Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Emily G Farrow

Showing results (41-50 of 58) with videos related to

Pageof 6
Sort By:
Genome Medicine|October 1, 2015
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseasesNeil A Miller, Emily G Farrow, Margaret Gibson, et al.
The Lancet. Respiratory Medicine|May 5, 2015
Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findingsLaurel K Willig, Josh E Petrikin, Laurie D Smith, et al.
Haematologica|August 19, 2017
Erythropoietin stimulates murine and human fibroblast growth factor-23, revealing novel roles for bone and bone marrowErica L Clinkenbeard, Mark R Hanudel, Keith R Stayrook, et al.
The Journal of Experimental Medicine|May 23, 2024
Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humansVictoria E Rael, Julian A Yano, John P Huizar, et al.
Human Mutation|October 17, 2025
One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient MatchmakingMatthew Osmond, E Magda Price, Orion J Buske, et al.
Research Square|February 20, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Plos Genetics|September 14, 2018
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Plos Genetics|July 13, 2018
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
HGG Advances|June 14, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Science Translational Medicine|December 5, 2014
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disordersSarah E Soden, Carol J Saunders, Laurel K Willig, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Genome Medicine|October 1, 2015
A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseasesNeil A Miller, Emily G Farrow, Margaret Gibson, et al.
The Lancet. Respiratory Medicine|May 5, 2015
Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findingsLaurel K Willig, Josh E Petrikin, Laurie D Smith, et al.
Haematologica|August 19, 2017
Erythropoietin stimulates murine and human fibroblast growth factor-23, revealing novel roles for bone and bone marrowErica L Clinkenbeard, Mark R Hanudel, Keith R Stayrook, et al.
The Journal of Experimental Medicine|May 23, 2024
Large-scale mutational analysis identifies UNC93B1 variants that drive TLR-mediated autoimmunity in mice and humansVictoria E Rael, Julian A Yano, John P Huizar, et al.
Human Mutation|October 17, 2025
One-Sided Matching Portal (OSMP): A Tool to Facilitate Rare Disease Patient MatchmakingMatthew Osmond, E Magda Price, Orion J Buske, et al.
Research Square|February 20, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Plos Genetics|September 14, 2018
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Plos Genetics|July 13, 2018
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
HGG Advances|June 14, 2025
Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia PigmentiMonica H Wojcik, Robin D Clark, Abdallah F Elias, et al.
Science Translational Medicine|December 5, 2014
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disordersSarah E Soden, Carol J Saunders, Laurel K Willig, et al.
Pageof 6