Results
|
181.
|
A genetic risk factor for periodic limb movements in sleep. [electronic resource] by
- Stefansson, Hreinn
- Rye, David B
- Hicks, Andrew
- Petursson, Hjorvar
- Ingason, Andres
- Thorgeirsson, Thorgeir E
- Palsson, Stefan
- Sigmundsson, Thordur
- Sigurdsson, Albert P
- Eiriksdottir, Ingibjorg
- Soebech, Emilia
- Bliwise, Donald
- Beck, Joseph M
- Rosen, Ami
- Waddy, Salina
- Trotti, Lynn M
- Iranzo, Alex
- Thambisetty, Madhav
- Hardarson, Gudmundur A
- Kristjansson, Kristleifur
- Gudmundsson, Larus J
- Thorsteinsdottir, Unnur
- Kong, Augustine
- Gulcher, Jeffrey R
- Gudbjartsson, Daniel
- Stefansson, Kari
Producer: 20070824
In:
The New England journal of medicine vol. 357
Availability: No items available.
|
|
182.
|
Two newly identified genetic determinants of pigmentation in Europeans. [electronic resource] by
- Sulem, Patrick
- Gudbjartsson, Daniel F
- Stacey, Simon N
- Helgason, Agnar
- Rafnar, Thorunn
- Jakobsdottir, Margret
- Steinberg, Stacy
- Gudjonsson, Sigurjon A
- Palsson, Arnar
- Thorleifsson, Gudmar
- Pálsson, Snaebjörn
- Sigurgeirsson, Bardur
- Thorisdottir, Kristin
- Ragnarsson, Rafn
- Benediktsdottir, Kristrun R
- Aben, Katja K
- Vermeulen, Sita H
- Goldstein, Alisa M
- Tucker, Margaret A
- Kiemeney, Lambertus A
- Olafsson, Jon H
- Gulcher, Jeffrey
- Kong, Augustine
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20080722
In:
Nature genetics vol. 40
Availability: No items available.
|
|
183.
|
Large scale replication study of the association between HLA class II/BTNL2 variants and osteoarthritis of the knee in European-descent populations. [electronic resource] by
- Valdes, Ana M
- Styrkarsdottir, Unnur
- Doherty, Michael
- Morris, David L
- Mangino, Massimo
- Tamm, Agu
- Doherty, Sally A
- Kisand, Kalle
- Kerna, Irina
- Tamm, Ann
- Wheeler, Margaret
- Maciewicz, Rose A
- Zhang, Weiya
- Muir, Kenneth R
- Dennison, Elaine M
- Hart, Deborah J
- Metrustry, Sarah
- Jonsdottir, Ingileif
- Jonsson, Gudbjorn F
- Jonsson, Helgi
- Ingvarsson, Thorvaldur
- Cooper, Cyrus
- Vyse, Timothy J
- Spector, Tim D
- Stefansson, Kari
- Arden, Nigel K
Producer: 20111219
In:
PloS one vol. 6
Availability: No items available.
|
|
184.
|
A mutation in APP protects against Alzheimer's disease and age-related cognitive decline. [electronic resource] by
- Jonsson, Thorlakur
- Atwal, Jasvinder K
- Steinberg, Stacy
- Snaedal, Jon
- Jonsson, Palmi V
- Bjornsson, Sigurbjorn
- Stefansson, Hreinn
- Sulem, Patrick
- Gudbjartsson, Daniel
- Maloney, Janice
- Hoyte, Kwame
- Gustafson, Amy
- Liu, Yichin
- Lu, Yanmei
- Bhangale, Tushar
- Graham, Robert R
- Huttenlocher, Johanna
- Bjornsdottir, Gyda
- Andreassen, Ole A
- Jönsson, Erik G
- Palotie, Aarno
- Behrens, Timothy W
- Magnusson, Olafur T
- Kong, Augustine
- Thorsteinsdottir, Unnur
- Watts, Ryan J
- Stefansson, Kari
Producer: 20120904
In:
Nature vol. 488
Availability: No items available.
