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Cecily Q Bernales

Showing results (11-20 of 27) with videos related to

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European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Neurobiology of Aging|October 22, 2013
SLC1A2 rs3794087 does not associate with essential tremorJay P Ross, Sruti Rayaprolu, Cecily Q Bernales, et al.
Human Mutation|March 23, 2017
Purinergic receptors P2RX4 and P2RX7 in familial multiple sclerosisA Dessa Sadovnick, Ben J Gu, Anthony L Traboulsee, et al.
Neuron|October 21, 2016
Case-Control Studies Are Not Familial StudiesZhe Wang, A Dessa Sadovnick, Anthony L Traboulsee, et al.
JCO Precision Oncology|May 4, 2022
Genomic Features of Lung-Recurrent Hormone-Sensitive Prostate CancerNicolette M Fonseca, Kim Van der Eecken, Cameron Herberts, et al.
Neuron|June 3, 2016
Nuclear Receptor NR1H3 in Familial Multiple SclerosisZhe Wang, A Dessa Sadovnick, Anthony L Traboulsee, et al.
NPJ Precision Oncology|March 14, 2023
A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomesElie J Ritch, Cameron Herberts, Evan W Warner, et al.
NPJ Precision Oncology|June 13, 2025
Clonal hematopoiesis in metastatic urothelial and renal cell carcinomaAslı D Munzur, Jack V W Bacon, Francine Fishbein, et al.
Cancer Research|December 9, 2024
Plasma Cell-Free DNA Chromatin Immunoprecipitation Profiling Depicts Phenotypic and Clinical Heterogeneity in Advanced Prostate CancerJoonatan Sipola, Aslı D Munzur, Edmond M Kwan, et al.
Nature|July 21, 2022
Deep whole-genome ctDNA chronology of treatment-resistant prostate cancerCameron Herberts, Matti Annala, Joonatan Sipola, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|August 14, 2014
VPS35 and DNAJC13 disease-causing variants in essential tremorAlex Rajput, Jay P Ross, Cecily Q Bernales, et al.
Neurobiology of Aging|October 22, 2013
SLC1A2 rs3794087 does not associate with essential tremorJay P Ross, Sruti Rayaprolu, Cecily Q Bernales, et al.
Human Mutation|March 23, 2017
Purinergic receptors P2RX4 and P2RX7 in familial multiple sclerosisA Dessa Sadovnick, Ben J Gu, Anthony L Traboulsee, et al.
Neuron|October 21, 2016
Case-Control Studies Are Not Familial StudiesZhe Wang, A Dessa Sadovnick, Anthony L Traboulsee, et al.
JCO Precision Oncology|May 4, 2022
Genomic Features of Lung-Recurrent Hormone-Sensitive Prostate CancerNicolette M Fonseca, Kim Van der Eecken, Cameron Herberts, et al.
Neuron|June 3, 2016
Nuclear Receptor NR1H3 in Familial Multiple SclerosisZhe Wang, A Dessa Sadovnick, Anthony L Traboulsee, et al.
NPJ Precision Oncology|March 14, 2023
A generalizable machine learning framework for classifying DNA repair defects using ctDNA exomesElie J Ritch, Cameron Herberts, Evan W Warner, et al.
NPJ Precision Oncology|June 13, 2025
Clonal hematopoiesis in metastatic urothelial and renal cell carcinomaAslı D Munzur, Jack V W Bacon, Francine Fishbein, et al.
Cancer Research|December 9, 2024
Plasma Cell-Free DNA Chromatin Immunoprecipitation Profiling Depicts Phenotypic and Clinical Heterogeneity in Advanced Prostate CancerJoonatan Sipola, Aslı D Munzur, Edmond M Kwan, et al.
Nature|July 21, 2022
Deep whole-genome ctDNA chronology of treatment-resistant prostate cancerCameron Herberts, Matti Annala, Joonatan Sipola, et al.
Pageof 3