Kyle C. Retterer
Impact in
- Genetics top 1%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Vascular Anomalies and Treatments
- Rheumatology top 1%
- Otitis Media and Relapsing Polychondritis
Papers in
- Genetics 49
- Genomics and Rare Diseases 33
- Genetics and Neurodevelopmental Disorders 22
- Genomic variations and chromosomal abnormalities 14
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- Mitochondrial Function and Pathology 6
- RNA modifications and cancer 5
- Congenital heart defects research 5
- Co-authors
- Gabriele Richard (4 shared papers)Dianalee McKnight (5 shared papers)Elizabeth A. Butler (2 shared papers)Amanda S. Lindy (2 shared papers)Jane Juusola (11 shared papers)Donald Mitchell (3 shared papers)Edmond C. Roelof (2 shared papers)Douglas Hamilton (3 shared papers)
- Journals
- The American Journal of Human Genetics (20 papers)Genetics in Medicine (10 papers)Neurogenetics (4 papers)Human Genetics (3 papers)Nature Genetics (3 papers)
- Partner nations
- United StatesFranceNetherlands
In The Last Decade
Kyle C. Retterer
69 papers receiving 5.7k citations
Kyle C. Retterer's Hit Papers
Peers
Comparison fields: 5 of 137
- Genetics 2.4k
- Genetics 475
- Rheumatology 649
- Molecular Biology 2.3k
- Clinical Biochemistry 195
Countries citing papers authored by Kyle C. Retterer
This map shows the geographic impact of Kyle C. Retterer'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 Kyle C. Retterer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kyle C. Retterer more than expected).
Fields of papers citing papers by Kyle C. Retterer
This network shows the impact of papers produced by Kyle C. Retterer. 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 Kyle C. Retterer. The network helps show where Kyle C. Retterer may publish in the future.
Co-authors
The 25 scholars most cited alongside Kyle C. Retterer, 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 77 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease Hit paper breakdown → | 2020 | 827 |
| 2 | Clinical application of whole-exome sequencing across clinical indications Hit paper breakdown → | 2015 | 800 |
| 3 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 402 |
| 4 | High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies Hit paper breakdown → | 2017 | 362 |
| 5 | 2018 | 225 | |
| 6 | 2015 | 218 | |
| 7 | 2017 | 139 | |
| 8 | 2017 | 137 | |
| 9 | 2017 | 132 | |
| 10 | 2015 | 127 | |
| 11 | 2020 | 119 | |
| 12 | 2003 | 112 | |
| 13 | 2014 | 108 | |
| 14 | 2019 | 104 | |
| 15 | 2003 | 102 | |
| 16 | 2017 | 102 | |
| 17 | 2021 | 90 | |
| 18 | 2017 | 90 | |
| 19 | 2021 | 83 | |
| 20 | 2023 | 83 |
About Kyle C. Retterer
Kyle C. Retterer is a scholar working on Genetics, Molecular Biology, Clinical Biochemistry, Cognitive Neuroscience and Genetics, having authored 77 papers that have together received 5.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (33 papers), Genetics and Neurodevelopmental Disorders (22 papers), Genomic variations and chromosomal abnormalities (14 papers), Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (6 papers), RNA modifications and cancer (5 papers), Autism Spectrum Disorder Research (5 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Genetics (2.4k citations), Genetics (475 citations), Rheumatology (649 citations), Molecular Biology (2.3k citations) and Clinical Biochemistry (195 citations). Kyle C. Retterer has collaborated with scholars based in United States, France and Netherlands. Frequent co-authors include Gabriele Richard, Dianalee McKnight, Elizabeth A. Butler, Amanda S. Lindy, Jane Juusola, Donald Mitchell, Edmond C. Roelof, Douglas Hamilton, Steven B. Mende and Pontus Brandt. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Neurogenetics, Human Genetics and Nature 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.