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Sulem

Showing results (121-130 of 322) with videos related to

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Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Plos Genetics|September 2, 2015
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery DiseaseSolveig Gretarsdottir, Hannes Helgason, Anna Helgadottir, et al.
Nature Genetics|May 20, 2008
Two newly identified genetic determinants of pigmentation in EuropeansPatrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, 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.
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.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 27, 2009
Association of folate-pathway gene polymorphisms with the risk of prostate cancer: a population-based nested case-control study, systematic review, and meta-analysisSimon M Collin, Chris Metcalfe, Luisa Zuccolo, et al.
Nature|July 18, 2012
A mutation in APP protects against Alzheimer's disease and age-related cognitive declineThorlakur Jonsson, Jasvinder K Atwal, Stacy Steinberg, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, 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.
Communications Biology|June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysisErna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, et al.
Pageof 33

Showing results (121-130 of 322) with videos related to

Sort By:
Pageof 33
Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Plos Genetics|September 2, 2015
A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery DiseaseSolveig Gretarsdottir, Hannes Helgason, Anna Helgadottir, et al.
Nature Genetics|May 20, 2008
Two newly identified genetic determinants of pigmentation in EuropeansPatrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, 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.
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.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|August 27, 2009
Association of folate-pathway gene polymorphisms with the risk of prostate cancer: a population-based nested case-control study, systematic review, and meta-analysisSimon M Collin, Chris Metcalfe, Luisa Zuccolo, et al.
Nature|July 18, 2012
A mutation in APP protects against Alzheimer's disease and age-related cognitive declineThorlakur Jonsson, Jasvinder K Atwal, Stacy Steinberg, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, 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.
Communications Biology|June 10, 2021
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysisErna V Ivarsdottir, Hilma Holm, Stefania Benonisdottir, et al.
Pageof 33