Search Results - "Jóhannsdóttir, Hrefna S."

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A susceptibility gene for late-onset idiopathic Parkinson's disease by Hicks, Andrew A., Pétursson, Hjörvar, Jónsson, Thorlákur, Stefánsson, Hreinn, Jóhannsdóttir, Hrefna S., Sainz, Jesus, Frigge, Michael L., Kong, Augustine, Gulcher, Jeffrey R., Stefánsson, Kári, Sveinbjörnsdóttir, Sigurlaug

Published in Annals of neurology (01-11-2002)

“…Eight regions of the genome (PARK1‐8) have been implicated in autosomal dominant and autosomal recessive forms of early‐onset Parkinson's disease. These forms…”
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Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis by Styrkarsdottir, Unnur, Helgason, Hannes, Sigurdsson, Asgeir, Norddahl, Gudmundur L, Agustsdottir, Arna B, Reynard, Louise N, Villalvilla, Amanda, Halldorsson, Gisli H, Jonasdottir, Aslaug, Magnusdottir, Audur, Oddson, Asmundur, Sulem, Gerald, Zink, Florian, Sveinbjornsson, Gardar, Helgason, Agnar, Johannsdottir, Hrefna S, Helgadottir, Anna, Stefansson, Hreinn, Gretarsdottir, Solveig, Rafnar, Thorunn, Almdahl, Ina S, Brækhus, Anne, Fladby, Tormod, Selbæk, Geir, Hosseinpanah, Farhad, Azizi, Fereidoun, Koh, Jung Min, Tang, Nelson L S, Daneshpour, Maryam S, Mayordomo, Jose I, Welt, Corrine, Braund, Peter S, Samani, Nilesh J, Kiemeney, Lambertus A, Lohmander, L Stefan, Christiansen, Claus, Andreassen, Ole A, Magnusson, Olafur, Masson, Gisli, Kong, Augustine, Jonsdottir, Ingileif, Gudbjartsson, Daniel, Sulem, Patrick, Jonsson, Helgi, Loughlin, John, Ingvarsson, Thorvaldur, Thorsteinsdottir, Unnur, Stefansson, Kari

Published in Nature genetics (01-05-2017)

“…Kari Stefansson, Unnur Styrkarsdottir and colleagues identify rare genotypes in COMP and CHADL associated with high risk of total hip replacement due to…”
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Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis by Styrkarsdottir, Unnur, Helgason, Hannes, Sigurdsson, Asgeir, Norddahl, Gudmundur L, Agustsdottir, Arna B, Reynard, Louise N, Villalvilla, Amanda, Halldorsson, Gisli H, Jonasdottir, Aslaug, Magnusdottir, Audur, Oddson, Asmundur, Sulem, Gerald, Zink, Florian, Sveinbjornsson, Gardar, Helgason, Agnar, Johannsdottir, Hrefna S, Helgadottir, Anna, Stefansson, Hreinn, Gretarsdottir, Solveig, Rafnar, Thorunn, Almdahl, Ina S, Brækhus, Anne, Fladby, Tormod, Selbæk, Geir, Hosseinpanah, Farhad, Azizi, Fereidoun, Koh, Jung Min, Tang, Nelson L S, Daneshpour, Maryam S, Mayordomo, Jose I, Welt, Corrine, Braund, Peter S, Samani, Nilesh J, Kiemeney, Lambertus A, Lohmander, L Stefan, Christiansen, Claus, Andreassen, Ole A, Magnusson, Olafur, Masson, Gisli, Kong, Augustine, Jonsdottir, Ingileif, Gudbjartsson, Daniel, Sulem, Patrick, Jonsson, Helgi, Loughlin, John, Ingvarsson, Thorvaldur, Thorsteinsdottir, Unnur, Stefansson, Kari

Published in Nature genetics (01-05-2017)

“…The evolutionary cost of gene loss is a central question in genetics and has been investigated in model organisms and human cell lines1-3. In humans, tolerance…”
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Correction: Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis by Styrkarsdottir, Unnur, Helgason, Hannes, Sigurdsson, Asgeir, Norddahl, Gudmundur L, Agustsdottir, Arna B, Reynard, Louise N, Villalvilla, Amanda, Halldorsson, Gisli H, Jonasdottir, Aslaug, Magnusdottir, Audur, Oddson, Asmundur, Sulem, Gerald, Zink, Florian, Sveinbjornsson, Gardar, Helgason, Agnar, Johannsdottir, Hrefna S, Helgadottir, Anna, Stefansson, Hreinn, Gretarsdottir, Solveig, Rafnar, Thorunn, Almdahl, Ina S, Brækhus, Anne, Fladby, Tormod, Selbæk, Geir, Hosseinpanah, Farhad, Azizi, Fereidoun, Koh, Jung Min, Tang, Nelson L S, Danesphour, Maryams, Mayordomo, Jose I, Welt, Corrine, Braund, Peter S, Samani, Nilesh J, Kiemeney, Lambertus A, Lohmander, L Stefan, Christiansen, Claus, Andreassen, Ole A, consortium, arcOGEN, Magnusson, Olafur, Masson, Gisli, Kong, Augustine, Jonsdottir, Ingileif, Gudbjartsson, Daniel, Sulem, Patrick, Jonsson, Helgi, Loughlin, John, Ingvarsson, Thorvaldur, Thorsteinsdottir, Unnur, Stefansson, Kari

Published in Nature genetics (01-08-2017)

“…Nat. Genet.; doi:10.1038/ng.3816; corrected online 17 April 2017 In the version of this article initially published online, the name of author Maryam S…”
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