June 23-30, 2016
Last Updated: Jun 23, 2016
- Comparison of genome sequencing and clinical genotyping for pharmacogenes.
Yang Wenjian et al. Clinical pharmacology and therapeutics 2016 Jun - Use of Whole Genome Sequencing and Patient Interviews To Link a Case of Sporadic Listeriosis to Consumption of Prepackaged Lettuce.
Jackson K A et al. Journal of food protection 2016 May 79(5) 806-9 - Genes and Athletic Performance: An Update.
Ahmetov Ildus I et al. Medicine and sport science 2016 6141-54 - Whole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back Again.
Szego Michael J et al. Journal of the Canadian Academy of Child and Adolescent Psychiatry = Journal de l'Acade´mie canadienne de psychiatrie de l'enfant et de l'adolescent 2016 25(2) 116-21 - The genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discovery.
Hahn M M, et al. Cellular oncology (Dordrecht) 2016 6 - Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants.
Xi Ruibin, et al. Nucleic acids research 2016 6 - Genomic Test Results and the Courtroom: The Roles of Experts and Expert Testimony.
Ramos Edward et al. The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics 2016 Mar 44(1) 205-15 - Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study.
Warren-Gash Charlotte et al. Hereditary cancer in clinical practice 2016 1412 - Identification of Rare Variants in Metabolites of the Carnitine Pathway by Whole Genome Sequencing Analysis.
Yazdani Akram, et al. Genetic epidemiology 2016 6 - Implementation of Whole Genome Sequencing (WGS) for Identification and Characterization of Shiga Toxin-Producing Escherichia coli (STEC) in the United States.
Lindsey Rebecca L et al. Frontiers in microbiology 2016 766 - Investigation of SLA4A3 as a candidate gene for human retinal disease.
Downs Louise M, et al. Journal of negative results in biomedicine 2016 0 (1) 11 - Patient-specific factors influence somatic variation patterns in von Hippel-Lindau disease renal tumours.
Fei Suzanne S, et al. Nature communications 2016 0 11588 - Very low depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation.
Gilly Arthur, et al. Human molecular genetics 2016 5 - Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patiets.
Yoo Eun-Hyung, et al. Journal of clinical laboratory analysis 2016 5 - HPV16 Sublineage Associations With Histology-Specific Cancer Risk Using HPV Whole-Genome Sequences in 3200 Women.
Mirabello Lisa, et al. Journal of the National Cancer Institute 2016 9 (9) - CFTR and/or pancreatitis susceptibility genes mutations as risk factors of pancreatitis in cystic fibrosis patients?
Gaitch Natacha, et al. Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] 2016 4 - AMD Projects: Analyzing Emerging Epidemics
Whole genome sequencing to assess epidemic potential of emerging meningococcal strains and monitor changes in vaccine immunogen and virulence-related genes - Whole-Genome Sequencing of a Healthy Aging Cohort: Cell
GA Erikson et al, Cell, April 2016 - Implementation of Nationwide Real-Time Whole-Genome Sequencing to Enhance Listeriosis Outbreak Detection and Investigation.
Jackson Brendan R et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2016 Apr - The implications of whole-genome sequencing in the control of tuberculosis
RS Lee, Ther Adv Infect Dis. 2016 Apr; 3(2): 47?62. - Whole-genome re-sequencing for the identification of high contribution susceptibility gene variants in patients with type 2 diabetes.
Sun Xiaojuan, et al. Molecular medicine reports 2016 3 - Whole genome and exome sequencing realignment supports the assignment of KCNJ12, KCNJ17, and KCNJ18 paralogous genes in thyrotoxic periodic paralysis locus: functional characterization of two polymorphic Kir2.6 isoforms.
Paninka Rolf M, et al. Molecular genetics and genomics : MGG 2016 3 - Rare EN1 Variants and Pediatric Bone Mass.
Mitchell Jonathan A, et al. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2016 3 - Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis.
Boppudi Sangamitra, et al. Clinical genetics 2016 3 - Whole-Genome Sequencing to Determine Origin of Multinational Outbreak of Sarocladium kiliense Bloodstream Infections.
Etienne Kizee A et al. Emerging infectious diseases 2016 Mar 22(3) - [Genome-Wide Association Studies for life-style related diseases].
Maeda Shiro, et al. Clinical calcium 2016 0 (3) 419-25 - Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
Zhang Yong-Biao, et al. Nature communications 2016 0 10605 - Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.
Kristjansson Ragnar P, et al. Nature communications 2016 0 10572 - Using whole genome sequencing and metagenomics to identify and track tickborne pathogens
- HLA class II sequence variants influence tuberculosis risk in populations of European ancestry.
Sveinbjornsson Gardar, et al. Nature genetics 2016 2
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