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Gisli Masson

Showing results (31-40 of 119) with videos related to

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Communications Biology|October 2, 2018
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobinGudjon R Oskarsson, Ragnar P Kristjansson, Amy L Lee, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Nature Genetics|October 24, 2018
Insights into imprinting from parent-of-origin phased methylomes and transcriptomesFlorian Zink, Droplaug N Magnusdottir, Olafur T Magnusson, et al.
Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Nature Genetics|January 18, 2005
A common inversion under selection in EuropeansHreinn Stefansson, Agnar Helgason, Gudmar Thorleifsson, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, et al.
Nature Communications|May 4, 2017
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L Frankel, et al.
Plos Genetics|June 12, 2013
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasetsNiels Grarup, Patrick Sulem, Camilla H Sandholt, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Genetics|October 31, 2018
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritisUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
Pageof 12

Showing results (31-40 of 119) with videos related to

Sort By:
Pageof 12
Communications Biology|October 2, 2018
A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobinGudjon R Oskarsson, Ragnar P Kristjansson, Amy L Lee, et al.
Nature Communications|February 4, 2016
Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenaseRagnar P Kristjansson, Asmundur Oddsson, Hannes Helgason, et al.
Nature Genetics|October 24, 2018
Insights into imprinting from parent-of-origin phased methylomes and transcriptomesFlorian Zink, Droplaug N Magnusdottir, Olafur T Magnusson, et al.
Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Nature Genetics|January 18, 2005
A common inversion under selection in EuropeansHreinn Stefansson, Agnar Helgason, Gudmar Thorleifsson, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, et al.
Nature Communications|May 4, 2017
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L Frankel, et al.
Plos Genetics|June 12, 2013
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasetsNiels Grarup, Patrick Sulem, Camilla H Sandholt, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Genetics|October 31, 2018
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritisUnnur Styrkarsdottir, Sigrun H Lund, Gudmar Thorleifsson, et al.
Pageof 12