Lesley C. Adès

8.7k citations

58 papers · 2.2k indexed · h-index 23

Genetics top 1%
Molecular Biology top 10%
Pulmonary and Respiratory Medicine top 5%
Surgery top 10%
Cardiology and Cardiovascular Medicine top 10%

Co-authors: Eric Haan Meredith Wilson Nicole Chia Katherine Holman John C. Mulley Michael C. Edwards Peter Meinecke Antônio Richieri‐Costa
Topics: Connective tissue disorders research (21 papers)Genomic variations and chromosomal abnormalities (9 papers)Aortic Disease and Treatment Approaches (6 papers)
Cited by: Genetics Developmental Biology Molecular Biology
Journals: Nucleic Acids Research Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Australia United States United Kingdom

In The Last Decade

Lesley C. Adès

54 papers receiving 2.1k citations

Peers

Countries citing papers authored by Lesley C. Adès

Since Specialization

Citations

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

Fields of papers citing papers by Lesley C. Adès

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lesley C. Adès. 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 Lesley C. Adès. The network helps show where Lesley C. Adès may publish in the future.

Co-authorship network of co-authors of Lesley C. Adès

This figure shows the co-authorship network connecting the top 25 collaborators of Lesley C. Adès. A scholar is included among the top collaborators of Lesley C. Adès 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 Lesley C. Adès. Lesley C. Adès 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	Case Report: A rare case of bilateral molar natal teeth in a term newborn 2024 ·SHILAP Revista de lepidopterología ·(unknown),Lesley C. Adès,(unknown)	0
2	De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction 2010 ·American Journal of Medical Genetics Part A ·Dianna M. Milewicz,John R. Østergaard,Leena Ala‐Kokko,Nadia Khan,Dorothy K. Grange,Roberto Mendoza‐Londono,Timothy J. Bradley,Ann Haskins Olney,Lesley C. Adès,Joseph F. Maher,Dongchuan Guo,L. Maximilian Buja,Dong Kim,James Hyland,Ellen S. Regalado	178
3	Evolution of the face in Loeys–Dietz syndrome type II: longitudinal observations from infancy in seven cases 2008 ·Clinical Dysmorphology ·Lesley C. Adès	12
4	Nanophthalmos in a Melanesian population 2007 ·Clinical and Experimental Ophthalmology ·(unknown),James E. Smith,Yemima Berman,Lesley C. Adès,(unknown),(unknown),Frank Martin,Paul Mitchell,David Taylor	12
5	Deletion 22q11.2 syndrome—Implications for the intensive care physician* 2007 ·Pediatric Critical Care Medicine ·(unknown),Jonathan Gillis,(unknown),Lesley C. Adès	20
6	EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype–phenotype correlation? 2007 ·American Journal of Medical Genetics Part A ·Kenneth N. Maclean,(unknown),Elizabeth Gilmour,Mark G. Taylor,Hans Scheffer,Nicole Graf,Grahame Smith,Ella Onikul,Hans van Bokhoven,Celia Moss,Lesley C. Adès	10
7	FBN1, TGFBR1, and the Marfan‐craniosynostosis/mental retardation disorders revisited 2006 ·American Journal of Medical Genetics Part A ·Lesley C. Adès,Kathleen E. Sullivan,Andrew Biggin,Eric Haan,Maggie Brett,Katherine Holman,Joanne Dixon,Stephen P. Robertson,Anthony D. Holmes,John Rogers,Bruce Bennetts	69
8	Histopathology and fibrillin‐1 distribution in severe early onset Marfan syndrome 2005 ·American Journal of Medical Genetics Part A ·Kim Summers,Maria Nataatmadja,Dongming Xu,MJ West,(unknown),(unknown),Andrew Colley,Lesley C. Adès	17
9	Enamel defects and Lyonization in focal dermal hypoplasia 2004 ·Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology ·Richard Balmer,A. Colin Cameron,Lesley C. Adès,Michael J. Aldred	11
