Michael Gonzalez

5.8k citations

47 papers · 1.9k indexed · h-index 26

Molecular Biology top 10%
Cellular and Molecular Neuroscience top 2%
Cell Biology top 5%
Neurology top 2%
Genetics top 10%

Co-authors: Stephan Züchner Rebecca Schüle Martin J. Pinter Rita J. Balice‐Gordon Qiang Chang William F. Collins Fiorella Speziani Matthis Synofzik
Topics: Hereditary Neurological Disorders (17 papers)Neurological diseases and metabolism (10 papers)Genetic Neurodegenerative Diseases (8 papers)
Cited by: Neurology Cellular and Molecular Neuroscience Sensory Systems
Journals: Proceedings of the National Academy of Sciences Journal of Clinical Oncology Journal of Neuroscience
Partner nations: United States Germany United Kingdom

In The Last Decade

Michael Gonzalez

46 papers receiving 1.9k 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-authorship network of co-authors of Michael Gonzalez

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Gonzalez. A scholar is included among the top collaborators of Michael Gonzalez 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 Gonzalez. Michael Gonzalez 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	Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey 2020 ·Neurologia i Neurochirurgia Polska ·(unknown),(unknown),Michael Gonzalez,(unknown),Esra Battaloğlu,Yeşim Parman	2
2	Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach 2019 ·European Journal of Human Genetics ·Chao Wu,Batsal Devkota,Perry Evans,Xiaonan Zhao,Samuel W. Baker,(unknown),Kajia Cao,Michael Gonzalez,Pushkala Jayaraman,Laura K. Conlin,Bryan L. Krock,Matthew A. Deardorff,Nancy B. Spinner,Ian D. Krantz,Avni Santani,Ahmad Abou Tayoun,Mahdi Sarmady	10
3	The Development and Validation of Clinical Exome-Based Panels Using ExomeSlicer 2018 ·Journal of Molecular Diagnostics ·(unknown),Michael Gonzalez,Jorune Balciuniene,Perry Evans,Mahdi Sarmady,Ahmad Abou Tayoun	18
4	Genetic background of the hereditary spastic paraplegia phenotypes in Hungary — An analysis of 58 probands 2016 ·Journal of the Neurological Sciences ·(unknown),Zoltán Grosz,Michael Gonzalez,(unknown),(unknown),Anikó Gál,Edina Varga,Péter Klivènyi,Júlia Koller,Stephan Züchner,Mária Judit Molnár	24
5	De novo PMP2mutations in families with type 1 Charcot–Marie–Tooth disease 2016 ·Brain ·William W. Motley,(unknown),Sabrina W. Yum,Michael Gonzalez,Feifei Tao,Julia Wanschitz,Alleene V. Strickland,Wolfgang N. Löscher,Els De Vriendt,Stefan Koppi,Līvija Medne,Andreas Janecke,Albena Jordanova,Stephan Züchner,Steven S. Scherer	30
6	Rare Manifestation of a c.290 C>T, p.Gly97GluVCPMutation 2015 ·SHILAP Revista de lepidopterología ·Nivedita U. Jerath,(unknown),Steven A. Moore,Michael E. Shy,Conrad C. Weihl,Tsui‐Fen Chou,Tiffany Grider,Michael Gonzalez,Stephan Züchner,Andrea Swenson	16
7	Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot–Marie–Tooth disease 2015 ·Neuromuscular Disorders ·Kathryn M. Brennan,Yunhong Bai,Chiara Pisciotta,(unknown),Shawna Feely,Mark J. Hoegger,Laurie Gutmann,Steven A. Moore,Michael Gonzalez,Diane L. Sherman,Peter Brophy,Stephan Züchner,Michael E. Shy	22
8	Adult-onset painful axonal polyneuropathy caused by a dominantNAGLUmutation 2015 ·Brain ·Martine Tétreault,Michael Gonzalez,(unknown),Pierre Allard,Kalle Gehring,(unknown),(unknown),Ronald Schondorf,Jean Mathieu,Stephan Züchner,Bernard Brais	20
9	Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration 2015 ·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	3
