Martin Paucar

2.1k total citations
52 papers, 412 citations indexed

About

Martin Paucar is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Martin Paucar has authored 52 papers receiving a total of 412 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 27 papers in Cellular and Molecular Neuroscience and 13 papers in Neurology. Recurrent topics in Martin Paucar's work include Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (16 papers) and DNA Repair Mechanisms (6 papers). Martin Paucar is often cited by papers focused on Genetic Neurodegenerative Diseases (25 papers), Mitochondrial Function and Pathology (16 papers) and DNA Repair Mechanisms (6 papers). Martin Paucar collaborates with scholars based in Sweden, United States and United Kingdom. Martin Paucar's co-authors include Per Svenningsson, José Miguel Laffita‐Mesa, Johan Brask, Håkan Karlsson, Krister Kristensson, Helena Malmgren, A. Malcolm R. Taylor, Ruth H. Walker, Inger Nennesmo and Ingemar Björkhem and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Martin Paucar

48 papers receiving 408 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Martin Paucar Sweden	11	221	142	98	60	45	52	412
Gui Zhang China	11	240 1.1×	70 0.5×	64 0.7×	35 0.6×	63 1.4×	26	509
Mika H. Martikainen Finland	13	205 0.9×	95 0.7×	130 1.3×	47 0.8×	61 1.4×	34	418
Niranjanan Nirmalananthan United Kingdom	11	293 1.3×	159 1.1×	177 1.8×	30 0.5×	61 1.4×	23	537
Daniel García‐Pérez Spain	13	132 0.6×	152 1.1×	68 0.7×	17 0.3×	34 0.8×	43	402
Katherine G. Meilleur United States	14	301 1.4×	92 0.6×	46 0.5×	125 2.1×	60 1.3×	38	545
Nadiya Byts Finland	10	141 0.6×	85 0.6×	134 1.4×	34 0.6×	79 1.8×	13	449
Lemuel Racacho Canada	14	262 1.2×	164 1.2×	192 2.0×	116 1.9×	66 1.5×	18	547
Mahima Kapoor United Kingdom	9	119 0.5×	94 0.7×	125 1.3×	35 0.6×	54 1.2×	25	341
Hanna Mierzewska Poland	15	444 2.0×	105 0.7×	98 1.0×	127 2.1×	82 1.8×	57	728
Shin Okazaki Japan	12	243 1.1×	112 0.8×	80 0.8×	160 2.7×	83 1.8×	79	620

Countries citing papers authored by Martin Paucar

Since Specialization

Citations

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

Fields of papers citing papers by Martin Paucar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Paucar

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Thonberg, Håkan, Aida Paivandy, Lars Feuk, et al.. (2025). Acute Vestibular Syndrome Unmasking an RFC1 -Spectrum Disorder. Neurology Genetics. 11(1). e200238–e200238.

Sundblom, Jimmy, et al.. (2024). Cerebrospinal fluid glial fibrillary acidic protein, in contrast to amyloid beta protein, is associated with disease symptoms in Huntington's disease. Journal of the Neurological Sciences. 459. 122979–122979.

Paucar, Martin, Daniel Nilsson, Martin Engvall, et al.. (2024). Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs. Journal of Internal Medicine. 296(3). 234–248. 7 indexed citations

Svensson, Eva, et al.. (2024). The clinical spectrum of ataxia telangiectasia in a cohort in Sweden. Heliyon. 10(4). e26073–e26073. 2 indexed citations

Kvarnung, Malin, Wolfgang Sperker, Helene Bruhn, et al.. (2023). Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3. Neurology Genetics. 9(6). e200100–e200100. 1 indexed citations

Paucar, Martin, et al.. (2023). Neuropathy with Cerebral Features Induced by Nitrous Oxide Abuse—A Case Report. Toxics. 11(12). 959–959. 2 indexed citations

Paucar, Martin, et al.. (2022). Are ATXN2 variants modifying our understanding about neural pathogenesis, phenotypes, and diagnostic?. Neural Regeneration Research. 17(11). 2445–2445. 1 indexed citations

Laffita‐Mesa, José Miguel, Martin Paucar, & Per Svenningsson. (2021). Ataxin-2 gene: a powerful modulator of neurological disorders. Current Opinion in Neurology. 34(4). 578–588. 22 indexed citations

Paucar, Martin, Bianca Tesi, Saeed Eshtad, et al.. (2021). Adult-Onset Ataxia With Neuropathy and White Matter Abnormalities Due to a Novel SAMD9L Variant. Neurology Genetics. 7(6). e628–e628. 2 indexed citations

10.

Landtblom, Anne‐Marie, Dag Nyholm, Radu Constantinescu, et al.. (2020). Proenkephalin Decreases in Cerebrospinal Fluid with Symptom Progression of Huntington's Disease. Movement Disorders. 36(2). 481–491. 18 indexed citations

11.

Einarsdóttir, Elísabet, Hans Matsson, Harriet E. Nilsson, et al.. (2020). Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report. BMC Medical Genetics. 21(1). 87–87. 4 indexed citations

12.

Paucar, Martin, Håkan Almqvist, Ingemar Björkhem, & Per Svenningsson. (2020). Hyperkinesias and Echolalia in Primary Familial Brain Calcification. Annals of Neurology. 89(2). 418–419. 3 indexed citations

13.

Sveinsson, Ólafur, Bjarne Udd, Per Svenningsson, et al.. (2019). Involuntary movements, vocalizations and cognitive decline. Parkinsonism & Related Disorders. 79. 135–137. 2 indexed citations

14.

Paucar, Martin, Inger Nennesmo, & Per Svenningsson. (2018). Pathological Study of a FMR1 Premutation Carrier With Progressive Supranuclear Palsy. Frontiers in Genetics. 9. 317–317. 5 indexed citations

15.

Paucar, Martin, Peter Gustavsson, Magnus Nordenskjöld, et al.. (2018). Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19. The Cerebellum. 17(4). 465–476. 11 indexed citations

16.

Paucar, Martin, Martin Engvall, Lisa Gordon, et al.. (2016). POLG-Associated Ataxia Presenting as a Fragile X Tremor/Ataxia Phenocopy Syndrome. The Cerebellum. 15(5). 632–635. 1 indexed citations

17.

Paucar, Martin, et al.. (2016). Hypospadias as a novel feature in spinal bulbar muscle atrophy. Journal of Neurology. 263(4). 703–706. 2 indexed citations

18.

Paucar, Martin, et al.. (2016). PSP-CBS with Dopamine Deficiency in a Female with a FMR1 Premutation. The Cerebellum. 15(5). 636–640. 7 indexed citations

19.

Paucar, Martin, Per‐Åke Lindestad, Ruth H. Walker, & Per Svenningsson. (2015). Teaching Video Neuro Images : Feeding dystonia in chorea-acanthocytosis. Neurology. 85(19). e143–4. 6 indexed citations

20.

Saeed, Ahmed, Jan Andersson, Irina A. Pikuleva, et al.. (2013). 7α-hydroxy-3-oxo-4-cholestenoic acid in cerebrospinal fluid reflects the integrity of the blood-brain barrier. Journal of Lipid Research. 55(2). 313–318. 38 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.

Explore authors with similar magnitude of impact