Gad Hatem

Malmoe, M, Sweden

Last Updated: 09/26/2026

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Found 14 publications

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorder.

Journal: medRxiv : the preprint server for health sciences

Published: May 18, 2026

Sex-specific signatures of fetal programming for gestational diabetes mellitus in umbilical cord: A cohort study from Tanzania.

Sex-specific signatures of fetal programming for gestational diabetes mellitus in umbilical cord: A cohort study from Tanzania.

Journal: BMC medicine

Published: January 25, 2026

Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects.

Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects.

Journal: Nature communications

Published: December 14, 2025

Parent-of-origin effects in the life-course evolution of cardiometabolic traits.

Parent-of-origin effects in the life-course evolution of cardiometabolic traits.

Journal: Diabetologia

Published: December 13, 2024

E2F transcription factors promote tumorigenicity in pancreatic ductal adenocarcinoma.

E2F transcription factors promote tumorigenicity in pancreatic ductal adenocarcinoma.

Journal: Cancer medicine

Published: September 18, 2023

Genetic architecture of oral glucose-stimulated insulin release provides biological insights into type 2 diabetes aetiology.

Genetic architecture of oral glucose-stimulated insulin release provides biological insights into type 2 diabetes aetiology.

Journal: Nature metabolism

Published: July 30, 2023

Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake.

Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake.

Journal: Nature genetics

Published: August 04, 2022

Islet Gene View-a tool to facilitate islet research.

Islet Gene View-a tool to facilitate islet research.

Journal: Life science alliance

Published: January 19, 2022

Lipid-Associated Variants near ANGPTL3 and LPL Show Parent-of-Origin Specific Effects on Blood Lipid Levels and Obesity.

Lipid-Associated Variants near ANGPTL3 and LPL Show Parent-of-Origin Specific Effects on Blood Lipid Levels and Obesity.

Journal: Genes

Published: November 22, 2021

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.

Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.

Journal: Human molecular genetics

Published: November 11, 2021

Mapping the Cord Blood Transcriptome of Pregnancies Affected by Early Maternal Anemia to Identify Signatures of Fetal Programming.

Mapping the Cord Blood Transcriptome of Pregnancies Affected by Early Maternal Anemia to Identify Signatures of Fetal Programming.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 23, 2021

SCRT1 is a novel beta cell transcription factor with insulin regulatory properties.

SCRT1 is a novel beta cell transcription factor with insulin regulatory properties.

Journal: Molecular and cellular endocrinology

Published: June 05, 2020

Showing 1-12 of 14

Last Updated: 09/26/2026