Tine Deconinck

3.8k total citations
28 papers, 733 citations indexed

About

Tine Deconinck is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Tine Deconinck has authored 28 papers receiving a total of 733 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 18 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Tine Deconinck's work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (8 papers) and Hereditary Neurological Disorders (8 papers). Tine Deconinck is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (8 papers) and Hereditary Neurological Disorders (8 papers). Tine Deconinck collaborates with scholars based in Belgium, United States and Germany. Tine Deconinck's co-authors include Peter De Jonghe, Jonathan Baets, Katrien Smets, Arvid Suls, Tine Van Dyck, Liesbet Deprez, Lieve Claes, Albena Jordanova, Stephan Züchner and Rebecca Schüle and has published in prestigious journals such as Brain, Neurology and Scientific Reports.

In The Last Decade

Tine Deconinck

26 papers receiving 726 citations

Peers

Countries citing papers authored by Tine Deconinck

Since Specialization

Citations

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

Fields of papers citing papers by Tine Deconinck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tine Deconinck

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

#	Work	Indexed citations
1	A heterozygous 9q34 deletion encompassing SPTAN1 as a cause of distal myopathy 2025 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), (unknown), Tine Deconinck, Katrien Janssens, (unknown), Alicia Alonso‐Jiménez, German Demidov, Steven Laurie, Willem De Ridder, (unknown), Vincent Timmerman, Jonathan Baets	0
2	TBP Repeat Expansion Analysis in Patients Carrying Heterozygous STUB1 Variants 2025 ·Movement Disorders ·(unknown), (unknown), Kristof Van Schil, Tine Deconinck, Katrien Storm, (unknown), (unknown), David Crosiers, (unknown), Willem De Ridder, Peter De Jonghe, (unknown)	0
3	Vitamin D3 deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis 2024 ·Scientific Reports ·Sabrina Ehnert, Stefan Hauser, Holger Hengel, (unknown), Rebecca Schüle, Tobias Lindig, Jonathan Baets, Tine Deconinck, Peter De Jonghe, Tina Histing, Andreas K. Nüssler, Lüdger Schöls, Tim W. Rattay	1
4	Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1-associated diseases 2024 ·Brain Communications ·Danique Beijer, (unknown), (unknown), Willem De Ridder, (unknown), Abigail L. D. Tadenev, (unknown), Tine Deconinck, Richard Macdonell, Wilson Marques, Peter De Jonghe, (unknown), Rebecca Meyer‐Schuman, Stephan Züchner, Anthony Antonellis, Robert W. Burgess, Jonathan Baets	7
5	A homozygous loss of function variant in POPDC3: From invalidating exercise intolerance to a limb-girdle muscular dystrophy phenotype 2023 ·Neuromuscular Disorders ·Willem De Ridder, Geert de Vries, Kristof Van Schil, Tine Deconinck, Vincent Mouly, Volker Straub, Jonathan Baets	1
6	Distinct features in adult polyglucosan body disease: a case series 2022 ·Neuromuscular Disorders ·(unknown), (unknown), Edwin H. Jacobs, (unknown), Tine Deconinck, Willem De Ridder, Sven Dekeyzer, Jonathan Baets	3
7	Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response 2021 ·Life Science Alliance ·Danique Beijer, Thomas Agnew, J.G.M. Rack, Evgeniia Prokhorova, Tine Deconinck, Berten Ceulemans, Stojan Perić, Vedrana Milić Rašić, Peter De Jonghe, Ivan Ahel, Jonathan Baets	16
8	Pathogenic variants in the AFG3L2 proteolytic domain cause SCA28 through haploinsufficiency and proteostatic stress-driven OMA1 activation 2019 ·Journal of Medical Genetics ·(unknown), (unknown), (unknown), Davide Mazza, Franca Codazzi, Tyler Mark Pierson, Alessandro Ambrosi, Dagmar Nolte, Cyril Goizet, Camilo Toro, Jonathan Baets, Tine Deconinck, (unknown), Paola Mandich, Giorgio Casari, Francesca Maltecca	19
