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Research participants' perspectives about the return of uninformative genomic test results in a clinical research setting

Journal of genetic counseling, 2024-06, Vol.33 (3), p.689-698

2024

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Feasibility, face validity, and sensitivity of a web‐based simulation tool for assessing genetic counseling communication

Journal of genetic counseling, 2020-12, Vol.29 (6), p.1200-1209

2020

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Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict

Journal of genetic counseling, 2021-06, Vol.30 (3), p.766-773

2021

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eP512: Identifying clinical and psychological factors associated with genomics-related outcomes in a centralized sequencing protocol

Genetics in medicine, 2022-03, Vol.24 (3), p.S326-S327

2022

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PRESENTING A MULTIDISCIPLINARY FRAMEWORK FOR RESEARCH GENOME SEQUENCING COUPLED WITH GENETIC COUNSELING AND RETURN OF CLINICALLY VALIDATED PRIMARY AND SECONDARY FINDINGS FOR INDIVIDUALS WITH PSYCHIATRIC DISORDERS

European neuropsychopharmacology, 2022-10, Vol.63, p.e126-e127

2022

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T102. IDENTIFYING NEW TREATMENT TARGETS FOR ALCOHOL USE DISORDER THROUGH GENETIC AND ELECTRONIC HEALTH RECORDS DATA APPROACHES

European neuropsychopharmacology, 2023-10, Vol.75, p.S217-S217

2023

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Patient Perspectives on Adaptation to Inborn Errors of Immunity

Clinical immunology (Orlando, Fla.), 2023-05, Vol.250, p.109388, Article 109388

2023

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Assessing genetic counselor communication in response to virtual, asynchronous simulated video prompts

Journal of genetic counseling, 2022-04, Vol.31 (2), p.424-432

2022

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Perceived control is significantly associated with psychological adaptation in individuals with known or suspected inborn errors of immunity

Journal of community genetics, 2023-12, Vol.14 (6), p.639-647

2023

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CONTRIBUTION OF GENOME SEQUENCING IN THE EVALUATION OF CHILDREN AND ADOLESCENTS WITH SUSPECTED SERONEGATIVE AUTOIMMUNE ENCEPHALITIS

European neuropsychopharmacology, 2022-10, Vol.63, p.e151-e152

2022

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Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations

Journal of allergy and clinical immunology, 2022-10, Vol.150 (4), p.947-954

2022

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T61. PERSONAL UTILITY OF POLYGENIC RISK SCORES: ATTITUDES AND INTEREST AMONG INDIVIDUALS WITH MAJOR DEPRESSIVE DISORDER AND TREATMENT RESISTANT DEPRESSION

European neuropsychopharmacology, 2022-10, Vol.63, p.e201-e202

2022

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eP133: Genome sequencing and chromosomal microarray as a tool for evaluating phenotypic variability in individuals with X and Y chromosome variations

Genetics in medicine, 2022-03, Vol.24 (3), p.S83-S83

2022

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eP083: Chromosomal microarray analysis as a supplement to exome sequencing in pediatric patients with suspected inborn errors of immunity

Genetics in medicine, 2022-03, Vol.24 (3), p.S55-S55

2022

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OP019: A tertiary care clinical sequencing program for patients with suspected immune defects: Results from the first 1000 families

Genetics in medicine, 2022-03, Vol.24 (3), p.S350-S350

2022

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eP400: Utility of genome sequencing in CNV identification in an immune disorders cohort

Genetics in medicine, 2022-03, Vol.24 (3), p.S252-S252

2022

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Psychological state at the time of psychiatric genetic counseling impacts patient empowerment: A pre-post analysis

Journal of genetic counseling, 2024-07

2024

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Clinical Exome Sequencing of 1000 Families with Complex Immune Phenotypes: Towards comprehensive genomic evaluations

Journal of allergy and clinical immunology, 2022-06, Vol.150 (4), p.947-954

2022

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The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome

