Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Miika Mehine"'
Autor:
Sangeetha Kandoi, Cassandra Martinez, Kevin Xu Chen, Miika Mehine, L Vinod K Reddy, Brian C Mansfield, Jacque L Duncan, Deepak A Lamba
Publikováno v:
eLife, Vol 12 (2024)
Retinitis pigmentosa (RP), a heterogenous group of inherited retinal disorder, causes slow progressive vision loss with no effective treatments available. Mutations in the rhodopsin gene (RHO) account for ~25% cases of autosomal dominant RP (adRP). I
Externí odkaz:
https://doaj.org/article/7450c3797a71493d85bdb55da0488e53
Autor:
Diana Mandelker, Antonio Marra, Nikita Mehta, Pier Selenica, Zarina Yelskaya, Ciyu Yang, Joshua Somar, Miika Mehine, Maksym Misyura, Olca Basturk, Alicia Latham, Maria Carlo, Michael Walsh, Zsofia K. Stadler, Kenneth Offit, Chaitanya Bandlamudi, Meera Hameed, Ping Chi, Jorge S. Reis-Filho, Ozge Ceyhan-Birsoy
Publikováno v:
npj Precision Oncology, Vol 7, Iss 1, Pp 1-6 (2023)
Abstract Traditional genetic testing for patients with gastrointestinal stromal tumors (GISTs) focus on those with syndromic features. To assess whether expanded genetic testing of GIST patients could identify hereditary cancer predisposition, we ana
Externí odkaz:
https://doaj.org/article/8ed49bc9d2174d23ac73af0621960d66
Autor:
Miika Mehine, Terhi Ahvenainen, Sara Khamaiseh, Jouni Härkönen, Siiri Reinikka, Tuomas Heikkinen, Anna Äyräväinen, Päivi Pakarinen, Päivi Härkki, Annukka Pasanen, Anna-Liisa Levonen, Ralf Bützow, Pia Vahteristo
Publikováno v:
Oncogenesis, Vol 11, Iss 1, Pp 1-10 (2022)
Abstract Uterine leiomyomas, or fibroids, are the most common tumors in women of reproductive age. Uterine leiomyomas can be classified into at least three main molecular subtypes according to mutations affecting MED12, HMGA2, or FH. FH-deficient lei
Externí odkaz:
https://doaj.org/article/199d3f3126b54a4fbad0c263ac974ff4
Autor:
Sami Belhadj, Aliya Khurram, Chaitanya Bandlamudi, Guillermo Palou-Márquez, Vignesh Ravichandran, Zoe Steinsnyder, Temima Wildman, Amanda Catchings, Yelena Kemel, Semanti Mukherjee, Benjamin Fesko, Kanika Arora, Miika Mehine, Sita Dandiker, Aalin Izhar, John Petrini, Susan Domchek, Katherine L. Nathanson, Jamie Brower, Fergus Couch, Zsofia Stadler, Mark Robson, Michael Walsh, Joseph Vijai, Michael Berger, Fran Supek, Rachid Karam, Sabine Topka, Kenneth Offit
Publikováno v:
Clinical Cancer Research. 29:422-431
Purpose: To explore the role of NBN as a pan-cancer susceptibility gene. Experimental Design: Matched germline and somatic DNA samples from 34,046 patients were sequenced using Memorial Sloan Kettering-Integrated Mutation Profiling of Actionable Canc
Autor:
Kanika Arora, Thinh N. Tran, Yelena Kemel, Miika Mehine, Ying L. Liu, Subhiksha Nandakumar, Shaleigh A. Smith, A. Rose Brannon, Irina Ostrovnaya, Konrad H. Stopsack, Pedram Razavi, Anton Safonov, Hira A. Rizvi, Matthew D. Hellmann, Joseph Vijai, Thomas C. Reynolds, James A. Fagin, Jian Carrot-Zhang, Kenneth Offit, David B. Solit, Marc Ladanyi, Nikolaus Schultz, Ahmet Zehir, Carol L. Brown, Zsofia K. Stadler, Debyani Chakravarty, Chaitanya Bandlamudi, Michael F. Berger
Publikováno v:
Cancer Discov
Accurate ancestry inference is critical for identifying genetic contributors of cancer disparities among populations. Although methods to infer genetic ancestry have historically relied upon genome-wide markers, the adaptation to targeted clinical se
Autor:
