Pages that link to "Q36817316"
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The following pages link to eXclusion: toward integrating the X chromosome in genome-wide association analyses (Q36817316):
Displaying 50 items.
- Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness (Q21131974) (← links)
- Genetic Research and Women's Heart Disease: a Primer (Q28069638) (← links)
- Integration of genome-wide association and extant brain expression QTL identifies candidate genes influencing prepulse inhibition in inbred F1 mice. (Q30383534) (← links)
- High-resolution genetic mapping of complex traits from a combined analysis of F2 and advanced intercross mice (Q30587743) (← links)
- XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome (Q30987029) (← links)
- Modeling X Chromosome Data Using Random Forests: Conquering Sex Bias (Q31030396) (← links)
- Heritability and genomics of gene expression in peripheral blood (Q33575322) (← links)
- Genetics of coronary artery disease: an update (Q33732873) (← links)
- X-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation (Q34021819) (← links)
- A Review of Autoimmune Disease Hypotheses with Introduction of the "Nucleolus" Hypothesis (Q34047060) (← links)
- Discovery and refinement of muscle weight QTLs in B6 × D2 advanced intercross mice (Q34062919) (← links)
- Sex and gender differences in the causes of dementia: a narrative review (Q34214272) (← links)
- X-inactivation informs variance-based testing for X-linked association of a quantitative trait (Q34472075) (← links)
- Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases (Q34639949) (← links)
- Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population (Q35063837) (← links)
- Learning about the X from our parents (Q35067109) (← links)
- Chromosome X-wide association study identifies Loci for fasting insulin and height and evidence for incomplete dosage compensation (Q35091275) (← links)
- Genetics of cardiovascular disease: Importance of sex and ethnicity (Q35738812) (← links)
- Influence of Feature Encoding and Choice of Classifier on Disease Risk Prediction in Genome-Wide Association Studies. (Q35749062) (← links)
- Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X Chromosome (Q36172690) (← links)
- A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration (Q36468916) (← links)
- Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos (Q36473454) (← links)
- Novel loci and pathways significantly associated with longevity (Q36615898) (← links)
- Impact of the X Chromosome and sex on regulatory variation (Q36959192) (← links)
- No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis (Q37330353) (← links)
- Genetic and epigenetic studies of FOXP3 in asthma and allergy (Q37481048) (← links)
- Identification of loci affecting teat number by genome-wide association studies on three pig populations (Q37548765) (← links)
- Sex differences in attention Deficit Hyperactivity Disorder: candidate genetic and endocrine mechanisms. (Q38200373) (← links)
- Detecting epistasis in human complex traits (Q38247072) (← links)
- Human Y-chromosome variation in the genome-sequencing era. (Q38757668) (← links)
- X chromosome-wide association study identifies a susceptibility locus for inflammatory bowel disease in Koreans (Q38883868) (← links)
- Suggestive association between variants in IL1RAPL and asthma symptoms in Latin American children. (Q39216721) (← links)
- Genetic Basis for Sex Differences in Obesity and Lipid Metabolism (Q39382856) (← links)
- Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder (Q39732399) (← links)
- HbA1c for type 2 diabetes diagnosis in Africans and African Americans: Personalized medicine NOW! (Q40045609) (← links)
- A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts (Q40055740) (← links)
- Potentially functional variants in lncRNAs are associated with breast cancer risk in a Chinese population. (Q40248157) (← links)
- An imputation-based genome-wide association study on traits related to male reproduction in a White Duroc × Erhualian F2 population. (Q40478814) (← links)
- A Bayesian test for Hardy-Weinberg equilibrium of biallelic X-chromosomal markers (Q41643181) (← links)
- From sexless to sexy: Why it is time for human genetics to consider and report analyses of sex. (Q42355531) (← links)
- Sex, Gender, and Transgender: Metabolic Impact of Cross Hormone Therapy (Q46190351) (← links)
- Absent CNKSR2 causes seizures and intellectual, attention, and language deficits (Q48029963) (← links)
- Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors (Q49487202) (← links)
- How to include chromosome X in your genome-wide association study (Q51124802) (← links)
- Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2. (Q52665584) (← links)
- Sex Differences in HIV Infection: Mystique Versus Machismo (Q56996082) (← links)
- Genome wide association analysis in a mouse advanced intercross line (Q59794227) (← links)
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness (Q60182871) (← links)
- Genetic Association and Altered Gene Expression of in Multiple Sclerosis Patients (Q60949388) (← links)
- The role of sex in the genomics of human complex traits (Q62477829) (← links)