Julie McGaughran

7.2k total citations · 1 hit paper
79 papers, 2.4k citations indexed

About

Julie McGaughran is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Julie McGaughran has authored 79 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 29 papers in Molecular Biology and 21 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Julie McGaughran's work include Cardiomyopathy and Myosin Studies (17 papers), Genomic variations and chromosomal abnormalities (15 papers) and Cardiovascular Effects of Exercise (12 papers). Julie McGaughran is often cited by papers focused on Cardiomyopathy and Myosin Studies (17 papers), Genomic variations and chromosomal abnormalities (15 papers) and Cardiovascular Effects of Exercise (12 papers). Julie McGaughran collaborates with scholars based in Australia, United Kingdom and New Zealand. Julie McGaughran's co-authors include Dian Donnai, Christopher Semsarian, Jodie Ingles, Ingrid Winship, J. Atherton, William C. Nichols, Lisa Wheeler, James E. Loyd, Rajiv D. Machado and Michael W. Pauciulo and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Circulation.

In The Last Decade

Julie McGaughran

75 papers receiving 2.3k 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.

Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia

2001 518 citations Ingrid Winship, Julie McGaughran et al. profile →

Peers

Countries citing papers authored by Julie McGaughran

Since Specialization

Citations

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

Fields of papers citing papers by Julie McGaughran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julie McGaughran. 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 Julie McGaughran. The network helps show where Julie McGaughran may publish in the future.

