F. Kutlar

University of North Carolina at Chapel Hill — United States

Medicine · Health Sciences

38h-index4.2kcitations196works0.02yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(166), Iron Metabolism and Disorders(84), Blood groups and transfusion(43), Neonatal Health and Biochemistry(35), Erythrocyte Function and Pathophysiology(33)

Publications196 total

Coagulation activation in sickle cell trait: an exploratory study
UNC Libraries·2020Open Access
Hydroxyurea differentially modulates activator and repressors of γ-globin gene in erythroblasts of responsive and non-responsive patients with sickle cell disease in correlation with Index of Hydroxyurea Responsiveness
UKnowledge (University of Kentucky)·2017Open Access
Hydroxyurea differentially modulates activator and repressors of γ-globin gene in erythroblasts of responsive and non-responsive patients with sickle cell disease in correlation with Index of Hydroxyurea Responsiveness
Haematologica·2017· 17 citedOpen Access
Coinheritance of Alpha-3.7 Deletion and Hb Questembert [131alpha-2 Tct > CCT](Ser131>Pro)] in an African American Patient Results in an Alpha Thalassemia Phenotype
Blood·2015
Hemoglobin F Only Syndrome at Birth
Journal of Pediatric Hematology/Oncology·2015· 2 cited
Coagulation activation in sickle cell trait: an exploratory study
British Journal of Haematology·2015· 34 citedOpen Access
A New<sup>A</sup>γ-Globin Chain Variant: Hb F-Sykesville MD [<sup>A</sup>γ113(G15)Val → Ile;<i>HBG1</i>: c.340G&gt;A] Detected in a Caucasian Baby
Hemoglobin·2015· 1 cited
Diagnostic Challenges in a Low a2 β-Thalassemia Case
Blood·2014
Two New γ Chain Variants: Hb F-Augusta GA [<sup>G</sup>γ59(E3)Lys → Arg;<i>HBG2</i>: c.179A &gt; G] and Hb F-Port Royal-II [<sup>A</sup>γ125(H3)Glu → Ala;<i>HBG1</i>: c.377A &gt; C]
Hemoglobin·2014· 1 cited
Two New Hemoglobin Variants: Hb Tallahassee [α3(A1)Ser→Tyr;<i>HBA2</i>: c.11C&gt;A] and Hb Madison-NC [β119(GH2)Gly→Ser;<i>HBB</i>: c.358G&gt;A]
Hemoglobin·2014· 1 cited
Nondeletional α-Thalassemia (α2- IVS-1-116, A&gt;G HBA2): An α2 Gene Point Mutation Detected in an African-American Female for the First Time
Acta Haematologica·2013· 1 cited
Hb Fulton-Georgia [α20(B1)His→Pro;<i>HBA1</i>: c.62A&gt;C]: A New α-Globin Variant Coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC Disease
Hemoglobin·2013· 2 cited
Improving the Accuracy of BCR-ABL Transcript Quantitation: Pitfalls of Using a Common Standard for b3a2 and b2a2 Transcripts
Blood·2012
Homozygous Expression of a Novel Senegalese-Type Partial Deletion of the Beta and Delta Genes Causes a Delta0 Beta+ Thalassemia.
Blood·2012
Exploratory Study of Haptoglobin Levels by Genotype in Adult Sickle Cell Patients
Blood·2011· 6 cited
BCL11A Polymorphism and HbF Response to Hydroxyurea in Adult Patients with Sickle Cell Disease
Blood·2011· 1 cited
Thalassemia-like Phenotype in a Novel Complex Hemoglobinopathy With α, β, δ Globin Chain Abnormalities
Journal of Pediatric Hematology/Oncology·2011· 2 cited
Pomalidomide augments fetal hemoglobin production without the myelosuppressive effects of hydroxyurea in transgenic sickle cell mice
Blood·2011· 84 citedOpen Access
The Quest for Hb Questembert: A Challenging Case of An Unstable Hb Variant
Blood·2010
Potential Pitfalls In Quantitative Real-Time PCR for Molecular Monitoring of BCR-ABL In the Management of CML.
Blood·2010
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Frequent Co-authors

Abdullah Kutlar(26), T. H. J. Huisman(12), T. H. J. Huisman(11), T. A. Stoming(10), J. M. Gonzalez‐Redondo(8), Aytemiz Gürgey(7), KD Lanclos(5), M Aksoy(5), Virgil McKie(5), T. Nakatsuji(4), Yurdanur Kılınç(4), R. Öner(4), Çiğdem Altay(4), Y. Hattori(4), E. Baysal(4), T. Harano(4), C Altay(3), J. B. Wilson(3), A. L. Reese(3), Aleksandar Dimovski(3)