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Developmental Pathways from Genetic, Prenatal, Parenting and Emotional/Behavioral Risk to Cortisol Reactivity and Adolescent Substance Use: A TRAILS Study

Journal of youth and adolescence, 2020-01, Vol.49 (1), p.17-31

2020

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Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth

Development and psychopathology, 2021-02, Vol.33 (1), p.76-86

2021

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Overlapping genetic effects between suicidal ideation and neurocognitive functioning

Journal of affective disorders, 2019-04, Vol.249, p.104-111

2019

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Inhibitory Control in Siblings Discordant for Exposure to Maternal Smoking During Pregnancy

Developmental psychology, 2018-02, Vol.54 (2), p.199-208

2018

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Shared additive genetic influences on DSM-IV criteria for alcohol dependence in subjects of European ancestry

Addiction (Abingdon, England), 2015-12, Vol.110 (12), p.1922-1931

2015

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Examining the role of common genetic variants on alcohol, tobacco, cannabis and illicit drug dependence: genetics of vulnerability to drug dependence

Addiction (Abingdon, England), 2015-03, Vol.110 (3), p.530-537

2015

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Interactions between Genetic, Prenatal, Cortisol, and Parenting Influences on Adolescent Substance Use and Frequency: A TRAILS Study

European addiction research, 2022, Vol.28 (3), p.176-185

2022

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The etiology of DSM-5 alcohol use disorder: Evidence of shared and non-shared additive genetic effects

Drug and alcohol dependence, 2019-08, Vol.201, p.147-154

2019

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Associations Between Depression-Relevant Genetic Risk and Youth Stress Exposure: Evidence of Gene-Environment Correlations

Journal of psychopathology and clinical science, 2022-07, Vol.131 (5), p.457-466

2022

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Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes

Brain (London, England : 1878), 2024-05, Vol.147 (5), p.1837-1855

2024

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New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases

Journal of medical genetics, 2011-11, Vol.48 (11), p.752-760

2011

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Evidence of Shared Genome-Wide Additive Genetic Effects on Interpersonal Trauma Exposure and Generalized Vulnerability to Drug Dependence in a Population of Substance Users

Journal of traumatic stress, 2016-06, Vol.29 (3), p.197-204

2016

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DYRK1A Overexpression in Mice Downregulates the Gonadotropic Axis and Disturbs Early Stages of Spermatogenesis

Genes, 2021-11, Vol.12 (11), p.1800

2021

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A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis

Acta neuropathologica communications, 2018-10, Vol.6 (1), p.109-109, Article 109

2018

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NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos

Disease models & mechanisms, 2013-03, Vol.6 (2), p.537-543

2013

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A Preliminary Study of Genetic Variation in the Dopaminergic and Serotonergic Systems and Genome-Wide Additive Genetic Effects on Depression Severity and Treatment Response

Clinical psychological science, 2017-01, Vol.5 (1), p.158-165

2017

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Learning "graph-mer" motifs that predict gene expression trajectories in development

PLoS computational biology, 2010-04, Vol.6 (4), p.e1000761-e1000761

2010

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HPA Axis Multilocus Genetic Profile Score Moderates the Impact of Interpersonal Stress on Prospective Increases in Depressive Symptoms for Offspring of Depressed Mothers

Journal of abnormal psychology (1965), 2017-11, Vol.126 (8), p.1017-1028

2017

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The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

Genetics in medicine, 2021-09, Vol.23 (9), p.1726-1737

2021

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Enlarging the Amino Acid Set of Escherichia coli by Infiltration of the Valine Coding Pathway

Science (American Association for the Advancement of Science), 2001-04, Vol.292 (5516), p.501-504

2001

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Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma

PloS one, 2020-09, Vol.15 (9), p.e0237792

2020

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Learning "graph-mer" Motifs that Predict Gene Expression Trajectories in Development: e1000761

PLoS computational biology, 2010-04, Vol.6 (4)

2010

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Additive Genetic Contribution to Symptom Dimensions in Major Depressive Disorder

Journal of abnormal psychology (1965), 2016-05, Vol.125 (4), p.495-501

2016

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Phenotype and imaging features associated with APP duplications

Alzheimer's research & therapy, 2023-05, Vol.15 (1), p.93-93, Article 93

2023

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Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating

Human mutation, 2008-06, Vol.29 (6), p.E13-E26

2008

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Developmental Pathways from Genetic, Prenatal, Parenting and Emotional/Behavioral Risk to Cortisol Reactivity and Adolescent Substance Use: A TRAILS Study

Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth

Overlapping genetic effects between suicidal ideation and neurocognitive functioning

Inhibitory Control in Siblings Discordant for Exposure to Maternal Smoking During Pregnancy

Shared additive genetic influences on DSM-IV criteria for alcohol dependence in subjects of European ancestry

Examining the role of common genetic variants on alcohol, tobacco, cannabis and illicit drug dependence: genetics of vulnerability to drug dependence

Interactions between Genetic, Prenatal, Cortisol, and Parenting Influences on Adolescent Substance Use and Frequency: A TRAILS Study

The etiology of DSM-5 alcohol use disorder: Evidence of shared and non-shared additive genetic effects

Associations Between Depression-Relevant Genetic Risk and Youth Stress Exposure: Evidence of Gene-Environment Correlations

Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes

New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases

Evidence of Shared Genome-Wide Additive Genetic Effects on Interpersonal Trauma Exposure and Generalized Vulnerability to Drug Dependence in a Population of Substance Users

DYRK1A Overexpression in Mice Downregulates the Gonadotropic Axis and Disturbs Early Stages of Spermatogenesis

A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis

NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos

A Preliminary Study of Genetic Variation in the Dopaminergic and Serotonergic Systems and Genome-Wide Additive Genetic Effects on Depression Severity and Treatment Response

Learning "graph-mer" motifs that predict gene expression trajectories in development

HPA Axis Multilocus Genetic Profile Score Moderates the Impact of Interpersonal Stress on Prospective Increases in Depressive Symptoms for Offspring of Depressed Mothers

The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

Enlarging the Amino Acid Set of Escherichia coli by Infiltration of the Valine Coding Pathway

Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma

Learning "graph-mer" Motifs that Predict Gene Expression Trajectories in Development: e1000761

Additive Genetic Contribution to Symptom Dimensions in Major Depressive Disorder

Phenotype and imaging features associated with APP duplications

Update of the Pompe disease mutation database with 107 sequence variants and a format for severity rating

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