Whole-exome sequencing of a pedigree segregating asthma

scientific article

Whole-exome sequencing of a pedigree segregating asthma is …
instance of (P31):
scholarly articleQ13442814

External links are
P6179Dimensions Publication ID1026438999
P356DOI10.1186/1471-2350-13-95
P932PMC publication ID3563469
P698PubMed publication ID23046476
P5875ResearchGate publication ID232224548

P50authorAndrew T DeWanQ56233414
P2093author name stringMichael B Bracken
Kyle M Walsh
Karen Hellenbrand
Kathryn Brigham Egan
Keli Sorrentino
Nicole Pizzoferrato
P2860cites workGenome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regionsQ33669033
Lack of MEF2A mutations in coronary artery diseaseQ33726939
Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism.Q34037256
Variants of DENND1B associated with asthma in childrenQ34089817
c-Cbl and Cbl-b regulate T cell responsiveness by promoting ligand-induced TCR down-modulationQ34157660
Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degenerationQ34561066
Transcription factor MEF2A mutations in patients with coronary artery diseaseQ35054057
PDE11A associations with asthma: results of a genome-wide association scanQ35096782
Is survival possible without arachidonate metabolites in the brain during systemic infection?Q35180269
Protein-protein interactions involving inducible nitric oxide synthaseQ35544106
Association of inducible nitric oxide synthase with asthma severity, total serum immunoglobulin E and blood eosinophil levelsQ36203321
The search for genetic variants and epigenetics related to asthmaQ37941708
dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictionsQ42059080
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 peopleQ43136367
Hereditary sensory autonomic neuropathy caused by a mutation in dystonin.Q44805368
On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association testQ45288594
Attempted replication of 50 reported asthma risk genes identifies a SNP in RAD50 as associated with childhood atopic asthmaQ45349008
An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.Q48940291
Glucocorticoid-related genetic susceptibility for Alzheimer's disease.Q53361460
Finding the missing heritability of complex diseasesQ22122198
Myomegalin is a novel protein of the golgi/centrosome that interacts with a cyclic nucleotide phosphodiesteraseQ24290674
Myomegalin is a novel A-kinase anchoring protein involved in the phosphorylation of cardiac myosin binding protein CQ24302222
A common variant of HMGA2 is associated with adult and childhood height in the general populationQ24603211
Mutation of MEF2A in an inherited disorder with features of coronary artery diseaseQ24669679
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing dataQ27860742
The Sequence Alignment/Map format and SAMtoolsQ27860966
Patterns and rates of exonic de novo mutations in autism spectrum disordersQ28264242
Genetic heterogeneity in human diseaseQ28280100
A large-scale, consortium-based genomewide association study of asthmaQ28293885
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarctionQ28308221
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility geneQ28943322
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing dataQ29547161
Fast and accurate long-read alignment with Burrows-Wheeler transformQ29547193
A framework for variation discovery and genotyping using next-generation DNA sequencing dataQ29547262
De novo mutations revealed by whole-exome sequencing are strongly associated with autismQ29547269
Personal genomes: The case of the missing heritabilityQ29614582
Missing heritability and strategies for finding the underlying causes of complex diseaseQ29614586
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthmaQ29614903
Evolution and functional impact of rare coding variation from deep sequencing of human exomesQ29617587
Common variants in the GDF5-UQCC region are associated with variation in human heightQ30435234
Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican childrenQ33497893
P921main subjectasthmaQ35869
P304page(s)95
P577publication date2012-10-09
P1433published inBMC Medical GeneticsQ15759918
P1476titleWhole-exome sequencing of a pedigree segregating asthma
P478volume13

Reverse relations

cites work (P2860)
Q47292997A Schizophrenia-Linked KALRN Coding Variant Alters Neuron Morphology, Protein Function, and Transcript Stability.
Q38806101Are genetic tests informative in predicting food allergy?
Q35735738Cbl-b: Roles in T Cell Tolerance, Proallergic T Cell Development, and Cancer Immunity
Q26864326Complex genetics of pulmonary diseases: lessons from genome-wide association studies and next-generation sequencing
Q38420848Contributing factors to the development of childhood asthma: working toward risk minimization.
Q33953086E3 ubiquitin ligase Cbl-b in innate and adaptive immunity
Q35023033Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma
Q38207119Genetic risk factors for the development of allergic disease identified by genome-wide association
Q40859008Genetics of adolescent idiopathic scoliosis in the post-genome-wide association study era
Q35556785Genetics of allergic diseases
Q64236058Genomic Predictors of Asthma Phenotypes and Treatment Response
Q37734509Identification of miRNA biomarkers of pneumonia using RNA-sequencing and bioinformatics analysis
Q64883360Identification of rare variants of allergic rhinitis based on whole genome sequencing and gene expression profiling: A preliminary investigation in four families.
Q35862462In Utero Cigarette Smoke Affects Allergic Airway Disease But Does Not Alter the Lung Methylome
Q28087013Mapping asthma-associated variants in admixed populations
Q49538238Methylene-tetrahydrofolate reductase contributes to allergic airway disease.
Q38393275Modulation of Immune Cell Functions by the E3 Ligase Cbl-b.
Q36085898Sequencing study on familial lung squamous cancer
Q38360676Unravelling the complex genetic background of atopic dermatitis: from genetic association results towards novel therapeutic strategies

Search more.