Áslaug Jónasdóttir

20.2k total citations · 1 hit paper
19 papers, 1.9k citations indexed

About

Áslaug Jónasdóttir is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Áslaug Jónasdóttir has authored 19 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Áslaug Jónasdóttir's work include Multiple Sclerosis Research Studies (5 papers), Genomics and Rare Diseases (4 papers) and T-cell and Retrovirus Studies (3 papers). Áslaug Jónasdóttir is often cited by papers focused on Multiple Sclerosis Research Studies (5 papers), Genomics and Rare Diseases (4 papers) and T-cell and Retrovirus Studies (3 papers). Áslaug Jónasdóttir collaborates with scholars based in Iceland, United Kingdom and United States. Áslaug Jónasdóttir's co-authors include Kāri Stefánsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Augustine Kong, Gísli Másson, Aðalbjörg Jónasdóttir, Guðmar Þorleifsson, Sigurjón A. Guðjónsson, Agnar Helgason and G. Bragi Walters and has published in prestigious journals such as Nature, Science and Nature Genetics.

In The Last Decade

Áslaug Jónasdóttir

19 papers receiving 1.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma

2007 478 citations Guðmar Þorleifsson, Kristinn P. Magnússon et al. Science profile →

Peers

Countries citing papers authored by Áslaug Jónasdóttir

Since Specialization

Citations

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

Fields of papers citing papers by Áslaug Jónasdóttir

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Áslaug Jónasdóttir

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

All Works

Sort: Min cites: Since: Top N: Style:

