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The Lancet. Neurology
|
November 9, 2019
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A Nalls, Cornelis Blauwendraat, Costanza L Vallerga, et al.
The Oncologist
|
July 19, 2022
Implementation and Clinical Adoption of Precision Oncology Workflows Across a Healthcare Network
Dora Dias-Santagata, Rebecca S Heist, Adam Z Bard, et al.
Plos One
|
November 22, 2023
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe
Nicolas Garnier, Joanne Berghout, Aldona Zygmunt, et al.
Plos One
|
January 10, 2024
Researching COVID to enhance recovery (RECOVER) tissue pathology study protocol: Rationale, objectives, and design
Andrea B Troxel, Marie-Abele C Bind, Thomas J Flotte, et al.
Plos Genetics
|
March 23, 2012
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
Christina M Lill, Johannes T Roehr, Matthew B McQueen, et al.
Cell
|
July 23, 2019
An Integrative Model of Cellular States, Plasticity, and Genetics for Glioblastoma
Cyril Neftel, Julie Laffy, Mariella G Filbin, et al.
Advances in Experimental Medicine and Biology
|
September 16, 2024
Global Challenges After a Global Challenge: Lessons Learned from the COVID-19 Pandemic
Niloufar Yazdanpanah, Constantine Sedikides, Hans D Ochs, et al.
Archives of Neurology
|
April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
Alice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Progress in Brain Research
|
February 27, 2021
Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI
Winfried Schlee, Stefan Schoisswohl, Susanne Staudinger, et al.
Nature Genetics
|
February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
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of 47
Search research articles
Search
Showing results (451-460 of 463) with videos related to
Sort By:
Page
of 47
The Lancet. Neurology
|
November 9, 2019
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Mike A Nalls, Cornelis Blauwendraat, Costanza L Vallerga, et al.
The Oncologist
|
July 19, 2022
Implementation and Clinical Adoption of Precision Oncology Workflows Across a Healthcare Network
Dora Dias-Santagata, Rebecca S Heist, Adam Z Bard, et al.
Plos One
|
November 22, 2023
Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe
Nicolas Garnier, Joanne Berghout, Aldona Zygmunt, et al.
Plos One
|
January 10, 2024
Researching COVID to enhance recovery (RECOVER) tissue pathology study protocol: Rationale, objectives, and design
Andrea B Troxel, Marie-Abele C Bind, Thomas J Flotte, et al.
Plos Genetics
|
March 23, 2012
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database
Christina M Lill, Johannes T Roehr, Matthew B McQueen, et al.
Cell
|
July 23, 2019
An Integrative Model of Cellular States, Plasticity, and Genetics for Glioblastoma
Cyril Neftel, Julie Laffy, Mariella G Filbin, et al.
Advances in Experimental Medicine and Biology
|
September 16, 2024
Global Challenges After a Global Challenge: Lessons Learned from the COVID-19 Pandemic
Niloufar Yazdanpanah, Constantine Sedikides, Hans D Ochs, et al.
Archives of Neurology
|
April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration
Alice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Progress in Brain Research
|
February 27, 2021
Towards a unification of treatments and interventions for tinnitus patients: The EU research and innovation action UNITI
Winfried Schlee, Stefan Schoisswohl, Susanne Staudinger, et al.
Nature Genetics
|
February 16, 2010
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions
Vivianna M Van Deerlin, Patrick M A Sleiman, Maria Martinez-Lage, et al.
Page
of 47