Kaitlin E. Samocha
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 19
- Genomics and Rare Diseases 13
- Genetic Associations and Epidemiology 5
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Genetic Mapping and Diversity in Plants and Animals 3
-
- RNA and protein synthesis mechanisms 4
- Genomics and Phylogenetic Studies 4
- Co-authors
- Mark J. Daly (14 shared papers)Daniel G. MacArthur (7 shared papers)Benjamin M. Neale (8 shared papers)Konrad J. Karczewski (5 shared papers)Monkol Lek (3 shared papers)Shamil Sunyaev (3 shared papers)Douglas M. Ruderfer (2 shared papers)Tymor Hamamsy (2 shared papers)
- Journals
- Nature Genetics (3 papers)Nature Communications (2 papers)Proceedings of the National Academy of Sciences (2 papers)Clinical Cancer Research (1 paper)Nature Medicine (1 paper)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
Kaitlin E. Samocha
22 papers receiving 1.9k citations
Kaitlin E. Samocha's Hit Papers
Peers
Comparison fields: 5 of 118
- Genetics 1.3k
- Cancer Research 210
- Molecular Biology 917
- Cognitive Neuroscience 178
- Aging 13
Countries citing papers authored by Kaitlin E. Samocha
This map shows the geographic impact of Kaitlin E. Samocha'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 Kaitlin E. Samocha with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kaitlin E. Samocha more than expected).
Fields of papers citing papers by Kaitlin E. Samocha
This network shows the impact of papers produced by Kaitlin E. Samocha. 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 Kaitlin E. Samocha. The network helps show where Kaitlin E. Samocha may publish in the future.
Co-authors
The 25 scholars most cited alongside Kaitlin E. Samocha, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The ExAC browser: displaying reference data information from over 60 000 exomes Hit paper breakdown → | 2016 | 452 |
| 2 | 2014 | 375 | |
| 3 | 2015 | 242 | |
| 4 | 2017 | 183 | |
| 5 | 2016 | 104 | |
| 6 | 2014 | 85 | |
| 7 | 2010 | 82 | |
| 8 | 2017 | 79 | |
| 9 | 2015 | 43 | |
| 10 | 2019 | 39 | |
| 11 | 2010 | 32 | |
| 12 | 2016 | 30 | |
| 13 | 2022 | 29 | |
| 14 | 2018 | 29 | |
| 15 | 2009 | 29 | |
| 16 | 2022 | 29 | |
| 17 | 2016 | 16 | |
| 18 | 2015 | 14 | |
| 19 | 2015 | 14 | |
| 20 | 2016 | 10 |
About Kaitlin E. Samocha
Kaitlin E. Samocha is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Surgery and Plant Science, having authored 23 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genetic Associations and Epidemiology (5 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA and protein synthesis mechanisms (4 papers), Genomics and Phylogenetic Studies (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (4 papers) and Genetic Mapping and Diversity in Plants and Animals (3 papers). The work is most often cited by research in Genetics (1.3k citations), Cancer Research (210 citations), Molecular Biology (917 citations), Cognitive Neuroscience (178 citations) and Aging (13 citations). Kaitlin E. Samocha has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include Mark J. Daly, Daniel G. MacArthur, Benjamin M. Neale, Konrad J. Karczewski, Monkol Lek, Shamil Sunyaev, Douglas M. Ruderfer, Tymor Hamamsy, David Kavanagh and Or Zuk. Their work appears in journals such as Nature Genetics, Nature Communications, Proceedings of the National Academy of Sciences, Clinical Cancer Research and Nature Medicine.
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.