Dena G. Hernandez

11.5k citations

15 papers · 731 indexed · h-index 13

Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments 10
- Neurological diseases and metabolism 3
Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments 10
- Neurological diseases and metabolism 3
Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases 6
- Nuclear Receptors and Signaling 4
Physiology
- Alzheimer's disease research and treatments 2
Genetics
Molecular Biology
- RNA regulation and disease 3
- Genomics and Chromatin Dynamics 1
Epidemiology
- Autophagy in Disease and Therapy 1

Co-authors: Andrew Singleton John Hardy J. Raphael Gibbs Mark Cookson Javier Simón‐Sánchez Roberto Weiser Melissa Hanson Katrina Gwinn
Cited by: Neurology Cellular and Molecular Neuroscience
Partner nations: United States United Kingdom Finland

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

The 25 scholars most cited alongside Dena G. Hernandez, 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 Dena G. Hernandez Line = papers co-authored together Dena G. Hernandez links everyone, so they are left out of the graph.

All Works

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15 of 15 papers shown

#	Work
1	Cerebellum mitochondrial DNA copy number is increased in Parkinson’s disease Talia Beglarian,David R. Tyrpak,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	2025	0
2	Finnish Parkinson’s disease study integrating protein-protein interaction network data with exome sequencing analysis Ari Siitonen,Laura Kytövuori,Mike A. Nalls,J. Raphael Gibbs,Dena G. Hernandez,Pauli Ylikotila,Markku Peltonen,Andrew Singleton,Kari Majamaa	2019	7
3	Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study Ari Siitonen,Michael A. Nalls,Dena G. Hernandez,J. Raphael Gibbs,Jinhui Ding,Pauli Ylikotila,Connor Edsall,Andrew Singleton,Kari Majamaa	2017	33
4	Comprehensive promoter level expression quantitative trait loci analysis of the human frontal lobe 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	2016	14
5	EIF4G1 mutations do not cause Parkinson's disease Noah Nichols,José Brás,Dena G. Hernandez,Iris E. Jansen,Suzanne Lesage,Steven Lubbe,Andrew B. Singleton	2015	15
6	Canine Hereditary Ataxia in Old English Sheepdogs and Gordon Setters Is Associated with a Defect in the Autophagy Gene Encoding RAB24 Caryline Agler,Dahlia M. Nielsen,Ganokon Urkasemsin,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	2014	35
7	A 7.5‐Mb duplication at chromosome 11q21‐11q22.3 is associated with a novel spastic ataxia syndrome 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	2014	22
8	An exploratory analysis on gene-environment interactions for Parkinson disease Jianjun Gao,Michael A. Nalls,Min Shi,Bonnie R. Joubert,Dena G. Hernandez,Xuemei Huang,Albert R. Hollenbeck,Andrew Singleton,Honglei Chen	2012	37
9	Genome Wide Assessment of Young Onset Parkinson’s Disease from Finland Dena G. Hernandez,Michael A. Nalls,Pauli Ylikotila,Margaux F. Keller,John Hardy,Kari Majamaa,Andrew Singleton	2012	24
10	Siblings With Ischemic Stroke Study 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,M. Keller,Bradford B. Worrall,(unknown)	2011	20
11	Genome-wide Screen Identifies rs646776 near Sortilin as a Regulator of Progranulin Levels in Human Plasma 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	2010	112
12	DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA 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	2008	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 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	2005	32
14	Early‐onset Parkinson's disease caused by a compound heterozygous DJ‐1 mutation Stephen Hague,Ekaterina Rogaeva,Dena G. Hernandez,Cindy Gulick,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	2003	190
15	Case‐control study of the extended tau gene haplotype in Parkinson's disease Demetrius M. Maraganore,Dena G. Hernandez,Andrew B. Singleton,Matthew J. Farrer,Shannon K. McDonnell,Michael Hutton,John Hardy,Walter A. Rocca	2001	47

About Dena G. Hernandez

Dena G. Hernandez is a scholar working on Neurology, Cellular and Molecular Neuroscience and Neurology, having authored 15 papers that have together received 731 indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (10 papers), Genetic Neurodegenerative Diseases (6 papers), Nuclear Receptors and Signaling (4 papers), Neurological diseases and metabolism (3 papers), RNA regulation and disease (3 papers), Alzheimer's disease research and treatments (2 papers), Genomics and Chromatin Dynamics (1 paper) and Autophagy in Disease and Therapy (1 paper). The work is most often cited by research in Neurology (481 citations), Neurology (170 citations) and Cellular and Molecular Neuroscience (301 citations). Dena G. Hernandez has collaborated with scholars based in United States, United Kingdom and Finland. Frequent 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.

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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