Author

Danna Hull

Observed names: D. Hull, Hull, D., Hull, Danna

Institutions: Newborn Screening Ontario, BORN Ontario

Observed institutions: Queen's University, Kingston General Hospital, Newborn Screening Ontario, Royal Victoria Hospital, Kingston Health Sciences Centre, BORN Ontario

ORCID: 0000-0002-9237-2949

Observed ORCID: 0000-0002-9237-2949

OpenAlex ID: A5036427944

Mobile element insertion detection in 89,874 clinical exomes

2020 · Rebecca I. Torene, Kevin Galens, et al. · Genetics in Medicine · 67

Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5

2013 · P. Kannu, A.B. Campos-Xavier, et al. · European Journal of Medical Genetics · 21

Survey of the Definition of Fetal Viability and the Availability, Indications, and Decision Making Processes for Post‐Viability Termination of Pregnancy for Fetal Abnormalities and Health Conditions in Canada

2015 · Danna Hull, Gregory Davies, et al. · Journal of Genetic Counseling · 16

Expression of Heat Shock Protein 70 Is Insufficient To Extend Drosophila melanogaster Longevity

2019 · Chengfeng Xiao, Danna Hull, et al. · G3 Genes Genomes Genetics · 14

Familial Hemolytic Anemia Due to Hb Sabine [β91(F7)Leu←Pro] Identified BY Polymerase Chain Reaction

1998 · D. Hull, P. C. Winter, et al. · Hemoglobin · 8

First and second trimester maternal serum markers for prenatal aneuploidy screening: An update on the adjustment factors for race, smoking, and insulin dependent diabetes mellitus

2023 · Tianhua Huang, Kara Bellai-Dussault, et al. · Clinical Biochemistry · 7

Survey of Prenatal Counselling Practices Regarding Aneuploidy Risk Modification, Invasive Diagnostic Procedure Risks, and Procedure Eligibility Criteria in Canadian Centres

2012 · Danna Hull, Gregory Davies, et al. · Journal of Obstetrics and Gynaecology Canada · 3

Noninvasive Prenatal Detection of Trisomy 21 by Targeted Semiconductor Sequencing: A Technical Feasibility Study

2017 · Yanwei Xi, Aryan Arbabi, et al. · Fetal Diagnosis and Therapy · 2

Investigating the outcomes of pregnancies with atypical results following SNP-based cfDNA screening: a population-based cohort study

2026 · Kara Bellai-Dussault, Shelley D. Dougan, et al. · American Journal of Obstetrics & Gynecology MFM

Understanding imposter phenomenon in genetic counselors: Impact and strategies for mitigation

2026 · Susan Creighton, Alison M. Elliott, et al. · Journal of Genetic Counseling

Contents Vol. 42, 2017

2017 · Fernando Viñals, Flavia Correa, et al. · Fetal Diagnosis and Therapy

Acknowledgement to the Reviewers

2017 · Fernando Viñals, Flavia Correa, et al. · Fetal Diagnosis and Therapy

Supplementary Material for: Noninvasive Prenatal Detection of Trisomy 21 by Targeted Semiconductor Sequencing: A Technical Feasibility Study

2017 · Xi, Y., Arbabi, A., et al. · Figshare

Corrigendum to “Post-axial polydactyly type A2, overgrowth and autistic traits associated with a chromosome 13q31.3 microduplication encompassing miR-17-92 and GPC5” [Eur J Med Genet 56 (8) (2013) 452–457]

2014 · P. Kannu, A.B. Campos-Xavier, et al. · European Journal of Medical Genetics

OP34.09: Counselling practices regarding aneuploidy risk modification, invasive procedure risks, and procedure eligibility criteria across Canadian centres

2012 · G. Davies, D. Hull, et al. · Ultrasound in Obstetrics and Gynecology

Works count: 16

Citation count: 138

H-index: 6

I10-index: 4