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0218 Sleep and Circadian Polygenic Risk Scores Predict Actigraphy-derived Traits and Cognition in Older Adults

Sleep (New York, N.Y.), 2024-04, Vol.47 (Supplement_1), p.A94-A94

2024

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29. EPIGENOME-WIDE ASSOCIATION META-ANALYSIS OF ADULT ATTENTION-DEFICIT/HYPERACTIVITY DISORDER

European neuropsychopharmacology, 2022-10, Vol.63, p.e61

2022

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44. META-ANALYSIS OF GENOME-WIDE DNA METHYLATION IN SCHIZOPHRENIA: DOES SEX STRATIFICATION IMPROVE DISCOVERY?

European neuropsychopharmacology, 2023-10, Vol.75, p.S79-S80

2023

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5.23 Leveraging the Genetics of ADHD Symptom Dimensions in Child Psychiatric Outpatients

Journal of the American Academy of Child and Adolescent Psychiatry, 2023-10, Vol.62 (10), p.S266-S266

2023

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6.71 ATTENTION IS PREDICTED BY ALZHEIMER’S DISEASE POLYGENIC RISK SCORE IN TYPICALLY DEVELOPING CHILDREN MORE THAN IN CHILDREN WITH ADHD

Journal of the American Academy of Child and Adolescent Psychiatry, 2019-10, Vol.58 (10), p.S294-S294

2019

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74 GENETICS OF ADHD DIMENSIONS: BIOLOGICAL AND CLINICAL IMPLICATIONS FOR ADHD

European neuropsychopharmacology, 2019-10, Vol.29, p.S101-S101

Zayats, Tetyana

2019

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76 GENETIC ARCHITECTURE OF PERSISTENT ATTENTION DEFICIT/HYPERACTIVITY DISORDER

European neuropsychopharmacology, 2019-10, Vol.29, p.S102-S103

2019

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87. EXPLORATION OF BRAIN-HERITABLE METHYLATION IN SCHIZOPHRENIA CASES AND CONTROLS

European neuropsychopharmacology, 2022-10, Vol.63, p.e92

2022

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89 CROSS-DISORDER META-ANALYSIS OF GENOMEWIDE ASSOCIATION STUDIES SHEDS LIGHT INTO POTENTIALLY SHARED NEUROBIOLOGY ACROSS ADHD, ASD, OCD, AND TS

European neuropsychopharmacology, 2019-10, Vol.29, p.S109-S109

2019

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Assessing the contribution of genetic nurture to refractive error

European journal of human genetics : EJHG, 2022-11, Vol.30 (11), p.1226-1232

2022

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ATTENTION IS PREDICTED BY ALZHEIMER’S DISEASE POLYGENIC RISK SCORE IN TYPICALLY DEVELOPING CHILDREN MORE THAN CHILDREN WITH ATTENTION/DEFICIT-HYPERACTIVITY DISORDER

Alzheimer's & dementia, 2019-07, Vol.15 (7), p.P975-P976

2019

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Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

Nature communications, 2021-02, Vol.12 (1), p.1166-1166, Article 1166

2021

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Axes of astigmatism in fellow eyes show mirror rather than direct symmetry

Ophthalmic & physiological optics, 2008-07, Vol.28 (4), p.327-333

2008

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The (Broad-Sense) Genetic Correlations Among Four Measures of Inattention and Hyperactivity in 12 Year Olds

Behavior genetics, 2020-07, Vol.50 (4), p.273-288

2020

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A candidate gene investigation of methylphenidate response in adult attention-deficit/hyperactivity disorder patients: results from a naturalistic study

Journal of Neural Transmission, 2016-08, Vol.123 (8), p.859-865

2016

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COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study

Osteoarthritis and cartilage open, 2024-03, Vol.6 (1), p.100424-100424, Article 100424

2024

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COL1A1 and COL2A1 Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the COL2A1 Locus

Investigative ophthalmology & visual science, 2009-09, Vol.50 (9), p.4080-4086

2009

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COLIA1 and COL2A1 Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the COL2A1 Locus

Investigative ophthalmology & visual science, 2009, Vol.50 (9), p.4080-4086

2009

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A CONTRIBUTION OF RARE COPY NUMBER VARIATIONS TO THE DEVELOPMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER: GENOME-WIDE META-ANALYSES IN 12548 INDIVIDUALS

