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Asta Försti

Name	Asta Försti
Ort	Finnland
Akademischer Grad bzw. Titel	Dr. PhD
Beziehung	Deutsches Krebsforschungszentrum. Abteilung Molekulargenetische Epidemiologie Universität Heidelberg. Medizinische Fakultät (Lehrbeauftragte)
Weitere Angaben	1984 M.Sc. in Biochemie und1992 PhD in Biochemie und Biotechnologie an der Universität Kuopio, Finnland; Wissenschaftlerin am DKFZ in Heidelberg und Lehrbeauftragte der Medizinischen Fakultät der Universität Heidelberg
Quelle	16/250
Datensatztyp	Person
GND-Nummer	1155331672
Datensatz-ID	1155331672
Beteiligt an alle anzeigen Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance Deciphering the genetics and mechanisms of predisposition to multiple myeloma Identification of novel genetic loci for risk of multiple myeloma by functional annotation The complementary roles of genome-wide approaches in identifying genes linked to an inherited risk of colorectal cancer Investigation of rare non-coding variants in familial multiple myeloma Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk Survival trends in hematological malignancies in the Nordic countries through 50 years Functional dissection of inherited non-coding variation influencing multiple myeloma risk Germline variants of CYBA and TRPM4 predispose to familial colorectal cancer Whole-exome sequencing identifies a novel germline variant in PTK7 gene in familial colorectal cancer A rare large duplication of MLH1 identified in Lynch syndrome A novel low-risk germline variant in the SH2 domain of the SRC gene affects multiple pathways in familial colorectal cancer Characterization of rare germline variants in familial multiple myeloma Combinations of low-frequency genetic variants might predispose to familial pancreatic cancer Whole exome sequencing identifies APCDD1 and HDAC5 genes as potentially cancer predisposing in familial colorectal cancer Cancer predisposition genes in cancer-free families Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients Multiple myeloma: family history and mortality in second primary cancers Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family Familial Ovarian Cancer Clusters with Other Cancers Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma [Letter] Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility Pedigree based DNA sequencing pipeline for germline genomes of cancer families Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

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Asta Försti

Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance

Deciphering the genetics and mechanisms of predisposition to multiple myeloma

Identification of novel genetic loci for risk of multiple myeloma by functional annotation

The complementary roles of genome-wide approaches in identifying genes linked to an inherited risk of colorectal cancer

Investigation of rare non-coding variants in familial multiple myeloma

Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk

Survival trends in hematological malignancies in the Nordic countries through 50 years

Functional dissection of inherited non-coding variation influencing multiple myeloma risk

Germline variants of CYBA and TRPM4 predispose to familial colorectal cancer

Whole-exome sequencing identifies a novel germline variant in PTK7 gene in familial colorectal cancer

A rare large duplication of MLH1 identified in Lynch syndrome

A novel low-risk germline variant in the SH2 domain of the SRC gene affects multiple pathways in familial colorectal cancer

Characterization of rare germline variants in familial multiple myeloma

Combinations of low-frequency genetic variants might predispose to familial pancreatic cancer

Whole exome sequencing identifies APCDD1 and HDAC5 genes as potentially cancer predisposing in familial colorectal cancer

Cancer predisposition genes in cancer-free families

Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes

Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients

Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma

Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology

Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients

Multiple myeloma: family history and mortality in second primary cancers

Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family

Familial Ovarian Cancer Clusters with Other Cancers

Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study

Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma [Letter]

Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study