Matthew P. Schultz
Allegheny General Hospital
20 Papers
17 Citations
Matthew P. Schultz is an academic researcher from Allegheny General Hospital. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 2, co-authored 2 publications.
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Papers
Comparative Genomic Analyses of the Moraxella catarrhalis Serosensitive and Seroresistant Lineages Demonstrate Their Independent Evolution
Joshua P. Earl,Stefan P. W. de Vries,Azad Ahmed,Evan Powell,Matthew P. Schultz,Peter W. M. Hermans,Darryl J. Hill,Zhemin Zhou,Crystala I. Constantinidou,Fen Z. Hu,Hester J. Bootsma,Garth D. Ehrlich +11 more
TL;DR: The bacterial species Moraxella catarrhalis has been hypothesized as being composed of two distinct lineages with separate evolutionary histories based on several molecular typing methods, but it is shown that there are three lineages—the SR, SS, and the divergent.
Design and validation of a supragenome array for determination of the genomic content of Haemophilus influenzae isolates
Rory A. Eutsey,N. Luisa Hiller,N. Luisa Hiller,Joshua P. Earl,Benjamin Janto,Benjamin Janto,Margaret E. Dahlgren,Azad Ahmed,Evan Powell,Matthew P. Schultz,Janet R. Gilsdorf,Lixin Zhang,Arnold L. Smith,Timothy F. Murphy,Sanjay Sethi,Kai Shen,Kai Shen,J. Christopher Post,J. Christopher Post,Fen Z. Hu,Fen Z. Hu,Garth D. Ehrlich,Garth D. Ehrlich +22 more
TL;DR: These analyses provided the most comprehensive and detailed genomic/phylogenetic look at this species to date, and identified a subset of highly divergent strains that form a separate lineage within the species.
A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties.
Mariam Thomas Mathew,Austin A. Antoniou,Naveen Ramesh,Min Hu,Jeffrey B Gaither,Danielle Mouhlas,Sayaka Hashimoto,M. Humphrey,Theodora Matthews,Jesse M. Hunter,Shalini C. Reshmi,Matthew P. Schultz,Kristy Lee,Ruthann B. Pfau,Catherine E. Cottrell,Kim L. McBride,Nicholas Navin,Bimal P. Chaudhari,Marco L. Leung +18 more
TL;DR: In this article , the authors performed a database search for all CMA testing performed from 2010 to 2020, and delineated the diagnostic yield based on patient characteristics, including sex, age, clinical specialty of providers, indication of testing, and pathogenic finding.
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P004: Urine polyols for diagnosis of sorbitol dehydrogenase (SORD) deficiency-related peripheral neuropathy*
Amy L. White,Jordan Bontrager,William Laxen,Perry R. Loken,Tiffany Grider,Josef Alawneh,Vincent Carson,Emily Lauer,Angela Pickart,Zhiyv Niu,Devin Oglesbee,Dimitar Gavrilov,Silvia Torelli,Patricia Hall,Dietrich Matern,Michael Shy,David Herrmann,Matthew P. Schultz +17 more
TL;DR: Sorbitol dehydrogenase (SORD) deficiency, a genetic cause of progressive peripheral neuropathy, is diagnosed through plasma sorbitol testing, but a clinical biochemical assay is lacking; urine polyols may provide a novel diagnostic tool for this autosomal recessive neurometabolic disorder.
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