Janet Hoenicka

10.2k total citations · 1 hit paper
76 papers, 3.8k citations indexed

About

Janet Hoenicka is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Janet Hoenicka has authored 76 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Cellular and Molecular Neuroscience, 30 papers in Molecular Biology and 18 papers in Neurology. Recurrent topics in Janet Hoenicka's work include Neurotransmitter Receptor Influence on Behavior (20 papers), Parkinson's Disease Mechanisms and Treatments (11 papers) and Genetic Neurodegenerative Diseases (11 papers). Janet Hoenicka is often cited by papers focused on Neurotransmitter Receptor Influence on Behavior (20 papers), Parkinson's Disease Mechanisms and Treatments (11 papers) and Genetic Neurodegenerative Diseases (11 papers). Janet Hoenicka collaborates with scholars based in Spain, United Kingdom and United States. Janet Hoenicka's co-authors include Israel Ampuero, Justo Garcı́a de Yébenes, Raquel Ros, Lídice Vidal, Teodoro del Ser, Javier Alegre‐Abarrategui, Juan Carlos Gómez‐Esteban, Elena Lezcano, Begoña Atarés and Verónica Llorens and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Janet Hoenicka

73 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia

2003 2.1k citations Raquel Ros, Israel Ampuero et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Janet Hoenicka Spain	26	2.2k	1.6k	967	868	486	76	3.8k
J.J. Zarranz Spain	27	3.1k 1.4×	1.4k 0.8×	1.1k 1.1×	743 0.9×	749 1.5×	76	4.1k
Jenna C. Carroll United States	23	1.6k 0.7×	1.5k 0.9×	1.8k 1.9×	1.2k 1.3×	762 1.6×	25	4.8k
Kalpana Merchant United States	39	1.1k 0.5×	2.1k 1.3×	1.0k 1.1×	1.8k 2.1×	357 0.7×	79	4.2k
Pierre‐Olivier Fernagut France	39	3.0k 1.4×	2.4k 1.5×	815 0.8×	1.2k 1.4×	909 1.9×	90	5.1k
Patrick M. Abou‐Sleiman United Kingdom	23	2.2k 1.0×	1.2k 0.8×	733 0.8×	1.4k 1.6×	681 1.4×	36	3.7k
Charles K. Meshul United States	39	1.7k 0.8×	2.7k 1.6×	546 0.6×	1.5k 1.7×	523 1.1×	130	4.9k
Daniel G. Healy United Kingdom	20	3.3k 1.5×	1.3k 0.8×	630 0.7×	799 0.9×	678 1.4×	30	4.1k
Andréas Hartmann France	30	1.6k 0.7×	1.4k 0.8×	363 0.4×	1.0k 1.2×	633 1.3×	47	3.4k
Sheng‐Han Kuo United States	37	2.6k 1.2×	2.3k 1.4×	828 0.9×	1.6k 1.8×	653 1.3×	163	5.4k
Emmanuel N. Pothos United States	36	1.3k 0.6×	3.0k 1.8×	1.3k 1.3×	1.8k 2.0×	390 0.8×	53	5.9k

Countries citing papers authored by Janet Hoenicka

Since Specialization

Citations

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

Fields of papers citing papers by Janet Hoenicka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janet Hoenicka

This figure shows the co-authorship network connecting the top 25 collaborators of Janet Hoenicka. A scholar is included among the top collaborators of Janet Hoenicka 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 Janet Hoenicka. Janet Hoenicka 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

Cantarero, Lara, Elena Garrido, Sara Fernández‐Lizarbe, et al.. (2024). ANKK1 Is a Wnt/PCP Scaffold Protein for Neural F-ACTIN Assembly. International Journal of Molecular Sciences. 25(19). 10705–10705.

