Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Aayushi, Srivastava"'
Autor:
Kari Hemminki, Aayushi Srivastava, Sivaramakrishna Rachakonda, Obul Bandapalli, Eduardo Nagore, Akseli Hemminki, Rajiv Kumar
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 18, Iss 1, Pp 1-6 (2020)
Abstract Background When germline mutations are suspected as causal in cancer, patient DNA may be sequenced to detect variants in relevant genes. If a particular mutation has not been reported in reliable family studies, genetic counselors are facing
Externí odkaz:
https://doaj.org/article/769447fee5474b8db79bbb73597feb36
Autor:
Aayushi Srivastava, Sara Giangiobbe, Diamanto Skopelitou, Beiping Miao, Nagarajan Paramasivam, Chiara Diquigiovanni, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Familial inheritance in non-medullary thyroid cancer (NMTC) is an area that has yet to be adequately explored. Despite evidence suggesting strong familial clustering of non-syndromic NMTC, known variants still account for a very small percentage of t
Externí odkaz:
https://doaj.org/article/23c65b19eb464b2c85226e7343289103
Autor:
Aayushi Srivastava, Sara Giangiobbe, Abhishek Kumar, Nagarajan Paramasivam, Dagmara Dymerska, Wolfgang Behnisch, Mathias Witzens-Harig, Jan Lubinski, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 8 (2020)
Hodgkin lymphoma (HL) is a lymphoproliferative malignancy of B-cell origin that accounts for 10% of all lymphomas. Despite evidence suggesting strong familial clustering of HL, there is no clear understanding of the contribution of genes predisposing
Externí odkaz:
https://doaj.org/article/8dd35bfecde94fb981e63ac60497ced8
Autor:
Aayushi Srivastava, Abhishek Kumar, Sara Giangiobbe, Elena Bonora, Kari Hemminki, Asta Försti, Obul Reddy Bandapalli
Publikováno v:
Biomolecules, Vol 9, Iss 10, p 605 (2019)
Evidence of familial inheritance in non-medullary thyroid cancer (NMTC) has accumulated over the last few decades. However, known variants account for a very small percentage of the genetic burden. Here, we focused on the identification of common pat
Externí odkaz:
https://doaj.org/article/e8cf342d24f54b02a96c7a5db8760e4c
Publikováno v:
Transactions on Computational Science XXXIX ISBN: 9783662664902
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc16a48400314d82bea4121234813fa9
https://doi.org/10.1007/978-3-662-66491-9_4
https://doi.org/10.1007/978-3-662-66491-9_4
Autor:
Beiping, Miao, Diamanto, Skopelitou, Aayushi, Srivastava, Sara, Giangiobbe, Dagmara, Dymerska, Nagarajan, Paramasivam, Abhishek, Kumar, Magdalena, Kuświk, Wojciech, Kluźniak, Katarzyna, Paszkowska-Szczur, Matthias, Schlesner, Jan, Lubinski, Kari, Hemminki, Asta, Försti, Obul Reddy, Bandapalli
Publikováno v:
International journal of molecular sciences. 23(3)
Colorectal cancer (CRC) is the third most frequently diagnosed malignancy worldwide. Only 5% of all CRC cases are due to germline mutations in known predisposition genes, and the remaining genetic burden still has to be discovered. In this study, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81afa39d167e055c725cf8ceaf98440a
https://pubmed.ncbi.nlm.nih.gov/35163215
https://pubmed.ncbi.nlm.nih.gov/35163215
Autor:
Abhishek Kumar, Jan Lubinski, Kari Hemminki, Asta Försti, Nagarajan Paramasivam, Diamanto Skopelitou, Beiping Miao, Dagmara Dymerska, Magdalena Kuswick, Aayushi Srivastava, Matthias Schlesner, Obul Reddy Bandapalli
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1837, p 1837 (2021)
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1837, p 1837 (2021)
Germline mutations in predisposition genes account for only 20% of all familial colorectal cancers (CRC) and the remaining genetic burden may be due to rare high- to moderate-penetrance germline variants that are not explored. With the aim of identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78b4e620d1f5f00e0f3541a136e0dd7b
Autor:
Beiping Miao, Jan Lubinski, Diamanto Skopelitou, Matthias Schlesner, Magdalena Kuświk, Nagarajan Paramasivam, Abhishek Kumar, Kari Hemminki, Asta Försti, Aayushi Srivastava, Obul Reddy Bandapalli, Dagmara Dymerska
Publikováno v:
Journal of Personalized Medicine
Volume 11
Issue 4
Volume 11
Issue 4
Colorectal cancer (CRC) shows one of the largest proportions of familial cases among different malignancies, but only 5–10% of all CRC cases are linked to mutations in established predisposition genes. Thus, familial CRC constitutes a promising tar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e8afa3057f2a5d513e49588dbb205f
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/92391
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/92391
Autor:
Aayushi, Srivastava, Sara, Giangiobbe, Diamanto, Skopelitou, Beiping, Miao, Nagarajan, Paramasivam, Chiara, Diquigiovanni, Elena, Bonora, Kari, Hemminki, Asta, Försti, Obul Reddy, Bandapalli
Publikováno v:
Frontiers in Endocrinology
Familial inheritance in non-medullary thyroid cancer (NMTC) is an area that has yet to be adequately explored. Despite evidence suggesting strong familial clustering of non-syndromic NMTC, known variants still account for a very small percentage of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ebe1d2e0ab571b88d74d5bcdd00df098
https://pubmed.ncbi.nlm.nih.gov/33692755
https://pubmed.ncbi.nlm.nih.gov/33692755
Autor:
Aayushi, Srivastava, Beiping, Miao, Diamanto, Skopelitou, Varun, Kumar, Abhishek, Kumar, Nagarajan, Paramasivam, Elena, Bonora, Kari, Hemminki, Asta, Försti, Obul Reddy, Bandapalli
Publikováno v:
Cancers
Non-medullary thyroid cancer (NMTC) is a common endocrine malignancy with a genetic basis that has yet to be unequivocally established. In a recent whole-genome sequencing study of five families with occurrence of NMTCs, we shortlisted promising vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5db78eac21ecbe45754eb5c55300add
https://pubmed.ncbi.nlm.nih.gov/32492864
https://pubmed.ncbi.nlm.nih.gov/32492864