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Author Details
Full Name
Peter Ryabinin
Affiliation
Knight Cancer Institute Oregon Health & Science University Portland Oregon USA.
ORCID
Career Start Year
2013
Papers
13
H Index
6
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36645612
Youth Polygenic Scores, Youth ADHD Symptoms, and Parenting Dimensions: An Evocative Gene-Environment Correlation Study.
Res Child Adolesc Psychopathol
2023
37753156
Joint polygenic and environmental risks for childhood attention-deficit/hyperactivity disorder (ADHD) and ADHD symptom dimensions.
JCPP Adv
2023
37500827
Trans-ancestry meta-analysis of genome wide association studies of inhibitory control.
Mol Psychiatry
2023
36848718
The Oregon ADHD-1000: A new longitudinal data resource enriched for clinical cases and multiple levels of analysis.
Dev Cogn Neurosci
2023
35102487
Longitudinal Temperament Pathways to ADHD Between Childhood and Adolescence.
Res Child Adolesc Psychopathol
2022
35427730
Attention-Deficit/Hyperactivity Disorder: Restricted Phenotypes Prevalence, Comorbidity, and Polygenic Risk Sensitivity in the ABCD Baseline Cohort.
J Am Acad Child Adolesc Psychiatry
2022
35868306
Integrative analysis of drug response and clinical outcome in acute myeloid leukemia.
Cancer Cell
2022
31973781
Smaller total brain volume but not subcortical structure volume related to common genetic risk for ADHD.
Psychol Med
2021
31605387
Evaluating chronic emotional dysregulation and irritability in relation to ADHD and depression genetic risk in children with ADHD.
J Child Psychol Psychiatry
2020
32066674
Large epigenome-wide association study of childhood ADHD identifies peripheral DNA methylation associated with disease and polygenic risk burden.
Transl Psychiatry
2020
29496126
Working Memory and Vigilance as Multivariate Endophenotypes Related to Common Genetic Risk for Attention-Deficit/Hyperactivity Disorder.
J Am Acad Child Adolesc Psychiatry
2018
29211761
Prophetic Granger Causality to infer gene regulatory networks.
PLoS One
2017
24286512
Comparison of methods to identify aberrant expression patterns in individual patients: augmenting our toolkit for precision medicine.
Genome Med
2013
1 - 13 of 13
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