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Eric Haan

6PUBLICATIONS

150CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Neurogenetics

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Publications (6)

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|Aug 12, 2025

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Renee Johnson, Robert A Fletcher, Stacey Peters

|Dec 29, 2022

Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (<i>DSP</i>) Truncating Variant.

Edgar T Hoorntje, Charlotte Burns, Luisa Marsili

|Apr 20, 2021

Marfan syndrome resulting from a rare pathogenic FBN1 variant, ascertained through a proband with IgG4-related arteriopathy.

Eric A Haan, Francois H Chamalaun, Steven A J Chamuleau

|Oct 04, 2019

Disruptive variants of <i>CSDE1</i> associate with autism and interfere with neuronal development and synaptic transmission.

Hui Guo, Ying Li, Lu Shen

|May 06, 2018

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.

Suzanna G M Frints, Aysegul Ozanturk, Germán Rodríguez Criado

|Jun 20, 2017

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

Madeleine R Geisheker, Gabriel Heymann, Tianyun Wang

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Frequent Collaborators

3 joint publications

Jozef Gecz

2 joint publications

Nicholas Pachter

2 joint publications

Christopher Semsarian

2 joint publications

Corrado Romano

2 joint publications

J Peter van Tintelen

2 joint publications

Jan D H Jongbloed

2 joint publications

Euan A Ashley

2 joint publications

Tina Thompson

2 joint publications

Richard D Bagnall

2 joint publications

Victoria N Parikh

Frequent Collaborators

3 joint publications

Jozef Gecz

2 joint publications

Nicholas Pachter

2 joint publications

Christopher Semsarian

2 joint publications

Corrado Romano

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