Tyler Reimschisel
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
- Family Practice top 10%
Papers in
-
- Congenital heart defects research 4
- Mitochondrial Function and Pathology 3
- Metabolomics and Mass Spectrometry Studies 2
-
- Metabolism and Genetic Disorders 10
- Co-authors
- Jennifer Huang (1 shared paper)Anna L. Herring (1 shared paper)Stephan 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 (7 shared papers)Shanthi Krishnaswami (5 shared papers)
- Journals
- The Journal of Pediatrics (3 papers)European Journal of Human Genetics (2 papers)Human Molecular Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)Molecular Genetics and Metabolism (1 paper)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Tyler Reimschisel
22 papers receiving 784 citations
Tyler Reimschisel's Hit Papers
Peers
Comparison fields: 5 of 103
- Clinical Biochemistry 156
- Family Practice 16
- Orthopedics and Sports Medicine 62
- Biochemistry 43
- Developmental Biology 13
Countries citing papers authored by Tyler Reimschisel
This map shows the geographic impact of Tyler 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 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 Reimschisel more than expected).
Fields of papers citing papers by Tyler Reimschisel
This network shows the impact of papers produced by Tyler 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 Reimschisel. The network helps show where Tyler Reimschisel may publish in the future.
Co-authors
The 25 scholars most cited alongside Tyler 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A systematic review of the published literature on team-based learning in health professions education Hit paper breakdown → | 2017 | 187 |
| 2 | 2008 | 94 | |
| 3 | 2010 | 86 | |
| 4 | 2008 | 81 | |
| 5 | 2010 | 50 | |
| 6 | 2009 | 50 | |
| 7 | 2012 | 39 | |
| 8 | 2011 | 39 | |
| 9 | 2015 | 31 | |
| 10 | 2006 | 28 | |
| 11 | 2018 | 25 | |
| 12 | 2004 | 25 | |
| 13 | 2012 | 22 | |
| 14 | 2012 | 19 | |
| 15 | 2012 | 17 | |
| 16 | Adjuvant Treatment for Phenylketonuria (PKU) | 2012 | 14 |
| 17 | 2019 | 10 | |
| 18 | 2013 | 10 | |
| 19 | Adjuvant Treatment for Phenylketonuria: Future Research Needs: Identification of Future Research Needs From Comparative Effectiveness Review No. 56 | 2012 | 3 |
| 20 | 2012 | 2 |
About Tyler Reimschisel
Tyler Reimschisel is a scholar working on Molecular Biology, Clinical Biochemistry, Genetics, Pediatrics, Perinatology and Child Health and Biochemistry, having authored 23 papers that have together received 834 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (10 papers), Congenital heart defects research (4 papers), Amino Acid Enzymes and Metabolism (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Mitochondrial Function and Pathology (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Metabolomics and Mass Spectrometry Studies (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Clinical Biochemistry (156 citations), Family Practice (16 citations), Orthopedics and Sports Medicine (62 citations), Biochemistry (43 citations) and Developmental Biology (13 citations). Tyler Reimschisel has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Jennifer Huang, Anna L. Herring, Stephan Böhm, Christina A. Gurnett, Matthew B. Dobbs, Anne M. Connolly, Melissa L McPheeters, Shanthi Krishnaswami, Dennis J. Dietzen and Michael Landt. Their work appears in journals such as The Journal of Pediatrics, European Journal of Human Genetics, Human Molecular Genetics, Journal of Inherited Metabolic Disease and Molecular Genetics and Metabolism.
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.