Michael D. Briggs

5.0k citations

75 papers · 3.5k · 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

Genetics 39
- Connective tissue disorders research 37
Molecular Biology 36
- Ubiquitin and proteasome pathways 16
- RNA Research and Splicing 6

Co-authors: Kathryn Chapman (6 shared papers)Ray Boot-Handford (22 shared papers)Geert Mortier (12 shared papers)Karl E. Kadler (7 shared papers)David L. Rimoin (8 shared papers)Michael E. Grant (3 shared papers)Ralph S. Lachman (5 shared papers)Robert G. Knowlton (7 shared papers)
Journals: Human Mutation (7 papers)Human Molecular Genetics (5 papers)European Journal of Human 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

73 papers receiving 3.4k 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-authors

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

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#	Work
1	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, E. Gaines, J.A. Cekleniak, Robert G. Knowlton, D.H. Cohn	1995	398
2	Pseudoachondroplasia and multiple epiphyseal dysplasia: Mutation review, molecular interactions, and genotype to phenotype correlations Human Mutation ·Michael D. Briggs, Kathryn Chapman	2002	218
3	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	188
4	Mutations in the region encoding the von Willebrand factor A domain of matrilin-3 are associated with multiple epiphyseal dysplasia Nature Genetics ·Kathryn Chapman, Geert Mortier, Kay Chapman, John Loughlin, Michael E. Grant, Michael D. Briggs	2001	158
5	Diverse Mutations in the Gene for Cartilage Oligomeric Matrix Protein in the Pseudoachondroplasia–Multiple Epiphyseal Dysplasia Disease Spectrum The American Journal of Human Genetics ·Michael D. Briggs, Geert Mortier, William G. Cole, Lily King, Steven S. Golik, Jacky Bonaventure, Lieve Nuytinck, Anne De Paepe, Jules G. Leroy, Leslie G. Biesecker, Mark Lipson, William R. Wilcox, Ralph S. Lachman, David L. Rimoin, Robert G. Knowlton, Daniel H. Cohn	1998	136
6	Differential regulation of peroxisome proliferator activated receptor gamma1 (PPARgamma1) and PPARgamma2 messenger RNA expression in the early stages of adipogenesis. PubMed ·Régis Saladin, Lluís Fajas, Sharon Dana, Y D Halvorsen, Johan Auwerx, Michael D. Briggs	1999	119
7	The unfolded protein response and its relevance to connective tissue diseases Cell and Tissue Research ·Ray Boot-Handford, Michael D. Briggs	2009	110
8	Targeted Induction of Endoplasmic Reticulum Stress Induces Cartilage Pathology PLoS Genetics ·M. Helen Rajpar, Ben McDermott, Louise H. W. Kung, Rachel Eardley, Lynette Knowles, Mel C. Heeran, David J. Thornton, Richard Wilson, John F. Bateman, Richard Poulsom, Peter Arvan, Karl E. Kadler, Michael D. Briggs, Ray Boot-Handford	2009	108
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	104
10	Reduced cell proliferation and increased apoptosis are significant pathological mechanisms in a murine model of mild pseudoachondroplasia resulting from a mutation in the C-terminal domain of COMP Human Molecular Genetics ·Katarzyna A. Piróg, Roger S. Meadows, Lynette Knowles, Dick Heinegård, David J. Thornton, Karl E. Kadler, Ray Boot-Handford, Michael D. Briggs	2007	86
11	Pseudoachondroplasia and multiple epiphyseal dysplasia: A 7‐year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution Human Mutation ·Gail C. Jackson, Lauréane Mittaz‐Crettol, Jacqueline Taylor, Geert Mortier, J Spranger, Bernhard Zabel, Martine Le Merrer, Valérie Cormier‐Daire, Christine M Hall, Amaka C Offiah, Michael Wright, Ravi Savarirayan, Gen Nishimura, Simon Ramsden, Rob Elles, Luisa Bonafé, Andrea Superti‐Furga, Sheila Unger, Andreas Zankl, Michael D. Briggs	2011	81
12	Identification in Vitreous and Molecular Cloning of Opticin, a Novel Member of the Family of Leucine-rich Repeat Proteins of the Extracellular Matrix Journal of Biological Chemistry ·Anthony Reardon, Magali Le Goff, Michael D. Briggs, David McLeod, John K. Sheehan, David J. Thornton, (unknown)	2000	72
