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Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations.
Johnston, Jennifer J; Lewis, Katie L; Ng, David; Singh, Larry N; Wynter, Jamila; Brewer, Carmen; Brooks, Brian P; Brownell, Isaac; Candotti, Fabio; Gonsalves, Steven G; Hart, Suzanne P; Kong, Heidi H; Rother, Kristina I; Sokolic, Robert; Solomon, Benjamin D; Zein, Wadih M; Cooper, David N; Stenson, Peter D; Mullikin, James C; Biesecker, Leslie G.
Affiliation
  • Johnston JJ; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Lewis KL; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Ng D; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Singh LN; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Wynter J; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Brewer C; National Institute for Deafness and Other Communication Disorders, NIH, Bethesda, MD 20892, USA.
  • Brooks BP; National Eye Institute, NIH, Bethesda, MD 20892, USA.
  • Brownell I; National Cancer Institute, NIH, Bethesda, MD 20892, USA.
  • Candotti F; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Gonsalves SG; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Hart SP; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Kong HH; National Cancer Institute, NIH, Bethesda, MD 20892, USA.
  • Rother KI; National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892, USA.
  • Sokolic R; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Solomon BD; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA.
  • Zein WM; National Eye Institute, NIH, Bethesda, MD 20892, USA.
  • Cooper DN; Institute of Medical Genetics, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.
  • Stenson PD; Institute of Medical Genetics, School of Medicine, Cardiff University, Heath Park, Cardiff CF14 4XN, UK.
  • Mullikin JC; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA; NIH Intramural Sequencing Center, NIH, Bethesda, MD 20892, USA.
  • Biesecker LG; National Human Genome Research Institute, NIH, Bethesda, MD 20892, USA; NIH Intramural Sequencing Center, NIH, Bethesda, MD 20892, USA. Electronic address: lesb@mail.nih.gov.
Am J Hum Genet ; 96(6): 913-25, 2015 Jun 04.
Article in En | MEDLINE | ID: mdl-26046366
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Atherosclerosis / Genome-Wide Association Study / Precision Medicine / High-Throughput Nucleotide Sequencing / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Am J Hum Genet Year: 2015 Type: Article Affiliation country: United States
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Atherosclerosis / Genome-Wide Association Study / Precision Medicine / High-Throughput Nucleotide Sequencing / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Male / Middle aged Language: En Journal: Am J Hum Genet Year: 2015 Type: Article Affiliation country: United States