10	Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy 2014 ·The American Journal of Human Genetics ·D. Herrmann,Rita Horváth,Janet E. Sowden,Michael Gonzalez,Avencia Sánchez-Mejías,Zhuo Guan,Roger G. Whittaker,(unknown),(unknown),Boglárka Bánsági,Angela Pyle,Veronika Boczonadi,Hanns Lochmüller,Helen Griffin,Patrick F. Chinnery,Thomas E. Lloyd,J. Troy Littleton,(unknown)	2
11	Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration 2014 ·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	82
12	A Novel p.Leu(381)Phe Mutation in Presenilin 1 is Associated with Very Early Onset and Unusually Fast Progressing Dementia as well as Lysosomal Inclusions Typically Seen in Kufs Disease 2014 ·Journal of Alzheimer s Disease ·Natalia Dolzhanskaya,Michael Gonzalez,(unknown),Shannon Stefl,Jeffrey M. Messing,G. Y. Wen,Emil Alexov,Stephan Züchner,Milen Velinov	19
13	A novel mutation in VCP causes Charcot–Marie–Tooth Type 2 disease 2014 ·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	98
14	Identifying novel genes and genetic/phenotypic spectra for inherited neurodegenerative disorders using next-generation sequencing 2014 ·Nature Computational Science ·Michael Gonzalez	1
15	Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54) 2013 ·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	56
16	GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis 2013 ·Human Mutation ·Michael Gonzalez,(unknown),Derek Van Booven,(unknown),Eric Powell,Fiorella Speziani,Mustafa Tekin,Rebecca Schüle,Stephan Züchner	48
17	Do Not Trust the Pedigree: Reduced and Sex-Dependent Penetrance at a Novel Mutation Hotspot in ATL1 Blurs Autosomal Dominant Inheritance of Spastic Paraplegia 2013 ·Human Mutation ·(unknown),Rebecca Schüle,(unknown),Irene Valenzuela,Fiorella Speziani,Michael Gonzalez,(unknown),Gudrun Nürnberg,Hölger Thiele,Janine Altmüller,Victoria Álvarez,Josep Gámez,James Garbern,Peter Nürnberg,Stephan Züchner,Christian Beetz	19
18	Correction: Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families 2012 ·PLoS ONE ·Milen Velinov,Natalia Dolzhanskaya,Michael Gonzalez,Eric Powell,Ioanna Konidari,William Hulme,John F. Staropoli,Winnie Xin,G. Y. Wen,(unknown),(unknown),Katherine B. Sims,W. Ted Brown,(unknown)	7
19	Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss 2012 ·PLoS ONE ·Oscar Diaz‐Horta,Duygu Duman,Joseph Foster,Aslı Sırmacı,Michael Gonzalez,Nejat Mahdieh,(unknown),Mortaza Bonyadi,Filiz Başak Cengiz,Ibis Menéndez,(unknown),Yvonne J. K. Edwards,Stephan Züchner,Susan H. Blanton,Mustafa Tekin	127
20	From genome to vaccine: in silico predictions, ex vivo verification 2001 ·Vaccine ·Anne S. De Groot,(unknown),(unknown),Julie Frost,Bill M. Jesdale,Michael Gonzalez,William Martin,(unknown)	143

About Michael Gonzalez

Michael Gonzalez is a scholar working on Neurology, Cellular and Molecular Neuroscience and Genetics, having authored 47 papers that have together received 1.9k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (17 papers), Neurological diseases and metabolism (10 papers) and Genetic Neurodegenerative Diseases (8 papers). The work is most often cited by research in Neurology (365 citations), Cellular and Molecular Neuroscience (727 citations) and Sensory Systems (127 citations). Michael Gonzalez has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include Stephan Züchner, Rebecca Schüle, Martin J. Pinter, Rita J. Balice‐Gordon, Qiang Chang, William F. Collins, Fiorella Speziani, Matthis Synofzik, Lüdger Schöls and Bill M. Jesdale. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and Journal of Neuroscience.

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