Marc Sultan

Basel, BS, Switzerland

Last Updated: 09/26/2026

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Found 32 publications

Spatial transcriptomics and single-nucleus RNA sequencing reveal rAAV2- and rAAV9-specific transduction signatures in the mouse liver.

Spatial transcriptomics and single-nucleus RNA sequencing reveal rAAV2- and rAAV9-specific transduction signatures in the mouse liver.

Journal: Gene therapy
Published: April 16, 2025

Mini Review: Spatial Transcriptomics to Decode the Central Nervous System.

Mini Review: Spatial Transcriptomics to Decode the Central Nervous System.

Journal: Toxicologic pathology
Published: March 22, 2025

Comparison of single-cell RNA-seq methods to enable transcriptome profiling of neutrophils in clinical samples.

Comparison of single-cell RNA-seq methods to enable transcriptome profiling of neutrophils in clinical samples.

Journal: Cell reports methods
Published: October 24, 2024

A Simple, Quick, and Partially Automated Protocol for the Isolation of Single Nuclei from Frozen Mammalian Tissues for Single Nucleus Sequencing.

A Simple, Quick, and Partially Automated Protocol for the Isolation of Single Nuclei from Frozen Mammalian Tissues for Single Nucleus Sequencing.

Journal: Journal of visualized experiments : JoVE
Published: August 14, 2023

Profiling the heterogeneity of colorectal cancer consensus molecular subtypes using spatial transcriptomics.

Profiling the heterogeneity of colorectal cancer consensus molecular subtypes using spatial transcriptomics.

Journal: NPJ precision oncology
Published: February 24, 2023

TET2-Driven Clonal Hematopoiesis and Response to Canakinumab: An Exploratory Analysis of the CANTOS Randomized Clinical Trial.

TET2-Driven Clonal Hematopoiesis and Response to Canakinumab: An Exploratory Analysis of the CANTOS Randomized Clinical Trial.

Journal: JAMA cardiology
Published: April 06, 2022

Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains.

Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains.

Journal: Journal of clinical immunology
Published: February 17, 2022

Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study.

Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study.

Journal: Scientific data
Published: March 23, 2021

Full exome sequencing of 11 families with Hidradenitis suppurativa.

Full exome sequencing of 11 families with Hidradenitis suppurativa.

Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: May 26, 2020

Detection of CSF1 rearrangements deleting the 3' UTR in tenosynovial giant cell tumors.

Detection of CSF1 rearrangements deleting the 3' UTR in tenosynovial giant cell tumors.

Journal: Genes, chromosomes & cancer
Published: July 17, 2019

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing.

Journal: Nature biotechnology
Published: May 02, 2019

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing.

Journal: Nature biotechnology
Published: September 26, 2018
Showing 1-12 of 32

Last Updated: 09/26/2026