Michael D. Briggs

4.9k citations

75 papers · 3.4k indexed · h-index 35

Impact in

Immunology and Allergy top 0.5%
- Cell Adhesion Molecules Research
Rheumatology top 0.5%
- Osteoarthritis Treatment and Mechanisms

Papers in

Immunology and Allergy 24
- Cell Adhesion Molecules Research 24
Rheumatology 28
- Osteoarthritis Treatment and Mechanisms 26

Co-authors: Kathryn Chapman Ray Boot-Handford Geert Mortier Karl E. Kadler David L. Rimoin Michael E. Grant Ralph S. Lachman Roger S. Meadows
Journals: Human Mutation (7 papers)European Journal of Human Genetics (5 papers)Human Molecular Genetics (5 papers)Journal of Biological Chemistry (5 papers)PLoS ONE (4 papers)
Partner nations: United Kingdom United States Belgium

In The Last Decade

Michael D. Briggs

74 papers receiving 3.3k citations

Peers

Countries citing papers authored by Michael D. Briggs

Since Specialization

Citations

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

Fields of papers citing papers by Michael D. Briggs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael D. Briggs. 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 Michael D. Briggs. The network helps show where Michael D. Briggs may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Michael D. Briggs, 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 Michael D. Briggs Line = papers co-authored together Michael D. Briggs links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Multiple epiphyseal dysplasia and related disorders: Molecular genetics, disease mechanisms, and therapeutic avenues Developmental Dynamics ·Kulbir Singh Redhu, Anuraj Karakkath, Michael D. Briggs	2020	20
2	XBP1 signalling is essential for alleviating mutant protein aggregation in ER-stress related skeletal disease PLoS Genetics ·Katarzyna A. Piróg, Kulbir Singh Redhu, Claire Hartley, Robert M. Jackson, Jamie Soul, Jean‐Marc Schwartz, John F. Bateman, Ray Boot-Handford, Michael D. Briggs	2019	16
3	Genomic profiling of a Hepatocyte growth factor-dependent signature for MET-targeted therapy in glioblastoma Journal of Translational Medicine ·Jennifer Johnson, Maria Libera Ascierto, Sandeep Mittal, David Newsome, Liang Kang, Michael D. Briggs, Kirk Tanner, Francesco M. Marincola, Michael E. Berens, George F. Vande Woude, Qian Xie	2015	18
4	Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation Arthritis & Rheumatism ·Peter A. Bell, Katarzyna A. Piróg, Maryline Fresquet, David J. Thornton, Ray Boot-Handford, Michael D. Briggs	2011	8
5	Collagen XXVII Organises the Pericellular Matrix in the Growth Plate PLoS ONE ·Darren A. Plumb, 信夫松下, BC Choudhary, Lee Mina-A, Mironov Aa, Karl E. Kadler, Michael D. Briggs, Ray Boot-Handford	2011	34
6	Type IX collagen gene mutations can result in multiple epiphyseal dysplasia that is associated with osteochondritis dissecans and a mild myopathy American Journal of Medical Genetics Part A ·Gail C. Jackson, 寺島薫, Irene Stolte‐Dijkstra, Aad Verrips, Jacqueline Taylor, Michael D. Briggs	2010	38
7	Structural and Functional Investigations of Matrilin-1 A-domains Reveal Insights into Their Role in Cartilage ECM Assembly* Journal of Biological Chemistry ·Maryline Fresquet, Thomas A. Jowitt, Louise A. Stephen, Joni Ylöstalo, Michael D. Briggs	2010	17
8	The unfolded protein response and its relevance to connective tissue diseases Cell and Tissue Research ·Ray Boot-Handford, Michael D. Briggs	2009	107
9	A Recessive Skeletal Dysplasia, SEMD Aggrecan Type, Results from a Missense Mutation Affecting the C-Type Lectin Domain of Aggrecan The American Journal of Human Genetics ·Stuart W. Tompson, Barry Merriman, Vincent Funari, Maryline Fresquet, Ralph S. Lachman, David L. Rimoin, Stanley F. Nelson, Michael D. Briggs, Daniel H. Cohn, Deborah Krakow	2008	101
10	Structural and Functional Characterization of Recombinant Matrilin-3 A-domain and Implications for Human Genetic Bone Diseases Journal of Biological Chemistry ·Maryline Fresquet, Thomas A. Jowitt, Joni Ylöstalo, Paul Coffey, Roger S. Meadows, Leena Ala‐Kokko, David J. Thornton, Michael D. Briggs	2007	37
