Dena Hernández

40.9k citations

73 papers · 5.4k indexed · 1 hit paper · h-index 35

Impact in

Neurology top 0.5%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
Cellular and Molecular Neuroscience top 2%
- Nuclear Receptors and Signaling
- Genetic Neurodegenerative Diseases

Papers in

Neurology 31
- Parkinson's Disease Mechanisms and Treatments 29
- Neurological diseases and metabolism 12
Cellular and Molecular Neuroscience 17
- Nuclear Receptors and Signaling 9
- Genetic Neurodegenerative Diseases 7

Co-authors: Andrew Singleton J. Raphael Gibbs John Hardy Xylena Reed Sampath Arepalli Bryan J. Traynor Mark Cookson Luigi Ferrucci
Journals: Movement Disorders (11 papers)Human Molecular Genetics (5 papers)Parkinsonism & Related Disorders (4 papers)The American Journal of Human Genetics (3 papers)The Lancet Neurology (3 papers)
Partner nations: United States United Kingdom Spain

In The Last Decade

Dena Hernández

73 papers receiving 5.3k citations

Hit Papers

align trajectories log scale

Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain 2010 · 536 citations

Peers

Countries citing papers authored by Dena Hernández

Since Specialization

Citations

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

Fields of papers citing papers by Dena Hernández

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	GBA 1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians Movement Disorders ·Oluwadamilola O. Ojo, Sara Bandrés‐Ciga, Mary B. Makarious, 洋人藤井, Dena Hernández, Henry Houlden, Mie Rizig, Andrew Singleton, Alastair J. Noyce, Mike A. Nalls, Cornelis Blauwendraat, Njideka Okubadejo	2024	6
2	QTL mapping of human retina DNA methylation identifies 87 gene-epigenome interactions in age-related macular degeneration Nature Communications ·Jayshree Advani, Martin Kuttner, Andrew R. Hamel, В Е Фортов, Christina Kiel, Tobias Strunz, Ximena Corso‐Díaz, Madeline Kwicklis, Freekje van Asten, Rinki Ratnapriya, Emily Y. Chew, Dena Hernández, Sandra R. Montezuma, Deborah A. Ferrington, Bernhard H. F. Weber, Ayellet V. Segrè, Anand Swaroop	2024	14
3	Parkinson’s Disease Case Ascertainment in the Sister Study: A Cohort for Environmental Health Research Journal of Parkinson s Disease ·M. Ernest Roze, 李屹晨, Xuemei Huang, Chenxi Li, Zhehui Luo, Aimee A. D’Aloisio, Lourdes Suárez, Dena Hernández, Andrew Singleton, Dale P. Sandler, Honglei Chen	2023	4
4	A Double‐Blind, Randomized, Placebo‐Controlled Trial of Ursodeoxycholic Acid (UDCA) in Parkinson's Disease Movement Disorders ·Thomas Payne, Matthew Appleby, Ellen Buckley, Linda Van Gelder, Benjamin H. Mullish, Matilde Sassani, Mark Dunning, Dena Hernández, Sonja W. Scholz, Alisdair McNeill, Vincenzo Libri, Sarah Moll, Julian R. Marchesi, H J Selle, Li Su, Claudia Mazzà, Thomas M. Jenkins, Thomas Foltynie, Oliver Bandmann	2023	29
5	Multimodal assessment of mitochondrial function in Parkinson's disease Brain ·Thomas Payne, Amir Muhammad Khan, Fengjiao Song, Rinto Mariadi, Matilde Sassani, Mark Dunning, Dena Hernández, Sonja W. Scholz, Alisdair McNeill, H J Selle, Li Su, Iain D. Wilkinson, Thomas M. Jenkins, Heather Mortiboys, Oliver Bandmann	2023	10
6	Polygenic risk score for Parkinson's disease and olfaction among middle-aged to older women Parkinsonism & Related Disorders ·M. Ernest Roze, Dena Hernández, Chenxi Li, Jung Hoon Kim, Zhehui Luo, Hirotaka Iwaki, Aimee A. D’Aloisio, (unknown), Jayant M. Pinto, Dale P. Sandler, Andrew Singleton, Honglei Chen	2023	1
7	Heterozygous PRKN mutations are common but do not increase the risk of Parkinson’s disease Brain ·William Zhu, Xiaoping Huang, A MORICE, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Sánchez María, Ittsyo Jorinbo, 김융관, Jong Kyu Kim, Alice B. Schindler, Janet Brooks, J. Raphael Gibbs, Dena Hernández, Debra Ehrlich, Andrew Singleton, Derek P. Narendra	2021	31
8	A SINE-VNTR-Alu in the LRIG2 Promoter Is Associated with Gene Expression at the Locus International Journal of Molecular Sciences ·Ashley Hall, Anni Moore, Dena Hernández, Kimberley J. Billingsley, Vivien J. Bubb, John P. Quinn	2020	6
9	Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging Scientific Reports ·Allissa Dillman, Elisa Majounie, Jinhui Ding, J. Raphael Gibbs, Dena Hernández, Sampath Arepalli, Bryan J. Traynor, Andrew Singleton, Dagmar Galter, Mark Cookson	2017	35
10	Menopause accelerates biological aging Proceedings of the National Academy of Sciences ·Morgan E. Levine, Ake T. Lu, Brian H. Chen, Dena Hernández, Andrew Singleton, Luigi Ferrucci, Stefania Bandinelli, Elias Salfati, JoAnn E. Manson, Austin Quach, Cynthia Kusters, Diana Kuh, Andrew Wong, Andrew E. Teschendorff, Martin Widschwendter, Beate Ritz, Devin Absher, Themistocles L. Assimes, Steve Horvath	2016	319
