Pages that link to "Q24618492"

The following pages link to In search of low-frequency and rare variants affecting complex traits (Q24618492):

Displaying 44 items.

• Association claims in the sequencing era (Q24273315) (← links)
• Genetic Risk Factors for Ischemic and Hemorrhagic Stroke (Q28079249) (← links)
• Whole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertension (Q28237461) (← links)
• Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate (Q28657831) (← links)
• Novel SNP markers in InvGE and SssI genes are associated with natural variation of sugar contents and frying color in Solanum tuberosum Group Phureja. (Q30378239) (← links)
• Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm (Q30405930) (← links)
• Combining powers of linkage and association mapping for precise dissection of QTL controlling resistance to gray leaf spot disease in maize (Zea mays L.). (Q31020982) (← links)
• Clinical Applicability of Whole-Exome Sequencing Exemplified by a Study in Young Adults with the Advanced Cryptogenic Cholestatic Liver Diseases. (Q33775587) (← links)
• On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows. (Q33925543) (← links)
• Validation and assessment of variant calling pipelines for next-generation sequencing (Q34030865) (← links)
• Genetics, genomics, and their relevance to pathology and therapy (Q34108958) (← links)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants (Q34146799) (← links)
• Exome sequencing from nanogram amounts of starting DNA: comparing three approaches (Q35200827) (← links)
• Genetics of allergic diseases (Q35556785) (← links)
• Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. (Q35906336) (← links)
• Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells (Q36131690) (← links)
• Is Whole Exome Sequencing Clinically Practical in the Management of Pediatric Crohn's Disease? (Q36223434) (← links)
• Whole-exome sequencing in an isolated population from the Dalmatian island of Vis (Q37108926) (← links)
• A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans (Q37393239) (← links)
• LipidSeq: a next-generation clinical resequencing panel for monogenic dyslipidemias (Q37665490) (← links)
• Current concepts and clinical applications of stroke genetics (Q38197434) (← links)
• Genetic counseling practice in next generation sequencing research: implications for the ethical oversight of the informed consent process (Q38199059) (← links)
• Considerations for rare variants in drug metabolism genes and the clinical implications (Q38199740) (← links)
• Genetics and brain morphology (Q38379199) (← links)
• Genetic architectures of seropositive and seronegative rheumatic diseases (Q38439633) (← links)
• A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity (Q38687787) (← links)
• Genetics of Gestational Diabetes Mellitus and Maternal Metabolism (Q38709349) (← links)
• BayesPI-BAR: a new biophysical model for characterization of regulatory sequence variations (Q38850146) (← links)
• MicroRNAs as biomarkers for psychiatric disorders with a focus on autism spectrum disorder: Current progress in genetic association studies, expression profiling, and translational research (Q39248707) (← links)
• Chronic Periodontitis Genome-wide Association Study in the Hispanic Community Health Study / Study of Latinos. (Q39416305) (← links)
• An exome-wide analysis of low frequency and rare variants in relation to risk of breast cancer in African American Women: the AMBER Consortium (Q39706039) (← links)
• Two PALB2 germline mutations found in both BRCA1+ and BRCAx familial breast cancer (Q41126310) (← links)
• De Novo FGF12 (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia (Q41628411) (← links)
• Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation (Q46734706) (← links)
• Mutational analysis of IZUMO1R in women with fertilization failure and polyspermy after in vitro fertilization (Q47564637) (← links)
• Genetics of Alzheimer's Disease: the Importance of Polygenic and Epistatic Components (Q48146731) (← links)
• Estimating the mutational load for cardiovascular diseases in Pakistani population (Q50114231) (← links)
• Nature and nurture: a case of transcending haematological pre-malignancies in a pair of monozygotic twins adding possible clues on the pathogenesis of B-cell proliferations. (Q53590128) (← links)
• What Does This Mutation Mean? The Tools and Pitfalls of Variant Interpretation in Lymphoid Malignancies. (Q55170341) (← links)
• Whole Exome Sequencing of Patients from Multicase Families with Systemic Lupus Erythematosus Identifies Multiple Rare Variants. (Q55449353) (← links)
• Genetic predisposition to necrotizing enterocolitis in premature infants: Current knowledge, challenges, and future directions (Q57192831) (← links)
• Improved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers (Q91286786) (← links)
• Clinical-pathological correlations of BAV and the attendant thoracic aortopathies. Part 2: Pluridisciplinary perspective on their genetic and molecular origins (Q92599834) (← links)
• Genetic factors for alcohol dependence and schizophrenia: common and rare variants (Q94423560) (← links)