Author details

Full Name

Mark J Rieder

Affiliation

ORCID

Career Start Year

1995

Papers

131

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
35169816	Interactions among 17 respiratory pathogens: a cross-sectional study using clinical and community surveillance data.	medRxiv	2022
32511368	SwabExpress: An end-to-end protocol for extraction-free COVID-19 testing.	bioRxiv	2021
34286830	SwabExpress: An End-to-End Protocol for Extraction-Free COVID-19 Testing.	Clin Chem	2021
34115094	Comparison of Symptoms and RNA Levels in Children and Adults With SARS-CoV-2 Infection in the Community Setting.	JAMA Pediatr	2021
33941621	Viral genomes reveal patterns of the SARS-CoV-2 outbreak in Washington State.	Sci Transl Med	2021
33563599	Evaluating Specimen Quality and Results from a Community-Wide, Home-Based Respiratory Surveillance Study.	J Clin Microbiol	2021
33597259	Comparable Specimen Collection from Both Ends of At-Home Midturbinate Swabs.	J Clin Microbiol	2021
33330895	Comparable specimen collection from both ends of at-home mid-turbinate swabs.	medRxiv	2020
32356944	Early Detection of Covid-19 through a Citywide Pandemic Surveillance Platform.	N Engl J Med	2020
33444172	Diagnostic accuracy of an app-guided, self-administered test for influenza among individuals presenting to general practice with influenza-like illness: study protocol.	BMJ Open	2020
33033018	The Seattle Flu Study: a multiarm community-based prospective study protocol for assessing influenza prevalence, transmission and genomic epidemiology.	BMJ Open	2020
33024981	Viral genomes reveal patterns of the SARS-CoV-2 outbreak in Washington State.	medRxiv	2020
28369038	Immunosequencing identifies signatures of cytomegalovirus exposure history and HLA-mediated effects on the T cell repertoire.	Nat Genet	2017
26284524	Correction: Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis.	PLoS Genet	2015
25592578	Measures of exposure impact genetic association studies: an example in vitamin K levels and VKORC1.	Pac Symp Biocomput	2015
25415970	Rare variation facilitates inferences of fine-scale population structure in humans.	Mol Biol Evol	2015
26047157	Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis.	PLoS Genet	2015
26596423	Annotation of pseudogenic gene segments by massively parallel sequencing of rearranged lymphocyte receptor loci.	Genome Med	2015
26290413	High-throughput pairing of T cell receptor Î± and Î² sequences.	Sci Transl Med	2015
24507775	Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.	Am J Hum Genet	2014
24282029	Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.	Hum Mol Genet	2014
24970842	Detection of minimal residual disease in B lymphoblastic leukemia by high-throughput sequencing of IGH.	Clin Cancer Res	2014
23201682	Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.	Nature	2013
22584458	Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes.	Pharmacogenomics J	2013
23778323	Pharmacogenetics in American Indian populations: analysis of CYP2D6, CYP3A4, CYP3A5, and CYP2C9 in the Confederated Salish and Kootenai Tribes.	Pharmacogenet Genomics	2013
23910461	Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.	Am J Hum Genet	2013
23995691	A statin-dependent QTL for GATM expression is associated with statin-induced myopathy.	Nature	2013
24157944	Using synthetic templates to design an unbiased multiplex PCR assay.	Nat Commun	2013
24027095	High-throughput sequencing of T-cell receptors reveals a homogeneous repertoire of tumour-infiltrating lymphocytes in ovarian cancer.	J Pathol	2013
23755828	Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.	Lancet	2013
24013571	Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families.	Anesthesiology	2013
23239648	"Mandibulofacial dysostosis with microcephaly" caused by EFTUD2 mutations: expanding the phenotype.	Am J Med Genet A	2013
22095694	Evidence for involvement of GNB1L in autism.	Am J Med Genet B Neuropsychiatr Genet	2012
22479202	Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.	PLoS Genet	2012
22495309	Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.	Nature	2012
22337857	Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.	Circ Cardiovasc Genet	2012
22782511	Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5.	Arch Neurol	2012
22772371	TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.	Nat Genet	2012
22772370	Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.	Nat Genet	2012
22863193	Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies.	Am J Hum Genet	2012
22560091	A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.	Am J Hum Genet	2012
22604720	Evolution and functional impact of rare coding variation from deep sequencing of human exomes.	Science	2012
23086943	Ligand directed signaling differences between rodent and human Îº-opioid receptors.	Journal of Biological Chemistry	2012
22179552	Detection of structural variants and indels within exome data.	Nat Methods	2011
21353195	Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.	Am J Hum Genet	2011
21305047	Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey.	PLoS One	2011
21204214	IGF1R variants associated with isolated single suture craniosynostosis.	Am J Med Genet A	2011
21572417	Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.	Nat Genet	2011
21757428	Linkage and association of phospholipid transfer protein activity to LASS4.	J Lipid Res	2011
21949389	Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers.	Proc Natl Acad Sci U S A	2011