Marten Jager
Berlin, BE 10117, Germany
Last Updated: 09/26/2026
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Found 18 publications
Small intestinal neuroendocrine tumors lack early genomic drivers, acquire DNA repair defects and harbor hallmarks of low REST expression.
Journal: Scientific reports
Published: December 08, 2024
Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid features.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 14, 2022
Combining callers improves the detection of copy number variants from whole-genome sequencing.
Journal: European journal of human genetics : EJHG
Published: November 18, 2020
Live-cell imaging of circadian clock protein dynamics in CRISPR-generated knock-in cells.
Journal: Nature communications
Published: May 27, 2020
Complement and inflammasome overactivation mediates paroxysmal nocturnal hemoglobinuria with autoinflammation.
Journal: The Journal of clinical investigation
Published: July 19, 2018
Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation.
Journal: Scientific reports
Published: May 25, 2018
An integrative systems approach identifies novel candidates in Marfan syndrome-related pathophysiology.
Journal: Journal of cellular and molecular medicine
Published: May 20, 2018
Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis.
Journal: Leukemia
Published: September 01, 2017
Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis.
Journal: Genome medicine
Published: August 02, 2017
De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.
Journal: American journal of human genetics
Published: May 19, 2017
L1Base 2: more retrotransposition-active LINE-1s, more mammalian genomes.
Journal: Nucleic acids research
Published: August 13, 2016
Alternate-locus aware variant calling in whole genome sequencing.
Journal: Genome medicine
Published: August 08, 2016
Last Updated: 09/26/2026