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International Journal of Cancer
|
May 25, 2019
A novel combined miRNA and methylation marker panel (miMe) for prediction of prostate cancer outcome after radical prostatectomy
Siri H Strand, Elham Bavafaye-Haghighi, Helle Kristensen, et al.
European Journal of Human Genetics : EJHG
|
January 23, 2014
Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population
Shengting Li, Soren Besenbacher, Yingrui Li, et al.
Nature
|
August 24, 2012
Rate of de novo mutations and the importance of father's age to disease risk
Augustine Kong, Michael L Frigge, Gisli Masson, et al.
Nature
|
December 18, 2009
Parental origin of sequence variants associated with complex diseases
Augustine Kong, Valgerdur Steinthorsdottir, Gisli Masson, et al.
Scientific Data
|
September 22, 2017
Whole genome characterization of sequence diversity of 15,220 Icelanders
Hákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Genetics
|
October 11, 2011
Identification of low-frequency variants associated with gout and serum uric acid levels
Patrick Sulem, Daniel F Gudbjartsson, G Bragi Walters, et al.
Cancer Research
|
February 10, 2011
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk
Thorunn Rafnar, Patrick Sulem, Soren Besenbacher, et al.
Nature Genetics
|
October 4, 2011
Mutations in BRIP1 confer high risk of ovarian cancer
Thorunn Rafnar, Daniel F Gudbjartsson, Patrick Sulem, et al.
Nature Genetics
|
March 26, 2015
Large-scale whole-genome sequencing of the Icelandic population
Daniel F Gudbjartsson, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Science Translational Medicine
|
December 17, 2010
Genetic correction of PSA values using sequence variants associated with PSA levels
Julius Gudmundsson, Soren Besenbacher, Patrick Sulem, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
International Journal of Cancer
|
May 25, 2019
A novel combined miRNA and methylation marker panel (miMe) for prediction of prostate cancer outcome after radical prostatectomy
Siri H Strand, Elham Bavafaye-Haghighi, Helle Kristensen, et al.
European Journal of Human Genetics : EJHG
|
January 23, 2014
Variation and association to diabetes in 2000 full mtDNA sequences mined from an exome study in a Danish population
Shengting Li, Soren Besenbacher, Yingrui Li, et al.
Nature
|
August 24, 2012
Rate of de novo mutations and the importance of father's age to disease risk
Augustine Kong, Michael L Frigge, Gisli Masson, et al.
Nature
|
December 18, 2009
Parental origin of sequence variants associated with complex diseases
Augustine Kong, Valgerdur Steinthorsdottir, Gisli Masson, et al.
Scientific Data
|
September 22, 2017
Whole genome characterization of sequence diversity of 15,220 Icelanders
Hákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Nature Genetics
|
October 11, 2011
Identification of low-frequency variants associated with gout and serum uric acid levels
Patrick Sulem, Daniel F Gudbjartsson, G Bragi Walters, et al.
Cancer Research
|
February 10, 2011
Genome-wide significant association between a sequence variant at 15q15.2 and lung cancer risk
Thorunn Rafnar, Patrick Sulem, Soren Besenbacher, et al.
Nature Genetics
|
October 4, 2011
Mutations in BRIP1 confer high risk of ovarian cancer
Thorunn Rafnar, Daniel F Gudbjartsson, Patrick Sulem, et al.
Nature Genetics
|
March 26, 2015
Large-scale whole-genome sequencing of the Icelandic population
Daniel F Gudbjartsson, Hannes Helgason, Sigurjon A Gudjonsson, et al.
Science Translational Medicine
|
December 17, 2010
Genetic correction of PSA values using sequence variants associated with PSA levels
Julius Gudmundsson, Soren Besenbacher, Patrick Sulem, et al.
Page
of 2