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

Jamie Allen

Showing results (11-20 of 47) with videos related to

Pageof 5
Sort By:
CJEM|March 26, 2021
Spontaneous compartment syndrome in a patient with hemophilia BJoseph Levi, Tara Stansbury, Matthew D Marschall, et al.
Journal of the American Society for Mass Spectrometry|April 16, 2023
MALDI IMS-Derived Molecular Contour Maps: Augmenting Histology Whole-Slide ImagesKavya Sharman, Nathan Heath Patterson, Lukasz G Migas, et al.
BMC Genomics|June 6, 2023
SUsPECT: a pipeline for variant effect prediction based on custom long-read transcriptomes for improved clinical variant annotationRenee Salz, Nuno Saraiva-Agostinho, Emil Vorsteveld, et al.
Human Molecular Genetics|January 12, 2018
Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genesXingyi Guo, Jiajun Shi, Qiuyin Cai, et al.
Journal of Medical Genetics|August 6, 2017
Rare, protein-truncating variants in <i>ATM</i>, <i>CHEK2</i> and <i>PALB2</i>, but not <i>XRCC2</i>, are associated with increased breast cancer risksBrennan Decker, Jamie Allen, Craig Luccarini, et al.
Cancers|July 2, 2021
<i>RAD51D</i> Aberrant Splicing in Breast Cancer: Identification of Splicing Regulatory Elements and Minigene-Based Evaluation of 53 DNA VariantsElena Bueno-Martínez, Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 16, 2019
Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case-Control StudyBrennan Decker, Jamie Allen, Craig Luccarini, et al.
Cancer Research|November 3, 2018
Differential Burden of Rare and Common Variants on Tumor Characteristics, Survival, and Mode of Detection in Breast CancerJingmei Li, Emilio Ugalde-Morales, Wei Xiong Wen, et al.
The Journal of Pathology|June 18, 2022
Minigene-based splicing analysis and ACMG/AMP-based tentative classification of 56 ATM variantsElena Bueno-Martínez, Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, et al.
Cancers|December 18, 2020
Comprehensive Functional Characterization and Clinical Interpretation of 20 Splice-Site Variants of the <i>RAD51C</i> GeneLara Sanoguera-Miralles, Alberto Valenzuela-Palomo, Elena Bueno-Martínez, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
CJEM|March 26, 2021
Spontaneous compartment syndrome in a patient with hemophilia BJoseph Levi, Tara Stansbury, Matthew D Marschall, et al.
Journal of the American Society for Mass Spectrometry|April 16, 2023
MALDI IMS-Derived Molecular Contour Maps: Augmenting Histology Whole-Slide ImagesKavya Sharman, Nathan Heath Patterson, Lukasz G Migas, et al.
BMC Genomics|June 6, 2023
SUsPECT: a pipeline for variant effect prediction based on custom long-read transcriptomes for improved clinical variant annotationRenee Salz, Nuno Saraiva-Agostinho, Emil Vorsteveld, et al.
Human Molecular Genetics|January 12, 2018
Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genesXingyi Guo, Jiajun Shi, Qiuyin Cai, et al.
Journal of Medical Genetics|August 6, 2017
Rare, protein-truncating variants in <i>ATM</i>, <i>CHEK2</i> and <i>PALB2</i>, but not <i>XRCC2</i>, are associated with increased breast cancer risksBrennan Decker, Jamie Allen, Craig Luccarini, et al.
Cancers|July 2, 2021
<i>RAD51D</i> Aberrant Splicing in Breast Cancer: Identification of Splicing Regulatory Elements and Minigene-Based Evaluation of 53 DNA VariantsElena Bueno-Martínez, Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 16, 2019
Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case-Control StudyBrennan Decker, Jamie Allen, Craig Luccarini, et al.
Cancer Research|November 3, 2018
Differential Burden of Rare and Common Variants on Tumor Characteristics, Survival, and Mode of Detection in Breast CancerJingmei Li, Emilio Ugalde-Morales, Wei Xiong Wen, et al.
The Journal of Pathology|June 18, 2022
Minigene-based splicing analysis and ACMG/AMP-based tentative classification of 56 ATM variantsElena Bueno-Martínez, Lara Sanoguera-Miralles, Alberto Valenzuela-Palomo, et al.
Cancers|December 18, 2020
Comprehensive Functional Characterization and Clinical Interpretation of 20 Splice-Site Variants of the <i>RAD51C</i> GeneLara Sanoguera-Miralles, Alberto Valenzuela-Palomo, Elena Bueno-Martínez, et al.
Pageof 5