Timothy Drumheller

838 total citations
10 papers, 662 citations indexed

About

Timothy Drumheller is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Timothy Drumheller has authored 10 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Surgery. Recurrent topics in Timothy Drumheller's work include Chromatin Remodeling and Cancer (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Heavy Metal Exposure and Toxicity (1 paper). Timothy Drumheller is often cited by papers focused on Chromatin Remodeling and Cancer (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Heavy Metal Exposure and Toxicity (1 paper). Timothy Drumheller collaborates with scholars based in United States, Sweden and Canada. Timothy Drumheller's co-authors include Birgit Claus Henn, Asa Bradman, Cynthia J. Curry, Dana Boyd Barr, Brenda Eskenazi, Gregory T. Wolf, Thomas E. Carey, Michael S. Benninger, D L Van Dyke and Maria J. Worsham and has published in prestigious journals such as Environmental Health Perspectives, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Timothy Drumheller

10 papers receiving 642 citations

Peers

Timothy Drumheller
Rebecca E. Slager United States
Paul E. Perry United Kingdom
Adéle Kruger United States
L. Renzi Italy
Alicia B. Moore United States
Diane Rebourcet United Kingdom
Margaux McBirney United States
Timothy Drumheller
Citations per year, relative to Timothy Drumheller Timothy Drumheller (= 1×) peers Shiari Nozawa

Countries citing papers authored by Timothy Drumheller

Since Specialization
Citations

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

Fields of papers citing papers by Timothy Drumheller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Timothy Drumheller

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

All Works

10 of 10 papers shown
1.
Takagishi, Jennifer, Katherine A. Rauen, Timothy Drumheller, Boris G. Kousseff, & Maxine J. Sutcliffe. (2006). Chromosome 3p25 deletion in mother and daughter with minimal phenotypic effect. American Journal of Medical Genetics Part A. 140A(14). 1587–1593. 17 indexed citations
2.
Bradman, Asa, Dana Boyd Barr, Birgit Claus Henn, et al.. (2003). Measurement of pesticides and other toxicants in amniotic fluid as a potential biomarker of prenatal exposure: a validation study.. Environmental Health Perspectives. 111(14). 1779–1782. 206 indexed citations
3.
Gripp, Karen W., Viera Kasparcova, Donna M. McDonald‐McGinn, et al.. (2001). A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: Fluorescence in situ hybridization and dosage-sensitive Southern blot analysis. Genetics in Medicine. 3(2). 102–108. 13 indexed citations
4.
Campo, Miguel Del, Marilyn C. Jones, Alexey Veraksa, et al.. (1999). Monodactylous Limbs and Abnormal Genitalia Are Associated with Hemizygosity for the Human 2q31 Region That Includes the HOXD Cluster. The American Journal of Human Genetics. 65(1). 104–110. 69 indexed citations
5.
Drumheller, Timothy, Barbara McGillivray, Patrick MacLeod, et al.. (1996). Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.. Journal of Medical Genetics. 33(10). 842–847. 45 indexed citations
6.
Kumlien, Johan, et al.. (1994). Identification of human chromosome region 3p14.2–21.3-specific YAC clones using Alu-PCR products from a radiation hybrid. Somatic Cell and Molecular Genetics. 20(2). 137–142. 1 indexed citations
7.
Dyke, D L Van, Maria J. Worsham, Timothy Drumheller, et al.. (1994). Recurrent cytogenetic abnormalities in squamous cell carcinomas of the head and neck region. Genes Chromosomes and Cancer. 9(3). 192–206. 177 indexed citations
8.
Powell, Cynthia M., R. Thomas Taggart, Timothy Drumheller, et al.. (1994). Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature. American Journal of Medical Genetics. 52(1). 19–26. 108 indexed citations
9.
Rock, Jack, et al.. (1993). Cytogenetic findings in pituitary adenoma: Results of a pilot study. Surgical Neurology. 40(3). 224–229. 22 indexed citations
10.
Babu, V. Ramesh, et al.. (1989). A prospective study of 92 bladder cancer patients: Cytogenetics, histopathology, and tumor behavior. Cancer Genetics and Cytogenetics. 41(2). 232–232. 4 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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