Results
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121.
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Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility. [electronic resource] by
- Gianfrancesco, Milena A
- Glymour, M Maria
- Walter, Stefan
- Rhead, Brooke
- Shao, Xiaorong
- Shen, Ling
- Quach, Hong
- Hubbard, Alan
- Jónsdóttir, Ingileif
- Stefánsson, Kári
- Strid, Pernilla
- Hillert, Jan
- Hedström, Anna
- Olsson, Tomas
- Kockum, Ingrid
- Schaefer, Catherine
- Alfredsson, Lars
- Barcellos, Lisa F
Producer: 20170629
In:
American journal of epidemiology vol. 185
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122.
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Sequence variants from whole genome sequencing a large group of Icelanders. [electronic resource] by
- Gudbjartsson, Daniel F
- Sulem, Patrick
- Helgason, Hannes
- Gylfason, Arnaldur
- Gudjonsson, Sigurjon A
- Zink, Florian
- Oddson, Asmundur
- Magnusson, Gisli
- Halldorsson, Bjarni V
- Hjartarson, Eirikur
- Sigurdsson, Gunnar Th
- Kong, Augustine
- Helgason, Agnar
- Masson, Gisli
- Magnusson, Olafur Th
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20151215
In:
Scientific data vol. 2
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123.
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Profiling of genes expressed in peripheral blood mononuclear cells predicts glucocorticoid sensitivity in asthma patients. [electronic resource] by
- Hakonarson, Hakon
- Bjornsdottir, Unnur S
- Halapi, Eva
- Bradfield, Jonathan
- Zink, Florian
- Mouy, Magali
- Helgadottir, Hildur
- Gudmundsdottir, Asta S
- Andrason, Hjalti
- Adalsteinsdottir, Asdis E
- Kristjansson, Kristleifur
- Birkisson, Illugi
- Arnason, Thor
- Andresdottir, Margret
- Gislason, David
- Gislason, Thorarinn
- Gulcher, Jeffrey R
- Stefansson, Kari
Producer: 20060420
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 102
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124.
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Sequence variants in the RNF212 gene associate with genome-wide recombination rate. [electronic resource] by
- Kong, Augustine
- Thorleifsson, Gudmar
- Stefansson, Hreinn
- Masson, Gisli
- Helgason, Agnar
- Gudbjartsson, Daniel F
- Jonsdottir, Gudrun M
- Gudjonsson, Sigurjon A
- Sverrisson, Sverrir
- Thorlacius, Theodora
- Jonasdottir, Aslaug
- Hardarson, Gudmundur A
- Palsson, Stefan T
- Frigge, Michael L
- Gulcher, Jeffrey R
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20080321
In:
Science (New York, N.Y.) vol. 319
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125.
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Reproductive fitness and genetic risk of psychiatric disorders in the general population. [electronic resource] by
- Mullins, Niamh
- Ingason, Andrés
- Porter, Heather
- Euesden, Jack
- Gillett, Alexandra
- Ólafsson, Sigurgeir
- Gudbjartsson, Daniel F
- Lewis, Cathryn M
- Sigurdsson, Engilbert
- Saemundsen, Evald
- Gudmundsson, Ólafur Ó
- Frigge, Michael L
- Kong, Augustine
- Helgason, Agnar
- Walters, G Bragi
- Gustafsson, Omar
- Stefansson, Hreinn
- Stefansson, Kari
Producer: 20181214
In:
Nature communications vol. 8
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126.
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Linkage of osteoporosis to chromosome 20p12 and association to BMP2. [electronic resource] by
- Styrkarsdottir, Unnur
- Cazier, Jean-Baptiste
- Kong, Augustine
- Rolfsson, Ottar
- Larsen, Helene
- Bjarnadottir, Emma
- Johannsdottir, Vala D
- Sigurdardottir, Margret S
- Bagger, Yu
- Christiansen, Claus
- Reynisdottir, Inga
- Grant, Struan F A
- Jonasson, Kristjan
- Frigge, Michael L
- Gulcher, Jeffrey R
- Sigurdsson, Gunnar
- Stefansson, Kari
Producer: 20060113
In:
PLoS biology vol. 1
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127.
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Identification of a large set of rare complete human knockouts. [electronic resource] by
- Sulem, Patrick
- Helgason, Hannes
- Oddson, Asmundur
- Stefansson, Hreinn
- Gudjonsson, Sigurjon A
- Zink, Florian
- Hjartarson, Eirikur
- Sigurdsson, Gunnar Th
- Jonasdottir, Adalbjorg
- Jonasdottir, Aslaug
- Sigurdsson, Asgeir
- Magnusson, Olafur Th
- Kong, Augustine
- Helgason, Agnar
- Holm, Hilma
- Thorsteinsdottir, Unnur
- Masson, Gisli
- Gudbjartsson, Daniel F
- Stefansson, Kari
Producer: 20150706
In:
Nature genetics vol. 47
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128.
