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Enrique Audain

Showing results (11-20 of 28) with videos related to

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Clinical Epigenetics|June 13, 2019
DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMsKirstin Hoff, Marta Lemme, Anne-Karin Kahlert, et al.
Journal of Pharmaceutical and Biomedical Analysis|December 30, 2014
Bio-analytical method based on MALDI-MS analysis for the quantification of CIGB-300 anti-tumor peptide in human plasmaAnia Cabrales-Rico, Beatriz G de la Torre, Hilda E Garay, et al.
Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.
Journal of Proteome Research|April 23, 2025
Open-Source and FAIR Research Software for ProteomicsYasset Perez-Riverol, Wout Bittremieux, William S Noble, et al.
Nucleic Acids Research|November 6, 2018
The PRIDE database and related tools and resources in 2019: improving support for quantification dataYasset Perez-Riverol, Attila Csordas, Jingwen Bai, et al.
Genome Medicine|October 14, 2024
A validated heart-specific model for splice-disrupting variants in childhood heart diseaseRobert Lesurf, Jeroen Breckpot, Jade Bouwmeester, et al.
Nature Genetics|December 18, 2019
Loss of ADAMTS19 causes progressive non-syndromic heart valve diseaseFlorian Wünnemann, Asaf Ta-Shma, Christoph Preuss, et al.
NPJ Genomic Medicine|June 2, 2026
Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome studyEnrique Audain, Anna Wilsdon, Gregor Dombrowsky, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2022
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysmsEva S van Walree, Gregor Dombrowsky, Iris E Jansen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 22, 2020
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysmsEva S van Walree, Gregor Dombrowsky, Iris E Jansen, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Clinical Epigenetics|June 13, 2019
DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMsKirstin Hoff, Marta Lemme, Anne-Karin Kahlert, et al.
Journal of Pharmaceutical and Biomedical Analysis|December 30, 2014
Bio-analytical method based on MALDI-MS analysis for the quantification of CIGB-300 anti-tumor peptide in human plasmaAnia Cabrales-Rico, Beatriz G de la Torre, Hilda E Garay, et al.
Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.
Journal of Proteome Research|April 23, 2025
Open-Source and FAIR Research Software for ProteomicsYasset Perez-Riverol, Wout Bittremieux, William S Noble, et al.
Nucleic Acids Research|November 6, 2018
The PRIDE database and related tools and resources in 2019: improving support for quantification dataYasset Perez-Riverol, Attila Csordas, Jingwen Bai, et al.
Genome Medicine|October 14, 2024
A validated heart-specific model for splice-disrupting variants in childhood heart diseaseRobert Lesurf, Jeroen Breckpot, Jade Bouwmeester, et al.
Nature Genetics|December 18, 2019
Loss of ADAMTS19 causes progressive non-syndromic heart valve diseaseFlorian Wünnemann, Asaf Ta-Shma, Christoph Preuss, et al.
NPJ Genomic Medicine|June 2, 2026
Assessing the contribution of rare variants to congenital heart disease through a large-scale case-control exome studyEnrique Audain, Anna Wilsdon, Gregor Dombrowsky, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 8, 2022
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysmsEva S van Walree, Gregor Dombrowsky, Iris E Jansen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 22, 2020
Germline variants in HEY2 functional domains lead to congenital heart defects and thoracic aortic aneurysmsEva S van Walree, Gregor Dombrowsky, Iris E Jansen, et al.
Pageof 3