Lea M. Coon

Most-cited papers

1. Genotype–phenotype correlation of hereditary erythrocytosis mutations, a single center experience

   J. Oliveira, Lea M. Coon, L. Frederick, Molly S. Hein +9 more

   2018American journal of hematology/oncology46 citations Open access

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2. Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family

   Juliana Perez Botero, Dong Chen, R. He, D. Viswanatha +9 more

   2016Platelets23 citations

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3. Severe Bleeding with Subclinical Oculocutaneous Albinism in a Patient with a Novel HPS6 Missense Variant

   C. Han, K. O'Brien, Lea M. Coon, J. Majerus +10 more

   2018American Journal of Medical Genetics. Part A13 citations Open access

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4. Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia

   Juliana Perez Botero, Dong Chen, M. Cousin, J. Majerus +6 more

   2017Leukemia and Lymphoma12 citations

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5. Hermansky-Pudlak syndrome subtype 5 (HPS-5) novel mutation in a 65 year-old with oculocutaneous hypopigmentation and mild bleeding diathesis: The importance of recognizing a subtle phenotype

   J. P. Botero, Dong Chen, J. Majerus, Lea M. Coon +4 more

   2018Platelets11 citations

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6. Practice patterns in the diagnosis of inherited platelet disorders within a single institution

   Juliana Perez Botero, R. Pruthi, J. Majerus, Lea M. Coon +3 more

   2017Blood Coagulation and Fibrinolysis8 citations

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7. Factor V Deficiency with a Thrombotic Clinical Phenotype

   Meera Sridharan, Lea M. Coon, Dong Chen, R. Pruthi

   2019Seminars in Thrombosis and Hemostasis6 citations Open access

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8. Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience

   Juliana Perez Botero, Lea M. Coon, J. Majerus, Dong Chen +1 more

   2017Seminars in Thrombosis and Hemostasis5 citations

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9. A Novel β-Globin Chain Hemoglobin Variant, Hb Allentown [β137(H15)Val→Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Intermittent Aplastic Crises and Splenomegaly

   A. Collier, Lea M. Coon, P. Monteleone, S. Umaru +3 more

   2016Hemoglobin4 citations

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10. Deletional HPFH Vs. Delta Beta Thalassemia: Closing in on a Possible Hb F Silencer Location

    Molly S. Hein, Kenneth C. Swanson, P. Lundquist, Joella A Yungerberg +6 more

    20153 citations

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11. Hereditary Thrombotic Thrombocytopenic Purpura in a 9-Month Old: Diagnosing and Managing an Ultra-rare Disorder.

    Kirk D. Wyatt, Mira A. Kohorst, Lea M. Coon, R. Hurley +2 more

    2020Journal of pediatric hematology/oncology2 citations Open access

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12. Further Characterization of Hb Bronovo [α103(G10)His→Leu; HBA2: c.311A>T] and First Report of the Homozygous State

    Nikita Mehta, J. Johnston, Molly S. Hein, B. Kipp +7 more

    2020Hemoglobin2 citations

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13. Spectrum of Mutations Associated with Hereditary Erythrocytosis

    J. Oliveira, Lori S. Frederick, Lea M. Coon, Molly S. Hein +6 more

    20152 citations

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14. Autosomal-Recessive LMNA Dilated Cardiomyopathy

    Rosalie M. Sterner, Lea M. Coon, John L. Black, Ann M. Moyer +2 more

    2025JACC Case Reports1 citations Open access

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15. An Erythrocytosis-Associated Mutation in the Zinc Finger of PHD2 Provides Insights into Its Binding of p23

    Daisheng Song, W. Guan, Lea M. Coon, A. Al-Kali +2 more

    2019Hypoxia1 citations Open access

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16. HP_A_230502 81..86

    W. Guan, Lea M. Coon, A. Al-Kali, J. Oliveira +1 more

    20190 citations

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17. Case Report: Development of Factor VIII Inhibitor in a Patient with an Uncommon de novo Mutation in the Factor VIII Gene

    Kirk D. Wyatt, Lea M. Coon, Dawn Rusk, V. Rodriguez +1 more

    2019Acta Haematologica0 citations

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18. Comparison of αLEPRA and αLELY Co-Inheritance with a SPTA1 Whole Gene Deletion, a Family Study

    Molly S. Hein, Lea M. Coon, Tavanna R. Porter, R. He +8 more

    2019Blood0 citations Open access

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19. Large Deletions Involving the Beta Globin Gene Complex: Genotype-Phenotype Correlation of 119 Cases

    Molly S. Hein, J. Oliveira, Kenneth C. Swanson, P. Lundquist +6 more

    20150 citations

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