Josja Graafland

837 total citations
4 papers, 358 citations indexed

About

Josja Graafland is a scholar working on Cellular and Molecular Neuroscience, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Josja Graafland has authored 4 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Cellular and Molecular Neuroscience, 2 papers in Neurology and 2 papers in Nutrition and Dietetics. Recurrent topics in Josja Graafland's work include Parkinson's Disease Mechanisms and Treatments (2 papers), Neurological disorders and treatments (1 paper) and Hemoglobinopathies and Related Disorders (1 paper). Josja Graafland is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (2 papers), Neurological disorders and treatments (1 paper) and Hemoglobinopathies and Related Disorders (1 paper). Josja Graafland collaborates with scholars based in Netherlands, Italy and Denmark. Josja Graafland's co-authors include Simone Olgiati, Vincenzo Bonifati, Marialuisa Quadri, Guido J. Breedveld, Bin Wu, Fengping Xu, Hsin Fen Chien, Mingyan Fang, Marianna Amboni and Roberto Erro and has published in prestigious journals such as Movement Disorders, Human Mutation and Parkinsonism & Related Disorders.

In The Last Decade

Josja Graafland

4 papers receiving 356 citations

Peers

Countries citing papers authored by Josja Graafland

Since Specialization

Citations

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

Fields of papers citing papers by Josja Graafland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Josja Graafland

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

All Works

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4 of 4 papers shown

#	Work	Indexed citations
1	The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN 2017 ·Parkinsonism & Related Disorders ·Simone Olgiati, Okan Doğu, Zeynep Tüfekçıoğlu, (unknown), Esen Saka, Murat Gültekin, Hakan Kaleağası, (unknown), Josja Graafland, Guido J. Breedveld, Marialuisa Quadri, (unknown), (unknown), (unknown), (unknown), Başar Bılgıç, Bülent Elibol, Murat Emre, Haşmet Hanağası, Vincenzo Bonifati	31
2	Early-onset parkinsonism caused by alpha-synuclein gene triplication: Clinical and genetic findings in a novel family 2015 ·Parkinsonism & Related Disorders ·Simone Olgiati, Astrid Thomas, Marialuisa Quadri, Guido J. Breedveld, Josja Graafland, (unknown), Hannie Douben, Annelies de Klein, Marco Onofrj, Vincenzo Bonifati	47
3	Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes 2015 ·Movement Disorders ·Marialuisa Quadri, (unknown), Suvasini Sharma, Simone Olgiati, Josja Graafland, Guido J. Breedveld, (unknown), (unknown), Puneet Jain, Satinder Aneja, Atin Kumar, (unknown), (unknown), Bibek Talukdar, Vincenzo Bonifati	49
4	Mutation in theSYNJ1Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism 2013 ·Human Mutation ·Marialuisa Quadri, Mingyan Fang, Marina Picillo, Simone Olgiati, Guido J. Breedveld, Josja Graafland, Bin Wu, Fengping Xu, Roberto Erro, Marianna Amboni, (unknown), Mario Quarantelli, Grazia Annesi, Aldo Quattrone, Hsin Fen Chien, Egberto Reis Barbosa, (unknown), Ben A. Oostra, Paolo Barone, Jun Wang, Vincenzo Bonifati	231

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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