Helmut Fuchs

Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome

Single-cell, whole-embryo phenotyping of mammalian developmental disorders

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain

Identifying causal serum protein–cardiometabolic trait relationships using whole genome sequencing

A resource of targeted mutant mouse lines for 5,061 genes

Offspring born to influenza A virus infected pregnant mice have increased susceptibility to viral and bacterial infections in early life

Human and mouse essentiality screens as a resource for disease gene discovery

Irp2 regulates insulin production through iron-mediated Cdkal1-catalyzed tRNA modification

Physiological relevance of the neuronal isoform of inositol-1,4,5-trisphosphate 3-kinases in mice

Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice

Bacterial encapsulins as orthogonal compartments for mammalian cell engineering

RNase H2 Loss in Murine Astrocytes Results in Cellular Defects Reminiscent of Nucleic Acid-Mediated Autoinflammation

Prevalence of sexual dimorphism in mammalian phenotypic traits

Noncanonical thyroid hormone signaling mediates cardiometabolic effects in vivo

Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice

High-throughput discovery of novel developmental phenotypes

Cardioprotection and lifespan extension by the natural polyamine spermidine

Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease

CIP2A Promotes T-Cell Activation and Immune Response to Listeria monocytogenes Infection

MFAP4 Promotes Vascular Smooth Muscle Migration, Proliferation and Accelerates Neointima Formation

Aberrant methylation of t <scp>RNA</scp> s links cellular stress to neuro‐developmental disorders

Mitochondrial Dysfunction and Decrease in Body Weight of a Transgenic Knock-in Mouse Model for TDP-43

Abnormal Brain Iron Metabolism in Irp2 Deficient Mice Is Associated with Mild Neurological and Behavioral Impairments

<scp>M</scp>i<scp>R</scp>‐34a deficiency accelerates medulloblastoma formation <i>in vivo</i>

Rapamycin extends murine lifespan but has limited effects on aging

IFIT2 Is an Effector Protein of Type I IFN–Mediated Amplification of Lipopolysaccharide (LPS)-Induced TNF-α Secretion and LPS-Induced Endotoxin Shock

High Mobility Group N Proteins Modulate the Fidelity of the Cellular Transcriptional Profile in a Tissue- and Variant-specific Manner