9	De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function 2018 ·European Journal of Human Genetics ·Matthis Synofzik, Katherine L. Helbig, Florian Harmuth, Tine Deconinck, Pranoot Tanpaiboon, Bo Sun, Wenting Guo, Ruiwu Wang, Erika Palmaer, Sha Tang, G. Bradley Schaefer, Janina Gburek‐Augustat, Stephan Züchner, Ingeborg Krägeloh‐Mann, Jonathan Baets, Peter De Jonghe, Peter Bauer, S.R. Wayne Chen, Lüdger Schöls, Rebecca Schüle	30
10	GDAP2 mutations implicate susceptibility to cellular stress in a new form of cerebellar ataxia 2018 ·Brain ·Ilse Eidhof, Jonathan Baets, Erik-Jan Kamsteeg, Tine Deconinck, (unknown), Jean‐Jacques Martin, Rebecca Schüle, Stephan Züchner, Peter De Jonghe, Annette Schenck, Bart P.C. van de Warrenburg	14
11	STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations 2017 ·Orphanet Journal of Rare Diseases ·Stefanie N. Hayer, Tine Deconinck, Benjamin Bender, Katrien Smets, Stephan Züchner, Selina Reich, Lüdger Schöls, Rebecca Schüle, Peter De Jonghe, Jonathan Baets, Matthis Synofzik	45
12	Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes 2017 ·Neurobiology of Aging ·Carlo Wilke, Jonathan Baets, Jan De Bleecker, Tine Deconinck, Saskia Biskup, Stefanie N. Hayer, Stephan Züchner, Rebecca Schüle, Peter De Jonghe, Matthis Synofzik	27
13	Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48) 2016 ·Neurology Genetics ·Jennifer Hirst, Marianna Madeo, Katrien Smets, James R. Edgar, Lüdger Schöls, Jun Li, (unknown), Tine Deconinck, Jonathan Baets, Elisabeth Van Aken, Jan De Bleecker, Manuel B. Datiles, Ricardo H. Roda, Joachim Liepert, Stephan Züchner, Caterina Mariotti, Peter De Jonghe, Craig Blackstone, Michael C. Kruer	24
14	Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions 2016 ·Brain ·Paola S. Denora, Katrien Smets, (unknown), (unknown), Carlo Casali, Tine Deconinck, Anne Sieben, Michael Gonzales, Stephan Züchner, Frédéric Darios, D. Peeters, Alexis Brice, Alessandro Malandrini, Peter De Jonghe, Filippo M. Santorelli, Giovanni Stévanin, Jean‐Jacques Martin, Khalid Hamid El Hachimi	49
15	Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses 2016 ·Mitochondrion ·Arnaud Vanlander, Laura Muiño Mosquera, Joseph Panzer, Tine Deconinck, Joél Smet, Sara Seneca, Jo Van Dorpe, Liesbeth Ferdinande, Chantal Ceuterick‐de Groote, Peter De Jonghe, Rudy Van Coster, Jonathan Baets	10
16	Cerebrotendinous xanthomatosis presenting with asymmetric parkinsonism: a case with I-123-FP-CIT SPECT imaging 2012 ·Acta Neurologica Belgica ·(unknown), (unknown), Jonathan Baets, Sarah Ceyssens, Luc van den Hauwe, Tine Deconinck, (unknown)	5
17	Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation 2011 ·European Journal of Paediatric Neurology ·(unknown), Arvid Suls, Tine Deconinck, Peter De Jonghe, Ilan Linder, Sara Kivity, Ron Dabby, Esther Leshinsky‐Silver, Dorit Lev, Tally Lerman‐Sagie	19
18	TheSCN1Avariant database: a novel research and diagnostic tool 2009 ·Human Mutation ·Lieve Claes, Liesbet Deprez, Arvid Suls, Jonathan Baets, Katrien Smets, Tine Van Dyck, Tine Deconinck, Albena Jordanova, Peter De Jonghe	103
19	Epilepsy as part of the phenotype associated with ATP1A2 mutations 2007 ·Epilepsia ·Liesbet Deprez, Sarah Weckhuysen, (unknown), Tine Deconinck, Kristl G. Claeys, Lieve Claes, Arvid Suls, Tine Van Dyck, André Palmini, Gert Matthijs, Wim Van Paesschen, Peter De Jonghe	80
20	Spastin gene mutations in Bulgarian patients with hereditary spastic paraplegia 2006 ·Clinical Genetics ·(unknown), Ann Löfgren, (unknown), (unknown), (unknown), Albena Jordanova, (unknown), Tine Deconinck, Vincent Timmerman, Ivo Kremensky, Peter De Jonghe, Vanio Mitev	6

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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