The human gene connectome as a map of short cuts for morbid allele discovery.
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Inherited BCL10 deficiency impairs hematopoietic and nonhematopoietic immunityHuman Knockout Carriers: Dead, Diseased, Healthy, or Improved?Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndromeHGCS: an online tool for prioritizing disease-causing gene variants by biological distanceEngineering crassulacean acid metabolism to improve water-use efficiencyMiningABs: mining associated biomarkers across multi-connected gene expression datasetsProteomics in immunity and herpes simplex encephalitis.Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies.Mycobacterium simiae infection in two unrelated patients with different forms of inherited IFN-γR2 deficiency.Novel primary immunodeficiency candidate genes predicted by the human gene connectomeNetwork propagation with dual flow for gene prioritization.Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.Inherited IL-17RC deficiency in patients with chronic mucocutaneous candidiasisNovel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome.Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia.Can the impact of human genetic variations be predicted?The human gene damage index as a gene-level approach to prioritizing exome variants.TLR3 immunity to infection in mice and humansWhole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.Application of high-throughput sequencing for studying genomic variations in congenital heart disease.Exome and genome sequencing for inborn errors of immunity.Evolutionary Genomics.Whole-exome sequencing for detecting inborn errors of immunity: overview and perspectives.Properties of human genes guided by their enrichment in rare and common variants.Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.CDG: An Online Server for Detecting Biologically Closest Disease-Causing Genes and its Application to Primary Immunodeficiency.Simulation of the Dynamics of Primary Immunodeficiencies in B Cells
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P2860
The human gene connectome as a map of short cuts for morbid allele discovery.
description
2013 nî lūn-bûn
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2013年の論文
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2013年論文
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2013年論文
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2013年論文
@zh-hk
2013年論文
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2013年論文
@zh-tw
2013年论文
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2013年论文
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2013年论文
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name
The human gene connectome as a map of short cuts for morbid allele discovery.
@en
type
label
The human gene connectome as a map of short cuts for morbid allele discovery.
@en
prefLabel
The human gene connectome as a map of short cuts for morbid allele discovery.
@en
P2093
P2860
P50
P356
P1476
The human gene connectome as a map of short cuts for morbid allele discovery.
@en
P2093
Avinash Abhyankar
Dror Fried
Patrick Nitschke
Yuval Itan
P2860
P304
P356
10.1073/PNAS.1218167110
P407
P50
P577
2013-03-18T00:00:00Z