Andrea H. Németh

12.1k total citations · 1 hit paper
93 papers, 3.2k citations indexed

About

Andrea H. Németh is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Andrea H. Németh has authored 93 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 54 papers in Molecular Biology, 34 papers in Cellular and Molecular Neuroscience and 16 papers in Neurology. Recurrent topics in Andrea H. Németh's work include Genetic Neurodegenerative Diseases (29 papers), Mitochondrial Function and Pathology (19 papers) and Neurological disorders and treatments (12 papers). Andrea H. Németh is often cited by papers focused on Genetic Neurodegenerative Diseases (29 papers), Mitochondrial Function and Pathology (19 papers) and Neurological disorders and treatments (12 papers). Andrea H. Németh collaborates with scholars based in United Kingdom, Hungary and United States. Andrea H. Németh's co-authors include Edit I. Buzás, Xabier Osteikoetxea, Barbara W. Sódar, Katalin Szabó-Taylor, Krisztina Pálóczi, Ágnes Kittel, Éva Pállinger, Krisztina V Vukman, Zoltán Wiener and Károly Vékey and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and PLoS ONE.

In The Last Decade

Andrea H. Németh

91 papers receiving 3.1k 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.

Low-density lipoprotein mimics blood plasma-derived exosomes and microvesicles during isolation and detection

2016 414 citations Barbara W. Sódar, Ágnes Kittel et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrea H. Németh United Kingdom	30	2.1k	768	558	442	413	93	3.2k
John D. Heiss United States	39	1.1k 0.5×	1.2k 1.6×	315 0.6×	755 1.7×	220 0.5×	153	4.8k
Dimitris G. Placantonakis United States	30	1.2k 0.6×	452 0.6×	316 0.6×	444 1.0×	158 0.4×	103	3.1k
Mahlon D. Johnson United States	38	1.7k 0.8×	315 0.4×	353 0.6×	837 1.9×	212 0.5×	142	4.8k
Mel Ziman Australia	38	2.1k 1.0×	475 0.6×	1.0k 1.8×	308 0.7×	185 0.4×	159	4.5k
Yazhen Zhu United States	26	3.2k 1.5×	1.5k 1.9×	434 0.8×	374 0.8×	1.2k 3.0×	72	4.7k
Ting Lei China	30	1.0k 0.5×	376 0.5×	375 0.7×	487 1.1×	123 0.3×	234	3.3k
Andreas F. Mack Germany	44	2.6k 1.3×	945 1.2×	267 0.5×	371 0.8×	276 0.7×	160	5.7k
Dong‐Eog Kim South Korea	33	1.2k 0.6×	382 0.5×	350 0.6×	734 1.7×	199 0.5×	117	4.5k
William J. Kupsky United States	36	1.4k 0.7×	837 1.1×	218 0.4×	1.1k 2.5×	389 0.9×	132	4.9k
Kyu‐Chang Wang South Korea	44	1.4k 0.7×	1.1k 1.4×	359 0.6×	2.2k 5.0×	446 1.1×	335	7.2k

Countries citing papers authored by Andrea H. Németh

Since Specialization

Citations

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

Fields of papers citing papers by Andrea H. Németh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrea H. Németh. 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 Andrea H. Németh. The network helps show where Andrea H. Németh may publish in the future.

Co-authorship network of co-authors of Andrea H. Németh

This figure shows the co-authorship network connecting the top 25 collaborators of Andrea H. Németh. A scholar is included among the top collaborators of Andrea H. Németh 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 Andrea H. Németh. Andrea H. Németh 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

Garcés, Pilar, Chrystalina A. Antoniades, Anna Sobańska, et al.. (2023). Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes. The Cerebellum. 23(1). 121–135. 10 indexed citations

Evangelisti, Stefania, J F Betts, Mark Jenkinson, et al.. (2023). Subthalamic nucleus shows opposite functional connectivity pattern in Huntington’s and Parkinson’s disease. Brain Communications. 5(6). fcad282–fcad282. 5 indexed citations

Steel, Dora, Federica Rachele Danti, Benjamin Kamien, et al.. (2023). Clinical Phenotype in Individuals With Birk-Landau-Perez Syndrome Associated With Biallelic SLC30A9 Pathogenic Variants. Neurology. 100(21). e2214–e2223. 1 indexed citations

Magrinelli, Francesca, Clarissa Rocca, Roberto Simone, et al.. (2022). Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2‐1‐Related Disorder. Movement Disorders. 38(2). 347–353. 4 indexed citations

Broadgate, Suzanne, et al.. (2021). Whole genome sequencing in a Knobloch syndrome family confirms the molecular diagnosis. Ophthalmic Genetics. 43(2). 201–209.

