Eric Schmitt

3.7k citations

68 papers · 2.0k indexed · h-index 24

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Neuropsychology and Physiological Psychology top 5%

Papers in ⓘ

Neuropsychology and Physiological Psychology 5
Clinical Biochemistry 19
- Metabolism and Genetic Disorders 19

Co-authors: Lee‐Jun C. Wong (15 shared papers)Andreas Kruse (8 shared papers)Leisa Johnson (1 shared paper)Karen Cichowski (1 shared paper)Tyler Jacks (1 shared paper)Elizabeth A. Murphy (1 shared paper)Kim L. Mercer (1 shared paper)Doron C. Greenbaum (1 shared paper)
Journals: Molecular Genetics and Metabolism (10 papers)Genetics in Medicine (5 papers)Human Mutation (5 papers)Mitochondrion (2 papers)Functional Ecology (1 paper)
Partner nations: United States Germany France

In The Last Decade

Eric Schmitt

65 papers receiving 2.0k citations

Peers

Countries citing papers authored by Eric Schmitt

Since Specialization

Citations

This map shows the geographic impact of Eric Schmitt'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 Eric Schmitt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Schmitt more than expected).

Fields of papers citing papers by Eric Schmitt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric Schmitt. 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 Eric Schmitt. The network helps show where Eric Schmitt may publish in the future.

