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Plos One
|
June 30, 2009
Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array
Siim Sõber, Elin Org, Katrin Kepp, et al.
Human Molecular Genetics
|
March 24, 2009
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations
Elin Org, Susana Eyheramendy, Peeter Juhanson, et al.
American Journal of Human Genetics
|
February 7, 2015
COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency
Gloria Brea-Calvo, Tobias B Haack, Daniela Karall, et al.
The Journal of Clinical Investigation
|
November 17, 2020
Congenital heart disease risk loci identified by genome-wide association study in European patients
Harald Lahm, Meiwen Jia, Martina Dreßen, et al.
Heart Rhythm
|
July 4, 2020
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand
Pattarapong Makarawate, Charlotte Glinge, Apichai Khongphatthanayothin, et al.
Brain : a Journal of Neurology
|
April 30, 2025
Pleiotropic effects of MORC2 derive from its epigenetic signature
Fatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, et al.
Nature Communications
|
February 15, 2018
Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway
Elisa Benedetti, Maja Pučić-Baković, Toma Keser, et al.
Nature Communications
|
June 13, 2017
Genetic diagnosis of Mendelian disorders via RNA sequencing
Laura S Kremer, Daniel M Bader, Christian Mertes, et al.
Nature Genetics
|
July 29, 2008
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
Barbara Schormair, David Kemlink, Darina Roeske, et al.
Nature Communications
|
November 15, 2017
Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway
Elisa Benedetti, Maja Pučić-Baković, Toma Keser, et al.
Page
of 51
Search research articles
Search
Showing results (271-280 of 508) with videos related to
Sort By:
Page
of 51
Plos One
|
June 30, 2009
Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array
Siim Sõber, Elin Org, Katrin Kepp, et al.
Human Molecular Genetics
|
March 24, 2009
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations
Elin Org, Susana Eyheramendy, Peeter Juhanson, et al.
American Journal of Human Genetics
|
February 7, 2015
COQ4 mutations cause a broad spectrum of mitochondrial disorders associated with CoQ10 deficiency
Gloria Brea-Calvo, Tobias B Haack, Daniela Karall, et al.
The Journal of Clinical Investigation
|
November 17, 2020
Congenital heart disease risk loci identified by genome-wide association study in European patients
Harald Lahm, Meiwen Jia, Martina Dreßen, et al.
Heart Rhythm
|
July 4, 2020
Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand
Pattarapong Makarawate, Charlotte Glinge, Apichai Khongphatthanayothin, et al.
Brain : a Journal of Neurology
|
April 30, 2025
Pleiotropic effects of MORC2 derive from its epigenetic signature
Fatemeh Peymani, Tomohiro Ebihara, Dmitrii Smirnov, et al.
Nature Communications
|
February 15, 2018
Publisher Correction: Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway
Elisa Benedetti, Maja Pučić-Baković, Toma Keser, et al.
Nature Communications
|
June 13, 2017
Genetic diagnosis of Mendelian disorders via RNA sequencing
Laura S Kremer, Daniel M Bader, Christian Mertes, et al.
Nature Genetics
|
July 29, 2008
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome
Barbara Schormair, David Kemlink, Darina Roeske, et al.
Nature Communications
|
November 15, 2017
Network inference from glycoproteomics data reveals new reactions in the IgG glycosylation pathway
Elisa Benedetti, Maja Pučić-Baković, Toma Keser, et al.
Page
of 51