Blood advances, 2022-07, Vol.6 (13), p.3974-3978

2022

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The Contribution of Rare Copy Number Variants in FAS Towards Pathogenesis of Autoimmune Lymphoproliferative Syndrome

Blood advances, 2022-04

2022

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Multi-site integrated optical addressing of trapped ions

Nature communications, 2024-05, Vol.15 (1), p.3709-3709, Article 3709

2024

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The Next Generation Blueprint of Computational Toxicology at the U.S. Environmental Protection Agency

Toxicological sciences, 2019-06, Vol.169 (2), p.317-332

2019

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Evaluating In Vitro-In Vivo Extrapolation of Toxicokinetics

Toxicological sciences, 2018-05, Vol.163 (1), p.152-169

2018

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Cytotoxicity of the Essential Oil of Fennel (Foeniculum vulgare) from Tajikistan

Foods, 2017-08, Vol.6 (9), p.73

2017

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Research participants' perspectives about the return of uninformative genomic test results in a clinical research setting

Feasibility, face validity, and sensitivity of a web‐based simulation tool for assessing genetic counseling communication

Exome sequencing study in a clinical research setting finds general acceptance of study returning secondary genomic findings with little decisional conflict

Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity

eP512: Identifying clinical and psychological factors associated with genomics-related outcomes in a centralized sequencing protocol

PRESENTING A MULTIDISCIPLINARY FRAMEWORK FOR RESEARCH GENOME SEQUENCING COUPLED WITH GENETIC COUNSELING AND RETURN OF CLINICALLY VALIDATED PRIMARY AND SECONDARY FINDINGS FOR INDIVIDUALS WITH PSYCHIATRIC DISORDERS

T102. IDENTIFYING NEW TREATMENT TARGETS FOR ALCOHOL USE DISORDER THROUGH GENETIC AND ELECTRONIC HEALTH RECORDS DATA APPROACHES

Patient Perspectives on Adaptation to Inborn Errors of Immunity

Assessing genetic counselor communication in response to virtual, asynchronous simulated video prompts

Perceived control is significantly associated with psychological adaptation in individuals with known or suspected inborn errors of immunity

CONTRIBUTION OF GENOME SEQUENCING IN THE EVALUATION OF CHILDREN AND ADOLESCENTS WITH SUSPECTED SERONEGATIVE AUTOIMMUNE ENCEPHALITIS

Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations

T61. PERSONAL UTILITY OF POLYGENIC RISK SCORES: ATTITUDES AND INTEREST AMONG INDIVIDUALS WITH MAJOR DEPRESSIVE DISORDER AND TREATMENT RESISTANT DEPRESSION

eP133: Genome sequencing and chromosomal microarray as a tool for evaluating phenotypic variability in individuals with X and Y chromosome variations

eP083: Chromosomal microarray analysis as a supplement to exome sequencing in pediatric patients with suspected inborn errors of immunity

OP019: A tertiary care clinical sequencing program for patients with suspected immune defects: Results from the first 1000 families

eP400: Utility of genome sequencing in CNV identification in an immune disorders cohort

Psychological state at the time of psychiatric genetic counseling impacts patient empowerment: A pre-post analysis

Clinical Exome Sequencing of 1000 Families with Complex Immune Phenotypes: Towards comprehensive genomic evaluations

The contribution of rare copy number variants in FAS toward pathogenesis of autoimmune lymphoproliferative syndrome

The Contribution of Rare Copy Number Variants in FAS Towards Pathogenesis of Autoimmune Lymphoproliferative Syndrome

Multi-site integrated optical addressing of trapped ions

The Next Generation Blueprint of Computational Toxicology at the U.S. Environmental Protection Agency

Evaluating In Vitro-In Vivo Extrapolation of Toxicokinetics

Cytotoxicity of the Essential Oil of Fennel (Foeniculum vulgare) from Tajikistan

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