Julia Parrish
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
- Oral Surgery top 10%
Papers in
-
- RNA regulation and disease 4
- RNA Research and Splicing 3
- Genomics and Chromatin Dynamics 3
- Congenital heart defects research 2
- Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Genetic and rare skin diseases. 3
- Co-authors
- David L. Nelson (2 shared papers)Annemieke J.M.H. Verkerk (1 shared paper)Ben A. Oostra (1 shared paper)Lisa G. Shaffer (1 shared paper)Aimee S. Spikes (1 shared paper)C. Sue Richards (1 shared paper)James B. Reynolds (1 shared paper)Dan E. Wells (5 shared papers)
- Journals
- Human Molecular Genetics (5 papers)Genomics (5 papers)Human Mutation (2 papers)Mammalian Genome (1 paper)Genetic Analysis Biomolecular Engineering (1 paper)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Julia Parrish
20 papers receiving 700 citations
Peers
Comparison fields: 5 of 66
- Genetics 364
- Oral Surgery 39
- Molecular Biology 411
- Rheumatology 62
- Cancer Research 54
Countries citing papers authored by Julia Parrish
This map shows the geographic impact of Julia Parrish'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 Julia Parrish with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julia Parrish more than expected).
Fields of papers citing papers by Julia Parrish
This network shows the impact of papers produced by Julia Parrish. 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 Julia Parrish. The network helps show where Julia Parrish may publish in the future.
Co-authors
The 25 scholars most cited alongside Julia Parrish, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 1994 | 164 | |
| 2 | 1995 | 99 | |
| 3 | 1996 | 90 | |
| 4 | 1992 | 61 | |
| 5 | 1995 | 48 | |
| 6 | 1995 | 45 | |
| 7 | 1995 | 40 | |
| 8 | 2008 | 36 | |
| 9 | 2007 | 32 | |
| 10 | 1991 | 25 | |
| 11 | 1998 | 23 | |
| 12 | 2009 | 16 | |
| 13 | 1993 | 16 | |
| 14 | 1997 | 13 | |
| 15 | 1993 | 11 | |
| 16 | 1995 | 10 | |
| 17 | 1994 | 6 | |
| 18 | 1997 | 2 | |
| 19 | 1994 | 1 | |
| 20 | 2021 | 1 |
About Julia Parrish
Julia Parrish is a scholar working on Molecular Biology, Genetics, Cell Biology, Physiology and Oncology, having authored 20 papers that have together received 739 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), RNA regulation and disease (4 papers), Alzheimer's disease research and treatments (3 papers), RNA Research and Splicing (3 papers), Genetic and rare skin diseases. (3 papers), Genomics and Chromatin Dynamics (3 papers), melanin and skin pigmentation (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (364 citations), Oral Surgery (39 citations), Molecular Biology (411 citations), Rheumatology (62 citations) and Cancer Research (54 citations). Julia Parrish has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include David L. Nelson, Annemieke J.M.H. Verkerk, Ben A. Oostra, Lisa G. Shaffer, Aimee S. Spikes, C. Sue Richards, James B. Reynolds, Dan E. Wells, Manfred Wehnert and M.J. Wagner. Their work appears in journals such as Human Molecular Genetics, Genomics, Human Mutation, Mammalian Genome and Genetic Analysis Biomolecular Engineering.
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.