about
De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.Family-based association tests for sequence data, and comparisons with population-based association tests.Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autismComparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data.Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modeling.Joint study of genetic regulators for expression traits related to breast cancer.Constructing gene association networks for rheumatoid arthritis using the backward genotype-trait association (BGTA) algorithm.On quality control measures in genome-wide association studies: a test to assess the genotyping quality of individual probands in family-based association studies and an application to the HapMap data.Linkage disequilibrium mapping of the chromosome 6q21-22.31 bipolar I disorder susceptibility locusA new testing strategy to identify rare variants with either risk or protective effect on disease.Small sample properties of rare variant analysis methods.Finding disease variants in Mendelian disorders by using sequence data: methods and applications.Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches.Rare variant analysis for family-based design.Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autismCopy number variation genotyping using family information.Study designs for identification of rare disease variants in complex diseases: the utility of family-based designsRefinement of primate copy number variation hotspots identifies candidate genomic regions evolving under positive selection.Genetic variants within the serotonin transporter associated with familial risk for major depression.Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAFGenomewide weighted hypothesis testing in family-based association studies, with an application to a 100K scanScan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets.A spectral approach integrating functional genomic annotations for coding and noncoding variants.Does rate of progression run in essential tremor families? Slower vs. faster progressorsDe Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and SchizophreniaA General and Robust Framework for Secondary Traits Analysis.Sequence kernel association tests for the combined effect of rare and common variants.On the frequency of copy number variants.Estimating the number of unseen variants in the human genome.Genetic association analysis of copy-number variation (CNV) in human disease pathogenesisIdentification of candidate genes for familial early-onset essential tremor.Essential Tremor in a Charcot-Marie-Tooth Type 2C Kindred Does Not Segregate with the TRPV4 R269H Mutation.Unified Sequence-Based Association Tests Allowing for Multiple Functional Annotations and Meta-Analysis of Noncoding Variation in Metabochip Data.Empirical Bayes scan statistics for detecting clusters of disease risk variants in genetic studies.On the optimal design of genetic variant discovery studiesOn the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.Rare-variant association tests in longitudinal studies, with an application to the Multi-Ethnic Study of Atherosclerosis (MESA).Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.QRank: a novel quantile regression tool for eQTL discovery.Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
P50
Q30454132-988CA008-D847-4B5A-84DD-69753D789A5FQ30587122-8B83CBD5-EE1E-4F83-8617-C2F8B3BD27DCQ30717096-195C8650-4A2D-497D-8DB9-98EDFC96F30BQ30879444-F2E3ED9A-D782-44D0-94BC-17570D2D47E5Q30958077-D68061F2-F079-43D9-9E01-086EDBEBCB7DQ33332757-C375117E-556A-4E80-B924-475AF77FB3B8Q33332815-11B1ABF1-2630-4FE4-ABD5-A67453D56515Q33486490-BFB71E9E-6147-4440-9E5E-E40402271DB4Q33793490-02503C6E-53DC-40EF-B62D-747AE609DFFDQ33815362-A7098BB3-552D-44FA-85BE-68219B021447Q34085632-D90975FC-11D2-487F-BBB0-39447FBDB513Q34089812-7F1D791C-4984-4F60-BCD9-7A75BFC21C3FQ34175438-9620C303-9431-4F9C-8FC0-A4C20AB42FCAQ34558081-00060D2A-3600-4713-BD2D-695A72FDB583Q34682335-7EA70C0A-914D-4553-BC53-EDF5B29BEE78Q34711165-FEA62D49-386C-44E7-BBEE-481CE26F11B2Q35542036-5448E201-21BD-432E-B077-3666B593649EQ35561178-4023EDB2-C799-4C10-AC60-144672D548B2Q35671605-20EEECBB-5EA3-4816-AEBA-72B94488ACBEQ35758502-71B276B7-AE8C-48B0-B49F-562E4E94E1F6Q35946334-6B82A606-6DA3-4351-921D-D817420582ACQ36017094-04791DEA-050D-4CDC-AF10-F41B5BB1B9FAQ36515609-A5FD595C-0E9F-4B4A-9276-9E3E70B10E6AQ36625556-82C14E96-1F57-4051-BF79-06AC1B990573Q36692253-3BDC9814-19F0-4271-8EDB-872E9237CE6EQ36787358-0B715FF8-6A72-4B18-A73A-93D0F16B149CQ36909285-6E951F22-9BBF-4F4D-A772-BF5C78D3F19EQ36924050-CB677D23-54C8-4782-856A-69D6B094A5F9Q37146925-B44302A8-F4C3-4260-A0D7-A9AC0A5FEBB6Q37281239-D41BC62A-06E8-4EAB-905F-063CB1E3844DQ37351438-4A3FBA3E-3144-422F-9716-0407473C7939Q37603156-223C1685-6912-4D19-9869-4426B0FA2643Q38606760-AB81659B-2806-4189-A71F-847C9DD4195FQ40879974-C0A4BDF7-C799-40B2-BBBD-8A89890DA7F7Q42424982-FC38597B-94F1-48A1-8A1E-D1B86E65F66BQ45288594-59DE0FFD-3904-406A-BAB6-6659532F2CBBQ46655315-D2FC7E42-F84B-4707-97DA-BA7873E7032FQ47073818-F28579A7-CC12-4144-8C40-77D5750863F7Q47354901-B702D176-F255-498C-98DA-139FF519BD05Q50001526-7D08931D-EC4A-48FC-B18A-6B5926EFFCCD
P50
name
Iuliana Ionita-Laza
@en
type
label
Iuliana Ionita-Laza
@en
prefLabel
Iuliana Ionita-Laza
@en