Jennefer N. Kohler
- Genetics top 10%
- Genomics and Rare Diseases 6
- BRCA gene mutations in cancer 6
- Genomic variations and chromosomal abnormalities 2
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- Prenatal Screening and Diagnostics 2
- Childhood Cancer Survivors' Quality of Life 1
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- Health Systems, Economic Evaluations, Quality of Life 2
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- Neurological diseases and metabolism 1
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- Platelet Disorders and Treatments 1
- Co-authors
- Erin TurbittBarbara B. BieseckerKatie L. LewisBenjamin S. WilfondMatthew T. WheelerJonathan A. BernsteinHolly L. PeayLeila Jamal
- Cited by
- GeneticsPediatrics, Perinatology and Child HealthPublic Health, Environmental and Occupational Health
- Partner nations
- United StatesAustraliaIndia
In The Last Decade
Jennefer N. Kohler
15 papers receiving 359 citations
Peers
Comparison fields: 5 of 67
- Genetics 245
- Pediatrics, Perinatology and Child Health 55
- Public Health, Environmental and Occupational Health 59
- Cancer Research 29
- Economics and Econometrics 39
Countries citing papers authored by Jennefer N. Kohler
This map shows the geographic impact of Jennefer N. Kohler'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 Jennefer N. Kohler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jennefer N. Kohler more than expected).
Fields of papers citing papers by Jennefer N. Kohler
This network shows the impact of papers produced by Jennefer N. Kohler. 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 Jennefer N. Kohler. The network helps show where Jennefer N. Kohler may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Jennefer N. Kohler, 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 | 2023 | 6 | |
| 2 | 2023 | 7 | |
| 3 | 2022 | 26 | |
| 4 | 2022 | 23 | |
| 5 | 2022 | 3 | |
| 6 | 2021 | 13 | |
| 7 | 2021 | 4 | |
| 8 | 2019 | 5 | |
| 9 | 2019 | 16 | |
| 10 | 2019 | 5 | |
| 11 | 2019 | 12 | |
| 12 | 2018 | 62 | |
| 13 | 2017 | 113 | |
| 14 | 2017 | 63 | |
| 15 | 2016 | 4 |
About Jennefer N. Kohler
Jennefer N. Kohler is a scholar working on Genetics, Immunology and Allergy and Speech and Hearing, having authored 15 papers that have together received 362 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (6 papers), Prenatal Screening and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Health Systems, Economic Evaluations, Quality of Life (2 papers), Neurological diseases and metabolism (1 paper), Childhood Cancer Survivors' Quality of Life (1 paper) and Platelet Disorders and Treatments (1 paper). The work is most often cited by research in Genetics (245 citations), Pediatrics, Perinatology and Child Health (55 citations) and Public Health, Environmental and Occupational Health (59 citations). Jennefer N. Kohler has collaborated with scholars based in United States, Australia and India. Frequent co-authors include Erin Turbitt, Barbara B. Biesecker, Katie L. Lewis, Benjamin S. Wilfond, Matthew T. Wheeler, Jonathan A. Bernstein, Holly L. Peay, Leila Jamal, Leslie G. Biesecker and Michael C. Leo.
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.