Virtual International Authority File


Albert de la Chapelle suomalainen lääketieteellisen genetiikan emeritusprofessori (Helsingin yliopisto), tutkimusprofessori ja tieteen akateemikko (Suomen Akatemia) Wikidata

De la Chapelle, Albert National Library of France Sudoc [ABES], France Library of Congress/NACO National Library of Israel

Albert de la Chapelle ISNI

Chapelle, Albert de la National Library of the Netherlands

La Chapelle, Albert de BIBSYS

La Chapelle, Albert de 1933- German National Library

VIAF ID: 46778744 (Personal)


Open Section Close Section Preferred Forms





Open Section Close Section 4xx's: Alternate Name Forms (13)

Open Section Close SectionWorks

Title Sources
Bidrag till kännedomen om de s.k. primära, akuta streptokockperitoniterna BIBSYS Sudoc [ABES], France
Cytogenetical and clinical observations in female gonadal dysgenesis Sudoc [ABES], France National Library of the Netherlands
Discovery of common variants associated with low TSH levels and thyroid cancer risk Wikidata
Dissection of the Major Hematopoietic Quantitative Trait Locus in Chromosome 6q23.3 Identifies miR-3662 as a Player in Hematopoiesis and Acute Myeloid Leukemia. Wikidata
Frequent PIK3CA Mutations in Colorectal and Endometrial Tumors With 2 or More Somatic Mutations in Mismatch Repair Genes Wikidata
The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless Wikidata
Gene expression and functional evidence of epithelial-to-mesenchymal transition in papillary thyroid carcinoma invasion. Wikidata
Genetic predisposition to colorectal cancer. Wikidata
A genome-wide association study yields five novel thyroid cancer risk loci. Wikidata
Genome-Wide Expression Screening Discloses Long Noncoding RNAs Involved in Thyroid Carcinogenesis Wikidata
Genomic sequence matters: a SNP in microRNA-146a can turn anti-apoptotic. Wikidata
Hereditary intrinsic factor deficiency in chaldeans. Wikidata
Heritable polymorphism predisposes to high BAALC expression in acute myeloid leukemia Wikidata
Identification and characterization of genomic rearrangements of MSH2 and MLH1 in Lynch syndrome (HNPCC) by novel techniques. Wikidata
Identification of a novel noncoding RNA gene, NAMA, that is downregulated in papillary thyroid carcinoma with BRAF mutation and associated with growth arrest. Wikidata
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease. Wikidata
Immunodepletion plasma proteomics by tripleTOF 5600 and Orbitrap elite/LTQ-Orbitrap Velos/Q exactive mass spectrometers. Wikidata
Immunoglobulin transcript sequence and somatic hypermutation computation from unselected RNA-seq reads in chronic lymphocytic leukemia. Wikidata
Implication des récepteurs à dépendance de la nétrine-1 dans les cancers colorectaux Sudoc [ABES], France
In-depth characterization of the microRNA transcriptome in normal thyroid and papillary thyroid carcinoma. Wikidata
The incidence of Lynch syndrome. Wikidata
Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients Wikidata
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. Wikidata
Int. Wks. on Human Gene Mapping (8th : 1985 : University of Helsinki). Human gene mapping 8, 1985: Sudoc [ABES], France National Library of France National Library of the Netherlands Library of Congress/NACO National Library of Israel
Intronic miR-3151 within BAALC drives leukemogenesis by deregulating the TP53 pathway. Wikidata
Involvement of netrin-1 dependence receptors in colorectal tumorigenesis. Sudoc [ABES], France
Low cancer incidence rates in Ohio Amish. Wikidata
MicroRNA-3151 inactivates TP53 in BRAF-mutated human malignancies. Wikidata
MicroRNA signature in thyroid fine needle aspiration cytology applied to "atypia of undetermined significance" cases Wikidata
miR-3151 interplays with its host gene BAALC and independently affects outcome of patients with cytogenetically normal acute myeloid leukemia Wikidata
Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation. Wikidata
