Christine Patch
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Kidney Cyst Diseases
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- Prenatal Screening and Diagnostics
- Ethics and Legal Issues in Pediatric Healthcare
Papers in
- Genetics 51
- BRCA gene mutations in cancer 37
- Genomics and Rare Diseases 28
- Genomic variations and chromosomal abnormalities 7
- Nutrition, Genetics, and Disease 6
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- Ethics and Legal Issues in Pediatric Healthcare 10
- Co-authors
- Anna Middleton (12 shared papers)Heather Skirton (13 shared papers)Alison Metcalfe (8 shared papers)Celine Lewis (14 shared papers)Saskia C. Sanderson (12 shared papers)Melissa Hill (12 shared papers)Martina C. Cornel (5 shared papers)Lyn S. Chitty (9 shared papers)
- Journals
- European Journal of Human Genetics (20 papers)Genetics in Medicine (4 papers)Journal of Medical Genetics (2 papers)Journal of Nursing Scholarship (2 papers)Frontiers in Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
Christine Patch
84 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 105
- Genetics 1.1k
- Pediatrics, Perinatology and Child Health 359
- Public Health, Environmental and Occupational Health 231
- Hematology 61
- Cancer Research 76
Countries citing papers authored by Christine Patch
This map shows the geographic impact of Christine Patch'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 Christine Patch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christine Patch more than expected).
Fields of papers citing papers by Christine Patch
This network shows the impact of papers produced by Christine Patch. 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 Christine Patch. The network helps show where Christine Patch may publish in the future.
Co-authors
The 25 scholars most cited alongside Christine Patch, 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 85 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 124 | |
| 2 | 2018 | 98 | |
| 3 | 2005 | 95 | |
| 4 | 2020 | 86 | |
| 5 | 2011 | 74 | |
| 6 | 2012 | 58 | |
| 7 | 2016 | 49 | |
| 8 | 1994 | 47 | |
| 9 | 2021 | 41 | |
| 10 | 2020 | 41 | |
| 11 | 2018 | 40 | |
| 12 | 2020 | 40 | |
| 13 | 2009 | 39 | |
| 14 | 2022 | 37 | |
| 15 | 2013 | 37 | |
| 16 | 2015 | 35 | |
| 17 | 2023 | 34 | |
| 18 | 2022 | 30 | |
| 19 | 2017 | 29 | |
| 20 | 2019 | 29 |
About Christine Patch
Christine Patch is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Molecular Biology and Hematology, having authored 85 papers that have together received 1.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (37 papers), Genomics and Rare Diseases (28 papers), Ethics in Clinical Research (12 papers), Ethics and Legal Issues in Pediatric Healthcare (10 papers), Iron Metabolism and Disorders (9 papers), Genomic variations and chromosomal abnormalities (7 papers), Nutrition, Genetics, and Disease (6 papers) and Health Systems, Economic Evaluations, Quality of Life (5 papers). The work is most often cited by research in Genetics (1.1k citations), Pediatrics, Perinatology and Child Health (359 citations), Public Health, Environmental and Occupational Health (231 citations), Hematology (61 citations) and Cancer Research (76 citations). Christine Patch has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Anna Middleton, Heather Skirton, Alison Metcalfe, Celine Lewis, Saskia C. Sanderson, Melissa Hill, Martina C. Cornel, Lyn S. Chitty, Judith Charlton and Beverly Searle. Their work appears in journals such as European Journal of Human Genetics, Genetics in Medicine, Journal of Medical Genetics, Journal of Nursing Scholarship and Frontiers in 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.