Susan E. Holmes

4.4k total citations · 1 hit paper
39 papers, 2.6k citations indexed

About

Susan E. Holmes is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Susan E. Holmes has authored 39 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 22 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in Susan E. Holmes's work include Genetic Neurodegenerative Diseases (22 papers), Mitochondrial Function and Pathology (17 papers) and Ubiquitin and proteasome pathways (5 papers). Susan E. Holmes is often cited by papers focused on Genetic Neurodegenerative Diseases (22 papers), Mitochondrial Function and Pathology (17 papers) and Ubiquitin and proteasome pathways (5 papers). Susan E. Holmes collaborates with scholars based in United States, France and Portugal. Susan E. Holmes's co-authors include Russell L. Margolis, Haig H. Kazazian, Christopher A. Ross, Jef D. Boeke, Ralph J. DeBerardinis, Thierry Naas, John V. Moran, Elizabeth O’Hearn, Dobrila D. Rudnicki and Hyon S. Hwang and has published in prestigious journals such as Cell, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Susan E. Holmes

38 papers receiving 2.6k 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.

High Frequency Retrotransposition in Cultured Mammalian Cells

1996 809 citations John V. Moran, Susan E. Holmes et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Susan E. Holmes United States	22	2.1k	1.0k	965	387	365	39	2.6k
Tamae Ohye Japan	27	1.4k 0.6×	697 0.7×	287 0.3×	569 1.5×	463 1.3×	71	2.6k
D.L. Browne United States	16	977 0.5×	575 0.6×	123 0.1×	250 0.6×	200 0.5×	31	1.3k
Elsa Vera Spain	19	1.8k 0.8×	278 0.3×	140 0.1×	162 0.4×	160 0.4×	19	3.2k
J. Ott United States	15	1.2k 0.6×	231 0.2×	174 0.2×	1.0k 2.6×	57 0.2×	27	2.2k
Andrew S. McCallion United States	25	1.7k 0.8×	173 0.2×	168 0.2×	698 1.8×	67 0.2×	48	2.5k
Lorena Pantano United States	24	1.4k 0.6×	222 0.2×	150 0.2×	332 0.9×	73 0.2×	36	2.0k
Jessica L. Buxton United Kingdom	17	1.2k 0.5×	612 0.6×	198 0.2×	570 1.5×	261 0.7×	27	1.7k
T. Serikawa Japan	23	942 0.4×	397 0.4×	163 0.2×	791 2.0×	68 0.2×	62	2.0k
Penelope E. Bonnen United States	19	1.8k 0.8×	1.2k 1.2×	34 0.0×	389 1.0×	463 1.3×	37	2.4k
Bertold Schrank Germany	16	1.4k 0.7×	171 0.2×	160 0.2×	120 0.3×	344 0.9×	31	2.2k

Countries citing papers authored by Susan E. Holmes

Since Specialization

Citations

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

Fields of papers citing papers by Susan E. Holmes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Susan E. Holmes. 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 Susan E. Holmes. The network helps show where Susan E. Holmes may publish in the future.

Co-authorship network of co-authors of Susan E. Holmes

This figure shows the co-authorship network connecting the top 25 collaborators of Susan E. Holmes. A scholar is included among the top collaborators of Susan E. Holmes 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 Susan E. Holmes. Susan E. Holmes 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

Boice, D. C., et al.. (2018). The Urban Heat Island of San Antonio, Texas, from 1991 to 2010. Journal of Geography Environment and Earth Science International. 17(2). 1–13. 6 indexed citations

O’Hearn, Elizabeth, Susan E. Holmes, & Russell L. Margolis. (2011). Spinocerebellar ataxia type 12. Handbook of clinical neurology. 103. 535–547. 41 indexed citations

Seixas, Ana I., Susan E. Holmes, Hiroshi Takeshima, et al.. (2011). Loss of junctophilin‐3 contributes to huntington disease‐like 2 pathogenesis. Annals of Neurology. 71(2). 245–257. 60 indexed citations

