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Patrick Sulem

Showing results (61-70 of 280) with videos related to

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Circulation. Genomic and Precision Medicine|October 26, 2018
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac DeathGardar Sveinbjornsson, Eva F Olafsdottir, Rosa B Thorolfsdottir, et al.
Nature Communications|June 7, 2017
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitisSnaevar Sigurdsson, Kristjan F Alexandersson, Patrick Sulem, et al.
BMC Medical Genetics|November 16, 2017
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPABrynjar O Jensson, Sif Hansdottir, Gudny A Arnadottir, et al.
Nature Communications|February 23, 2017
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniationGyda Bjornsdottir, Stefania Benonisdottir, Gardar Sveinbjornsson, et al.
Biological Psychiatry Global Open Science|January 6, 2026
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia MedicationGudmundur Einarsson, Hannes K Arnason, Rosa S Gisladottir, et al.
European Journal of Human Genetics : EJHG|July 4, 2024
Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genesNoor Smal, Fatma Majdoub, Katrien Janssens, et al.
Nature Genetics|June 30, 2009
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityGudmar Thorleifsson, Hilma Holm, Vidar Edvardsson, et al.
NPJ Parkinson'S Disease|August 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's diseaseAstros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Genetics|October 24, 2007
Genetic determinants of hair, eye and skin pigmentation in EuropeansPatrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, 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.
Pageof 28

Showing results (61-70 of 280) with videos related to

Sort By:
Pageof 28
Circulation. Genomic and Precision Medicine|October 26, 2018
Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac DeathGardar Sveinbjornsson, Eva F Olafsdottir, Rosa B Thorolfsdottir, et al.
Nature Communications|June 7, 2017
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitisSnaevar Sigurdsson, Kristjan F Alexandersson, Patrick Sulem, et al.
BMC Medical Genetics|November 16, 2017
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPABrynjar O Jensson, Sif Hansdottir, Gudny A Arnadottir, et al.
Nature Communications|February 23, 2017
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniationGyda Bjornsdottir, Stefania Benonisdottir, Gardar Sveinbjornsson, et al.
Biological Psychiatry Global Open Science|January 6, 2026
Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia MedicationGudmundur Einarsson, Hannes K Arnason, Rosa S Gisladottir, et al.
European Journal of Human Genetics : EJHG|July 4, 2024
Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genesNoor Smal, Fatma Majdoub, Katrien Janssens, et al.
Nature Genetics|June 30, 2009
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral densityGudmar Thorleifsson, Hilma Holm, Vidar Edvardsson, et al.
NPJ Parkinson'S Disease|August 15, 2024
Loss-of-function variants in ITSN1 confer high risk of Parkinson's diseaseAstros Th Skuladottir, Vinicius Tragante, Gardar Sveinbjornsson, et al.
Nature Genetics|October 24, 2007
Genetic determinants of hair, eye and skin pigmentation in EuropeansPatrick Sulem, Daniel F Gudbjartsson, Simon N Stacey, 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.
Pageof 28