Jessica E Harris - JoVE Visualize

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Spine|November 10, 2025

Reoperation Risk Between Plated and Stand-Alone Anterior Cervical Discectomy and Fusion: A National Spine Registry-Based Cohort StudyEhsan Tabaraee, Heather A Prentice, Jessica E Harris, et al.

Spine|November 3, 2025

Reoperation Risks Between Cervical Disc Arthroplasty and Anterior Cervical Discectomy With Fusion: It is Not Always About Adjacent Segment DiseaseSamir Alsalek, Richard N Chang, Maya Harary, et al.

Human Molecular Genetics|October 26, 2014

Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defectsAideen M McInerney-Leo, Duncan B Sparrow, Jessica E Harris, et al.

Joint Commission Journal on Quality and Patient Safety|February 17, 2024

Improvements in Quality, Safety and Costs Associated with Use of Implant Registries Within a Health SystemHeather A Prentice, Jessica E Harris, Kenneth Sucher, et al.

Scientific Reports|April 21, 2016

Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 functionClaudio R Cortés, Aideen M McInerney-Leo, Ida Vogel, et al.

Human Mutation|April 3, 2016

Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate FamiliesAideen M McInerney-Leo, Jessica E Harris, Michael Gattas, et al.

Journal of Medical Genetics|April 13, 2016

Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasiaAideen M McInerney-Leo, Carine Le Goff, Paul J Leo, et al.

Pediatric Diabetes|September 8, 2018

Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohortStephanie R Johnson, Jonathan J Ellis, Paul J Leo, et al.

The Journal of Clinical Endocrinology and Metabolism|December 28, 2020

Multiple Endocrine Tumors Associated with Germline MAX Mutations: Multiple Endocrine Neoplasia Type 5?Amanda J Seabrook, Jessica E Harris, Sofia B Velosa, et al.

Human Molecular Genetics|July 18, 2021

Germline ERBB3 mutation in familial non-small-cell lung carcinoma: expanding ErbB's role in oncogenesisAideen M McInerney-Leo, Hui Yi Chew, Po-Ling Inglis, et al.

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Showing results (21-30 of 30) with videos related to

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You have reached the last page of results.This site can display upto 30 results.

Spine|November 10, 2025

Reoperation Risk Between Plated and Stand-Alone Anterior Cervical Discectomy and Fusion: A National Spine Registry-Based Cohort StudyEhsan Tabaraee, Heather A Prentice, Jessica E Harris, et al.

Spine|November 3, 2025

Reoperation Risks Between Cervical Disc Arthroplasty and Anterior Cervical Discectomy With Fusion: It is Not Always About Adjacent Segment DiseaseSamir Alsalek, Richard N Chang, Maya Harary, et al.

Human Molecular Genetics|October 26, 2014

Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defectsAideen M McInerney-Leo, Duncan B Sparrow, Jessica E Harris, et al.

Joint Commission Journal on Quality and Patient Safety|February 17, 2024

Improvements in Quality, Safety and Costs Associated with Use of Implant Registries Within a Health SystemHeather A Prentice, Jessica E Harris, Kenneth Sucher, et al.

Scientific Reports|April 21, 2016

Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 functionClaudio R Cortés, Aideen M McInerney-Leo, Ida Vogel, et al.

Human Mutation|April 3, 2016

Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate FamiliesAideen M McInerney-Leo, Jessica E Harris, Michael Gattas, et al.

Journal of Medical Genetics|April 13, 2016

Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasiaAideen M McInerney-Leo, Carine Le Goff, Paul J Leo, et al.

Pediatric Diabetes|September 8, 2018

Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohortStephanie R Johnson, Jonathan J Ellis, Paul J Leo, et al.

The Journal of Clinical Endocrinology and Metabolism|December 28, 2020

Multiple Endocrine Tumors Associated with Germline MAX Mutations: Multiple Endocrine Neoplasia Type 5?Amanda J Seabrook, Jessica E Harris, Sofia B Velosa, et al.

Human Molecular Genetics|July 18, 2021

Germline ERBB3 mutation in familial non-small-cell lung carcinoma: expanding ErbB's role in oncogenesisAideen M McInerney-Leo, Hui Yi Chew, Po-Ling Inglis, et al.

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