Výsledky vyhledávání - Rodrigo Gularte‐Mérida

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  1. 1
    Recurrent<i>MED12</i>exon 2 mutations in benign breast fibroepithelial lesions in adolescents and young adults

    Recurrent<i>MED12</i>exon 2 mutations in benign breast fibroepithelial lesions in adolescents and young adults Autor Fresia Pareja, Arnaud Da Cruz Paula, Melissa P. Murray, Timothy Hoang, Rodrigo Gularte‐Mérida, David Brown, Edaise M. da Silva, Ana Paula Martins Sebastião, Dilip D. Giri, Britta Weigelt, Jorge S. Reis‐Filho, Edi Brogi

    Vydáno 2018
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  2. 2
    Solid papillary breast carcinomas resembling the tall cell variant of papillary thyroid neoplasms (solid papillary carcinomas with reverse polarity) harbour recurrent mutations affecting <i><scp>IDH</scp>2</i> and <i><scp>PIK</scp>3<scp>CA</scp></i>: a validation cohort

    Solid papillary breast carcinomas resembling the tall cell variant of papillary thyroid neoplasms (solid papillary carcinomas with reverse polarity) harbour recurrent mutations aff... Autor John R. Lozada, Thais Basili, Fresia Pareja, Bárbara Alemar, Arnaud Da Cruz Paula, Rodrigo Gularte‐Mérida, Dilip D. Giri, Patricia Querzoli, Gábor Cserni, Emad A. Rakha, Maria Pia Foschini, Jorge S. Reis‐Filho, Edi Brogi, Britta Weigelt, Felipe C. Geyer

    Vydáno 2018
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  3. 3
    <i>MYBL1</i> rearrangements and <i>MYB</i> amplification in breast adenoid cystic carcinomas lacking the <i>MYB</i>–<i>NFIB</i> fusion gene

    <i>MYBL1</i> rearrangements and <i>MYB</i> amplification in breast adenoid cystic carcinomas lacking the <i>MYB</i>–<i>NFIB</i> fusion gene Autor Jisun Kim, Felipe C. Geyer, Luciano G. Martelotto, Charlotte K.Y. Ng, Raymond S. Lim, Pier Selenica, Anqi Li, Fresia Pareja, Nicola Fusco, Marcia Edelweiss, Rahul Kumar, Rodrigo Gularte‐Mérida, Andre Neil Forbes, Ekta Khurana, Odette Mariani, Sunil Badve, Anne Vincent‐Salomon, Larry Norton, Jorge S. Reis‐Filho, Britta Weigelt

    Vydáno 2017
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  4. 4
    Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing

    Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing Autor Timour Baslan, Jude Kendall, Konstantin Volyanskyy, Katherine McNamara, Hilary Cox, Sean D'Italia, Frank Ambrosio, M Riggs, Linda Rodgers, Anthony Leotta, Junyan Song, Yong Mao, Jie Wu, Ronak Shah, Rodrigo Gularte‐Mérida, Kalyani Chadalavada, Gouri J. Nanjangud, Vinay Varadan, Assaf Gordon, Christina Curtis, A. Krasnitz, Nevenka Dimitrova, Lyndsay N. Harris, Michael Wigler, James Hicks

    Vydáno 2020
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  5. 5
    The Genomic Landscape of Mucinous Breast Cancer

    The Genomic Landscape of Mucinous Breast Cancer Autor Fresia Pareja, Ju Youn Lee, David Brown, Salvatore Piscuoglio, Rodrigo Gularte‐Mérida, Pier Selenica, Arnaud Da Cruz Paula, Sasi Arunachalam, Rahul Kumar, Felipe C. Geyer, Catarina Silveira, Edaise M. da Silva, Anqi Li, Caterina Marchiò, Charlotte K.Y. Ng, Odette Mariani, Laetitia Fuhrmann, Hannah Y. Wen, Larry Norton, Anne Vincent‐Salomon, Edi Brogi, Jorge S. Reis‐Filho, Britta Weigelt

    Vydáno 2018
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  6. 6
    PAX8–GLIS3 gene fusion is a pathognomonic genetic alteration of hyalinizing trabecular tumors of the thyroid

    PAX8–GLIS3 gene fusion is a pathognomonic genetic alteration of hyalinizing trabecular tumors of the thyroid Autor Caterina Marchiò, Arnaud Da Cruz Paula, Rodrigo Gularte‐Mérida, Thais Basili, Alissa Brandes, Edaise M. da Silva, Catarina Silveira, Lorenzo Ferrando, Jasna Metović, Francesca Maletta, Laura Annaratone, Fresia Pareja, Brian P. Rubin, Aaron P. Hoschar, Gaetano De Rosa, Stefano La Rosa, Massimo Bongiovanni, Bibianna Purgina, Simonetta Piana, Marco Volante, Britta Weigelt, Jorge S. Reis‐Filho, Mauro Papotti

    Vydáno 2019
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  7. 7
    Identification of recurrent FHL2-GLI2 oncogenic fusion in sclerosing stromal tumors of the ovary

    Identification of recurrent FHL2-GLI2 oncogenic fusion in sclerosing stromal tumors of the ovary Autor Sarah H. Kim, Arnaud Da Cruz Paula, Thais Basili, Higinio Dopeso, Rui Bi, Fresia Pareja, Edaise M. da Silva, Rodrigo Gularte‐Mérida, Zhen Sun, Sho Fujisawa, Caitlin G. Smith, Lorenzo Ferrando, Ana Paula Martins Sebastião, Yonina Bykov, Anqi Li, Catarina Silveira, Charles Ashley, Anthe A. Stylianou, Pier Selenica, Wesley Samore, Achim A. Jungbluth, Dmitriy Zamarin, Nadeem R. Abu‐Rustum, Kristian Helin, Robert A. Soslow, Jorge S. Reis‐Filho, Esther Oliva, Britta Weigelt