|
|
185.
|
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease. [electronic resource] by
- Gretarsdottir, Solveig
- Helgason, Hannes
- Helgadottir, Anna
- Sigurdsson, Asgeir
- Thorleifsson, Gudmar
- Magnusdottir, Audur
- Oddsson, Asmundur
- Steinthorsdottir, Valgerdur
- Rafnar, Thorunn
- de Graaf, Jacqueline
- Daneshpour, Maryam S
- Hedayati, Mehdi
- Azizi, Fereidoun
- Grarup, Niels
- Jørgensen, Torben
- Vestergaard, Henrik
- Hansen, Torben
- Eyjolfsson, Gudmundur
- Sigurdardottir, Olof
- Olafsson, Isleifur
- Kiemeney, Lambertus A
- Pedersen, Oluf
- Sulem, Patrick
- Thorgeirsson, Gudmundur
- Gudbjartsson, Daniel F
- Holm, Hilma
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20160531
In:
PLoS genetics vol. 11
Availability: No items available.
|
|
186.
|
Sequence variant at 4q25 near PITX2 associates with appendicitis. [electronic resource] by
- Kristjansson, Ragnar P
- Benonisdottir, Stefania
- Oddsson, Asmundur
- Galesloot, Tessel E
- Thorleifsson, Gudmar
- Aben, Katja K
- Davidsson, Olafur B
- Jonsson, Stefan
- Arnadottir, Gudny A
- Jensson, Brynjar O
- Walters, G Bragi
- Sigurdsson, Jon K
- Sigurdsson, Snaevar
- Holm, Hilma
- Arnar, David O
- Thorgeirsson, Gudmundur
- Alexiusdottir, Kristin
- Jonsdottir, Ingileif
- Thorsteinsdottir, Unnur
- Kiemeney, Lambertus A
- Jonsson, Thorvaldur
- Gudbjartsson, Daniel F
- Rafnar, Thorunn
- Sulem, Patrick
- Stefansson, Kari
Producer: 20181231
In:
Scientific reports vol. 7
Availability: No items available.
|
|
187.
|
A common inversion under selection in Europeans. [electronic resource] by
- Stefansson, Hreinn
- Helgason, Agnar
- Thorleifsson, Gudmar
- Steinthorsdottir, Valgerdur
- Masson, Gisli
- Barnard, John
- Baker, Adam
- Jonasdottir, Aslaug
- Ingason, Andres
- Gudnadottir, Vala G
- Desnica, Natasa
- Hicks, Andrew
- Gylfason, Arnaldur
- Gudbjartsson, Daniel F
- Jonsdottir, Gudrun M
- Sainz, Jesus
- Agnarsson, Kari
- Birgisdottir, Birgitta
- Ghosh, Shyamali
- Olafsdottir, Adalheidur
- Cazier, Jean-Baptiste
- Kristjansson, Kristleifur
- Frigge, Michael L
- Thorgeirsson, Thorgeir E
- Gulcher, Jeffrey R
- Kong, Augustine
- Stefansson, Kari
Producer: 20050301
In:
Nature genetics vol. 37
Availability: No items available.
|
|
188.
|
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2. [electronic resource] by
- Haraldsdottir, Sigurdis
- Rafnar, Thorunn
- Frankel, Wendy L
- Einarsdottir, Sylvia
- Sigurdsson, Asgeir
- Hampel, Heather
- Snaebjornsson, Petur
- Masson, Gisli
- Weng, Daniel
- Arngrimsson, Reynir
- Kehr, Birte
- Yilmaz, Ahmet
- Haraldsson, Stefan
- Sulem, Patrick
- Stefansson, Tryggvi
- Shields, Peter G
- Sigurdsson, Fridbjorn
- Bekaii-Saab, Tanios
- Moller, Pall H
- Steinarsdottir, Margret
- Alexiusdottir, Kristin
- Hitchins, Megan
- Pritchard, Colin C
- de la Chapelle, Albert
- Jonasson, Jon G
- Goldberg, Richard M
- Stefansson, Kari
Producer: 20181211
In:
Nature communications vol. 8
Availability: No items available.
