Seguir
Hannes Pétur Eggertsson
Hannes Pétur Eggertsson
Dirección de correo verificada de decode.is
Título
Citado por
Citado por
Año
Parental influence on human germline de novo mutations in 1,548 trios from Iceland
H Jónsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ...
Nature 549 (7673), 519, 2017
8242017
Characterizing mutagenic effects of recombination through a sequence-level genetic map
BV Halldorsson, G Palsson, OA Stefansson, H Jonsson, MT Hardarson, ...
Science 363 (6425), eaau1043, 2019
2482019
Graphtyper enables population-scale genotyping using pangenome graphs
HP Eggertsson, H Jonsson, S Kristmundsdottir, E Hjartarson, B Kehr, ...
Nature genetics 49 (11), 1654, 2017
2002017
DNA methylation as a mediator of HLA-DRB1* 15: 01 and a protective variant in multiple sclerosis
L Kular, Y Liu, S Ruhrmann, G Zheleznyakova, F Marabita, ...
Nature communications 9 (1), 2397, 2018
1782018
Whole genome characterization of sequence diversity of 15,220 Icelanders
H Jónsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ...
Scientific data 4, 170115, 2017
1282017
Multiple transmissions of de novo mutations in families
H Jónsson, P Sulem, GA Arnadottir, G Pálsson, HP Eggertsson, ...
Nature genetics 50 (12), 1674, 2018
1002018
Identification of Lynch syndrome risk variants in the Romanian population
PD Iordache, D Mates, B Gunnarsson, HP Eggertsson, P Sulem, ...
Journal of cellular and molecular medicine 22 (12), 6068-6076, 2018
132018
PopDel identifies medium-size deletions jointly in tens of thousands of genomes
S Roskosch, H Jónsson, E Björnsson, D Beyter, HP Eggertsson, P Sulem, ...
bioRxiv, 740225, 2019
82019
Profile of common prostate cancer risk variants in an unscreened Romanian population
PD Iordache, D Mates, B Gunnarsson, HP Eggertsson, P Sulem, ...
Journal of cellular and molecular medicine 22 (3), 1574-1582, 2018
62018
Recurrence of de novo mutations in families
H Jonsson, P Sulem, GA Arnadottir, G Palsson, HP Eggertsson, ...
bioRxiv, 221259, 2017
22017
Gyper: A graph-based HLA genotyper using aligned DNA sequences
HP Eggertsson
22015
Characterizing mutagenic effects of recombination through a sequence-level genetic map (vol 363, eaaw8705, 2019)
BV Halldorsson, G Palsson, OA Stefansson, H Jonsson, MT Hardarson, ...
Science 363 (6430), 939-939, 2019
12019
Graphtyper: Population-scale genotyping using pangenome graphs
HP Eggertsson, H Jonsson, S Kristmundsdottir, E Hjartarson, B Kehr, ...
bioRxiv, 148403, 2017
12017
PopDel calls medium-size deletions jointly in tens of thousands of genomes
S Roskosch, D Beyter, H Jonsson, HP Eggertsson, BV Halldorsson, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1717-1717, 2019
2019
GraphTyper: A pangenome method for identifyingsequence variants at a population scale
HP Eggertsson
University of Iceland, School of Engineering and Natural Sciences, Faculty …, 2019
2019
Aging oocytes accelerate regional sequence diversity in humans and African apes
H Jonsson, P Sulem, B Kehr, S Kristmundsdottir, F Zink, E Hjartarson, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 26, 80-80, 2018
2018
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–16