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Thomas Meitinger

Showing results (321-330 of 508) with videos related to

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Hypertension (Dallas, Tex. : 1979)|August 9, 2017
Transcriptome-Wide Analysis Identifies Novel Associations With Blood PressureTanja Zeller, Claudia Schurmann, Katharina Schramm, et al.
Plos One|May 9, 2009
Genetic structure of Europeans: a view from the North-EastMari Nelis, Tõnu Esko, Reedik Mägi, et al.
Brain : a Journal of Neurology|May 21, 2013
β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulationSusan J Hayflick, Michael C Kruer, Allison Gregory, et al.
Nature Neuroscience|March 25, 2015
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementiaAxel Freischmidt, Thomas Wieland, Benjamin Richter, et al.
Cephalalgia : an International Journal of Headache|December 15, 2015
Gene-based pleiotropy across migraine with aura and migraine without aura patient groupsHuiying Zhao, Else Eising, Boukje de Vries, et al.
European Heart Journal|November 20, 2010
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23Jeanette Erdmann, Christina Willenborg, Janja Nahrstaedt, et al.
Molecular Systems Biology|September 27, 2012
Novel biomarkers for pre-diabetes identified by metabolomicsRui Wang-Sattler, Zhonghao Yu, Christian Herder, et al.
American Journal of Human Genetics|December 20, 2016
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe EncephalopathySamira Ait-El-Mkadem, Manal Dayem-Quere, Mirjana Gusic, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathyXiaowu Gai, Daniele Ghezzi, Mark A Johnson, et al.
Nature Genetics|March 24, 2009
Common variants at ten loci modulate the QT interval duration in the QTSCD StudyArne Pfeufer, Serena Sanna, Dan E Arking, et al.
Pageof 51

Showing results (321-330 of 508) with videos related to

Sort By:
Pageof 51
Hypertension (Dallas, Tex. : 1979)|August 9, 2017
Transcriptome-Wide Analysis Identifies Novel Associations With Blood PressureTanja Zeller, Claudia Schurmann, Katharina Schramm, et al.
Plos One|May 9, 2009
Genetic structure of Europeans: a view from the North-EastMari Nelis, Tõnu Esko, Reedik Mägi, et al.
Brain : a Journal of Neurology|May 21, 2013
β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulationSusan J Hayflick, Michael C Kruer, Allison Gregory, et al.
Nature Neuroscience|March 25, 2015
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementiaAxel Freischmidt, Thomas Wieland, Benjamin Richter, et al.
Cephalalgia : an International Journal of Headache|December 15, 2015
Gene-based pleiotropy across migraine with aura and migraine without aura patient groupsHuiying Zhao, Else Eising, Boukje de Vries, et al.
European Heart Journal|November 20, 2010
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23Jeanette Erdmann, Christina Willenborg, Janja Nahrstaedt, et al.
Molecular Systems Biology|September 27, 2012
Novel biomarkers for pre-diabetes identified by metabolomicsRui Wang-Sattler, Zhonghao Yu, Christian Herder, et al.
American Journal of Human Genetics|December 20, 2016
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe EncephalopathySamira Ait-El-Mkadem, Manal Dayem-Quere, Mirjana Gusic, et al.
American Journal of Human Genetics|September 3, 2013
Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathyXiaowu Gai, Daniele Ghezzi, Mark A Johnson, et al.
Nature Genetics|March 24, 2009
Common variants at ten loci modulate the QT interval duration in the QTSCD StudyArne Pfeufer, Serena Sanna, Dan E Arking, et al.
Pageof 51