Author

Meredith Hanna

Institutions: Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences

Observed institutions: Brigham and Women's Hospital, Harvard University, Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences

OpenAlex ID: A5103787782

An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery

2018 · Alireza Haghighi, Joel B. Krier, et al. · npj Genomic Medicine · 26

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

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

Hb F-SickKids ( HBG2 : C.308A > G): A Novel γ-Globin Variant Associated with Transient Neonatal Cyanosis

2026 · Landry E. Nfonsam, Meredith Hanna, et al. · Hemoglobin

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

Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia

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: 14

Citation count: 39

H-index: 3

I10-index: 1