The components of type A behaviour and its genetic determinants

Genotype-environment correlations in late childhood and early adolescence: antisocial behavioral problems and coercive parenting.

Developmental psychology·1998

Changes in degree of sclerosis as a function of prophylactic treatment in cancer-prone and CHD-prone probands.

Behaviour research and therapy·1991

Specific deficits in component reading and language skills: genetic and environmental influences.

Journal of learning disabilities·1989

Genotype x age interaction for neuroticism.

Behavior genetics·1976

Genetic and environmental components of inconsistency and unrepeatability in twins' responses to a neuroticism questionnaire.

Behavior genetics·1976

The nature of extraversion: a genetical analysis.

Journal of personality and social psychology·1975

Detection and interpolation of outliers in biosignals.

Activitas nervosa superior·1990

Precopulatory behaviour of male rats: developmental aspects and dependence on female's solicitation.

Activitas nervosa superior·1990

An easy method to record slow potential shifts (SPS) in rabbits using the "oddball" paradigm.

Activitas nervosa superior·1990

Site of motor pathway excitation during cervical spinal stimulation.

Activitas nervosa superior·1990

Late EEG after-effects in humans following hyperventilation. II. A comparison between subjects with different level of adaptation to hypoxia.

Activitas nervosa superior·1990

Late EEG after-effects in humans following hyperventilation. I. A comparison between intero- and exteroceptive influences.

Activitas nervosa superior·1990

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease.

Science translational medicine·2026

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The components of type A behaviour and its genetic determinants

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Genotype-environment correlations in late childhood and early adolescence: antisocial behavioral problems and coercive parenting.

Changes in degree of sclerosis as a function of prophylactic treatment in cancer-prone and CHD-prone probands.

Specific deficits in component reading and language skills: genetic and environmental influences.

Genotype x age interaction for neuroticism.

Genetic and environmental components of inconsistency and unrepeatability in twins' responses to a neuroticism questionnaire.

The nature of extraversion: a genetical analysis.

Detection and interpolation of outliers in biosignals.

Precopulatory behaviour of male rats: developmental aspects and dependence on female's solicitation.

An easy method to record slow potential shifts (SPS) in rabbits using the "oddball" paradigm.

Site of motor pathway excitation during cervical spinal stimulation.

Late EEG after-effects in humans following hyperventilation. II. A comparison between subjects with different level of adaptation to hypoxia.

Late EEG after-effects in humans following hyperventilation. I. A comparison between intero- and exteroceptive influences.

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease.

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The components of type A behaviour and its genetic determinants

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