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Patrick Sulem

Showing results (41-50 of 280) with videos related to

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Brain Communications|March 5, 2025
Biallelic variants in <i>GTF3C3</i> encoding a subunit of the TFIIIC2 complex are associated with neurodevelopmental phenotypes in humans and zebrafishMohamed S Abdel-Hamid, Adeline Paimboeuf, Maha S Zaki, et al.
European Heart Journal|March 29, 2018
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aortaThorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
The Lancet. Oncology|August 7, 2010
GPC5 rs2352028 variant and risk of lung cancer in never smokersMaria Teresa Landi, Nilanjan Chatterjee, Neil E Caporaso, et al.
Plos Medicine|June 14, 2006
The BARD1 Cys557Ser variant and breast cancer risk in IcelandSimon N Stacey, Patrick Sulem, Oskar T Johannsson, et al.
BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
Nature|August 24, 2012
Rate of de novo mutations and the importance of father's age to disease riskAugustine Kong, Michael L Frigge, Gisli Masson, et al.
Nature Genetics|October 14, 2008
Male-pattern baldness susceptibility locus at 20p11J Brent Richards, Xin Yuan, Frank Geller, et al.
Science (New York, N.Y.)|August 11, 2007
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucomaGudmar Thorleifsson, Kristinn P Magnusson, Patrick Sulem, et al.
The Journal of Clinical Endocrinology and Metabolism|December 20, 2023
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral DensityUnnur Styrkarsdottir, Vinicius Tragante, Lilja Stefansdottir, et al.
Nature Genetics|March 28, 2017
Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibilityDaniel J Wright, Felix R Day, Nicola D Kerrison, et al.
Pageof 28

Showing results (41-50 of 280) with videos related to

Sort By:
Pageof 28
Brain Communications|March 5, 2025
Biallelic variants in <i>GTF3C3</i> encoding a subunit of the TFIIIC2 complex are associated with neurodevelopmental phenotypes in humans and zebrafishMohamed S Abdel-Hamid, Adeline Paimboeuf, Maha S Zaki, et al.
European Heart Journal|March 29, 2018
A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aortaThorsteinn Bjornsson, Rosa B Thorolfsdottir, Gardar Sveinbjornsson, et al.
The Lancet. Oncology|August 7, 2010
GPC5 rs2352028 variant and risk of lung cancer in never smokersMaria Teresa Landi, Nilanjan Chatterjee, Neil E Caporaso, et al.
Plos Medicine|June 14, 2006
The BARD1 Cys557Ser variant and breast cancer risk in IcelandSimon N Stacey, Patrick Sulem, Oskar T Johannsson, et al.
BMC Medical Genetics|October 3, 2017
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sistersGudny A Arnadottir, Brynjar O Jensson, Sigurdur E Marelsson, et al.
Nature|August 24, 2012
Rate of de novo mutations and the importance of father's age to disease riskAugustine Kong, Michael L Frigge, Gisli Masson, et al.
Nature Genetics|October 14, 2008
Male-pattern baldness susceptibility locus at 20p11J Brent Richards, Xin Yuan, Frank Geller, et al.
Science (New York, N.Y.)|August 11, 2007
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucomaGudmar Thorleifsson, Kristinn P Magnusson, Patrick Sulem, et al.
The Journal of Clinical Endocrinology and Metabolism|December 20, 2023
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral DensityUnnur Styrkarsdottir, Vinicius Tragante, Lilja Stefansdottir, et al.
Nature Genetics|March 28, 2017
Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibilityDaniel J Wright, Felix R Day, Nicola D Kerrison, et al.
Pageof 28