Ulfarsson, Magnus O.

Large-scale integration of the plasma proteome with genetics and disease

Ferkingstad, E., Sulem, P., Atlason, B. A., Sveinbjornsson, G., Magnusson, M. I., Styrmisdottir, E. L., Gunnarsdottir, K., Helgason, A., Oddsson, A., Halldorsson, B. V., et al. (2021) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 1,697

Large-scale plasma proteomics comparisons through genetics and disease associations

Eldjarn, G. H., Ferkingstad, E., Lund, S. H., Helgason, H., Magnusson, O. T., Gunnarsdottir, K., Olafsdottir, T. A., Halldorsson, B. V., Olason, P. I., Zink, F., et al. (2023) · Nature

Genetic Associations and EpidemiologyBioinformatics and Genomic Networks

Cited by 583

The sequences of 150,119 genomes in the UK Biobank

Halldorsson, B. V., Eggertsson, H. P., Moore, K. H. S., Hauswedell, H., Eiriksson, O., Ulfarsson, M. O., Palsson, G., Hardarson, M. T., Oddsson, A., Jensson, B. O., et al. (2022) · Nature

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 448

Multispectral and Hyperspectral Image Fusion Using a 3-D-Convolutional Neural Network

Palsson, F., Sveinsson, J. R., & Ulfarsson, M. O. (2017) · IEEE Geoscience and Remote Sensing Letters

Advanced Image Fusion TechniquesRemote-Sensing Image Classification

Cited by 364

Blind Hyperspectral Unmixing Using Autoencoders: A Critical Comparison

Palsson, B., Sveinsson, J. R., & Ulfarsson, M. O. (2022) · IEEE Journal of Selected Topics in Applied Earth Observations and Remote Sensing

Remote-Sensing Image ClassificationGeochemistry and Geologic Mapping

Cited by 107

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

Ulfarsson, M. O., Walters, G. B., Gustafsson, O., Steinberg, S., Silva, A., Doyle, O. M., Brammer, M., Gudbjartsson, D. F., Arnarsdottir, S., Jonsdottir, G. A., et al. (2017) · Translational Psychiatry

Genomic variations and chromosomal abnormalitiesReading and Literacy Development

Cited by 78

Effects of copy number variations on brain structure and risk for psychiatric illness: Large‐scale studies from the ENIGMA working groups on CNVs

Sønderby, I. E., Ching, C. R. K., Thomopoulos, S. I., van der Meer, D., Sun, D., Villalon‐Reina, J. E., Agartz, I., Amunts, K., Arango, C., Armstrong, N. J., et al. (2022) · Human Brain Mapping

Genomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Cited by 67

Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

Sønderby, I. E., Gústafsson, Ó., Doan, N. T., Hibar, D. P., Martin-Brevet, S., Abdellaoui, A., Ames, D., Amunts, K., Andersson, M., Armstrong, N. J., et al. (2020) · Molecular Psychiatry

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

Cited by 66

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study

Silva, A. I., Ulfarsson, M. O., Stefansson, H., Gustafsson, O., Walters, G. B., Linden, D. E. J., Wilkinson, L. S., Drakesmith, M., Owen, M. J., Hall, J., et al. (2019) · Biological Psychiatry

Genomic variations and chromosomal abnormalitiesAdvanced Neuroimaging Techniques and Applications

Cited by 36