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Translational Psychiatry
|
April 26, 2017
15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia
M O Ulfarsson, G B Walters, O Gustafsson, et al.
Molecular Psychiatry
|
March 9, 2016
A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
T E Thorgeirsson, S Steinberg, G W Reginsson, et al.
Journal of Dental Research
|
January 25, 2018
Rare and Common Variants Conferring Risk of Tooth Agenesis
L Jonsson, T E Magnusson, A Thordarson, et al.
Molecular Psychiatry
|
August 21, 2013
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene
X-J Luo, M Li, L Huang, et al.
Translational Psychiatry
|
October 7, 2015
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence
D B Hancock, G W Reginsson, N C Gaddis, et al.
Molecular Psychiatry
|
October 4, 2017
Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence
D B Hancock, Y Guo, G W Reginsson, et al.
Molecular Psychiatry
|
February 18, 2015
Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus
R S Desikan, A J Schork, Y Wang, et al.
Molecular Psychiatry
|
September 30, 2009
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
A Ingason, D Rujescu, S Cichon, et al.
Osteoarthritis and Cartilage
|
November 10, 2010
Recommendations for standardization and phenotype definitions in genetic studies of osteoarthritis: the TREAT-OA consortium
H J M Kerkhof, I Meulenbelt, T Akune, et al.
Molecular Psychiatry
|
August 31, 2011
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM
N Amin, E Byrne, J Johnson, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 113) with videos related to
Sort By:
Page
of 12
Translational Psychiatry
|
April 26, 2017
15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia
M O Ulfarsson, G B Walters, O Gustafsson, et al.
Molecular Psychiatry
|
March 9, 2016
A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
T E Thorgeirsson, S Steinberg, G W Reginsson, et al.
Journal of Dental Research
|
January 25, 2018
Rare and Common Variants Conferring Risk of Tooth Agenesis
L Jonsson, T E Magnusson, A Thordarson, et al.
Molecular Psychiatry
|
August 21, 2013
Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene
X-J Luo, M Li, L Huang, et al.
Translational Psychiatry
|
October 7, 2015
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence
D B Hancock, G W Reginsson, N C Gaddis, et al.
Molecular Psychiatry
|
October 4, 2017
Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence
D B Hancock, Y Guo, G W Reginsson, et al.
Molecular Psychiatry
|
February 18, 2015
Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus
R S Desikan, A J Schork, Y Wang, et al.
Molecular Psychiatry
|
September 30, 2009
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
A Ingason, D Rujescu, S Cichon, et al.
Osteoarthritis and Cartilage
|
November 10, 2010
Recommendations for standardization and phenotype definitions in genetic studies of osteoarthritis: the TREAT-OA consortium
H J M Kerkhof, I Meulenbelt, T Akune, et al.
Molecular Psychiatry
|
August 31, 2011
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM
N Amin, E Byrne, J Johnson, et al.
Page
of 12