Defining the phenotype in human genetic studies: forward genetics and reverse phenotyping.
about
Genome-wide association with bone mass and geometry in the Framingham Heart StudyGenome-wide association studies: a primerProgress in genetic studies of pain and analgesiaDisruptive CHD8 mutations define a subtype of autism early in developmentSerotonin transporter variant drives preventable gastrointestinal abnormalities in development and function.Feasibility of a bilateral 4000-6000 Hz notch as a phenotype for genetic association analysis.The bowel and beyond: the enteric nervous system in neurological disordersEvidence for pleiotropic factors in genetics of the musculoskeletal systemGenetics of the musculoskeletal system: a pleiotropic approachHow pleiotropic genetics of the musculoskeletal system can inform genomics and phenomics of agingAutosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma.Are "functionally related polymorphisms" of renin-angiotensin-aldosterone system gene polymorphisms associated with hypertension?Genetic research into bipolar disorder: the need for a research framework that integrates sophisticated molecular biology and clinically informed phenotype characterization.A genotype-first approach to defining the subtypes of a complex diseaseApplication of genetic/genomic approaches to allergic disorders.Querying phenotype-genotype relationships on patient datasets using semantic web technology: the example of Cerebrotendinous xanthomatosis.An official American Thoracic Society Statement: pulmonary hypertension phenotypesEvidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.Greater prevalence of proposed DSM-5 nicotine use disorder compared to DSM-IV nicotine dependence in treated adolescents and young adultsIdentification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associationsContributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions.Computer-assisted phenotype characterization for genetic research in psychiatry.Neurocognitive endophenotypes for bipolar disorder identified in multiplex multigenerational familiesTargeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3Heritability and Familiality of Temperament and Character Dimensions in Korean Families with Schizophrenic Linkage Disequilibrium.Bringing a developmental perspective to anxiety geneticsA latent modeling approach to genotype-phenotype relationships: maternal problem behavior clusters, prenatal smoking, and MAOA genotype.Age, Gene/Environment Susceptibility-Reykjavik Study: multidisciplinary applied phenomics.Diagnostic use of Massively Parallel Sequencing in Neuromuscular Diseases: Towards an Integrated Diagnosis.Frequency of hybridization between Ostrinia nubilalis E-and Z-pheromone races in regions of sympatry within the United States.Early-onset dementias: diagnostic and etiological considerations.Unlocking Mendelian disease using exome sequencing.Importance of multi-modal approaches to effectively identify cataract cases from electronic health recordsNeuroimaging as a potential biomarker to optimize psychiatric research and treatment.Whole genome/exome sequencing in mood and psychotic disorders.The biological coherence of human phenome databases.Genetic tests in major psychiatric disorders-integrating molecular medicine with clinical psychiatry-why is it so difficult?"Forward genetics" as a method to maximize power and cost-efficiency in studies of human complex traitsDissecting the phenotype in genome-wide association studies of psychiatric illness
P2860
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P2860
Defining the phenotype in human genetic studies: forward genetics and reverse phenotyping.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Defining the phenotype in huma ...... etics and reverse phenotyping.
@ast
Defining the phenotype in huma ...... etics and reverse phenotyping.
@en
type
label
Defining the phenotype in huma ...... etics and reverse phenotyping.
@ast
Defining the phenotype in huma ...... etics and reverse phenotyping.
@en
prefLabel
Defining the phenotype in huma ...... etics and reverse phenotyping.
@ast
Defining the phenotype in huma ...... etics and reverse phenotyping.
@en
P2860
P356
P1433
P1476
Defining the phenotype in huma ...... etics and reverse phenotyping.
@en
P2093
Thomas G Schulze
P2860
P304
P356
10.1159/000083539
P577
2004-01-01T00:00:00Z