Author

Betty-Ann Hohenadel

Observed names: B.-A. Hohenadel, Betty‐Ann Hohenadel

Institutions: Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences

Observed institutions: Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences

OpenAlex ID: A5085986945

Normal Hb A2β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) inCiswith the Hb A2’δ-Globin Gene Missense Mutation (HBD: c.49G>C)

2013 · John S. Waye, Barry Eng, et al. · Hemoglobin · 7

Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the locus control region

2015 · A. Amid, M. Cheong, et al. · Haematologica · 6

Characterization of Three Novel δ Chain Hemoglobin Variants and Two δ-Thalassemia Alleles

2010 · Hannes Frischknecht, Heinz Troxler, et al. · Hemoglobin · 4

Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene

2017 · John S. Waye, Meredith Hanna, et al. · Hemoglobin · 3

Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion

2015 · John S. Waye, Barry Eng, et al. · Hemoglobin · 3

β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T]

2024 · John S. Waye, Meredith Hanna, et al. · Hemoglobin · 2

Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of theβ-Globin Gene Promoter (HBB: c.-133G > A)

2014 · John S. Waye, Barry Eng, et al. · Hemoglobin · 2

Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)

2013 · John S. Waye, Barry Eng, et al. · Hemoglobin · 2

α0-Thalassemia Due to a 90.7 kb Deletion (– –NFLD)

2017 · John S. Waye, Barry Eng, et al. · Hemoglobin · 1

Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG orHBA1:c.2T>A)

2016 · John S. Waye, Barry Eng, et al. · Hemoglobin · 1

α+-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup]

2015 · John S. Waye, Barry Eng, et al. · Hemoglobin · 1

Characterization of a Novel, Recurrent 40.6 kb α 0 ‐Thalassemia Deletion in Canadians of East Indian Descent

2026 · John S. Waye, Meredith Hanna, et al. · International Journal of Laboratory Hematology

Optimized Test Utilization Significantly Increased the Positive Detection Rate for Myeloproliferative Neoplasms

2026 · Landry E. Nfonsam, Melody (Zhenchen) Qi, et al. · Cancers

Choosing wisely-directed HFE testing improves diagnostic yield and test utilization in hereditary hemochromatosis

2026 · Landry E. Nfonsam, Betty-Ann Hohenadel, et al. · Clinical Biochemistry

Novel δβ Fusion Gene in Individuals of Bhutanese and Nepalese Origin

2026 · John S. Waye, Meredith Hanna, et al. · International Journal of Laboratory Hematology

Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup)

2024 · John S. Waye, Meredith Hanna, et al. · Hemoglobin

Compound Heterozygosity for Hb S and a Novel Deletion of Dnase I Hypersensitivity Sites HS3 and HS4 of β-Globin Locus Control Region Results in Hb S/β+-Thalassemia Phenotype

2014 · Ali Amid, Barry Eng, et al. · Blood

Works count: 17

Citation count: 32

H-index: 3

I10-index: