Jonathan P. Park
Impact in
-
- Lymphoma Diagnosis and Treatment
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Chronic Lymphocytic Leukemia Research
Papers in
- Genetics 22
- Genomic variations and chromosomal abnormalities 17
- Chronic Lymphocytic Leukemia Research 4
- Genetic Syndromes and Imprinting 3
- Co-authors
- Doris H. Wurster‐Hill (13 shared papers)T. Mohandas (10 shared papers)John B. Moeschler (12 shared papers)Walter W. Noll (6 shared papers)C. Harker Rhodes (3 shared papers)John M. Graham (2 shared papers)John M. Graham (4 shared papers)Cindy L. Vnencak‐Jones (1 shared paper)
- Journals
- Archives of Pathology & Laboratory Medicine (4 papers)Clinical Genetics (4 papers)Prenatal Diagnosis (3 papers)Genetics in Medicine (2 papers)American Journal of Medical Genetics (10 papers)
- Partner nations
- United StatesQatarUnited Kingdom
In The Last Decade
Jonathan P. Park
39 papers receiving 960 citations
Peers
Comparison fields: 5 of 85
- Pathology and Forensic Medicine 196
- Genetics 305
- Genetics 105
- Pediatrics, Perinatology and Child Health 131
- Molecular Biology 446
Countries citing papers authored by Jonathan P. Park
This map shows the geographic impact of Jonathan P. Park'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 Jonathan P. Park with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan P. Park more than expected).
Fields of papers citing papers by Jonathan P. Park
This network shows the impact of papers produced by Jonathan P. Park. 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 Jonathan P. Park. The network helps show where Jonathan P. Park may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan P. Park, 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 41 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 133 | |
| 2 | 1999 | 102 | |
| 3 | Clinical laboratory assays for HER-2/neu amplification and overexpression: Quality assurance, standardization, and proficiency testing | 2002 | 65 |
| 4 | 1998 | 58 | |
| 5 | 2007 | 45 | |
| 6 | 1994 | 43 | |
| 7 | 1998 | 42 | |
| 8 | 2001 | 38 | |
| 9 | 2006 | 37 | |
| 10 | 1987 | 30 | |
| 11 | 2005 | 26 | |
| 12 | 1992 | 26 | |
| 13 | 1991 | 23 | |
| 14 | 1996 | 22 | |
| 15 | 1998 | 22 | |
| 16 | 1989 | 21 | |
| 17 | 1996 | 21 | |
| 18 | An MCL1-overexpressing Burkitt lymphoma subline exhibits enhanced survival on exposure to serum deprivation, topoisomerase inhibitors, or staurosporine but remains sensitive to 1-beta-D-arabinofuranosylcytosine. | 2002 | 20 |
| 19 | 1988 | 18 | |
| 20 | 1993 | 18 |
About Jonathan P. Park
Jonathan P. Park is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Genetics, having authored 41 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Prenatal Screening and Diagnostics (10 papers), Chronic Lymphocytic Leukemia Research (4 papers), Tumors and Oncological Cases (3 papers), Acute Myeloid Leukemia Research (3 papers), Genetic Syndromes and Imprinting (3 papers), Chromosomal and Genetic Variations (3 papers) and Gestational Trophoblastic Disease Studies (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (196 citations), Genetics (305 citations), Genetics (105 citations), Pediatrics, Perinatology and Child Health (131 citations) and Molecular Biology (446 citations). Jonathan P. Park has collaborated with scholars based in United States, Qatar and United Kingdom. Frequent co-authors include Doris H. Wurster‐Hill, T. Mohandas, John B. Moeschler, Walter W. Noll, C. Harker Rhodes, John M. Graham, John M. Graham, Cindy L. Vnencak‐Jones, William B. Kinlaw and Matthew Edwards. Their work appears in journals such as Archives of Pathology & Laboratory Medicine, Clinical Genetics, Prenatal Diagnosis, Genetics in Medicine and American Journal of Medical 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.