Damien L. Bruno

3.3k total citations
29 papers, 1.5k citations indexed

About

Damien L. Bruno is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Damien L. Bruno has authored 29 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 12 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Damien L. Bruno's work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (8 papers) and Genomics and Rare Diseases (5 papers). Damien L. Bruno is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (8 papers) and Genomics and Rare Diseases (5 papers). Damien L. Bruno collaborates with scholars based in Australia, United States and Netherlands. Damien L. Bruno's co-authors include Howard R. Slater, Alison G. Compton, Elena J. Tucker, David R. Thorburn, Vamsi K. Mootha, Sarah E. Calvo, Trent Burgess, John Christodoulou, Sze Chern Lim and Caterina Garone and has published in prestigious journals such as Nature Genetics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Damien L. Bruno

28 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Damien L. Bruno Australia 19 917 526 353 164 129 29 1.5k
Nadine Gigarel France 18 1.8k 2.0× 282 0.5× 711 2.0× 248 1.5× 78 0.6× 39 2.2k
Mohammed A. Aldahmesh Saudi Arabia 32 1.2k 1.3× 815 1.5× 63 0.2× 68 0.4× 113 0.9× 61 2.0k
Reeval Segel Israel 18 649 0.7× 249 0.5× 174 0.5× 211 1.3× 87 0.7× 40 1.1k
Elena J. Tucker Australia 19 1.3k 1.4× 348 0.7× 580 1.6× 71 0.4× 25 0.2× 41 1.7k
Dorota Piekutowska‐Abramczuk Poland 17 773 0.8× 181 0.3× 353 1.0× 52 0.3× 62 0.5× 59 1.0k
Isabelle Thiffault United States 23 822 0.9× 482 0.9× 132 0.4× 85 0.5× 67 0.5× 65 1.4k
Patricia Ybot‐González Spain 21 973 1.1× 239 0.5× 27 0.1× 152 0.9× 118 0.9× 39 1.4k
Xiangdong Kong China 16 376 0.4× 288 0.5× 84 0.2× 310 1.9× 69 0.5× 150 874
Lora Jh Bean United States 24 862 0.9× 606 1.2× 70 0.2× 216 1.3× 139 1.1× 58 1.6k
Natalia Martín United States 13 372 0.4× 160 0.3× 52 0.1× 42 0.3× 17 0.1× 17 794

Countries citing papers authored by Damien L. Bruno

Since Specialization
Citations

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

Fields of papers citing papers by Damien L. Bruno

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Damien L. Bruno. 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 Damien L. Bruno. The network helps show where Damien L. Bruno may publish in the future.

Co-authorship network of co-authors of Damien L. Bruno

This figure shows the co-authorship network connecting the top 25 collaborators of Damien L. Bruno. A scholar is included among the top collaborators of Damien L. Bruno 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 Damien L. Bruno. Damien L. Bruno is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Whitlam, John, Ling Ling, Alison Skene, et al.. (2018). Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunction. American Journal of Transplantation. 19(4). 1037–1049. 86 indexed citations
3.
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Chandrananda, Dineika, Natalie Thorne, Devika Ganesamoorthy, et al.. (2014). Investigating and Correcting Plasma DNA Sequencing Coverage Bias to Enhance Aneuploidy Discovery. PLoS ONE. 9(1). e86993–e86993. 21 indexed citations
5.
Lim, Sze Chern, Justine E. Marum, Elena J. Tucker, et al.. (2013). Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes. Human Molecular Genetics. 22(22). 4460–4473. 81 indexed citations
6.
Tucker, Elena J., Bas F.J. Wanschers, Radek Szklarczyk, et al.. (2013). Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression. PLoS Genetics. 9(12). e1004034–e1004034. 85 indexed citations
7.
Tan, Tiong Yang, Amanda Collins, Paul A. James, et al.. (2011). Phenotypic variability of distal 22q11.2 copy number abnormalities. American Journal of Medical Genetics Part A. 155(7). 1623–1633. 54 indexed citations
8.
Bruno, Damien L., Stuart White, Devika Ganesamoorthy, et al.. (2011). Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping. Journal of Medical Genetics. 48(12). 831–839. 64 indexed citations
9.
Bruno, Damien L., Zornitza Stark, David J. Amor, et al.. (2011). Extending the scope of diagnostic chromosome analysis: Detection of single gene defects using high-resolution SNP microarrays. Human Mutation. 32(12). 1500–1506. 32 indexed citations
10.
Traylor, Ryan N., Damien L. Bruno, Trent Burgess, et al.. (2010). A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33. PLoS ONE. 5(8). e12462–e12462. 21 indexed citations
11.
Stark, Zornitza, Monique M. Ryan, Damien L. Bruno, Trent Burgess, & Ravi Savarirayan. (2010). Atypical Silver–Russell phenotype resulting from maternal uniparental disomy of chromosome 7. American Journal of Medical Genetics Part A. 152A(9). 2342–2345. 9 indexed citations
12.
Calvo, Sarah E., Elena J. Tucker, Alison G. Compton, et al.. (2010). High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nature Genetics. 42(10). 851–858. 279 indexed citations
13.
Kogelenberg, Margriet van, Sondhya Ghedia, George McGillivray, et al.. (2010). Periventricular Heterotopia in Common Microdeletion Syndromes. Molecular Syndromology. 1(1). 35–41. 32 indexed citations
14.
Yeung, Alison, Damien L. Bruno, Ingrid E. Scheffer, et al.. (2009). 4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment. European Journal of Medical Genetics. 52(6). 440–442. 49 indexed citations
15.
Hunter, Matthew F., Damien L. Bruno, & David J. Amor. (2009). Functional disomy of proximal Xp causes a distinct phenotype comprising early hypotonia, hypertelorism, small hands and feet, ear abnormalities, myopia and cognitive impairment. American Journal of Medical Genetics Part A. 149A(8). 1763–1767. 3 indexed citations
16.
Thomas, N. Simon, John F. Harvey, David J. Bunyan, et al.. (2009). Clinical and molecular characterization of duplications encompassing the human SHOX gene reveal a variable effect on stature. American Journal of Medical Genetics Part A. 149A(7). 1407–1414. 43 indexed citations
17.
Bruno, Damien L., et al.. (2006). Management of Postmenopausal Symptoms in Breast Cancer Survivors. Seminars in Oncology. 33(6). 696–707. 14 indexed citations
18.
Bruno, Damien L., Trent Burgess, Hua Ren, et al.. (2006). High‐throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy. American Journal of Medical Genetics Part A. 140A(24). 2786–2793. 45 indexed citations
19.
20.
Slater, Howard R., Damien L. Bruno, Hua Ren, et al.. (2004). Improved testing for CMT1A and HNPP using multiplex ligation-dependent probe amplification (MLPA) with rapid DNA preparations: Comparison with the interphase FISH Method. Human Mutation. 24(2). 164–171. 54 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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