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Epilepsia
|
November 21, 2014
Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-convergence on axonal guidance
Sanne S Kaalund, Morten T Venø, Mads Bak, et al.
Journal of Medical Genetics
|
July 27, 2014
Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes
Malene B Rasmussen, Jakob V Nielsen, Charles M Lourenço, et al.
Plos Genetics
|
November 13, 2018
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization
Lusine Nazaryan-Petersen, Jesper Eisfeldt, Maria Pettersson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 14, 2014
Immature truncated O-glycophenotype of cancer directly induces oncogenic features
Prakash Radhakrishnan, Sally Dabelsteen, Frey Brus Madsen, et al.
American Journal of Human Genetics
|
May 29, 2018
Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes
Christina Halgren, Nete M Nielsen, Lusine Nazaryan-Petersen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 14, 2022
DNA methylation episignature in Gabriele-de Vries syndrome
Florian Cherik, Jack Reilly, Jennifer Kerkhof, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 15, 2025
Childhood Cancer Predisposition and Evolutionary Constraints: Novel lessons from Germline Genomes from 1,127 Children with Cancer
Ulrik Kristoffer Stoltze, Thomas van Overeem Hansen, Jon Foss-Skiftesvik, et al.
Plos Genetics
|
September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Nature
|
February 12, 2010
Ancient human genome sequence of an extinct Palaeo-Eskimo
Morten Rasmussen, Yingrui Li, Stinus Lindgreen, et al.
Plos Genetics
|
July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Page
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Search research articles
Search
Showing results (71-80 of 84) with videos related to
Sort By:
Page
of 9
Epilepsia
|
November 21, 2014
Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-convergence on axonal guidance
Sanne S Kaalund, Morten T Venø, Mads Bak, et al.
Journal of Medical Genetics
|
July 27, 2014
Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes
Malene B Rasmussen, Jakob V Nielsen, Charles M Lourenço, et al.
Plos Genetics
|
November 13, 2018
Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization
Lusine Nazaryan-Petersen, Jesper Eisfeldt, Maria Pettersson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 14, 2014
Immature truncated O-glycophenotype of cancer directly induces oncogenic features
Prakash Radhakrishnan, Sally Dabelsteen, Frey Brus Madsen, et al.
American Journal of Human Genetics
|
May 29, 2018
Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes
Christina Halgren, Nete M Nielsen, Lusine Nazaryan-Petersen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 14, 2022
DNA methylation episignature in Gabriele-de Vries syndrome
Florian Cherik, Jack Reilly, Jennifer Kerkhof, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
August 15, 2025
Childhood Cancer Predisposition and Evolutionary Constraints: Novel lessons from Germline Genomes from 1,127 Children with Cancer
Ulrik Kristoffer Stoltze, Thomas van Overeem Hansen, Jon Foss-Skiftesvik, et al.
Plos Genetics
|
September 21, 2021
Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
Nature
|
February 12, 2010
Ancient human genome sequence of an extinct Palaeo-Eskimo
Morten Rasmussen, Yingrui Li, Stinus Lindgreen, et al.
Plos Genetics
|
July 29, 2021
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
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of 9