Author

Asta Försti

German Cancer Research CenterORCID 0000-0002-9857-4728Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Aayushi SrivastavaiD· 2 shared Abhishek KumariD· 2 shared Kari HemminkiiD· 2 shared Nagarajan ParamasivamiD· 2 shared Obul Reddy BandapalliiD· 2 shared Albert de la ChapelleiD· 1 shared Anne BolandiD· 1 shared Anne‐Louise LeuteneggeriD· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersGenomics

Aayushi SrivastavaORCID

Mutual co-authors in cluster

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3 papers

Recent·Most cited

Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium

Thérèse Truong, Fabienne Lesueur, Pierre‐Emmanuel Sugier, Julie Guibon, Constance Xhaard, Mojgan Karimi, Om Kulkarni, Elise A. Lucotte, Delphine Bacq‐Daian, Anne Boland, Claire Mulot, Pierre Laurent‐Puig, Claire Schvartz, Anne‐Valérie Guizard, Yan Xin Ren, , Florent de Vathaire

This study identifies genetic risk loci for differentiated thyroid cancer in multiethnic populations, finding novel associations and allele frequency differences between Oceanian and European ancestry groups.

International Journal of Cancer · Feb 3, 2021Peer-reviewedGenetic & Genomic Medicine

A novel germline mutation in the POT1 gene predisposes to familial non-medullary thyroid cancer

Aayushi Srivastava, Beiping Miao, Diamanto Skopelitou, Varun Kumar, Abhishek Kumar, Nagarajan Paramasivam, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli

This study identifies a novel germline POT1 mutation (p.V29L) associated with familial non-medullary thyroid cancer and shows it causes telomere dysfunction.

Cancers · Jun 1, 2020Peer-reviewedGenomics

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing

Aayushi Srivastava, Sara Giangiobbe, Abhishek Kumar, Nagarajan Paramasivam, Dagmara Dymerska, Wolfgang Behnisch, Mathias Witzens‐Harig, Jan Lubiński, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli

This study uses whole genome sequencing to identify potential familial Hodgkin lymphoma predisposing genes in three families, finding a novel DICER1 variant in one family.

Frontiers in Bioengineering and Biotechnology · Mar 5, 2020Peer-reviewedGenetic & Genomic Medicine