Benito, Daniel Natera‐de, Carla Garcia‐Cabau, Cristina Jou, et al.. (2023). Common pathophysiology for ANXA11 disorders caused by aspartate 40 variants. Annals of Clinical and Translational Neurology. 10(3). 408–425. 7 indexed citations

Cantarero, Lara, et al.. (2023). Differential effects of Mendelian GDAP1 clinical variants on mitochondria-lysosome membrane contacts sites. Biology Open. 12(4). 8 indexed citations

Vela, Lydia, et al.. (2022). Non-Motor Symptoms in PLA2G6-Associated Dystonia-Parkinsonism: A Case Report and Literature Review. Journal of Clinical Medicine. 11(6). 1590–1590. 1 indexed citations

Casas‐Alba, Dídac, et al.. (2022). Diagnostic strategies in patients with undiagnosed and rare diseases. 6. 322–332. 3 indexed citations

Carrera‐García, Laura, et al.. (2022). Genetic approaches and pathogenic pathways in the clinical management of Charcot-Marie-Tooth disease. 6. 333–352. 5 indexed citations

Nuevo‐Tapioles, Cristina, Fulvio Santacatterina, Cristina Núñez de Arenas, et al.. (2021). Effective therapeutic strategies in a preclinical mouse model of Charcot–Marie–Tooth disease. Human Molecular Genetics. 30(24). 2441–2455. 5 indexed citations

Domı́nguez, Laura, et al.. (2021). Mitochondria and calcium defects correlate with axonal dysfunction in GDAP1-related Charcot-Marie-Tooth mouse model. Neurobiology of Disease. 152. 105300–105300. 18 indexed citations

Ponce, G., et al.. (2020). Ankyrin Repeat and Kinase Domain Containing 1 Gene, and Addiction Vulnerability. International Journal of Molecular Sciences. 21(7). 2516–2516. 18 indexed citations

10.

Montero‐Pedrazuela, Ana, Rebeca Vidal, Inés García‐Consuegra, et al.. (2016). The Addiction-Related Protein ANKK1 is Differentially Expressed During the Cell Cycle in Neural Precursors. Cerebral Cortex. 27(5). 2809–2819. 12 indexed citations

11.

Ponce, G., et al.. (2015). The Addiction-Related Gene Ankk1 is Oppositely Regulated by D1R- and D2R-Like Dopamine Receptors. Neurotoxicity Research. 29(3). 345–350. 15 indexed citations

12.

Hsu, Janet, Janet Hoenicka, & Silvia Muro. (2014). Targeting, Endocytosis, and Lysosomal Delivery of Active Enzymes to Model Human Neurons by ICAM-1-Targeted Nanocarriers. Pharmaceutical Research. 32(4). 1264–1278. 17 indexed citations

13.

Ponce, G., Roberto Rodríguez–Jiménez, Diana Taboada, et al.. (2010). High frequency of childhood ADHD history in women with fibromyalgia. European Psychiatry. 26(8). 482–483. 29 indexed citations

14.

Hoenicka, Janet, María Aragüés, G. Ponce, et al.. (2007). From dopaminergic genes to psychiatric disorders. Neurotoxicity Research. 11(1). 61–71. 19 indexed citations

15.

Rodríguez–Jiménez, Roberto, César Ávila, Miguel Ángel Jiménez‐Arriero, et al.. (2006). Impulsivity and Sustained Attention in Pathological Gamblers: Influence of Childhood ADHD History. Journal of Gambling Studies. 22(4). 451–461. 82 indexed citations

16.

Ponce, G., Miguel Ángel Jiménez‐Arriero, Gabriel Rubio, et al.. (2003). The A1 allele of the DRD2 gene (TaqI A polymorphisms) is associated with antisocial personality in a sample of alcohol-dependent patients. European Psychiatry. 18(7). 356–360. 83 indexed citations

17.

Carmona, Jenny Andrea, et al.. (2003). Unique origin and low penetrance of the 946delGAG mutation in Valencian DYT1 families. Clinical Genetics. 64(2). 153–159. 1 indexed citations

18.

Morales, Blas, Armando Martínez, Isabel Gonzalo, et al.. (2002). Steele‐Richardson‐Olszewski syndrome in a patient with a single C212Y mutation in the parkin protein. Movement Disorders. 17(6). 1374–1380. 41 indexed citations

19.

Hoenicka, Janet, Lídice Vidal, Blas Morales, et al.. (2002). Molecular Findings in Familial Parkinson Disease in Spain. Archives of Neurology. 59(6). 966–966. 38 indexed citations

20.

Hoenicka, Janet, Pilar Rodríguez‐Pombo, Celia Pérez‐Cerdá, et al.. (1998). New frequent mutation in the PCCB gene in Spanish propionic acidemia patients. Human Mutation. 11(S1). S234–S236. 11 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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