|
|
189.
|
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.
|
|
190.
|
A polygenic resilience score moderates the genetic risk for schizophrenia. [electronic resource] by
- Hess, Jonathan L
- Tylee, Daniel S
- Mattheisen, Manuel
- Børglum, Anders D
- Als, Thomas D
- Grove, Jakob
- Werge, Thomas
- Mortensen, Preben Bo
- Mors, Ole
- Nordentoft, Merete
- Hougaard, David M
- Byberg-Grauholm, Jonas
- Bækvad-Hansen, Marie
- Greenwood, Tiffany A
- Tsuang, Ming T
- Curtis, David
- Steinberg, Stacy
- Sigurdsson, Engilbert
- Stefánsson, Hreinn
- Stefánsson, Kári
- Edenberg, Howard J
- Holmans, Peter
- Faraone, Stephen V
- Glatt, Stephen J
Producer: 20210514
In:
Molecular psychiatry vol. 26
Availability: No items available.
|
|
191.
|
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures. [electronic resource] by
- Styrkarsdottir, Unnur
- Thorleifsson, Gudmar
- Gudjonsson, Sigurjon A
- Sigurdsson, Asgeir
- Center, Jacqueline R
- Lee, Seung Hun
- Nguyen, Tuan V
- Kwok, Timothy C Y
- Lee, Jenny S W
- Ho, Suzanne C
- Woo, Jean
- Leung, Ping-C
- Kim, Beom-Jun
- Rafnar, Thorunn
- Kiemeney, Lambertus A
- Ingvarsson, Thorvaldur
- Koh, Jung-Min
- Tang, Nelson L S
- Eisman, John A
- Christiansen, Claus
- Sigurdsson, Gunnar
- Thorsteinsdottir, Unnur
- Stefansson, Kari
Producer: 20160609
In:
Nature communications vol. 7
Availability: No items available.
|
|
192.
|
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke. [electronic resource] by
- Helgadottir, Anna
- Manolescu, Andrei
- Thorleifsson, Gudmar
- Gretarsdottir, Solveig
- Jonsdottir, Helga
- Thorsteinsdottir, Unnur
- Samani, Nilesh J
- Gudmundsson, Gudmundur
- Grant, Struan F A
- Thorgeirsson, Gudmundur
- Sveinbjornsdottir, Sigurlaug
- Valdimarsson, Einar M
- Matthiasson, Stefan E
- Johannsson, Halldor
- Gudmundsdottir, Olof
- Gurney, Mark E
- Sainz, Jesus
- Thorhallsdottir, Margret
- Andresdottir, Margret
- Frigge, Michael L
- Topol, Eric J
- Kong, Augustine
- Gudnason, Vilmundur
- Hakonarson, Hakon
- Gulcher, Jeffrey R
- Stefansson, Kari
Producer: 20040503
In:
Nature genetics vol. 36
Availability: No items available.
|
|
193.
|
Association of folate-pathway gene polymorphisms with the risk of prostate cancer: a population-based nested case-control study, systematic review, and meta-analysis. [electronic resource] by
- Collin, Simon M
- Metcalfe, Chris
- Zuccolo, Luisa
- Lewis, Sarah J
- Chen, Lina
- Cox, Angela
- Davis, Michael
- Lane, J Athene
- Donovan, Jenny
- Smith, George Davey
- Neal, David E
- Hamdy, Freddie C
- Gudmundsson, Julius
- Sulem, Patrick
- Rafnar, Thorunn
- Benediktsdottir, Kristrun R
- Eeles, Rosalind A
- Guy, Michelle
- Kote-Jarai, Zsofia
- Morrison, Jonathan
- Al Olama, Ali Amin
- Stefansson, Kari
- Easton, Douglas F
- Martin, Richard M
Producer: 20091215
In:
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology vol. 18
Availability: No items available.
