Marie T. Lott

13.7k total citations · 3 hit papers
53 papers, 9.8k citations indexed

About

Marie T. Lott is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Marie T. Lott has authored 53 papers receiving a total of 9.8k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 33 papers in Clinical Biochemistry and 10 papers in Genetics. Recurrent topics in Marie T. Lott's work include Mitochondrial Function and Pathology (42 papers), Metabolism and Genetic Disorders (33 papers) and ATP Synthase and ATPases Research (20 papers). Marie T. Lott is often cited by papers focused on Mitochondrial Function and Pathology (42 papers), Metabolism and Genetic Disorders (33 papers) and ATP Synthase and ATPases Research (20 papers). Marie T. Lott collaborates with scholars based in United States, Italy and France. Marie T. Lott's co-authors include Douglas C. Wallace, John M. Shoffner, Angela Maria Serena Lezza, Gurparkash Singh, Marisol Corral‐Debrinski, Scott W. Ballinger, Louis J. Elsas, Eeva Nikoskelainen, Theodore G. Schurr and Michael D. Brown and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Marie T. Lott

52 papers receiving 9.5k citations

Hit Papers

align trajectories sort by overperformance

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, Marie T. Lott 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 — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marie T. Lott United States	38	8.4k	4.2k	1.3k	860	754	53	9.8k
Orly Elpeleg Israel	56	7.0k 0.8×	3.2k 0.8×	1.6k 1.3×	917 1.1×	728 1.0×	244	10.4k
Sara Shanske United States	60	9.6k 1.1×	6.2k 1.5×	1.2k 0.9×	1.3k 1.5×	1.1k 1.5×	188	12.1k
Ian Holt United Kingdom	60	10.0k 1.2×	4.7k 1.1×	657 0.5×	1.1k 1.3×	486 0.6×	160	11.0k
Gavin Hudson United Kingdom	37	3.3k 0.4×	1.4k 0.3×	359 0.3×	555 0.6×	451 0.6×	81	4.5k
Emma L. Blakely United Kingdom	38	4.8k 0.6×	2.6k 0.6×	467 0.4×	587 0.7×	379 0.5×	100	5.3k
Gerald V. Raymond United States	46	5.1k 0.6×	2.2k 0.5×	970 0.8×	333 0.4×	1.6k 2.1×	137	7.2k
Jan‐Willem Taanman United Kingdom	43	5.8k 0.7×	1.9k 0.4×	604 0.5×	1.3k 1.5×	864 1.1×	115	7.6k
Anne Chomyn United States	33	6.0k 0.7×	2.4k 0.6×	244 0.2×	444 0.5×	722 1.0×	51	6.6k
Maria Falkenberg Sweden	46	8.3k 1.0×	2.9k 0.7×	579 0.5×	528 0.6×	923 1.2×	91	9.4k
Jutta Gärtner Germany	49	3.6k 0.4×	761 0.2×	944 0.7×	1.0k 1.2×	952 1.3×	217	7.6k

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

Parca, Luca, Tommaso Biagini, Massimo Carella, et al.. (2023). APOGEE 2: multi-layer machine-learning model for the interpretable prediction of mitochondrial missense variants. Nature Communications. 14(1). 5058–5058. 20 indexed citations

Wallace, Douglas C. & Marie T. Lott. (2017). Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease. Handbook of experimental pharmacology. 240. 339–376. 51 indexed citations

Wallace, Douglas C., Michael D. Brown, & Marie T. Lott. (1999). Mitochondrial DNA variation in human evolution and disease. Gene. 238(1). 211–230. 349 indexed citations

Wallace, Douglas C., Michael D. Brown, Simon Melov, Brett H. Graham, & Marie T. Lott. (1998). Mitochondrial biology, degenerative diseases and aging. BioFactors. 7(3). 187–190. 98 indexed citations

Wallace, Douglas C., John M. Shoffner, Ian A. Trounce, et al.. (1995). Mitochondrial DNA mutations in human degenerative diseases and aging. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1271(1). 141–151. 190 indexed citations

Torroni, Antonio, et al.. (1995). African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Human Mutation. 5(4). 310–317. 20 indexed citations

Wallace, Douglas C., Marie T. Lott, John M. Shoffner, & Scott W. Ballinger. (1994). Mitochondrial DNA Mutations in Epilepsy and Neurological Disease. Epilepsia. 35(s1). S43–50. 44 indexed citations

Torroni, Antonio, Ornella Semino, C. Ronald Scott, et al.. (1994). mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico.. PubMed. 54(2). 303–18. 119 indexed citations

Torroni, Antonio, et al.. (1994). mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.. PubMed. 55(4). 760–76. 234 indexed citations

10.

Weiner, Norman, Nancy J. Newman, Simmons Lessell, et al.. (1993). Atypical Leber's Hereditary Optic Neuropathy With Molecular Confirmation. Archives of Neurology. 50(5). 470–473. 35 indexed citations

11.

Brown, M.D., Alexander S. Voljavec, Marie T. Lott, et al.. (1992). Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.. Genetics. 130(1). 163–173. 230 indexed citations

12.

Corral‐Debrinski, Marisol, et al.. (1992). Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age. Nature Genetics. 2(4). 324–329. 709 indexed citations breakdown →

13.

Brown, M.D., Chih-Ting Yang, Ian A. Trounce, et al.. (1992). A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.. PubMed. 51(2). 378–85. 57 indexed citations

14.

Corral‐Debrinski, Marisol, John M. Shoffner, Marie T. Lott, & Douglas C. Wallace. (1992). Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease. Mutation Research/DNAging. 275(3-6). 169–180. 289 indexed citations

15.

Lott, Marie T., et al.. (1991). The Clinical Characteristics of Pedigrees of Leber's Hereditary Optic Neuropathy With the 11778 Mutation. American Journal of Ophthalmology. 111(6). 750–762. 304 indexed citations

16.

Lott, Marie T., et al.. (1990). Variable Genotype of Leber's Hereditary Optic Neuropathy Patients. American Journal of Ophthalmology. 109(6). 625–631. 93 indexed citations

17.

Wallace, Douglas C., Marie T. Lott, Angela Maria Serena Lezza, et al.. (1990). Mitochondrial DNA Mutations Associated with Neuromuscular Diseases: Analysis and Diagnosis Using the Polymerase Chain Reaction. Pediatric Research. 28(5). 525–528. 22 indexed citations

18.

Lott, Marie T., et al.. (1990). Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation. Cell. 61(6). 931–937. 1150 indexed citations breakdown →

19.

Shoffner, John M., et al.. (1989). Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.. Proceedings of the National Academy of Sciences. 86(20). 7952–7956. 400 indexed citations

20.

Wallace, Douglas C., Xianxian Zheng, Marie T. Lott, et al.. (1988). Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease. Cell. 55(4). 601–610. 401 indexed citations

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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