Vilja Jokinen, Miika Mehine, Siiri Reinikka, Sara Khamaiseh, Terhi Ahvenainen, Anna Äyräväinen, Päivi Härkki, Ralf Bützow, Annukka Pasanen, Pia Vahteristo
Publikováno v:
Genes, Chromosomes and Cancer. 62:27-38
Autor:
Michael F. Berger, Chaitanya Bandlamudi, Debyani Chakravarty, Zsofia K. Stadler, Carol L. Brown, Ahmet Zehir, Nikolaus Schultz, Marc Ladanyi, David B. Solit, Kenneth Offit, Jian Carrot-Zhang, James A. Fagin, Thomas C. Reynolds, Joseph Vijai, Matthew D. Hellmann, Hira A. Rizvi, Anton Safonov, Pedram Razavi, Konrad H. Stopsack, Irina Ostrovnaya, A. Rose Brannon, Shaleigh A. Smith, Subhiksha Nandakumar, Ying L. Liu, Miika Mehine, Yelena Kemel, Thinh N. Tran, Kanika Arora
Supplementary Figure from Genetic Ancestry Correlates with Somatic Differences in a Real-World Clinical Cancer Sequencing Cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25f537c0312ea4d4c178b97338c02ac3
https://doi.org/10.1158/2159-8290.22542027
https://doi.org/10.1158/2159-8290.22542027
Autor:
Michael F. Berger, Chaitanya Bandlamudi, Debyani Chakravarty, Zsofia K. Stadler, Carol L. Brown, Ahmet Zehir, Nikolaus Schultz, Marc Ladanyi, David B. Solit, Kenneth Offit, Jian Carrot-Zhang, James A. Fagin, Thomas C. Reynolds, Joseph Vijai, Matthew D. Hellmann, Hira A. Rizvi, Anton Safonov, Pedram Razavi, Konrad H. Stopsack, Irina Ostrovnaya, A. Rose Brannon, Shaleigh A. Smith, Subhiksha Nandakumar, Ying L. Liu, Miika Mehine, Yelena Kemel, Thinh N. Tran, Kanika Arora
Accurate ancestry inference is critical for identifying genetic contributors of cancer disparities among populations. Although methods to infer genetic ancestry have historically relied upon genome-wide markers, the adaptation to targeted clinical se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a0ff42c45d37323a5e274c7bb307c29
https://doi.org/10.1158/2159-8290.c.6549786.v1
https://doi.org/10.1158/2159-8290.c.6549786.v1
Autor:
Michael F. Berger, Chaitanya Bandlamudi, Debyani Chakravarty, Zsofia K. Stadler, Carol L. Brown, Ahmet Zehir, Nikolaus Schultz, Marc Ladanyi, David B. Solit, Kenneth Offit, Jian Carrot-Zhang, James A. Fagin, Thomas C. Reynolds, Joseph Vijai, Matthew D. Hellmann, Hira A. Rizvi, Anton Safonov, Pedram Razavi, Konrad H. Stopsack, Irina Ostrovnaya, A. Rose Brannon, Shaleigh A. Smith, Subhiksha Nandakumar, Ying L. Liu, Miika Mehine, Yelena Kemel, Thinh N. Tran, Kanika Arora
Supplementary Data from Genetic Ancestry Correlates with Somatic Differences in a Real-World Clinical Cancer Sequencing Cohort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::047cb47eac6510b37d505956dfd9093b
https://doi.org/10.1158/2159-8290.22542033.v1
https://doi.org/10.1158/2159-8290.22542033.v1
Autor:
Kenneth Offit, Sabine Topka, Rachid Karam, Fran Supek, Michael Berger, Joseph Vijai, Michael Walsh, Mark Robson, Zsofia Stadler, Fergus Couch, Jamie Brower, Katherine L. Nathanson, Susan Domchek, John Petrini, Aalin Izhar, Sita Dandiker, Miika Mehine, Kanika Arora, Benjamin Fesko, Semanti Mukherjee, Yelena Kemel, Amanda Catchings, Temima Wildman, Zoe Steinsnyder, Vignesh Ravichandran, Guillermo Palou-Márquez, Chaitanya Bandlamudi, Aliya Khurram, Sami Belhadj
Supplementary Figure S1. Germline and somatic data from The Cancer Genome Atlas (TCGA) project, representing 10,268 cancer patients with whole exome sequencing data.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::692cfa22cc2afd66084d69faebdf809c
https://doi.org/10.1158/1078-0432.22489497.v1
https://doi.org/10.1158/1078-0432.22489497.v1