Partial trisomy of C11q and its effect on affective disorder segregating in a three generation family

Functionality appreciation in young children.

Body image·2024

Evaluating the effectiveness and acceptability of two positive body image media micro-interventions among children aged 4-6 years old - a study protocol.

BMC public health·2024

Perinatal sleep disruption and postpartum psychosis in bipolar disorder: Findings from the UK BDRN Pregnancy Study.

Journal of affective disorders·2023

Does a greater training load increase the risk of injury and illness in ultramarathon runners? : A prospective, descriptive, longitudinal design.

South African journal of sports medicine·2023

Postpartum psychosis in bipolar disorder: no evidence of association with personality traits, cognitive style or affective temperaments.

BMC psychiatry·2019

Interaction between childhood maltreatment on immunogenetic risk in depression: Discovery and replication in clinical case-control samples.

Brain, behavior, and immunity·2017

Female-specific associations of glyoxalase 1 polymorphisms with schizophrenia in a Han Chinese case-control study.

Psychiatric genetics·2026

Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability.

Psychiatric genetics·2026

Prenatal diagnosis and genetic counseling of a de novo 10q11.22q11.23 duplication associated with a normal development at 12 months of age.

Psychiatric genetics·2026

Severe self-injury in a young girl with autism spectrum disorder and Helsmoortel-van der Aa syndrome responding to naltrexone.

Psychiatric genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Contrasting outcomes of 16p11.2 microdeletion and microduplication in prenatal diagnosis: phenotypic variability and genetic counseling strategies.

Psychiatric genetics·2026

The genome sequence of the Lapland Ringlet, Erebia embla (Thunberg, 1791) (Lepidoptera: Nymphalidae).

Wellcome open research·2026

Protracted Fate Acquisition and Epigenetic De-Aging During Induced Neural Stem Cell Conversion of Human Blood Cells.

Aging cell·2026

Association between RANK gene polymorphism and early femoral neck bone loss in kidney transplant recipients.

Journal of bone and mineral metabolism·2026

Cell-free DNA fragmentomics: from chromatin biology to clinical stratification.

Epigenomics·2026

Histological Differentiation of Neovascularisation and Residual Veins in Groin Recurrence.

Annals of vascular surgery·2026

CRISPR-based genome editing of smooth muscle cells: Disease models, therapeutic applications, and future perspectives.

Vascular pharmacology·2026

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Partial trisomy of C11q and its effect on affective disorder segregating in a three generation family

Related Concept Videos

Functionality appreciation in young children.

Evaluating the effectiveness and acceptability of two positive body image media micro-interventions among children aged 4-6 years old - a study protocol.

Perinatal sleep disruption and postpartum psychosis in bipolar disorder: Findings from the UK BDRN Pregnancy Study.

Does a greater training load increase the risk of injury and illness in ultramarathon runners? : A prospective, descriptive, longitudinal design.

Postpartum psychosis in bipolar disorder: no evidence of association with personality traits, cognitive style or affective temperaments.

Interaction between childhood maltreatment on immunogenetic risk in depression: Discovery and replication in clinical case-control samples.

Female-specific associations of glyoxalase 1 polymorphisms with schizophrenia in a Han Chinese case-control study.

Disruption of GAD1 protein architecture by a novel missense variant in a consanguineous family with autosomal recessive intellectual disability.

Prenatal diagnosis and genetic counseling of a de novo 10q11.22q11.23 duplication associated with a normal development at 12 months of age.

Severe self-injury in a young girl with autism spectrum disorder and Helsmoortel-van der Aa syndrome responding to naltrexone.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Contrasting outcomes of 16p11.2 microdeletion and microduplication in prenatal diagnosis: phenotypic variability and genetic counseling strategies.

The genome sequence of the Lapland Ringlet, Erebia embla (Thunberg, 1791) (Lepidoptera: Nymphalidae).

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Partial trisomy of C11q and its effect on affective disorder segregating in a three generation family

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