Dena G. Hernandez

11.5k total citations
15 papers, 731 citations indexed

About

Dena G. Hernandez is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Dena G. Hernandez has authored 15 papers receiving a total of 731 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 10 papers in Cellular and Molecular Neuroscience and 6 papers in Molecular Biology. Recurrent topics in Dena G. Hernandez's work include Parkinson's Disease Mechanisms and Treatments (10 papers), Genetic Neurodegenerative Diseases (6 papers) and Nuclear Receptors and Signaling (4 papers). Dena G. Hernandez is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (10 papers), Genetic Neurodegenerative Diseases (6 papers) and Nuclear Receptors and Signaling (4 papers). Dena G. Hernandez collaborates with scholars based in United States, United Kingdom and Finland. Dena G. Hernandez's co-authors include Andrew Singleton, John Hardy, J. Raphael Gibbs, Mark Cookson, Javier Simón‐Sánchez, Roberto Weiser, Melissa Hanson, Katrina Gwinn, Marisol Gallardo and Jinhui Ding and has published in prestigious journals such as PLoS ONE, Stroke and Annals of Neurology.

In The Last Decade

Dena G. Hernandez

14 papers receiving 707 citations

Peers

Countries citing papers authored by Dena G. Hernandez

Since Specialization

Citations

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

Fields of papers citing papers by Dena G. Hernandez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dena G. Hernandez. 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 Dena G. Hernandez. The network helps show where Dena G. Hernandez may publish in the future.

Co-authorship network of co-authors of Dena G. Hernandez

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Cerebellum mitochondrial DNA copy number is increased in Parkinson’s disease 2025 ·Brain Communications ·(unknown), (unknown), J. Raphael Gibbs, J. Andrew MacKay, Sonja W. Scholz, Bryan Traynor, Marilyn S. Albert, Liana S. Rosenthal, Ted M. Dawson, Juan C. Troncoso, Dena G. Hernandez, (unknown), Charles H. Adler, Geidy E. Serrano, Andrew B. Singleton, Thomas G. Beach, Brooke E. Hjelm	0
2	Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis 2019 ·Scientific Reports ·Ari Siitonen, (unknown), Mike A. Nalls, J. Raphael Gibbs, Dena G. Hernandez, Pauli Ylikotila, Markku Peltonen, Andrew Singleton, Kari Majamaa	7
3	Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study 2017 ·Neurobiology of Aging ·Ari Siitonen, Michael A. Nalls, Dena G. Hernandez, J. Raphael Gibbs, Jinhui Ding, Pauli Ylikotila, Connor Edsall, Andrew Singleton, Kari Majamaa	33
4	Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe 2016 ·Genome Medicine ·Cornelis Blauwendraat, Margherita Francescatto, J. Raphael Gibbs, Iris E. Jansen, Javier Simón‐Sánchez, Dena G. Hernandez, Allissa Dillman, Andrew Singleton, Mark Cookson, Patrizia Rizzu, Peter Heutink	14
5	EIF4G1 mutations do not cause Parkinson's disease 2015 ·Neurobiology of Aging ·Noah Nichols, José Brás, Dena G. Hernandez, Iris E. Jansen, Suzanne Lesage, Steven Lubbe, Andrew B. Singleton	15
6	Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24 2014 ·PLoS Genetics ·(unknown), Dahlia M. Nielsen, (unknown), Andrew Singleton, Noriko Tonomura, Snævar Sigurðsson, Ruqi Tang, Keith E. Linder, Sampath Arepalli, Dena G. Hernandez, Kerstin Lindblad‐Toh, Joyce van de Leemput, Alison A. Motsinger‐Reif, Dennis P. O’Brien, Jerold S. Bell, Tonya Harris, Steven J. Steinberg, Natasha J. Olby	35
7	A 7.5‐Mb duplication at chromosome 11q21‐11q22.3 is associated with a novel spastic ataxia syndrome 2014 ·Movement Disorders ·Janel O. Johnson, Giovanni Stévanin, Joyce van de Leemput, Dena G. Hernandez, Sampath Arepalli, Sylvie Forlani, Reza Zonozi, J. Raphael Gibbs, Alexis Brice, Alexandra Dürr, Andrew B. Singleton	22
8	An exploratory analysis on gene-environment interactions for Parkinson disease 2012 ·Neurobiology of Aging ·Jianjun Gao, Michael A. Nalls, Min Shi, Bonnie R. Joubert, Dena G. Hernandez, Xuemei Huang, Albert R. Hollenbeck, Andrew Singleton, Honglei Chen	37
9	Genome Wide Assessment of Young Onset Parkinson’s Disease from Finland 2012 ·PLoS ONE ·Dena G. Hernandez, Michael A. Nalls, Pauli Ylikotila, Margaux F. Keller, John Hardy, Kari Majamaa, Andrew Singleton	24
10	Siblings With Ischemic Stroke Study 2011 ·Stroke ·James F. Meschia, Michael A. Nalls, Mar Matarín, Thomas G. Brott, Robert D. Brown, John Hardy, Brett Kissela, Stephen S. Rich, Andrew Singleton, Dena G. Hernandez, Luigi Ferrucci, Kerra Pearce, (unknown), Bradford B. Worrall, (unknown)	20
11	Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma 2010 ·The American Journal of Human Genetics ·Minerva M. Carrasquillo, Alexandra M. Nicholson, NiCole A. Finch, J. Raphael Gibbs, Matt Baker, Nicola J. Rutherford, Talisha A. Hunter, Mariely DeJesus‐Hernandez, Gina Bisceglio, Ian R. Mackenzie, Andrew Singleton, Mark Cookson, Julia E. Crook, Allissa Dillman, Dena G. Hernandez, Ronald C. Petersen, Neill R. Graff‐Radford, Steven G. Younkin, Rosa Rademakers	112
12	DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA 2008 ·The Lancet Neurology ·Sarah Camargos, Sonja W. Scholz, Javier Simón‐Sánchez, Coro Paisán‐Ruíz, Patrick A. Lewis, Dena G. Hernandez, Jinhui Ding, J. Raphael Gibbs, Mark Cookson, José Brás, Rita Guerreiro, Catarina R. Oliveira, Andrew J. Lees, John Hardy, Francisco Cardoso, Andrew Singleton	143
13	Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease 2005 ·Neuroscience Letters ·Javier Simón‐Sánchez, Melissa Hanson, Amanda Singleton, Dena G. Hernandez, Aideen McInerney‐Leo, Robert Nussbaum, John S. Werner, Marisol Gallardo, Roberto Weiser, Katrina Gwinn, Andrew B. Singleton, Jordi Clarimón	32
14	Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation 2003 ·Annals of Neurology ·Stephen Hague, Ekaterina Rogaeva, Dena G. Hernandez, (unknown), Amanda Singleton, Melissa Hanson, Janel Johnson, Roberto Weiser, Marisol Gallardo, Bernard Ravina, Katrina Gwinn, Anthony Crawley, Peter St George‐Hyslop, Anthony E. Lang, Peter Heutink, Vincenzo Bonifati, John Hardy, Andrew Singleton	190
15	Case‐control study of the extended tau gene haplotype in Parkinson's disease 2001 ·Annals of Neurology ·Demetrius M. Maraganore, Dena G. Hernandez, (unknown), Matthew J. Farrer, Shannon K. McDonnell, Michael Hutton, John Hardy, Walter A. Rocca	47

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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