about
Common variants at five new loci associated with early-onset inflammatory bowel diseaseCommon genetic variants on 5p14.1 associate with autism spectrum disordersA landscape of driver mutations in melanomaMutational heterogeneity in cancer and the search for new cancer-associated genesAutism genome-wide copy number variation reveals ubiquitin and neuronal genesStrong synaptic transmission impact by copy number variations in schizophrenia.Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effectsDiverse genome-wide association studies associate the IL12/IL23 pathway with Crohn DiseaseLoci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel diseaseOncogenic and sorafenib-sensitive ARAF mutations in lung adenocarcinomaGenome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorderMapping the hallmarks of lung adenocarcinoma with massively parallel sequencingMeta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated lociFollow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.Signatures of mutational processes in human cancerThe cancer precision medicine knowledge base for structured clinical-grade mutations and interpretationsDistinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas.Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder.Variants of DENND1B associated with asthma in children.Identification of focally amplified lineage-specific super-enhancers in human epithelial cancers.Insertions and Deletions Target Lineage-Defining Genes in Human Cancers.Genetic modifiers of EGFR dependence in non-small cell lung cancer.Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2.High-throughput Phenotyping of Lung Cancer Somatic MutationsA pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing eventsInvestigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry.High-throughput Phenotyping of Lung Cancer Somatic Mutations.Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47Erratum: Corrigendum: Signatures of mutational processes in human cancer17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestrySelective and mechanistic sources of recurrent rearrangements across the cancer genome
P50
Q24600801-4F63E5BB-5F1A-4E32-A354-8458B61BFE84Q24603204-47AADA39-0D5F-45ED-9DFF-B44EA4387FB3Q24603357-3C293E49-1EB8-4937-8D1A-825EADDF28AFQ24606956-40E119BB-D04A-4268-8A31-864AC0EB5FAAQ24629598-81B9B33B-1083-430E-9B60-D3A5BA8C6ECBQ24630444-CAFD289D-264C-4449-90BE-F5883C782844Q24631241-B8A671DC-9696-45F5-82F9-584D428D4568Q24644398-BD39E983-5712-4BB1-BAA9-7755E800298FQ24646902-8D510E38-E37E-4721-ABA1-DE1C20C180B0Q27852873-5BFDAB34-305B-4A14-AEF6-061C79AAA8BAQ28254567-EFF74359-3085-4B6B-A914-B249F168A757Q28275103-00909502-B631-495E-9C95-27C94CC7E678Q28943305-9133E46A-F588-4E79-9F1D-69AC90EC4C2EQ28943424-9BFF0D7C-4760-4BC6-BAAA-1C899B7421EBQ29417127-C8FA09FB-7A6E-491F-BFF6-9CC0FEB7C093Q29547191-1FD491F5-076B-4351-9B4B-7CF838DF1C84Q30490259-527FC970-D9D2-4CC1-B57C-A81272DC3FBDQ30762699-5C9C3B9A-B385-4E0F-AF1E-9F80F585F111Q33323357-6A6CCFDE-44DE-4CF3-8364-E4802B407EC3Q33474877-9965104D-9204-478C-8E63-5D443A32A141Q33769815-036AE74F-F984-491E-9145-1F98F33D7335Q34089817-CEEE820A-273E-4BB8-AAD7-34F6093306BDQ34504751-5B17B235-F991-4E1D-A4CA-7A085CA01B07Q34549348-06F8308A-D86F-417B-8895-FB764CF62D09Q34832117-6CBF7D91-89FF-41D7-A73B-21FAD6C1118EQ36221780-9568D24F-C51E-48C6-81C1-02CDD13525CCQ38754469-68AEF8F7-CD36-4968-9BE1-5A97F42B162DQ39027040-4528D1A5-7D5B-4F43-AA92-E1BF9D3DE6A9Q40234047-EF1CA921-D84E-4057-A546-3769CFB57845Q49895349-9208DC63-8EC9-49CC-8525-CCA0D01FD34DQ56968576-8DE26832-0298-45C1-9B3D-70E85A0466F8Q57082606-AA67AD2B-395F-41E6-BA0D-FFE3BFD3225DQ57638160-B14BBD32-A5D7-41DC-AB75-53322F1E1F62Q58323720-855DEF6B-ACF3-45AB-A142-6F2E1AC4BD21
P50
description
onderzoeker
@nl
name
Marcin Imielinski
@en
Marcin Imielinski
@es
Marcin Imielinski
@sl
type
label
Marcin Imielinski
@en
Marcin Imielinski
@es
Marcin Imielinski
@sl
prefLabel
Marcin Imielinski
@en
Marcin Imielinski
@es
Marcin Imielinski
@sl