|
|
194.
|
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease. [electronic resource] by
- Bjornsson, Eythor
- Helgason, Hannes
- Halldorsson, Gisli
- Helgadottir, Anna
- Gylfason, Arnaldur
- Kehr, Birte
- Jonasdottir, Adalbjorg
- Jonasdottir, Aslaug
- Sigurdsson, Asgeir
- Oddsson, Asmundur
- Thorleifsson, Gudmar
- Magnusson, Olafur Th
- Gretarsdottir, Solveig
- Zink, Florian
- Kristjansson, Ragnar P
- Asgeirsdottir, Margret
- Swinkels, Dorine W
- Kiemeney, Lambertus A
- Eyjolfsson, Gudmundur I
- Sigurdardottir, Olof
- Masson, Gisli
- Olafsson, Isleifur
- Thorgeirsson, Gudmundur
- Holm, Hilma
- Thorsteinsdottir, Unnur
- Gudbjartsson, Daniel F
- Sulem, Patrick
- Stefansson, Kari
Producer: 20171012
In:
Human molecular genetics vol. 26
Availability: No items available.
|
|
195.
|
Multiple transmissions of de novo mutations in families. [electronic resource] by
- Jónsson, Hákon
- Sulem, Patrick
- Arnadottir, Gudny A
- Pálsson, Gunnar
- Eggertsson, Hannes P
- Kristmundsdottir, Snaedis
- Zink, Florian
- Kehr, Birte
- Hjorleifsson, Kristjan E
- Jensson, Brynjar Ö
- Jonsdottir, Ingileif
- Marelsson, Sigurdur Einar
- Gudjonsson, Sigurjon Axel
- Gylfason, Arnaldur
- Jonasdottir, Adalbjorg
- Jonasdottir, Aslaug
- Stacey, Simon N
- Magnusson, Olafur Th
- Thorsteinsdottir, Unnur
- Masson, Gisli
- Kong, Augustine
- Halldorsson, Bjarni V
- Helgason, Agnar
- Gudbjartsson, Daniel F
- Stefansson, Kari
Producer: 20190424
In:
Nature genetics vol. 50
Availability: No items available.
|
|
196.
|
Identification of Genetic Loci Shared Between Attention-Deficit/Hyperactivity Disorder, Intelligence, and Educational Attainment. [electronic resource] by
- O'Connell, Kevin S
- Shadrin, Alexey
- Smeland, Olav B
- Bahrami, Shahram
- Frei, Oleksandr
- Bettella, Francesco
- Krull, Florian
- Fan, Chun C
- Askeland, Ragna B
- Knudsen, Gun Peggy S
- Halmøy, Anne
- Steen, Nils Eiel
- Ueland, Torill
- Walters, G Bragi
- Davíðsdóttir, Katrín
- Haraldsdóttir, Gyða S
- Guðmundsson, Ólafur Ó
- Stefánsson, Hreinn
- Reichborn-Kjennerud, Ted
- Haavik, Jan
- Dale, Anders M
- Stefánsson, Kári
- Djurovic, Srdjan
- Andreassen, Ole A
Producer: 20210106
In:
Biological psychiatry vol. 87
Availability: No items available.
|
|
197.