    Vydáno 2020
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  8. 8
    Loss-of-function mutations in ATP6AP1 and ATP6AP2 in granular cell tumors

    Loss-of-function mutations in ATP6AP1 and ATP6AP2 in granular cell tumors Autor Fresia Pareja, Alissa Brandes, Thais Basili, Pier Selenica, Felipe C. Geyer, Dan Fan, Arnaud Da Cruz Paula, Rahul Kumar, David Brown, Rodrigo Gularte‐Mérida, Bárbara Alemar, Rui Bi, Raymond S. Lim, Ino de Bruijn, Sho Fujisawa, Rui Gardner, Elvin Feng, Anqi Li, Edaise M. da Silva, John R. Lozada, Pedro Blecua, Leona Cohen‐Gould, Achim A. Jungbluth, Emad A. Rakha, Ian O. Ellis, Maria I. Edelweiss, Juan Palazzo, Larry Norton, Travis J. Hollmann, Marcia Edelweiss, Brian P. Rubin, Britta Weigelt, Jorge S. Reis‐Filho

    Vydáno 2018
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  9. 9
    Clinical sequencing of soft tissue and bone sarcomas delineates diverse genomic landscapes and potential therapeutic targets

    Clinical sequencing of soft tissue and bone sarcomas delineates diverse genomic landscapes and potential therapeutic targets Autor Benjamin A. Nacev, Francisco Sánchez-Vega, Shaleigh Smith, Cristina R. Antonescu, Evan Rosenbaum, Hongyu Shi, Cerise Tang, Nicholas D. Socci, Satshil Rana, Rodrigo Gularte‐Mérida, Ahmet Zehir, Mrinal M. Gounder, Timothy G. Bowler, Anisha Luthra, Bhumika Jadeja, Azusa Okada, Jonathan A. Strong, Jake Stoller, Jason E. Chan, Ping Chi, Sandra P. D’Angelo, Mark A. Dickson, Ciara M. Kelly, Mary Louise Keohan, Sujana Movva, Katherine A. Thornton, Paul A. Meyers, Leonard H. Wexler, Emily K. Slotkin, Julia Glade Bender, Neerav Shukla, Martee L. Hensley, John H. Healey, Michael P. LaQuaglia, Kaled M. Alektiar, Aimeé M. Crago, Sam S. Yoon, Brian R. Untch, Sarah Chiang, Narasimhan P. Agaram, Meera Hameed, Michael F. Berger, David B. Solit, Nikolaus Schultz, Marc Ladanyi, Samuel Singer, William D. Tap

    Vydáno 2022
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  10. 10
    Homologous recombination DNA repair defects in PALB2-associated breast cancers

    Homologous recombination DNA repair defects in PALB2-associated breast cancers Autor Anqi Li, Felipe C. Geyer, Pedro Blecua, Ju Youn Lee, Pier Selenica, David Brown, Fresia Pareja, Simon S. K. Lee, Rahul Kumar, Bárbara Rivera, Rui Bi, Salvatore Piscuoglio, Hannah Y. Wen, John R. Lozada, Rodrigo Gularte‐Mérida, Luca Cavallone, Zoulikha Rezoug, Tú Nguyen‐Dumont, Paolo Peterlongo, Carlo Tondini, Thorkild Terkelsen, Karina Rønlund, Susanne E. Boonen, Arto Mannerma, Robert Winqvist, Markéta Janatová, Pathmanathan Rajadurai, Bing Xia, Larry Norton, Mark E. Robson, Pei-Sze Ng, Lai‐Meng Looi, Melissa C. Southey, Britta Weigelt, Teo Soo-Hwang, Marc Tischkowitz, William D. Foulkes, Jorge S. Reis‐Filho, Morteza Aghmesheh, David J. Amor, Leslie Andrews, Yoland Antill, Rosemary L. Balleine, Jonathan Beesley, Anneke C. Blackburn, Michael Bogwitz, Matthew A. Brown, Matthew Burgess, Jo Burke, Phyllis Butow, Liz Caldon, Ian Campbell, Alice Christian, Christine L. Clarke, Paul A. Cohen, Ashley Crook, James Cui, Margaret C. Cummings, Sarah‐Jane Dawson, Anna de Fazio, Martin B. Delatycki, Alexander Dobrovic, Tracy Dudding, Pascal H. G. Duijf, Edward Edkins, Stacey L. Edwards, Gelareh Farshid, Andrew Fellows, Michael Field, James M. Flanagan, Peter C.C. Fong, John Forbes, Laura Forrest, Stephen B. Fox, Juliet D. French, Michael Friedlander, David Gallego‐Ortega, Michael Gattas, Graham G. Giles, Grantley Gill, Margaret Gleeson, Sian Greening, Eric Haan, Marion Harris, Nicholas K. Hayward, Ian B. Hickie, John L. Hopper, Clare Hunt, Paul A. James, Mark A. Jenkins, Richard Kefford, Maira Kentwell, Judy Kirk, James Kollias, Sunil R. Lakhani, Geoffrey J. Lindeman, Lara Lipton, Lizz Lobb, Sheau Wen Lok, Finlay Macrea

    Vydáno 2019
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