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Diversity in non-repetitive human sequences not found in the reference genome. [electronic resource] by
- Kehr, Birte
- Helgadottir, Anna
- Melsted, Pall
- Jonsson, Hakon
- Helgason, Hannes
- Jonasdottir, Adalbjörg
- Jonasdottir, Aslaug
- Sigurdsson, Asgeir
- Gylfason, Arnaldur
- Halldorsson, Gisli H
- Kristmundsdottir, Snaedis
- Thorgeirsson, Gudmundur
- Olafsson, Isleifur
- Holm, Hilma
- Thorsteinsdottir, Unnur
- Sulem, Patrick
- Helgason, Agnar
- Gudbjartsson, Daniel F
- Halldorsson, Bjarni V
- Stefansson, Kari
Producer: 20170905
In:
Nature genetics vol. 49
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129.
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Reconstructing an African haploid genome from the 18th century. [electronic resource] by
- Jagadeesan, Anuradha
- Gunnarsdóttir, Ellen D
- Ebenesersdóttir, S Sunna
- Guðmundsdóttir, Valdis B
- Thordardottir, Elisabet Linda
- Einarsdóttir, Margrét S
- Jónsson, Hákon
- Dugoujon, Jean-Michel
- Fortes-Lima, Cesar
- Migot-Nabias, Florence
- Massougbodji, Achille
- Bellis, Gil
- Pereira, Luisa
- Másson, Gísli
- Kong, Augustine
- Stefánsson, Kári
- Helgason, Agnar
Producer: 20190513
In:
Nature genetics vol. 50
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130.
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. [electronic resource] by
- Nalls, Michael A
- Plagnol, Vincent
- Hernandez, Dena G
- Sharma, Manu
- Sheerin, Una-Marie
- Saad, Mohamad
- Simón-Sánchez, J
- Schulte, Claudia
- Lesage, Suzanne
- Sveinbjörnsdóttir, Sigurlaug
- Stefánsson, Kári
- Martinez, Maria
- Hardy, John
- Heutink, Peter
- Brice, Alexis
- Gasser, Thomas
- Singleton, Andrew B
- Wood, Nicholas W
Producer: 20110329
In:
Lancet (London, England) vol. 377
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131.
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Multiple genetic loci for bone mineral density and fractures. [electronic resource] by
- Styrkarsdottir, Unnur
- Halldorsson, Bjarni V
- Gretarsdottir, Solveig
- Gudbjartsson, Daniel F
- Walters, G Bragi
- Ingvarsson, Thorvaldur
- Jonsdottir, Thorbjorg
- Saemundsdottir, Jona
- Center, Jacqueline R
- Nguyen, Tuan V
- Bagger, Yu
- Gulcher, Jeffrey R
- Eisman, John A
- Christiansen, Claus
- Sigurdsson, Gunnar
- Kong, Augustine
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20080603
In:
The New England journal of medicine vol. 358
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132.
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Several common variants modulate heart rate, PR interval and QRS duration. [electronic resource] by
- Holm, Hilma
- Gudbjartsson, Daniel F
- Arnar, David O
- Thorleifsson, Gudmar
- Thorgeirsson, Gudmundur
- Stefansdottir, Hrafnhildur
- Gudjonsson, Sigurjon A
- Jonasdottir, Aslaug
- Mathiesen, Ellisiv B
- Njølstad, Inger
- Nyrnes, Audhild
- Wilsgaard, Tom
- Hald, Erin M
- Hveem, Kristian
- Stoltenberg, Camilla
- Løchen, Maja-Lisa
- Kong, Augustine
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20100217
In:
Nature genetics vol. 42
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133.
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An analysis of single nucleotide polymorphisms of 125 DNA repair genes in the Texas genome-wide association study of lung cancer with a replication for the XRCC4 SNPs. [electronic resource] by
- Yu, Hongping
- Zhao, Hui
- Wang, Li-E
- Han, Younghun
- Chen, Wei V
- Amos, Christopher I
- Rafnar, Thorunn
- Sulem, Patrick
- Stefansson, Kari
- Landi, Maria Teresa
- Caporaso, Neil
- Albanes, Demetrius
- Thun, Michael
- McKay, James D
- Brennan, Paul
- Wang, Yufei
- Houlston, Richard S
- Spitz, Margaret R
- Wei, Qingyi
Producer: 20110701
In:
DNA repair vol. 10
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134.
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Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability. [electronic resource] by
- Ivarsdottir, Erna V
- Steinthorsdottir, Valgerdur
- Daneshpour, Maryam S
- Thorleifsson, Gudmar
- Sulem, Patrick
- Holm, Hilma
- Sigurdsson, Snaevar
- Hreidarsson, Astradur B
- Sigurdsson, Gunnar
- Bjarnason, Ragnar
- Thorsson, Arni V
- Benediktsson, Rafn
- Eyjolfsson, Gudmundur
- Sigurdardottir, Olof
- Olafsson, Isleifur
- Zeinali, Sirous
- Azizi, Fereidoun
- Thorsteinsdottir, Unnur
- Gudbjartsson, Daniel F
- Stefansson, Kari
Producer: 20171025
In:
Nature genetics vol. 49
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135.
