Pages that link to "Q35239173"
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The following pages link to Magnitude of type I error when single-locus linkage analysis is maximized over models: a simulation study. (Q35239173):
Displaying 50 items.
- Linkage analysis in the next-generation sequencing era (Q24289003) (← links)
- Identification of a new candidate locus for uric acid nephrolithiasis (Q24533463) (← links)
- Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26. (Q24533776) (← links)
- Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4). (Q24648625) (← links)
- Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata (Q24680203) (← links)
- An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder (Q30494147) (← links)
- The importance of modelling heterogeneity in complex disease: application to NIMH Schizophrenia Genetics Initiative data (Q30987745) (← links)
- Using linkage analysis to detect gene-gene interaction by stratifying family data on known disease, or disease-associated, alleles. (Q31155143) (← links)
- Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families (Q33188524) (← links)
- Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations (Q33232734) (← links)
- Linkage analysis of alcohol dependence using MOD scores (Q33232756) (← links)
- Y chromosome lineage- and village-specific genes on chromosomes 1p22 and 6q27 control visceral leishmaniasis in Sudan. (Q33284534) (← links)
- All LODs are not created equal (Q33908550) (← links)
- Linkage at 12q24 with systemic lupus erythematosus (SLE) is established and confirmed in Hispanic and European American families (Q33909567) (← links)
- Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12 (Q33910053) (← links)
- A major lung cancer susceptibility locus maps to chromosome 6q23-25. (Q33910059) (← links)
- Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results (Q33926291) (← links)
- Evidence for linkage and association of GABRB3 and GABRA5 to panic disorder (Q34068930) (← links)
- False-positive rates in two-point parametric linkage analysis (Q34085231) (← links)
- Genomewide scan and fine-mapping linkage studies in four European samples with bipolar affective disorder suggest a new susceptibility locus on chromosome 1p35-p36 and provides further evidence of loci on chromosome 4q31 and 6q24. (Q34137467) (← links)
- Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family (Q34142114) (← links)
- Significant linkage for Tourette syndrome in a large French Canadian family (Q34144080) (← links)
- Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy (Q34145085) (← links)
- Linkage of familial schizophrenia to chromosome 13q32 (Q34145743) (← links)
- The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy. (Q34345047) (← links)
- A new Graves disease-susceptibility locus maps to chromosome 20q11.2. International Consortium for the Genetics of Autoimmune Thyroid Disease (Q34388225) (← links)
- Further evidence for the increased power of LOD scores compared with nonparametric methods (Q34388663) (← links)
- The essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches (Q34389357) (← links)
- Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity (Q34389602) (← links)
- Power comparison of parametric and nonparametric linkage tests in small pedigrees (Q34390464) (← links)
- Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization (Q34390667) (← links)
- Identification of epilepsy genes in human and mouse (Q34432267) (← links)
- Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. (Q34627021) (← links)
- A linkage search for joint panic disorder/bipolar genes (Q34683418) (← links)
- Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q. (Q34807127) (← links)
- Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22. (Q35109839) (← links)
- Using Linkage Analysis to Detect Gene-Gene Interactions. 2. Improved Reliability and Extension to More-Complex Models (Q35890482) (← links)
- Linkage Analysis of Genomic Regions Contributing to the Expression of Type 1 Diabetes Microvascular Complications and Interaction with HLA (Q36204486) (← links)
- 'Linkage analysis of thyroid antibody production: evidence for shared susceptibility to clinical autoimmune thyroid disease (Q36938349) (← links)
- The power and robustness of maximum LOD score statistics (Q36950118) (← links)
- Autoimmune thyroiditis and diabetes: dissecting the joint genetic susceptibility in a large cohort of multiplex families. (Q37193226) (← links)
- A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide search (Q37203153) (← links)
- Investigation of parent-of-origin effect in comitant strabismus using MOD score analysis (Q37258692) (← links)
- A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13. (Q37259295) (← links)
- Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13. (Q39806687) (← links)
- Significance levels in complex inheritance (Q41787286) (← links)
- Multipoint lods provide reliable linkage evidence despite unknown limiting distribution: type I error probabilities decrease with sample size for multipoint lods and mods (Q41917744) (← links)
- Novel loci interacting epistatically with bone morphogenetic protein receptor 2 cause familial pulmonary arterial hypertension (Q42925160) (← links)
- Direct power comparisons between simple LOD scores and NPL scores for linkage analysis in complex diseases (Q43218606) (← links)
- Genetic linkage of systemic lupus erythematosus to 13q32 in African American families with affected male members. (Q53655610) (← links)