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Schizophrenia Research
|
October 18, 2016
Schizophrenia is associated with a pattern of spatial working memory deficits consistent with cortical disinhibition
Martina Starc, John D Murray, Nicole Santamauro, et al.
Frontiers in Psychiatry
|
January 9, 2014
Connectivity, pharmacology, and computation: toward a mechanistic understanding of neural system dysfunction in schizophrenia
Alan Anticevic, Michael W Cole, Grega Repovs, et al.
Digital Health
|
October 9, 2023
A feasibility study on the efficacy of a patient-owned wound surveillance system for diabetic foot ulcer care (ePOWS study)
Zhiwen J Lo, Keerthi B Harish, Elaine Tan, et al.
Journal of Genetic Counseling
|
September 24, 2020
Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force
Leigha Senter, Jehannine C Austin, Meghan Carey, et al.
Journal of Abnormal Psychology
|
October 19, 2018
Effects of reward on spatial working memory in schizophrenia
Youngsun T Cho, Norman H Lam, Martina Starc, et al.
Neuroimage
|
March 29, 2022
Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
Youngsun T Cho, Flora Moujaes, Charles H Schleifer, et al.
Neurogenetics
|
August 5, 2015
Mutations in ARID2 are associated with intellectual disabilities
Linshan Shang, Megan T Cho, Kyle Retterer, et al.
American Journal of Medical Genetics. Part A
|
September 24, 2017
Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series
Anya Revah-Politi, Mythily Ganapathi, Louise Bier, et al.
Transplantation Proceedings
|
May 29, 2016
Short-Term Outcomes of ABO-Incompatible Living Donor Kidney Transplantation With Uniform Protocol: Significance of Baseline Anti-ABO Titer
K W Lee, J B Park, D K Oh, et al.
Clinical Genetics
|
August 30, 2016
De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females
R Webster, M T Cho, K Retterer, et al.
Page
of 38
Search research articles
Search
Showing results (251-260 of 375) with videos related to
Sort By:
Page
of 38
Schizophrenia Research
|
October 18, 2016
Schizophrenia is associated with a pattern of spatial working memory deficits consistent with cortical disinhibition
Martina Starc, John D Murray, Nicole Santamauro, et al.
Frontiers in Psychiatry
|
January 9, 2014
Connectivity, pharmacology, and computation: toward a mechanistic understanding of neural system dysfunction in schizophrenia
Alan Anticevic, Michael W Cole, Grega Repovs, et al.
Digital Health
|
October 9, 2023
A feasibility study on the efficacy of a patient-owned wound surveillance system for diabetic foot ulcer care (ePOWS study)
Zhiwen J Lo, Keerthi B Harish, Elaine Tan, et al.
Journal of Genetic Counseling
|
September 24, 2020
Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force
Leigha Senter, Jehannine C Austin, Meghan Carey, et al.
Journal of Abnormal Psychology
|
October 19, 2018
Effects of reward on spatial working memory in schizophrenia
Youngsun T Cho, Norman H Lam, Martina Starc, et al.
Neuroimage
|
March 29, 2022
Reward and loss incentives improve spatial working memory by shaping trial-by-trial posterior frontoparietal signals
Youngsun T Cho, Flora Moujaes, Charles H Schleifer, et al.
Neurogenetics
|
August 5, 2015
Mutations in ARID2 are associated with intellectual disabilities
Linshan Shang, Megan T Cho, Kyle Retterer, et al.
American Journal of Medical Genetics. Part A
|
September 24, 2017
Loss-of-function variants in NFIA provide further support that NFIA is a critical gene in 1p32-p31 deletion syndrome: A four patient series
Anya Revah-Politi, Mythily Ganapathi, Louise Bier, et al.
Transplantation Proceedings
|
May 29, 2016
Short-Term Outcomes of ABO-Incompatible Living Donor Kidney Transplantation With Uniform Protocol: Significance of Baseline Anti-ABO Titer
K W Lee, J B Park, D K Oh, et al.
Clinical Genetics
|
August 30, 2016
De novo loss of function mutations in KIAA2022 are associated with epilepsy and neurodevelopmental delay in females
R Webster, M T Cho, K Retterer, et al.
Page
of 38