Marie T. Lott

13.7k citations

53 papers · 9.8k indexed · 3 hit papers · h-index 38

Molecular Biology top 0.5%
Clinical Biochemistry top 0.01%
Genetics top 1%
Cellular and Molecular Neuroscience top 2%
Physiology top 5%

Co-authors: Douglas C. Wallace John M. Shoffner Angela Maria Serena Lezza Gurparkash Singh Marisol Corral‐Debrinski Scott W. Ballinger Theodore G. Schurr Eeva Nikoskelainen
Topics: Mitochondrial Function and Pathology (42 papers)Metabolism and Genetic Disorders (33 papers)ATP Synthase and ATPases Research (20 papers)
Cited by: Clinical Biochemistry Molecular Biology Aging
Journals: Science New England Journal of Medicine Cell
Partner nations: United States Italy France

In The Last Decade

Marie T. Lott

52 papers receiving 9.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy

1988 1.8k citations Douglas C. Wallace, Gurparkash Singh et al. profile →
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation

1990 1.1k citations Marie T. Lott, Angela Maria Serena Lezza et al. Cell profile →
Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

1992 709 citations Marisol Corral‐Debrinski, Terzah M. Horton et al. Nature Genetics profile →

Peers

Countries citing papers authored by Marie T. Lott

Since Specialization

Citations

This map shows the geographic impact of Marie T. Lott's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marie T. Lott with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marie T. Lott more than expected).

Fields of papers citing papers by Marie T. Lott

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marie T. Lott. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marie T. Lott. The network helps show where Marie T. Lott may publish in the future.

Co-authorship network of co-authors of Marie T. Lott

This figure shows the co-authorship network connecting the top 25 collaborators of Marie T. Lott. A scholar is included among the top collaborators of Marie T. Lott based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marie T. Lott. Marie T. Lott is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	P704: A virtual registry of 9K Leigh syndrome and primary mitochondrial disease cases constructed through semi-automated literature mining and expert curation 2025 ·Genetics in Medicine Open ·Li Shen,Marie T. Lott,Elizabeth M. McCormick,Colleen Muraresku,(unknown),Douglas C. Wallace,Zarazuela Zolkipli‐Cunningham,Shamima Rahman,Marni J. Falk,Xiaowu Gai	0
2	APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants 2023 ·Nature Communications ·(unknown),Luca Parca,(unknown),Tommaso Biagini,(unknown),(unknown),(unknown),Massimo Carella,Vincent Procaccio,Marie T. Lott,(unknown),Angelo L. Vescovi,Douglas C. Wallace,Viviana Caputo,Tommaso Mazza	20
3	Predicting the pathogenicity of novel variants in mitochondrial tRNA with MitoTIP 2017 ·PLoS Computational Biology ·(unknown),Jeremy Leipzig,Marie T. Lott,Shiping Zhang,Vincent Procaccio,Douglas C. Wallace,Neal Sondheimer	87
4	Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease 2017 ·Handbook of experimental pharmacology ·Douglas C. Wallace,Marie T. Lott	51
5	Mitochondrial DNA variation in human evolution and disease 1999 ·Gene ·Douglas C. Wallace,Michael D. Brown,Marie T. Lott	349
6	Mitochondrial biology, degenerative diseases and aging 1998 ·BioFactors ·Douglas C. Wallace,Michael D. Brown,Simon Melov,Brett H. Graham,Marie T. Lott	98
7	MITOMAP: an update on the status of the human mitochondrial genome database 1997 ·Nucleic Acids Research ·Andreas M. Kogelnik,Marie T. Lott,M.D. Brown,(unknown),Douglas C. Wallace	46
8	Mitochondrial DNA mutations in human degenerative diseases and aging 1995 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Douglas C. Wallace,John M. Shoffner,Ian A. Trounce,Michael D. Brown,Scott W. Ballinger,Marisol Corral‐Debrinski,Terzah M. Horton,Albert S. Jun,Marie T. Lott	190
9	African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba 1995 ·Human Mutation ·Antonio Torroni,Michael D. Brown,Marie T. Lott,Nancy J. Newman,Douglas C. Wallace,(unknown)	20
10	Mitochondrial DNA Mutations in Epilepsy and Neurological Disease 1994 ·Epilepsia ·Douglas C. Wallace,Marie T. Lott,John M. Shoffner,Scott W. Ballinger	44
11	Atypical Leber's Hereditary Optic Neuropathy With Molecular Confirmation 1993 ·Archives of Neurology ·Norman Weiner,Nancy J. Newman,Simmons Lessell,D. R. Johns,Marie T. Lott,Douglas C. Wallace	35
12	Mitochondrial DNA deletions in human brain: regional variability and increase with advanced agebreakdown → 1992 ·Nature Genetics ·Marisol Corral‐Debrinski,Terzah M. Horton,Marie T. Lott,John M. Shoffner,M. Flint Beal,(unknown)	709
13	Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease 1992 ·Mutation Research/DNAging ·Marisol Corral‐Debrinski,John M. Shoffner,Marie T. Lott,Douglas C. Wallace	289
14	Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. 1992 ·Genetics ·M.D. Brown,Alexander S. Voljavec,Marie T. Lott,Antonio Torroni,Chih-Ting Yang,Douglas C. Wallace	230
15	The Clinical Characteristics of Pedigrees of Leber's Hereditary Optic Neuropathy With the 11778 Mutation 1991 ·American Journal of Ophthalmology ·(unknown),Marie T. Lott,(unknown)	304
16	Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutationbreakdown → 1990 ·Cell ·(unknown),Marie T. Lott,Angela Maria Serena Lezza,Peter Seibel,Scott W. Ballinger,Douglas C. Wallace	1150
17	Mitochondrial DNA Mutations Associated with Neuromuscular Diseases: Analysis and Diagnosis Using the Polymerase Chain Reaction 1990 ·Pediatric Research ·Douglas C. Wallace,Marie T. Lott,Angela Maria Serena Lezza,Peter Seibel,Alexander S. Voljavec,John M. Shoffner	22
18	Variable Genotype of Leber's Hereditary Optic Neuropathy Patients 1990 ·American Journal of Ophthalmology ·Marie T. Lott,Alexander S. Voljavec,(unknown)	93
19	A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy 1989 ·New England Journal of Medicine ·Gurparkash Singh,Marie T. Lott,Douglas C. Wallace	117
20	Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease 1988 ·Cell ·Douglas C. Wallace,Xianxian Zheng,Marie T. Lott,John M. Shoffner,(unknown),Richard I. Kelley,Charles M. Epstein,Linton C. Hopkins	401

About Marie T. Lott

Marie T. Lott is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics, having authored 53 papers that have together received 9.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (42 papers), Metabolism and Genetic Disorders (33 papers) and ATP Synthase and ATPases Research (20 papers). The work is most often cited by research in Clinical Biochemistry (4.2k citations), Molecular Biology (8.4k citations) and Aging (181 citations). Marie T. Lott has collaborated with scholars based in United States, Italy and France. Frequent co-authors include Douglas C. Wallace, John M. Shoffner, Angela Maria Serena Lezza, Gurparkash Singh, Marisol Corral‐Debrinski, Scott W. Ballinger, Theodore G. Schurr, Eeva Nikoskelainen, Louis J. Elsas and Michael D. Brown. Their work appears in journals such as Science, New England Journal of Medicine and Cell.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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