Results
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Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis. [electronic resource] by
- Sigurdsson, Snaevar
- Alexandersson, Kristjan F
- Sulem, Patrick
- Feenstra, Bjarke
- Gudmundsdottir, Steinunn
- Halldorsson, Gisli H
- Olafsson, Sigurgeir
- Sigurdsson, Asgeir
- Rafnar, Thorunn
- Thorgeirsson, Thorgeir
- Sørensen, Erik
- Nordholm-Carstensen, Andreas
- Burcharth, Jakob
- Andersen, Jens
- Jørgensen, Henrik Stig
- Possfelt-Møller, Emma
- Ullum, Henrik
- Thorleifsson, Gudmar
- Masson, Gisli
- Thorsteinsdottir, Unnur
- Melbye, Mads
- Gudbjartsson, Daniel F
- Stefansson, Tryggvi
- Jonsdottir, Ingileif
- Stefansson, Kari
Producer: 20181218
In:
Nature communications vol. 8
Availability: No items available.
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Insights into imprinting from parent-of-origin phased methylomes and transcriptomes. [electronic resource] by
- Zink, Florian
- Magnusdottir, Droplaug N
- Magnusson, Olafur T
- Walker, Nicolas J
- Morris, Tiffany J
- Sigurdsson, Asgeir
- Halldorsson, Gisli H
- Gudjonsson, Sigurjon A
- Melsted, Pall
- Ingimundardottir, Helga
- Kristmundsdottir, Snædis
- Alexandersson, Kristjan F
- Helgadottir, Anna
- Gudmundsson, Julius
- Rafnar, Thorunn
- Jonsdottir, Ingileif
- Holm, Hilma
- Eyjolfsson, Gudmundur Ingi
- Sigurdardottir, Olof
- Olafsson, Isleifur
- Masson, Gisli
- Gudbjartsson, Daniel F
- Thorsteinsdottir, Unnur
- Halldorsson, Bjarni V
- Stacey, Simon N
- Stefansson, Kari
Producer: 20190423
In:
Nature genetics vol. 50
Availability: No items available.
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Epigenetic and genetic components of height regulation. [electronic resource] by
- Benonisdottir, Stefania
- Oddsson, Asmundur
- Helgason, Agnar
- Kristjansson, Ragnar P
- Sveinbjornsson, Gardar
- Oskarsdottir, Arna
- Thorleifsson, Gudmar
- Davidsson, Olafur B
- Arnadottir, Gudny A
- Sulem, Gerald
- Jensson, Brynjar O
- Holm, Hilma
- Alexandersson, Kristjan F
- Tryggvadottir, Laufey
- Walters, G Bragi
- Gudjonsson, Sigurjon A
- Ward, Lucas D
- Sigurdsson, Jon K
- Iordache, Paul D
- Frigge, Michael L
- Rafnar, Thorunn
- Kong, Augustine
- Masson, Gisli
- Helgason, Hannes
- Thorsteinsdottir, Unnur
- Gudbjartsson, Daniel F
- Sulem, Patrick
- Stefansson, Kari
Producer: 20180905
In:
Nature communications vol. 7
Availability: No items available.
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5.
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A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease. [electronic resource] by
- Arnadottir, Gudny A
- Norddahl, Gudmundur L
- Gudmundsdottir, Steinunn
- Agustsdottir, Arna B
- Sigurdsson, Snaevar
- Jensson, Brynjar O
- Bjarnadottir, Kristbjorg
- Theodors, Fannar
- Benonisdottir, Stefania
- Ivarsdottir, Erna V
- Oddsson, Asmundur
- Kristjansson, Ragnar P
- Sulem, Gerald
- Alexandersson, Kristjan F
- Juliusdottir, Thorhildur
- Gudmundsson, Kjartan R
- Saemundsdottir, Jona
- Jonasdottir, Adalbjorg
- Jonasdottir, Aslaug
- Sigurdsson, Asgeir
- Manzanillo, Paolo
- Gudjonsson, Sigurjon A
- Thorisson, Gudmundur A
- Magnusson, Olafur Th
- Masson, Gisli
- Orvar, Kjartan B
- Holm, Hilma
- Bjornsson, Sigurdur
- Arngrimsson, Reynir
- Gudbjartsson, Daniel F
- Thorsteinsdottir, Unnur
- Jonsdottir, Ingileif
- Haraldsson, Asgeir
- Sulem, Patrick
- Stefansson, Kari
Producer: 20190107
In:
Nature communications vol. 9
Availability: No items available.
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