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Matthew J Ferber

Showing results (21-30 of 41) with videos related to

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Oncogene|October 17, 2003
Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinomaMatthew J Ferber, Erik C Thorland, Antoinette A T P Brink, et al.
Hereditary Cancer in Clinical Practice|February 5, 2015
High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case reportMaria Fernanda Noriega-Iriondo, Gerardo Colon-Otero, Benjamin R Kipp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity FrameworkBryce A Seifert, Jennifer L McGlaughon, Sarah A Jackson, et al.
Genetics in Medicine Open|December 13, 2024
Combining rare and common genetic variants improves population risk stratification for breast cancerAlexandre Bolze, Daniel Kiser, Kelly M Schiabor Barrett, et al.
Mayo Clinic Proceedings|June 20, 2014
Genomic medicine and incidental findings: balancing actionability and patient autonomyJennifer B McCormick, Richard R Sharp, Gianrico Farrugia, et al.
The Journal of Molecular Diagnostics : JMD|March 8, 2016
Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping CascadeYuan Ji, Jennifer M Skierka, Joseph H Blommel, et al.
Mayo Clinic Proceedings|October 6, 2015
Whole-Exome Sequencing of 10 Scientists: Evaluation of the Process and OutcomesNoralane M Lindor, Kimberly A Schahl, Kiley J Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2021
One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementationStephen E Lincoln, Tina Hambuch, Justin M Zook, et al.
Mayo Clinic Proceedings|March 6, 2016
Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic ExperienceKonstantinos N Lazaridis, Kimberly A Schahl, Margot A Cousin, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Implementing individualized medicine into the medical practiceKonstantinos N Lazaridis, Tammy M McAllister, Dusica Babovic-Vuksanovic, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Oncogene|October 17, 2003
Preferential integration of human papillomavirus type 18 near the c-myc locus in cervical carcinomaMatthew J Ferber, Erik C Thorland, Antoinette A T P Brink, et al.
Hereditary Cancer in Clinical Practice|February 5, 2015
High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case reportMaria Fernanda Noriega-Iriondo, Gerardo Colon-Otero, Benjamin R Kipp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity FrameworkBryce A Seifert, Jennifer L McGlaughon, Sarah A Jackson, et al.
Genetics in Medicine Open|December 13, 2024
Combining rare and common genetic variants improves population risk stratification for breast cancerAlexandre Bolze, Daniel Kiser, Kelly M Schiabor Barrett, et al.
Mayo Clinic Proceedings|June 20, 2014
Genomic medicine and incidental findings: balancing actionability and patient autonomyJennifer B McCormick, Richard R Sharp, Gianrico Farrugia, et al.
The Journal of Molecular Diagnostics : JMD|March 8, 2016
Preemptive Pharmacogenomic Testing for Precision Medicine: A Comprehensive Analysis of Five Actionable Pharmacogenomic Genes Using Next-Generation DNA Sequencing and a Customized CYP2D6 Genotyping CascadeYuan Ji, Jennifer M Skierka, Joseph H Blommel, et al.
Mayo Clinic Proceedings|October 6, 2015
Whole-Exome Sequencing of 10 Scientists: Evaluation of the Process and OutcomesNoralane M Lindor, Kimberly A Schahl, Kiley J Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 19, 2021
One in seven pathogenic variants can be challenging to detect by NGS: an analysis of 450,000 patients with implications for clinical sensitivity and genetic test implementationStephen E Lincoln, Tina Hambuch, Justin M Zook, et al.
Mayo Clinic Proceedings|March 6, 2016
Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic ExperienceKonstantinos N Lazaridis, Kimberly A Schahl, Margot A Cousin, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Implementing individualized medicine into the medical practiceKonstantinos N Lazaridis, Tammy M McAllister, Dusica Babovic-Vuksanovic, et al.
Pageof 5