Common variants conferring risk of schizophrenia (2009)
Stefansson, Hreinn, Ophoff, Roel A, Steinberg, Stacy, Andreassen, Ole A, Cichon, Sven, Rujescu, Dan, ...
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Gudbjartsson, Daniel F, Bjornsdottir, Unnur S, Halapi, Eva, Helgadottir, Anna, Sulem, Patrick, Jonsdottir, Gudrun M, ...
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Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009)
Stefansson, Hreinn, Steinberg, Stacy, Petursson, Hjorvar, Gustafsson, Omar, Gudjonsdottir, Iris H, Jonsdottir, Gudrun A, ...
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Disruption of the neurexin 1 gene is associated with schizophrenia (2009)
Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietiläinen, Olli P H, Barnes, Michael R, Toulopoulou, Timothea, ...
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Variant in the sequence of the LINGO1 gene confers risk of essential tremor (2009)
Stefansson, Hreinn, Steinberg, Stacy, Petursson, Hjorvar, Gustafsson, Omar, Gudjonsdottir, Iris H, Jonsdottir, Gudrun A, ...
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Entesarian, Miriam, Carlsson, Birgit, Mansouri, Mahmoud Reza, Stattin, Eva-Lena, Holmberg, Eva, Golovleva, Irina, ...
We identified a paracentric inversion of chromosome 10 [inv(10)(q11.22q21.1)] in 0.20% of Swedish individuals (15/7,439) referred for cytogenetic analysis. A retrospective analysis of 8,896...
Disruption of the neurexin 1 gene is associated with schizophrenia (2009)
Rujescu, Dan, Ingason, Andres, Cichon, Sven, Pietiläinen, Olli P.H., Barnes, Michael R., Toulopoulou, Timothea, ...
Deletions within the neurexin 1 gene (NRXN1; 2p16.3) are associated with autism and have also been reported in two families with schizophrenia. We examined NRXN1, and the closely related NRXN2 and...
Large recurrent microdeletions associated with schizophrenia (2008)
Stefansson, Hreinn, Rujescu, Dan, Cichon, Sven, Pietiläinen, Olli P H, Ingason, Andres, Steinberg, Stacy, ...
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Many sequence variants affecting diversity of adult human height (2008)
Gudbjartsson, Daniel F, Walters, G Bragi, Thorleifsson, Gudmar, Stefansson, Hreinn, Halldorsson, Bjarni V, Zusmanovich, Pasha, ...
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A variant associated with nicotine dependence, lung cancer and peripheral arterial disease (2008)
Thorgeirsson, Thorgeir E, Geller, Frank, Sulem, Patrick, Rafnar, Thorunn, Wiste, Anna, Magnusson, Kristinn P, ...
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Genetics of gene expression and its effect on disease (2008)
Emilsson, Valur, Thorleifsson, Gudmar, Zhang, Bin, Leonardson, Amy S, Zink, Florian, Zhu, Jun, ...
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Helgadottir, Anna, Thorleifsson, Gudmar, Magnusson, Kristinn P, Grétarsdottir, Solveig, Steinthorsdottir, Valgerdur, Manolescu, Andrei, ...
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Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma (2007)
Thorleifsson, Gudmar, Magnusson, Kristinn P, Sulem, Patrick, Walters, G Bragi, Gudbjartsson, Daniel F, Stefansson, Hreinn, ...
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A genetic risk factor for periodic limb movements in sleep (2007)
Stefansson, Hreinn, Rye, David B, Hicks, Andrew, Petursson, Hjorvar, Ingason, Andres, Thorgeirsson, Thorgeir E, ...
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Support for involvement of the AHI1 locus in schizophrenia (2007)
Ingason, Andres, Sigmundsson, Thordur, Steinberg, Stacy, Sigurdsson, Engilbert, Haraldsson, Magnus, Magnusdottir, Brynja B, ...
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Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. (2006)
Grant, Struan F A, Thorleifsson, Gudmar, Reynisdottir, Inga, Benediktsson, Rafn, Manolescu, Andrei, Sainz, Jesus, ...
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CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD. (2006)
Magnusson, Kristinn P, Duan, Shan, Sigurdsson, Haraldur, Petursson, Hjorvar, Yang, Zhenglin, Zhao, Yu, ...
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CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD (2006)
Kristinn P. Magnusson, Shan Duan, Haraldur Sigurdsson, Hjorvar Petursson, Zhenglin Yang, Yu Zhao, ...
A common missense variant, Y402H, in the Complement Factor H gene is associated strongly with soft drusen, a precursor of advanced age-related macular degeneration
CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD (2006)
Kristinn P. Magnusson, Shan Duan, Haraldur Sigurdsson, Hjorvar Petursson, Zhenglin Yang, Yu Zhao, ...
