Flip M. Mulder

Utrecht, UT 3584CX, Netherlands

Last Updated: 09/26/2026

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Found 11 publications

The Lettuce Expression Browser: from lab to LEB.

The Lettuce Expression Browser: from lab to LEB.

Journal: The Plant journal : for cell and molecular biology
Published: October 27, 2025

Lactuca super-pangenome reduces bias towards reference genes in lettuce research.

Lactuca super-pangenome reduces bias towards reference genes in lettuce research.

Journal: BMC plant biology
Published: July 01, 2024

Long RNA Sequencing and Ribosome Profiling of Inflamed β-Cells Reveal an Extensive Translatome Landscape.

Long RNA Sequencing and Ribosome Profiling of Inflamed β-Cells Reveal an Extensive Translatome Landscape.

Journal: Diabetes
Published: November 04, 2020

Clinical and genetic correlates of islet-autoimmune signatures in juvenile-onset type 1 diabetes.

Clinical and genetic correlates of islet-autoimmune signatures in juvenile-onset type 1 diabetes.

Journal: Diabetologia
Published: June 07, 2019

Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.

Influence of common SCN1A promoter variants on the severity of SCN1A-related phenotypes.

Journal: Molecular genetics & genomic medicine
Published: November 19, 2018

Modifier genes in SCN1A-related epilepsy syndromes.

Modifier genes in SCN1A-related epilepsy syndromes.

Journal: Molecular genetics & genomic medicine
Published: November 19, 2018

Assessment of parental mosaicism in SCN1A-related epilepsy by single-molecule molecular inversion probes and next-generation sequencing.

Assessment of parental mosaicism in SCN1A-related epilepsy by single-molecule molecular inversion probes and next-generation sequencing.

Journal: Journal of medical genetics
Published: August 08, 2018

Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes.

Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes.

Journal: Epilepsia
Published: January 16, 2018

Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population.

Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population.

Journal: PloS one
Published: June 18, 2015

A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.

A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.

Journal: Human molecular genetics
Published: June 25, 2014

Increased paternal age and the influence on burden of genomic copy number variation in the general population.

Increased paternal age and the influence on burden of genomic copy number variation in the general population.

Journal: Human genetics
Published: August 29, 2012
Showing 1-11 of 11

Last Updated: 09/26/2026