David L. Nelson
Impact in
- Genetics top 0.05%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases
Papers in
- Genetics 122
- Genetics and Neurodevelopmental Disorders 92
- Genomic variations and chromosomal abnormalities 19
-
- Neurotransmitter Receptor Influence on Behavior 39
- Co-authors
- Stephen T. WarrenMaura PierettiC. Thomas CaskeyLaurence A. RubinJames S. SutcliffeCarole C. KurmanYing‐Hui FuRaymond G. Fenwick
- Journals
- Human Molecular Genetics (20 papers)The Journal of Immunology (15 papers)Journal of Pharmacology and Experimental Therapeutics (12 papers)Proceedings of the National Academy of Sciences (10 papers)The American Journal of Human Genetics (9 papers)
- Partner nations
- United StatesNetherlandsItaly
In The Last Decade
David L. Nelson
309 papers receiving 21.4k citations
Hit Papers
Peers
Comparison fields: 5 of 184
- Genetics 9.2k
- Cellular and Molecular Neuroscience 3.9k
- Cognitive Neuroscience 3.8k
- Molecular Biology 11.8k
- Immunology 3.1k
Countries citing papers authored by David L. Nelson
This map shows the geographic impact of David L. Nelson'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 L. Nelson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David L. Nelson more than expected).
Fields of papers citing papers by David L. Nelson
This network shows the impact of papers produced by David L. Nelson. 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 L. Nelson. The network helps show where David L. Nelson may publish in the future.
Co-authors
The 25 scholars most cited alongside David L. Nelson, 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 | 2022 | 26 | |
| 2 | 2019 | 2 | |
| 3 | 2013 | 256 | |
| 4 | 2009 | 83 | |
| 5 | 2008 | 100 | |
| 6 | 2008 | 38 | |
| 7 | 2007 | 34 | |
| 8 | 2006 | 97 | |
| 9 | Lecture notebook for Lehninger principles of biochemistry | 2005 | 3 |
| 10 | 2003 | 3 | |
| 11 | 2002 | 35 | |
| 12 | A Universal Technique for Relating Heterogeneous Data Models | 2001 | 2 |
| 13 | 1998 | 59 | |
| 14 | Large domains of apparent delayed replication timing associated with triplet repeat expansion at FRAXA and FRAXE. | 1996 | 63 |
| 15 | 1996 | 34 | |
| 16 | FMR1 in global populations. | 1996 | 65 |
| 17 | 1995 | 6 | |
| 18 | Absence of FMR1 protein in two mentally retarded fragile X males without CGG repeat expansion | 1994 | 2 |
| 19 | 1993 | 35 | |
| 20 | A sagebrush wilt disease of unknown cause | 1981 | 4 |
About David L. Nelson
David L. Nelson is a scholar working on Genetics, Cellular and Molecular Neuroscience, Molecular Biology, Immunology and Cell Biology, having authored 316 papers that have together received 22.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (92 papers), Neurotransmitter Receptor Influence on Behavior (39 papers), Autism Spectrum Disorder Research (38 papers), Receptor Mechanisms and Signaling (26 papers), Immune Cell Function and Interaction (25 papers), Genomic variations and chromosomal abnormalities (19 papers), Cellular Mechanics and Interactions (16 papers) and RNA modifications and cancer (16 papers). The work is most often cited by research in Genetics (9.2k citations), Cellular and Molecular Neuroscience (3.9k citations), Cognitive Neuroscience (3.8k citations), Molecular Biology (11.8k citations) and Immunology (3.1k citations). David L. Nelson has collaborated with scholars based in United States, Netherlands and Italy. Frequent co-authors include Stephen T. Warren, Maura Pieretti, C. Thomas Caskey, Laurence A. Rubin, James S. Sutcliffe, Stephen T. Warren, Carole C. Kurman, Ying‐Hui Fu, Raymond G. Fenwick and Antonio Pizzuti. Their work appears in journals such as Human Molecular Genetics, The Journal of Immunology, Journal of Pharmacology and Experimental Therapeutics, Proceedings of the National Academy of Sciences and The American Journal of Human 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.