Molecular profiling of chronic lymphocytic leukaemia: genetics meets epigenetics to identify predisposing genes. Wikidata
Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer. Wikidata
Mutational Landscape and Gene Expression Patterns in Adult Acute Myeloid Leukemias with Monosomy 7 as a Sole Abnormality. Wikidata
Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD I Wikidata
MYH9 binds to lncRNA gene PTCSC2 and regulates FOXE1 in the 9q22 thyroid cancer risk locus. Wikidata
NRAS isoforms differentially affect downstream pathways, cell growth, and cell transformation. Wikidata
The Olympic Games and Athletic Sex Assignment. Wikidata
Overexpression of the ETS-related gene, ERG, predicts a worse outcome in acute myeloid leukemia with normal karyotype: a Cancer and Leukemia Group B study. Wikidata
Papillary and follicular thyroid carcinomas show distinctly different microarray expression profiles and can be distinguished by a minimum of five genes. Wikidata
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein. Wikidata
Patients with colorectal cancer associated with Lynch syndrome and MLH1 promoter hypermethylation have similar prognoses. Wikidata
PD-1 Blockade in Tumors with Mismatch-Repair Deficiency Wikidata
Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications. Wikidata
PMS2 monoallelic mutation carriers: the known unknown Wikidata
Polymorphic mature microRNAs from passenger strand of pre-miR-146a contribute to thyroid cancer. Wikidata
The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor type. Wikidata
Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer. Wikidata
Primary Cell Culture Systems for Human Thyroid Studies. Wikidata
PTCSC3 Is Involved in Papillary Thyroid Carcinoma Development by Modulating S100A4 Gene Expression. Wikidata
PTEN mutational spectra, expression levels, and subcellular localization in microsatellite stable and unstable colorectal cancers. Wikidata
Reprogramming of miRNA networks in cancer and leukemia. Wikidata
Risk factors for colorectal cancer in patients with multiple serrated polyps: a cross-sectional case series from genetics clinics Wikidata
Role of cancer-associated stromal fibroblasts in metastatic colon cancer to the liver and their expression profiles. Wikidata
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer). Wikidata
The search for unaffected individuals with Lynch syndrome: do the ends justify the means? Wikidata
Somatic acquisition and signaling of TGFBR1*6A in cancer. Wikidata
Somatic MED12 mutations are associated with poor prognosis markers in chronic lymphocytic leukemia Wikidata
Structural characterization of NRAS isoform 5 Wikidata
Study of p.N247S KERA mutation in a British family with cornea plana. Wikidata
Telomere length and telomerase reverse transcriptase gene copy number in patients with papillary thyroid carcinoma. Wikidata
Tgfbr1 haploinsufficiency is a potent modifier of colorectal cancer development Wikidata
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina Wikidata
Thyroid hormone receptor beta (THRB) is a major target gene for microRNAs deregulated in papillary thyroid carcinoma (PTC) Wikidata
Über die Wernicke'sche Enzephalopathie und die Bedeutung des Gehirnstammes für die Persönlichkeit / Über Muskelkrämpfe und Crampuskrankheit / [von] Eero Hillbom und Eero Rechardt. Creutzfeldt Jakob disease / [by] Eero Hillbom, Matti Tuovinen and Albert de la Chapelle. National Library of the Netherlands
Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetrance Wikidata
Variants in the ATM-CHEK2-BRCA1 axis determine genetic predisposition and clinical presentation of papillary thyroid carcinoma. Wikidata
Variants in the netrin-1 receptor UNC5C prevent apoptosis and increase risk of familial colorectal cancer. Wikidata

Open Section Close Section Selected Co-authors

Open Section Close Section Countries and Regions of Publication (3)

Open Section Close Section Publication Statistics

Open Section Close Section Selected Publishers (4)

Open Section Close Section History of VIAF ID:46778744 (10)