Damien L. Bruno

3.3k citations

29 papers · 1.5k indexed · h-index 19

Molecular Biology top 10%
Genetics top 5%
Clinical Biochemistry top 1%
Pediatrics, Perinatology and Child Health top 10%
Surgery

Co-authors: Howard R. Slater David R. Thorburn Elena J. Tucker Alison G. Compton Vamsi K. Mootha Sarah E. Calvo Trent Burgess John Christodoulou
Topics: Genomic variations and chromosomal abnormalities (18 papers)Prenatal Screening and Diagnostics (8 papers)Genomics and Rare Diseases (5 papers)
Cited by: Clinical Biochemistry Transplantation Genetics
Journals: Nature Genetics PLoS ONE Human Molecular Genetics
Partner nations: Australia United States Netherlands

In The Last Decade

Damien L. Bruno

28 papers receiving 1.4k citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Diagnostic application of kidney allograft-derived absolute cell-free DNA levels during transplant dysfunction 2018 ·American Journal of Transplantation ·John Whitlam,Ling Ling,Alison Skene,John Kanellis,(unknown),Howard R. Slater,Damien L. Bruno,David A. Power	86
2	Higher Levels of Exhaled Dimethylcyclopropane in Patients with Small Intestinal Bowel Overgrowth, Periodontitis when Associated with a Medical History of Cancer 2018 ·Damien L. Bruno,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	1
3	Use of ubiquitous, highly heterozygous copy number variants and digital droplet polymerase chain reaction to monitor chimerism after allogeneic haematopoietic stem cell transplantation 2017 ·Experimental Hematology ·John Whitlam,Ling Ling,(unknown),(unknown),(unknown),Ian Brooks,(unknown),(unknown),Vida Petrovic,Damien L. Bruno,Françoise Méchinaud,Rachel Conyers,Howard R. Slater	6
4	Investigating and Correcting Plasma DNA Sequencing Coverage Bias to Enhance Aneuploidy Discovery 2014 ·PLoS ONE ·Dineika Chandrananda,Natalie Thorne,Devika Ganesamoorthy,Damien L. Bruno,Yuval Benjamini,Terence P. Speed,Howard R. Slater,Melanie Bahlo	21
5	Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes 2013 ·Human Molecular Genetics ·Sze Chern Lim,(unknown),Justine E. Marum,Elena J. Tucker,Damien L. Bruno,Lisa G. Riley,John Christodoulou,Edwin P. Kirk,Avihu Boneh,(unknown),Michael Springer,Vamsi K. Mootha,Tracey A. Rouault,Silke Leimkühler,David R. Thorburn,Alison G. Compton	81
6	Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression 2013 ·PLoS Genetics ·Elena J. Tucker,Bas F.J. Wanschers,Radek Szklarczyk,Hayley S. Mountford,(unknown),Mariël A.M. van den Brand,(unknown),Richard J. Rodenburg,Boris Reljić,Alison G. Compton,Ann E. Frazier,Damien L. Bruno,John Christodoulou,Hitoshi Endo,Michael T. Ryan,Leo Nijtmans,Martijn A. Huynen,David R. Thorburn	85
7	Phenotypic variability of distal 22q11.2 copy number abnormalities 2011 ·American Journal of Medical Genetics Part A ·Tiong Yang Tan,Amanda Collins,Paul A. James,George McGillivray,Zornitza Stark,Christopher T. Gordon,Richard J. Leventer,Kate Pope,Robin Forbes,John A. Crolla,Devika Ganesamoorthy,Trent Burgess,Damien L. Bruno,Howard R. Slater,Peter G. Farlie,David J. Amor	54
8	Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping 2011 ·Journal of Medical Genetics ·Damien L. Bruno,Stuart White,Devika Ganesamoorthy,Trent Burgess,(unknown),(unknown),David Francis,(unknown),(unknown),(unknown),F Norris,(unknown),Mark D. Pertile,Zornitza Stark,David J. Amor,Howard R. Slater	64
9	Extending the scope of diagnostic chromosome analysis: Detection of single gene defects using high-resolution SNP microarrays 2011 ·Human Mutation ·Damien L. Bruno,Zornitza Stark,David J. Amor,Trent Burgess,(unknown),(unknown),David Francis,Devika Ganesamoorthy,(unknown),Paul A. James,Darren D. O’Rielly,(unknown),Ravi Savarirayan,(unknown),(unknown),Howard R. Slater	32
