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Graham McLennan

Showing results (1-10 of 16) with videos related to

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Prenatal Diagnosis|July 18, 2020
Cell-free DNA screening in twin pregnancies: A more accurate and reliable screening toolJason Chibuk, Jill Rafalko, Theresa Boomer, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 2, 2024
Developing a Prospective Gestational Lyme Disease StudyGraham McLennan, Suzanne E Dale, Laura Gillim, et al.
Molecular Cytogenetics|June 10, 2023
Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarrayErica Soster, John Tynan, Clare Gibbons, et al.
Plos One|March 12, 2021
Application of mosaicism ratio to multifetal gestationsJill Rafalko, Samantha Caldwell, Erica Soster, et al.
Cancers|April 3, 2021
Early, On-Treatment Levels and Dynamic Changes of Genomic Instability in Circulating Tumor DNA Predict Response to Treatment and Outcome in Metastatic Breast Cancer PatientsAdriana Aguilar-Mahecha, Josiane Lafleur, Susie Brousse, et al.
American Journal of Obstetrics and Gynecology|February 23, 2016
Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variantsRoy B Lefkowitz, John A Tynan, Tong Liu, et al.
Molecular Cancer Therapeutics|December 8, 2018
Genome-Wide Sequencing of Cell-Free DNA Identifies Copy-Number Alterations That Can Be Used for Monitoring Response to Immunotherapy in Cancer PatientsTaylor J Jensen, Aaron M Goodman, Shumei Kato, et al.
Transplantation and Cellular Therapy|October 16, 2021
Assessing CAR T-Cell Therapy Response Using Genome-Wide Sequencing of Cell-Free DNA in Patients With B-Cell LymphomasAaron M Goodman, Kimberly A Holden, Ah-Reum Jeong, et al.
Molecular Cancer Therapeutics|September 1, 2021
Genome-wide Sequencing of Cell-free DNA Enables Detection of Copy-number Alterations in Patients with Cancer Where Tissue Biopsy is Not FeasibleTaylor J Jensen, Aaron M Goodman, Christopher K Ellison, et al.
Prenatal Diagnosis|April 18, 2013
Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasmaAmin R Mazloom, Željko Džakula, Paul Oeth, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Prenatal Diagnosis|July 18, 2020
Cell-free DNA screening in twin pregnancies: A more accurate and reliable screening toolJason Chibuk, Jill Rafalko, Theresa Boomer, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 2, 2024
Developing a Prospective Gestational Lyme Disease StudyGraham McLennan, Suzanne E Dale, Laura Gillim, et al.
Molecular Cytogenetics|June 10, 2023
Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarrayErica Soster, John Tynan, Clare Gibbons, et al.
Plos One|March 12, 2021
Application of mosaicism ratio to multifetal gestationsJill Rafalko, Samantha Caldwell, Erica Soster, et al.
Cancers|April 3, 2021
Early, On-Treatment Levels and Dynamic Changes of Genomic Instability in Circulating Tumor DNA Predict Response to Treatment and Outcome in Metastatic Breast Cancer PatientsAdriana Aguilar-Mahecha, Josiane Lafleur, Susie Brousse, et al.
American Journal of Obstetrics and Gynecology|February 23, 2016
Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variantsRoy B Lefkowitz, John A Tynan, Tong Liu, et al.
Molecular Cancer Therapeutics|December 8, 2018
Genome-Wide Sequencing of Cell-Free DNA Identifies Copy-Number Alterations That Can Be Used for Monitoring Response to Immunotherapy in Cancer PatientsTaylor J Jensen, Aaron M Goodman, Shumei Kato, et al.
Transplantation and Cellular Therapy|October 16, 2021
Assessing CAR T-Cell Therapy Response Using Genome-Wide Sequencing of Cell-Free DNA in Patients With B-Cell LymphomasAaron M Goodman, Kimberly A Holden, Ah-Reum Jeong, et al.
Molecular Cancer Therapeutics|September 1, 2021
Genome-wide Sequencing of Cell-free DNA Enables Detection of Copy-number Alterations in Patients with Cancer Where Tissue Biopsy is Not FeasibleTaylor J Jensen, Aaron M Goodman, Christopher K Ellison, et al.
Prenatal Diagnosis|April 18, 2013
Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasmaAmin R Mazloom, Željko Džakula, Paul Oeth, et al.
Pageof 2