Mazzone, Roberta, Irene del Molino del Barrio, Annalidia Donato, et al.. (2020). Inhibition of the SUV4-20 H1 histone methyltransferase increases frataxin expression in Friedreich's ataxia patient cells. Journal of Biological Chemistry. 295(52). 17973–17985. 9 indexed citations

Taylor, John, E Blair, Sarah Wordsworth, et al.. (2019). Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series. Genome Medicine. 11(1). 46–46. 21 indexed citations

Watson, Lauren M., Ricardo Parolin Schnekenberg, Jonathan P. Williams, et al.. (2017). Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44. The American Journal of Human Genetics. 101(3). 451–458. 55 indexed citations

Matula, Zsolt, Andrea H. Németh, Péter Lőrincz, et al.. (2016). The Role of Extracellular Vesicle and Tunneling Nanotube-Mediated Intercellular Cross-Talk Between Mesenchymal Stem Cells and Human Peripheral T Cells. Stem Cells and Development. 25(23). 1818–1832. 46 indexed citations

10.

Osteikoetxea, Xabier, Andrea H. Németh, Barbara W. Sódar, Krisztina V Vukman, & Edit I. Buzás. (2016). Extracellular vesicles in cardiovascular disease: are they Jedi or Sith?. The Journal of Physiology. 594(11). 2881–2894. 41 indexed citations

11.

Osteikoetxea, Xabier, Andrea Balogh, Katalin Szabó-Taylor, et al.. (2015). Improved Characterization of EV Preparations Based on Protein to Lipid Ratio and Lipid Properties. PLoS ONE. 10(3). e0121184–e0121184. 152 indexed citations

12.

Szabó-Taylor, Katalin, Brent J. Ryan, Xabier Osteikoetxea, et al.. (2015). Oxidative and other posttranslational modifications in extracellular vesicle biology. Seminars in Cell and Developmental Biology. 40. 8–16. 43 indexed citations

13.

Anand, Geetha, Shelley Segal, Andrea H. Németh, et al.. (2014). H1N1 Triggered Recurrent Acute Necrotizing Encephalopathy in a Family With a T653I Mutation in the RANBP2 Gene. The Pediatric Infectious Disease Journal. 34(3). 318–320. 13 indexed citations

14.

Collett, Johnny, Patrick Esser, Hanan Khalil, et al.. (2014). Insights into gait disorders: Walking variability using phase plot analysis, Huntington's disease. Gait & Posture. 40(4). 694–700. 38 indexed citations

15.

Dawes, Helen, Johnny Collett, Lori Quinn, et al.. (2014). Exercise testing and training in people with Huntington’s disease. Clinical Rehabilitation. 29(2). 196–206. 19 indexed citations

16.

Apáti, Ágota, Tamás I. Orbán, Nóra Varga, et al.. (2008). High level functional expression of the ABCG2 multidrug transporter in undifferentiated human embryonic stem cells. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1778(12). 2700–2709. 71 indexed citations

17.

Németh, Andrea H., et al.. (2005). Gastrointestinal Manifestations of Common Variable Immunodeficiency Diagnosed by Video- and Capsule Endoscopy. Endoscopy. 37(6). 603–604. 4 indexed citations

18.

Barbot, Clara, Nobutada Tachi, Pascale Bomont, et al.. (2002). Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34. European Journal of Human Genetics. 10. 272–273. 3 indexed citations

19.

Rampoldi, Luca, Carol Dobson‐Stone, Justin P. Rubio, et al.. (2001). A conserved sorting-associated protein is mutant in chorea-acanthocytosis. Nature Genetics. 28(2). 119–120. 223 indexed citations

20.

Worth, Paul, Eimear Dunne, Andrea H. Németh, & Nicholas Wood. (1999). Autosomal dominant cerebellar ataxia type III: No evidence for a large pathological CAG repeat expansion in the SCA 11 gene.. UCL Discovery (University College London). 1 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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