Conxi Lazaro Garcia (Conxi Lázaro, Conxi Lázaro Garcia, Conxi Lazaro)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Topics

Breast Cancer Risk

Peripheral Nerve

Papillary Thyroid

Top Venues

European journal of human genetics : EJHG

JCO precision oncology

Journal of medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Cristina Fortuno, Bing-Jian Feng, Courtney Carroll, Giovanni Innella, Wendy K Kohlmann, Conxi Lazaro Garcia, Joan Brunet, Lidia Feliubadaló, Silvia Iglesias, Mireia Menéndez, Alex Teulé, Mandy L Ballinger, David M Thomas, Ainsley Campbell, Michael J Field, Marion Harris, Judy Kirk, Nicholas Pachter, Nicola K Poplawski, Rachel Susman, Katherine Tucker, Mathew J Wallis, Rachel Williams, Elisa Cops, David E Goldgar, null null, Paul A James, Amanda B Spurdle
Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum. JCO precision oncology 8 (2024)
Cristina Fortuno, Bing-Jian Feng, Courtney Carroll, Giovanni Innella, Wendy K Kohlmann, Conxi Lazaro Garcia, Joan Brunet, Lidia Feliubadaló, Silvia Iglesias, Mireia Menéndez, Alex Teulé, Mandy L Ballinger, David M Thomas, Ainsley Campbell, Michael J Field, Marion Harris, Judy Kirk, Nicholas Pachter, Nicola K Poplawski, Rachel Susman, Katherine Tucker, Mathew J Wallis, Rachel Williams, Elisa Cops, David E Goldgar, null null, Paul A James, Amanda B Spurdle
Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum. JCO precision oncology 8 (2024)
Cristina Fortuno, Bing-Jian Feng, Courtney Carroll, Giovanni Innella, Wendy K Kohlmann, Conxi Lazaro Garcia, Joan Brunet, Lidia Feliubadaló, Silvia Iglesias, Mireia Menéndez, Alex Teulé, Mandy L Ballinger, David M Thomas, Ainsley Campbell, Michael J Field, Marion Harris, Judy Kirk, Nicholas Pachter, Nicola K Poplawski, Rachel Susman, Katherine Tucker, Mathew J Wallis, Rachel Williams, Elisa Cops, David E Goldgar, null null, Paul A James, Amanda B Spurdle
Cancer Risks Associated With TP53 Pathogenic Variants: Maximum Likelihood Analysis of Extended Pedigrees for Diagnosis of First Cancers Beyond the Li-Fraumeni Syndrome Spectrum. JCO precision oncology 8 (2024)
Lenka Stolarova, Petra Kleiblova, Petra Zemankova, Barbora Stastna, Marketa Janatova, Jana Soukupova, Maria Isabel Waddington Achatz, Christine B Ambrosone, Paraskevi Apostolou, Banu K Arun, Paul L Auer, Mollie E Barnard, Birgitte Bertelsen, null null, Marinus J Blok, Nicholas J Boddicker, Joan Brunet, Elizabeth S Burnside, Mariarosaria Calvello, Ian G Campbell, Sock Hoai Chan, Fei Chen, Jian Bang Chiang, Anna Coppa, Laura Cortesi, Ana Crujeiras-González, null null, Kim De Leeneer, Robin de Putter, Allison DePersia, Lisa Devereux, Susan M Domchek, Anna Efremidis, Christoph Engel, Corinna Ernst, Dafydd Gareth Evans, Lidia Feliubadaló, Florentia Fostira, Olivia Fuentes-Ríos, Encarna B Gómez-García, Sara González, Christopher A Haiman, Thomas Van Overeem Hansen, Jan Hauke, James M Hodge, Chunling Hu, Hongyan Huang, Nur Diana Binte Ishak, Yusuke Iwasaki, Irene Konstantopoulou, Peter Kraft, James V Lacey, Conxi Lazaro Garcia, Na Li, Weng Khong Lim, Sara Lindström, Adriana Lori, María Elena Martínez, Alexandra Martins, Koichi Matsuda, Giuseppe Matullo, Simone McInerny, Kyriaki Michailidou, Marco Montagna, Alvaro N A Monteiro, Luigi Mori, Katherine L Nathanson, Susan L Neuhausen, Heli Nevanlinna, Janet E Olson, Julie R Palmer, Barbara Pasini, Alpa V Patel, Maria Piane, Bruce Poppe, Paolo Radice, Alessandra Renieri, Nicoletta Resta, Marcy E Richardson, Toon Rosseel, Kathryn J Ruddy, Marta Santamariña, Elizabeth Santana Dos Santos, Lauren R Teras, Amanda Ewart Toland, Amy Trentham-Dietz, Celine M Vachon, Alexander E Volk, Nana Weber-Lassalle, Jeffrey N Weitzel, Lisa Wiesmuller, Stacey J Winham, Siddhartha Yadav, Drakoulis Yannoukakos, Song Yao, Valentina Zampiga, Magnus Zethoven, Ze Wen Zhang, Tomáš Zima, Amanda B Spurdle, Ana Vega, Maria Rossing, Jesús Del Valle, Arcangela De Nicolo, Eric Hahnen, Kathleen B M Claes, Joanne Ngeow Yuen Yie, Yukihide Momozawa, Paul A James, Fergus J Couch, Libor Macůrek, Zdenek Kleibl