10	Atypical Silver–Russell phenotype resulting from maternal uniparental disomy of chromosome 7 2010 ·American Journal of Medical Genetics Part A ·Zornitza Stark,Monique M. Ryan,Damien L. Bruno,Trent Burgess,Ravi Savarirayan	9
11	A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33 2010 ·PLoS ONE ·Ryan N. Traylor,Damien L. Bruno,Trent Burgess,Robert S. Wildin,(unknown),Devika Ganesamoorthy,David J. Amor,Matthew F. Hunter,Michael S. Caplan,Jill A. Rosenfeld,Aaron Theisen,Beth S. Torchia,Lisa G. Shaffer,Blake C. Ballif,Howard R. Slater	21
12	Periventricular Heterotopia in Common Microdeletion Syndromes 2010 ·Molecular Syndromology ·Margriet van Kogelenberg,Sondhya Ghedia,George McGillivray,Damien L. Bruno,Richard J. Leventer,K D MacDermot,James T. Nelson,L Nagarajan,Joris A. Veltman,Arjan Pm de Brouwer,R. J McKinlay Gardner,Hans van Bokhoven,Edwin P. Kirk,Stephen P. Robertson	32
13	High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency 2010 ·Nature Genetics ·Sarah E. Calvo,Elena J. Tucker,Alison G. Compton,Denise M. Kirby,Gabriel Crawford,Noël P. Burtt,Manuel A. Rivas,Candace Guiducci,Damien L. Bruno,Olga Goldberger,(unknown),Esko Wiltshire,Callum Wilson,David Altshuler,Stacey B. Gabriel,Mark J. Daly,David R. Thorburn,Vamsi K. Mootha	279
14	4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairment 2009 ·European Journal of Medical Genetics ·Alison Yeung,Damien L. Bruno,Ingrid E. Scheffer,(unknown),Trent Burgess,Howard R. Slater,David J. Amor	49
15	Functional disomy of proximal Xp causes a distinct phenotype comprising early hypotonia, hypertelorism, small hands and feet, ear abnormalities, myopia and cognitive impairment 2009 ·American Journal of Medical Genetics Part A ·Matthew F. Hunter,Damien L. Bruno,David J. Amor	3
16	Clinical and molecular characterization of duplications encompassing the human SHOX gene reveal a variable effect on stature 2009 ·American Journal of Medical Genetics Part A ·N. Simon Thomas,John F. Harvey,David J. Bunyan,Julia Rankin,Giedré Grigelioniené,Damien L. Bruno,Tiong Yang Tan,Susan Tomkins,Robert Hastings	43
17	Management of Postmenopausal Symptoms in Breast Cancer Survivors 2006 ·Seminars in Oncology ·Damien L. Bruno,(unknown)	14
18	High‐throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy 2006 ·American Journal of Medical Genetics Part A ·Damien L. Bruno,Trent Burgess,Hua Ren,Sara Nouri,Mark D. Pertile,David Francis,Fiona Norris,(unknown),Jan Schouten,K. H. Andy Choo,Howard R. Slater	45
19	Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay 2005 ·Human Mutation ·Emma L. Northrop,Hua Ren,Damien L. Bruno,(unknown),(unknown),Jan Schouten,K.H. Andy Choo,Howard R. Slater	25
20	Improved testing for CMT1A and HNPP using multiplex ligation-dependent probe amplification (MLPA) with rapid DNA preparations: Comparison with the interphase FISH Method 2004 ·Human Mutation ·Howard R. Slater,Damien L. Bruno,Hua Ren,(unknown),Trent Burgess,(unknown),Sara Nouri,Jan Schouten,K. H. Andy Choo	54

About Damien L. Bruno

Damien L. Bruno is a scholar working on Genetics, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 29 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (8 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Clinical Biochemistry (353 citations), Transplantation (93 citations) and Genetics (526 citations). Damien L. Bruno has collaborated with scholars based in Australia, United States and Netherlands. Frequent co-authors include Howard R. Slater, David R. Thorburn, Elena J. Tucker, Alison G. Compton, Vamsi K. Mootha, Sarah E. Calvo, Trent Burgess, John Christodoulou, Sze Chern Lim and Adrienne Laskowski. Their work appears in journals such as Nature Genetics, PLoS ONE and Human Molecular Genetics.

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.

Explore authors with similar magnitude of impact