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Magnus K. O. Burstedt

Observed names: Burstedt, M Burstedt, M. K. O. Burstedt, M.K.O. Burstedt, Magnus Burstedt
ORCID: 0000-0001-5550-0633
Observed ORCID: 0000-0001-5550-0633
OpenAlex ID: A5084086602
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
2016 · Asbjørg Stray-Pedersen, Hanne Sørmo Sorte, et al. · Journal of Allergy and Clinical Immunology · 289
Control of Grasp Stability in Humans Under Different Frictional Conditions During Multidigit Manipulation
1999 · Magnus K. O. Burstedt, J. Randall Flanagan, et al. · Journal of Neurophysiology · 181
Control of Fingertip Forces in Multidigit Manipulation
1999 · J. Randall Flanagan, Magnus K. O. Burstedt, et al. · Journal of Neurophysiology · 149
Coordination of fingertip forces during human manipulation can emerge from independent neural networks controlling each engaged digit
1997 · M. K. O. Burstedt, Benoni B. Edin, et al. · Experimental Brain Research · 78
Control of grasp stability during pronation and supination movements
1999 · R. S. Johansson, Jenny L. Backlin, et al. · Experimental Brain Research · 72
Mechanisms for Force Adjustments to Unpredictable Frictional Changes at Individual Digits During Two-Fingered Manipulation
1998 · Ingvars Birznieks, Magnus K. O. Burstedt, et al. · Journal of Neurophysiology · 50
Genomic screening in rare disorders: New mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability
2018 · Malin Kvarnung, Fulya Taylan, et al. · Clinical Genetics · 35
Precision grip function after hand replantation and digital nerve injury
2006 · M. Schenker, M.K.O. Burstedt, et al. · Journal of Plastic Reconstructive & Aesthetic Surgery · 27
Control of Forces Applied by Individual Fingers Engaged in Restraint of an Active Object
1997 · Magnus K. O. Burstedt, Ingvars Birznieks, et al. · Journal of Neurophysiology · 27
A national long-read sequencing study on chromosomal rearrangements uncovers hidden complexities
2024 · Jesper Eisfeldt, Adam Ameur, et al. · Genome Research · 22
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Pre‐ and postnatal growth failure with microcephaly due to two novel heterozygous IGF1R mutations and response to growth hormone treatment
2020 · Alexandra Gkourogianni, Anenisia C. Andrade, et al. · Acta Paediatrica · 6
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Qualitative Interviews To Inform Development Of A Patient Reported Outcome (PRO) Strategy In RLBP1 Retinitis Pigmentosa (RLBP1 RP)
2017 · C Tolley, A Mullins, et al. · Value in Health · 5
Acral Peeling Skin Syndrome: Two Unusual Cases and the Therapeutic Potential of Botulinum Toxin
2024 · Anna-Lotta Stjernbrandt, Magnus Burstedt, et al. · Acta Dermato Venereologica · 4
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Control of grasp stability in humans under various frictional conditions during multi‐digit lifting
1999 · Burstedt, Flanagan, et al. · Acta Physiologica Scandinavica · 4
Towards routine long-read sequencing for rare disease: a national pilot study on chromosomal rearrangements
2023 · Jesper Eisfeldt, Adam Ameur, et al. · medRxiv · 3
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Hyperinsulinemia in Sotos Syndrome with a de novo NSD1 Deletion
2024 · Elena Lundberg, Magnus Burstedt, et al. · Journal of Clinical Research in Pediatric Endocrinology · 2
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Phenotypic and transcriptomic characterization of biallelic RNU2‐2 developmental and epileptic encephalopathy
2026 · Olivia J. Henry, Nadja Pekkola Pacheco, et al. · Epilepsia · 1
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Extracting homogenous data from heterogenous diseases: RaraSwed, the Swedish national rare disease quality registry
2026 · Sanna Mansoob, Dan Hellström, et al. · BMC Global and Public Health
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Front Cover
2018 · Malin Kvarnung, Fulya Taylan, et al. · Clinical Genetics
Works count: 19
Citation count: 955
H-index: 10
I10-index: 10
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