D.C. Wallace

1.0k total citations
16 papers, 609 citations indexed

About

D.C. Wallace is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, D.C. Wallace has authored 16 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 4 papers in Clinical Biochemistry. Recurrent topics in D.C. Wallace's work include Mitochondrial Function and Pathology (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Metabolism and Genetic Disorders (4 papers). D.C. Wallace is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Metabolism and Genetic Disorders (4 papers). D.C. Wallace collaborates with scholars based in Australia, United States and Russia. D.C. Wallace's co-authors include John M. Shoffner, Marie T. Lott, Antonio Torroni, Abdelaziz Heddi, Grzegorz J. Stępień, Patrick Lestienne, A. Kaufman, Marisol Corral‐Debrinski, Brett H. Graham and M. F. Beal and has published in prestigious journals such as Journal of Biological Chemistry, Brain and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

D.C. Wallace

16 papers receiving 574 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D.C. Wallace Australia	13	470	231	122	86	53	16	609
R. Kálmánchey Hungary	10	206 0.4×	105 0.5×	49 0.4×	80 0.9×	25 0.5×	27	422
William Craigen United States	9	290 0.6×	114 0.5×	34 0.3×	81 0.9×	53 1.0×	13	443
Mika H. Martikainen Finland	13	205 0.4×	135 0.6×	95 0.8×	47 0.5×	61 1.2×	34	418
Rajith de Silva United Kingdom	14	487 1.0×	68 0.3×	127 1.0×	34 0.4×	54 1.0×	29	687
J.F. de Rijk-van Andel Netherlands	10	246 0.5×	155 0.7×	146 1.2×	106 1.2×	75 1.4×	15	497
Divya Pathak India	6	303 0.6×	64 0.3×	192 1.6×	30 0.3×	112 2.1×	8	480
Laurence Lion‐François France	13	160 0.3×	87 0.4×	74 0.6×	66 0.8×	31 0.6×	32	535
Jyrki Kaukonen Finland	6	1.1k 2.3×	655 2.8×	234 1.9×	144 1.7×	56 1.1×	7	1.2k
Takayuki Mito Japan	12	339 0.7×	90 0.4×	28 0.2×	98 1.1×	70 1.3×	17	525
Emily Moon United States	7	228 0.5×	98 0.4×	58 0.5×	80 0.9×	28 0.5×	7	326

Countries citing papers authored by D.C. Wallace

Since Specialization

Citations

This map shows the geographic impact of D.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 D.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 D.C. Wallace more than expected).

Fields of papers citing papers by D.C. Wallace

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of D.C. Wallace. A scholar is included among the top collaborators of D.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 D.C. Wallace. D.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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16 of 16 papers shown

Volodko, Natalia, Maria Lvova, Elena B. Starikovskaya, et al.. (2006). Spectrum of pathogenic mtDNA mutations in Leber’s hereditary optic neuropathy families from Siberia. Russian Journal of Genetics. 42(1). 76–83. 12 indexed citations

Derbeneva, Olga, et al.. (2002). [Mitochondrial DNA variation in Kets and Nganasans and the early peoples of Northern Eurasia].. PubMed. 38(11). 1554–60. 25 indexed citations

Horton, Terzah M., Brett H. Graham, Marisol Corral‐Debrinski, et al.. (1995). Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients. Neurology. 45(10). 1879–1883. 87 indexed citations

Shoffner, John M., Martin G. Bialer, Steven G. Pavlakis, et al.. (1995). Mitochondria1 encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNA ^Leu(UUR) gene. Neurology. 45(2). 286–292. 48 indexed citations

Shoffner, John M. & D.C. Wallace. (1994). Heart disease and mitochondrial DNA mutations.. PubMed. 1(4). 235–41. 17 indexed citations

Heddi, Abdelaziz, Patrick Lestienne, D.C. Wallace, & Grzegorz J. Stępień. (1993). Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP production. Journal of Biological Chemistry. 268(16). 12156–12163. 85 indexed citations

Logue, F.C., et al.. (1992). Sleep shift dissociates the nocturnal peaks of parathyroid hormone (1-84), nephrogenous cyclic adenosine monophosphate, and prolactin in normal men.. The Journal of Clinical Endocrinology & Metabolism. 75(1). 25–29. 18 indexed citations

Shoffner, John M., Marie T. Lott, & D.C. Wallace. (1991). MERRF: a model disease for understanding the principles of mitochondrial genetics.. PubMed. 147(6-7). 431–5. 16 indexed citations

Wallace, D.C., et al.. (1990). Report of the committee on human mitochondrial DNA. Cytogenetic and Genome Research. 55(1-4). 395–405. 121 indexed citations

10.

Brackenridge, C. J., et al.. (1978). A linkage study of the loci for Huntington's disease and some common polymorphic markers. Annals of Human Genetics. 42(2). 203–211. 10 indexed citations

11.

Wallace, D.C.. (1976). The social effect of Huntington's Chorea on reproductive effectiveness. Annals of Human Genetics. 39(3). 375–379. 17 indexed citations

12.

Wallace, D.C.. (1972). HUNTINGTON'S CHOREA IN QUEENSLAND A NOT UNCOMMON DISEASE. The Medical Journal of Australia. 1(7). 299–307. 19 indexed citations

13.

Wallace, D.C. & Anita Hall. (1972). Evidence of genetic heterogeneity in Huntington's chorea. Journal of Neurology Neurosurgery & Psychiatry. 35(6). 789–800. 20 indexed citations

14.

Wallace, D.C.. (1970). Leber's Optic Atrophy: A Possible Example of Vertical Transmission of a Slow Virus in Man. Australasian Annals of Medicine. 19(3). 259–262. 20 indexed citations

15.

Wallace, D.C.. (1970). A NEW MANIFESTATION OF LEBER'S DISEASE AND A NEW EXPLANATION FOR THE AGENCY RESPONSIBLE FOR ITS UNUSUAL PATTERN OF INHERITANCE. Brain. 93(1). 121–132. 91 indexed citations

16.

Wallace, D.C., et al.. (1970). Severe achondroplasia: demonstration of probable heterogeneity within this clinical syndrome.. Journal of Medical Genetics. 7(1). 22–26. 3 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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