David O. Sillence

1.1k total citations
16 papers, 782 citations indexed

About

David O. Sillence is a scholar working on Molecular Biology, Genetics and Orthopedics and Sports Medicine. According to data from OpenAlex, David O. Sillence has authored 16 papers receiving a total of 782 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Orthopedics and Sports Medicine. Recurrent topics in David O. Sillence's work include Hedgehog Signaling Pathway Studies (3 papers), Bone health and treatments (2 papers) and Mitochondrial Function and Pathology (2 papers). David O. Sillence is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Bone health and treatments (2 papers) and Mitochondrial Function and Pathology (2 papers). David O. Sillence collaborates with scholars based in Australia, United States and Hong Kong. David O. Sillence's co-authors include P W Lu, Jane Allen, Julie Briody, Graham D. Ogle, IAN R. J. HUMPHRIES, Christopher T. Cowell, Robert Howman‐Giles, Ági K. Gedeon, Meredith Wilson and John C. Mulley and has published in prestigious journals such as The Journal of Cell Biology, Human Molecular Genetics and Journal of Bone and Mineral Research.

In The Last Decade

David O. Sillence

16 papers receiving 754 citations

Peers

Countries citing papers authored by David O. Sillence

Since Specialization

Citations

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

Fields of papers citing papers by David O. Sillence

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David O. Sillence. 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 David O. Sillence. The network helps show where David O. Sillence may publish in the future.

Co-authorship network of co-authors of David O. Sillence

This figure shows the co-authorship network connecting the top 25 collaborators of David O. Sillence. A scholar is included among the top collaborators of David O. Sillence 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 David O. Sillence. David O. Sillence 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:

16 of 16 papers shown

#	Work	Indexed citations
1	A novel intermediate mucolipidosis II/IIIαβ caused by GNPTAB mutation in the cytosolic N-terminal domain 2013 ·European Journal of Human Genetics ·Jules G. Leroy, David O. Sillence, Tim Wood, Jarrod W. Barnes, Robert Roger Lebel, Michael J. Friez, Roger E. Stevenson, Richard Steet, Sara Cathey	17
2	COL10A1 nonsense and frame-shift mutations have a gain-of-function effect on the growth plate in human and mouse metaphyseal chondrodysplasia type Schmid 2007 ·Human Molecular Genetics ·Matthew Ho, Kwok Yeung Tsang, (unknown), Miki Susic, Outi Mäkitie, (unknown), Vivian Ng, David O. Sillence, Ray Boot-Handford, Gary Gibson, Kmc Cheung, William G. Cole, Kathryn S.E. Cheah, Danny Chan	55
3	Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctata. 1998 ·Journal of Medical Genetics ·Leslie J. Sheffield, Amelia H. Osborn, Wendy Hutchison, David O. Sillence, Sue Forrest, Stefan J. White, H H Dahl	19
4	Abnormal Compartmentalization of Cartilage Matrix Components in Mice Lacking Collagen X: Implications for Function 1997 ·The Journal of Cell Biology ·Kin Ming Kwan, (unknown), Sheila X. Zhou, (unknown), Richard Yuen Chong Kong, (unknown), Bjørn R. Olsen, David O. Sillence, Patrick Tam, Kathryn S.E. Cheah	156
5	The Wolf-Hirschhorn syndrome in adulthood: Evaluation of a 24-year-old man with a rec(4) chromosome 1996 ·American Journal of Medical Genetics ·Robert Ogle, David O. Sillence, (unknown), (unknown), (unknown), Lisa Robson, (unknown)	12
6	X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome. 1995 ·Journal of Medical Genetics ·Ági K. Gedeon, Meredith Wilson, (unknown), David O. Sillence, John C. Mulley	46
7	Bone mineral density of total body, spine, and femoral neck in children and young adults: A cross-sectional and longitudinal study 1994 ·Journal of Bone and Mineral Research ·P W Lu, Julie Briody, Graham D. Ogle, (unknown), IAN R. J. HUMPHRIES, Jane Allen, Robert Howman‐Giles, David O. Sillence, Christopher T. Cowell	246
8	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
9	An X‐Linked Reticulate Pigmentary Disorder With Systemic Manifestations: Report of a Second Family 1993 ·Pediatric Dermatology ·Lesley C. Adès, Maureen Rogers, David O. Sillence	15
10	Axenfeld anomaly in association with hypomelanosis of Ito 1991 ·Ophthalmic Paediatrics and Genetics ·Maree Flaherty, Carmencita D. Padilla, David O. Sillence	4
11	Unusual radiographic manifestations of chondrodysplasia punctata 1989 ·Skeletal Radiology ·(unknown), A Schlesinger, K. Kozlowski, A. K. Poznanski, (unknown), G Dreyer, (unknown), David O. Sillence, (unknown)	10
12	A colour atlas of clinical genetics 1984 ·The Medical Journal of Australia ·David O. Sillence	1
13	ANIRIDIA RESULTING FROM CHROMOSOME 11p13 DELETION (MILLER'S SYNDROME): REPORT OF A CASE 1984 ·(unknown), (unknown), David O. Sillence	1
14	Spondylohumerofemoral hypoplasia (giant cell chondrodysplasia): A neonatally lethal short‐limb skeletal dysplasia 1982 ·American Journal of Medical Genetics ·David O. Sillence, Ralph S. Lachman, T Jenkins, Vincent M. Riccardi, David L. Rimoin	35
15	Non‐Majewski short rib‐polydactyly syndrome 1980 ·American Journal of Medical Genetics ·David O. Sillence, J. Herrmann, John M. Optiz	29
16	An Embedding Method for Histochemical Studies of Undecalcified Skeletal Growth Plate 1980 ·Stain Technology ·William A. Horton, (unknown), David O. Sillence, David L. Rimoin	32

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