Harm Boer

Long noncoding RNAs in mammalian cells: what, where, and why?

Epigenetics in human disease and prospects for epigenetic therapy

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

Intellectual disability and its relationship to autism spectrum disorders

The predictive value of numerical magnitude comparison for individual differences in mathematics achievement

22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features

Prader–Willi syndrome and Angelman syndrome

Circular Intronic Long Noncoding RNAs

DNA Methylation and Its Basic Function

A gene expression atlas of the central nervous system based on bacterial artificial chromosomes

Obsessive-compulsive disorder phenotypes: implications for genetic studies

Unique features of long non-coding RNA biogenesis and function

The hallmarks of cancer

The epidemiology of obsessive-compulsive disorder in the National Comorbidity Survey Replication

Prevalence of psychiatric diagnoses in children with mental retardation: data from a population-based study

Prader-Willi syndrome

Down syndrome

22q11.2 deletion syndrome

DNA methylation and human disease

Quadruplex DNA: sequence, topology and structure

Assessment of mental health problems in people with Down syndrome: key considerations

AnFgf8mouse mutant phenocopies human 22q11 deletion syndrome

Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management

Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome

Maladaptive behaviour in Prader‐Willi syndrome in adult life

Prevalence of, and risk factors for, physical ill‐health in people with Prader‐Willi syndrome: a population‐based study

Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study

Academic underachievement by people with Prader–Willi syndrome

Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter

Prader–Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey

Cognitive abilities and genotype in a population‐based sample of people with Prader–Willi syndrome

The course and outcome of psychiatric illness in people with Prader–Willi syndrome: implications for management and treatment

A study of the influence of different genotypes on the physical and behavioral phenotypes of children and adults ascertained clinically as having PWS

Psychopathology in adults with 22q11 deletion syndrome and moderate and severe intellectual disability