Michael Gonzalez

5.9k citations

47 papers · 2.0k · h-index 26

Impact in

Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
Neurology top 2%
- Neurological diseases and metabolism

Papers in

Cellular and Molecular Neuroscience 20
- Hereditary Neurological Disorders 16
- Genetic Neurodegenerative Diseases 5
Molecular Biology 18
- RNA Research and Splicing 4
- Mitochondrial Function and Pathology 4

Co-authors: Stephan Züchner (25 shared papers)Rebecca Schüle (12 shared papers)Rita J. Balice‐Gordon (1 shared paper)Martin J. Pinter (1 shared paper)Qiang Chang (1 shared paper)William F. Collins (1 shared paper)Fiorella Speziani (5 shared papers)Matthis Synofzik (7 shared papers)
Journals: Human Mutation (5 papers)Brain (4 papers)PLoS ONE (4 papers)Neurology (3 papers)The American Journal of Human Genetics (3 papers)
Partner nations: United States Germany United Kingdom

In The Last Decade

Michael Gonzalez

46 papers receiving 2.0k citations

Peers

Countries citing papers authored by Michael Gonzalez

Since Specialization

Citations

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

Fields of papers citing papers by Michael Gonzalez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Michael Gonzalez, 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 Michael Gonzalez Line = papers co-authored together Michael Gonzalez 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 47 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Gap Junctional Coupling and Patterns of Connexin Expression among Neonatal Rat Lumbar Spinal Motor Neurons Journal of Neuroscience ·Qiang Chang, Michael Gonzalez, Martin J. Pinter, Rita J. Balice‐Gordon	1999	174
2	From genome to vaccine: in silico predictions, ex vivo verification Vaccine ·Anne S. De Groot, Andrew Bosma, Natasha Chinai, Julie Frost, Bill M. Jesdale, Michael Gonzalez, William Martin, Caitlin Saint-Aubin	2001	151
3	PNPLA6 mutations cause Boucher-Neuhäuser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum Brain ·Matthis Synofzik, Michael Gonzalez, Charles Marques Lourenço, Marie Coutelier, Tobias B. Haack, Adriana Rebelo, Didier Hannequin, Tim M. Strom, Holger Prokisch, Christoph Kernstock, Alexandra Dürr, Lüdger Schöls, Marcos M. Lima-Martínez, Amjad Farooq, Rebecca Schüle, Giovanni Stévanin, Wilson Marques, Stephan Züchner	2013	148
4	Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss PLoS ONE ·Oscar Diaz‐Horta, Duygu Duman, Joseph Foster, Aslı Sırmacı, Michael Gonzalez, Nejat Mahdieh, Nikou Fotouhi, Mortaza Bonyadi, Filiz Başak Cengiz, Ibis Menéndez, Rick H. Ulloa, Yvonne J. K. Edwards, Stephan Züchner, Susan H. Blanton, Mustafa Tekin	2012	128
5	A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease Brain ·Michael Gonzalez, Shawna Feely, Fiorella Speziani, Alleene V. Strickland, Matt C. Danzi, Chelsea Bacon, Youjin Lee, Tsui‐Fen Chou, Susan H. Blanton, Conrad C. Weihl, Stephan Züchner, Michael E. Shy	2014	101
6	Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2 Journal of Neurology Neurosurgery & Psychiatry ·Michael Gonzalez, Heather M. McLaughlin, Henry Houlden, Min Guo, Yo‐Tsen Liu, Marios Hadjivassilious, Fiorella Speziani, Xiang‐Lei Yang, Anthony Antonellis, Mary M. Reilly, Stephan Züchner	2013	100
7	Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated Cardiomyopathy Circulation Cardiovascular Genetics ·Nadine Norton, Duanxiang Li, Evadnie Rampersaud, Ana Morales, Eden R. Martin, Stephan Züchner, Shengru Guo, Michael Gonzalez, Dale J. Hedges, Peggy D. Robertson, Niklas Krumm, Deborah A. Nickerson, Ray E. Hershberger	2013	89
8	Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration The American Journal of Human Genetics ·Matthis Synofzik, Tobias B. Haack, Robert Kopajtich, Matteo Gorza, Doron Rapaport, Markus Greiner, Caroline Schönfeld, Clemens Freiberg, Stefan Schorr, Reinhard W. Holl, Michael Gonzalez, Andreas Fritsche, Petra Fallier‐Becker, Richard Zimmermann, Tim M. Strom, Thomas Meitinger, Stephan Züchner, Rebecca Schüle, Lüdger Schöls, Holger Prokisch	2014	83
9	Modulation of Motoneuron Excitability by Brain-Derived Neurotrophic Factor Journal of Neurophysiology ·Michael Gonzalez, William F. Collins	1997	77