European neuropsychopharmacology, 2019, Vol.29, p.S1042-S1042

2019

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A DNA METHYLATION STUDY OF THE ANTIPSYCHOTIC QUETIAPINE (SEROQUEL): TREATMENT EFFECTS IN SCHIZOPHRENIA AND BIPOLAR DISORDER

European neuropsychopharmacology, 2022-10, Vol.63, p.e131-e132

2022

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Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

Immunity (Cambridge, Mass.), 2015-06, Vol.42 (6), p.1185-1196

2015

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The Examination of Remodeling Processes of Hard Periodontal Tissues in Rats with Disorders of Pancreatic Incretory Function

Archive of Clinical Medicine, 2022-12, Vol.28 (2), p.32-36

2022

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F6GENETICS OF TREATMENT RESPONSE FOR ATOMOXETINE IN ADHD

European neuropsychopharmacology, 2019, Vol.29, p.S1113-S1113

2019

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0218 Sleep and Circadian Polygenic Risk Scores Predict Actigraphy-derived Traits and Cognition in Older Adults

29. EPIGENOME-WIDE ASSOCIATION META-ANALYSIS OF ADULT ATTENTION-DEFICIT/HYPERACTIVITY DISORDER

44. META-ANALYSIS OF GENOME-WIDE DNA METHYLATION IN SCHIZOPHRENIA: DOES SEX STRATIFICATION IMPROVE DISCOVERY?

5.23 Leveraging the Genetics of ADHD Symptom Dimensions in Child Psychiatric Outpatients

6.71 ATTENTION IS PREDICTED BY ALZHEIMER’S DISEASE POLYGENIC RISK SCORE IN TYPICALLY DEVELOPING CHILDREN MORE THAN IN CHILDREN WITH ADHD

74 GENETICS OF ADHD DIMENSIONS: BIOLOGICAL AND CLINICAL IMPLICATIONS FOR ADHD

76 GENETIC ARCHITECTURE OF PERSISTENT ATTENTION DEFICIT/HYPERACTIVITY DISORDER

87. EXPLORATION OF BRAIN-HERITABLE METHYLATION IN SCHIZOPHRENIA CASES AND CONTROLS

89 CROSS-DISORDER META-ANALYSIS OF GENOMEWIDE ASSOCIATION STUDIES SHEDS LIGHT INTO POTENTIALLY SHARED NEUROBIOLOGY ACROSS ADHD, ASD, OCD, AND TS

Assessing the contribution of genetic nurture to refractive error

ATTENTION IS PREDICTED BY ALZHEIMER’S DISEASE POLYGENIC RISK SCORE IN TYPICALLY DEVELOPING CHILDREN MORE THAN CHILDREN WITH ATTENTION/DEFICIT-HYPERACTIVITY DISORDER

Author Correction: Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

Axes of astigmatism in fellow eyes show mirror rather than direct symmetry

The (Broad-Sense) Genetic Correlations Among Four Measures of Inattention and Hyperactivity in 12 Year Olds

A candidate gene investigation of methylphenidate response in adult attention-deficit/hyperactivity disorder patients: results from a naturalistic study

COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study

COL11A1 is associated with developmental dysplasia of the hip and secondary osteoarthritis in the HUNT study

COL1A1 and COL2A1 Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the COL2A1 Locus

COLIA1 and COL2A1 Genes and Myopia Susceptibility: Evidence of Association and Suggestive Linkage to the COL2A1 Locus

A CONTRIBUTION OF RARE COPY NUMBER VARIATIONS TO THE DEVELOPMENT OF ATTENTION DEFICIT HYPERACTIVITY DISORDER: GENOME-WIDE META-ANALYSES IN 12548 INDIVIDUALS

Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder

A DNA METHYLATION STUDY OF THE ANTIPSYCHOTIC QUETIAPINE (SEROQUEL): TREATMENT EFFECTS IN SCHIZOPHRENIA AND BIPOLAR DISORDER

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases

The Examination of Remodeling Processes of Hard Periodontal Tissues in Rats with Disorders of Pancreatic Incretory Function

F6GENETICS OF TREATMENT RESPONSE FOR ATOMOXETINE IN ADHD

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