Tim Donlon
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Hematology top 5%
- Acute Myeloid Leukemia Research
- Hematopoietic Stem Cell Transplantation
Papers in
-
- Cancer-related gene regulation 3
- DNA Repair Mechanisms 2
- Kruppel-like factors research 2
- Genetics 6
- Genetic Syndromes and Imprinting 4
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Marc Lalande (2 shared papers)S.A. Latt (6 shared papers)Uta Francke (2 shared papers)Arnon Nagler (2 shared papers)Albert Schinzel (1 shared paper)G.A.P. Bruns (2 shared papers)Arlene R. Wyman (1 shared paper)Wendy P. Robinson (1 shared paper)
- Journals
- Genomics (2 papers)Human Genetics (2 papers)Proceedings of the National Academy of Sciences (2 papers)Cold Spring Harbor Symposia on Quantitative Biology (1 paper)PROTEOMICS (1 paper)
- Partner nations
- United StatesCanadaSwitzerland
In The Last Decade
Tim Donlon
23 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 89
- Genetics 672
- Hematology 200
- Pediatrics, Perinatology and Child Health 231
- Molecular Biology 600
- Physical Therapy, Sports Therapy and Rehabilitation 37
Countries citing papers authored by Tim Donlon
This map shows the geographic impact of Tim Donlon'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 Tim Donlon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tim Donlon more than expected).
Fields of papers citing papers by Tim Donlon
This network shows the impact of papers produced by Tim Donlon. 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 Tim Donlon. The network helps show where Tim Donlon may publish in the future.
Co-authors
The 25 scholars most cited alongside Tim Donlon, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 222 | |
| 2 | 1990 | 191 | |
| 3 | 2006 | 184 | |
| 4 | 1986 | 138 | |
| 5 | 1988 | 84 | |
| 6 | 1985 | 75 | |
| 7 | 1986 | 67 | |
| 8 | 1985 | 66 | |
| 9 | 1986 | 63 | |
| 10 | 1999 | 57 | |
| 11 | Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization. | 1983 | 37 |
| 12 | Effects of recombinant human granulocyte colony stimulating factor and granulocyte-monocyte colony stimulating factor on in vitro hemopoiesis in the myelodysplastic syndromes. | 1990 | 32 |
| 13 | 1990 | 29 | |
| 14 | 1985 | 25 | |
| 15 | 1991 | 22 | |
| 16 | 1996 | 20 | |
| 17 | Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma. | 1986 | 19 |
| 18 | 2010 | 11 | |
| 19 | 2018 | 9 | |
| 20 | 1989 | 3 |
About Tim Donlon
Tim Donlon is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Hematology and Cell Biology, having authored 28 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (4 papers), Prenatal Screening and Diagnostics (4 papers), Microtubule and mitosis dynamics (3 papers), Cancer-related gene regulation (3 papers), DNA Repair Mechanisms (2 papers), Neuroblastoma Research and Treatments (2 papers), Kruppel-like factors research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (672 citations), Hematology (200 citations), Pediatrics, Perinatology and Child Health (231 citations), Molecular Biology (600 citations) and Physical Therapy, Sports Therapy and Rehabilitation (37 citations). Tim Donlon has collaborated with scholars based in United States, Canada and Switzerland. Frequent co-authors include Marc Lalande, S.A. Latt, Uta Francke, Arnon Nagler, Albert Schinzel, G.A.P. Bruns, Arlene R. Wyman, Wendy P. Robinson, Tayfun Özçelık and Stuart E. Leff. Their work appears in journals such as Genomics, Human Genetics, Proceedings of the National Academy of Sciences, Cold Spring Harbor Symposia on Quantitative Biology and PROTEOMICS.
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.