Cagnoli, Claudia, Giovanni Stévanin, Alessandro Brussino, et al.. (2010). Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. Human Mutation. 31(10). 1117–1124. 53 indexed citations

Sachs, Nancy A., Dobrila D. Rudnicki, Virginia L. Willour, et al.. (2009). Long tandem repeats as a form of genomic copy number variation: structure and length polymorphism of a chromosome 5p repeat in control and schizophrenia populations. Psychiatric Genetics. 19(2). 64–71. 20 indexed citations

Holmes, Susan E., Jill S. Wentzell, Ana I. Seixas, et al.. (2006). A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array. Human Genetics. 120(2). 193–200.

Sachs, Nancy A., Akira Sawa, Susan E. Holmes, et al.. (2005). A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder. Molecular Psychiatry. 10(8). 758–764. 161 indexed citations

Bahl, S., Uma Mittal, M.P. Sachdeva, et al.. (2005). Evidence of a Common Founder for SCA12 in the Indian Population. Annals of Human Genetics. 69(5). 528–534. 52 indexed citations

Nicholas, Anthony P., Elizabeth O’Hearn, Susan E. Holmes, Dung‐Tsa Chen, & Russell L. Margolis. (2004). Clinical signs and symptoms in a large hereditary spastic paraparesis pedigree with a novel spastin mutation. Movement Disorders. 19(6). 641–648. 5 indexed citations

10.

Cagnoli, Claudia, Tohru Matsuura, Tetsuo Ashizawa, et al.. (2004). Detection of Large Pathogenic Expansions in FRDA1, SCA10, and SCA12 Genes Using a Simple Fluorescent Repeat-Primed PCR Assay. Journal of Molecular Diagnostics. 6(2). 96–100. 43 indexed citations

11.

Holmes, Susan E., Melvin G. McInnis, Akira Sawa, et al.. (2003). Novel CAG/CTG repeat expansion mutations do not contribute to the genetic risk for most cases of bipolar disorder or schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 124B(1). 15–19. 7 indexed citations

12.

Holmes, Susan E., et al.. (2003). Why is SCA12 different from other SCAs?. Cytogenetic and Genome Research. 100(1-4). 189–197. 53 indexed citations

13.

Holmes, Susan E., et al.. (2001). SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia. Brain Research Bulletin. 56(3-4). 397–403. 69 indexed citations

14.

Margolis, Russell L., Elizabeth O’Hearn, Adam Rosenblatt, et al.. (2001). A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion. Annals of Neurology. 50(6). 373–380. 123 indexed citations

15.

Fujigasaki, Hiroto, Ishwar C. Verma, A. Camuzat, et al.. (2001). SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family. Annals of Neurology. 49(1). 117–121. 72 indexed citations

16.

Holmes, Susan E., Wànkuí Gǒng, Heather E. McDermid, et al.. (1997). Disruption of the Clathrin Heavy Chain-Like Gene (CLTCL) Associated with Features of DGS/VCFS: A Balanced (21;22)(p12;q11) Translocation. Human Molecular Genetics. 6(3). 357–367. 39 indexed citations

17.

Holmes, Susan E., et al.. (1997). Blood Lead Levels in a Continuity Clinic Population. Journal of Toxicology Clinical Toxicology. 35(2). 181–186. 4 indexed citations

18.

Moran, John V., Susan E. Holmes, Thierry Naas, et al.. (1996). High Frequency Retrotransposition in Cultured Mammalian Cells. Cell. 87(5). 917–927. 809 indexed citations breakdown →

19.

Holmes, Susan E., et al.. (1994). A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion. Nature Genetics. 7(2). 143–148. 189 indexed citations

20.

Holmes, Susan E.. (1986). Comments on this Special Issue. Evaluation & the Health Professions. 9(2). 131–136. 1 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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