David W. Mohr

1.1k total citations
13 papers, 303 citations indexed

About

David W. Mohr is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, David W. Mohr has authored 13 papers receiving a total of 303 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Epidemiology. Recurrent topics in David W. Mohr's work include Genomics and Phylogenetic Studies (5 papers), Genetic diversity and population structure (3 papers) and Genetic and phenotypic traits in livestock (2 papers). David W. Mohr is often cited by papers focused on Genomics and Phylogenetic Studies (5 papers), Genetic diversity and population structure (3 papers) and Genetic and phenotypic traits in livestock (2 papers). David W. Mohr collaborates with scholars based in United States, United Kingdom and Denmark. David W. Mohr's co-authors include Amy E. DeZern, J. Brooks Jackson, Susan E. Stanley, Mary Armanios, Robert A. Brodsky, Clifford M. Takemoto, James F. Casella, Stephen G. Bolton, Carol W. Greider and Carolyn Applegate and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Scientific Reports.

In The Last Decade

David W. Mohr

13 papers receiving 301 citations

Peers

David W. Mohr

PHYSI

GENET

PRM

IMMUN

Prajakta Jogdand Sweden

Andrew Huang United States

Caroline End Germany

Lauren Stevenson United States

Kelly Robinson United States

Sara Stier Germany

H Küpper Germany

Birte Zurek Germany

Melva L. Gonzalez United States

Troy Mitchell Canada

Prajakta Jogdand Sweden

David W. Mohr

89 ×0.9

64 ×0.7

PHYSI

38 ×0.5

GENET

41 ×0.8

PRM

90 ×2.4

IMMUN

Citations per year, relative to David W. Mohr David W. Mohr (= 1×) peers Prajakta Jogdand

Countries citing papers authored by David W. Mohr

Since Specialization

Citations

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

Fields of papers citing papers by David W. Mohr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David W. Mohr

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Shapira, Guy, David W. Mohr, Maria Bettinotti, et al.. (2023). Genomic Markers Associated with Cytomegalovirus DNAemia in Kidney Transplant Recipients. Viruses. 15(11). 2227–2227. 1 indexed citations

Mohr, David W., Stephen J. Gaughran, Justin Paschall, et al.. (2022). A Chromosome-Length Assembly of the Hawaiian Monk Seal (Neomonachus schauinslandi): A History of “Genetic Purging” and Genomic Stability. Genes. 13(7). 1270–1270. 4 indexed citations

Kandathil, Abraham J., Andrea L. Cox, Kimberly Page, et al.. (2021). Plasma virome and the risk of blood-borne infection in persons with substance use disorder. Nature Communications. 12(1). 6909–6909. 13 indexed citations

Verratti, Kathleen, et al.. (2021). A novel canis lupus familiaris reference genome improves variant resolution for use in breed-specific GWAS. Life Science Alliance. 4(4). e202000902–e202000902. 9 indexed citations

Randad, Pranay R., Jesper Larsen, Hülya Kaya, et al.. (2021). Transmission of Antimicrobial-Resistant Staphylococcus aureus Clonal Complex 9 between Pigs and Humans, United States. Emerging infectious diseases. 27(3). 740–748. 15 indexed citations

Tamazian, Gaik, Pavel Dobrynin, Daria V. Zhernakova, et al.. (2021). Draftde novoGenome Assembly of the Elusive Jaguarundi,Puma yagouaroundi. Journal of Heredity. 112(6). 540–548. 5 indexed citations

Humble, Emily, Pavel Dobrynin, Helen Senn, et al.. (2020). Chromosomal‐level genome assembly of the scimitar‐horned oryx: Insights into diversity and demography of a species extinct in the wild. Molecular Ecology Resources. 20(6). 1668–1681. 22 indexed citations

Randad, Pranay R., Carly Dillen, Roger V. Ortines, et al.. (2019). Comparison of livestock-associated and community-associated Staphylococcus aureus pathogenicity in a mouse model of skin and soft tissue infection. Scientific Reports. 9(1). 6774–6774. 7 indexed citations

Alder, Jonathan K., Vidya Sagar Hanumanthu, Margaret A. Strong, et al.. (2018). Diagnostic utility of telomere length testing in a hospital-based setting. Proceedings of the National Academy of Sciences. 115(10). E2358–E2365. 144 indexed citations

10.

Ferrer, Marc, Sara J.C. Gosline, Marigo Stathis, et al.. (2018). Pharmacological and genomic profiling of neurofibromatosis type 1 plexiform neurofibroma-derived schwann cells. Scientific Data. 5(1). 180106–180106. 23 indexed citations

11.

Scott, Alan F., David W. Mohr, Laura Kasch, et al.. (2014). Identification of anHMGB3Frameshift Mutation in a Family With an X-linked Colobomatous Microphthalmia Syndrome Using Whole-Genome and X-Exome Sequencing. JAMA Ophthalmology. 132(10). 1215–1215. 18 indexed citations

12.

Scott, Alan F., David W. Mohr, Hua Ling, et al.. (2014). Characterization of the Genomic Architecture and Mutational Spectrum of a Small Cell Prostate Carcinoma. Genes. 5(2). 366–384. 6 indexed citations

13.

Azarian, Taj, Afsar Ali, Judith A. Johnson, et al.. (2014). Phylodynamic Analysis of Clinical and Environmental Vibrio cholerae Isolates from Haiti Reveals Diversification Driven by Positive Selection. mBio. 5(6). 36 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.

Explore authors with similar magnitude of impact