Michael Woontner

1.6k total citations
36 papers, 1.0k citations indexed

About

Michael Woontner is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Michael Woontner has authored 36 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 28 papers in Clinical Biochemistry and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Michael Woontner's work include Metabolism and Genetic Disorders (28 papers), Mitochondrial Function and Pathology (18 papers) and Biochemical and Molecular Research (9 papers). Michael Woontner is often cited by papers focused on Metabolism and Genetic Disorders (28 papers), Mitochondrial Function and Pathology (18 papers) and Biochemical and Molecular Research (9 papers). Michael Woontner collaborates with scholars based in United States, Brazil and Uruguay. Michael Woontner's co-authors include Judith A. Jaehning, Stephen I. Goodman, Paul A. Wade, David M. Koeller, Moaçir Wajner, Gunter B. Kohlhaw, J. José Bonner, Frank E. Frerman, Diogo O. Souza and Jelena Lazović and has published in prestigious journals such as Science, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Michael Woontner

35 papers receiving 997 citations

Peers

Countries citing papers authored by Michael Woontner

Since Specialization

Citations

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

Fields of papers citing papers by Michael Woontner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Woontner

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Woontner. A scholar is included among the top collaborators of Michael Woontner 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 Michael Woontner. Michael Woontner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Increased susceptibility to quinolinic acid‐induced seizures and long‐term changes in brain oscillations in an animal model of glutaric acidemia type I 2021 ·Journal of Neuroscience Research ·(unknown), (unknown), Bianca Seminotti, Michael Woontner, Moaçir Wajner, María Elisa Calcagnotto	0
2	REVIEW: Practical strategies to maintain anabolism by intravenous nutritional management in children with inborn metabolic diseases 2021 ·Molecular Genetics and Metabolism ·(unknown), Peter R. Baker, Janet A. Thomas, Heather E. Skillman, Laurie Bernstein, Sommer Gaughan, (unknown), Curtis R. Coughlin, Shawn E. McCandless, Austin Larson, (unknown), (unknown), Erica Wymore, (unknown), Michael Woontner, Johan L.K. Van Hove	6
3	An explanation for metabolite excretion in high- and low-excretor patients with glutaric acidemia type 1 2019 ·Molecular Genetics and Metabolism ·Stephen I. Goodman, Michael Woontner	2
4	Long Lasting High Lysine Diet Aggravates White Matter Injury in Glutaryl-CoA Dehydrogenase Deficient (Gcdh−/−) Mice 2018 ·Molecular Neurobiology ·Silvia Olivera‐Bravo, Bianca Seminotti, (unknown), César Augusto João Ribeiro, Guilhian Leipnitz, Michael Woontner, Stephen I. Goodman, Diogo O. Souza, Luis Barbeito, Moaçir Wajner	11
5	Maternal obesity and increased neonatal adiposity correspond with altered infant mesenchymal stem cell metabolism 2017 ·JCI Insight ·Peter R. Baker, Zachary W. Patinkin, Allison Shapiro, Becky A. de la Houssaye, Michael Woontner, Kristen E. Boyle, Lauren A. Vanderlinden, Dana Dabelea, Jacob E. Friedman	32
6	Higher Vulnerability of Menadione-Exposed Cortical Astrocytes of Glutaryl-CoA Dehydrogenase Deficient Mice to Oxidative Stress, Mitochondrial Dysfunction, and Cell Death: Implications for the Neurodegeneration in Glutaric Aciduria Type I 2016 ·Molecular Neurobiology ·(unknown), Bianca Seminotti, Ângela Zanatta, (unknown), Bruna Bellaver, Alexandre Umpierrez Amaral, André Quincozes‐Santos, Stephen I. Goodman, Michael Woontner, Diogo O. Souza, Moaçir Wajner	11
7	The M405V allele of the glutaryl-CoA dehydrogenase gene is an important marker for glutaric aciduria type I (GA-I) low excretors 2016 ·Molecular Genetics and Metabolism ·(unknown), Carol L. Greene, Erin T. Strovel, (unknown), Elaine Spector, Michael Woontner, Gunter Scharer, Gregory M. Enns, Renata C. Gallagher, Arthur B. Zinn, Shawn E. McCandless, Charles L. Hoppel, Stephen I. Goodman, Jirair K. Bedoyan	11
8	Experimental evidence that overexpression of NR2B glutamate receptor subunit is associated with brain vacuolation in adult glutaryl-CoA dehydrogenase deficient mice: A potential role for glutamatergic-induced excitotoxicity in GA I neuropathology 2015 ·Journal of the Neurological Sciences ·(unknown), Bianca Seminotti, Alexandre Umpierrez Amaral, Guilhian Leipnitz, Stephen I. Goodman, Michael Woontner, Diogo O. Souza, Moaçir Wajner	14
