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Tavanna R. Porter

Observed names: Tavanna Porter, Tavanna R Porter
Institution: Mayo Clinic
Observed institution: Mayo Clinic
ORCID: 0000-0003-3796-1473
Observed ORCID: 0000-0003-3796-1473
OpenAlex ID: A5015035371
Genotype–phenotype correlation of hereditary erythrocytosis mutations, a single center experience
2018 · Jennifer L. Oliveira, Lea M. Coon, et al. · American Journal of Hematology · 46
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Interpreting sulfhemoglobin and methemoglobin in patients with cyanosis: An overview of patients with M‐hemoglobin variants
2021 · Aruna Rangan, Michelle E. Savedra, et al. · International Journal of Laboratory Hematology · 26
Erythrocytosis associated with EPAS1(HIF2A), EGLN1(PHD2), VHL, EPOR or BPGM mutations: The Mayo Clinic experience
2022 · Naseema Gangat, Jennifer L. Oliveira, et al. · Haematologica · 12
Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing
2021 · Aruna Rangan, Molly S. Hein, et al. · Journal of Molecular Diagnostics · 12
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Effects of Voxelotor (GBT440) Therapy on Laboratory Testing of Sickle Cell Patients
2019 · Michelle E. Savedra, Jessica L. Szuberski, et al. · Blood · 2
P734: Hemoglobin S coinheritance with unusual clinically significant beta globin variants
2024 · Tavanna Porter, Kenneth Swanson, et al. · Genetics in Medicine Open · 1
Hb F-Wentzville [Gγ24(B6)Gly→Glu; HBG2: c.74G>A, p.Gly25Glu]: An Unstable Gγ-Globin Variant Associated with Neonatal Hemolytic Anemia
2020 · Katarina M. Semkiu, Jennifer L. Oliveira, et al. · Hemoglobin · 1
Long Range Sequencing Shows Improved Resolution in the Detection of Beta Globin Cluster Variants
2019 · Aruna Rangan, Molly S. Hein, et al. · Blood · 1
Novel Double Fusion (βδβ) Hemoglobin Variant with Comparison to Lepore Hemoglobins
2023 · Aruna Rangan, Kenneth C. Swanson, et al. · Blood
Large β Globin Gene Cluster Deletions and Implications on Transcription Factor Regulation in Hemoglobin Switching - Α Novel ε Gγ Αγ Deletion with Intact LCR
2021 · Christineil Thompson, Mira A Kohorst, et al. · Blood
Comparison of αLEPRA and αLELY Co-Inheritance with a SPTA1 Whole Gene Deletion, a Family Study
2019 · Molly S. Hein, Lea Coon, et al. · Blood
Works count: 11
Citation count: 101
H-index: 4
I10-index: 4
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