Tessa Wassenberg

1.0k total citations
19 papers, 372 citations indexed

About

Tessa Wassenberg is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience and Surgery. According to data from OpenAlex, Tessa Wassenberg has authored 19 papers receiving a total of 372 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Clinical Biochemistry, 6 papers in Cellular and Molecular Neuroscience and 4 papers in Surgery. Recurrent topics in Tessa Wassenberg's work include Metabolism and Genetic Disorders (8 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological disorders and treatments (3 papers). Tessa Wassenberg is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological disorders and treatments (3 papers). Tessa Wassenberg collaborates with scholars based in Netherlands, Germany and Canada. Tessa Wassenberg's co-authors include Michèl A.A.P. Willemsen, Marcel M. Verbeek, Roser Pons, Kathrin Jeltsch, Thomas Opladen, Wang‐Tso Lee, Mario Mastrangelo, Manju A. Kurian, Toni S. Pearson and Ángeles García‐Cazorla and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Movement Disorders.

In The Last Decade

Tessa Wassenberg

18 papers receiving 369 citations

Peers

Countries citing papers authored by Tessa Wassenberg

Since Specialization

Citations

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

Fields of papers citing papers by Tessa Wassenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tessa Wassenberg

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase ( TH ) Deficiency 2025 ·Journal of Inherited Metabolic Disease ·(unknown), Oya Kuseyri Hübschmann, (unknown), Roser Pons, Toni S. Pearson, Kathrin Jeltsch, (unknown), Tessa Wassenberg, Gabriella Horváth, (unknown), Manju A. Kurian, Elisenda Cortès‐Saladelafont, Agathe Roubertie, Vincenzo Leuzzi, Mariarita Bertoldi, Mario Mastrangelo, (unknown), (unknown), Ángeles García‐Cazorla, Thomas Opladen	0
2	Consensus Recommendations for the Clinical Management of Hematological Malignancies in Patients with DNA Double Stranded Break Disorders 2022 ·Cancers ·Agata Pastorczak, Andishe Attarbaschi, Simon Bomken, Arndt Borkhardt, Jutte van der Werff ten Bosch, Sarah Elitzur, Andrew R. Gennery, Eva Hlaváčková, (unknown), Zdenka Křenová, Wojciech Młynarski, Tomasz Szczepański, Tessa Wassenberg, Jan Loeffen	11
3	Hypocalcemia as a Cause of Complex Febrile Seizures in a Toddler 2021 ·SHILAP Revista de lepidopterología ·(unknown), Tessa Wassenberg, Jesse Vanbesien	1
4	Blood, urine and cerebrospinal fluid analysis in TH and AADC deficiency and the effect of treatment 2021 ·Molecular Genetics and Metabolism Reports ·Tessa Wassenberg, (unknown), L.A.H. Monnens, Ron A. Wevers, Michèl A.A.P. Willemsen, Marcel M. Verbeek	4
5	Autosomal dominant GCH1 mutations causing spastic paraplegia at disease onset 2020 ·Parkinsonism & Related Disorders ·Tessa Wassenberg, Meyke Schouten, Rick C. Helmich, Michèl A.A.P. Willemsen, Erik‐Jan Kamsteeg, Bart P.C. van de Warrenburg	8
6	Clinical presentation and long‐term follow‐up of dopamine beta hydroxylase deficiency 2020 ·Journal of Inherited Metabolic Disease ·Tessa Wassenberg, Jaap Deinum, Frans J. van Ittersum, Erik‐Jan Kamsteeg, Maartje Pennings, Marcel M. Verbeek, Ron A. Wevers, Mirjam E. van Albada, Ido P. Kema, Jorie Versmissen, (unknown), Jacques W.M. Lenders, L.A.H. Monnens, Michèl A.A.P. Willemsen	11
7	Novel Protein Biomarkers of Monoamine Metabolism Defects Correlate with Disease Severity 2020 ·Movement Disorders ·(unknown), Eva Borràs, Marta Molero-Luís, Tessa Wassenberg, (unknown), Marcel M. Verbeek, Michèl A.A.P. Willemsen, Thomas Opladen, Kathrin Jeltsch, Roser Pons, Beat Thöny, Gabriella Horváth, Zühal Yapıcı, Jennifer Friedman, Keith Hyland, Guillermo Agosta, Eduardo López‐Laso, Rafael Artuch, Eduard Sabidó, Àngels García‐Cazorla	10
