David Schlessinger
Impact in
- Genetics top 0.02%
- Genetic Associations and Epidemiology
- Nutrition, Genetics, and Disease
- Bacterial Genetics and Biotechnology
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic and phenotypic traits in livestock
- Hemoglobinopathies and Related Disorders
- Aging top 0.5%
Papers in
- Genetics 162
- Genetic Associations and Epidemiology 77
- Genomic variations and chromosomal abnormalities 33
- Bacterial Genetics and Biotechnology 28
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 24
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- RNA and protein synthesis mechanisms 103
- RNA Research and Splicing 21
- Genomics and Chromatin Dynamics 18
- Co-authors
- David Apirion (23 shared papers)Gerald Medoff (30 shared papers)Chang‐Yi Cui (21 shared papers)Manuela Uda (25 shared papers)Alfred Tissieres (2 shared papers)Giuseppe Pilia (20 shared papers)Antonino Forabosco (15 shared papers)G S Kobayashi (16 shared papers)
- Journals
- Nature Genetics (29 papers)Genomics (27 papers)Proceedings of the National Academy of Sciences (26 papers)Journal of Molecular Biology (20 papers)Journal of Bacteriology (18 papers)
- Partner nations
- United StatesItalyUnited Kingdom
In The Last Decade
David Schlessinger
443 papers receiving 49.2k citations
David Schlessinger's Hit Papers
Peers
Comparison fields: 5 of 195
- Genetics 21.5k
- Aging 307
- Molecular Biology 11.8k
- Cardiology and Cardiovascular Medicine 3.4k
- Genetics 1.1k
Countries citing papers authored by David Schlessinger
This map shows the geographic impact of David Schlessinger'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 David Schlessinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Schlessinger more than expected).
Fields of papers citing papers by David Schlessinger
This network shows the impact of papers produced by David Schlessinger. 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 David Schlessinger. The network helps show where David Schlessinger may publish in the future.
Co-authors
The 25 scholars most cited alongside David Schlessinger, 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 446 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 | 2966 |
| 2 | Next-generation genotype imputation service and methods Hit paper breakdown → | 2016 | 2789 |
| 3 | Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index Hit paper breakdown → | 2010 | 2434 |
| 4 | A reference panel of 64,976 haplotypes for genotype imputation Hit paper breakdown → | 2016 | 2110 |
| 5 | Hundreds of variants clustered in genomic loci and biological pathways affect human height Hit paper breakdown → | 2010 | 1569 |
| 6 | Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits Hit paper breakdown → | 2007 | 1441 |
| 7 | Defining the role of common variation in the genomic and biological architecture of adult human height Hit paper breakdown → | 2014 | 1408 |
| 8 | Newly identified loci that influence lipid concentrations and risk of coronary artery disease Hit paper breakdown → | 2008 | 1363 |
| 9 | Common variants at 30 loci contribute to polygenic dyslipidemia Hit paper breakdown → | 2008 | 1180 |
| 10 | Genome-wide association study identifies eight loci associated with blood pressure Hit paper breakdown → | 2009 | 1023 |
| 11 | The DNA sequence of the human X chromosome Hit paper breakdown → | 2005 | 855 |
| 12 | The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome Hit paper breakdown → | 2001 | 836 |
| 13 | Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution Hit paper breakdown → | 2010 | 788 |
| 14 | Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses Hit paper breakdown → | 2016 | 768 |
| 15 | Complex genetic signatures in immune cells underlie autoimmunity and inform therapy Hit paper breakdown → | 2020 | 705 |
| 16 | Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome Hit paper breakdown → | 1996 | 659 |
| 17 | Ribonucleoprotein particles from Escherichia coli Hit paper breakdown → | 1959 | 627 |
| 18 | 1996 | 592 | |
| 19 | 2008 | 565 | |
| 20 | Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations Hit paper breakdown → | 2009 | 552 |
About David Schlessinger
David Schlessinger is a scholar working on Genetics, Molecular Biology, Urology, Cardiology and Cardiovascular Medicine and Endocrinology, Diabetes and Metabolism, having authored 446 papers that have together received 51.7k indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (103 papers), Genetic Associations and Epidemiology (77 papers), Genomic variations and chromosomal abnormalities (33 papers), Bacterial Genetics and Biotechnology (28 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (24 papers), RNA Research and Splicing (21 papers), Chromosomal and Genetic Variations (19 papers) and Genomics and Chromatin Dynamics (18 papers). The work is most often cited by research in Genetics (21.5k citations), Aging (307 citations), Molecular Biology (11.8k citations), Cardiology and Cardiovascular Medicine (3.4k citations) and Genetics (1.1k citations). David Schlessinger has collaborated with scholars based in United States, Italy and United Kingdom. Frequent co-authors include David Apirion, Gerald Medoff, Chang‐Yi Cui, Manuela Uda, Alfred Tissieres, Giuseppe Pilia, Antonino Forabosco, G S Kobayashi, James Dewey Watson and Antonio Cao. Their work appears in journals such as Nature Genetics, Genomics, Proceedings of the National Academy of Sciences, Journal of Molecular Biology and Journal of Bacteriology.
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.