Kristin Ørstavik

1.8k total citations
51 papers, 1.2k citations indexed

About

Kristin Ørstavik is a scholar working on Neurology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Kristin Ørstavik has authored 51 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Neurology, 17 papers in Cellular and Molecular Neuroscience and 17 papers in Physiology. Recurrent topics in Kristin Ørstavik's work include Pain Mechanisms and Treatments (13 papers), Botulinum Toxin and Related Neurological Disorders (12 papers) and Genetic Neurodegenerative Diseases (9 papers). Kristin Ørstavik is often cited by papers focused on Pain Mechanisms and Treatments (13 papers), Botulinum Toxin and Related Neurological Disorders (12 papers) and Genetic Neurodegenerative Diseases (9 papers). Kristin Ørstavik collaborates with scholars based in Norway, Germany and Sweden. Kristin Ørstavik's co-authors include Ellen Jørum, Martin Schmelz, Roland Schmidt, Barbara Namer, Marita Hilliges, Christian Weidner, Hermann O. Handwerker, H. E. Torebjörk, Richard W. Carr and Inge Petter Kleggetveit and has published in prestigious journals such as Journal of Neuroscience, Brain and Neurology.

In The Last Decade

Kristin Ørstavik

47 papers receiving 1.2k citations

Peers

Countries citing papers authored by Kristin Ørstavik

Since Specialization

Citations

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

Fields of papers citing papers by Kristin Ørstavik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kristin Ørstavik

