Search Results - Joshua D. Smith
- Showing 1 - 20 results of 74
- Go to Next Page
-
1
-
2
-
3
-
4
High Rates of<i>Rickettsia parkeri</i>Infection in Gulf Coast Ticks (<i>Amblyomma maculatum</i>) and Identification of “<i>Candidatus</i>Rickettsia Andeanae” from Fairfax County, V... by Christen Fornadel, Xing Zhang, Joshua D. Smith, Christopher D. Paddock, Jorge R. Arias, Douglas E. Norris
Published 2011Artigo -
5
-
6
Soluble Transforming Growth Factor-β Type II Receptor Inhibits Negative Remodeling, Fibroblast Transdifferentiation, and Intimal Lesion Formation But Not Endothelial Growth by Joshua D. Smith, Shane R. Bryant, Leslie L. Couper, Calvin Vary, Philip J. Gotwals, Victor Koteliansky, Volkhard Lindner
Published 1999Artigo -
7
-
8
A Multivariate Genome-Wide Association Analysis of 10 LDL Subfractions, and Their Response to Statin Treatment, in 1868 Caucasians by Heejung Shim, Daniel I. Chasman, Joshua D. Smith, Samia Mora, Paul M. Ridker, Deborah A. Nickerson, Ronald M. Krauss, Matthew Stephens
Published 2015Artigo -
9
Genetic Variation Is Associated With C-Reactive Protein Levels in the Third National Health and Nutrition Examination Survey by Dana C. Crawford, Christopher Sanders, Xiaoting Qin, Joshua D. Smith, Cynthia Shephard, Michelle Wong, Laura Witrak, Mark J. Rieder, Deborah A. Nickerson
Published 2006Artigo -
10
-
11
-
12
-
13
Haplotype Diversity across 100 Candidate Genes for Inflammation, Lipid Metabolism, and Blood Pressure Regulation in Two Populations by Dana C. Crawford, Christopher S. Carlson, Mark J. Rieder, Dana P. Carrington, Yi Qian, Joshua D. Smith, Michael A. Eberle, Leonid Kruglyak, Deborah A. Nickerson
Published 2004Artigo -
14
Tracing Sub-Structure in the European American Population with PCA-Informative Markers by Peristera Paschou, Petros Drineas, Jamey Lewis, Caroline M. Nievergelt, Deborah A. Nickerson, Joshua D. Smith, Paul M. Ridker, Daniel I. Chasman, Ronald M. Krauss, Elad Ziv
Published 2008Artigo -
15
Combined Influence of <i>LDLR</i> and <i>HMGCR</i> Sequence Variation on Lipid-Lowering Response to Simvastatin by Lara M. Mangravite, Marisa W. Medina, Jinrui Cui, Sheila Pressman, Joshua D. Smith, Mark J. Rieder, Xiuqing Guo, Deborah A. Nickerson, Jerome I. Rotter, Ronald M. Krauss
Published 2010Artigo -
16
Mutations in DCDC2 (doublecortin domain containing protein 2) in neonatal sclerosing cholangitis by Tassos Grammatikopoulos, Melissa Sambrotta, Sandra Strautnieks, Pierre Foskett, A. S. Knisely, Bart Wagner, Maesha Deheragoda, Chris Starling, Giorgina Mieli‐Vergani, Joshua D. Smith, Laura N. Bull, Richard J. Thompson
Published 2016Artigo -
17
Exome Sequencing Identifies a Recurrent De Novo ZSWIM6 Mutation Associated with Acromelic Frontonasal Dysostosis by Joshua D. Smith, Anne Hing, Christine M. Clarke, Nathan M. Johnson, Francisco A. Perez, Sarah S. Park, Jeremy A. Horst, Brig Mecham, Lisa Maves, Deborah A. Nickerson, Michael L. Cunningham
Published 2014Artigo -
18
A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease by Heather C Mefford, Gregory M. Cooper, Troy Zerr, Joshua D. Smith, Carl Baker, Neil Shafer, Erik C. Thorland, Cindy Skinner, Charles E. Schwartz, Deborah A. Nickerson, Evan E. Eichler
Published 2009Artigo -
19
A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex by Marie‐Estelle Losfeld, Bobby G. Ng, Martin Kircher, Kati J. Buckingham, Emily H. Turner, Alexey M. Eroshkin, Joshua D. Smith, Jay Shendure, D. A. Nickerson, Michael J. Bamshad, Hudson H. Freeze
Published 2013Artigo -
20
De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism by Ash Zawerton, Baojin Yao, J. Paige Yeager, Tommaso Pippucci, Abdul Haseeb, Joshua D. Smith, Lisa Wischmann, Susanne J. Kühl, John Dean, Daniela T. Pilz, Susan Holder, Alisdair McNeill, Claudio Graziano, Véronique Lefebvre
Published 2019Artigo
Search Tools:
Related Subjects
Biology
Genetics
Gene
Medicine
Mutation
Genotype
Internal medicine
Single-nucleotide polymorphism
Exome sequencing
Computational biology
Endocrinology
Exome
Phenotype
Population
Bioinformatics
Genetic association
Genome-wide association study
Missense mutation
Biochemistry
Genome
Allele
Environmental health
Pathology
Autism
Cholesterol
Computer science
Demography
Evolutionary biology
Haplotype
Psychiatry