Background Age-related macular degeneration (AMD) is the most common cause of irreversible visual impairment in the developed world. The two forms of advanced AMD, geographic atrophy and neovascular...
Fossdal, Ragnheidur, Jonasson, Fridbert, Kristjansdottir, Gudlaug T, Kong, Augustine, Stefansson, Hreinn, Gosh, Shyamali, ...
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Fossdal, Ragnheidur, Jonasson, Fridbert, Kristjansdottir, Gudlaug Thora, Kong, Augustine, Stefansson, Hreinn, Gosh, Shyamali, ...
Sveinsson's Chorioretinal Atrophy (SCRA) also referred to as Helicoid Peripapillary Chorioretinal Degeneration (HPCD) or Atrophia Areata (AA) is an autosomal dominant eye disease, characterized by...
Fossdal, Ragnheidur, Jonasson, Fridbert, Kristjansdottir, Gudlaug T., Kong, Augustine, Stefansson, Hreinn, Gosh, Shyamali, ...
Sveinsson's chorioretinal atrophy (SCRA), also referred to as helicoid peripapillary chorioretinal degeneration or atrophia areata, is an autosomal dominant eye disease, characterized by symmetrical...
Fossdal, Ragnheidur, Jonasson, Fridbert, Kristjansdottir, Gudlaug Thora, Kong, Augustine, Stefansson, Hreinn, Gosh, Shyamali, ...
Sveinsson's Chorioretinal Atrophy (SCRA) also referred to as Helicoid Peripapillary Chorioretinal Degeneration (HPCD) or Atrophia Areata (AA) is an autosomal dominant eye disease, characterized by...
A susceptibility gene for late-onset idiopathic Parkinson's disease (2002)
Hicks, Andrew A, Petursson, Hjorvar, Jonsson, Thorlakur, Stefansson, Hreinn, Johannsdottir, Hrefna S, Sainz, Jesus, ...
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Neuregulin 1 and susceptibility to schizophrenia (2002)
Stefansson, Hreinn, Sigurdsson, Engilbert, Steinthorsdottir, Valgerdur, Bjornsdottir, Soley, Sigmundsson, Thordur, Ghosh, Shyamali, ...
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A genome-wide scan for preeclampsia in the Netherlands (2001)
Lachmeijer, Augusta M. A., Arngrimsson, Reynir, Bastiaans, Esther B., Frigge, Michael. L., Pals, Gerard, Sigurdardottir, Sigrun, ...
A genome-wide scan for preeclampsia in the Netherlands (2001)
Lachmeijer, Augusta M. A., Arngrimsson, Reynir, Bastiaans, Esther B., Frigge, Michael. L., Pals, Gerard, Sigurdardottir, Sigrun, ...
Mamedov, Fikret, Stefansson, Hreinn, Albertsson, Per-Åke, Styring, Stenbjörn
The electron transport properties of photosystem II (PSII) from five different domains of the thylakoid membrane were analyzed by flash-induced fluorescence kinetics. These domains are the entire...
CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD
Magnusson, Kristinn P, Duan, Shan, Sigurdsson, Haraldur, Petursson, Hjorvar, Yang, Zhenglin, Zhao, Yu, ...
A common missense variant, Y402H, in the Complement Factor H gene is associated strongly with soft drusen, a precursor of advanced age-related macular degeneration
Neuregulin 1 and Susceptibility to Schizophrenia
Stefansson, Hreinn, Sigurdsson, Engilbert, Steinthorsdottir, Valgerdur, Bjornsdottir, Soley, Sigmundsson, Thordur, Ghosh, Shyamali, ...
The cause of schizophrenia is unknown, but it has a significant genetic component. Pharmacologic studies, studies of gene expression in man, and studies of mouse mutants suggest involvement of...
Association of Neuregulin 1 with Schizophrenia Confirmed in a Scottish Population
Stefansson, Hreinn, Sarginson, Jane, Kong, Augustine, Yates, Phil, Steinthorsdottir, Valgerdur, Gudfinnsson, Einar, ...
Recently, we identified neuregulin 1 (NRG1) as a susceptibility gene for schizophrenia in the Icelandic population, by a combined linkage and association approach. Here, we report the first study...
CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD
Magnusson, Kristinn P, Duan, Shan, Sigurdsson, Haraldur, Petursson, Hjorvar, Yang, Zhenglin, Zhao, Yu, ...
A common missense variant, Y402H, in the Complement Factor H gene is associated strongly with soft drusen, a precursor of advanced age-related macular degeneration
The Impact of Divergence Time on the Nature of Population Structure: An Example from Iceland
Price, Alkes L., Helgason, Agnar, Palsson, Snaebjorn, Stefansson, Hreinn, St. Clair, David, Andreassen, Ole A., ...
The Icelandic population has been sampled in many disease association studies, providing a strong motivation to understand the structure of this population and its ramifications for disease gene...