Julia E. Parrish
Impact in
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and rare skin diseases.
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Developmental Biology top 5%
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 9
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 3
- Genetic Associations and Epidemiology 3
- Genetic Mapping and Diversity in Plants and Animals 2
- Genetics and Neurodevelopmental Disorders 2
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- Muscle Physiology and Disorders 3
- Genomics and Phylogenetic Studies 2
- Co-authors
- David L. Nelson (5 shared papers)Ben A. Oostra (1 shared paper)Annemieke J.M.H. Verkerk (1 shared paper)C. Sue Richards (1 shared paper)Aimee S. Spikes (1 shared paper)Lisa G. Shaffer (1 shared paper)Dan E. Wells (5 shared papers)M.J. Wagner (3 shared papers)
- Journals
- Genomics (5 papers)Human Molecular Genetics (5 papers)Nature (2 papers)Human Mutation (2 papers)Mammalian Genome (1 paper)
- Partner nations
- United StatesGermanyUnited Kingdom
In The Last Decade
Julia E. Parrish
20 papers receiving 1.5k citations
Julia E. Parrish's Hit Papers
Peers
Comparison fields: 5 of 83
- Genetics 933
- Developmental Biology 45
- Rheumatology 88
- Molecular Biology 350
- Reproductive Medicine 40
Countries citing papers authored by Julia E. Parrish
This map shows the geographic impact of Julia E. 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 E. 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 E. Parrish more than expected).
Fields of papers citing papers by Julia E. Parrish
This network shows the impact of papers produced by Julia E. 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 E. Parrish. The network helps show where Julia E. Parrish may publish in the future.
Co-authors
The 25 scholars most cited alongside Julia E. 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 | The DNA sequence of the human X chromosome Hit paper breakdown → | 2005 | 855 |
| 2 | 1994 | 163 | |
| 3 | 1995 | 102 | |
| 4 | 1996 | 95 | |
| 5 | 1992 | 61 | |
| 6 | 1995 | 49 | |
| 7 | 1995 | 44 | |
| 8 | 2006 | 39 | |
| 9 | 1995 | 37 | |
| 10 | 1991 | 25 | |
| 11 | 1998 | 22 | |
| 12 | 1993 | 13 | |
| 13 | 1997 | 13 | |
| 14 | 1993 | 11 | |
| 15 | 1995 | 8 | |
| 16 | 1994 | 5 | |
| 17 | 1997 | 2 | |
| 18 | 1994 | 1 | |
| 19 | 2021 | 1 | |
| 20 | 2026 | 1 |
About Julia E. Parrish
Julia E. Parrish is a scholar working on Genetics, Molecular Biology, Internal Medicine, Ophthalmology and Cell Biology, having authored 20 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetic Associations and Epidemiology (3 papers), Muscle Physiology and Disorders (3 papers), Genetic Mapping and Diversity in Plants and Animals (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genomics and Phylogenetic Studies (2 papers) and Ocular Oncology and Treatments (1 paper). The work is most often cited by research in Genetics (933 citations), Developmental Biology (45 citations), Rheumatology (88 citations), Molecular Biology (350 citations) and Reproductive Medicine (40 citations). Julia E. Parrish has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include David L. Nelson, Ben A. Oostra, Annemieke J.M.H. Verkerk, C. Sue Richards, Aimee S. Spikes, Lisa G. Shaffer, Dan E. Wells, M.J. Wagner, Manfred S. Wehnert and Bernhard Horsthemke. Their work appears in journals such as Genomics, Human Molecular Genetics, Nature, Human Mutation and Mammalian Genome.
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.