Co-authorship network of co-authors of Julie McGaughran

This figure shows the co-authorship network connecting the top 25 collaborators of Julie McGaughran. A scholar is included among the top collaborators of Julie McGaughran 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 Julie McGaughran. Julie McGaughran 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	Use of Advanced Echocardiographic Modalities to Discriminate Preclinical Hypertrophic Cardiomyopathy Mutation Carriers From Non-Carriers 2025 ·Circulation Genomic and Precision Medicine ·(unknown), (unknown), (unknown), (unknown), Arun Dahiya, Arnold C.T. Ng, Julie McGaughran, Louise McCormack, S. Prasad, J. Atherton	0
2	Assessing the unmet needs of genomic testing in Australia: a geospatial exploration 2024 ·European Journal of Human Genetics ·(unknown), Felicity Collins, Susan M. White, (unknown), Mathew Wallis, Nicholas Pachter, Julie McGaughran, Chris Barnett, Stephanie Best	1
3	Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services 2024 ·European Journal of Human Genetics ·Stephanie Best, (unknown), C. Richards, Michael C. Quinn, Sebastian Lunke, Amanda B. Spurdle, Karin S. Kassahn, Chirag Patel, Danya F. Vears, Ilias Goranitis, Fiona Lynch, Alan J. Robertson, Emma Tudini, John Christodoulou, Hamish S. Scott, Julie McGaughran, Zornitza Stark	2
4	Factors influencing uptake of familial long QT syndrome genetic testing 2015 ·American Journal of Medical Genetics Part A ·Charlotte Burns, Julie McGaughran, Andrew M. Davis, Christopher Semsarian, Jodie Ingles	37
5	Abstract 20544: Family History Characteristics as Risk Factors for Sudden Cardiac Death Events in Hypertrophic Cardiomyopathy 2014 ·Circulation ·Jodie Ingles, Charlotte Burns, C. Medi, Laura Yeates, Louise McCormack, L. Hunt, Julie McGaughran, J. Atherton, Christopher Semsarian	0
6	CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling 2013 ·Journal of Clinical Investigation ·Petro Starokadomskyy, Nathan Gluck, Haiying Li, Baozhi Chen, Mathew Wallis, Gabriel N. Maine, Xicheng Mao, Iram Waris Zaidi, Marco Y. Hein, Fiona J. McDonald, Steffen Lenzner, (unknown), Hans‐Hilger Ropers, Andreas W. Kuß, Julie McGaughran, Jozef Gécz, Ezra Burstein	77
7	Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy 2013 ·Genetics in Medicine ·Jodie Ingles, Tanya Sarina, Laura Yeates, L. Hunt, Ivan Macciocca, Louise McCormack, Ingrid Winship, Julie McGaughran, J. Atherton, Christopher Semsarian	85
8	Improving identification of lynch syndrome patients: A comparison of research data with clinical records 2012 ·International Journal of Cancer ·Yen Y. Tan, Julie McGaughran, Kaltin Ferguson, Michael D. Walsh, Daniel D. Buchanan, Joanne Young, Penelope M. Webb, Andreas Obermair, Amanda B. Spurdle, (unknown)	24
9	Lung Fibrosis, Premature Graying, and Macrocytosis 2012 ·American Journal of Respiratory and Critical Care Medicine ·Daniel C. Chambers, Belinda E. Clarke, Julie McGaughran, Christine Kim Garcia	7
10	A cost-effectiveness model of genetic testing for the evaluation of families with hypertrophic cardiomyopathy 2011 ·Heart ·Jodie Ingles, Julie McGaughran, Paul Scuffham, J. Atherton, Christopher Semsarian	90
11	Elements of morphology: Standard terminology for the head and face 2009 ·American Journal of Medical Genetics Part A ·Judith Allanson, Christopher Cunniff, H. Eugene Hoyme, Julie McGaughran, Maximilian Muenke, Giovanni Neri	115
12	Non‐pathological paternal isodisomy of chromosome 2 detected from a genome‐wide SNP scan 2009 ·American Journal of Medical Genetics Part A ·Matthew C. Keller, Allan F. McRae, Julie McGaughran, Peter M. Visscher, Nicholas G. Martin, Grant W. Montgomery	27
13	Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome 2008 ·Human Mutation ·May Tassabehji, Zhi Fang, Emma Hilton, Julie McGaughran, Zhongming Zhao, Charles E. de Bock, Emma Howard, (unknown), Dian Donnai, Ashish D. Diwan, Forbes Manson, (unknown), Raymond A. Clarke	148
14	Recurrence of Mowat–Wilson syndrome in siblings with the same proven mutation 2005 ·American Journal of Medical Genetics Part A ·Julie McGaughran, (unknown), Florence Dastot‐Le Moal, Meredith Wilson, David Mowat, (unknown), Michel Goossens	32
15	Prenatal diagnosis of mosaic trisomy 20 in New Zealand 2002 ·Australian and New Zealand Journal of Obstetrics and Gynaecology ·Paul A. James, Kate Gibson, Julie McGaughran	22
16	Compound Heterozygosity at the FMR1 Gene 2001 ·PubMed ·Madhuri Hegde, (unknown), Belinda Chong, Julie McGaughran, (unknown), Donald R. Love	7
17	Malignant peripheral nerve sheath tumors in neurofibromatosis 1. 2001 ·The American Journal of Human Genetics ·D. Gareth Evans, (unknown), (unknown), Julie McGaughran, Barry G. Timms, Anthony Moran	15
18	Clinical phenotypes of nine cases of Kabuki syndrome from New Zealand 2001 ·Clinical Dysmorphology ·Julie McGaughran, Salim Aftimos, Craig Jefferies, Ingrid Winship	24
19	Alveolar capillary dysplasia with antenatal anomalies mimicking trisomy 21 2001 ·Journal of Paediatrics and Child Health ·Julie McGaughran, (unknown), (unknown)	12
20	Delineation of the Critical Deletion Region for Congenital Heart Defects, on Chromosome 8p23.1 1999 ·The American Journal of Human Genetics ·Koenraad Devriendt, Gert Matthijs, (unknown), Marc Gewillig, Bénédicte Eyskens, Helle Hjalgrim, (unknown), Julie McGaughran, Karen Brøndum‐Nielsen, Peter Marynen, Jean‐Pierre Fryns, Joris Vermeesch	98

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