|
Variant in the sequence of the LINGO1 gene confers risk of essential tremor. [electronic resource] by
- Stefansson, Hreinn
- Steinberg, Stacy
- Petursson, Hjorvar
- Gustafsson, Omar
- Gudjonsdottir, Iris H
- Jonsdottir, Gudrun A
- Palsson, Stefan T
- Jonsson, Thorlakur
- Saemundsdottir, Jona
- Bjornsdottir, Gyda
- Böttcher, Yvonne
- Thorlacius, Theodora
- Haubenberger, Dietrich
- Zimprich, Alexander
- Auff, Eduard
- Hotzy, Christoph
- Testa, Claudia M
- Miyatake, Lisa A
- Rosen, Ami R
- Kristleifsson, Kristleifur
- Rye, David
- Asmus, Friedrich
- Schöls, Ludger
- Dichgans, Martin
- Jakobsson, Finnbogi
- Benedikz, John
- Thorsteinsdottir, Unnur
- Gulcher, Jeffrey
- Kong, Augustine
- Stefansson, Kari
Producer: 20090402
In:
Nature genetics vol. 41
Availability: No items available.
|
|
198.
|
Parental influence on human germline de novo mutations in 1,548 trios from Iceland. [electronic resource] by
- Jónsson, Hákon
- Sulem, Patrick
- Kehr, Birte
- Kristmundsdottir, Snaedis
- Zink, Florian
- Hjartarson, Eirikur
- Hardarson, Marteinn T
- Hjorleifsson, Kristjan E
- Eggertsson, Hannes P
- Gudjonsson, Sigurjon Axel
- Ward, Lucas D
- Arnadottir, Gudny A
- Helgason, Einar A
- Helgason, Hannes
- Gylfason, Arnaldur
- Jonasdottir, Adalbjorg
- Jonasdottir, Aslaug
- Rafnar, Thorunn
- Frigge, Mike
- Stacey, Simon N
- Th Magnusson, Olafur
- Thorsteinsdottir, Unnur
- Masson, Gisli
- Kong, Augustine
- Halldorsson, Bjarni V
- Helgason, Agnar
- Gudbjartsson, Daniel F
- Stefansson, Kari
Producer: 20180226
In:
Nature vol. 549
Availability: No items available.
|
|
199.
|
Association analysis of 29,956 individuals confirms that a low-frequency variant at CCND2 halves the risk of type 2 diabetes by enhancing insulin secretion. [electronic resource] by
- Yaghootkar, Hanieh
- Stancáková, Alena
- Freathy, Rachel M
- Vangipurapu, Jagadish
- Weedon, Michael N
- Xie, Weijia
- Wood, Andrew R
- Ferrannini, Ele
- Mari, Andrea
- Ring, Susan M
- Lawlor, Debbie A
- Davey Smith, George
- Jørgensen, Torben
- Hansen, Torben
- Pedersen, Oluf
- Steinthorsdottir, Valgerdur
- Guðbjartsson, Daniel F
- Thorleifsson, Gudmar
- Thorsteinsdottir, Unnur
- Stefansson, Kari
- Hattersley, Andrew T
- Walker, Mark
- Morris, Andrew D
- McCarthy, Mark I
- Palmer, Colin N A
- Laakso, Markku
- Frayling, Timothy M
Producer: 20150819
In:
Diabetes vol. 64
Availability: No items available.
|
|
200.
|
MAP1B mutations cause intellectual disability and extensive white matter deficit. [electronic resource] by
- Walters, G Bragi
- Gustafsson, Omar
- Sveinbjornsson, Gardar
- Eiriksdottir, Valgerdur K
- Agustsdottir, Arna B
- Jonsdottir, Gudrun A
- Steinberg, Stacy
- Gunnarsson, Arni F
- Magnusson, Magnus I
- Unnsteinsdottir, Unnur
- Lee, Amy L
- Jonasdottir, Adalbjorg
- Sigurdsson, Asgeir
- Jonasdottir, Aslaug
- Skuladottir, Astros
- Jonsson, Lina
- Nawaz, Muhammad S
- Sulem, Patrick
- Frigge, Mike
- Ingason, Andres
- Love, Askell
- Norddhal, Gudmundur L
- Zervas, Mark
- Gudbjartsson, Daniel F
- Ulfarsson, Magnus O
- Saemundsen, Evald
- Stefansson, Hreinn
- Stefansson, Kari
Producer: 20181217
In:
Nature communications vol. 9
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