Nelson B. Freimer
- Genetics top 0.2%
- Genetic Associations and Epidemiology 35
- Genetic Mapping and Diversity in Plants and Animals 17
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 7
- Cognitive Neuroscience top 2%
- Oncology top 2%
- Drug Transport and Resistance Mechanisms 8
- Music top 1%
- Plant Science top 1%
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- Pediatric Hepatobiliary Diseases and Treatments 8
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- Bipolar Disorder and Treatment 8
- Co-authors
- Montgomery SlatkinSusan K. ServiceAna M. ValdesChiara SabattiJae Hoon SulHyun Min KangNoah ZaitlenEleazar Eskin
- Journals
- The American Journal of Human Genetics (10 papers)Nature Genetics (8 papers)Human Molecular Genetics (7 papers)
- Partner nations
- United StatesUnited KingdomNetherlands
In The Last Decade
Nelson B. Freimer
133 papers receiving 9.8k citations
Hit Papers
Peers
Comparison fields: 5 of 173
- Genetics 4.4k
- Cognitive Neuroscience 1.2k
- Oncology 1.4k
- Music 136
- Plant Science 1.4k
Countries citing papers authored by Nelson B. Freimer
This map shows the geographic impact of Nelson B. Freimer'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 Nelson B. Freimer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nelson B. Freimer more than expected).
Fields of papers citing papers by Nelson B. Freimer
This network shows the impact of papers produced by Nelson B. Freimer. 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 Nelson B. Freimer. The network helps show where Nelson B. Freimer may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Nelson B. Freimer, 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 | 2024 | 6 | |
| 2 | 2024 | 15 | |
| 3 | 2022 | 2 | |
| 4 | 2020 | 55 | |
| 5 | 2020 | 14 | |
| 6 | 2018 | 30 | |
| 7 | Population genomics disentangles taxonomic relationships and identifies ancient hybridization in the genus Chlorocebus | 2017 | 2 |
| 8 | 2016 | 30 | |
| 9 | 2015 | 24 | |
| 10 | 2011 | 79 | |
| 11 | 2009 | 54 | |
| 12 | Genome-wide association (GWA) analysis in 4000 members of a Finnish birth cohort identifies common variants associated with fasting insulin levels and related metabolic traits | 2008 | 1 |
| 13 | Meta-analysis of genome-wide association data involving 6,100 adults of European origin identifies common variants associated with fasting glucose levels | 2008 | 1 |
| 14 | 2008 | 54 | |
| 15 | 2007 | 24 | |
| 16 | 2005 | 49 | |
| 17 | Clinical and biochemical features of FIC1 (ATP8B1) and BSEP (ABCB11) disease. | 2002 | 6 |
| 18 | 2000 | 63 | |
| 19 | 1999 | 84 | |
| 20 | 1996 | 5 |
About Nelson B. Freimer
Nelson B. Freimer is a scholar working on Genetics, Aging and Virology, having authored 136 papers that have together received 10.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (35 papers), Genetic Mapping and Diversity in Plants and Animals (17 papers), Genomic variations and chromosomal abnormalities (11 papers), Pediatric Hepatobiliary Diseases and Treatments (8 papers), Drug Transport and Resistance Mechanisms (8 papers), Bipolar Disorder and Treatment (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (4.4k citations), Cognitive Neuroscience (1.2k citations) and Oncology (1.4k citations). Nelson B. Freimer has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Montgomery Slatkin, Susan K. Service, Ana M. Valdes, Chiara Sabatti, Jae Hoon Sul, Hyun Min Kang, Noah Zaitlen, Eleazar Eskin, Amy Peterson and Anna Di Rienzo. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Human Molecular Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Journal of Virology.
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.