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Pediatric Neurology
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October 2, 2007
Novel de novo mutation of a conserved SCN1A amino-acid residue (R1596)
Dennis J Dlugos, Thomas N Ferraro, Russell J Buono
Expert Review of Neurotherapeutics
|
December 22, 2006
Role of genetics in the diagnosis and treatment of epilepsy
Thomas N Ferraro, Dennis J Dlugos, Russell J Buono
Biology
|
March 26, 2025
Enhancing Single-Cell and Bulk Hi-C Data Using a Generative Transformer Model
Ruoying Gao, Thomas N Ferraro, Liang Chen, et al.
Briefings in Bioinformatics
|
June 23, 2021
Consensus clustering of single-cell RNA-seq data by enhancing network affinity
Yaxuan Cui, Shaoqiang Zhang, Ying Liang, et al.
Briefings in Bioinformatics
|
September 26, 2022
Decoding brain memory formation by single-cell RNA sequencing
Atlas M Sardoo, Shaoqiang Zhang, Thomas N Ferraro, et al.
Brain Research
|
January 28, 2019
Deletion of the vesicular monoamine transporter 1 (vmat1/slc18a1) gene affects dopamine signaling
Falk W Lohoff, Gregory V Carr, Bethany Brookshire, et al.
Neuroscience Letters
|
February 6, 2008
Association between variation in the vesicular monoamine transporter 1 gene on chromosome 8p and anxiety-related personality traits
Falk W Lohoff, Marion Lautenschlager, Johannes Mohr, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
June 7, 2021
Effectiveness of a Team-Based Learning exercise in the learning outcomes of a medical pharmacology course: insight from struggling students
Gonzalo A Carrasco, Kathryn C Behling, Matthew Gentile, et al.
Psychiatric Genetics
|
January 6, 2006
Analysis of variations in the NAPG gene on chromosome 18p11 in bipolar disorder
Andrew E Weller, John P Dahl, Falk W Lohoff, et al.
Frontiers in Neurology
|
July 28, 2020
The Molecular Genetic Interaction Between Circadian Rhythms and Susceptibility to Seizures and Epilepsy
Christopher J Re, Alexander I Batterman, Jason R Gerstner, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 86) with videos related to
Sort By:
Page
of 9
Pediatric Neurology
|
October 2, 2007
Novel de novo mutation of a conserved SCN1A amino-acid residue (R1596)
Dennis J Dlugos, Thomas N Ferraro, Russell J Buono
Expert Review of Neurotherapeutics
|
December 22, 2006
Role of genetics in the diagnosis and treatment of epilepsy
Thomas N Ferraro, Dennis J Dlugos, Russell J Buono
Biology
|
March 26, 2025
Enhancing Single-Cell and Bulk Hi-C Data Using a Generative Transformer Model
Ruoying Gao, Thomas N Ferraro, Liang Chen, et al.
Briefings in Bioinformatics
|
June 23, 2021
Consensus clustering of single-cell RNA-seq data by enhancing network affinity
Yaxuan Cui, Shaoqiang Zhang, Ying Liang, et al.
Briefings in Bioinformatics
|
September 26, 2022
Decoding brain memory formation by single-cell RNA sequencing
Atlas M Sardoo, Shaoqiang Zhang, Thomas N Ferraro, et al.
Brain Research
|
January 28, 2019
Deletion of the vesicular monoamine transporter 1 (vmat1/slc18a1) gene affects dopamine signaling
Falk W Lohoff, Gregory V Carr, Bethany Brookshire, et al.
Neuroscience Letters
|
February 6, 2008
Association between variation in the vesicular monoamine transporter 1 gene on chromosome 8p and anxiety-related personality traits
Falk W Lohoff, Marion Lautenschlager, Johannes Mohr, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology
|
June 7, 2021
Effectiveness of a Team-Based Learning exercise in the learning outcomes of a medical pharmacology course: insight from struggling students
Gonzalo A Carrasco, Kathryn C Behling, Matthew Gentile, et al.
Psychiatric Genetics
|
January 6, 2006
Analysis of variations in the NAPG gene on chromosome 18p11 in bipolar disorder
Andrew E Weller, John P Dahl, Falk W Lohoff, et al.
Frontiers in Neurology
|
July 28, 2020
The Molecular Genetic Interaction Between Circadian Rhythms and Susceptibility to Seizures and Epilepsy
Christopher J Re, Alexander I Batterman, Jason R Gerstner, et al.
Page
of 9