Mei Baker
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders
Papers in
- Genetics 17
- Genetics and Neurodevelopmental Disorders 14
- Neurogenetic and Muscular Disorders Research 5
- Immunology 13
- Immunodeficiency and Autoimmune Disorders 12
- Co-authors
- Jinkuk Hong (11 shared papers)Jan S. Greenberg (6 shared papers)Philip M. Farrell (7 shared papers)Gary Hoffman (7 shared papers)Matthew J. Maenner (2 shared papers)Charles D. Brokopp (6 shared papers)John M. Routes (7 shared papers)William J. Grossman (4 shared papers)
- Journals
- International Journal of Neonatal Screening (8 papers)Journal of Allergy and Clinical Immunology (4 papers)Genetics in Medicine (3 papers)The Journal of Pediatrics (3 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (3 papers)
- Partner nations
- United StatesSwitzerlandBrazil
In The Last Decade
Mei Baker
57 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 77
- Genetics 548
- Clinical Biochemistry 105
- Immunology 278
- Cognitive Neuroscience 222
- Genetics 101
Countries citing papers authored by Mei Baker
This map shows the geographic impact of Mei 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 Mei Baker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mei Baker more than expected).
Fields of papers citing papers by Mei Baker
This network shows the impact of papers produced by Mei 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 Mei Baker. The network helps show where Mei Baker may publish in the future.
Co-authors
The 25 scholars most cited alongside Mei 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 151 | |
| 2 | 2009 | 132 | |
| 3 | 2014 | 131 | |
| 4 | 2002 | 112 | |
| 5 | 2011 | 102 | |
| 6 | 2015 | 73 | |
| 7 | 2013 | 55 | |
| 8 | 2010 | 50 | |
| 9 | 2004 | 44 | |
| 10 | 2018 | 41 | |
| 11 | 2015 | 32 | |
| 12 | 2011 | 32 | |
| 13 | 2019 | 29 | |
| 14 | 2014 | 27 | |
| 15 | 2019 | 26 | |
| 16 | 2017 | 25 | |
| 17 | 2020 | 24 | |
| 18 | 2019 | 22 | |
| 19 | 2020 | 22 | |
| 20 | 2018 | 21 |
About Mei Baker
Mei Baker is a scholar working on Genetics, Immunology, Pulmonary and Respiratory Medicine, Cognitive Neuroscience and Epidemiology, having authored 57 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (14 papers), Immunodeficiency and Autoimmune Disorders (12 papers), Autism Spectrum Disorder Research (11 papers), Cystic Fibrosis Research Advances (11 papers), Metabolism and Genetic Disorders (8 papers), Respiratory viral infections research (7 papers), Thyroid Disorders and Treatments (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). The work is most often cited by research in Genetics (548 citations), Clinical Biochemistry (105 citations), Immunology (278 citations), Cognitive Neuroscience (222 citations) and Genetics (101 citations). Mei Baker has collaborated with scholars based in United States, Switzerland and Brazil. Frequent co-authors include Jinkuk Hong, Jan S. Greenberg, Philip M. Farrell, Gary Hoffman, Matthew J. Maenner, Charles D. Brokopp, John M. Routes, William J. Grossman, Daniel Mandel and Marsha Mailick Seltzer. Their work appears in journals such as International Journal of Neonatal Screening, Journal of Allergy and Clinical Immunology, Genetics in Medicine, The Journal of Pediatrics and American Journal of Medical Genetics Part B Neuropsychiatric 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.