Desirée du Sart

4.7k citations

39 papers · 2.0k indexed · h-index 26

Co-authors: Malgorzata Schmidt Paul Kalitsis K. H. Andy Choo Alyssa E. Barry Michael Cancilla Kellie M. Tainton John K. Olynyk Peter Gochee
Topics: Genetics and Neurodevelopmental Disorders (10 papers)Cancer Genomics and Diagnostics (7 papers)Genetic factors in colorectal cancer (6 papers)
Cited by: Genetics Hematology
Journals: The Lancet Nature Genetics Gastroenterology
Partner nations: Australia United States United Kingdom

In The Last Decade

Desirée du Sart

39 papers receiving 1.9k citations

Peers

Countries citing papers authored by Desirée du Sart

Since Specialization

Citations

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

Fields of papers citing papers by Desirée du Sart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Desirée du Sart. 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 Desirée du Sart. The network helps show where Desirée du Sart may publish in the future.

Co-authorship network of co-authors of Desirée du Sart

This figure shows the co-authorship network connecting the top 25 collaborators of Desirée du Sart. A scholar is included among the top collaborators of Desirée du Sart 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 Desirée du Sart. Desirée du Sart 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

#	Work	Indexed citations
1	EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias 2023 ·European Journal of Human Genetics ·(unknown),Zahurul A. Bhuiyan,Domenico Coviello,Desirée du Sart,(unknown),Maria Iascone,Déborah Morris-Rosendahl,(unknown),Marjon van Slegtenhorst,Kate Thomson	11
2	Molecular Inconsistencies in a Fragile X Male with Early Onset Ataxia 2016 ·Genes ·(unknown),Tracy Dudding,(unknown),Marta Arpone,David Francis,Xin Li,Howard R. Slater,Carolyn Rogers,Lesley Bretherton,Desirée du Sart,Robert Heard,David E. Godler	6
3	Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt Analysis 2015 ·Clinical Chemistry ·(unknown),Howard R. Slater,David Francis,Desirée du Sart,Xin Li,David J. Amor,(unknown),Lorena Santa María,Víctor Faúndes,(unknown),César Trigo,(unknown),(unknown),David E. Godler	25
4	A comprehensive evaluation of myocardial fibrosis in hypertrophic cardiomyopathy with cardiac magnetic resonance imaging: linking genotype with fibrotic phenotype 2014 ·European Heart Journal - Cardiovascular Imaging ·A. Ellims,L. Iles,Liang‐Han Ling,Belinda Chong,Ivan Macciocca,Glenn S. Slavin,James Hare,David M. Kaye,Silvana Marasco,Catriona McLean,Paul A. James,Desirée du Sart,Andrew J. Taylor	72
5	Premature arthritis is a distinct type II collagen phenotype 2010 ·Arthritis & Rheumatism ·Pekka Kannus,John F. Bateman,(unknown),Shannon Cowie,Desirée du Sart,Shaun McGrath,Matthew Edwards,Ravi Savarirayan	40
6	Familial adenomatous polyposis 2009 ·Best Practice & Research Clinical Gastroenterology ·Finlay Macrae,Desirée du Sart,Steven Nasioulas	12
7	Population screening and cascade testing for carriers of SMA 2007 ·European Journal of Human Genetics ·Melanie Smith,(unknown),Belinda Chong,(unknown),Shannon Cowie,Desirée du Sart	57
8	Detection of Mutations in Genes Associated with Hearing Loss Using a Microarray-Based Approach 2006 ·Journal of Molecular Diagnostics ·Kirby Siemering,Shehnaaz S.M. Manji,Wendy Hutchison,Desirée du Sart,Dean Phelan,Hans‐Henrik M. Dahl	18
9	Hyperplastic Polyposis Syndrome: Phenotypic Presentations and the Role of MBD4 and MYH 2006 ·Gastroenterology ·Elizabeth Chow,Lara Lipton,Elly Lynch,(unknown),C. Aragona,(unknown),Gregor J. Brown,Ingrid Winship,Melissa Barker,Daniel D. Buchanan,Shannon Cowie,(unknown),Desirée du Sart,Joanne Young,Barbara Leggett,Jeremy R. Jass,Finlay Macrae	124
