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John S Witte

Showing results (161-170 of 256) with videos related to

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Nature Communications|April 26, 2016
Identifying genetically driven clinical phenotypes using linear mixed modelsJonathan D Mosley, John S Witte, Emma K Larkin, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
The full spectrum of OCT1 (SLC22A1) mutations bridges transporter biophysics to drug pharmacogenomicsSook Wah Yee, Christian Macdonald, Darko Mitrovic, et al.
American Journal of Medical Genetics. Part A|April 22, 2022
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention StudySara R Rashkin, Mario Cleves, Gary M Shaw, et al.
Pediatrics|July 31, 2013
A genome-wide association study (GWAS) for bronchopulmonary dysplasiaHui Wang, Krystal R St Julien, David K Stevenson, et al.
Blood|October 3, 2015
MDS-associated somatic mutations and clonal hematopoiesis are common in idiopathic cytopenias of undetermined significanceBrian Kwok, Jeff M Hall, John S Witte, et al.
HGG Advances|February 6, 2025
Unraveling the genetic landscape of susceptibility to multiple primary cancersPooja Middha, Linda Kachuri, Jovia L Nierenberg, et al.
Medrxiv : the Preprint Server for Health Sciences|November 22, 2024
Unraveling the genetic landscape of susceptibility to multiple primary cancersPooja Middha, Linda Kachuri, Jovia L Nierenberg, et al.
Cancer Research|February 28, 2016
Mutational Landscape of Aggressive Prostate Tumors in African American MenKarla J Lindquist, Pamela L Paris, Thomas J Hoffmann, et al.
Molecular Cell|May 4, 2024
The full spectrum of SLC22 OCT1 mutations illuminates the bridge between drug transporter biophysics and pharmacogenomicsSook Wah Yee, Christian B Macdonald, Darko Mitrovic, et al.
International Journal of Cancer|June 22, 2019
A genome-wide association study of prostate cancer in LatinosZhaohui Du, Hannah Hopp, Sue A Ingles, et al.
Pageof 26

Showing results (161-170 of 256) with videos related to

Sort By:
Pageof 26
Nature Communications|April 26, 2016
Identifying genetically driven clinical phenotypes using linear mixed modelsJonathan D Mosley, John S Witte, Emma K Larkin, et al.
Biorxiv : the Preprint Server for Biology|June 19, 2023
The full spectrum of OCT1 (SLC22A1) mutations bridges transporter biophysics to drug pharmacogenomicsSook Wah Yee, Christian Macdonald, Darko Mitrovic, et al.
American Journal of Medical Genetics. Part A|April 22, 2022
A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention StudySara R Rashkin, Mario Cleves, Gary M Shaw, et al.
Pediatrics|July 31, 2013
A genome-wide association study (GWAS) for bronchopulmonary dysplasiaHui Wang, Krystal R St Julien, David K Stevenson, et al.
Blood|October 3, 2015
MDS-associated somatic mutations and clonal hematopoiesis are common in idiopathic cytopenias of undetermined significanceBrian Kwok, Jeff M Hall, John S Witte, et al.
HGG Advances|February 6, 2025
Unraveling the genetic landscape of susceptibility to multiple primary cancersPooja Middha, Linda Kachuri, Jovia L Nierenberg, et al.
Medrxiv : the Preprint Server for Health Sciences|November 22, 2024
Unraveling the genetic landscape of susceptibility to multiple primary cancersPooja Middha, Linda Kachuri, Jovia L Nierenberg, et al.
Cancer Research|February 28, 2016
Mutational Landscape of Aggressive Prostate Tumors in African American MenKarla J Lindquist, Pamela L Paris, Thomas J Hoffmann, et al.
Molecular Cell|May 4, 2024
The full spectrum of SLC22 OCT1 mutations illuminates the bridge between drug transporter biophysics and pharmacogenomicsSook Wah Yee, Christian B Macdonald, Darko Mitrovic, et al.
International Journal of Cancer|June 22, 2019
A genome-wide association study of prostate cancer in LatinosZhaohui Du, Hannah Hopp, Sue A Ingles, et al.
Pageof 26