Ines Dierick

3.1k total citations · 1 hit paper
14 papers, 1.2k citations indexed

About

Ines Dierick is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Ines Dierick has authored 14 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 4 papers in Genetics. Recurrent topics in Ines Dierick's work include Hereditary Neurological Disorders (10 papers), Heat shock proteins research (5 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Ines Dierick is often cited by papers focused on Hereditary Neurological Disorders (10 papers), Heat shock proteins research (5 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Ines Dierick collaborates with scholars based in Belgium, Australia and Austria. Ines Dierick's co-authors include Vincent Timmerman, Joy Irobi, Peter De Jonghe, Michaela Auer‐Grumbach, Klaus Wagner, Garth A. Nicholson, Craig L. Bennett, Phillip F. Chance, Kenneth H. Fischbeck and Ian P. Blair and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Ines Dierick

14 papers receiving 1.2k 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.

DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

2004 602 citations Craig L. Bennett, Ian P. Blair et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ines Dierick Belgium	9	677	460	453	362	278	14	1.2k
Mayana Zatz Brazil	6	504 0.7×	245 0.5×	523 1.2×	334 0.9×	154 0.6×	9	961
Elizabeth L. Tudor United Kingdom	7	752 1.1×	239 0.5×	593 1.3×	311 0.9×	129 0.5×	7	1.2k
Elisa Onesto Italy	17	819 1.2×	337 0.7×	715 1.6×	411 1.1×	101 0.4×	18	1.3k
Nathalie Verpoorten Belgium	8	391 0.6×	526 1.1×	254 0.6×	141 0.4×	231 0.8×	9	1.0k
Nicholas J. Kramer United States	11	715 1.1×	264 0.6×	688 1.5×	307 0.8×	101 0.4×	13	1.2k
Anna‐Lena Ström Sweden	15	540 0.8×	250 0.5×	503 1.1×	172 0.5×	108 0.4×	21	1.1k
Annette Abel United States	8	668 1.0×	475 1.0×	483 1.1×	375 1.0×	270 1.0×	8	1.2k
Kai Y. Soo Australia	12	463 0.7×	192 0.4×	788 1.7×	362 1.0×	111 0.4×	15	1.1k
Manal A. Farg Australia	13	548 0.8×	243 0.5×	996 2.2×	429 1.2×	152 0.5×	14	1.5k
Brett J Winborn United States	7	890 1.3×	323 0.7×	442 1.0×	244 0.7×	67 0.2×	8	1.2k

Countries citing papers authored by Ines Dierick

Since Specialization

Citations

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

Fields of papers citing papers by Ines Dierick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ines Dierick

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

All Works

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14 of 14 papers shown

Dierick, Ines, et al.. (2022). How to Successfully Generate an Alternative Approach to a Thorough QT Study: GLPG1972 as an Example. Clinical Pharmacology & Therapeutics. 113(2). 310–320. 1 indexed citations

Rakočević-Stojanović, Vidosava, Stojan Perić, Jonathan Baets, et al.. (2010). N88S mutation in the BSCL2 gene in a Serbian family with distal hereditary motor neuropathy type V or Silver syndrome. Journal of the Neurological Sciences. 296(1-2). 107–109. 7 indexed citations

Almeida‐Souza, Leonardo, Sofie Goethals, Vicky De Winter, et al.. (2010). Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy. Journal of Biological Chemistry. 285(17). 12778–12786. 86 indexed citations

Irobi, Joy, Leonardo Almeida‐Souza, Bob Asselbergh, et al.. (2010). Mutant HSPB8 causes motor neuron-specific neurite degeneration. Human Molecular Genetics. 19(16). 3254–3265. 68 indexed citations

Baets, Jonathan, Ines Dierick, Chantal Ceuterick‐de Groote, et al.. (2009). Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity. Neuromuscular Disorders. 19(2). 172–175. 8 indexed citations

Reddel, Stephen, Robert Ouvrier, Garth A. Nicholson, et al.. (2008). Autosomal dominant congenital spinal muscular atrophy – A possible developmental deficiency of motor neurones?. Neuromuscular Disorders. 18(7). 530–535. 8 indexed citations

Dierick, Ines, Joy Irobi, Sophie Janssens, et al.. (2007). Genetic variant in theHSPB1 promoter region impairs the HSP27 stress response. Human Mutation. 28(8). 830–830. 31 indexed citations

Irobi, Joy, Ines Dierick, Albena Jordanova, et al.. (2006). Unraveling the genetics of distal hereditary motor neuronopathies. NeuroMolecular Medicine. 8(1-2). 131–146. 47 indexed citations

Irobi, Joy, Ines Dierick, Albena Jordanova, et al.. (2006). Unraveling the Genetics of Distal Hereditary Motor Neuronopathies. NeuroMolecular Medicine. 8(1-2). 131–146. 9 indexed citations

10.

Irobi, Joy, Ines Dierick, Veerle De Corte, et al.. (2006). G.O.1 In vitro expression of small heat shock protein HSPB8 and HSPB1 mutations causing axonal neuropathy. Neuromuscular Disorders. 16(9-10). 645–646. 1 indexed citations

11.

Dierick, Ines, Joy Irobi, Peter De Jonghe, & Vincent Timmerman. (2005). Small heat shock proteins in inherited peripheral neuropathies. Annals of Medicine. 37(6). 413–422. 46 indexed citations

12.

Bennett, Craig L., Ian P. Blair, Imke Puls, et al.. (2004). DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4). The American Journal of Human Genetics. 74(6). 1128–1135. 602 indexed citations breakdown →

13.

Windpassinger, Christian, Michaela Auer‐Grumbach, Joy Irobi, et al.. (2004). Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome. Nature Genetics. 36(3). 271–276. 279 indexed citations

14.

Irobi, Joy, Eva Nelis, Kristien Verhoeven, et al.. (2002). Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3. Journal of the Peripheral Nervous System. 7(2). 87–95. 3 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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