arrest polyglutamine-dependent neurodegeneration in Drosophila Hit paper breakdown → | 2001 | 1052 |
| 12 | Mammalian multidrug resistance gene: Complete cDNA sequence indicates strong homology to bacterial transport proteins Hit paper breakdown → | 1986 | 950 |
| 13 | The Huntington's disease protein interacts with p53 and CREB-binding protein and represses transcription Hit paper breakdown → | 2000 | 909 |
| 14 | The candidate Wilms' tumour gene is involved in genitourinary development Hit paper breakdown → | 1990 | 757 |
| 15 | Isolation and expression of a complementary DNA that confers multidrug resistance Hit paper breakdown → | 1986 | 737 |
| 16 | Bipolar affective disorders linked to DNA markers on chromosome 11 Hit paper breakdown → | 1987 | 674 |
| 17 | The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB–binding protein Hit paper breakdown → | 1996 | 674 |
| 18 | Targeted integration of adeno‐associated virus (AAV) into human chromosome 19. Hit paper breakdown → | 1991 | 644 |
| 19 | Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy Hit paper breakdown → | 1992 | 627 |
| 20 | 1986 | 594 |
About David E. Housman
David E. Housman is a scholar working on Cellular and Molecular Neuroscience, Genetics, Molecular Biology, Genetics and Oncology, having authored 407 papers that have together received 58.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (65 papers), Genomic variations and chromosomal abnormalities (43 papers), Genetic Associations and Epidemiology (36 papers), Renal and related cancers (29 papers), Drug Transport and Resistance Mechanisms (24 papers), Hemoglobinopathies and Related Disorders (22 papers), Schizophrenia research and treatment (18 papers) and Acute Myeloid Leukemia Research (18 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (8.9k citations), Oncology (8.4k citations), Genetics (8.7k citations), Molecular Biology (18.4k citations) and Hematology (3.1k citations). David E. Housman has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Scott Lowe, Tyler Jacks, Philippe Gros, H. Earl Ruley, Jerry Pelletier, James M. Croop, Tom M. Glaser, Daniel A. Haber, Alan Buckler and Katherine M. Call. Their work appears in journals such as Proceedings of the National Academy of Sciences, Genomics, Molecular and Cellular Biology, Cell and Nature Genetics.
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.