Co-authors

The 25 scholars most cited alongside Eric Schmitt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eric Schmitt Line = papers co-authored together Eric Schmitt links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 68 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	K-ras is an essential gene in the mouse with partial functional overlap with N-ras Genes & Development ·Leisa Johnson, Doron C. Greenbaum, Karen Cichowski, Kim L. Mercer, Elizabeth A. Murphy, Eric Schmitt, Roderick T. Bronson, H Umanoff, W Edelmann, Raju Kucherlapati, Tyler Jacks	1997	449
2	Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase Human Mutation ·David Dimmock, Q. Zhang, Carlo Dionisi‐Vici, Rosalba Carrozzo, Joseph T.C. Shieh, L-Y Tang, Cavatina K. Truong, Eric Schmitt, Mara Sifry-Platt, S. Lucioli, Filippo M. Santorelli, (unknown), Maria Angeles Rodríguez, Klaas J. Wierenga, Gregory M. Enns, Nicola Longo, Mark Lipson, Hilary Vallance, W. J. Craigen, Fernando Scaglia, L-J. C. Wong	2008	123
3	Quantitative Evaluation of the Mitochondrial DNA Depletion Syndrome Clinical Chemistry ·David Dimmock, Lin-ya Tang, Eric Schmitt, Lee‐Jun C. Wong	2010	101
4	Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy Hepatology ·Lee-Jun Wong, Nicola Brunetti‐Pierri, Qing Zhang, Nada Yazigi, Kevin E. Bove, Beverly Barrett Dahms, Michelle A. Puchowicz, Ignacio González-Gómez, Eric Schmitt, Cavatina K. Truong, Charles L. Hoppel, Ping‐Chieh Chou, Jing Wang, Erin E. Baldwin, Darius J. Adams, Nancy Leslie, Richard G. Boles, Douglas S. Kerr, William J. Craigen	2007	94
5	Closely related families of genes code for the α and α‘ subunits of the soybean 7S storage protein complex Nucleic Acids Research ·Mary A. Schuler, Eric Schmitt, Roger N. Beachy	1982	89
6	Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects Human Mutation ·Sha Tang, Jing Wang, Victor Wei Zhang, Fangyuan Li, Megan Landsverk, Hong Cui, Cavatina K. Truong, Guoli Wang, Li Chieh Chen, Brett H. Graham, Fernando Scaglia, Eric Schmitt, William J. Craigen, Lee‐Jun C. Wong	2013	70
7	Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization Human Mutation ·Daniela del Gaudio, Yaping Yang, Barbara A. Boggs, Eric Schmitt, Jennifer A. Lee, Trilochan Sahoo, Hoang T. Pham, Joanna Wiszniewska, A. Craig Chinault, Arthur L. Beaudet, Christine M. Eng	2008	69
8	The prevalence of the 235delC GJB2 mutation in a Chinese deaf population Genetics in Medicine ·Pu Dai, Fei Yu, Bing Han, Yongyi Yuan, Qi Li, Guojian Wang, Xin Liu, Jia He, Deliang Huang, Dongyang Kang, Xin Zhang, Huijun Yuan, Eric Schmitt, Dongyi Han, Lee‐Jun C. Wong	2007	65
9	Genomic Analyses Yield Markers for Identifying Agronomically Important Genes in Potato Molecular Plant ·Yangping Li, Christophe Colleoni, Junjie Zhang, Qiqi Liang, Yufeng Hu, Holly Ruess, Reinhard Simon, Ying‐Hong Liu, Hanmei Liu, Guowu Yu, Eric Schmitt, Chloé Ponitzki, Guangjian Liu, Huanhuan Huang, Feilong Zhan, Lin Chen, Yubi Huang, David M. Spooner, Binquan Huang	2018	61
10	DNA sequence analysis of GJB2, encoding connexin 26: Observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls American Journal of Medical Genetics Part A ·Hsiao‐Yuan Tang, Ping Fang, Patricia A. Ward, Eric Schmitt, Sandra Darilek, Spiros Manolidis, John S. Oghalai, Benjamin B. Roa, Raye Lynn Alford	2006	60
11	MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: New patients and novel mutations Molecular Genetics and Metabolism ·Ayman W. El‐Hattab, Fang-Yuan Li, Eric Schmitt, Shulin Zhang, William J. Craigen, Lee-Jun Wong	2009	59
12	Molecular spectrum of SLC22A5 (OCTN2) gene mutations detected in 143 subjects evaluated for systemic carnitine deficiency Human Mutation ·Fangyuan Li, Ayman W. El‐Hattab, Erawati V. Bawle, Richard G. Boles, Eric Schmitt, Fernando Scaglia, Lee‐Jun C. Wong	2010	59
13	Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 gene Molecular Genetics and Metabolism ·Lindsay C. Burrage, Sha Tang, Jing Wang, Taraka Donti, Magdalena Walkiewicz, James M. Luchak, Li-Chieh Chen, Eric Schmitt, Zhiyv Niu, Rodrigo Eraña, Jill V. Hunter, Brett H. Graham, Lee-Jun Wong, Fernando Scaglia	2014	52
14	A multidimensional scale for the measurement of agreement with age stereotypes and the salience of age in social interaction Ageing and Society ·Andreas Kruse, Eric Schmitt	2006	46
15	Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes PLoS ONE ·Bekim Sadiković, Jing Wang, Ayman W. El‐Hattab, Megan Landsverk, Ganka Douglas, Ellen K. Brundage, William J. Craigen, Eric Schmitt, Lee‐Jun C. Wong	2010	41
16	Regional genomic instability predisposes to complex dystrophin gene rearrangements Human Genetics ·Junko Oshima, Daniel B. Magner, Jennifer A. Lee, Amy M. Breman, Eric Schmitt, Lisa D. White, Carol A. Crowe, Michelle Merrill, Parul Jayakar, Aparna Rajadhyaksha, Christine M. Eng, Daniela del Gaudio	2009	40
17	Interpretation of mitochondrial tRNA variants Genetics in Medicine ·Lee‐Jun C. Wong, Ting Chen, Jing Wang, Sha Tang, Eric Schmitt, Megan Landsverk, Fangyuan Li, Yue Wang, Shulin Zhang, Victor Wei Zhang, William J. Craigen	2020	37
18	Evolution of Young Sex Chromosomes in Two Dioecious Sister Plant Species with Distinct Sex Determination Systems Genome Biology and Evolution ·Hélène Martin, Fantin Carpentier, Sophie Gallina, Cécile Godé, Eric Schmitt, Aline Muyle, Gabriel Marais, Pascal Touzet	2019	33
19	An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory’s experience Genetics in Medicine ·Jing Wang, Eric Schmitt, Megan Landsverk, Victor Wei Zhang, Fangyuan Li, Brett H. Graham, William J. Craigen, Lee‐Jun C. Wong	2012	30
20	A Comprehensive Strategy for Accurate Mutation Detection of the Highly Homologous PMS2 Journal of Molecular Diagnostics ·Jianli Li, Hongzheng Dai, Yanming Feng, Jia Tang, Stella Chen, Tian Xia, Elizabeth Gorman, Eric Schmitt, Terah A.A. Hansen, Jing Wang, Sharon E. Plon, Victor Wei Zhang, Lee‐Jun C. Wong	2015	30

About Eric Schmitt

Eric Schmitt is a scholar working on Neuropsychology and Physiological Psychology, Clinical Biochemistry, Genetics, Ecology, Evolution, Behavior and Systematics and Molecular Biology, having authored 68 papers that have together received 2.0k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (19 papers), Mitochondrial Function and Pathology (13 papers), Plant and animal studies (7 papers), RNA modifications and cancer (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), ATP Synthase and ATPases Research (5 papers) and Biochemical and Molecular Research (5 papers). The work is most often cited by research in Clinical Biochemistry (547 citations), Neuropsychology and Physiological Psychology (64 citations), Sensory Systems (124 citations), Molecular Biology (1.4k citations) and Genetics (301 citations). Eric Schmitt has collaborated with scholars based in United States, Germany and France. Frequent co-authors include Lee‐Jun C. Wong, Andreas Kruse, Leisa Johnson, Karen Cichowski, Tyler Jacks, Elizabeth A. Murphy, Kim L. Mercer, Doron C. Greenbaum, Roderick T. Bronson and Raju Kucherlapati. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, Human Mutation, Mitochondrion and Functional Ecology.

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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