Patrick Sulem
Impact in
- Ophthalmology top 1%
- Glaucoma and retinal disorders
- Retinal Diseases and Treatments
- Genetics top 2%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
-
- DNA Repair Mechanisms 5
- Genomics and Chromatin Dynamics 5
- Epigenetics and DNA Methylation 4
- Genetics 19
- Genomics and Rare Diseases 9
- Genetic Associations and Epidemiology 8
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- Kāri Stefánsson (39 shared papers)Daníel F. Guðbjartsson (34 shared papers)Unnur Þorsteinsdóttir (30 shared papers)Augustine Kong (16 shared papers)Gísli Másson (16 shared papers)Guðmar Þorleifsson (14 shared papers)Hreinn Stefánsson (6 shared papers)Hilma Hólm (17 shared papers)
- Journals
- Nature Genetics (9 papers)Nature Communications (4 papers)PLoS Genetics (3 papers)PLoS Medicine (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- IcelandUnited StatesUnited Kingdom
In The Last Decade
Patrick Sulem
49 papers receiving 2.6k citations
Patrick Sulem's Hit Papers
Peers
Comparison fields: 5 of 143
- Ophthalmology 358
- Genetics 1.0k
- Nephrology 186
- Cancer Research 236
- Molecular Biology 974
Countries citing papers authored by Patrick Sulem
This map shows the geographic impact of Patrick Sulem'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 Patrick Sulem with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Sulem more than expected).
Fields of papers citing papers by Patrick Sulem
This network shows the impact of papers produced by Patrick Sulem. 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 Patrick Sulem. The network helps show where Patrick Sulem may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Sulem, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma Hit paper breakdown → | 2007 | 478 |
| 2 | 2008 | 231 | |
| 3 | 2004 | 207 | |
| 4 | 2010 | 155 | |
| 5 | 2015 | 142 | |
| 6 | 2015 | 120 | |
| 7 | 2017 | 118 | |
| 8 | 2018 | 104 | |
| 9 | 2017 | 84 | |
| 10 | 2016 | 82 | |
| 11 | 2016 | 80 | |
| 12 | 2016 | 61 | |
| 13 | 2013 | 56 | |
| 14 | 2017 | 56 | |
| 15 | 2018 | 54 | |
| 16 | 2016 | 52 | |
| 17 | 2018 | 50 | |
| 18 | 2003 | 49 | |
| 19 | 2006 | 47 | |
| 20 | 2021 | 40 |
About Patrick Sulem
Patrick Sulem is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Surgery, having authored 51 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Genetic Associations and Epidemiology (8 papers), DNA Repair Mechanisms (5 papers), Genomics and Chromatin Dynamics (5 papers), Epigenetics and DNA Methylation (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chronic Kidney Disease and Diabetes (4 papers) and Genetic factors in colorectal cancer (3 papers). The work is most often cited by research in Ophthalmology (358 citations), Genetics (1.0k citations), Nephrology (186 citations), Cancer Research (236 citations) and Molecular Biology (974 citations). Patrick Sulem has collaborated with scholars based in Iceland, United States and United Kingdom. Frequent co-authors include Kāri Stefánsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Augustine Kong, Gísli Másson, Guðmar Þorleifsson, Hreinn Stefánsson, Hilma Hólm, Aðalbjörg Jónasdóttir and Áslaug Jónasdóttir. Their work appears in journals such as Nature Genetics, Nature Communications, PLoS Genetics, PLoS Medicine and European Journal of Human 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.