8	CAPN1 mutations: Expanding the CAPN1-related phenotype: From hereditary spastic paraparesis to spastic ataxia 2018 ·European Journal of Medical Genetics ·(unknown), Ziv Gan‐Or, (unknown), Jennifer A. Ruskey, Bart van de Warrenburg, Tessa Wassenberg, Erik‐Jan Kamsteeg, Guy A. Rouleau, Oksana Suchowersky	18
9	CAPN1: novel mutations expanding the phenotype of hereditary spastic paraparesis. (P6.039) 2018 ·Neurology ·(unknown), (unknown), Ziv Gan‐Or, Bart van de Warrenburg, Tessa Wassenberg, Guy A. Rouleau, Oksana Suchowersky	1
10	Consensus guideline for the diagnosis and treatment of aromatic l-amino acid decarboxylase (AADC) deficiency 2017 ·Orphanet Journal of Rare Diseases ·Tessa Wassenberg, Marta Molero-Luís, Kathrin Jeltsch, Georg F. Hoffmann, Birgit Assmann, Nenad Blau, Ángeles García‐Cazorla, Rafael Artuch, Roser Pons, Toni S. Pearson, (unknown), Mario Mastrangelo, Phillip L. Pearl, Wang‐Tso Lee, Manju A. Kurian, Simon Heales, Lisa Flint, Marcel M. Verbeek, Michèl A.A.P. Willemsen, Thomas Opladen	156
11	Non-motor symptoms and quality of life in dopa-responsive dystonia patients 2017 ·Parkinsonism & Related Disorders ·(unknown), Anouk Kuiper, (unknown), Anna L. Bartels, D.J. Kamphuis, Nicole I. Wolf, Bwee Tien Poll‐The, Tessa Wassenberg, E Peeters, Tom J. de Koning, Marina A.J. Tijssen	16
12	l -Dopa in dystonia 2017 ·Neurology ·Roderick P.P.W.M. Maas, Tessa Wassenberg, Jean‐Pierre Lin, Bart P.C. van de Warrenburg, Michèl A.A.P. Willemsen	23
13	The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders 2016 ·Molecular Genetics and Metabolism Reports ·Thomas Opladen, Elisenda Cortès‐Saladelafont, Mario Mastrangelo, Gabriella Horváth, Roser Pons, Eduardo López‐Laso, Joaquín Alejandro Fernández‐Ramos, Tomáš Honzík, Toni S. Pearson, Jennifer Friedman, Sabine Scholl‐Bürgi, Tessa Wassenberg, Sabine Jung‐Klawitter, Oya Kuseyri Hübschmann, Kathrin Jeltsch, Manju A. Kurian, Àngels García‐Cazorla	39
14	Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Questions 2016 ·Pediatric Nephrology ·Tessa Wassenberg, Michèl A.A.P. Willemsen, Henry Dijkman, Jaap Deinum, L.A.H. Monnens	1
15	Neurodevelopmental outcome in full‐term newborns with refractory neonatal seizures 2011 ·Acta Paediatrica ·(unknown), Tessa Wassenberg, (unknown), Levinus A. Bok, (unknown), (unknown), Peter Andriessen	15
16	The Paradox of Hyperdopaminuria in Aromatic l-Amino Acid Deficiency Explained 2011 ·JIMD Reports ·Tessa Wassenberg, L.A.H. Monnens, (unknown), Ron A. Wevers, Marcel M. Verbeek, Michèl A.A.P. Willemsen	11
17	Multi-channel amplitude-integrated EEG characteristics in preterm infants with a normal neurodevelopment at two years of corrected age 2011 ·Early Human Development ·Hendrik J. Niemarkt, (unknown), (unknown), Tessa Wassenberg, (unknown), (unknown), Boris W. Kramer, Antonio W. D. Gavilanes, Luc J. I. Zimmermann, Sidarto Bambang Oetomo, Peter Andriessen	16
18	Urinary dopamine in aromatic L-amino acid decarboxylase deficiency: The unsolved paradox 2010 ·Molecular Genetics and Metabolism ·Tessa Wassenberg, Michèl A.A.P. Willemsen, (unknown), Martin Lammens, Kiek Verrijp, Martijn J. Wilmer, Wang‐Tso Lee, Ron A. Wevers, Marcel M. Verbeek	24
19	Neonatal airway obstruction caused by rapidly growing nasopharyngeal teratoma 2009 ·Acta Paediatrica ·(unknown), Tessa Wassenberg, (unknown), (unknown), Peter Andriessen	7

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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