John Rogers

7.8k citations

104 papers · 3.6k indexed · 1 hit paper · h-index 30

Impact in

Rheumatology top 0.5%
- Heterotopic Ossification and Related Conditions
- Bone and Dental Protein Studies
Nephrology top 2%
- Parathyroid Disorders and Treatments

Papers in

Rheumatology 23
- Heterotopic Ossification and Related Conditions 6
- Bone and Dental Protein Studies 6
Genetics 39
- Connective tissue disorders research 20
- Genomic variations and chromosomal abnormalities 11

Co-authors: John F. Bateman Danny Chan David Sillence Rolf Morhart J. M. Connor Patricia Delai Eileen M. Shore David L. Glaser
Journals: Journal of Medical Genetics (11 papers)The Journal of Pediatrics (5 papers)The Medical Journal of Australia (3 papers)European Journal of Pediatrics (3 papers)Journal of Mammalogy (3 papers)
Partner nations: Australia United States United Kingdom

In The Last Decade

John Rogers

99 papers receiving 3.4k citations

Hit Papers

align trajectories log scale

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva 2006 · 866 citations

Peers

Countries citing papers authored by John Rogers

Since Specialization

Citations

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

Fields of papers citing papers by John Rogers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside John Rogers, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with John Rogers Line = papers co-authored together John Rogers links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	Salivary characteristics and dental caries experience in remote Indigenous children in Australia: a cross-sectional study BMC Oral Health ·Ratilal Lalloo, Santosh Kumar Tadakamadla, Jeroen Kroon, LI Jie-ming, Sanjeewa Kularatna, J. F. Monaco, Kostas Kapellas, Verónica Jackelin, M. Da Silva, John Rogers, Newell W. Johnson	2019	13
2	What factors are associated with dental general anaesthetics for Australian children and what are the policy implications? A qualitative study BMC Oral Health ·John Rogers, Clare Delany, Clive Wright, Kaye Roberts‐Thomson, Mike Morgan	2018	18
3	“You're one of us now”: Young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP) American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Rony E. Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John Rogers, Martin B. Delatycki	2008	76
4	“Holding your breath”: Interviews with young people who have undergone predictive genetic testing for Huntington disease American Journal of Medical Genetics Part A ·Rony E. Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John Rogers, Martin B. Delatycki	2007	44
5	FBN1, TGFBR1, and the Marfan‐craniosynostosis/mental retardation disorders revisited 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	2006	69
6	A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva Nature Genetics ·Eileen M. Shore, Meiqi Xu, George Feldman, David Fenstermacher, Tae‐Joon Cho, In Ho Choi, J. M. Connor, Patricia Delai, David L. Glaser, Martine LeMerrer, Rolf Morhart, John Rogers, Roger Smith, James T. Triffitt, Jon Andoni Urtizberea, Michael Zasloff, Matthew A. Brown, Frederick S. Kaplan Hit paper breakdown →	2006	866
7	The Phenotype of Fibrodysplasia Ossificans Progressiva Clinical Reviews in Bone and Mineral Metabolism ·Frederick S. Kaplan, David L. Glaser, Eileen M. Shore, Gregory K. Deirmengian, Rishi Gupta, Patricia Delai, Rolf Morhart, Roger Smith, Martine Le Merrer, John Rogers, J. M. Connor, Joseph A. Kitterman	2005	85
8	Longterm follow‐up in chondrodysplasia punctata, tibia–metacarpal type, demonstrating natural history American Journal of Medical Genetics Part A ·Ravi Savarirayan, Robert Boyle, J. Masel, John Rogers, Leslie J. Sheffield	2003	12
9	Chronic Beryllium Disease and Beryllium Sensitization at Rocky Flats: A Case-Control Study PubMed ·Susan Marie Viet, 崔卫峰, John Rogers	2000	22
10	Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda Nature Genetics ·Ági K. Gedeon, Alison Colley, Robyn V. Jamieson, Elizabeth M. Thompson, John Rogers, David Sillence, George E. Tiller, John C. Mulley, Jozef Gécz	1999	145
11	Cerebrospinal fluid shunts in the management of behavioural problems in Sanfilippo syndrome (MPS III) European Journal of Pediatrics ·Stephen P. Robertson, Geoffrey L. Klug, John Rogers	1998	9
12	Pitt-Rogers-Dank syndrome: The result of a 4p microdeletion American Journal of Medical Genetics ·Michele Clemens, John T. Martsolf, John Rogers, Patricia Mowery‐Rushton, Urvashi Surti, Elizabeth McPherson	1996	23
13	Type X Collagen Multimer Assembly in Vitro Is Prevented by a Gly618 to Val Mutation in the α1(X) NC1 Domain Resulting in Schmid Metaphyseal Chondrodysplasia Journal of Biological Chemistry ·Danny Chan, William G. Cole, John Rogers, John F. Bateman	1995	69
14	The clinical features of spondyloepiphyseal dysplasia congenita resulting from the substitution of glycine 997 by serine in the alpha 1(II) chain of type II collagen. Journal of Medical Genetics ·William G. Cole, Roger K. Hall, John Rogers	1993	22
15	Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p 11.2 p 11.2) (Smith‐Magenis syndrome) Journal of Paediatrics and Child Health ·Andrew Colley, M. Leversha, Lucille Voullaire, John Rogers	1990	47
16	Autosomal recessive hydrocephalus with third ventricle obstruction American Journal of Medical Genetics ·C.W. Chow, Penelope McKelvie, R. McD. Anderson, Ethna Phelan, Geoffrey L. Klug, John Rogers	1990	19
17	Duplication of a small segment of 5p due to maternal recombination within a paracentric shift American Journal of Medical Genetics ·Graham C. Webb, Lucille Voullaire, John Rogers	1988	30
18	Tertiary lactic acidosis The Journal of Pediatrics ·John Rogers, R.G. Wilkinson, Guowe, D. M. Danks	1981	3
19	A postaxial polydactyly-dental-vertebral syndrome The Journal of Pediatrics ·John Rogers, L. Stefan Levin, John P. Dorst, Samia A. Temtamy	1977	7
20	Use and complications of high-dose disodium etidronate therapy in fibrodysplasia ossificans progressiva The Journal of Pediatrics ·John Rogers, John P. Dorst, 埃文思·朱利安	1977	40

About John Rogers

John Rogers is a scholar working on Rheumatology, Genetics, Clinical Biochemistry, Developmental Biology and Periodontics, having authored 104 papers that have together received 3.6k indexed citations. Recurring topics across this work include Connective tissue disorders research (20 papers), Genomic variations and chromosomal abnormalities (11 papers), Metabolism and Genetic Disorders (9 papers), Prenatal Screening and Diagnostics (8 papers), Medical Imaging and Pathology Studies (7 papers), Bone health and treatments (7 papers), Heterotopic Ossification and Related Conditions (6 papers) and Bone and Dental Protein Studies (6 papers). The work is most often cited by research in Rheumatology (1.3k citations), Nephrology (369 citations), Genetics (1.4k citations), Pulmonary and Respiratory Medicine (772 citations) and Developmental Biology (50 citations). John Rogers has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include John F. Bateman, Danny Chan, David Sillence, Rolf Morhart, J. M. Connor, Patricia Delai, Eileen M. Shore, David L. Glaser, Roger Smith and Frederick S. Kaplan. Their work appears in journals such as Journal of Medical Genetics, The Journal of Pediatrics, The Medical Journal of Australia, European Journal of Pediatrics and Journal of Mammalogy.

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