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AMIA ... Annual Symposium Proceedings. AMIA Symposium
|
April 21, 2020
Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants
Paul Dexter, Henry Ong, Amanda Elsey, et al.
The Journal of Pediatrics
|
April 16, 2013
Prompt control of an outbreak caused by extended-spectrum β-lactamase-producing Klebsiella pneumoniae in a neonatal intensive care unit
Joseph B Cantey, Pranavi Sreeramoju, Mambarambath Jaleel, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
October 23, 2012
Effectiveness of a school district closure for pandemic influenza A (H1N1) on acute respiratory illnesses in the community: a natural experiment
Daphne L Copeland, Ricardo Basurto-Davila, Wendy Chung, et al.
Cardiovascular Research
|
November 17, 2007
A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance
Earl Gordon, Gianina Panaghie, Liyong Deng, et al.
Diabetes
|
November 15, 2013
β-cell dysfunction due to increased ER stress in a stem cell model of Wolfram syndrome
Linshan Shang, Haiqing Hua, Kylie Foo, et al.
Breast Cancer Research and Treatment
|
May 16, 2015
Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry
Tehillah S Menes, Mary Beth Terry, David Goldgar, et al.
Journal of Genetic Counseling
|
June 25, 2013
Use of genetic tests among neurologists and psychiatrists: knowledge, attitudes, behaviors, and needs for training
Melissa Salm, Kristopher Abbate, Paul Appelbaum, et al.
Arxiv
|
May 7, 2024
GestaltMML: Enhancing Rare Genetic Disease Diagnosis through Multimodal Machine Learning Combining Facial Images and Clinical Texts
Da Wu, Jingye Yang, Cong Liu, et al.
Human Mutation
|
September 15, 2004
Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency
Vito Iacobazzi, Federica Invernizzi, Silvia Baratta, et al.
Neurology
|
April 16, 2017
Phenotype of GABA-transaminase deficiency
Mary Kay Koenig, Ryan Hodgeman, James J Riviello, et al.
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of 10
Search research articles
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Showing results (41-50 of 92) with videos related to
Sort By:
Page
of 10
AMIA ... Annual Symposium Proceedings. AMIA Symposium
|
April 21, 2020
Development of a Genomic Data Flow Framework: Results of a Survey Administered to NIH-NHGRI IGNITE and eMERGE Consortia Participants
Paul Dexter, Henry Ong, Amanda Elsey, et al.
The Journal of Pediatrics
|
April 16, 2013
Prompt control of an outbreak caused by extended-spectrum β-lactamase-producing Klebsiella pneumoniae in a neonatal intensive care unit
Joseph B Cantey, Pranavi Sreeramoju, Mambarambath Jaleel, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
October 23, 2012
Effectiveness of a school district closure for pandemic influenza A (H1N1) on acute respiratory illnesses in the community: a natural experiment
Daphne L Copeland, Ricardo Basurto-Davila, Wendy Chung, et al.
Cardiovascular Research
|
November 17, 2007
A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance
Earl Gordon, Gianina Panaghie, Liyong Deng, et al.
Diabetes
|
November 15, 2013
β-cell dysfunction due to increased ER stress in a stem cell model of Wolfram syndrome
Linshan Shang, Haiqing Hua, Kylie Foo, et al.
Breast Cancer Research and Treatment
|
May 16, 2015
Second primary breast cancer in BRCA1 and BRCA2 mutation carriers: 10-year cumulative incidence in the Breast Cancer Family Registry
Tehillah S Menes, Mary Beth Terry, David Goldgar, et al.
Journal of Genetic Counseling
|
June 25, 2013
Use of genetic tests among neurologists and psychiatrists: knowledge, attitudes, behaviors, and needs for training
Melissa Salm, Kristopher Abbate, Paul Appelbaum, et al.
Arxiv
|
May 7, 2024
GestaltMML: Enhancing Rare Genetic Disease Diagnosis through Multimodal Machine Learning Combining Facial Images and Clinical Texts
Da Wu, Jingye Yang, Cong Liu, et al.
Human Mutation
|
September 15, 2004
Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency
Vito Iacobazzi, Federica Invernizzi, Silvia Baratta, et al.
Neurology
|
April 16, 2017
Phenotype of GABA-transaminase deficiency
Mary Kay Koenig, Ryan Hodgeman, James J Riviello, et al.
Page
of 10