Tyler E. Reimschisel
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Metabolism and Genetic Disorders 12
- Genetics 9
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 5
- Co-authors
- Jennifer Chunyan Huang (1 shared paper)Anna L. Herring (1 shared paper)Stephan Karl Böhm (1 shared paper)Christina A. Gurnett (1 shared paper)Matthew B. Dobbs (1 shared paper)Anne M. Connolly (1 shared paper)Melissa L McPheeters (5 shared papers)Shanthi Krishnaswami (4 shared papers)
- Journals
- Genetics in Medicine (4 papers)The Journal of Pediatrics (3 papers)Mitochondrion (2 papers)European Journal of Human Genetics (2 papers)Human Mutation (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Tyler E. Reimschisel
28 papers receiving 1.9k citations
Tyler E. Reimschisel's Hit Papers
Peers
Comparison fields: 5 of 117
- Clinical Biochemistry 304
- Genetics 745
- Molecular Biology 874
- Pediatrics, Perinatology and Child Health 173
- Biochemistry 67
Countries citing papers authored by Tyler E. Reimschisel
This map shows the geographic impact of Tyler E. Reimschisel'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 Tyler E. Reimschisel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tyler E. Reimschisel more than expected).
Fields of papers citing papers by Tyler E. Reimschisel
This network shows the impact of papers produced by Tyler E. Reimschisel. 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 Tyler E. Reimschisel. The network helps show where Tyler E. Reimschisel may publish in the future.
Co-authors
The 25 scholars most cited alongside Tyler E. Reimschisel, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 503 | |
| 2 | 2017 | 230 | |
| 3 | 2010 | 210 | |
| 4 | A systematic review of the published literature on team-based learning in health professions education Hit paper breakdown → | 2017 | 194 |
| 5 | 2010 | 97 | |
| 6 | 2008 | 91 | |
| 7 | 2008 | 83 | |
| 8 | 2017 | 56 | |
| 9 | 2010 | 54 | |
| 10 | 2009 | 51 | |
| 11 | 2012 | 49 | |
| 12 | 2011 | 43 | |
| 13 | 2012 | 42 | |
| 14 | 2013 | 41 | |
| 15 | 2013 | 35 | |
| 16 | 2015 | 32 | |
| 17 | 2006 | 29 | |
| 18 | 2018 | 28 | |
| 19 | 2012 | 27 | |
| 20 | 2004 | 26 |
About Tyler E. Reimschisel
Tyler E. Reimschisel is a scholar working on Clinical Biochemistry, Genetics, Molecular Biology, Biochemistry and Pediatrics, Perinatology and Child Health, having authored 29 papers that have together received 2.0k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (12 papers), Mitochondrial Function and Pathology (7 papers), Congenital heart defects research (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (5 papers), Amino Acid Enzymes and Metabolism (2 papers), Metabolomics and Mass Spectrometry Studies (2 papers) and Pharmacological Effects and Toxicity Studies (2 papers). The work is most often cited by research in Clinical Biochemistry (304 citations), Genetics (745 citations), Molecular Biology (874 citations), Pediatrics, Perinatology and Child Health (173 citations) and Biochemistry (67 citations). Tyler E. Reimschisel has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Jennifer Chunyan Huang, Anna L. Herring, Stephan Karl Böhm, Christina A. Gurnett, Matthew B. Dobbs, Anne M. Connolly, Melissa L McPheeters, Shanthi Krishnaswami, Mary O. Carayannopoulos and Christopher Fonnesbeck. Their work appears in journals such as Genetics in Medicine, The Journal of Pediatrics, Mitochondrion, European Journal of Human Genetics and Human Mutation.
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.