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Patrick G. Gallagher

Patrick G. Gallagher

D-Index & Metrics

Molecular Biology

D-Index
63
Citations
12536
World Ranking
1816
National Ranking
910

Overview

Patrick G. Gallagher is affiliated with Yale University in the United States. Their research spans several interconnected fields, primarily focusing on medicine and biochemistry, genetics, and molecular biology.

Their subfields of study include:

  • Molecular Biology
  • Physiology
  • Hematology
  • Genetics
  • Pulmonary and Respiratory Medicine

Main topics of their work cover:

  • Erythrocyte Function and Pathophysiology
  • RNA modifications and cancer
  • Epigenetics and DNA Methylation
  • Hemoglobinopathies and Related Disorders
  • Blood groups and transfusion
  • Blood properties and coagulation
  • Neonatal Health and Biochemistry

Gallagher has contributed to scholarly literature in various notable venues, frequently publishing in:

  • Blood
  • Journal of Perinatology
  • American Journal of Hematology
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Blood Advances

Recent publications include:

  • "Recommendations for diagnosis and treatment of methemoglobinemia," 2021, American Journal of Hematology
  • "Perinatal aspects on the covid-19 pandemic: a practical resource for perinatal-neonatal specialists," 2020, Journal of Perinatology
  • "Histone Acetyltransferases p300 and CBP Coordinate Distinct Chromatin Remodeling Programs in Vascular Smooth Muscle Plasticity," 2022, Circulation
  • "Anemia in the pediatric patient," 2022, Blood
  • "Phase 3, multicentre, randomised, placebo-controlled study evaluating the efficacy and safety of ustekinumab in patients with systemic lupus erythematosus," 2022, Annals of the Rheumatic Diseases

Frequent collaborators include:

  • Vincent Schulz
  • Lionel Blanc
  • Laurie A. Steiner
  • Narla Mohandas
  • James Palis

Gallagher has also contributed to book publications, including one released by the American Psychological Association titled Portable PhD: Taking your psychology career beyond academia. in 2020.

Best Publications

  • Red cell membrane: past, present, and future

    Narla Mohandas;Patrick G. Gallagher

  • Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

    Ryan Zarychanski;Vincent P. Schulz;Brett L. Houston;Yelena Maksimova

  • Global transcriptome analyses of human and murine terminal erythroid differentiation

    Xiuli An;Xiuli An;Vincent P. Schulz;Jie Li;Kunlu Wu;Kunlu Wu

  • Sites of Regulated Phosphorylation that Control K-Cl Cotransporter Activity

    Jesse Rinehart;Yelena D. Maksimova;Jessica E. Tanis;Kathryn L. Stone

  • Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.

    Stefan W. Eber;Jennifer M. Gonzalez;Marcia L. Lux;Alphonse L. Scarpa

  • Hereditary elliptocytosis: spectrin and protein 4.1R

    Patrick G Gallagher

  • Piezo Proteins: Regulators of Mechanosensation and Other Cellular Processes

    Sviatoslav N. Bagriantsev;Elena O. Gracheva;Patrick G. Gallagher

  • Red cell membrane disorders.

    Patrick G. Gallagher

  • Telehealth interventions for the secondary prevention of coronary heart disease: A systematic review and meta-analysis

    Kai Jin;Sahar Khonsari;Robyn Gallagher;Patrick Gallagher

  • Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-E.

    Jie Li;John Hale;Pooja Bhagia;Pooja Bhagia;Fumin Xue

  • Novel role for EKLF in megakaryocyte lineage commitment

    Pilar Frontelo;Deepa Manwani;Mariann Galdass;Holger Karsunky

  • Proton Block and Voltage Gating Are Potassium-dependent in the Cardiac Leak Channel Kcnk3

    Coeli M.B. Lopes;Patrick G. Gallagher;Marianne E. Buck;Margaret H. Butler

  • Nonstochastic reprogramming from a privileged somatic cell state.

    Shangqin Guo;Xiaoyuan Zi;Vincent P. Schulz;Jijun Cheng

  • In vivo correction of anaemia in β-thalassemic mice by γPNA-mediated gene editing with nanoparticle delivery

    Raman Bahal;Nicole Ali McNeer;Elias Quijano;Yanfeng Liu

  • Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment

    Pratik Home;Biswarup Saha;Soma Ray;Debasree Dutta

  • Neonatal Sepsis 2004-2013: The Rise and Fall of Coagulase-Negative Staphylococci

    Matthew J. Bizzarro;Veronika Shabanova;Robert S. Baltimore;Louise-Marie Dembry

  • Perinatal aspects on the covid-19 pandemic: a practical resource for perinatal-neonatal specialists.

    Francis Mimouni;Satyan Lakshminrusimha;Stephen A. Pearlman;Tonse Raju

  • Failure of Terminal Erythroid Differentiation in EKLF-Deficient Mice Is Associated with Cell Cycle Perturbation and Reduced Expression of E2F2

    Andre M. Pilon;Murat O. Arcasoy;Holly K. Dressman;Serena E. Vayda

  • Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis

    Edyta Glogowska;Kimberly Lezon-Geyda;Yelena Maksimova;Vincent P. Schulz

  • Novel role for EKLF in megakaryocyte lineage commitment. Commentary

    Gerd A. Blobel;Pilar Frontelo;Deepa Manwani;Mariann Galdass

Frequent Co-Authors

Bernard G. Forget
Bernard G. Forget Yale University
David M. Bodine
David M. Bodine National Institutes of Health
Narla Mohandas
Narla Mohandas New York Blood Center
Xiuli An
Xiuli An New York Blood Center
David W. Speicher
David W. Speicher The Wistar Institute
Richard A. Ehrenkranz
Richard A. Ehrenkranz Yale University
Diane S. Krause
Diane S. Krause Yale University
Samuel E. Lux
Samuel E. Lux Harvard University
Jon S. Morrow
Jon S. Morrow Yale University
David H.K. Chui
David H.K. Chui Boston University

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