M
Matthew S. Edwards
Researcher at San Diego State University
Publications - 274
Citations - 9299
Matthew S. Edwards is an academic researcher from San Diego State University. The author has contributed to research in topics: Kelp forest & Kelp. The author has an hindex of 48, co-authored 254 publications receiving 7772 citations. Previous affiliations of Matthew S. Edwards include Moss Landing Marine Laboratories & John Hunter Hospital.
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Journal ArticleDOI
Global patterns of kelp forest change over the past half-century
Kira A. Krumhansl,Daniel K. Okamoto,Andrew Rassweiler,Mark Novak,John J. Bolton,Kyle C. Cavanaugh,Sean D. Connell,Craig R. Johnson,Brenda Konar,Scott D. Ling,Fiorenza Micheli,Kjell Magnus Norderhaug,Alejandro Pérez-Matus,Isabel Sousa-Pinto,Daniel C. Reed,Anne K. Salomon,Nick T. Shears,Thomas Wernberg,Robert J. Anderson,Nevell S. Barrett,Alejandro H. Buschmann,Mark H. Carr,Jennifer E. Caselle,Sandrine Derrien-Courtel,Graham J. Edgar,Matthew S. Edwards,James A. Estes,Claire Goodwin,Michael C. Kenner,David J. Kushner,Frithjof E. Moy,Julia Nunn,Robert S. Steneck,Julio A. Vásquez,Jane C. Watson,Jon D. Witman,Jarrett E. K. Byrnes +36 more
TL;DR: Although global drivers could be affecting kelp forests at multiple scales, local stressors and regional variation in the effects of these drivers dominate kelp dynamics, in contrast to many other marine and terrestrial foundation species.
Journal ArticleDOI
Prevalence of renovascular disease in the elderly: a population-based study
Kimberley J. Hansen,Matthew S. Edwards,Timothy E. Craven,Gregory S. Cherr,Sharon A. Jackson,Richard G. Appel,Gregory L. Burke,Richard H. Dean +7 more
TL;DR: This investigation provides the first population-based estimate of the prevalence of RVD among free-living, elderly black and white Americans, and its presence was significantly and independently associated with increasing age, low high-density lipoprotein cholesterol levels, and increasing systolic blood pressure.
Journal Article
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the patched protein, and no genotype-phenotype correlations are evident
Carol Wicking,Susan Shanley,Ian M. Smyth,Susan Gillies,Kylie Negus,Scott Graham,Graeme Suthers,Neva Haites,Matthew S. Edwards,Brandon J. Wainwright,Georgia Chenevix-Trench +10 more
TL;DR: The preponderance of truncation mutants in the germ line of NBCCS patients suggests that the developmental defects associated with the disorder are most likely due to haploinsufficiency, and the notion that PTCH may have a transport function is supported.
Journal ArticleDOI
The genetics of keratoconus.
TL;DR: The evidence that suggests keratoconus is primarily an inherited condition is considered, and research strategies aimed at unveiling the genetic predisposition, and the enigma of environmental influences on its phenotypic expression are examined.
Journal ArticleDOI
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
Mary L. Marazita,Jeffrey C. Murray,Andrew C. Lidral,Mauricio Arcos-Burgos,Margaret E. Cooper,Toby H Goldstein,Brion S. Maher,Sandra Daack-Hirsch,R. E. Schultz,M. Adela Mansilla,L. Leigh Field,You E. Liu,Natalie J. Prescott,Sue Malcolm,Robin M. Winter,Ajit Kisor Ray,Lina M. Moreno,Consuelo Valencia,Katherine Neiswanger,Diego F. Wyszynski,Joan E. Bailey-Wilson,Hasan Albacha-Hejazi,Terri H. Beaty,Iain McIntosh,Jacqueline B. Hetmanski,Gökhan Tunçbilek,Matthew S. Edwards,Louise A. Harkin,Rodney J. Scott,Laurence Roddick +29 more
TL;DR: These are the first genomewide significant linkage results ever reported for CL/P, and they represent an unprecedented demonstration of the power of linkage analysis to detect multiple genes simultaneously for a complex disorder.