Pages that link to "Q34707985"

The following pages link to FLAGS, frequently mutated genes in public exomes (Q34707985):

Displaying 33 items.

• The genotypic and phenotypic spectrum of PIGA deficiency (Q30935460) (← links)
• Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions (Q31060798) (← links)
• Mutations in HECW2 are associated with intellectual disability and epilepsy (Q34531736) (← links)
• Defects in fatty acid amide hydrolase 2 in a male with neurologic and psychiatric symptoms (Q35579901) (← links)
• Concurrent Mutations in ATM and Genes Associated with Common γ Chain Signaling in Peripheral T Cell Lymphoma (Q35832062) (← links)
• Germline Variants of Prostate Cancer in Japanese Families. (Q36152825) (← links)
• Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease (Q36167703) (← links)
• Uncovering disease mechanisms through network biology in the era of Next Generation Sequencing (Q36799563) (← links)
• Comprehensive mutational analysis of primary and relapse acute promyelocytic leukemia. (Q37150061) (← links)
• Optic atrophy, cataracts, lipodystrophy/lipoatrophy, and peripheral neuropathy caused by a de novo OPA3 mutation (Q37518618) (← links)
• An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a TUBB3 mutation (Q37678113) (← links)
• DOMINO: Using Machine Learning to Predict Genes Associated with Dominant Disorders. (Q45945168) (← links)
• Genomic analysis of atypical fibroxanthoma (Q46176867) (← links)
• Whole-exome sequencing for detecting inborn errors of immunity: overview and perspectives. (Q47097066) (← links)
• Molecular Autopsy for Sudden Death in the Young: Is Data Aggregation the Key? (Q47102396) (← links)
• Benchmarking distributed data warehouse solutions for storing genomic variant information (Q47113794) (← links)
• Correction to: FLAGS, frequently mutated genes in public exomes (Q47163680) (← links)
• Genome-wide genetic and epigenetic analyses of pancreatic acinar cell carcinomas reveal aberrations in genome stability. (Q47164606) (← links)
• Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability. (Q48028085) (← links)
• Settling the score: variant prioritization and Mendelian disease. (Q52544730) (← links)
• Calculating the statistical significance of rare variants causal for Mendelian and complex disorders. (Q55334031) (← links)
• Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia (Q58085842) (← links)
• Sialic acid catabolism by N-acetylneuraminate pyruvate lyase is essential for muscle function (Q61456223) (← links)
• Epigenetic age acceleration of cervical squamous cell carcinoma converged to human papillomavirus 16/18 expression, immunoactivation, and favourable prognosis (Q89635650) (← links)
• TAPES: A tool for assessment and prioritisation in exome studies (Q90716751) (← links)
• Lack of APC somatic mutation is associated with early-onset colorectal cancer in African Americans (Q91617920) (← links)
• Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects (Q92022430) (← links)
• Genetic Mutations Underlying Phenotypic Plasticity in Basosquamous Carcinoma (Q92809489) (← links)
• Proteogenomic Characterization of Ovarian HGSC Implicates Mitotic Kinases, Replication Stress in Observed Chromosomal Instability (Q96305534) (← links)
• Spontaneous mutations in the single TTN gene represent high tumor mutation burden (Q98613255) (← links)
• The genomic landscape of Mongolian hepatocellular carcinoma (Q98891422) (← links)
• Whole Exome Profiling of NSCLC Among African Americans (Q99547332) (← links)
• Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias (Q103827045) (← links)