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R Quinlan

Showing results (331-340 of 347) with videos related to

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Gait & Posture|October 1, 2017
A "HOLTER" for Parkinson's disease: Validation of the ability to detect on-off states using the REMPARK systemÀngels Bayés, Albert Samá, Anna Prats, et al.
Oncotarget|August 18, 2015
Expression profiling of nuclear receptors in breast cancer identifies TLX as a mediator of growth and invasion in triple-negative breast cancerMeng-Lay Lin, Hetal Patel, Judit Remenyi, et al.
Nature Biotechnology|February 13, 2018
Nanopore sequencing and assembly of a human genome with ultra-long readsMiten Jain, Sergey Koren, Karen H Miga, et al.
Nature Genetics|March 10, 2015
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancersSuna Onengut-Gumuscu, Wei-Min Chen, Oliver Burren, et al.
Molecular Genetics & Genomic Medicine|February 4, 2022
Comprehensive variant calling from whole-genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic herniaThomas J Nicholas, Najla Al-Sweel, Andrew Farrell, et al.
JAMA Neurology|May 12, 2015
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence ProjectPaul L Auer, Mike Nalls, James F Meschia, et al.
Genome Research|September 9, 2008
Rapid whole-genome mutational profiling using next-generation sequencing technologiesDouglas R Smith, Aaron R Quinlan, Heather E Peckham, et al.
Nature Communications|February 7, 2018
Publisher Correction: Combating subclonal evolution of resistant cancer phenotypesSamuel W Brady, Jasmine A McQuerry, Yi Qiao, et al.
Nature Communications|November 3, 2017
Combating subclonal evolution of resistant cancer phenotypesSamuel W Brady, Jasmine A McQuerry, Yi Qiao, et al.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Pageof 35

Showing results (331-340 of 347) with videos related to

Sort By:
Pageof 35
Gait & Posture|October 1, 2017
A "HOLTER" for Parkinson's disease: Validation of the ability to detect on-off states using the REMPARK systemÀngels Bayés, Albert Samá, Anna Prats, et al.
Oncotarget|August 18, 2015
Expression profiling of nuclear receptors in breast cancer identifies TLX as a mediator of growth and invasion in triple-negative breast cancerMeng-Lay Lin, Hetal Patel, Judit Remenyi, et al.
Nature Biotechnology|February 13, 2018
Nanopore sequencing and assembly of a human genome with ultra-long readsMiten Jain, Sergey Koren, Karen H Miga, et al.
Nature Genetics|March 10, 2015
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancersSuna Onengut-Gumuscu, Wei-Min Chen, Oliver Burren, et al.
Molecular Genetics & Genomic Medicine|February 4, 2022
Comprehensive variant calling from whole-genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic herniaThomas J Nicholas, Najla Al-Sweel, Andrew Farrell, et al.
JAMA Neurology|May 12, 2015
Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence ProjectPaul L Auer, Mike Nalls, James F Meschia, et al.
Genome Research|September 9, 2008
Rapid whole-genome mutational profiling using next-generation sequencing technologiesDouglas R Smith, Aaron R Quinlan, Heather E Peckham, et al.
Nature Communications|February 7, 2018
Publisher Correction: Combating subclonal evolution of resistant cancer phenotypesSamuel W Brady, Jasmine A McQuerry, Yi Qiao, et al.
Nature Communications|November 3, 2017
Combating subclonal evolution of resistant cancer phenotypesSamuel W Brady, Jasmine A McQuerry, Yi Qiao, et al.
Nature Methods|August 4, 2025
The Platinum Pedigree: a long-read benchmark for genetic variantsZev Kronenberg, Cillian Nolan, David Porubsky, et al.
Pageof 35