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Nature Protocols
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July 31, 2015
Population-specific genotype imputations using minimac or IMPUTE2
Elisabeth M van Leeuwen, Alexandros Kanterakis, Patrick Deelen, et al.
Frontiers in Genetics
|
November 24, 2016
A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study
Claudia T Silva, Irina V Zorkoltseva, Najaf Amin, et al.
Progress in Retinal and Eye Research
|
May 7, 2018
A new perspective on lipid research in age-related macular degeneration
Elisabeth M van Leeuwen, Eszter Emri, Benedicte M J Merle, et al.
Human Mutation
|
May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Adriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
European Journal of Human Genetics : EJHG
|
June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'
Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Human Molecular Genetics
|
June 7, 2015
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness
Gabriel Cuellar-Partida, Henriët Springelkamp, Sionne E M Lucas, et al.
Plos One
|
October 21, 2014
The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels
Elisabeth M van Leeuwen, Françoise A S Smouter, Tony Kam-Thong, et al.
Communications Biology
|
December 5, 2019
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters
Pieter W M Bonnemaijer, Elisabeth M van Leeuwen, Adriana I Iglesias, et al.
Human Molecular Genetics
|
February 1, 2015
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Henriët Springelkamp, Adriana I Iglesias, Gabriel Cuellar-Partida, et al.
Journal of the American College of Cardiology
|
April 7, 2016
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
Amit V Khera, Hong-Hee Won, Gina M Peloso, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
Nature Protocols
|
July 31, 2015
Population-specific genotype imputations using minimac or IMPUTE2
Elisabeth M van Leeuwen, Alexandros Kanterakis, Patrick Deelen, et al.
Frontiers in Genetics
|
November 24, 2016
A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study
Claudia T Silva, Irina V Zorkoltseva, Najaf Amin, et al.
Progress in Retinal and Eye Research
|
May 7, 2018
A new perspective on lipid research in age-related macular degeneration
Elisabeth M van Leeuwen, Eszter Emri, Benedicte M J Merle, et al.
Human Mutation
|
May 12, 2017
Haplotype reference consortium panel: Practical implications of imputations with large reference panels
Adriana I Iglesias, Sven J van der Lee, Pieter W M Bonnemaijer, et al.
European Journal of Human Genetics : EJHG
|
June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'
Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Human Molecular Genetics
|
June 7, 2015
WNT10A exonic variant increases the risk of keratoconus by decreasing corneal thickness
Gabriel Cuellar-Partida, Henriët Springelkamp, Sionne E M Lucas, et al.
Plos One
|
October 21, 2014
The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels
Elisabeth M van Leeuwen, Françoise A S Smouter, Tony Kam-Thong, et al.
Communications Biology
|
December 5, 2019
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters
Pieter W M Bonnemaijer, Elisabeth M van Leeuwen, Adriana I Iglesias, et al.
Human Molecular Genetics
|
February 1, 2015
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure
Henriët Springelkamp, Adriana I Iglesias, Gabriel Cuellar-Partida, et al.
Journal of the American College of Cardiology
|
April 7, 2016
Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia
Amit V Khera, Hong-Hee Won, Gina M Peloso, et al.
Page
of 4