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Clinical and Translational Science
|
July 10, 2025
Announcing the Biomedical Data Translator: Initial Public Release
Karamarie Fecho, Gwênlyn Glusman, Sergio E Baranzini, et al.
Vaccines
|
January 21, 2023
Reinfection with SARS-CoV-2 and Waning Humoral Immunity: A Case Report
Jason D Goldman, Kai Wang, Katharina Röltgen, et al.
Plos One
|
September 1, 2015
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Plos One
|
May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Nature Genetics
|
November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Julian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
December 4, 2018
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder
Monika Budde, Stefanie Friedrichs, Ney Alliey-Rodriguez, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
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Search research articles
Search
Showing results (61-70 of 67) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 67 results.
Clinical and Translational Science
|
July 10, 2025
Announcing the Biomedical Data Translator: Initial Public Release
Karamarie Fecho, Gwênlyn Glusman, Sergio E Baranzini, et al.
Vaccines
|
January 21, 2023
Reinfection with SARS-CoV-2 and Waning Humoral Immunity: A Case Report
Jason D Goldman, Kai Wang, Katharina Röltgen, et al.
Plos One
|
September 1, 2015
Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Plos One
|
May 22, 2015
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry
Louis Viollet, Gustavo Glusman, Kelley J Murphy, et al.
Nature Genetics
|
November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes
Julian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
December 4, 2018
Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder
Monika Budde, Stefanie Friedrichs, Ney Alliey-Rodriguez, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
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of 7