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Author Details
Full Name
Sabrina A Suckiel
Affiliation
Icahn School of Medicine at Mount Sinai
ORCID
Career Start Year
2015
Papers
34
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37897232
Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program.
Genet Med
2024
36563179
Detection of mosaic variants using genome sequencing in a large pediatric cohort.
Am J Med Genet A
2023
38006881
The NYCKidSeq randomized controlled trial: Impact of GUÃA digitally enhanced genetic results disclosure in diverse families.
Am J Hum Genet
2023
37461450
The NYCKidSeq randomized controlled trial: Impact of GUÃA digitally enhanced genetic counseling in racially and ethnically diverse families.
medRxiv
2023
37158195
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
Genet Med
2023
36993157
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
medRxiv
2023
36949526
The TeleKidSeq pilot study: incorporating telehealth into clinical care of children from diverse backgrounds undergoing whole genome sequencing.
Pilot Feasibility Stud
2023
37246632
Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.
Genet Med
2023
37334874
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.
Clin Genet
2023
36621880
Returning integrated genomic risk and clinical recommendations: The eMERGE study.
Genet Med
2023
36617640
Clinical genetic counseling and translation considerations for polygenic scores in personalized risk assessments: A Practice Resource from the National Society of Genetic Counselors.
J Genet Couns
2023
36575824
Elective genetic testing: Genetics professionals' perspectives and practices.
J Genet Couns
2023
35380538
Perspectives of diverse Spanish- and English-speaking patients on the clinical use of polygenic risk scores.
Genet Med
2022
33467513
Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis.
J Pers Med
2021
33546753
Implementing genomic screening in diverse populations.
Genome Med
2021
33593377
Correction to: The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.
Trials
2021
33640235
Hope versus reality: Parent expectations of genomic testing.
Patient Educ Couns
2021
33531665
GUÃA: a digital platform to facilitate result disclosure in genetic counseling.
Genet Med
2021
33805616
Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium.
J Pers Med
2021
33884375
"Is that something that should concern me?": a qualitative exploration of parent understanding of their child's genomic test results.
HGG Adv
2021
34058740
Development and Validation of a Comprehensive Genomics Knowledge Scale.
Public Health Genomics
2021
33278053
A review and definition of 'usual care' in genetic counseling trials to standardize use in research.
J Genet Couns
2021
33446240
The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children.
Trials
2021
33283134
Lynch Syndrome-Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank.
JCO Precis Oncol
2020
31892343
Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank.
Genome Med
2019
29382336
Impacts of incorporating personal genome sequencing into graduate genomics education: a longitudinal study over three course years.
BMC Med Genomics
2018
28051073
Psychological and behavioural impact of returning personal results from whole-genome sequencing: the HealthSeq project.
Eur J Hum Genet
2017
28124750
Commentary: "My Identical Twin Sequenced Our Genome".
J Genet Couns
2017
26036856
Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Eur J Hum Genet
2016
26334178
Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public.
Genet Med
2016
26508568
Motivations, concerns and preferences of personal genome sequencing research participants: Baseline findings from the HealthSeq project.
Eur J Hum Genet
2016
26898680
Impact of Genomic Counseling on Informed Decision-Making among ostensibly Healthy Individuals Seeking Personal Genome Sequencing: the HealthSeq Project.
J Genet Couns
2016
25634025
How do students react to analyzing their own genomes in a whole-genome sequencing course?: outcomes of a longitudinal cohort study.
Genet Med
2015
26264128
Preparing the next generation of genomicists: a laboratory-style course in medical genomics.
BMC Med Genomics
2015
1 - 34 of 34
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row(s) 1 - 30 of 30
Collaborators
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Co-authored papers
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Carol R Horowitz
Institute for Health Equity Research, Icahn School of Medicine at Mount Sinai
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13
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Icahn School of Medicine at Mount Sinai
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John M Greally
Co-authored papers
10
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Middlebury College
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Saskia C Sanderson
University College London
Co-authored papers
8
Eric E Schadt
Icahn School of Medicine at Mount Sinai
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7
Emily R Soper
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
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Bart S Ferket
Institute for Healthcare Delivery Science, Icahn School of Medicine at Mount Sinai
Co-authored papers
4
Patricia Kovatch
Co-authored papers
3
Charlotte Cunningham-Rundles
Precision Immunology Institute, Icahn School of Medicine at Mount Sinai
Co-authored papers
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Ali Bashir
Google Accelerated Science Team, Google Inc
Co-authored papers
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Gabrielle Bertier
The Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
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3
Rosamond Rhodes
Icahn School of Medicine at Mount Sinai
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Hardik Shah
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John J Connolly
Center for Applied Genomics, Children's Hospital of Philadelphia
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Rex L Chisholm
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