CNV Concordance in 1,097 MZ Twin Pairs

The Genome of the Netherlands: design, and project goals

(2013) Dorret I Boomsma et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome

(2013) Miyake Kunio et al.   PLoS One

Comprehensive analysis of copy number variation in monozygotic twins discordant for bipolar disorder or schizophrenia

(2013) Rachael J. Bloom et al.   SCHIZOPHRENIA RESEARCH

CNV Analysis in Monozygotic Twin Pairs Discordant for Urorectal Malformations

(2013) Friederike Baudisch et al.   Twin Research and Human Genetics

The Adult Netherlands Twin Register: Twenty-Five Years of Survey and Biological Data Collection

(2013) Gonneke Willemsen et al.   Twin Research and Human Genetics

Aging as Accelerated Accumulation of Somatic Variants: Whole-Genome Sequencing of Centenarian and Middle-Aged Monozygotic Twin Pairs

(2013) Kai Ye et al.   Twin Research and Human Genetics

Age-Related Somatic Structural Changes in the Nuclear Genome of Human Blood Cells

(2012) Lars A. Forsberg et al.   AMERICAN JOURNAL OF HUMAN GENETICS

De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems

(2012) Erik A Ehli et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Rate of de novo mutations and the importance of father’s age to disease risk

(2012) Augustine Kong et al.   NATURE

The Young Netherlands Twin Register (YNTR): Longitudinal Twin and Family Studies in Over 70,000 Children

(2012) Catharina E. M. van Beijsterveldt et al.   Twin Research and Human Genetics

Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size

(2012) Ashutosh Halder et al.   Molecular Cytogenetics

500K SNP array analyses in blood and saliva showed no differences in a pair of monozygotic twins discordant for cleft lip

(2011) Linda P. Jakobsen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Thought Problems from Adolescence to Adulthood: Measurement Invariance and Longitudinal Heritability

(2011) Abdel Abdellaoui et al.   BEHAVIOR GENETICS

Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts

(2011) Danielle Veenma et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

(2011) A. Abyzov et al.   GENOME RESEARCH

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

(2011) Rachel D. Burnside et al.   HUMAN GENETICS

Copy number imbalances in blood and hair in monozygotic twins discordant for amyotrophic lateral sclerosis

(2011) Roger Pamphlett et al.   JOURNAL OF CLINICAL NEUROSCIENCE

Ontogenetic De Novo Copy Number Variations (CNVs) as a Source of Genetic Individuality: Studies on Two Families with MZD Twins for Schizophrenia

(2011) Sujit Maiti et al.   PLoS One

Accuracy of CNV Detection from GWAS Data

(2011) Dandan Zhang et al.   PLoS One

Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy

(2011) Hidenao Sasaki et al.   Molecular Brain

De novo rates and selection of large copy number variation

(2010) A. Itsara et al.   GENOME RESEARCH

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

(2010) Nigel M Williams et al.   LANCET

Taking qPCR to a higher level: Analysis of CNV reveals the power of high throughput qPCR to enhance quantitative resolution

(2010) Suzanne Weaver et al.   METHODS

Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis

(2010) Sergio E. Baranzini et al.   NATURE

Timing of De Novo Mutagenesis — A Twin Study of Sodium-Channel Mutations

(2010) Lata Vadlamudi et al.   NEW ENGLAND JOURNAL OF MEDICINE

Failure to Confirm CNVs as of Aetiological Significance in Twin Pairs Discordant for Schizophrenia

(2010) Shinji Ono et al.   Twin Research and Human Genetics

The Netherlands Twin Register Biobank: A Resource for Genetic Epidemiological Studies

(2010) Gonneke Willemsen et al.   Twin Research and Human Genetics

Accurately Assessing the Risk of Schizophrenia Conferred by Rare Copy-Number Variation Affecting Genes with Brain Function

(2010) Soumya Raychaudhuri et al.   PLoS Genetics

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

(2009) C. G. F. de Kovel et al.   BRAIN

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances

(2009) Marianne Doornbos et al.   European Journal of Medical Genetics

Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles

(2008) Carl E.G. Bruder et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Somatic mosaicism for copy number variation in differentiated human tissues

(2008) Arkadiusz Piotrowski et al.   HUMAN MUTATION

Copy-number variations associated with neuropsychiatric conditions

(2008) Edwin H. Cook Jr et al.   NATURE

Large recurrent microdeletions associated with schizophrenia

(2008) Hreinn Stefansson et al.   NATURE

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS

Genetic Influences on Thought Problems in 7-Year-Olds: A Twin-Study of Genetic, Environmental and Rater Effects

(2008) Abdel Abdellaoui et al.   Twin Research and Human Genetics