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Matthias Haimel

Showing results (21-30 of 28) with videos related to

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Nature Communications|July 14, 2017
Platelet function is modified by common sequence variation in megakaryocyte super enhancersRomina Petersen, John J Lambourne, Biola M Javierre, et al.
American Journal of Respiratory and Critical Care Medicine|October 30, 2019
Characterization of <i>GDF2</i> Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial HypertensionJoshua Hodgson, Emilia M Swietlik, Richard M Salmon, et al.
Nature Communications|April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertensionStefan Gräf, Matthias Haimel, Marta Bleda, et al.
Nature|June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.
Cell|November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex DiseaseWilliam J Astle, Heather Elding, Tao Jiang, et al.
Genome Research|September 20, 2011
Assemblathon 1: a competitive assessment of de novo short read assembly methodsDent Earl, Keith Bradnam, John St John, et al.
Gigascience|July 23, 2013
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate speciesKeith R Bradnam, Joseph N Fass, Anton Alexandrov, et al.
The Lancet. Respiratory Medicine|December 12, 2018
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysisChristopher J Rhodes, Ken Batai, Marta Bleda, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Nature Communications|July 14, 2017
Platelet function is modified by common sequence variation in megakaryocyte super enhancersRomina Petersen, John J Lambourne, Biola M Javierre, et al.
American Journal of Respiratory and Critical Care Medicine|October 30, 2019
Characterization of <i>GDF2</i> Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial HypertensionJoshua Hodgson, Emilia M Swietlik, Richard M Salmon, et al.
Nature Communications|April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertensionStefan Gräf, Matthias Haimel, Marta Bleda, et al.
Nature|June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health systemErnest Turro, William J Astle, Karyn Megy, et al.
Cell|November 19, 2016
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex DiseaseWilliam J Astle, Heather Elding, Tao Jiang, et al.
Genome Research|September 20, 2011
Assemblathon 1: a competitive assessment of de novo short read assembly methodsDent Earl, Keith Bradnam, John St John, et al.
Gigascience|July 23, 2013
Assemblathon 2: evaluating de novo methods of genome assembly in three vertebrate speciesKeith R Bradnam, Joseph N Fass, Anton Alexandrov, et al.
The Lancet. Respiratory Medicine|December 12, 2018
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysisChristopher J Rhodes, Ken Batai, Marta Bleda, et al.
Pageof 3