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D-Index & Metrics

Molecular Biology

D-Index
44
Citations
17944
World Ranking
2886
National Ranking
1374

Overview

Marie T. Lott is affiliated with the Children's Hospital of Philadelphia in the United States. Their research primarily focuses on biochemistry, genetics, and molecular biology, with a significant emphasis on mitochondrial function and pathology. The scientist has contributed to various topics, including metabolism and genetic disorders, genomics and rare diseases, glycosylation and glycoproteins research, carbohydrate chemistry and synthesis, monoclonal and polyclonal antibodies research, and RNA modifications and cancer.

Marie T. Lott's recent publications cover multiple aspects of molecular biology and mitochondrial research. Some of the papers include:

  • Mitochondrial DNA variation and cancer, 2021, Nature reviews. Cancer
  • Specifications of the ACMG/AMP standards and guidelines for mitochondrial DNA variant interpretation, 2020, Human Mutation
  • Core mitochondrial genes are down-regulated during SARS-CoV-2 infection of rodent and human hosts, 2023, Science Translational Medicine
  • Targeted Down Regulation Of Core Mitochondrial Genes During SARS-CoV-2 Infection, 2022, bioRxiv (Cold Spring Harbor Laboratory)
  • Natural Glycoforms of Human Interleukin 6 Show Atypical Plasma Clearance, 2021, Angewandte Chemie International Edition

The scientist frequently publishes in venues such as bioRxiv (Cold Spring Harbor Laboratory), Nature reviews. Cancer, Human Mutation, Science Translational Medicine, and Nature Communications. These venues highlight a consistent focus on molecular biology and medical research.

Collaborations are an integral part of Marie T. Lott's work. Frequent co-authors include Douglas C. Wallace, Larry N. Singh, Vincent Procaccio, Deborah G. Murdock, and Shiping Zhang. These partnerships reflect a collaborative research environment centered on mitochondrial biology and related genetic studies.

Marie T. Lott's research spans multiple subfields including molecular biology, clinical biochemistry, genetics, organic chemistry, and radiology, nuclear medicine, and imaging. With a strong foundation in these areas, the scientist explores complex biological systems primarily through the lens of mitochondrial function.

Best Publications

  • Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

    Douglas C. Wallace;Gurparkash Singh;Marie T. Lott;Judy A. Hodge

  • Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation

    John M. Shoffner;Marie T. Lott;Angela M.S. Lezza;Peter Seibel

  • Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age.

    M Corral-Debrinski;T Horton;M T Lott;J M Shoffner

  • Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

    Douglas C. Wallace;Xianxian Zheng;Marie T. Lott;John M. Shoffner

  • An enhanced MITOMAP with a global mtDNA mutational phylogeny.

    Eduardo Ruiz-Pesini;Marie T. Lott;Vincent Procaccio;Jason C. Poole

  • Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

    John M. Shoffner;Marie T. Lott;Alexander S. Voljavec;Shawke A. Soueidan

  • Mitochondrial DNA variation in human evolution and disease.

    Douglas C. Wallace;Michael D. Brown;Marie T. Lott

  • Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients

    John M. Shoffner;Michael D. Brown;Antonio Torroni;Marie T. Lott

  • MITOMAP: a human mitochondrial genome database—2004 update

    Marty C. Brandon;Marie T. Lott;Kevin Cuong Nguyen;Syawal Spolim

  • mtDNA Variation and Analysis Using Mitomap and Mitomaster

    Marie T. Lott;Jeremy N. Leipzig;Olga Derbeneva;H. Michael Xie

  • The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

    Nancy J. Newman;Marie T. Lott;Douglas C. Wallace

  • Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease.

    M. Corral-Debrinski;J.M. Shoffner;M.T. Lott;D.C. Wallace

  • MITOMAP: A Human Mitochondrial Genome Database

    Andreas M. Kogelnik;Andreas M. Kogelnik;Marie T. Lott;Michael D. Brown;Shamkant B. Navathe

  • Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease.

    Marisol Corral-Debrinski;Georges Stepien;John M. Shoffner;Marie T. Lott

  • Marked changes in mitochondrial DNA deletion levels in Alzheimer brains

    M Corral-Debrinski;T Horton;M T Lott;J M Shoffner

  • Mitochondrial DNA Complex I and III Mutations Associated with Leber's Hereditary Optic Neuropathy

    Michael D. Brown;Alexander S. Voljavec;Marie T. Lott;Antonio Torroni

  • Mitochondrial DNA mutations in human degenerative diseases and aging

    Douglas C. Wallace;John M. Shoffner;Ian Trounce;Michael D. Brown

  • Mitochondrial DNA Diversity in Indigenous Populations of the Southern Extent of Siberia, and the Origins of Native American Haplogroups

    Elena B. Starikovskaya;Rem I. Sukernik;Olga A. Derbeneva;Olga A. Derbeneva;Natalia V. Volodko

  • Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.

    Michael D. Brown;Alexander S. Voljavec;Marie T. Lott;Ian Macdonald

  • mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico.

    Antonio Torroni;Yu-Sheng Chen;Ornella Semino;A. S. Santachiara-Beneceretti

Frequent Co-Authors

Douglas C. Wallace
Douglas C. Wallace Children's Hospital of Philadelphia
Vincent Procaccio
Vincent Procaccio University of Angers
Antonio Torroni
Antonio Torroni University of Pavia
Xiaowu Gai
Xiaowu Gai Children's Hospital of Los Angeles
Nancy J. Newman
Nancy J. Newman Emory University
Pierre Baldi
Pierre Baldi University of California, Irvine
Stephan Züchner
Stephan Züchner University of Miami
Shamkant B. Navathe
Shamkant B. Navathe Georgia Institute of Technology
David R. Thorburn
David R. Thorburn Murdoch Children's Research Institute
Holger Prokisch
Holger Prokisch Technical University of Munich

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