Neil E. Lamb
Impact in
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- Prenatal Screening and Diagnostics
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
Papers in
- Genetics 19
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 6
- BRCA gene mutations in cancer 5
- Genetic Mapping and Diversity in Plants and Animals 4
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- DNA Repair Mechanisms 5
- Genetics, Bioinformatics, and Biomedical Research 4
- Co-authors
- Stephanie L. Sherman (10 shared papers)Terry Hassold (3 shared papers)S. L. Sherman (2 shared papers)Eleanor Feingold (6 shared papers)Irfan M. Hisamuddin (1 shared paper)Vincent W. Yang (1 shared paper)Brian A. Babbin (1 shared paper)Weidong Zhao (1 shared paper)
- Journals
- The American Journal of Human Genetics (4 papers)Cytogenetic and Genome Research (2 papers)Nature Genetics (2 papers)Comprehensive physiology (2 papers)Mammalian Genome (1 paper)
- Partner nations
- United StatesDenmarkSpain
In The Last Decade
Neil E. Lamb
28 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 80
- Pediatrics, Perinatology and Child Health 524
- Genetics 660
- Aging 20
- Molecular Biology 765
- Public Health, Environmental and Occupational Health 290
Countries citing papers authored by Neil E. Lamb
This map shows the geographic impact of Neil E. Lamb'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 Neil E. Lamb with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Neil E. Lamb more than expected).
Fields of papers citing papers by Neil E. Lamb
This network shows the impact of papers produced by Neil E. Lamb. 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 Neil E. Lamb. The network helps show where Neil E. Lamb may publish in the future.
Co-authors
The 25 scholars most cited alongside Neil E. Lamb, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 309 | |
| 2 | 2004 | 259 | |
| 3 | 1997 | 174 | |
| 4 | 2004 | 157 | |
| 5 | 2005 | 130 | |
| 6 | 2004 | 104 | |
| 7 | 2013 | 100 | |
| 8 | 2005 | 75 | |
| 9 | 2006 | 54 | |
| 10 | 2006 | 27 | |
| 11 | 2004 | 27 | |
| 12 | 2006 | 25 | |
| 13 | 1997 | 22 | |
| 14 | Methods for genetic linkage analysis using trisomies. | 1995 | 16 |
| 15 | 2020 | 8 | |
| 16 | 2003 | 8 | |
| 17 | 2022 | 6 | |
| 18 | 2012 | 4 | |
| 19 | 2016 | 4 | |
| 20 | 2009 | 4 |
About Neil E. Lamb
Neil E. Lamb is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health and Plant Science, having authored 28 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (6 papers), DNA Repair Mechanisms (5 papers), BRCA gene mutations in cancer (5 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers), Genetics, Bioinformatics, and Biomedical Research (4 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (524 citations), Genetics (660 citations), Aging (20 citations), Molecular Biology (765 citations) and Public Health, Environmental and Occupational Health (290 citations). Neil E. Lamb has collaborated with scholars based in United States, Denmark and Spain. Frequent co-authors include Stephanie L. Sherman, Terry Hassold, S. L. Sherman, Eleanor Feingold, Irfan M. Hisamuddin, Vincent W. Yang, Brian A. Babbin, Weidong Zhao, Mandayam O. Nandan and Sallie B. Freeman. Their work appears in journals such as The American Journal of Human Genetics, Cytogenetic and Genome Research, Nature Genetics, Comprehensive physiology and Mammalian Genome.
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.