Haan, Eric

Genome-wide association study identifies novel breast cancer susceptibility loci

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Refining analyses of copy number variation identifies specific genes associated with developmental delay

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

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A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

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Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

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Frontotemporal dementia and its subtypes: a genome-wide association study

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YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction

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Health professionals' knowledge, practice and opinions about fetal alcohol syndrome and alcohol consumption in pregnancy

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Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

Swarup, V., Hinz, F. I., Rexach, J. E., Noguchi, K.-I., Toyoshiba, H., Oda, A., Hirai, K., Sarkar, A., Seyfried, N. T., Cheng, C., et al. (2019) · Nature Medicine

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Pain Characteristics and Their Association With Quality of Life and Self-concept in Children With Hemiplegic Cerebral Palsy Identified From a Population Register

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CCDC22: a novel candidate gene for syndromic X-linked intellectual disability

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