D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 81 Citations 20,125 370 World Ranking 11558 National Ranking 6052
Biology and Biochemistry D-index 86 Citations 21,944 340 World Ranking 1951 National Ranking 1094

Research.com Recognitions

Awards & Achievements

2018 - Fellow, National Academy of Inventors

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Internal medicine
  • DNA

Her primary areas of investigation include Muscular dystrophy, Dystrophin, Genetics, Molecular biology and Sarcoglycan. Her Muscular dystrophy study frequently draws connections to adjacent fields such as Limb-girdle muscular dystrophy. Her research in Dystrophin tackles topics such as Cell biology which are related to areas like Biochemistry.

Elizabeth M. McNally frequently studies issues relating to Cardiomyopathy and Genetics. Elizabeth M. McNally combines subjects such as Lamin, Gene expression, Gene, Virology and Emerin with her study of Molecular biology. Her research integrates issues of Sarcoglycans and Dystroglycan in her study of Sarcoglycan.

Her most cited work include:

  • The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses. (911 citations)
  • Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy (447 citations)
  • Myosin subfragment-1 is sufficient to move actin filaments in vitro (409 citations)

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

The scientist’s investigation covers issues in Muscular dystrophy, Internal medicine, Cell biology, Genetics and Cardiomyopathy. Her Muscular dystrophy research integrates issues from Limb-girdle muscular dystrophy and Duchenne muscular dystrophy. Her Internal medicine study combines topics in areas such as Endocrinology and Cardiology.

Within one scientific family, Elizabeth M. McNally focuses on topics pertaining to Skeletal muscle under Cell biology, and may sometimes address concerns connected to Cardiac muscle. Her Cardiomyopathy study integrates concerns from other disciplines, such as Genetic heterogeneity, Gene mutation, Dilated cardiomyopathy and Genetic testing. Her study looks at the relationship between Dystrophin and topics such as Molecular biology, which overlap with Myosin and Lamin.

She most often published in these fields:

  • Muscular dystrophy (35.07%)
  • Internal medicine (32.05%)
  • Cell biology (23.29%)

What were the highlights of her more recent work (between 2017-2021)?

  • Internal medicine (32.05%)
  • Cardiomyopathy (20.55%)
  • Gene (10.14%)

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

Her primary scientific interests are in Internal medicine, Cardiomyopathy, Gene, Heart failure and Genetics. Her Internal medicine research includes elements of Endocrinology and Cardiology. In her research on the topic of Cardiomyopathy, Regulatory sequence and Human heart is strongly related with Enhancer.

Elizabeth M. McNally works mostly in the field of Heart failure, limiting it down to concerns involving Intensive care medicine and, occasionally, Clinical trial, Disease, Duchenne muscular dystrophy, Muscular dystrophy and Genetic testing. She has researched Muscular dystrophy in several fields, including Point mutation, Deflazacort, Prednisone, Skeletal muscle and Myocyte. Her study in Genetics focuses on Phenotype, Genetic variation, Gene expression and Promoter.

Between 2017 and 2021, her most popular works were:

  • A promoter interaction map for cardiovascular disease genetics. (66 citations)
  • Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network (44 citations)
  • Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular Cardiomyopathy. (31 citations)

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

  • Gene
  • Internal medicine
  • DNA

Muscular dystrophy, Internal medicine, Cell biology, Dystrophin and Duchenne muscular dystrophy are her primary areas of study. Her work carried out in the field of Muscular dystrophy brings together such families of science as MBNL1, Cellular differentiation, Trinucleotide repeat expansion, Cardiac function curve and Myogenesis. Elizabeth M. McNally works mostly in the field of Internal medicine, limiting it down to topics relating to Cardiology and, in certain cases, Desmoplakin and Intermediate filament.

Her biological study spans a wide range of topics, including Exon skipping, Lamin, Chromosome 3 and Exon. Her Dystrophin research incorporates themes from Myocyte, Actin cytoskeleton and Myostatin. Her Duchenne muscular dystrophy study incorporates themes from Endocrinology, Glucocorticoid and Surrogate endpoint.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses.

David L. Boone;Emre E. Turer;Eric G. Lee;Regina Celeste Ahmad.
Nature Immunology (2004)

1286 Citations

Myosin subfragment-1 is sufficient to move actin filaments in vitro.

Yoko Yano Toyoshima;Stephen J. Kron;Elizabeth M. McNally;Kenneth R. Niebling.
Nature (1987)

633 Citations

Mutations in the dystrophin-associated protein γ-sarcoglycan in chromosome 13 muscular dystrophy

Satoru Noguchi;Elizabeth M. McNally;Kamel Ben Othmane;Yasuko Hagiwara.
Science (1995)

630 Citations

The Dystrophin Glycoprotein Complex: Signaling Strength and Integrity for the Sarcolemma

Karen A. Lapidos;Rahul Kakkar;Elizabeth M. McNally.
Circulation Research (2004)

580 Citations

β–sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

Carsten G. Bönnemann;Raju Modi;Satoru Noguchi;Yuji Mizuno.
Nature Genetics (1995)

543 Citations

Dilated Cardiomyopathy: Genetic Determinants and Mechanisms

Elizabeth M. McNally;Luisa Mestroni.
Circulation Research (2017)

452 Citations

Genetic mutations and mechanisms in dilated cardiomyopathy

Elizabeth M. McNally;Jessica R. Golbus;Megan J. Puckelwartz.
Journal of Clinical Investigation (2013)

420 Citations

Filamin 2 (FLN2): A Muscle-specific Sarcoglycan Interacting Protein

Terri G. Thompson;Yiu Mo Chan;Andrew A. Hack;Melissa Brosius.
Journal of Cell Biology (2000)

341 Citations

γ-Sarcoglycan Deficiency Leads to Muscle Membrane Defects and Apoptosis Independent of Dystrophin

Andrew A. Hack;Chantal T. Ly;Fang Jiang;Cynthia J. Clendenin.
Journal of Cell Biology (1998)

339 Citations

Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies.

Gregory Q. Wallace;Elizabeth M. McNally.
Annual Review of Physiology (2009)

337 Citations

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