Tyler Reimschisel

2.5k total citations
22 papers, 779 citations indexed

About

Tyler Reimschisel is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Tyler Reimschisel has authored 22 papers receiving a total of 779 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Tyler Reimschisel's work include Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (4 papers) and Congenital heart defects research (4 papers). Tyler Reimschisel is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (4 papers) and Congenital heart defects research (4 papers). Tyler Reimschisel collaborates with scholars based in United States, United Kingdom and Canada. Tyler Reimschisel's co-authors include Jennifer Huang, Anna L. Herring, Christina A. Gurnett, Matthew B. Dobbs, Stephanie Boehm, Anne M. Connolly, Melissa L McPheeters, Shanthi Krishnaswami, Michael Landt and Mary O. Carayannopoulos and has published in prestigious journals such as Neurology, PEDIATRICS and Human Molecular Genetics.

In The Last Decade

Tyler Reimschisel

21 papers receiving 737 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tyler Reimschisel United States 15 243 161 148 135 128 22 779
Andrea Paola Rojas Gil Greece 14 240 1.0× 78 0.5× 33 0.2× 177 1.3× 10 0.1× 77 778
Fahad A. Bashiri Saudi Arabia 12 131 0.5× 96 0.6× 92 0.6× 48 0.4× 14 0.1× 63 552
Giulia Frisso Italy 22 557 2.3× 146 0.9× 72 0.5× 42 0.3× 2 0.0× 89 1.3k
Guy Massa Belgium 23 536 2.2× 520 3.2× 28 0.2× 111 0.8× 3 0.0× 60 1.5k
John S. Fuqua United States 16 381 1.6× 294 1.8× 10 0.1× 130 1.0× 6 0.0× 45 1.1k
M. Suzuki Japan 13 145 0.6× 76 0.5× 53 0.4× 71 0.5× 3 0.0× 20 660
Nancy McNamara United States 15 173 0.7× 46 0.3× 31 0.2× 237 1.8× 10 0.1× 26 806
Paula Costello United Kingdom 12 160 0.7× 47 0.3× 37 0.3× 57 0.4× 46 0.4× 16 516
Shu‐Chuan Chiang Taiwan 14 186 0.8× 74 0.5× 92 0.6× 53 0.4× 4 0.0× 22 913
Merve İnanç Türkiye 15 129 0.5× 20 0.1× 73 0.5× 120 0.9× 12 0.1× 44 892

Countries citing papers authored by Tyler Reimschisel

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Tyler Reimschisel

This figure shows the co-authorship network connecting the top 25 collaborators of Tyler Reimschisel. A scholar is included among the top collaborators of Tyler Reimschisel based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Tyler Reimschisel. Tyler Reimschisel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Thurm, Cary, Matt Hall, Jonathan H. Soslow, et al.. (2019). Heart Transplantation in Children with Mitochondrial Disease. The Journal of Pediatrics. 217. 46–51.e4. 9 indexed citations
2.
Ferdinandusse, Sacha, Joy D. Cogan, D.N. Cooper, et al.. (2018). Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant. American Journal of Medical Genetics Part A. 176(3). 692–698. 23 indexed citations
3.
Reimschisel, Tyler, et al.. (2017). A systematic review of the published literature on team-based learning in health professions education. Medical Teacher. 39(12). 1227–1237. 169 indexed citations
4.
Krishnaswami, Shanthi, Tyler Reimschisel, Christopher Fonnesbeck, et al.. (2016). Systematic review of large neutral amino acids for treatment of phenylketonuria. 3(4). 181–186.
5.
Barber, John, Jill A. Rosenfeld, John M. Graham, et al.. (2015). Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance. American Journal of Medical Genetics Part A. 167(9). 2052–2064. 28 indexed citations
6.
Williams, S., Kathryn M. Edwards, Roger Baxter, et al.. (2013). Comprehensive Assessment of Serious Adverse Events Following Immunization by Health Care Providers. The Journal of Pediatrics. 162(6). 1276–1281.e1. 9 indexed citations
7.
Lindegren, Mary Lou, Shanthi Krishnaswami, Tyler Reimschisel, et al.. (2012). A Systematic Review of BH4 (Sapropterin) for the Adjuvant Treatment of Phenylketonuria. JIMD Reports. 8. 109–119. 21 indexed citations
8.
Dharmadhikari, Avinash V., Przemysław Szafrański, Richard Person, et al.. (2012). Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148. Human Molecular Genetics. 21(15). 3345–3355. 17 indexed citations
9.
Fleming, Amy, William B. Cutrer, Tyler Reimschisel, & Joseph Gigante. (2012). You Too Can Teach Clinical Reasoning!. PEDIATRICS. 130(5). 795–797. 17 indexed citations
10.
McPheeters, Melissa L, Mary Lou Lindegren, Nila A Sathe, & Tyler Reimschisel. (2012). Adjuvant Treatment for Phenylketonuria: Future Research Needs. 1 indexed citations
11.
Krishnaswami, Shanthi, Chris Fonnesbeck, Tyler Reimschisel, et al.. (2012). Adjuvant Treatment for Phenylketonuria (PKU) [Internet]. 1 indexed citations
12.
Fonnesbeck, Christopher, et al.. (2012). Estimating the probability of IQ impairment from blood phenylalanine for phenylketonuria patients: a hierarchical meta‐analysis. Journal of Inherited Metabolic Disease. 36(5). 757–766. 34 indexed citations
13.
Bartnik, Magdalena, Katarzyna Derwińska, Monika Goś, et al.. (2011). Early-onset seizures due to mosaic exonic deletions of CDKL5 in a male and two females. Genetics in Medicine. 13(5). 447–452. 38 indexed citations
14.
Schiffmann, Raphael, Rick A. Martin, Tyler Reimschisel, et al.. (2010). Four-Year Prospective Clinical Trial of Agalsidase Alfa in Children with Fabry Disease. The Journal of Pediatrics. 156(5). 832–837.e1. 49 indexed citations
15.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Patricia I. Bader, et al.. (2010). Phenotypic manifestations of copy number variation in chromosome 16p13.11. European Journal of Human Genetics. 19(3). 280–286. 83 indexed citations
16.
Shchelochkov, Oleg A., Fangyuan Li, Michael T. Geraghty, et al.. (2009). High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH. Molecular Genetics and Metabolism. 96(3). 97–105. 44 indexed citations
17.
Gurnett, Christina A., Stephanie Boehm, Anne M. Connolly, Tyler Reimschisel, & Matthew B. Dobbs. (2008). Impact of congenital talipes equinovarus etiology on treatment outcomes. Developmental Medicine & Child Neurology. 50(7). 498–502. 91 indexed citations
18.
Dietzen, Dennis J., et al.. (2008). Rapid comprehensive amino acid analysis by liquid chromatography/tandem mass spectrometry: comparison to cation exchange with post‐column ninhydrin detection. Rapid Communications in Mass Spectrometry. 22(22). 3481–3488. 78 indexed citations
19.
Williams, Michael A., Glenn A. Mackin, H. Richard Beresford, et al.. (2006). American Academy of Neurology qualifications and guidelines for the physician expert witness. Neurology. 66(1). 13–14. 27 indexed citations
20.
Reimschisel, Tyler, Yu‐Qiang Ding, Elizabeth Sweeney, et al.. (2004). A neurological phenotype in nail patella syndrome (NPS) patients illuminated by studies of murine Lmx1b expression. European Journal of Human Genetics. 13(3). 330–335. 23 indexed citations

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.

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