10	Distinct patterns of germ-line deletions inMLH1 andMSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC) 2006 ·Human Mutation ·(unknown),(unknown),Rami Younan,Ping Liang,Desirée du Sart,Philip H. Gordon,Pierre Hutter,Frans B.L. Hogervorst,George Chong,William D. Foulkes	43
11	Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis 2005 ·The Lancet ·MB Delatycki,Katrina J. Allen,Amy Nisselle,V. Collins,Sylvia A. Metcalfe,Desirée du Sart,Jane Halliday,(unknown),Ivan Macciocca,(unknown),A J Wakefield,(unknown),(unknown),(unknown),(unknown),R. Williamson	73
12	Identification ofAPCgene mutations in colorectal cancer using universal microarray-based combinatorial sequencing-by-hybridization 2004 ·Human Mutation ·Shannon Cowie,Snezana Drmanac,Donald A. Swanson,Kathleen Delgrosso,Steve Huang,Desirée du Sart,Radoje Drmanac,Saul Surrey,Paolo Fortina	14
13	Implementation of HaemScreen, a workplace‐based genetic screening program for hemochromatosis 2004 ·Clinical Genetics ·Amy Nisselle,MB Delatycki,V. Collins,Sylvia A. Metcalfe,(unknown),Desirée du Sart,Jane Halliday,Ivan Macciocca,A J Wakefield,(unknown),(unknown),(unknown),(unknown),R. Williamson,Katrina J. Allen	28
14	Hereditary Nonpolyposis Colorectal Cancer in 95 Families: Differences and Similarities between Mutation-Positive and Mutation-Negative Kindreds 2001 ·The American Journal of Human Genetics ·Rodney J. Scott,Mary McPhillips,Cliff Meldrum,Patrick Fitzgerald,(unknown),Allan D. Spigelman,Desirée du Sart,Kathy Tucker,Judy Kirk	152
15	Mosaic inv dup(8p) marker chromosome with stable neocentromere suggests neocentromerization is a post-zygotic event 2001 ·American Journal of Medical Genetics ·Lucille Voullaire,Richard Saffery,Elizabeth D. Earle,Danielle V. Irvine,Howard R. Slater,(unknown),Desirée du Sart,Tracy L. Fleming,K. H. Andy Choo	26
16	Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia 2000 ·American Journal of Medical Genetics ·Elsdon Storey,Desirée du Sart,(unknown),(unknown),Louise Kelly,Richard J. Gardner,Susan M. Forrest,(unknown),Garth A. Nicholson	72
17	Direct Cloning of Human 10q25 Neocentromere DNA Using Transformation-Associated Recombination (TAR) in Yeast 1998 ·Genomics ·Michael Cancilla,Kellie M. Tainton,Alyssa E. Barry,Vladimir Larionov,Natalya Kouprina,Michael A. Resnick,Desirée du Sart,K. H. Andy Choo	32
18	Noninactivation of a portion of Xq28 in a balanced X‐autosome translocation 1992 ·American Journal of Medical Genetics ·Desirée du Sart,Paul Kalitsis,Malgorzata Schmidt	25
19	Functional disomies of the X chromosome influence the cell selection and hence the X inactivation pattern in females with balanced X‐autosome translocations: A review of 122 cases 1992 ·American Journal of Medical Genetics ·Malgorzata Schmidt,Desirée du Sart	143
20	New polymorphic DNA marker close to the fragile site FRAXA 1990 ·Genomics ·B. A. Oostra,(unknown),(unknown),Coen A. M. van Bennekom,Egbert Bakker,D. J. J. Halley,Malgorzata Schmidt,Desirée du Sart,Anne Smits,Bé Wieringa,Bernard A. van Oost	49

About Desirée du Sart

Desirée du Sart is a scholar working on Genetics, Genetics and Cancer Research, having authored 39 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Cancer Genomics and Diagnostics (7 papers) and Genetic factors in colorectal cancer (6 papers). The work is most often cited by research in Genetics (394 citations), Hematology (257 citations) and Genetics (617 citations). Desirée du Sart has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Malgorzata Schmidt, Paul Kalitsis, K. H. Andy Choo, Alyssa E. Barry, Michael Cancilla, Kellie M. Tainton, John K. Olynyk, Peter Gochee, Enrico Rossi and Lawrie W. Powell. Their work appears in journals such as The Lancet, Nature Genetics and Gastroenterology.

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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