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Genome Research
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February 8, 2008
WGAViewer: software for genomic annotation of whole genome association studies
Dongliang Ge, Kunlin Zhang, Anna C Need, et al.
American Journal of Human Genetics
|
April 17, 2007
Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1A
Erin L Heinzen, Woohyun Yoon, Sarah K Tate, et al.
Neurology
|
July 31, 2013
JURaSSiC: accuracy of clinician vs risk score prediction of ischemic stroke outcomes
Gustavo Saposnik, Robert Cote, Muhammad Mamdani, et al.
Radiology
|
July 1, 1993
Elevated levels of amniotic fluid alpha-fetoprotein: sonographic evaluation
M Robbin, R A Filly, S Fell, et al.
Neurology
|
September 30, 2018
Outcomes after carotid endarterectomy among elderly dual Medicare-Medicaid-eligible patients
Erica C Leifheit, Yun Wang, George Howard, et al.
Genetic Epidemiology
|
February 12, 2020
Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analyses
Mengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
American Journal of Human Genetics
|
May 20, 2014
Utilizing population controls in rare-variant case-parent association tests
Yu Jiang, Glen A Satten, Yujun Han, et al.
Journal of the American Heart Association
|
July 21, 2022
Rural Residence and Antihypertensive Medication Use in US Stroke Survivors
Phoebe M Tran, Lam T Tran, Cenjing Zhu, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
November 11, 1998
Psychopathology in children of parents with opiate dependence and/or major depression
E V Nunes, M M Weissman, R B Goldstein, et al.
JAMA Internal Medicine
|
August 28, 2013
Risk of thyroid cancer based on thyroid ultrasound imaging characteristics: results of a population-based study
Rebecca Smith-Bindman, Paulette Lebda, Vickie A Feldstein, et al.
Page
of 144
Search research articles
Search
Showing results (861-870 of 1,434) with videos related to
Sort By:
Page
of 144
Genome Research
|
February 8, 2008
WGAViewer: software for genomic annotation of whole genome association studies
Dongliang Ge, Kunlin Zhang, Anna C Need, et al.
American Journal of Human Genetics
|
April 17, 2007
Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1A
Erin L Heinzen, Woohyun Yoon, Sarah K Tate, et al.
Neurology
|
July 31, 2013
JURaSSiC: accuracy of clinician vs risk score prediction of ischemic stroke outcomes
Gustavo Saposnik, Robert Cote, Muhammad Mamdani, et al.
Radiology
|
July 1, 1993
Elevated levels of amniotic fluid alpha-fetoprotein: sonographic evaluation
M Robbin, R A Filly, S Fell, et al.
Neurology
|
September 30, 2018
Outcomes after carotid endarterectomy among elderly dual Medicare-Medicaid-eligible patients
Erica C Leifheit, Yun Wang, George Howard, et al.
Genetic Epidemiology
|
February 12, 2020
Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analyses
Mengqi Zhang, Sahar Gelfman, Janice McCarthy, et al.
American Journal of Human Genetics
|
May 20, 2014
Utilizing population controls in rare-variant case-parent association tests
Yu Jiang, Glen A Satten, Yujun Han, et al.
Journal of the American Heart Association
|
July 21, 2022
Rural Residence and Antihypertensive Medication Use in US Stroke Survivors
Phoebe M Tran, Lam T Tran, Cenjing Zhu, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
November 11, 1998
Psychopathology in children of parents with opiate dependence and/or major depression
E V Nunes, M M Weissman, R B Goldstein, et al.
JAMA Internal Medicine
|
August 28, 2013
Risk of thyroid cancer based on thyroid ultrasound imaging characteristics: results of a population-based study
Rebecca Smith-Bindman, Paulette Lebda, Vickie A Feldstein, et al.
Page
of 144