10	Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families PLoS ONE ·Milen Velinov, Natalia Dolzhanskaya, Michael Gonzalez, Eric Powell, Ioanna Konidari, William Hulme, John F. Staropoli, Winnie Xin, G. Y. Wen, Rosemary Barone, Scott H. Coppel, Katherine B. Sims, W. Ted Brown, Stephan Züchner	2012	66
11	Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54) European Journal of Human Genetics ·Michael Gonzalez, Sheela Nampoothiri, Cornelia Kornblum, Andrés Caballero-Oteyza, Jochen Walter, Ioanna Konidari, William Hulme, Fiorella Speziani, Lüdger Schöls, Stephan Züchner, Rebecca Schüle	2013	60
12	Rapid in vivo forward genetic approach for identifying axon death genes in Drosophila Proceedings of the National Academy of Sciences ·Lukas J. Neukomm, Thomas C. Burdett, Michael Gonzalez, Stephan Züchner, Marc Freeman	2014	57
13	First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy BMC Medical Genetics ·Katrien Smets, Anna Duarri, Tine Deconinck, Berten Ceulemans, Bart P.C. van de Warrenburg, Stephan Züchner, Michael Gonzalez, Rebecca Schüle, Matthis Synofzik, Nathalie Van der Aa, Peter De Jonghe, Dineke S. Verbeek, Jonathan Baets	2015	54
14	Mutation screen reveals novel variants and expands the phenotypes associated with DYNC1H1 Journal of Neurology ·Alleene V. Strickland, Maria Schabhüttl, H. Offenbacher, Matthis Synofzik, Natalie Hauser, Michaela Brunner‐Krainz, U Gruber‐Sedlmayr, Steven A. Moore, Reinhard Windhager, Benjamin Bender, Matthew B. Harms, Stephan Klebe, Peter Young, Marina Kennerson, Avencia Sanchez Mejias Garcia, Michael Gonzalez, Stephan Züchner, Rebecca Schüle, Michael E. Shy, Michaela Auer‐Grumbach	2015	52
15	Innovative Genomic Collaboration Using the GENESIS (GEM.app) Platform Human Mutation ·Michael Gonzalez, Marni J. Falk, Xiaowu Gai, Richard Postrel, Rebecca Schüle, Stephan Züchner	2015	52
16	Impaired Function is a Common Feature of Neuropathy-Associated Glycyl-tRNA Synthetase Mutations Human Mutation ·Laurie B. Griffin, Reiko Sakaguchi, David B. McGuigan, Michael Gonzalez, Charles Searby, Stephan Züchner, Ya‐Ming Hou, Anthony Antonellis	2014	48
17	GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis Human Mutation ·Michael Gonzalez, Rafael F. Acosta Lebrigio, Derek Van Booven, Rick H. Ulloa, Eric Powell, Fiorella Speziani, Mustafa Tekin, Rebecca Schüle, Stephan Züchner	2013	48
18	Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts Orphanet Journal of Rare Diseases ·Matthis Synofzik, Rebecca Schüle, Martin Schulze, Janina Gburek‐Augustat, Roland Schweizer, Anja Schirmacher, Ingeborg Krägeloh‐Mann, Michael Gonzalez, Peter Young, Stephan Züchner, Lüdger Schöls, Peter Bauer	2014	42
19	Motor protein mutations cause a new form of hereditary spastic paraplegia Neurology ·Andrés Caballero-Oteyza, Esra Battaloğlu, Levent Öcek, Tobias Lindig, Jennifer Reichbauer, Adriana Rebelo, Michael Gonzalez, Yaşar Zorlu, Burçak Özeş, Dagmar Timmann, Benjamin Bender, Günther Woehlke, Stephan Züchner, Lüdger Schöls, Rebecca Schüle	2014	41
20	Thrombotic thrombocytopenic purpura subsequent to acute myelogenous leukemia chemotherapy American Journal of Hematology ·John Byrnes, Hernan Baquerizo, Michael Gonzalez, George T. Hensely	1986	40

About Michael Gonzalez

Michael Gonzalez is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Cell Biology and Genetics, having authored 47 papers that have together received 2.0k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (16 papers), Neurological diseases and metabolism (6 papers), Genomics and Rare Diseases (6 papers), Genetic Neurodegenerative Diseases (5 papers), Cellular transport and secretion (4 papers), RNA Research and Splicing (4 papers), Mitochondrial Function and Pathology (4 papers) and Lysosomal Storage Disorders Research (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (728 citations), Neurology (305 citations), Sensory Systems (126 citations), Cell Biology (352 citations) and Developmental Neuroscience (59 citations). Michael Gonzalez has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Stephan Züchner, Rebecca Schüle, Rita J. Balice‐Gordon, Martin J. Pinter, Qiang Chang, William F. Collins, Fiorella Speziani, Matthis Synofzik, Lüdger Schöls and Bill M. Jesdale. Their work appears in journals such as Human Mutation, Brain, PLoS ONE, Neurology and The American Journal of Human Genetics.

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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