Genetics of childhood disorders: XII. Genomic imprinting: breaking the rules

Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.

Clinical genetics·2017

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities.

Molecular psychiatry·2013

Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome.

Clinical genetics·2010

Nutrient intake and body composition variables in Prader-Willi syndrome--effect of growth hormone supplementation and genetic subtype.

Journal of pediatric endocrinology & metabolism : JPEM·2007

LADD syndrome is caused by FGF10 mutations.

Clinical genetics·2006

Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.

Human genetics·2001

Disambiguating Maternal versus Fetal Etiological Pathways Linking Perinatal and Neurodevelopmental Outcomes.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

Diagnostic Accuracy of the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule, Second Edition, in a Naturalistic High-Risk Autism Spectrum Disorder Sample Aged 6-25 Years.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

Systematic Review and Meta-Analysis: Lack of Early Improvement Predicts Inefficacy of Antipsychotics for Schizophrenia in Adolescents.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

Maternal Influenza Infection During Pregnancy and Risk of Attention-Deficit/Hyperactivity Disorder in Offspring.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

A Common Metric for the Emotion Dysregulation Inventory From Early Childhood Through Adolescence.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

Systematic Review and Meta-Analysis: Risk Factors for Suicide in Youth Psychological Autopsy Studies.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

Bile and capsid variation coregulate histo-blood group antigen recognition and serum neutralization potency in GII.12 human norovirus.

Journal of virology·2026

A comprehensive overview of genetic mutations in Iranian patients with Bardet-Biedl syndrome.

Molecular genetics and metabolism reports·2026

HLA allelic variation and COVID-19 severity in a Kuwait-based population: a high-resolution immunogenetic study.

Frontiers in immunology·2026

Association Between Visceral Adiposity Index and Metabolic Syndrome and Its Components: Evidence From the PERSIAN Guilan Cohort Study.

Endocrinology, diabetes & metabolism·2026

Shared non-HLA genetic architecture across diverse ancestries links insulin secretion and resistance to type 1 diabetes.

Diabetologia·2026

Hypothalamic representation of aggressiveness across mouse strains.

Nature communications·2026

Related Experiment Videos

Genetics of childhood disorders: XII. Genomic imprinting: breaking the rules

Related Concept Videos

Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities.

Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome.

Nutrient intake and body composition variables in Prader-Willi syndrome--effect of growth hormone supplementation and genetic subtype.

LADD syndrome is caused by FGF10 mutations.

Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.

Disambiguating Maternal versus Fetal Etiological Pathways Linking Perinatal and Neurodevelopmental Outcomes.

Diagnostic Accuracy of the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule, Second Edition, in a Naturalistic High-Risk Autism Spectrum Disorder Sample Aged 6-25 Years.

Systematic Review and Meta-Analysis: Lack of Early Improvement Predicts Inefficacy of Antipsychotics for Schizophrenia in Adolescents.

Maternal Influenza Infection During Pregnancy and Risk of Attention-Deficit/Hyperactivity Disorder in Offspring.

A Common Metric for the Emotion Dysregulation Inventory From Early Childhood Through Adolescence.

Systematic Review and Meta-Analysis: Risk Factors for Suicide in Youth Psychological Autopsy Studies.

Bile and capsid variation coregulate histo-blood group antigen recognition and serum neutralization potency in GII.12 human norovirus.

A comprehensive overview of genetic mutations in Iranian patients with Bardet-Biedl syndrome.

HLA allelic variation and COVID-19 severity in a Kuwait-based population: a high-resolution immunogenetic study.

Association Between Visceral Adiposity Index and Metabolic Syndrome and Its Components: Evidence From the PERSIAN Guilan Cohort Study.

Shared non-HLA genetic architecture across diverse ancestries links insulin secretion and resistance to type 1 diabetes.

Hypothalamic representation of aggressiveness across mouse strains.

Related Experiment Videos

Genetics of childhood disorders: XII. Genomic imprinting: breaking the rules

Related Concept Videos

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