Carl Baker
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 25
- Genomic variations and chromosomal abnormalities 20
- Genomics and Rare Diseases 7
- Genetic diversity and population structure 3
- Genetics and Neurodevelopmental Disorders 3
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- Genomics and Phylogenetic Studies 8
- Co-authors
- Evan E. Eichler (30 shared papers)Raphael Bernier (7 shared papers)Santhosh Girirajan (8 shared papers)Laura Vives (4 shared papers)Deborah A. Nickerson (6 shared papers)Jay Shendure (4 shared papers)Maika Malig (6 shared papers)William A. Catterall (3 shared papers)
- Journals
- Genome Research (5 papers)The American Journal of Human Genetics (5 papers)Nature Genetics (3 papers)Nature Communications (2 papers)Science (2 papers)
- Partner nations
- United StatesItalySpain
In The Last Decade
Carl Baker
34 papers receiving 4.9k citations
Carl Baker's Hit Papers
Peers
Comparison fields: 5 of 123
- Genetics 2.9k
- Cognitive Neuroscience 909
- Molecular Biology 2.5k
- Cellular and Molecular Neuroscience 421
- Plant Science 749
Countries citing papers authored by Carl Baker
This map shows the geographic impact of Carl Baker'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 Carl Baker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carl Baker more than expected).
Fields of papers citing papers by Carl Baker
This network shows the impact of papers produced by Carl Baker. 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 Carl Baker. The network helps show where Carl Baker may publish in the future.
Co-authors
The 25 scholars most cited alongside Carl Baker, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations Hit paper breakdown → | 2011 | 810 |
| 2 | Personalized copy number and segmental duplication maps using next-generation sequencing Hit paper breakdown → | 2009 | 508 |
| 3 | 2009 | 420 | |
| 4 | Excess of rare, inherited truncating mutations in autism Hit paper breakdown → | 2015 | 348 |
| 5 | 2010 | 328 | |
| 6 | 1996 | 233 | |
| 7 | 2014 | 227 | |
| 8 | 2011 | 222 | |
| 9 | 2016 | 218 | |
| 10 | 2013 | 212 | |
| 11 | 2009 | 167 | |
| 12 | 2013 | 108 | |
| 13 | 2013 | 105 | |
| 14 | 2009 | 101 | |
| 15 | 1998 | 100 | |
| 16 | 2019 | 84 | |
| 17 | 2018 | 82 | |
| 18 | 2009 | 69 | |
| 19 | 2011 | 69 | |
| 20 | 1997 | 66 |
About Carl Baker
Carl Baker is a scholar working on Genetics, Molecular Biology, Plant Science, Cognitive Neuroscience and Pediatrics, Perinatology and Child Health, having authored 34 papers that have together received 5.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Chromosomal and Genetic Variations (15 papers), Genomics and Phylogenetic Studies (8 papers), Genomics and Rare Diseases (7 papers), Autism Spectrum Disorder Research (6 papers), Prenatal Screening and Diagnostics (4 papers), Genetic diversity and population structure (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (2.9k citations), Cognitive Neuroscience (909 citations), Molecular Biology (2.5k citations), Cellular and Molecular Neuroscience (421 citations) and Plant Science (749 citations). Carl Baker has collaborated with scholars based in United States, Italy and Spain. Frequent co-authors include Evan E. Eichler, Raphael Bernier, Santhosh Girirajan, Laura Vives, Deborah A. Nickerson, Jay Shendure, Maika Malig, William A. Catterall, Bradley P. Coe and Can Alkan. Their work appears in journals such as Genome Research, The American Journal of Human Genetics, Nature Genetics, Nature Communications and Science.
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.