M. Lance Cooper
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 14
- Genetics and Neurodevelopmental Disorders 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genomics and Rare Diseases 2
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- Chromosomal and Genetic Variations 7
- Co-authors
- Sau Wai Cheung (19 shared papers)Ankita Patel (10 shared papers)Paweł Stankiewicz (9 shared papers)A. Craig Chinault (6 shared papers)Zhishuo Ou (9 shared papers)Chad A. Shaw (4 shared papers)James R. Lupski (4 shared papers)Carlos A. Bacino (5 shared papers)
- Journals
- American Journal of Medical Genetics Part A (11 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)Molecular Cytogenetics (1 paper)Journal of Heredity (1 paper)PLoS ONE (1 paper)
- Partner nations
- United StatesTaiwanCanada
In The Last Decade
M. Lance Cooper
19 papers receiving 791 citations
Peers
Comparison fields: 5 of 60
- Genetics 624
- Pediatrics, Perinatology and Child Health 183
- Molecular Biology 328
- Plant Science 167
- Developmental Biology 9
Countries citing papers authored by M. Lance Cooper
This map shows the geographic impact of M. Lance Cooper'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 M. Lance Cooper with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Lance Cooper more than expected).
Fields of papers citing papers by M. Lance Cooper
This network shows the impact of papers produced by M. Lance Cooper. 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 M. Lance Cooper. The network helps show where M. Lance Cooper may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Lance Cooper, 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 | 2005 | 185 | |
| 2 | 2007 | 148 | |
| 3 | 2010 | 81 | |
| 4 | 2007 | 62 | |
| 5 | 2010 | 58 | |
| 6 | 2008 | 45 | |
| 7 | 2007 | 45 | |
| 8 | 2005 | 38 | |
| 9 | 2016 | 32 | |
| 10 | 2008 | 32 | |
| 11 | 2008 | 30 | |
| 12 | 2008 | 19 | |
| 13 | 2010 | 17 | |
| 14 | 2007 | 15 | |
| 15 | 2008 | 11 | |
| 16 | 2010 | 10 | |
| 17 | 2006 | 9 | |
| 18 | 2005 | 7 | |
| 19 | 2006 | 3 |
About M. Lance Cooper
M. Lance Cooper is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 19 papers that have together received 847 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genetics and Neurodevelopmental Disorders (7 papers), Chromosomal and Genetic Variations (7 papers), Congenital heart defects research (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Autism Spectrum Disorder Research (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (624 citations), Pediatrics, Perinatology and Child Health (183 citations), Molecular Biology (328 citations), Plant Science (167 citations) and Developmental Biology (9 citations). M. Lance Cooper has collaborated with scholars based in United States, Taiwan and Canada. Frequent co-authors include Sau Wai Cheung, Ankita Patel, Paweł Stankiewicz, A. Craig Chinault, Zhishuo Ou, Chad A. Shaw, James R. Lupski, Carlos A. Bacino, Svetlana A. Yatsenko and Arthur L. Beaudet. Their work appears in journals such as American Journal of Medical Genetics Part A, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Molecular Cytogenetics, Journal of Heredity and PLoS ONE.
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.