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A Missense Variant in PLEC Increases Risk of Atrial Fibrillation. [electronic resource] by
- Thorolfsdottir, Rosa B
- Sveinbjornsson, Gardar
- Sulem, Patrick
- Helgadottir, Anna
- Gretarsdottir, Solveig
- Benonisdottir, Stefania
- Magnusdottir, Audur
- Davidsson, Olafur B
- Rajamani, Sridharan
- Roden, Dan M
- Darbar, Dawood
- Pedersen, Terje R
- Sabatine, Marc S
- Jonsdottir, Ingileif
- Arnar, David O
- Thorsteinsdottir, Unnur
- Gudbjartsson, Daniel F
- Holm, Hilma
- Stefansson, Kari
Producer: 20171027
In:
Journal of the American College of Cardiology vol. 70
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136.
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Rare mutations associating with serum creatinine and chronic kidney disease. [electronic resource] by
- Sveinbjornsson, Gardar
- Mikaelsdottir, Evgenia
- Palsson, Runolfur
- Indridason, Olafur S
- Holm, Hilma
- Jonasdottir, Aslaug
- Helgason, Agnar
- Sigurdsson, Snaevar
- Jonasdottir, Adalbjorg
- Sigurdsson, Asgeir
- Eyjolfsson, Gudmundur Ingi
- Sigurdardottir, Olof
- Magnusson, Olafur Th
- Kong, Augustine
- Masson, Gisli
- Sulem, Patrick
- Olafsson, Isleifur
- Thorsteinsdottir, Unnur
- Gudbjartsson, Daniel F
- Stefansson, Kari
Producer: 20150713
In:
Human molecular genetics vol. 23
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137.
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New sequence variants associated with bone mineral density. [electronic resource] by
- Styrkarsdottir, Unnur
- Halldorsson, Bjarni V
- Gretarsdottir, Solveig
- Gudbjartsson, Daniel F
- Walters, G Bragi
- Ingvarsson, Thorvaldur
- Jonsdottir, Thorbjorg
- Saemundsdottir, Jona
- Snorradóttir, Steinunn
- Center, Jacqueline R
- Nguyen, Tuan V
- Alexandersen, Peter
- Gulcher, Jeffrey R
- Eisman, John A
- Christiansen, Claus
- Sigurdsson, Gunnar
- Kong, Augustine
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20090123
In:
Nature genetics vol. 41
Availability: No items available.
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138.
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Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes. [electronic resource] by
- Small, Kerrin S
- Hedman, Asa K
- Grundberg, Elin
- Nica, Alexandra C
- Thorleifsson, Gudmar
- Kong, Augustine
- Thorsteindottir, Unnur
- Shin, So-Youn
- Richards, Hannah B
- Soranzo, Nicole
- Ahmadi, Kourosh R
- Lindgren, Cecilia M
- Stefansson, Kari
- Dermitzakis, Emmanouil T
- Deloukas, Panos
- Spector, Timothy D
- McCarthy, Mark I
Producer: 20110726
In:
Nature genetics vol. 43
Availability: No items available.
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139.
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Physical and neurobehavioral determinants of reproductive onset and success. [electronic resource] by
- Day, Felix R
- Helgason, Hannes
- Chasman, Daniel I
- Rose, Lynda M
- Loh, Po-Ru
- Scott, Robert A
- Helgason, Agnar
- Kong, Augustine
- Masson, Gisli
- Magnusson, Olafur Th
- Gudbjartsson, Daniel
- Thorsteinsdottir, Unnur
- Buring, Julie E
- Ridker, Paul M
- Sulem, Patrick
- Stefansson, Kari
- Ong, Ken K
- Perry, John R B
Producer: 20170628
In:
Nature genetics vol. 48
Availability: No items available.
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140.
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A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta. [electronic resource] by
- Bjornsson, Thorsteinn
- Thorolfsdottir, Rosa B
- Sveinbjornsson, Gardar
- Sulem, Patrick
- Norddahl, Gudmundur L
- Helgadottir, Anna
- Gretarsdottir, Solveig
- Magnusdottir, Audur
- Danielsen, Ragnar
- Sigurdsson, Emil L
- Adalsteinsdottir, Berglind
- Gunnarsson, Sverrir I
- Jonsdottir, Ingileif
- Arnar, David O
- Helgason, Hrodmar
- Gudbjartsson, Tomas
- Gudbjartsson, Daniel F
- Thorsteinsdottir, Unnur
- Holm, Hilma
- Stefansson, Kari
Producer: 20191120
In:
European heart journal vol. 39
Availability: No items available.
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