Hernán Gonorazky

2.6k total citations
43 papers, 710 citations indexed

About

Hernán Gonorazky is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Hernán Gonorazky has authored 43 papers receiving a total of 710 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 19 papers in Genetics and 10 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Hernán Gonorazky's work include Neurogenetic and Muscular Disorders Research (19 papers), Muscle Physiology and Disorders (16 papers) and RNA modifications and cancer (9 papers). Hernán Gonorazky is often cited by papers focused on Neurogenetic and Muscular Disorders Research (19 papers), Muscle Physiology and Disorders (16 papers) and RNA modifications and cancer (9 papers). Hernán Gonorazky collaborates with scholars based in Canada, United States and Saudi Arabia. Hernán Gonorazky's co-authors include James J. Dowling, Ronald D. Cohn, Craig Campbell, Carsten G. Bönnemann, Dwi U. Kemaladewi, Mark A. Tarnopolsky, Sergey Naumenko, Steven A. Moore, Michael D. Wilson and Katherine D. Mathews and has published in prestigious journals such as Journal of Clinical Investigation, Neurology and The American Journal of Human Genetics.

In The Last Decade

Hernán Gonorazky

38 papers receiving 705 citations

Peers

Hernán Gonorazky

GENET

CCM

Jaya Punetha United States

Teodora Chamova Bulgaria

Nicolas Wein United States

Daniel Natera‐de Benito Spain

Danielle A. Griffin United States

Juergen Scharner United Kingdom

Stéphanie Astord France

Hiroko Wada Japan

Anne Destrèe Belgium

Alexandre Méjat France

Jaya Punetha United States

Hernán Gonorazky

319 ×0.6

85 ×0.4

GENET

139 ×0.8

GENET

94 ×0.8

CCM

46 ×0.5

Citations per year, relative to Hernán Gonorazky Hernán Gonorazky (= 1×) peers Jaya Punetha

Countries citing papers authored by Hernán Gonorazky

Since Specialization

Citations

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

Fields of papers citing papers by Hernán Gonorazky

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hernán Gonorazky

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

All Works

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20 of 20 papers shown

Gonorazky, Hernán, et al.. (2024). Expanding the spectrum of LAMB2: Pierson syndrome associated with neuromuscular junction disorder in two patients. Neuromuscular Disorders. 39. 30–32. 1 indexed citations

Sondheimer, Neal, Jessie M. Cameron, Hernán Gonorazky, et al.. (2023). Biallelic pathogenic variants in the mitochondrial form of phosphoenolpyruvate carboxykinase cause peripheral neuropathy. Human Genetics and Genomics Advances. 4(2). 100182–100182. 1 indexed citations

Grunebaum, Eyal, Binita M. Kamath, Christoph Licht, et al.. (2023). Case report: A case of spinal muscular atrophy in a preterm infant: risks and benefits of treatment. Frontiers in Neurology. 14. 1230889–1230889. 9 indexed citations

Gonorazky, Hernán, et al.. (2023). Understanding caregiver experiences with disease-modifying therapies for spinal muscular atrophy: a qualitative study. Archives of Disease in Childhood. 108(11). 929–934. 5 indexed citations

Chong, Jessica X., Matthew C. Childers, Colby T. Marvin, et al.. (2023). Variants in ACTC1 underlie distal arthrogryposis accompanied by congenital heart defects. Human Genetics and Genomics Advances. 4(3). 100213–100213. 9 indexed citations

Gonorazky, Hernán, et al.. (2023). P66 Salbutamol therapy in a neuromuscular cohort. Neuromuscular Disorders. 33. S75–S75. 1 indexed citations

Gonorazky, Hernán, et al.. (2023). Muscle MRI patterns for limb girdle muscle dystrophies: systematic review. Journal of Neurology. 270(8). 3946–3957. 2 indexed citations

Chiang, Jackie, Lauren M. Weinstock, Nikolaus E. Wolter, et al.. (2023). Sleep disordered breathing in infants identified through newborn screening with spinal muscular atrophy. Sleep Medicine. 111. 161–169. 7 indexed citations

Gonorazky, Hernán, et al.. (2023). CAMK4‐related Case of Hyperkinetic Movement Disorder. Movement Disorders Clinical Practice. 10(4). 707–709. 1 indexed citations

10.

Sabha, Nesrin, Jonathan Volpatti, Emanuela Pannia, et al.. (2022). Natural history of a mouse model of X-linked myotubular myopathy. Disease Models & Mechanisms. 15(7). 9 indexed citations

11.

Gonorazky, Hernán, et al.. (2022). PURA syndrome: neuromuscular junction manifestations with potential therapeutic implications. Neuromuscular Disorders. 32(10). 842–844. 6 indexed citations

12.

Oskoui, Maryam, Hernán Gonorazky, Hugh J. McMillan, et al.. (2021). Guidance on Gene Replacement Therapy in Spinal Muscular Atrophy: A Canadian Perspective. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49(3). 398–401.

13.

Kernohan, Kristin D., Hugh J. McMillan, Melanie Lacaria, et al.. (2021). Ontario Newborn Screening for Spinal Muscular Atrophy: The First Year. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 49(6). 821–823. 12 indexed citations

14.

Costain, Gregory, Susan Blasér, Susan Walker, et al.. (2020). Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a PEX3 defect: Case report and literature review. Molecular Genetics and Metabolism Reports. 25. 100664–100664. 3 indexed citations

15.

Yan, Han, Carolina Gorodetsky, Hernán Gonorazky, et al.. (2020). The Child & Youth CompreHensIve Longitudinal Database for Deep Brain Stimulation (CHILD-DBS). Child s Nervous System. 37(2). 607–615. 12 indexed citations

16.

McMillan, Hugh J., Kristin D. Kernohan, Jennifer Boyd, et al.. (2020). Newborn Screening for Spinal Muscular Atrophy: Ontario Testing and Follow-up Recommendations. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48(4). 504–511. 26 indexed citations

17.

Gonorazky, Hernán, James J. Dowling, Jonathan Volpatti, & Jiri Vajsar. (2019). Signs and Symptoms in Congenital Myopathies. Seminars in Pediatric Neurology. 29. 3–11. 6 indexed citations

18.

Léveillé, Etienne, Hernán Gonorazky, Marie‐France Rioux, et al.. (2018). Triple A syndrome presenting as complicated hereditary spastic paraplegia. Molecular Genetics & Genomic Medicine. 6(6). 1134–1139. 8 indexed citations

19.

Willer, Tobias, Benjamin W. Darbro, Hernán Gonorazky, et al.. (2018). Uniparental disomy unveils a novel recessive mutation in POMT2. Neuromuscular Disorders. 28(7). 592–596. 14 indexed citations

20.

Bettini, Mariela, Hernán Gonorazky, E. Fulgenzi, et al.. (2016). Immune-mediated rippling muscle disease and myasthenia gravis. Journal of Neuroimmunology. 299. 59–61. 6 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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