World's Best Scientists 2026 revealed!

D-Index & Metrics

Medicine

D-Index
90
Citations
26199
World Ranking
12327
National Ranking
6312

Research.com Recognitions

  • 1998 - Member of the National Academy of Medicine (NAM)

Overview

What is he best known for?

The fields of study he is best known for:

  • Internal medicine
  • Disease
  • Surgery

Robert C. Griggs mostly deals with Internal medicine, Surgery, Endocrinology, Muscular dystrophy and Pathology. His Internal medicine research is multidisciplinary, relying on both Gastroenterology and Periodic paralysis. The Surgery study combines topics in areas such as Placebo, Anesthesia and Duchenne muscular dystrophy.

As a part of the same scientific family, Robert C. Griggs mostly works in the field of Placebo, focusing on Clinical trial and, on occasion, Natural history and Disease. Robert C. Griggs works mostly in the field of Endocrinology, limiting it down to concerns involving Myotonia and, occasionally, Muscle disorder. His biological study spans a wide range of topics, including Deflazacort, Physical therapy and Muscle biopsy.

His most cited work include:

  • Inclusion body myositis and myopathies. (646 citations)
  • Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy (423 citations)
  • Clinical trial in duchenne dystrophy. I. The design of the protocol (405 citations)

What are the main themes of his work throughout his whole career to date?

Robert C. Griggs focuses on Internal medicine, Endocrinology, Duchenne muscular dystrophy, Myotonia and Clinical trial. His Internal medicine study combines topics from a wide range of disciplines, such as Placebo, Weakness and Cardiology. His research integrates issues of Anesthesia and Adverse effect in his study of Placebo.

His work carried out in the field of Duchenne muscular dystrophy brings together such families of science as Randomized controlled trial, Muscular dystrophy, Prednisone, Physical therapy and Pediatrics. His Muscular dystrophy research is included under the broader classification of Genetics. His research in Myotonia focuses on subjects like Periodic paralysis, which are connected to Hypokalemic periodic paralysis.

He most often published in these fields:

  • Internal medicine (25.23%)
  • Endocrinology (14.35%)
  • Duchenne muscular dystrophy (11.57%)

What were the highlights of his more recent work (between 2008-2021)?

  • Internal medicine (25.23%)
  • Duchenne muscular dystrophy (11.57%)
  • Physical therapy (8.56%)

In recent papers he was focusing on the following fields of study:

His main research concerns Internal medicine, Duchenne muscular dystrophy, Physical therapy, Pediatrics and Clinical trial. His Internal medicine research is multidisciplinary, incorporating elements of Placebo, Periodic paralysis, Endocrinology and Cardiology. He interconnects Muscular dystrophy, Newborn screening, Bioinformatics and Spinal muscular atrophy in the investigation of issues within Duchenne muscular dystrophy.

His Pediatrics study integrates concerns from other disciplines, such as Neurology and Genetic testing. In his research, Orphan drug is intimately related to Intensive care medicine, which falls under the overarching field of Clinical trial. Robert C. Griggs has researched Myotonia in several fields, including Weakness and Pathology.

Between 2008 and 2021, his most popular works were:

  • Clinical research for rare disease: opportunities, challenges, and solutions. (234 citations)
  • The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment (137 citations)
  • Evidence-based guideline summary: Diagnosis and treatment of limb-girdle and distal dystrophies Report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine (115 citations)

In his most recent research, the most cited papers focused on:

  • Internal medicine
  • Disease
  • Gene

Physical therapy, Internal medicine, Myotonia, Duchenne muscular dystrophy and Pediatrics are his primary areas of study. He combines subjects such as Neurology, Clinical trial and Evidence-based medicine, MEDLINE with his study of Physical therapy. His research links Endocrinology with Internal medicine.

His Myotonia research is multidisciplinary, incorporating perspectives in Periodic paralysis, Mexiletine and Pathology. Robert C. Griggs has included themes like Muscular dystrophy, Newborn screening and Myostatin in his Duchenne muscular dystrophy study. His Pediatrics research includes themes of Muscle biopsy, Status epilepticus, Genetic testing and Subarachnoid hemorrhage.