This figure shows the co-authorship network connecting the top 25 collaborators of Kristin Ørstavik. A scholar is included among the top collaborators of Kristin Ørstavik 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 Kristin Ørstavik. Kristin Ørstavik 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	Small and large fiber neuropathy in adults with myotonic dystrophy type 1 2024 ·Frontiers in Neurology ·(unknown), Sissel Løseth, Jan C. Frich, Espen Dietrichs, Kristin Ørstavik	4
2	Type 1 spinal muscular atrophy treated with nusinersen in Norway, a five-year follow-up 2024 ·European Journal of Paediatric Neurology ·(unknown), Magnhild Rasmussen, Kristin Ørstavik, Henrik Zetterberg, (unknown), (unknown), (unknown), (unknown)	0
3	A scoping review of health literacy in rare disorders: key issues and research directions 2024 ·Orphanet Journal of Rare Diseases ·Una Stenberg, (unknown), (unknown), Kristin Ørstavik, Maria Flink, Heidi Holmen, (unknown), (unknown), Gry Velvin	1
4	Myotonic dystrophy type 1 – a multiorgan disorder 2024 ·Tidsskrift for Den norske legeforening ·Kristin Ørstavik, (unknown), Magnhild Rasmussen, (unknown), (unknown), (unknown), (unknown), (unknown), Arvid Heiberg	2
5	Rehabilitation technology in assessment and treatment of arm and hand function in myotonic dystrophy type 1: A single subject experimental design study 2024 ·Journal of Neuromuscular Diseases ·(unknown), Kristin Ørstavik, (unknown), Jan C. Frich, Hilde Stendal Robinson	1
6	Translation, reliability, and validity of the Norwegian version of the ABILHAND-NMD and the ACTIVLIM for Myotonic Dystrophy type 1 2023 ·Disability and Rehabilitation ·(unknown), Kristin Ørstavik, Jan C. Frich, Hilde Stendal Robinson	1
7	Cognitive function, behaviour and quality of life in children with myotonic dystrophy type 1 in South - Eastern Norway 2023 ·European Journal of Paediatric Neurology ·(unknown), (unknown), (unknown), Kristin Ørstavik, Magnhild Rasmussen	6
8	Polyneuropathy in Adolescent Childhood Cancer Survivors: The PACCS Study 2022 ·Pediatric Neurology ·(unknown), Kristin Ørstavik, Corina S. Rueegg, (unknown), Elisabeth Edvardsen, (unknown), Ingrid Kristin Torsvik, Truls Raastad, Ellen Ruud, Kristian Bernhard Nilsen	3
9	The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease 2021 ·Orphanet Journal of Rare Diseases ·Sólrún Sigurðardóttir, (unknown), Trond Jenssen, Per Mathisen, Charlotte von der Lippe, Kristin Ørstavik, Ketil Heimdal, Dag Olav Dahle, M.S. Weedon-Fekjær, (unknown), Hege Pihlstrøm	6
10	MRI of trunk muscles and motor and respiratory function in patients with myotonic dystrophy type 1 2019 ·BMC Neurology ·(unknown), Bård Bjørnarå, Eva Kirkhus, (unknown), Gunnar Hansen, Jan C. Frich, Kristin Ørstavik	14
11	Proprioceptive loss and the perception, control and learning of arm movements in humans: evidence from sensory neuronopathy 2018 ·Experimental Brain Research ·R. Chris Miall, (unknown), (unknown), (unknown), (unknown), Kristin Ørstavik, Jonathan Cole, Fabrice R. Sarlegna	44
12	A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia 2015 ·Journal of Neuromuscular Diseases ·Kristin Ørstavik, (unknown), T. Torbergsen, Angela Abicht, (unknown), Emı́lia Kerty, Magnhild Rasmussen	5
13	Specific changes in conduction velocity recovery cycles of single nociceptors in a patient with erythromelalgia with the I848T gain-of-function mutation of Nav1.7 2015 ·Pain ·Barbara Namer, Kristin Ørstavik, Roland Schmidt, (unknown), Christian Weidner, Cato Mørk, (unknown), Knut Kvernebo, Hugh Salter, T. Hedley Carr, Märta Segerdahl, H. Quiding, Stephen G. Waxman, Hermann O. Handwerker, H. E. Torebjörk, Ellen Jørum, Martin Schmelz	32
14	Exonic mutations in SCN9A (Na _V 1.7) are found in a minority of patients with erythromelalgia 2014 ·Scandinavian Journal of Pain ·Zhiping Zhang, Martin Schmelz, Märta Segerdahl, H. Quiding, (unknown), (unknown), T. Hedley Carr, (unknown), Hugh Salter, (unknown), Kristin Ørstavik, (unknown), (unknown), (unknown), Ellen Jørum	22
15	Tynnfibernevropati 2013 ·Tidsskrift for Den norske legeforening ·Ellen Jørum, Torhild Warncke, Kristin Ørstavik	0
16	En alvorlig syk pasient som ikke våknet etter respiratorbehandling 2012 ·Tidsskrift for Den norske legeforening ·Kristin Ørstavik, Sigrid Svalheim, Ragnar Gunnarsson, (unknown), T. Torbergsen	1
17	Hereditary motor neuron disease in a large Norwegian family with a “H46R” substitution in the superoxide dismutase 1 gene 2012 ·Neuromuscular Disorders ·(unknown), Toril Fagerheim, Kristin Ørstavik, Trygve Holmøy, Arvid Heiberg, (unknown), Tim M. Strom, Øivind Nilssen, Arve Dahl	12
18	Abnormal Function of C-Fibers in Patients with Diabetic Neuropathy 2006 ·Journal of Neuroscience ·Kristin Ørstavik, Barbara Namer, Roland Schmidt, Martin Schmelz, Marita Hilliges, Christian Weidner, Richard W. Carr, Hermann O. Handwerker, Ellen Jørum, H. E. Torebjörk	159
19	ATP responses in human C nociceptors 2002 ·Pain ·Marita Hilliges, Christian Weidner, Martin Schmelz, Roland Schmidt, Kristin Ørstavik, Erik Torebjörk, Hermann O. Handwerker	52
20	Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies 2001 ·Muscle & Nerve ·Kristin Ørstavik, Mona Skard Heier, (unknown), Florian Stögbauer	21

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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