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Linda Rodgers

Showing results (21-30 of 36) with videos related to

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Nature|March 15, 2011
Tumour evolution inferred by single-cell sequencingNicholas Navin, Jude Kendall, Jennifer Troge, et al.
Genome Research|November 12, 2009
Inferring tumor progression from genomic heterogeneityNicholas Navin, Alexander Krasnitz, Linda Rodgers, et al.
Journal of Genetic Counseling|February 26, 2022
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastrointestinal CancerRachel Hodan, Linda Rodgers-Fouche, Sanjeevani Arora, et al.
Neuron|June 11, 2011
Rare de novo and transmitted copy-number variation in autistic spectrum disordersDan Levy, Michael Ronemus, Boris Yamrom, et al.
Genome Research|April 11, 2015
Optimizing sparse sequencing of single cells for highly multiplex copy number profilingTimour Baslan, Jude Kendall, Brian Ward, et al.
Research Connections|April 30, 2026
Feasibility and acceptability of an electronic decision aid for genetic testing in ovarian and pancreatic cancer patientsDanielle A Lynch, Sarah Wiser, Devanshi Patel, et al.
JCO Precision Oncology|October 28, 2023
Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice SurveyLinda Rodgers-Fouche, Sanjeevani Arora, Charité Ricker, et al.
Frontiers in Oncology|June 9, 2023
Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice surveyKathryn A Mraz, Rachel Hodan, Linda Rodgers-Fouche, et al.
Familial Cancer|June 21, 2023
Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal CancerRachel Hodan, Linda Rodgers-Fouche, Anu Chittenden, et al.
Genome Research|September 17, 2003
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variationRobert Lucito, John Healy, Joan Alexander, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Nature|March 15, 2011
Tumour evolution inferred by single-cell sequencingNicholas Navin, Jude Kendall, Jennifer Troge, et al.
Genome Research|November 12, 2009
Inferring tumor progression from genomic heterogeneityNicholas Navin, Alexander Krasnitz, Linda Rodgers, et al.
Journal of Genetic Counseling|February 26, 2022
Patterns of germline and somatic testing after universal tumor screening for Lynch syndrome: A clinical practice survey of active members of the Collaborative Group of the Americas on Inherited Gastrointestinal CancerRachel Hodan, Linda Rodgers-Fouche, Sanjeevani Arora, et al.
Neuron|June 11, 2011
Rare de novo and transmitted copy-number variation in autistic spectrum disordersDan Levy, Michael Ronemus, Boris Yamrom, et al.
Genome Research|April 11, 2015
Optimizing sparse sequencing of single cells for highly multiplex copy number profilingTimour Baslan, Jude Kendall, Brian Ward, et al.
Research Connections|April 30, 2026
Feasibility and acceptability of an electronic decision aid for genetic testing in ovarian and pancreatic cancer patientsDanielle A Lynch, Sarah Wiser, Devanshi Patel, et al.
JCO Precision Oncology|October 28, 2023
Exploring Stakeholders' Perspectives on Implementing Universal Germline Testing for Colorectal Cancer: Findings From a Clinical Practice SurveyLinda Rodgers-Fouche, Sanjeevani Arora, Charité Ricker, et al.
Frontiers in Oncology|June 9, 2023
Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice surveyKathryn A Mraz, Rachel Hodan, Linda Rodgers-Fouche, et al.
Familial Cancer|June 21, 2023
Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal CancerRachel Hodan, Linda Rodgers-Fouche, Anu Chittenden, et al.
Genome Research|September 17, 2003
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variationRobert Lucito, John Healy, Joan Alexander, et al.
Pageof 4