Andrej Michalik

1.0k total citations
11 papers, 463 citations indexed

About

Andrej Michalik is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Andrej Michalik has authored 11 papers receiving a total of 463 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Cellular and Molecular Neuroscience, 9 papers in Molecular Biology and 2 papers in Neurology. Recurrent topics in Andrej Michalik's work include Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (7 papers) and Ubiquitin and proteasome pathways (4 papers). Andrej Michalik is often cited by papers focused on Genetic Neurodegenerative Diseases (9 papers), Mitochondrial Function and Pathology (7 papers) and Ubiquitin and proteasome pathways (4 papers). Andrej Michalik collaborates with scholars based in Belgium, United States and United Kingdom. Andrej Michalik's co-authors include Christine Van Broeckhoven, Olaf Ansorge, Paola Giunti, Francesco Scaravilli, Brian Harding, Nicholas Wood, Jurgen Del‐Favero, Bianca Van Broeck, Samir Kumar‐Singh and Hans Wils and has published in prestigious journals such as Annals of Neurology, Human Molecular Genetics and Neurobiology of Aging.

In The Last Decade

Andrej Michalik

11 papers receiving 454 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Andrej Michalik Belgium	8	370	366	84	65	39	11	463
M. Kéfi Tunisia	10	211 0.6×	143 0.4×	92 1.1×	38 0.6×	20 0.5×	14	326
Jana Boy Germany	8	317 0.9×	331 0.9×	107 1.3×	17 0.3×	30 0.8×	8	404
P. Thomas United States	6	468 1.3×	450 1.2×	138 1.6×	35 0.5×	32 0.8×	7	571
Antoine Duquette Canada	9	251 0.7×	214 0.6×	95 1.1×	70 1.1×	79 2.0×	21	394
Svitlana Yablonska United States	7	391 1.1×	175 0.5×	94 1.1×	83 1.3×	51 1.3×	10	512
Elena Sánchez-Ferrero Spain	8	161 0.4×	164 0.4×	86 1.0×	42 0.6×	101 2.6×	10	313
Lauren M. Watson United Kingdom	10	251 0.7×	185 0.5×	33 0.4×	53 0.8×	20 0.5×	13	355
Alex Osmand United States	6	669 1.8×	684 1.9×	224 2.7×	41 0.6×	26 0.7×	7	792
Francesca Maltecca Italy	14	644 1.7×	408 1.1×	121 1.4×	52 0.8×	77 2.0×	25	727
Wai Yan Yau Australia	8	255 0.7×	275 0.8×	112 1.3×	17 0.3×	50 1.3×	15	390

Countries citing papers authored by Andrej Michalik

Since Specialization

Citations

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

Fields of papers citing papers by Andrej Michalik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrej Michalik

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

All Works

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11 of 11 papers shown

1.

Broeck, Bianca Van, Daniel Pirici, Debby Van Dam, et al.. (2006). Intraneuronal amyloid β and reduced brain volume in a novel APP T714I mouse model for Alzheimer's disease. Neurobiology of Aging. 29(2). 241–252. 50 indexed citations

2.

Michalik, Andrej & Christine Van Broeckhoven. (2004). Proteasome degrades soluble expanded polyglutamine completely and efficiently. Neurobiology of Disease. 16(1). 202–211. 48 indexed citations

3.

Ansorge, Olaf, Paola Giunti, Andrej Michalik, et al.. (2004). Ataxin‐7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats. Annals of Neurology. 56(3). 448–452. 40 indexed citations

4.

Michalik, Andrej & Christine Van Broeckhoven. (2003). Pathogenesis of polyglutamine disorders: aggregation revisited. Human Molecular Genetics. 12(suppl 2). R173–R186. 177 indexed citations

5.

Michalik, Andrej, et al.. (2003). Spinocerebellar ataxia type 7 associated with pigmentary retinal dystrophy. European Journal of Human Genetics. 12(1). 2–15. 99 indexed citations

6.

Michalik, Andrej, Aleksey Kazantsev, & Christine Van Broeckhoven. (2001). Method to Introduce Stable, Expanded, Polyglutamine-Encoding CAG/CAA Trinucleotide Repeats into CAG Repeat-Containing Genes. BioTechniques. 31(2). 250–254. 10 indexed citations

7.

Del‐Favero, Jurgen, D. Goossens, Peter De Jonghe, et al.. (1999). Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation. Human Genetics. 105(3). 217–225. 4 indexed citations

8.

Michalik, Andrej, Jurgen Del‐Favero, C. Mauger, Ann Löfgren, & Christine Van Broeckhoven. (1999). Genomic organisation of the spinocerebellar ataxia type 7 ( SCA7 ) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration. Human Genetics. 105(5). 410–417. 15 indexed citations

9.

Michalik, Andrej, Jurgen Del‐Favero, C. Mauger, A. Löfgren, & Christine Van Broeckhoven. (1999). Genomic organisation of the spinocerebellar ataxia type 7 (SCA7) gene responsible for autosomal dominant cerebellar ataxia with retinal degeneration. Human Genetics. 105(5). 410–417. 5 indexed citations

10.

Del‐Favero, Jurgen, D. Goossens, Peter De Jonghe, et al.. (1999). Isolation of CAG/CTG repeats from within the chromosome 2p21-p24 locus for autosomal dominant spastic paraplegia (SPG4) by YAC fragmentation. Human Genetics. 105(3). 217–225. 2 indexed citations

11.

Jonghe, Peter De, Andrej Michalik, Jamïlé Hazan, et al.. (1996). Pure Familial Spastic Paraplegia:Clinical and Genetic Analysis ofNine Belgian Pedigrees. European Journal of Human Genetics. 4(5). 260–266. 13 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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