Ástrós Skúladóttir

Author

Ástrós Skúladóttir

Also Known As

Astros Skuladottir, Astros T Skuladottir, Astros Th Skuladottir, Astros Th. Skuladottir, Astros Th. Skuladóttir, G. Bragi Walters, Tannemaat, Martijn R., Ástrós Skúladóttir, Ástrós Th. Skúladóttir

Publications

581

Citations

H-Index

Concepts

All Affiliations

University of Iceland deCODE Genetics (Iceland)Reykjavík University National University Hospital of Iceland Aarhus University Hospital

ÁS

About

Ástrós Skúladóttir is an author at University of Iceland specializing in bioinformatics, genomics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	252
2	Public Health	1	1	210
3	Biostatistics	1	1	210
4	Molecular Genetics	1	1	42
5	Functional Genomics	1	1	42

Ástrós Skúladóttir

Publications

377

Citations

H-Index

Page 1

	Year	Citations
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs Hannes P. Eggertsson, Doruk Beyter, Hákon Jónsson, Nature Communications GeneticsGenetic EpidemiologyGenomicsGenotype-phenotype AssociationMolecular Ecology	2019	210
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura Mona Ameri Chalmer, Lilja Stefánsdóttir, Ástrós Skúladóttir, Nature Genetics	2023	47
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming Rósa S. Gísladóttir, Erna V. Ivarsdottir, Agnar Helgason, Current Biology Functional GenomicsSequence VariantsGeneticsSensory ScienceMolecular Genetics	2020	42
MAP1B mutations cause intellectual disability and extensive white matter deficit G. Bragi Walters, Ómar Gústafsson, Garðar Sveinbjörnsson, Nature Communications	2018	35
Sequence variants affecting voice pitch in humans Rósa S. Gísladóttir, Agnar Helgason, Bjarni V. Halldórsson, Science Advances	2023	18
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy Erna V. Ivarsdottir, Kristbjörg Bjarnadóttir, Stefania Benónísdóttir, Nature Communications	2019	14
Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease Ástrós Skúladóttir, Vinicius Tragante, Garðar Sveinbjörnsson, npj Parkinson s Disease	2024	11

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