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Drug and Alcohol Dependence
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November 16, 2019
Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults
Lun-Hsien Chang, John B Whitfield, Mengzhen Liu, et al.
Plos One
|
June 23, 2011
Educational attainment: a genome wide association study in 9538 Australians
Nicolas W Martin, Sarah E Medland, Karin J H Verweij, et al.
American Journal of Medical Genetics. Part A
|
October 10, 2020
Exome sequencing identifies novel missense and deletion variants in RTN4IP1 associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis
Alissa M D'Gama, Eleina England, Jill A Madden, et al.
Circulation. Genomic and Precision Medicine
|
May 13, 2020
Congenital Heart Defects Due to <i>TAF1</i> Missense Variants
Sarah U Morton, Radhika Agarwal, Jill A Madden, et al.
Journal of Primary Care & Community Health
|
May 30, 2026
Implementing the 3-Day Skilled Nursing Facility Waiver: Key Insights
James S Newman, Kristin S Johnson, Tia J Meyer, et al.
Clinical Genetics
|
November 6, 2020
PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations
Camille Tremblay-Laganière, Rauan Kaiyrzhanov, Reza Maroofian, et al.
International Journal of Molecular Sciences
|
October 31, 2020
The P72R Polymorphism in R248Q/W p53 Mutants Modifies the Mutant Effect on Epithelial to Mesenchymal Transition Phenotype and Cell Invasion via CXCL1 Expression
Cristabelle De Souza, Jill A Madden, Dennis Minn, et al.
European Journal of Human Genetics : EJHG
|
January 23, 2023
Reanalysis of clinical exome identifies the second variant in two individuals with recessive disorders
Qifei Li, Rohan Agrawal, Klaus Schmitz-Abe, et al.
JAMA
|
March 27, 1998
Primary care physician compensation method in medical groups: does it influence the use and cost of health services for enrollees in managed care organizations?
D A Conrad, C Maynard, A Cheadle, et al.
Nature Genetics
|
June 22, 2010
Common SNPs explain a large proportion of the heritability for human height
Jian Yang, Beben Benyamin, Brian P McEvoy, et al.
Page
of 54
Search research articles
Search
Showing results (431-440 of 531) with videos related to
Sort By:
Page
of 54
Drug and Alcohol Dependence
|
November 16, 2019
Associations between polygenic risk for tobacco and alcohol use and liability to tobacco and alcohol use, and psychiatric disorders in an independent sample of 13,999 Australian adults
Lun-Hsien Chang, John B Whitfield, Mengzhen Liu, et al.
Plos One
|
June 23, 2011
Educational attainment: a genome wide association study in 9538 Australians
Nicolas W Martin, Sarah E Medland, Karin J H Verweij, et al.
American Journal of Medical Genetics. Part A
|
October 10, 2020
Exome sequencing identifies novel missense and deletion variants in RTN4IP1 associated with optic atrophy, global developmental delay, epilepsy, ataxia, and choreoathetosis
Alissa M D'Gama, Eleina England, Jill A Madden, et al.
Circulation. Genomic and Precision Medicine
|
May 13, 2020
Congenital Heart Defects Due to <i>TAF1</i> Missense Variants
Sarah U Morton, Radhika Agarwal, Jill A Madden, et al.
Journal of Primary Care & Community Health
|
May 30, 2026
Implementing the 3-Day Skilled Nursing Facility Waiver: Key Insights
James S Newman, Kristin S Johnson, Tia J Meyer, et al.
Clinical Genetics
|
November 6, 2020
PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations
Camille Tremblay-Laganière, Rauan Kaiyrzhanov, Reza Maroofian, et al.
International Journal of Molecular Sciences
|
October 31, 2020
The P72R Polymorphism in R248Q/W p53 Mutants Modifies the Mutant Effect on Epithelial to Mesenchymal Transition Phenotype and Cell Invasion via CXCL1 Expression
Cristabelle De Souza, Jill A Madden, Dennis Minn, et al.
European Journal of Human Genetics : EJHG
|
January 23, 2023
Reanalysis of clinical exome identifies the second variant in two individuals with recessive disorders
Qifei Li, Rohan Agrawal, Klaus Schmitz-Abe, et al.
JAMA
|
March 27, 1998
Primary care physician compensation method in medical groups: does it influence the use and cost of health services for enrollees in managed care organizations?
D A Conrad, C Maynard, A Cheadle, et al.
Nature Genetics
|
June 22, 2010
Common SNPs explain a large proportion of the heritability for human height
Jian Yang, Beben Benyamin, Brian P McEvoy, et al.
Page
of 54