19 of 19 papers shown

#	Work	Indexed citations
1	A population-based survey of FBN1 variants in Iceland reveals underdiagnosis of Marfan syndrome 2023 ·European Journal of Human Genetics ·(unknown), Gudny A. Arnadottir, Brynjar Ö. Jensson, Aðalbjörg Jónasdóttir, Hildigunnur Katrínardóttir, Rún Friðriksdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Sigurjón A. Guðjónsson, Jón J. Jónsson, Vigdís Stefánsdóttir, Ragnar Daníelsen, Ástríður Pálsdóttir, Hákon Jónsson, Agnar Helgason, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Hans T. Björnsson, Kāri Stefánsson, Patrick Sulem	4
2	Graphtyper enables population-scale genotyping using pangenome graphs 2017 ·Nature Genetics ·Hannes P. Eggertsson, Hákon Jónsson, Snædís Kristmundsdóttir, Eirikur Hjartarson, Birte Kehr, Gísli Másson, Florian Zink, Kristján Eldjárn Hjörleifsson, Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Ingileif Jónsdóttir, Daníel F. Guðbjartsson, Páll Melsted, Kāri Stefánsson, Bjarni V. Halldórsson	113
3	Diversity in non-repetitive human sequences not found in the reference genome 2017 ·Nature Genetics ·Birte Kehr, Anna Helgadóttir, Páll Melsted, Hákon Jónsson, Hannes Helgason, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Arnaldur Gylfason, Gísli H. Halldórsson, Snædís Kristmundsdóttir, Guðmundur Þorgeirsson, Ísleifur Ólafsson, Hilma Hólm, Unnur Þorsteinsdóttir, Patrick Sulem, Agnar Helgason, Daníel F. Guðbjartsson, Bjarni V. Halldórsson, Kāri Stefánsson	38
4	Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters 2017 ·BMC Medical Genetics ·Gudny A. Arnadottir, Brynjar Ö. Jensson, (unknown), Gerald Sulem, Ásmundur Oddsson, Ragnar P. Kristjansson, Stefania Benónísdóttir, Sigurjón A. Guðjónsson, Gísli Másson, Guðmundur Á. Þórisson, Jona Saemundsdottir, Ólafur Þ. Magnússon, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Daníel F. Guðbjartsson, Unnur Þorsteinsdóttir, Reynir Arngrı́msson, Patrick Sulem, Kāri Stefánsson	29
5	The rate of meiotic gene conversion varies by sex and age 2016 ·Nature Genetics ·Bjarni V. Halldórsson, Marteinn T. Hardarson, Birte Kehr, Unnur Styrkársdóttir, Arnaldur Gylfason, Guðmar Þorleifsson, Florian Zink, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Patrick Sulem, Gísli Másson, Unnur Þorsteinsdóttir, Agnar Helgason, Augustine Kong, Daníel F. Guðbjartsson, Kāri Stefánsson	61
6	Multi-nucleotide de novo Mutations in Humans 2016 ·PLoS Genetics ·Søren Besenbacher, Patrick Sulem, Agnar Helgason, Hannes Helgason, (unknown), Áslaug Jónasdóttir, Aðalbjörg Jónasdóttir, Ólafur Þ. Magnússon, Unnur Þorsteinsdóttir, Gísli Másson, Augustine Kong, Daníel F. Guðbjartsson, Kāri Stefánsson	82
7	Identification of a large set of rare complete human knockouts 2015 ·Nature Genetics ·Patrick Sulem, Hannes Helgason, Asmundur Oddson, Hreinn Stefánsson, Sigurjón A. Guðjónsson, Florian Zink, Eirikur Hjartarson, Gunnar Sigurðsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Sigurðsson, Ólafur Þ. Magnússon, Augustine Kong, Agnar Helgason, Hilma Hólm, Unnur Þorsteinsdóttir, Gísli Másson, Daníel F. Guðbjartsson, Kāri Stefánsson	142
8	Rare mutations associating with serum creatinine and chronic kidney disease 2014 ·Human Molecular Genetics ·Garðar Sveinbjörnsson, Evgenia Mikaelsdottir, Runólfur Pálsson, Ólafur S. Indridason, Hilma Hólm, Áslaug Jónasdóttir, Agnar Helgason, Snævar Sigurðsson, Aðalbjörg Jónasdóttir, Ásgeir Sigurðsson, Guðmundur I. Eyjólfsson, Ólöf Sigurðardóttir, Ólafur Þ. Magnússon, Augustine Kong, Gísli Másson, Patrick Sulem, Ísleifur Ólafsson, Unnur Þorsteinsdóttir, Daníel F. Guðbjartsson, Kāri Stefánsson	38
9	Fine-scale recombination rate differences between sexes, populations and individuals 2010 ·Nature ·Augustine Kong, Guðmar Þorleifsson, Daníel F. Guðbjartsson, Gísli Másson, Ásgeir Sigurðsson, Áslaug Jónasdóttir, G. Bragi Walters, Aðalbjörg Jónasdóttir, Arnaldur Gylfason, Kári Kristinsson, Sigurjón A. Guðjónsson, Michael L. Frigge, Agnar Helgason, Unnur Þorsteinsdóttir, Kāri Stefánsson	406
10	Several common variants modulate heart rate, PR interval and QRS duration 2010 ·Nature Genetics ·Hilma Hólm, Daníel F. Guðbjartsson, Davíð O. Arnar, Guðmar Þorleifsson, Guðmundur Þorgeirsson, (unknown), Sigurjón A. Guðjónsson, Áslaug Jónasdóttir, Ellisiv B. Mathiesen, Inger Njølstad, Audhild Nyrnes, Tom Wilsgaard, Erin Mathiesen Hald, Kristian Hveem, Camilla Stoltenberg, Maja‐Lisa Løchen, Augustine Kong, Unnur Þorsteinsdóttir, Kāri Stefánsson	242
11	Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate 2008 ·Science ·Augustine Kong, Guðmar Þorleifsson, Hreinn Stefánsson, Gísli Másson, Agnar Helgason, Daníel F. Guðbjartsson, G.M. Jonsdottir, Sigurjón A. Guðjónsson, Sverrir T. Sverrisson, Theodora Thorlacius, Áslaug Jónasdóttir, (unknown), Stefan Palsson, Michael L. Frigge, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Kāri Stefánsson	151
12	Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma breakdown → 2007 ·Science ·Guðmar Þorleifsson, Kristinn P. Magnússon, Patrick Sulem, G. Bragi Walters, Daníel F. Guðbjartsson, Hreinn Stefánsson, (unknown), Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, (unknown), Gísli Másson, (unknown), Hjörvar Pétursson, Ársæll Már Arnarsson, Mehdi Motallebipour, Ola Wallerman, Claes Wadelius, (unknown), Unnur Þorsteinsdóttir, Augustine Kong, Friðbert Jónasson, Kāri Stefánsson	478
13	Polymorphism of PRNP codons in the normal Icelandic population 2006 ·Acta Neurologica Scandinavica ·G. Georgsson, (unknown), Áslaug Jónasdóttir, Sanna Gudmundsson, (unknown)	9
14	A whole genome association study in Finnish multiple sclerosis patients with 3669 markers 2003 ·Journal of Neuroimmunology ·Mikko Laaksonen, Áslaug Jónasdóttir, Ragnheiður Fossdal, Juhani Ruutiainen, Stephen Sawcer, Alastair Compston, (unknown), Theodora Thorlacius, Jeffrey R. Gulcher, Jorma Ilonen	12
15	A whole genome association study in multiple sclerosis patients from north Portugal 2003 ·Journal of Neuroimmunology ·Berta Martins da Silva, Theodora Thorlacius, (unknown), Clara Pereira, Ragnheiður Fossdal, Hjörtur H. Jónsson, Ana Silva, Isabel Cristina Gonçalves Leite, João Cerqueira, Paulo Costa, Mónica Marta, Thomas Foltynie, Stephen Sawcer, Alastair Compston, Áslaug Jónasdóttir	9
16	A genomic screen of Spanish multiple sclerosis patients reveals multiple loci associated with the disease 2003 ·Journal of Neuroimmunology ·Robert Goertsches, Pablo Villoslada, Manuel Comabella, Xavier Montalbán, Arcadi Navarro, Emilio G. de la Concha, Rafael Arroyo, Adolfo López de Munaín, David Otaegui, Ricardo Palácios, Jordi Pérez‐Tur, Áslaug Jónasdóttir, (unknown), Ragnheiður Fossdal, Stephen Sawcer, Efrosini Setakis, Alastair Compston	26
17	A genome-wide screen for association in Hungarian multiple sclerosis 2003 ·Journal of Neuroimmunology ·Cecília Rajda, Krisztina Bencsik, (unknown), Áslaug Jónasdóttir, Thomas Foltynie, Stephen Sawcer, (unknown), Ragnheiður Fossdal, Efrosini Setakis, Alastair Compston, László Vécsei	9
18	A whole genome association study in Icelandic multiple sclerosis patients with 4804 markers 2003 ·Journal of Neuroimmunology ·Áslaug Jónasdóttir, Theodora Thorlacius, Ragnheiður Fossdal, Aðalbjörg Jónasdóttir, (unknown), John Benedikz, Hjörtur H. Jónsson, Jesús Sainz, H Einarsdottir, (unknown), (unknown), Stephen Sawcer, Alastair Compston, Kāri Stefánsson, Jeffrey R. Gulcher	19
19	Genome-wide linkage screen of a consanguineous multiple sclerosis kinship 2003 ·Multiple Sclerosis Journal ·(unknown), Thomas Masterman, Theodora Thorlacius, Magnús Örn Stefánsson, Áslaug Jónasdóttir, Kāri Stefánsson, Jan Hillert, Jeffrey R. Gulcher	17

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.

Explore authors with similar magnitude of impact