Best Publications

  • Inclusion body myositis and myopathies.

    Robert C. Griggs;Valerie Askanas;Salvatore DiMauro;Andrew Engel

  • Clinical trial in duchenne dystrophy. I. The design of the protocol

    Michael H. Brooke;Robert C. Griggs;Jerry R. Mendell;Gerald M. Fenichel

  • Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy

    J.R. Mendell;R.T. Moxley;R.C. Griggs;M.H. Brooke

  • Effect of testosterone on muscle mass and muscle protein synthesis

    R. C. Griggs;W. Kingston;R. F. Jozefowicz;B. E. Herr

  • Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

    Louis J. Ptáček;Rabi Tawil;Robert C. Griggs;Andrew G. Engel

  • Clinical investigation in duchenne dystrophy: 2. Determination of the “power” of therapeutic trials based on the natural history

    Brooke Mh;Fenichel Gm;Griggs Rc;Mendell

  • Identification of a mutation in the gene causing hyperkalemic periodic paralysis.

    Louis J. Ptáček;Alfred L. George;Robert C. Griggs;Rabi Tawil

  • Duchenne muscular dystrophy Patterns of clinical progression and effects of supportive therapy

    M. H. Brooke;G. M. Fenichel;R. C. Griggs;J. R. Mendell

  • Clinical research for rare disease: opportunities, challenges, and solutions.

    Robert C. Griggs;Mark Batshaw;Mary Dunkle;Rashmi Gopal-Srivastava

  • Andersen's syndrome : potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features

    Rabi Tawil;Louis J. Ptacek;Steven G. Pavlakis;Darryl C. DeVivo

  • The primary periodic paralyses: diagnosis, pathogenesis and treatment

    S. L. Venance;S. C. Cannon;D. Fialho;B. Fontaine

  • Primary episodic ataxias: diagnosis, pathogenesis and treatment.

    J.C. Jen;T.D. Graves;E.J. Hess;M.G. Hanna

  • Prednisone in Duchenne Dystrophy: A Randomized, Controlled Trial Defining the Time Course and Dose Response

    Robert C. Griggs;Richard T. Moxley;Jerry R. Mendell;Gerald M. Fenichel

  • Long-term benefit from prednisone therapy in Duchenne muscular dystrophy

    G. M. Fenichel;J. M. Florence;A. Pestronk;J. R. Mendell

  • Correlating phenotype and genotype in the periodic paralyses

    T. M. Miller;M. R. Dias da Silva;H. A. Miller;H. Kwiecinski

  • Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita.

    Louis J. Ptáček;Alfred L. George;Alfred L. George;Robert L. Barchi;Robert C. Griggs

  • Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group.

    Rabi Tawil;James Forrester;Robert C. Griggs;Jerry Mendell

  • Myotonic dystrophy with no trinucleotide repeat expansion.

    Charles A. Thornton;Robert C. Griggs;Richard T. Moxley

  • Duchenne dystrophy: Randomized, controlled trial of prednisone (18 months) and azathioprine (12 months)

    Robert C. Griggs;R. T. Moxley;J. R. Mendell;G. M. Fenichel

  • Hereditary paroxysmal ataxia: response to acetazolamide.

    Robert C. Griggs;Richard T. Moxley;Richard A. Lafrance;James McQuillen

Frequent Co-Authors

Rabi Tawil
Rabi Tawil University of Rochester Medical Center
Michael G. Hanna
Michael G. Hanna University College London
Jerry R. Mendell
Jerry R. Mendell The Ohio State University
Michael P. McDermott
Michael P. McDermott University of Rochester
Anthony A. Amato
Anthony A. Amato Claude Bernard University Lyon 1
Richard J. Barohn
Richard J. Barohn University of Missouri
Louis J. Ptáček
Louis J. Ptáček University of California, San Francisco
Timothy A. Pedley
Timothy A. Pedley Columbia University
John T. Kissel
John T. Kissel The Ohio State University
Richard T. Johnson
Richard T. Johnson Johns Hopkins University School of Medicine

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