Scott A Peslak

Scott A Peslak

University of Pennsylvania

H-index: 11

North America-United States

About Scott A Peslak

Scott A Peslak, With an exceptional h-index of 11 and a recent h-index of 10 (since 2020), a distinguished researcher at University of Pennsylvania, specializes in the field of Hematology, sickle cell disease, thalassemia, erythropoiesis, fetal hemoglobin.

His recent articles reflect a diverse array of research interests and contributions to the field:

Let-7 miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching

Expansion of human hematopoietic stem cells by inhibiting translation

Adults with Transfusion-Dependent Thalassemia Have Variable Clinical Profiles Depending on Where They Receive Care: Thalassemia Treatment Center Vs Community

Patients with Non-Transfusion-Dependent Thalassemia May Evolve to Transfusion-Dependent Thalassemia in Adulthood

Protein Phosphatase 6 Complex: Novel Regulator of Fetal Hemoglobin and Potential Therapeutic Target in Sickle Cell Disease

Author Correction: HIC2 controls developmental hemoglobin switching by repressing BCL11A transcription

Forced enhancer-promoter rewiring to alter gene expression in animal models

A novel, effective, and efficient strategy for treating sickle cell vaso-occlusive events in the infusion center setting

Scott A Peslak Information

University

Position

Hematology/Oncology Fellow

Citations(all)

466

Citations(since 2020)

352

Cited By

197

hIndex(all)

11

hIndex(since 2020)

10

i10Index(all)

11

i10Index(since 2020)

10

Email

University Profile Page

Google Scholar

Scott A Peslak Skills & Research Interests

Hematology

sickle cell disease

thalassemia

erythropoiesis

fetal hemoglobin

Top articles of Scott A Peslak

Let-7 miRNAs repress HIC2 to regulate BCL11A transcription and hemoglobin switching

Blood

2024/2/18

Expansion of human hematopoietic stem cells by inhibiting translation

biorxiv

2023/11/28

Adults with Transfusion-Dependent Thalassemia Have Variable Clinical Profiles Depending on Where They Receive Care: Thalassemia Treatment Center Vs Community

Blood

2023/11/28

Scott A Peslak
Scott A Peslak

H-Index: 7

Jennifer Cohen
Jennifer Cohen

H-Index: 5

Patients with Non-Transfusion-Dependent Thalassemia May Evolve to Transfusion-Dependent Thalassemia in Adulthood

Blood

2023/11/28

Protein Phosphatase 6 Complex: Novel Regulator of Fetal Hemoglobin and Potential Therapeutic Target in Sickle Cell Disease

Blood

2023/11/28

Scott A Peslak
Scott A Peslak

H-Index: 7

Junwei Shi
Junwei Shi

H-Index: 9

Author Correction: HIC2 controls developmental hemoglobin switching by repressing BCL11A transcription

Nature Genetics

2023/9

Forced enhancer-promoter rewiring to alter gene expression in animal models

Molecular Therapy-Nucleic Acids

2023/3/14

A novel, effective, and efficient strategy for treating sickle cell vaso-occlusive events in the infusion center setting

Blood Advances

2023/2/14

Scott A Peslak
Scott A Peslak

H-Index: 7

Compositions and methods for hemoglobin production

2023/2/9

Hemoglobinopathies and thalassemias

2023/1/1

Identification and characterization of RBM12 as a novel regulator of fetal hemoglobin expression

Blood Advances

2022/12/13

Regulation of Fetal Hemoglobin Production in Adult Erythroid Cells By Protein Phosphatase 6C (PPP6C)

Blood

2022/11/15

Let-7 Inhibits HIC2 to Control BCL11A Transcription and Hemoglobin Switching

Blood

2022/11/15

Peng Huang
Peng Huang

H-Index: 10

Scott A Peslak
Scott A Peslak

H-Index: 7

Targeting the EIF2AK1 Signaling Pathway Rescues Red Blood Cell Production in SF3B1-Mutant Myelodysplastic Syndromes With Ringed Sideroblasts

Blood cancer discovery

2022/11/2

HIC2 controls developmental hemoglobin switching by repressing BCL11A transcription

Nature genetics

2022/9

Dual function NFI factors control fetal hemoglobin silencing in adult erythroid cells (May, 10.1038/s41588-022-01076-1, 2022)

Nature genetics

2022/6

Histone H2A. X phosphorylation and Caspase-Initiated Chromatin Condensation in late-stage erythropoiesis

Epigenetics & Chromatin

2021/12

Protein phosphatase 6c (PPP6C) loss significantly raises fetal hemoglobin levels and reduces cell sickling

Blood

2021/11/23

Interrogating Post-Transcriptional Mechanisms of Fetal Hemoglobin Regulation

Blood

2021/11/23

Isolated changes in chromatin accessibility and enhancer-promoter contacts at the β-globin locus distinguish fetal hemoglobin producing F-cells from A-cells

Blood

2021/11/23

See List of Professors in Scott A Peslak University(University of Pennsylvania)

Co-Authors

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