11	Mutations in the known genes are not the major cause of MED; distinctive phenotypic entities among patients with no identified mutations European Journal of Human Genetics ·Eveliina Jakkula, Outi Mäkitie, Malwina Czarny‐Ratajczak, Gail C. Jackson, 隅蔵康一, Miki Susic, Michael D. Briggs, William G. Cole, Leena Ala‐Kokko	2004	25
12	A disorder resembling pseudoachondroplasia but without COMP mutation American Journal of Medical Genetics Part A ·J Spranger, Bernhard Zabel, Jason Kennedy, Gail C. Jackson, Michael D. Briggs	2004	3
13	Screening for Mutations in Cartilage ECM Genes Humana Press eBooks ·Michael D. Briggs	2003	1
14	Multiple epiphyseal dysplasia: radiographic abnormalities correlated with genotype Pediatric Radiology ·Sheila Unger, Michael D. Briggs, Paul Holden, Bernhard Zabel, Leena Ala‐Kokko, Petteri Paassilta, Jaana Lohiniva, David L. Rimoin, Ralph S. Lachman, Daniel H. Cohn	2001	41
15	Cartilage Oligomeric Matrix Protein Interacts with Type IX Collagen, and Disruptions to These Interactions Identify a Pathogenetic Mechanism in a Bone Dysplasia Family Journal of Biological Chemistry ·Paul Holden, Roger S. Meadows, Kathryn Chapman, Michael E. Grant, Karl E. Kadler, Michael D. Briggs	2001	186
16	Identification of five novel mutations in cartilage oligomeric matrix protein gene in pseudoachondroplasia and multiple epiphyseal dysplasia Human Mutation ·John Loughlin, Catherine Irven, Zehra Mustafa, Michael D. Briggs, Andrew Carr, Sally Ann Lynch, Robert G. Knowlton, Georges Mongredien, Bryan Sykes	1998	35
17	High-Resolution Genetic and Physical Mapping of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Mutations at Chromosome 19p13.1-p12 Genomics ·Robert G. Knowlton, Jiaming Cao, Daniel H. Cohn, Michael D. Briggs, Susan M.G. Hoffman, Brigitte Brandriff, Anne S. Olsen	1995	11
18	Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene Nature Genetics ·Michael D. Briggs, Susan M.G. Hoffman, Lily King, A. Olsen, H.W. Mohrenweiser, J. G. Leroy, Geert Mortier, David L. Rimoin, Ralph S. Lachman, Jeong-Su Kang, Jiaming Cao, Robert G. Knowlton, D.H. Cohn	1995	395
19	A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrix Human Genetics ·David L. Rimoin, 植物品種保護戦略フォーラム事務局, Michael D. Briggs, Peter J. Roughley, Helen E. Gruber, 泰士北川, Aurele A. Joseph, Y. Edward Hsia, Juliet Yuen, Kent A. Reinker, Ann Garber, Judy Grover, Shiding Ying, Georges Mongredien	1994	33
20	Linkage of typical pseudoachondroplasia to chromosome 19 Genomics ·Jacqueline T. Hecht, Clair A. Francomano, Michael D. Briggs, Michelle Deere, Valentin Belissen, William A. Horton, Matthew L. Warman, Daniel H. Cohn, Susan H. Blanton	1993	43

About Michael D. Briggs

Michael D. Briggs is a scholar working on Immunology and Allergy, Rheumatology, Genetics, Cell Biology and Molecular Biology, having authored 75 papers that have together received 3.4k indexed citations. Recurring topics across this work include Connective tissue disorders research (38 papers), Osteoarthritis Treatment and Mechanisms (26 papers), Cell Adhesion Molecules Research (24 papers), Ubiquitin and proteasome pathways (17 papers), Endoplasmic Reticulum Stress and Disease (11 papers), Bone health and treatments (9 papers), interferon and immune responses (6 papers) and Proteoglycans and glycosaminoglycans research (6 papers). The work is most often cited by research in Immunology and Allergy (848 citations), Rheumatology (1.3k citations), Genetics (1.3k citations), Cell Biology (752 citations) and Equine (44 citations). Michael D. Briggs has collaborated with scholars based in United Kingdom, United States and Belgium. Frequent co-authors include Kathryn Chapman, Ray Boot-Handford, Geert Mortier, Karl E. Kadler, David L. Rimoin, Michael E. Grant, Ralph S. Lachman, Roger S. Meadows, Robert G. Knowlton and Daniel H. Cohn. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, Human Molecular Genetics, Journal of Biological Chemistry and PLoS ONE.

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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