Nelson B. Freimer
Impact in
- Genetics top 0.02%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Mapping and Diversity in Plants and Animals
- Biological Psychiatry top 0.2%
Papers in
- Genetics 115
- Genetic Associations and Epidemiology 83
- Genomic variations and chromosomal abnormalities 26
- Genetics and Neurodevelopmental Disorders 24
- Genomics and Rare Diseases 23
- Genetic Mapping and Diversity in Plants and Animals 21
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- Autism Spectrum Disorder Research 16
- Co-authors
- Montgomery Slatkin (4 shared papers)Ana Maria Valdes (2 shared papers)Amy C. Peterson (3 shared papers)John E. Garza (1 shared paper)Anna Di Rienzo (2 shared papers)Susan K. Service (25 shared papers)Chiara Sabatti (6 shared papers)Laura N. Bull (6 shared papers)
- Journals
- The American Journal of Human Genetics (20 papers)Nature Genetics (17 papers)Nature (10 papers)Human Molecular Genetics (8 papers)PLoS Genetics (8 papers)
- Partner nations
- United StatesUnited KingdomFinland
In The Last Decade
Nelson B. Freimer
225 papers receiving 35.1k citations
Nelson B. Freimer's Hit Papers
Peers
Comparison fields: 5 of 196
- Genetics 15.6k
- Biological Psychiatry 1.1k
- Psychiatry and Mental health 3.9k
- Cognitive Neuroscience 4.2k
- Molecular Biology 9.1k
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-authors
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
Showing the 20 most-cited of 229 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Biological, clinical and population relevance of 95 loci for blood lipids Hit paper breakdown → | 2010 | 2946 |
| 2 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs Hit paper breakdown → | 2013 | 1775 |
| 3 | Hundreds of variants clustered in genomic loci and biological pathways affect human height Hit paper breakdown → | 2010 | 1546 |
| 4 | Analysis of shared heritability in common disorders of the brain Hit paper breakdown → | 2018 | 1441 |
| 5 | Large recurrent microdeletions associated with schizophrenia Hit paper breakdown → | 2008 | 1412 |
| 6 | Common variants conferring risk of schizophrenia Hit paper breakdown → | 2009 | 1402 |
| 7 | Mutational processes of simple-sequence repeat loci in human populations. Hit paper breakdown → | 1994 | 1333 |
| 8 | Replicating genotype–phenotype associations Hit paper breakdown → | 2007 | 1129 |
| 9 | Genome-wide association study identifies 30 loci associated with bipolar disorder Hit paper breakdown → | 2019 | 1065 |
| 10 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology Hit paper breakdown → | 2021 | 938 |
| 11 | A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis Hit paper breakdown → | 1998 | 836 |
| 12 | Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence Hit paper breakdown → | 2018 | 806 |
| 13 | Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects Hit paper breakdown → | 2016 | 773 |
| 14 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index Hit paper breakdown → | 2010 | 761 |
| 15 | Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Hit paper breakdown → | 2008 | 730 |
| 16 | Mapping the human genetic architecture of COVID-19 Hit paper breakdown → | 2021 | 641 |
| 17 | The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data Hit paper breakdown → | 2014 | 627 |
| 18 | A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis Hit paper breakdown → | 1998 | 619 |
| 19 | Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group Hit paper breakdown → | 2017 | 580 |
| 20 | Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes Hit paper breakdown → | 2018 | 543 |
About Nelson B. Freimer
Nelson B. Freimer is a scholar working on Genetics, Cognitive Neuroscience, Psychiatry and Mental health, Clinical Psychology and Molecular Biology, having authored 229 papers that have together received 36.4k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (83 papers), Genomic variations and chromosomal abnormalities (26 papers), Genetics and Neurodevelopmental Disorders (24 papers), Genomics and Rare Diseases (23 papers), Genetic Mapping and Diversity in Plants and Animals (21 papers), Autism Spectrum Disorder Research (16 papers), Obsessive-Compulsive Spectrum Disorders (15 papers) and Bipolar Disorder and Treatment (14 papers). The work is most often cited by research in Genetics (15.6k citations), Biological Psychiatry (1.1k citations), Psychiatry and Mental health (3.9k citations), Cognitive Neuroscience (4.2k citations) and Molecular Biology (9.1k citations). Nelson B. Freimer has collaborated with scholars based in United States, United Kingdom and Finland. Frequent co-authors include Montgomery Slatkin, Ana Maria Valdes, Amy C. Peterson, John E. Garza, Anna Di Rienzo, Susan K. Service, Chiara Sabatti, Laura N. Bull, Siamak Baharloo and Carrie E. Bearden. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Nature, Human Molecular Genetics and PLoS 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.