H. Boer

发表

In search of the psychosis gene in people with Prader‐Willi syndrome

A. Holland, E. Maina, T. Webb, 2008, American journal of medical genetics. Part A.

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

A. Holland, E. Maina, T. Webb, 2007, Journal of intellectual disability research : JIDR.

Relationship between clinical and genetic diagnosis of Prader-Willi syndrome

A. Holland, T. Webb, J. Whittington, 2002, Journal of medical genetics.

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome.

A. Holland, T. Webb, J. Whittington, 2004, Journal of intellectual disability research : JIDR.

Academic underachievement by people with Prader-Willi syndrome.

A. Holland, T. Webb, J. Whittington, 2004, Journal of intellectual disability research : JIDR.

CD36 expression and its relationship with obesity in blood cells from people with and without Prader–Willi syndrome

A. Holland, B. Horsthemke, T. Webb, 2005, Clinical genetics.

The use of medical care and the prevalence of serious illness in an adult Prader-Willi syndrome cohort.

M. Sinnema, L. Curfs, M. Maaskant, 2013, European journal of medical genetics.

Behavioral phenotype in adults with Prader-Willi syndrome.

S. Einfeld, M. Sinnema, L. Curfs, 2011, Research in developmental disabilities.

Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region.

A. Holland, T. Webb, J. Whittington, 2001, Journal of medical genetics.

Aging in Prader–Willi syndrome: Twelve persons over the age of 50 years

M. Sinnema, L. Curfs, M. Maaskant, 2012, American journal of medical genetics. Part A.

Investigation of Prader-Willi-like Phenotype using a Whole Genome Array

A. Holland, J. Arrand, E. Maina, 2012 .

GENETIC AND BEHAVIOURAL ASPECTS OF PRADER‐WILLI SYNDROME: A REVIEW WITH A TRANSLATION OF THE ORIGINAL PAPER

T. Webb, H. Boer, D. Clarke, 2010 .

Development and Behaviour in Genetic Syndromes: Prader‐Willi Syndrome

H. Boer, D. Clarke, 1999 .

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

T. van Amelsvoort, L. Curfs, J. Engelen, 2014, Journal of intellectual disability research : JIDR.

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

A. Holland, T. Webb, J. Whittington, 2002, Psychological Medicine.

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

A. Holland, E. Maina, T. Webb, 2007, Journal of Human Genetics.

The phenomenology and diagnosis of psychiatric illness in people with Prader–Willi syndrome

A. Holland, E. Maina, T. Webb, 2008, Psychological Medicine.

Maladaptive behaviour in Prader-Willi syndrome in adult life.

P. Sturmey, M. Chung, T. Webb, 1996, Journal of intellectual disability research : JIDR.

Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader–Willi syndrome: an ERP study

J. Stauder, L. Curfs, J. Whittington, 2005, Clinical Neurophysiology.

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

A. Holland, T. Webb, J. Whittington, 2002, Clinical genetics.

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

A. Holland, T. Webb, J. Whittington, 2002, The British journal of psychiatry : the journal of mental science.

Prader–Willi syndrome and psychotic symptoms: I. Case descriptions and genetic studies*

L. Curfs, T. Webb, H. Boer, 1998 .

Development and Behaviour in Genetic Syndromes: Rubinstein‐Taybi Syndrome

H. Boer, D. Clarke, J. Langton, 1999 .

Psychiatric illness in a cohort of adults with Prader-Willi syndrome.

M. Sinnema, L. Curfs, M. Maaskant, 2011, Research in developmental disabilities.

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy

A. Holland, J. Whittington, H. Boer, 2002, The Lancet.

Problem behaviors associated with deletion Prader-Willi, Smith-Magenis, and cri du chat syndromes.

H. Boer, D. Clarke, 1998, American journal of mental retardation : AJMR.

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

A. Holland, T. Webb, J. Whittington, 2002, Developmental medicine and child neurology.

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

A. Holland, T. Webb, J. Whittington, 2002 .

Behavioural studies in Prader-Willi Syndrome

H. Boer, 2004 .

Prader-Willi syndrome and psychotic symptoms: 1. Case descriptions and genetic studies.

L. Curfs, T. Webb, H. Boer, 1998, Journal of Intellectual Disability Research.