Decheng Ren

Shanghai Key Laboratory Of Embryo Original Diseases
Shanghai, China

Last Updated: 09/26/2026

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Found 65 publications

De novo variants in MAGED1 suggest a role in intellectual disability pathogenesis.

De novo variants in MAGED1 suggest a role in intellectual disability pathogenesis.

Journal: Neurobiology of disease

Published: February 12, 2026

POMC neuron METTL14/m6A/YTHDC1/YTHDF2 pathways safeguard energy balance, body weight, and metabolism.

POMC neuron METTL14/m6A/YTHDC1/YTHDF2 pathways safeguard energy balance, body weight, and metabolism.

Journal: Nature communications

Published: July 20, 2025

Pathogenic mutations disrupt stress granules assembly in patients with DDX3X neurodevelopmental disorder.

Pathogenic mutations disrupt stress granules assembly in patients with DDX3X neurodevelopmental disorder.

Journal: Human molecular genetics

Published: April 13, 2025

Adipose m6A reader YTHDF2 promotes obesity, insulin resistance, and liver steatosis by suppressing β-adrenergic signaling and lipolysis.

Adipose m6A reader YTHDF2 promotes obesity, insulin resistance, and liver steatosis by suppressing β-adrenergic signaling and lipolysis.

Journal: Cell reports

Published: March 13, 2025

The role of CSNK1A1 and its de novo mutations in infantile spasms syndrome.

The role of CSNK1A1 and its de novo mutations in infantile spasms syndrome.

Journal: Human molecular genetics

Published: December 24, 2024

METTL14-Induced M6A Methylation Increases G6pc Biosynthesis, Hepatic Glucose Production and Metabolic Disorders in Obesity.

METTL14-Induced M6A Methylation Increases G6pc Biosynthesis, Hepatic Glucose Production and Metabolic Disorders in Obesity.

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

Published: December 21, 2024

Identification of Schizophrenia-Risk Regulatory Variant rs1399178 in the Non-coding Region With Its Impact on NRF1 Binding.

Identification of Schizophrenia-Risk Regulatory Variant rs1399178 in the Non-coding Region With Its Impact on NRF1 Binding.

Journal: CNS neuroscience & therapeutics

Published: September 19, 2024

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Journal: The Journal of clinical investigation

Published: August 20, 2024

Unraveling schizophrenia's genetic complexity through advanced causal inference and chromatin 3D conformation.

Unraveling schizophrenia's genetic complexity through advanced causal inference and chromatin 3D conformation.

Journal: Schizophrenia research

Published: January 18, 2024

Adipose METTL14-Elicited N6 -Methyladenosine Promotes Obesity, Insulin Resistance, and NAFLD Through Suppressing β Adrenergic Signaling and Lipolysis.

Adipose METTL14-Elicited N6 -Methyladenosine Promotes Obesity, Insulin Resistance, and NAFLD Through Suppressing β Adrenergic Signaling and Lipolysis.

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

Published: March 13, 2023

TULP4, a novel E3 ligase gene, participates in neuronal migration as a candidate in schizophrenia.

TULP4, a novel E3 ligase gene, participates in neuronal migration as a candidate in schizophrenia.

Journal: CNS neuroscience & therapeutics

Published: March 07, 2023

Reduction of mRNA m6A associates with glucose metabolism via YTHDC1 in human and mice.

Reduction of mRNA m6A associates with glucose metabolism via YTHDC1 in human and mice.

Journal: Diabetes research and clinical practice

Published: January 10, 2023

Showing 1-12 of 65

Last Updated: 09/26/2026