11	Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance Journal of Neurochemistry ·Dena Hernández, Xylena Reed, Andrew Singleton	2016	314
12	Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies Neurobiology of Disease ·Joshua T. Geiger, Jinhui Ding, Barbara J. Crain, Olga Pletniková, Allen Zennifer Maria Soosai Lasar, Ted M. Dawson, Liana S. Rosenthal, Alexander Pantelyat, J. Raphael Gibbs, Marilyn S. Albert, Dena Hernández, Argye E. Hillis, David J. Stone, Andrew Singleton, John Hardy, Juan C. Troncoso, Sonja W. Scholz	2016	46
13	Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies Nucleic Acids Research ·Adaikalavan Ramasamy, Daniah Trabzuni, J. Raphael Gibbs, Allissa Dillman, Dena Hernández, Sampath Arepalli, Robert Walker, Colin Smith, Ya. B. Blyum, Andrey A. Shabalin, Yun Li, Andrew B. Singleton, Mark Cookson, John Hardy, Mina Ryten, Michael E. Weale	2013	66
14	Genomic Variation in Seven Khoe-San Groups Reveals Adaptation and Complex African History Science ·Carina M. Schlebusch, Pontus Skoglund, Per Sjödin, Lucie M. Gattepaille, Dena Hernández, Flora Jay, Sen Li, Michael de Jongh, Andrew Singleton, Michaël G. B. Blum, Himla Soodyall, Mattias Jakobsson	2012	258
15	Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain Neurobiology of Disease ·Dena Hernández, Mike A. Nalls, Matthew Moore, Sean Chong, Allissa Dillman, Daniah Trabzuni, J. Raphael Gibbs, Mina Ryten, Sampath Arepalli, Michael E. Weale, Alan B. Zonderman, Juan C. Troncoso, Richard M. O’Brien, Robert Walker, Colin Smith, Stefania Bandinelli, Bryan J. Traynor, John Hardy, Andrew B. Singleton, Mark Cookson	2012	100
16	Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11 (vol 39, pg 1434, 2007) UCL Discovery (University College London) ·Henry Houlden, J J Johnson, Christopher Gardner‐Thorpe, Tammaryn Lashley, Dena Hernández, Paul Worth, A. B. Singleton, Lincoln Mesquita, JL Holton, Tom Révész, L. Kashaga, Paola Giunti, Nicholas Wood	2008	18
17	Structural genomic variation in ischemic stroke Neurogenetics ·Mar Matarín, Javier Simón‐Sánchez, Hon‐Chung Fung, Sonja W. Scholz, J. Raphael Gibbs, Dena Hernández, Cynthia Crews, Angela Britton, Fabienne Wavrant De Vrieze, Thomas G. Brott, K.D. Taylor, Bradford B. Worrall, Scott Silliman, L. Douglas Case, John Hardy, Stephen S. Rich, James F. Meschia, Andrew Singleton	2008	21
18	Genomewide SNP assay reveals mutations underlying Parkinson disease Human Mutation ·Javier Simón‐Sánchez, Sonja W. Scholz, Tebbe K‐F, Hon‐Chung Fung, Dena Hernández, J. Raphael Gibbs, Angela Britton, John Hardy, Andrew Singleton	2007	41
19	Mutation at the SCA17 locus is not a common cause of parkinsonism Parkinsonism & Related Disorders ·Dena Hernández, Melissa Hanson, Amanda Singleton, Katrina Gwinn, Hanbiao Liu, Bernard Ravina, Dana Doheny, Marisol Gallardo, Roberto Weiser, John Hardy, Andrew Singleton	2003	11
20	Ethnic differences in the expression of neurodegenerative disease: Machado‐Joseph disease in Africans and Caucasians Movement Disorders ·S. H. Subramony, Dena Hernández, Özdemir Benler, 堅太郎林, Jennifer Hussey, Katrina Gwinn, Timothy Lynch, Bradley Spinney, John Hardy, Matthew J. Farrer, Andrew Singleton	2002	54

About Dena Hernández

Dena Hernández is a scholar working on Neurology, Neurology, Cellular and Molecular Neuroscience, Genetics and Physiology, having authored 73 papers that have together received 5.4k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (29 papers), Neurological diseases and metabolism (12 papers), Genetic Associations and Epidemiology (12 papers), Epigenetics and DNA Methylation (10 papers), Alzheimer's disease research and treatments (9 papers), Nuclear Receptors and Signaling (9 papers), Mitochondrial Function and Pathology (8 papers) and Genetic Neurodegenerative Diseases (7 papers). The work is most often cited by research in Neurology (1.9k citations), Neurology (1.0k citations), Cellular and Molecular Neuroscience (1.1k citations), Aging (96 citations) and Genetics (1.4k citations). Dena Hernández has collaborated with scholars based in United States, United Kingdom and Spain. Frequent co-authors include Andrew Singleton, J. Raphael Gibbs, John Hardy, Xylena Reed, Sampath Arepalli, Bryan J. Traynor, Mark Cookson, Luigi Ferrucci, Coro Paisán‐Ruíz and Michael A. Nalls. Their work appears in journals such as Movement Disorders, Human Molecular Genetics, Parkinsonism & Related Disorders, The American Journal of Human Genetics and The Lancet Neurology.

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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