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Biology and Biochemistry

D-Index
68
Citations
19348
World Ranking
7702
National Ranking
3510

Overview

Steven A. Moore is affiliated with the University of Iowa in the United States. Their research primarily focuses on the fields of Biochemistry, Genetics and Molecular Biology, and Medicine. Within these disciplines, Moore's work includes extensive contributions to Molecular Biology, Genetics, Epidemiology, Cellular and Molecular Neuroscience, and Cardiology and Cardiovascular Medicine.

Their research covers several main topics, including:

  • Muscle Physiology and Disorders
  • Cardiomyopathy and Myosin Studies
  • RNA Research and Splicing
  • Genetic Neurodegenerative Diseases
  • Neurogenetic and Muscular Disorders Research
  • Nuclear Structure and Function
  • RNA modifications and cancer

Some of the recent papers associated with Moore include:

  • Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular Dystrophy (2021), published in Journal of Molecular Diagnostics
  • Making Sense of Missense Variants in TTN-related Congenital Myopathies (2021), published in Acta Neuropathologica
  • What Every Neuropathologist Needs to Know: The Muscle Biopsy (2020), published in Journal of Neuropathology & Experimental Neurology
  • Intron Mutations and Early Transcription Termination in Duchenne and Becker Muscular Dystrophy (2022), published in Human Mutation
  • The Inflammatory Pathology of Dysferlinopathy is Distinct from Calpainopathy, Becker Muscular Dystrophy, and Inflammatory Myopathies (2022), published in Acta Neuropathologica Communications

Moore frequently collaborates with other researchers including Katherine D. Mathews, Benjamin W. Darbro, Karra A. Jones, Rebecca D. Folkerth, and Nicol C. Voermans.

The researcher has published extensively in several scientific venues, with notable contributions in:

  • Journal of Neuropathology & Experimental Neurology
  • Neuromuscular Disorders
  • Science Advances
  • International Journal of Molecular Sciences
  • Child Neurology Open

Best Publications

  • Severe acute respiratory syndrome coronavirus infection causes neuronal death in the absence of encephalitis in mice transgenic for human ACE2.

    Jason Netland;David K. Meyerholz;Steven Moore;Martin Cassell

  • Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

    Daniel E. Michele;Rita Barresi;Motoi Kanagawa;Fumiaki Saito

  • Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy

    Steven A. Moore;Fumiaki Saito;Jianguo Chen;Daniel E. Michele

  • Ataluren treatment of patients with nonsense mutation dystrophinopathy

    Katharine Bushby;Richard Finkel;Brenda Wong;Richard Barohn

  • Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle: A Novel Mechanism for Cardiomyopathy and Muscular Dystrophy

    Ramon Coral-Vazquez;Ronald D Cohn;Steven A Moore;Joseph A Hill

  • Astrocytes, not neurons, produce docosahexaenoic acid (22:6 omega-3) and arachidonic acid (20:4 omega-6).

    Steven A. Moore;Elizabeth Yoder;Sean Murphy;Gary R. Dutton

  • An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.

    Catherine A. Brownstein;Alan H. Beggs;Nils Homer;Barry Merriman

  • CaMKII determines mitochondrial stress responses in heart

    Mei Ling A. Joiner;Olha M. Koval;Jingdong Li;Jingdong Li;B. Julie He

  • Hydroxyeicosatetraenoic acids (HETEs)

    Arthur A. Spector;Joel A. Gordon;Steven A. Moore

  • Progressive Muscular Dystrophy in α-Sarcoglycan–deficient Mice

    Franck Duclos;Volker Straub;Steven A. Moore;David P. Venzke

  • Rapid development of colitis in NSAID-treated IL-10–deficient mice

    Daniel J. Berg;Juan Zhang;Joel V. Weinstock;Hanan F. Ismail

  • Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.

    Ronald D. Cohn;Michael D. Henry;Daniel E. Michele;Rita Barresi

  • Sarcolemma-localized nNOS is required to maintain activity after mild exercise

    Yvonne M. Kobayashi;Erik P. Rader;Robert W. Crawford;Nikhil K. Iyengar

  • Identification of a Functional Peroxisome Proliferator-Activated Receptor Response Element in the Rat Catalase Promoter

    Geoffrey D. Girnun;Frederick E. Domann;Steven A. Moore;Mike E. C. Robbins

  • LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies

    Rita Barresi;Daniel E Michele;Motoi Kanagawa;Hollie A Harper

  • Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E

    Madeleine Durbeej;Ronald D. Cohn;Ronald F. Hrstka;Steven A. Moore

  • Unique Role of Dystroglycan in Peripheral Nerve Myelination, Nodal Structure, and Sodium Channel Stabilization

    Fumiaki Saito;Steven A Moore;Rita Barresi;Michael D Henry

  • ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

    Tobias Willer;Hane Lee;Mark Lommel;Takako Yoshida-Moriguchi

  • Mutations in GDP-mannose pyrophosphorylase b cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan

    Keren J. Carss;Elizabeth Stevens;A. Reghan Foley;Sebahattin Cirak;Sebahattin Cirak

  • Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease.

    Hernan D. Gonorazky;Sergey Naumenko;Arun K. Ramani;Viswateja Nelakuditi

Frequent Co-Authors

Kevin P. Campbell
Kevin P. Campbell University of Iowa
Arthur A. Spector
Arthur A. Spector University of Iowa
Francesco Muntoni
Francesco Muntoni University College London
Volker Straub
Volker Straub Newcastle University
Michael E. Shy
Michael E. Shy University of Iowa
Stanley F. Nelson
Stanley F. Nelson University of California, Los Angeles
William T. Talman
William T. Talman University of Iowa
Robert M. Weiss
Robert M. Weiss University of Iowa
Hane Lee
Hane Lee University of California, Los Angeles
Frank M. Faraci
Frank M. Faraci University of Iowa

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