Author

Gad Hatem

Lund UniversityORCID 0000-0003-1221-4981Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Cancer Biology· 1 Genomics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 5 Approach:statistical model· 4 Assay:bulk RNA-seq· 3 Research Focus:differential expression· 3 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Research Focus:GWAS / association mapping· 2 Research Focus:cancer & tumor microenvironment· 1

Frequent Co-Authors

Rashmi B. PrasadiD· 4 shared Olof AsplundiD· 3 shared Emma AhlqvistiD· 2 shared Isabella ArtneriD· 2 shared Leif GroopiD· 2 shared Ola HanssoniD· 2 shared Tiinamaija TuomiiD· 2 shared Ulrika Krus· 2 shared

Activity by Year

2020-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 35 mutual co-author links

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4 shared papersGenetic & Genomic Medicine

Rashmi B. PrasadORCID

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Author profile →

5 papers

Recent·Most cited

Genetic & Genomic MedicineNature CommunicationsPeer-reviewedJun 1, 2026

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

Caroline Brito Nunes, Valentina Rukins, Aminata Hallimat Cissé…·Gunn-Helen Moen

The paper conducts a multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycemic traits, identifying novel loci and highlighting limited pregnancy-specific genetic effects.

1 citation

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintMay 7, 2026

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

F. Kyle Satterstrom, Kiana Jodeiry, Behrang Mahjani…·David J. Cutler

The paper develops a model to analyze X-linked rare variation in ASD, identifying 9 genes associated with ASD and explaining how X-linked variation could contribute to sex-differential prevalence.

1 citation

humanwhole-exome sequencing

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Cancer BiologyCancer MedicinePeer-reviewedApr 30, 2024

E2F transcription factors promote tumorigenicity in pancreatic ductal adenocarcinoma

Ludivine Bertonnier‐Brouty, Jonas Andersson, Tuomas Kaprio…·Isabella Artner

This study identifies E2F1 and E2F8 as key regulators promoting cell proliferation, survival, and migration in pancreatic ductal adenocarcinoma.

6 citations

humanbulk RNA-seq

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Molecular BiologyLife Science AlliancePeer-reviewedAug 10, 2022

Islet Gene View - a tool to facilitate islet research

Olof Asplund, Petter Storm, Vikash Chandra…·Rashmi B. Prasad

The paper introduces Islet Gene View (IGW), a platform that integrates gene expression and phenotypic data from pancreatic islets to explore T2D-related gene expression changes and their functional implications.

53 citationstop 1%

humanbulk RNA-seq

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GenomicsNature CommunicationsPeer-reviewedSep 30, 2020

Influence of genetic variants on gene expression in human pancreatic islets - implications for type 2 diabetes

Ana Viñuela, Arushi Varshney, Martijn van de Bunt…·Mark I. McCarthy

The paper investigates how genetic variants affect gene expression in human pancreatic islets and identifies candidate genes linked to type 2 diabetes.

152 citationstop 1%

humanbulk RNA-seq

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