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Medicine

D-Index
82
Citations
18775
World Ranking
16341
National Ranking
8220

Overview

Arthur P. Hays is affiliated with Columbia University in the United States. Their research primarily spans the field of Medicine, with specific focus areas including Genetics, Cardiology and Cardiovascular Medicine, Surgery, Pediatrics, Perinatology and Child Health, and Speech and Hearing.

The research topics Arthur P. Hays has contributed to reflect a multidisciplinary approach within medicine. Key areas include:

  • Cardiomyopathy and Myosin Studies
  • Neurogenetic and Muscular Disorders Research
  • Cardiac Structural Anomalies and Repair
  • Human-Animal Interaction Studies
  • Pediatric Pain Management Techniques
  • Veterinary Practice and Education Studies

Their publication record includes papers in diverse venues, illustrating a range of scientific interests. Notable publication venues are:

  • UNC Libraries
  • Human-Animal Interactions

Arthur P. Hays has authored recent papers as follows:

  • "X-Linked Dominant Scapuloperoneal Myopathy Is Due to a Mutation in the Gene Encoding Four-and-a-Half-LIM Protein 1," 2020, UNC Libraries
  • "Hippotherapy practice and safety patterns for adult clients in the United States," 2025, Human-Animal Interactions

Their frequent collaborators include Catarina M. Quinzii, Tuan H. Vu, K. Christopher Min, Kurenai Tanji, and Sandra Barral, each having coauthored multiple works with them.

Best Publications

  • Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface

    Eduardo Bonilla;Craig E. Samitt;Armand F. Miranda;Armand F. Miranda;Arthur P. Hays;Arthur P. Hays

  • Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy.

    Cecelia Webster;Laura Silberstein;Arthur P. Hays;Helen M. Blau

  • Structural abnormalities of subicular dendrites in subjects with schizophrenia and mood disorders: preliminary findings.

    Gorazd Rosoklija;Glen Toomayan;Steven P. Ellis;John Keilp

  • Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder

    Michio Hirano;G. Silvestri;D. M. Blake;A. Lombes

  • The natural history of primary lateral sclerosis

    P. H. Gordon;B. Cheng;I. B. Katz;M. Pinto

  • Increased expression of the pro-inflammatory enzyme cyclooxygenase-2 in amyotrophic lateral sclerosis.

    Gabrielle Almer;Christelle Guégan;Peter Teismann;Ali Naini

  • Recruitment of the Mitochondrial-Dependent Apoptotic Pathway in Amyotrophic Lateral Sclerosis

    Christelle Guégan;Miquel Vila;Gorazd Rosoklija;Arthur P. Hays

  • Experimental demyelination of nerve induced by serum of patients with neuropathy and an anti‐MAG IgM M‐protein

    Arthur P. Hays;Norman Latov;Masami Takatsu;William H. Sherman

  • The spectrum of neurologic disease associated with anti‐GM1 antibodies

    S. A. Sadiq;F. P. Thomas;K. Kilidireas;S. Protopsaltis

  • Gangliosides GM1 and GD1b are antigens for IgM M-protein in a patient with motor neuron disease.

    L Freddo;R K Yu;N Latov;P D Donofrio

  • Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency.

    Salvatore Dimauro;John F. Nicholson;Arthur P. Hays;Abraham B. B

  • Acute quadriplegic myopathy: a complication of treatment with steroids, nondepolarizing blocking agents, or both.

    Michio Hirano;B. R. Ott;E. C. Raps;C. Minetti

  • Metastatic carcinoma to the pituitary gland.

    Paul c. McCormick;Kalmon d. Post;Alexander d. Kandji;Arthur P. Hays

  • Experimental conduction block induced by serum from a patient with anti‐GM1 antibodies

    Maria Santoro;Antonino Uncini;Massimo Corbo;Susan M. Staugaitis

  • Emery‐dreifuss muscular dystrophy

    L. P. Rowland;L. P. Rowland;M. Fetell;M. Fetell;M. Olarte;M. Olarte;A. Hays;A. Hays

  • Progressive multifocal leukoencephalopathy in a male homosexual with T-cell immune deficiency.

    James R. Miller;Robert E. Barrett;Carolyn B. Britton;Michael L. Tapper

  • Monoclonal IgM with unique specificity to gangliosides GM1 and GD1b and to lacto‐N ‐tetraose associated with human motor neuron disease

    N. Latov;A. P. Hays;P. D. Donofrio;J. Liao H. Ito

  • Quantitative objective markers for upper and lower motor neuron dysfunction in ALS

    H. Mitsumoto;A. M. Uluğ;S. L. Pullman;C. L. Gooch

  • IDENTIFICATION OF A NOVEL MUTATION IN THE MTDNA ND5 GENE ASSOCIATED WITH MELAS

    Filippo M. Santorelli;Kurenai Tanji;Romana Kulikova;Sara Shanske

  • Peripherin and neurofilament protein coexist in spinal spheroids of motor neuron disease.

    Massimo Corbo;Arthur P. Hays

Frequent Co-Authors

Norman Latov
Norman Latov Cornell University
Lewis P. Rowland
Lewis P. Rowland Columbia University Medical Center
Salvatore DiMauro
Salvatore DiMauro Columbia University
Gorazd Rosoklija
Gorazd Rosoklija Columbia University
Eduardo Bonilla
Eduardo Bonilla Columbia University
Michio Hirano
Michio Hirano Columbia University
Antonino Uncini
Antonino Uncini University of Chieti-Pescara
Serge Przedborski
Serge Przedborski Columbia University
Ann Marie Schmidt
Ann Marie Schmidt New York University
Sara Shanske
Sara Shanske Columbia University Medical Center

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