10	Primary trabeculodysgenesis in association with neonatal Marfan syndrome 2004 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Lesley C. Adès,Glen A. Gole,James E. Elder,Ravi Savarirayan	7
11	The Hunter–McAlpine syndrome results from duplication 5q35–qter 2004 ·Clinical Genetics ·(unknown),Barbara R. DuPont,Margaret E. McLaughlin,(unknown),Elizabeth Baker,Lesley C. Adès,E Haan,(unknown)	11
12	Short stature, sensorineural deafness, ocular abnormalities and severe mental retardation in two siblings. A new syndrome? 2004 ·Clinical Dysmorphology ·Ingrid Sinnerbrink,Lesley C. Adès	2
13	Novel Types of Mutation Responsible for the Dermatosparactic Type of Ehlers–Danlos Syndrome (Type VIIC) and Common Polymorphisms in the ADAMTS2 Gene 2004 ·Journal of Investigative Dermatology ·Alain Colige,Lieve Nuytinck,Ingrid Haußer,Anthonie J. van Essen,Marc Thiry,Christian Herens,Lesley C. Adès,Fransiska Malfait,Anne De Paepe,Peter Franck,G. Wolff,Jan C. Oosterwijk,J.H. Sillevis Smitt,Charles M. Lapière,Betty Nusgens	96
14	Issues arising from the prenatal diagnosis of some rare trisomy mosaics—the importance of cryptic fetal mosaicism 2004 ·Prenatal Diagnosis ·Art Daniel,Zhanhe Wu,Artur Darmanian,Paul Malafiej,Varsha Tembe,Greg B. Peters,Craig H. Kennedy,Lesley C. Adès	38
15	Detection of thirty novelFBN1mutations in patients with Marfan syndrome or a related fibrillinopathy 2003 ·Human Mutation ·Andrew Biggin,Katherine Holman,Maggie Brett,Bruce Bennetts,Lesley C. Adès	49
16	A case of partial trisomy 4p syndrome presenting as severe hydronephrosis in utero 2003 ·Clinical Dysmorphology ·Katherine Neas,Nicole Chia,(unknown),Gregory B. Peters,Lesley C. Adès	1
17	Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene 1997 ·Nucleic Acids Research ·Gwenaëlle Collod‐Béroud,Christophe Béroud,Lesley C. Adès,Casilda G. Black,M. Boxer,D. J. H. Brock,Maurice Godfrey,Caroline Hayward,Leena Karttunen,(unknown),Leena Peltonen,Robert I. Richards,(unknown),Claudine Junien,Cathérine Boileau	25
18	Clinicopathologic findings in congenital aneurysms of the great vessels 1996 ·American Journal of Medical Genetics ·Lesley C. Adès,(unknown),Roger W. Byard,John F. Bateman,(unknown),Roger B.B. Mee,Eric Haan,Dianna M. Milewicz	20
19	Neurological involvement in worth type endosteal hyperostosis: Report of a family 1994 ·American Journal of Medical Genetics ·Lesley C. Adès,Lloyd Morris,(unknown),(unknown)	15
20	Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28 1993 ·American Journal of Medical Genetics ·Lesley C. Adès,Ági K. Gedeon,Meredith Wilson,M. C. Latham,M. W. Partington,John C. Mulley,John W. Nelson,Kei Lui,David O. Sillence	104

About Lesley C. Adès

Lesley C. Adès is a scholar working on Genetics, Developmental Biology and Cancer Research, having authored 58 papers that have together received 2.2k indexed citations. Recurring topics across this work include Connective tissue disorders research (21 papers), Genomic variations and chromosomal abnormalities (9 papers) and Aortic Disease and Treatment Approaches (6 papers). The work is most often cited by research in Genetics (1.3k citations), Developmental Biology (75 citations) and Molecular Biology (915 citations). Lesley C. Adès has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Eric Haan, Meredith Wilson, Nicole Chia, Katherine Holman, John C. Mulley, Michael C. Edwards, Peter Meinecke, Antônio Richieri‐Costa, Karen W. Gripp and David Wotton. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and SHILAP Revista de lepidopterología.

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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