Christian F. Becker

Koeln, NW, Germany

Last Updated: 09/26/2026

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Found 76 publications

A biallelic MRPL42 variant causes a combined oxidative phosphorylation deficiency syndrome revealed by multi-omics.

A biallelic MRPL42 variant causes a combined oxidative phosphorylation deficiency syndrome revealed by multi-omics.

Journal: NPJ genomic medicine

Published: November 17, 2025

A bioinspired microdevice unifying energy storage and actuation through hydration control.

A bioinspired microdevice unifying energy storage and actuation through hydration control.

Journal: Nature communications

Published: September 03, 2025

Chromosome-scale genome dynamics reveal signatures of independent haplotype evolution in the ancient asexual mite Platynothrus peltifer.

Chromosome-scale genome dynamics reveal signatures of independent haplotype evolution in the ancient asexual mite Platynothrus peltifer.

Journal: Science advances

Published: January 24, 2025

Albumin nanocapsules and nanocrystals for efficient intracellular drug release.

Albumin nanocapsules and nanocrystals for efficient intracellular drug release.

Journal: Nanoscale horizons

Published: August 29, 2024

An Atomistic View on the Mechanism of Diatom Peptide-Guided Biomimetic Silica Formation.

An Atomistic View on the Mechanism of Diatom Peptide-Guided Biomimetic Silica Formation.

Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)

Published: February 02, 2024

Noninvasive minimal residual disease assessment in relapsed/refractory large B-cell lymphoma using digital droplet PCR.

Noninvasive minimal residual disease assessment in relapsed/refractory large B-cell lymphoma using digital droplet PCR.

Journal: European journal of haematology

Published: December 30, 2023

Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia.

Biallelic loss-of-function variants of ZFTRAF1 cause neurodevelopmental disorder with microcephaly and hypotonia.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 31, 2023

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.

Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions.

Journal: Genome medicine

Published: March 15, 2023

Temporal disturbance of a model stream ecosystem by high microbial diversity from treated wastewater.

Temporal disturbance of a model stream ecosystem by high microbial diversity from treated wastewater.

Journal: MicrobiologyOpen

Published: November 22, 2022

Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability.

Whole-Exome Sequencing of Pakistani Consanguineous Families Identified Pathogenic Variants in Genes of Intellectual Disability.

Journal: Genes

Published: October 30, 2022

Understanding Self-Assembly of Silica-Precipitating Peptides to Control Silica Particle Morphology.

Understanding Self-Assembly of Silica-Precipitating Peptides to Control Silica Particle Morphology.

Journal: Advanced materials (Deerfield Beach, Fla.)

Published: August 19, 2022

Full-Length Spatial Transcriptomics Reveals the Unexplored Isoform Diversity of the Myocardium Post-MI.

Full-Length Spatial Transcriptomics Reveals the Unexplored Isoform Diversity of the Myocardium Post-MI.

Journal: Frontiers in genetics

Published: April 04, 2022

Showing 1-12 of 76

Last Updated: 09/26/2026