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Showing results (771-780 of 959) with videos related to

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Plos One|November 9, 2013
A pilot study using next-generation sequencing in advanced cancers: feasibility and challengesGlen J Weiss, Winnie S Liang, Michael J Demeure, et al.
Neuroimage|January 27, 2010
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohortLi Shen, Sungeun Kim, Shannon L Risacher, et al.
Nanoscale Advances|July 13, 2026
Isolation of extracellular vesicles from minimal volume ascites fluid using strong anion exchange beadsTyler T Cooper, Lorena Veliz, Farzaneh Afzali, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Assessment of MYC Gene and WNT Pathway Alterations in Early-Onset Colorectal Cancer Among Hispanic/Latino Patients Using Integrated Multi-Omics ApproachesF G Carranza, B Waldrup, Y Jin, et al.
F1000Research|July 1, 2017
Case Report: Novel mutations in <i>TBC1D24</i> are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilityErika Banuelos, Keri Ramsey, Newell Belnap, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|December 2, 2015
Transcriptomics and the mechanisms of antidepressant efficacyKaren Hodgson, Katherine E Tansey, Timothy R Powell, et al.
Human Genetics|November 22, 2019
Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD)Lorida Llaci, Keri Ramsey, Newell Belnap, et al.
Research Square|September 5, 2025
The Curious Case of a Heterozygous Loss-of-Function PSEN1 variant associated with Early-Onset Alzheimer's DiseaseInmaculada Sanjuan Ruiz, Lutgarde Serneels, Katleen Craessaerts, et al.
American Journal of Human Genetics|February 24, 2009
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisIsabelle Schrauwen, Megan Ealy, Matthew J Huentelman, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 17, 2015
An integrated framework for reporting clinically relevant biomarkers from paired tumor/normal genomic and transcriptomic sequencing data in support of clinical trials in personalized medicineSara Nasser, Ahmet A Kurdolgu, Tyler Izatt, et al.
Pageof 96

Showing results (771-780 of 959) with videos related to

Sort By:
Pageof 96
Plos One|November 9, 2013
A pilot study using next-generation sequencing in advanced cancers: feasibility and challengesGlen J Weiss, Winnie S Liang, Michael J Demeure, et al.
Neuroimage|January 27, 2010
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohortLi Shen, Sungeun Kim, Shannon L Risacher, et al.
Nanoscale Advances|July 13, 2026
Isolation of extracellular vesicles from minimal volume ascites fluid using strong anion exchange beadsTyler T Cooper, Lorena Veliz, Farzaneh Afzali, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Assessment of MYC Gene and WNT Pathway Alterations in Early-Onset Colorectal Cancer Among Hispanic/Latino Patients Using Integrated Multi-Omics ApproachesF G Carranza, B Waldrup, Y Jin, et al.
F1000Research|July 1, 2017
Case Report: Novel mutations in <i>TBC1D24</i> are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilityErika Banuelos, Keri Ramsey, Newell Belnap, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|December 2, 2015
Transcriptomics and the mechanisms of antidepressant efficacyKaren Hodgson, Katherine E Tansey, Timothy R Powell, et al.
Human Genetics|November 22, 2019
Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD)Lorida Llaci, Keri Ramsey, Newell Belnap, et al.
Research Square|September 5, 2025
The Curious Case of a Heterozygous Loss-of-Function PSEN1 variant associated with Early-Onset Alzheimer's DiseaseInmaculada Sanjuan Ruiz, Lutgarde Serneels, Katleen Craessaerts, et al.
American Journal of Human Genetics|February 24, 2009
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisIsabelle Schrauwen, Megan Ealy, Matthew J Huentelman, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|January 17, 2015
An integrated framework for reporting clinically relevant biomarkers from paired tumor/normal genomic and transcriptomic sequencing data in support of clinical trials in personalized medicineSara Nasser, Ahmet A Kurdolgu, Tyler Izatt, et al.
Pageof 96