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Gregory M Cooper

Showing results (131-140 of 195) with videos related to

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Tissue Engineering. Part A|November 8, 2014
Transforming growth factor beta 1 augments calvarial defect healing and promotes suture regenerationSameer Shakir, Zoe M MacIsaac, Sanjay Naran, et al.
The Journal of Craniofacial Surgery|October 20, 2018
Reconstruction of a Calvarial Wound Complicated by Infection: Comparing the Effects of Biopatterned Bone Morphogenetic Protein 2 and Vascular Endothelial Growth FactorJack E Brooker, Liliana B Camison, Michael R Bykowski, et al.
Plos Genetics|September 1, 2017
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamusPatricia Blanchet, Martina Bebin, Shaam Bruet, et al.
Blood|June 7, 2008
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance doseGregory M Cooper, Julie A Johnson, Taimour Y Langaee, et al.
Genome Medicine|November 22, 2022
Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencingKevin M Bowling, Michelle L Thompson, Melissa A Kelly, et al.
Nature Neuroscience|June 3, 2024
Multiomic profiling of transcription factor binding and function in human brainJacob M Loupe, Ashlyn G Anderson, Lindsay F Rizzardi, et al.
Neurology. Genetics|November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
Biorxiv : the Preprint Server for Biology|December 23, 2024
StarPhase: Comprehensive Phase-Aware Pharmacogenomic Diplotyper for Long-Read Sequencing DataJames M Holt, John Harting, Xiao Chen, et al.
American Journal of Human Genetics|April 25, 2020
Non-coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative DiseasesJ Nicholas Cochran, Ethan G Geier, Luke W Bonham, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLsBelle A Moyers, Jacob M Loupe, Stephanie A Felker, et al.
Pageof 20

Showing results (131-140 of 195) with videos related to

Sort By:
Pageof 20
Tissue Engineering. Part A|November 8, 2014
Transforming growth factor beta 1 augments calvarial defect healing and promotes suture regenerationSameer Shakir, Zoe M MacIsaac, Sanjay Naran, et al.
The Journal of Craniofacial Surgery|October 20, 2018
Reconstruction of a Calvarial Wound Complicated by Infection: Comparing the Effects of Biopatterned Bone Morphogenetic Protein 2 and Vascular Endothelial Growth FactorJack E Brooker, Liliana B Camison, Michael R Bykowski, et al.
Plos Genetics|September 1, 2017
MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamusPatricia Blanchet, Martina Bebin, Shaam Bruet, et al.
Blood|June 7, 2008
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance doseGregory M Cooper, Julie A Johnson, Taimour Y Langaee, et al.
Genome Medicine|November 22, 2022
Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experiences in genomic sequencingKevin M Bowling, Michelle L Thompson, Melissa A Kelly, et al.
Nature Neuroscience|June 3, 2024
Multiomic profiling of transcription factor binding and function in human brainJacob M Loupe, Ashlyn G Anderson, Lindsay F Rizzardi, et al.
Neurology. Genetics|November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
Biorxiv : the Preprint Server for Biology|December 23, 2024
StarPhase: Comprehensive Phase-Aware Pharmacogenomic Diplotyper for Long-Read Sequencing DataJames M Holt, John Harting, Xiao Chen, et al.
American Journal of Human Genetics|April 25, 2020
Non-coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative DiseasesJ Nicholas Cochran, Ethan G Geier, Luke W Bonham, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Allele biased transcription factor binding across human brain regions gives mechanistic insight into eQTLsBelle A Moyers, Jacob M Loupe, Stephanie A Felker, et al.
Pageof 20