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Tropical Medicine and Health
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June 25, 2022
Genetic variation in CSF2 (5q31.1) is associated with longitudinal susceptibility to pediatric malaria, severe malarial anemia, and all-cause mortality in a high-burden malaria and HIV region of Kenya
Lily E Kisia, Qiuying Cheng, Evans Raballah, et al.
Plos One
|
January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population
Nori Matsunami, Dexter Hadley, Charles H Hensel, et al.
Peerj
|
July 1, 2024
TIN-X version 3: update with expanded dataset and modernized architecture for enhanced illumination of understudied targets
Vincent T Metzger, Daniel C Cannon, Jeremy J Yang, et al.
Drug Safety
|
July 3, 2014
Bridging islands of information to establish an integrated knowledge base of drugs and health outcomes of interest
Richard D Boyce, Patrick B Ryan, G Niklas Norén, et al.
JMIR Mental Health
|
June 26, 2019
Preferences of Information Dissemination on Treatment for Bipolar Disorder: Patient-Centered Focus Group Study
Berit Kerner, Annette S Crisanti, Jason L DeShaw, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
May 2, 2022
Elevated SARS-CoV-2 in peripheral blood and increased COVID-19 severity in American Indians/Alaska Natives
Douglas J Perkins, Alexandra V Yingling, Qiuying Cheng, et al.
Bipolar Disorders
|
September 14, 2017
Systemic challenges in bipolar disorder management: A patient-centered approach
Anastasiya Nestsiarovich, Nathaniel G Hurwitz, Stuart J Nelson, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
November 29, 2021
Complement component 3 mutations alter the longitudinal risk of pediatric malaria and severe malarial anemia
Evans Raballah, Samuel B Anyona, Qiuying Cheng, et al.
Communications Medicine
|
July 17, 2023
Toxicology knowledge graph for structural birth defects
John Erol Evangelista, Daniel J B Clarke, Zhuorui Xie, et al.
Molecular Autism
|
January 29, 2014
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population
Nori Matsunami, Charles H Hensel, Lisa Baird, et al.
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of 6
Search research articles
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Showing results (31-40 of 52) with videos related to
Sort By:
Page
of 6
Tropical Medicine and Health
|
June 25, 2022
Genetic variation in CSF2 (5q31.1) is associated with longitudinal susceptibility to pediatric malaria, severe malarial anemia, and all-cause mortality in a high-burden malaria and HIV region of Kenya
Lily E Kisia, Qiuying Cheng, Evans Raballah, et al.
Plos One
|
January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population
Nori Matsunami, Dexter Hadley, Charles H Hensel, et al.
Peerj
|
July 1, 2024
TIN-X version 3: update with expanded dataset and modernized architecture for enhanced illumination of understudied targets
Vincent T Metzger, Daniel C Cannon, Jeremy J Yang, et al.
Drug Safety
|
July 3, 2014
Bridging islands of information to establish an integrated knowledge base of drugs and health outcomes of interest
Richard D Boyce, Patrick B Ryan, G Niklas Norén, et al.
JMIR Mental Health
|
June 26, 2019
Preferences of Information Dissemination on Treatment for Bipolar Disorder: Patient-Centered Focus Group Study
Berit Kerner, Annette S Crisanti, Jason L DeShaw, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
May 2, 2022
Elevated SARS-CoV-2 in peripheral blood and increased COVID-19 severity in American Indians/Alaska Natives
Douglas J Perkins, Alexandra V Yingling, Qiuying Cheng, et al.
Bipolar Disorders
|
September 14, 2017
Systemic challenges in bipolar disorder management: A patient-centered approach
Anastasiya Nestsiarovich, Nathaniel G Hurwitz, Stuart J Nelson, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
November 29, 2021
Complement component 3 mutations alter the longitudinal risk of pediatric malaria and severe malarial anemia
Evans Raballah, Samuel B Anyona, Qiuying Cheng, et al.
Communications Medicine
|
July 17, 2023
Toxicology knowledge graph for structural birth defects
John Erol Evangelista, Daniel J B Clarke, Zhuorui Xie, et al.
Molecular Autism
|
January 29, 2014
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population
Nori Matsunami, Charles H Hensel, Lisa Baird, et al.
Page
of 6