Douglas C. Wallace

4.4k total citations · 1 hit paper
23 papers, 3.4k citations indexed

About

Douglas C. Wallace is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Douglas C. Wallace has authored 23 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 14 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Douglas C. Wallace's work include Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (9 papers). Douglas C. Wallace is often cited by papers focused on Mitochondrial Function and Pathology (18 papers), Metabolism and Genetic Disorders (14 papers) and ATP Synthase and ATPases Research (9 papers). Douglas C. Wallace collaborates with scholars based in United States, France and South Africa. Douglas C. Wallace's co-authors include Vincent Procaccio, Weiwei Fan, John M. Shoffner, Marie T. Lott, M.D. Brown, Michael D. Brown, A. S. Jun, Alexander S. Voljavec, Antonio Torroni and Ian A. Trounce and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Douglas C. Wallace

23 papers receiving 3.3k 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 Energetics and Therapeutics

2010 550 citations Douglas C. Wallace, Weiwei Fan et al. Annual Review of Pathology Mechanisms of Disease profile →

Peers

Douglas C. Wallace

GENET

PHYSI

CMN

Khaled K. Abu‐Amero Saudi Arabia

Sabine Hofmann Germany

Kirby D. Smith United States

Valentino Romano Italy

Robert N. Lightowlers United Kingdom

Christian Becker Germany

Pio D’Adamo Italy

Marie T. Lott United States

Jürgen Horst Germany

Maria Lucia Valentino Italy

Khaled K. Abu‐Amero Saudi Arabia

Douglas C. Wallace

1.7k ×0.6

379 ×0.3

791 ×1.2

GENET

137 ×0.5

PHYSI

182 ×0.9

CMN

Citations per year, relative to Douglas C. Wallace Douglas C. Wallace (= 1×) peers Khaled K. Abu‐Amero

Countries citing papers authored by Douglas C. Wallace

Since Specialization

Citations

This map shows the geographic impact of Douglas C. Wallace'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 Douglas C. Wallace with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Douglas C. Wallace more than expected).

Fields of papers citing papers by Douglas C. Wallace

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Douglas C. Wallace. 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 Douglas C. Wallace. The network helps show where Douglas C. Wallace may publish in the future.

Co-authorship network of co-authors of Douglas C. Wallace

This figure shows the co-authorship network connecting the top 25 collaborators of Douglas C. Wallace. A scholar is included among the top collaborators of Douglas C. Wallace 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 Douglas C. Wallace. Douglas C. Wallace 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

Wallace, Douglas C.. (2015). Mitochondrial DNA Variation in Human Radiation and Disease. Cell. 163(1). 33–38. 176 indexed citations

Elson, Joanna L., M G Sweeney, Vincent Procaccio, et al.. (2012). Toward a mtDNA locus-specific mutation database using the LOVD platform. Human Mutation. 33(9). 1352–1358. 7 indexed citations

Wallace, Douglas C.. (2011). Bioenergetic Origins of Complexity and Disease. Cold Spring Harbor Symposia on Quantitative Biology. 76(0). 1–16. 102 indexed citations

Wallace, Douglas C., Weiwei Fan, & Vincent Procaccio. (2010). Mitochondrial Energetics and Therapeutics. Annual Review of Pathology Mechanisms of Disease. 5(1). 297–348. 550 indexed citations breakdown →

Su, Hailing, Weiwei Fan, Pınar Coşkun, et al.. (2009). Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome. Neuroscience Letters. 487(2). 129–133. 60 indexed citations

Wallace, Douglas C.. (2001). Mitochondrial defects in neurodegenerative disease. Mental Retardation and Developmental Disabilities Research Reviews. 7(3). 158–166. 54 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

Heddi, Abdelaziz, Hélène Faure, Douglas C. Wallace, & Georges Stepien. (1996). Coordinate expression of nuclear and mitochondrial genes involved in energy production in carcinoma and oncocytoma. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1316(3). 203–209. 58 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

10.

Wallace, Douglas C.. (1994). Mitochondrial DNA mutations in diseases of energy metabolism. Journal of Bioenergetics and Biomembranes. 26(3). 241–250. 143 indexed citations

11.

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

12.

Jun, A. S., M.D. Brown, & Douglas C. Wallace. (1994). A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.. Proceedings of the National Academy of Sciences. 91(13). 6206–6210. 247 indexed citations

13.

Trounce, Ian A., Stewart G. Neill, & Douglas C. Wallace. (1994). Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.. Proceedings of the National Academy of Sciences. 91(18). 8334–8338. 155 indexed citations

14.

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

15.

Merriwether, D. Andrew, Andrew G. Clark, Scott W. Ballinger, et al.. (1991). The structure of human mitochondrial DNA variation. Journal of Molecular Evolution. 33(6). 543–555. 183 indexed citations

16.

Shoffner, John M., et al.. (1990). Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1019(1). 1–10. 116 indexed citations

17.

Wallace, Douglas C., et al.. (1987). Sequence analysis of cDNAs for the human and bovine ATP synthase β subunit: mitochondrial DNA genes sustain seventeen times more mutations. Current Genetics. 12(2). 81–90. 190 indexed citations

18.

Oliver, Noëlynn, Barry Greenberg, & Douglas C. Wallace. (1983). Assignment of a polymorphic polypeptide to the human mitochondrial DNA unidentified reading frame 3 gene by a new peptide mapping strategy.. Journal of Biological Chemistry. 258(9). 5834–5839. 39 indexed citations

19.

Webster, Keith A., et al.. (1982). Assignment of an oligomycin-resistance locus to human chromosome 10. Somatic Cell and Molecular Genetics. 8(2). 223–244. 8 indexed citations

20.

Denaro, Maurizio, et al.. (1981). Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA.. Proceedings of the National Academy of Sciences. 78(9). 5768–5772. 118 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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