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Author Details

Stacey Pereira
Baylor College of Medicine.
2013
51
14
PMIDPaper TitleJournal TitlePublished Year
36434257Key drivers of family-level utility of pediatric genomic sequencing: a qualitative analysis to support preference research.Eur J Hum Genet2023
35435795Researcher Views on Changes in Personality, Mood, and Behavior in Next-Generation Deep Brain Stimulation.AJOB Neurosci2023
37279760Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project.Am J Hum Genet2023
37339287Curiosity and Uncertainty Resolution: Inflating the Perceived Utility of Genetic Information.Am J Bioeth2023
37468037Clinically Indicated Genomic Sequencing of Children in Foster Care: Legal and Ethical Issues.J Pediatr2023
37238322Framing the Family: A Qualitative Exploration of Factors That Shape Family-Level Experience of Pediatric Genomic Sequencing.Children (Basel)2023
37172398Child and adolescent psychiatrists' use, attitudes, and understanding of genetic testing and pharmacogenetics in clinical practice.Psychiatry Res2023
37131804Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study Protocol.medRxiv2023
37330169Participant perceptions of changes in psychosocial domains following participation in an adaptive deep brain stimulation trial.Brain Stimul2023
36919541The Need for Diverse Empirical Data to Inform the Use of Polygenic Risk Scores in Prenatal Screening.Am J Bioeth2023
34309124Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression.J Genet Couns2022
35604365Polygenic embryo screening: four clinical considerations warrant further attention.Hum Reprod2022
35792502Psychiatric polygenic risk scores: Child and adolescent psychiatrists' knowledge, attitudes, and experiences.Am J Med Genet B Neuropsychiatr Genet2022
35496073Researchers' Ethical Concerns About Using Adaptive Deep Brain Stimulation for Enhancement.Front Hum Neurosci2022
35571041Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study.Front Genet2022
35926784Post-trial access in implanted neural device research: Device maintenance, abandonment, and cost.Brain Stimul2022
36282588Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study.Circ Genom Precis Med2022
35216680Family secrets: Experiences and outcomes of participating in direct-to-consumer genetic relative-finder services.Am J Hum Genet2022
35089838Capacities and Limitations of Using Polygenic Risk Scores for Reproductive Decision Making.Am J Bioeth2022
33011736Perceptions of best practices for return of results in an international survey of psychiatric genetics researchers.Eur J Hum Genet2021
33609654Child and Adolescent Psychiatrists' Perceptions of Utility and Self-rated Knowledge of Genetic Testing Predict Usage for Autism Spectrum Disorder.J Am Acad Child Adolesc Psychiatry2021
34690676Patient, Caregiver, and Decliner Perspectives on Whether to Enroll in Adaptive Deep Brain Stimulation Research.Front Neurosci2021
34424265Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial.JAMA Pediatr2021
34207141Pediatric Oncologists' Experiences Returning and Incorporating Genomic Sequencing Results into Cancer Care.J Pers Med2021
34363016Genetic testing in ambulatory cardiology clinics reveals high rate of findings with clinical management implications.Genet Med2021
33106616Screening embryos for polygenic conditions and traits: ethical considerations for an emerging technology.Genet Med2021
31477844Psychiatric genomics researchers' perspectives on best practices for returning results to individual participants.Genet Med2020
33281581Researcher Perspectives on Ethical Considerations in Adaptive Deep Brain Stimulation Trials.Front Hum Neurosci2020
33424563Researcher Perspectives on Data Sharing in Deep Brain Stimulation.Front Hum Neurosci2020
30358063Psychiatric genetics researchers' views on offering return of results to individual participants.Am J Med Genet B Neuropsychiatr Genet2019
30209271Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project.Genet Med2019
31186522Responsibility, culpability, and parental views on genomic testing for seriously ill children.Genet Med2019
31329079Neuroethics at 15: Keep the Kant but Add More Bacon.AJOB Neurosci2019
31307366"DNA Is Information, and Genetics Is Information Technology": Reconsidering the Genetic Code.Am J Bioeth2019
30808425Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium.Genome Med2019
30600270Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project.Pediatrics2019
30600265Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project.Pediatrics2019
30531563An Ethical Framework for Research in Maternal-Fetal Intervention in the Presence of Maternal Human Immunodeficiency Virus or Hepatitis B and C Infection.Obstet Gynecol2019
29986673The BabySeq project: implementing genomic sequencing in newborns.BMC Pediatr2018
30133724Commercial Interests, the Technological Imperative, and Advocates: Three Forces Driving Genomic Sequencing in Newborns.Hastings Cent Rep2018
28072771Should you profit from your genome?Nat Biotechnol2017
28096516Newborn Sequencing in Genomic Medicine and Public Health.Pediatrics2017
28926626Do privacy and security regulations need a status update? Perspectives from an intergenerational survey.PLoS One2017
26729699Potential Psychosocial Risks of Sequencing Newborns.Pediatrics2016
27329739Return of individual genomic research results: what do consent forms tell participants?Eur J Hum Genet2016
27412853The ethics of conducting molecular autopsies in cases of sudden death in the young.Genome Res2016
26882539An open access pilot freely sharing cancer genomic data from participants in Texas.Sci Data2016
24188662Adult genetic risk screening.Annu Rev Med2014
25178093Open access data sharing in genomic research.Genes (Basel)2014
24082139Personalized genomic disease risk of volunteers.Proc Natl Acad Sci U S A2013
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Collaborators

Baylor College of Medicine.
Co-authored papers 33
Baylor College of Medicine.
Co-authored papers 17
Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
Co-authored papers 10
Harvard Medical School
Co-authored papers 9
Broad Institute of MIT and Harvard
Co-authored papers 9
Center for Medical Ethics and Health Policy, Baylor College of Medicine
Co-authored papers 8
University of California-San Francisco.
Co-authored papers 7
Boston Children's Hospital
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
Harvard Medical School, Harvard Pilgrim Health Care Institute
Co-authored papers 5
Harvard Medical School
Co-authored papers 4
Broad Institute of MIT and Harvard
Co-authored papers 4
The Broad Institute of MIT and Harvard
Co-authored papers 4
University of California-San Francisco.
Co-authored papers 3
Co-authored papers 3
University of Washington School of Public Health.
Co-authored papers 3
University of California san francisco
Co-authored papers 3
Norman Fixel Institute for Neurological Diseases, University of Florida
Co-authored papers 3
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
Baylor College of Medicine.
Co-authored papers 2
Texas Children's Hospital
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
College of Medicine, University of Arizona
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
Center for Medical Ethics and Health Policy, Baylor College of Medicine
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
Harvard Medical School
Co-authored papers 1