D Housman

845 total citations
15 papers, 680 citations indexed

About

D Housman is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, D Housman has authored 15 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Neurology. Recurrent topics in D Housman's work include Mitochondrial Function and Pathology (4 papers), Renal and related cancers (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). D Housman is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Renal and related cancers (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). D Housman collaborates with scholars based in United States, Canada and United Kingdom. D Housman's co-authors include Nicholas C. Dracopoli, Pauline T. Merrill, Conrad T. O. Fong, G M Brodeur, Peter S. White, Rogers C. Griffith, Ben Z. Stanger, Elise Rose, M. Kœnig and Eric S. Lander and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Annual Review of Neuroscience and Genome Research.

In The Last Decade

D Housman

15 papers receiving 667 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
D Housman United States	11	438	233	208	118	90	15	680
Ngan Ching Cheng Australia	13	681 1.6×	206 0.9×	186 0.9×	236 2.0×	109 1.2×	20	899
Keiko Tadokoro Japan	14	633 1.4×	94 0.4×	160 0.8×	50 0.4×	78 0.9×	19	856
Deborah Hughes United Kingdom	11	424 1.0×	102 0.4×	327 1.6×	95 0.8×	61 0.7×	11	792
J. Wasson United States	12	443 1.0×	197 0.8×	207 1.0×	71 0.6×	46 0.5×	13	764
Magali Fernandez United States	8	612 1.4×	122 0.5×	112 0.5×	185 1.6×	66 0.7×	9	863
Isuzu Ikeda Japan	9	292 0.7×	71 0.3×	85 0.4×	66 0.6×	137 1.5×	12	487
Shirley M. Myers Canada	13	380 0.9×	99 0.4×	188 0.9×	92 0.8×	218 2.4×	26	820
Loen M. Hansford Canada	15	417 1.0×	379 1.6×	94 0.5×	257 2.2×	237 2.6×	20	767
Renata Lonigro Italy	14	631 1.4×	53 0.2×	234 1.1×	49 0.4×	117 1.3×	23	952
Elisabeth Castellanos Spain	13	319 0.7×	144 0.6×	139 0.7×	95 0.8×	78 0.9×	26	620

Countries citing papers authored by D Housman

Since Specialization

Citations

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

Fields of papers citing papers by D Housman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D Housman

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

All Works

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15 of 15 papers shown

Hunter, Kent W., Laura Riba, Leonard C. Schalkwyk, et al.. (1996). Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics.. Genome Research. 6(4). 290–299. 14 indexed citations

Dackowski, William R., Timothy D. Connors, Vincent P. Stanton, et al.. (1996). The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval.. Genome Research. 6(6). 515–524. 8 indexed citations

Xu, Yali, et al.. (1995). Molecular characterization of a chromosome translocation breakpoint t(11;14)(p13;q11) from the cell line KOPT-K1.. PubMed. 9(11). 1812–7. 13 indexed citations

Ton, Carl C.T., Robert F. Mueller, Maria Luiza Petzl‐Erler, et al.. (1994). Absence of PAX6 Gene Mutations in Gillespie Syndrome (Partial Aniridia, Cerebellar Ataxia, and Mental Retardation). Genomics. 19(1). 145–148. 43 indexed citations

Stanger, Ben Z., et al.. (1992). The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice. Immunogenetics. 35(2). 97–101. 33 indexed citations

Krolewski, A S, Alessandro Doria, Jocelyne Magré, James H. Warram, & D Housman. (1992). Molecular genetic approaches to the identification of genes involved in the development of nephropathy in insulin-dependent diabetes mellitus.. Journal of the American Society of Nephrology. 3(4). S9–S9. 20 indexed citations

Rose, Elise, et al.. (1991). Molecular Approaches to Hereditary Diseases of the Nervous System: Huntington's Disease as a Paradigm. Annual Review of Neuroscience. 14(1). 503–529. 30 indexed citations

Hudson, John W., et al.. (1989). Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively. Genomics. 5(3). 510–521. 42 indexed citations

Driscoll, Daniel J., et al.. (1989). A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome. Genomics. 5(4). 880–893. 10 indexed citations

10.

Fong, Conrad T. O., Nicholas C. Dracopoli, Peter S. White, et al.. (1989). Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.. Proceedings of the National Academy of Sciences. 86(10). 3753–3757. 318 indexed citations

11.

Dracopoli, Nicholas C., Ben Z. Stanger, Caryn Y. Ito, et al.. (1988). A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I.. PubMed. 43(4). 462–70. 56 indexed citations

12.

Housman, D, et al.. (1986). Mapping of Human Chromosome 11: Organization of Genes within the Wilms' Tumor Region of the Chromosome. Cold Spring Harbor Symposia on Quantitative Biology. 51(0). 837–841. 4 indexed citations

13.

Bruns, G.A.P., et al.. (1985). Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.. PubMed. 37(2). 235–49. 76 indexed citations

14.

Wong, Wing C., et al.. (1982). Commitment of murine erythroleukemia (MEL) cells to terminal differentiation is associated with coordinated expression of globin and ribosomal genes.. PubMed. 102 pt A. 69–79. 8 indexed citations

15.

Housman, D & J.F. Gusella. (1982). Molecular genetic approaches to neural degenerative disorders. 415–422. 5 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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