13	Armet/Manf and Creld2 are components of a specialized ER stress response provoked by inappropriate formation of disulphide bonds: implications for genetic skeletal diseases Human Molecular Genetics ·Claire Hartley, Sarah Edwards, Lorna Mullan, Peter A. Bell, Maryline Fresquet, Ray Boot-Handford, Michael D. Briggs	2013	67
14	Decreased chondrocyte proliferation and dysregulated apoptosis in the cartilage growth plate are key features of a murine model of epiphyseal dysplasia caused by a matn3 mutation Human Molecular Genetics ·Matthew Leighton, Seema Nundlall, Tobias Starborg, Roger S. Meadows, Farhana E. Suleman, Lynette Knowles, Raimund Wagener, David J. Thornton, Karl E. Kadler, Ray Boot-Handford, Michael D. Briggs	2007	66
15	Multiple epiphyseal dysplasia mutations inMATN3 cause misfolding of the A-domain and prevent secretion of mutant matrilin-3 Human Mutation ·Sally L. Cotterill, Gail C. Jackson, Matthew Leighton, Raimund Wagener, Outi Mäkitie, William G. Cole, Michael D. Briggs	2005	60
16	An unfolded protein response is the initial cellular response to the expression of mutant matrilin-3 in a mouse model of multiple epiphyseal dysplasia Cell Stress and Chaperones ·Seema Nundlall, M. Helen Rajpar, Peter A. Bell, Christopher Clowes, Leo A.H. Zeeff, Benjamin Gardner, David J. Thornton, Ray Boot-Handford, Michael D. Briggs	2010	56
17	The aggrecanopathies; an evolving phenotypic spectrum of human genetic skeletal diseases Orphanet Journal of Rare Diseases ·Beth Gibson, Michael D. Briggs	2016	56
18	Identification of Novel pro-α2(IX) Collagen Gene Mutations in Two Families with Distinctive Oligo-Epiphyseal Forms of Multiple Epiphyseal Dysplasia The American Journal of Human Genetics ·Paul Holden, Elizabeth G. Canty, Geert Mortier, Bernhard Zabel, Jürgen W. Spranger, Andrew Carr, Michael E. Grant, John Loughlin, Michael D. Briggs	1999	53
19	Increased intracellular proteolysis reduces disease severity in an ER stress–associated dwarfism Journal of Clinical Investigation ·Lorna Mullan, Ewa Mularczyk, Louise H. W. Kung, Mitra Forouhan, Jordan Ma Wragg, Royston Goodacre, John F. Bateman, Eileithyia Swanton, Michael D. Briggs, Ray Boot-Handford	2017	50
20	Collagen XXVII Is Developmentally Regulated and Forms Thin Fibrillar Structures Distinct from Those of Classical Vertebrate Fibrillar Collagens Journal of Biological Chemistry ·Darren A. Plumb, Vivek Dhir, Mironov Aa, Laila Ferrara, Richard Poulsom, Karl E. Kadler, David J. Thornton, Michael D. Briggs, Ray Boot-Handford	2007	49

About Michael D. Briggs

Michael D. Briggs is a scholar working on Genetics, Molecular Biology, Rheumatology, Immunology and Allergy and Cell Biology, having authored 75 papers that have together received 3.5k indexed citations. Recurring topics across this work include Connective tissue disorders research (37 papers), Osteoarthritis Treatment and Mechanisms (26 papers), Cell Adhesion Molecules Research (24 papers), Ubiquitin and proteasome pathways (16 papers), Bone health and treatments (9 papers), Endoplasmic Reticulum Stress and Disease (9 papers), RNA Research and Splicing (6 papers) and Proteoglycans and glycosaminoglycans research (6 papers). The work is most often cited by research in Immunology and Allergy (740 citations), Rheumatology (1.3k citations), Cell Biology (722 citations), Genetics (1.2k citations) and Cancer Research (349 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, Robert G. Knowlton, Roger S. Meadows and Daniel H. Cohn. Their work appears in journals such as Human Mutation, Human Molecular Genetics, European Journal of Human 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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