9	Experimental evidence that bioenergetics disruption is not mainly involved in the brain injury of glutaryl-CoA dehydrogenase deficient mice submitted to lysine overload 2015 ·Brain Research ·Alexandre Umpierrez Amaral, Cristiane Cecatto, Bianca Seminotti, César Augusto João Ribeiro, (unknown), (unknown), Francine Hehn de Oliveira, Diogo O. Souza, Stephen I. Goodman, Michael Woontner, Moaçir Wajner	15
10	New Cases of DHTKD1 Mutations in Patients with 2-Ketoadipic Aciduria 2015 ·JIMD Reports ·Ashlee R. Stiles, (unknown), (unknown), (unknown), Michael Woontner, Stephen I. Goodman, José E. Abdenur	27
11	Disturbance of the glutamatergic system by glutaric acid in striatum and cerebral cortex of glutaryl-CoA dehydrogenase-deficient knockout mice: Possible implications for the neuropathology of glutaric acidemia type I 2014 ·Journal of the Neurological Sciences ·Estela Natacha Brandt Busanello, Carolina Gonçalves Fernandes, R. Martell, (unknown), Stephen I. Goodman, Michael Woontner, Diogo O. Souza, Moaçir Wajner	14
12	Increased Glutamate Receptor and Transporter Expression in the Cerebral Cortex and Striatum of Gcdh-/- Mice: Possible Implications for the Neuropathology of Glutaric Acidemia Type I 2014 ·PLoS ONE ·(unknown), Úrsula da Silveira Matte, Talita Giacomet de Carvalho, Bianca Seminotti, (unknown), David M. Koeller, Michael Woontner, Stephen I. Goodman, Diogo O. Souza, Moaçir Wajner	20
13	Acute lysine overload provokes protein oxidative damage and reduction of antioxidant defenses in the brain of infant glutaryl-CoA dehydrogenase deficient mice: A role for oxidative stress in GA I neuropathology 2014 ·Journal of the Neurological Sciences ·Bianca Seminotti, Rafael Teixeira Ribeiro, Alexandre Umpierrez Amaral, (unknown), (unknown), Guilhian Leipnitz, David M. Koeller, Stephen I. Goodman, Michael Woontner, Moaçir Wajner	14
14	Induction of oxidative stress in brain of glutaryl-CoA dehydrogenase deficient mice by acute lysine administration 2012 ·Molecular Genetics and Metabolism ·Bianca Seminotti, (unknown), Carolina Gonçalves Fernandes, Alexandre Umpierrez Amaral, (unknown), Guilhian Leipnitz, Diogo O. Souza, Michael Woontner, David M. Koeller, Stephen I. Goodman, Moaçir Wajner	26
15	Disruption of brain redox homeostasis in glutaryl-CoA dehydrogenase deficient mice treated with high dietary lysine supplementation 2012 ·Molecular Genetics and Metabolism ·Bianca Seminotti, Alexandre Umpierrez Amaral, (unknown), Carolina Gonçalves Fernandes, Guilhian Leipnitz, Silvia Olivera‐Bravo, Luis Barbeito, César Augusto João Ribeiro, Diogo O. Souza, Michael Woontner, Stephen I. Goodman, David M. Koeller, Moaçir Wajner	26
16	Neurodevelopmental and cognitive behavior of glutaryl-CoA dehydrogenase deficient knockout mice 2012 ·Life Sciences ·Estela Natacha Brandt Busanello, Letícia Ferreira Pettenuzzo, Paulo Henrique S. Botton, Pablo Pandolfo, Diogo O. Souza, Michael Woontner, Stephen I. Goodman, David M. Koeller, Moaçir Wajner	7
17	Marked reduction of Na+, K+-ATPase and creatine kinase activities induced by acute lysine administration in glutaryl-CoA dehydrogenase deficient mice 2012 ·Molecular Genetics and Metabolism ·Alexandre Umpierrez Amaral, Cristiane Cecatto, Bianca Seminotti, Ângela Zanatta, Carolina Gonçalves Fernandes, Estela Natacha Brandt Busanello, (unknown), César Augusto João Ribeiro, Diogo O. Souza, Michael Woontner, David M. Koeller, Stephen I. Goodman, Moaçir Wajner	24
18	Management of a patient with holocarboxylase synthetase deficiency 2008 ·Molecular Genetics and Metabolism ·Johan L.K. Van Hove, (unknown), (unknown), Janet A. Thomas, (unknown), Bruce A. Barshop, Michael Woontner, Donald M. Mock, Pei-Wen Chiang, Elaine Spector, Iván Meneses‐Morales, (unknown), Alfonso León‐Del‐Río	24
19	The role of the mitochondrion in cellular iron homeostasis 2001 ·Mitochondrion ·(unknown), Michael Woontner, David M. Koeller	30
20	Mutations in ARS1 increase the rate of simple loss of plasmids in Saccharomyces cerevisiae 1986 ·Yeast ·Randy Strich, Michael Woontner, John F. Scott	39

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.

Explore authors with similar magnitude of impact