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk. Clinical cancer research : an official journal of the American Association for Cancer Research (2023)
Edgar Creus-Bachiller, Juana Fernández-Rodríguez, Miriam Magallón-Lorenz, Sara Ortega-Bertran, Susana Navas-Rutete, Cleofe Romagosa, Tulio M Silva, Maria Pané Foix, Anna Estival, Diana Perez Sidelnikova, Mireia Morell, Helena Mazuelas, Meritxell Carrió, Tereza Lausová, David Reuss, Bernat Gel, Alberto Villanueva, Eduard Serra, Conxi Lazaro Garcia
Expanding a precision medicine platform for malignant peripheral nerve sheath tumors: new patient-derived orthotopic xenografts, cell lines and tumor entities. Molecular oncology (2023)
Juana Fernández-Rodríguez, Edgar Creus-Bachiller, Xiaohu Zhang, Maria Martinez-Iniesta, Sara Ortega-Bertran, Rajarashi Guha, Craig J Thomas, Margaret R Wallace, Cleofe Romagosa, Lourdes Salazar-Huayna, Karlyne M Reilly, Jaishri O Blakely, Jordi Serra-Musach, Miguel Angel Pujana, Eduard Serra, Alberto Villanueva, Marc Ferrer, Conxi Lazaro Garcia
A High-Throughput Screening Platform Identifies Novel Combination Treatments for Malignant Peripheral Nerve Sheath Tumors. Molecular cancer therapeutics 21 (7) (2022)
Belen Garcia, Nuria Catasus, Andrea Ros, Inma Rosas, Alejandro Negro, Mercedes Guerrero-Murillo, Ana Maria Valero, Anna Duat-Rodriguez, Juan Luis Becerra, Sandra Bonache, Conxi Lazaro Garcia, Carmina Comas, Isabel Bielsa, Eduard Serra, Concepción Hernández-Chico, Yolanda Martin, Elisabeth Castellanos, Ignacio Blanco
Neurofibromatosis type 1 families with first-degree relatives harbouring distinct <i>NF1</i> pathogenic variants. Genetic counselling and familial diagnosis: what should be offered? Journal of medical genetics 59 (10) (2022)
Francesca Mateo, Zhengcheng He, Lin Mei, Gorka Ruiz de Garibay, Carmen Herranz, Nadia García, Amanda Lorentzian, Alexandra Baiges, Eline Blommaert, Antonio Gómez, Oriol Mirallas, Anna Garrido-Utrilla, Luis Palomero, Roderic Espín, Ana I Extremera, M Teresa Soler-Monsó, Anna Petit, Rong Li, Joan Brunet, Ke Chen, Susanna Tan, Connie J Eaves, Curtis McCloskey, Razq Hakem, Rama Khokha, Philipp F Lange, Conxi Lazaro Garcia, Christopher A Maxwell, Miguel Angel Pujana
Modification of BRCA1-associated breast cancer risk by HMMR overexpression. Nature communications 13 (1) (2022)
Eileen O Dareng, Jonathan P Tyrer, Daniel R Barnes, Michelle R Jones, Xin Yang, Katja K H Aben, Muriel A Adank, Simona Agata, Irene L Andrulis, Hoda Anton-Culver, Natalia N Antonenkova, Gerasimos Aravantinos, Banu K Arun, Annelie Augustinsson, Judith Balmaña, Elisa V Bandera, Rosa B Barkardottir, Daniel Barrowdale, Matthias W Beckmann, Alicia Beeghly-Fadiel, Javier Benitez, Marina Bermisheva, Marcus Q Bernardini, Line Bjorge, Amanda Black, Natalia V Bogdanova, Bernardo Bonanni, Ake Borg, James D Brenton, Agnieszka Budzilowska, Ralf Bützow, Saundra S Buys, Hui Cai, Maria A Caligo, Ian G Campbell, Rikki Cannioto, Hayley Cassingham, Jenny Chang-Claude, Stephen J Chanock, Kexin Chen, Yoke-Eng Chiew, Wendy K Chung, Kathleen B M Claes, Sarah Colonna, null null, null null, null null, Linda S Cook, Fergus J Couch, Mary B Daly, Fanny Dao, Eleanor Davies, Miguel de la Hoya, Robin de Putter, Joe G Dennis, Allison DePersia, Peter Devilee, Orland Diez, Yuan Chun Ding, Jennifer A Doherty, Susan M Domchek, Thilo Dörk, Andreas du Bois, Matthias Dürst, Diana M Eccles, Heather A Eliassen, Christoph Engel, Gareth D Evans, Peter A Fasching, James M Flanagan, Renée T Fortner, Eva Macháčková, Eitan Friedman, Patricia A Ganz, Judy Garber, Francesca Gensini, Graham G Giles, Gord Glendon, Andrew K Godwin, Marc T Goodman, Mark H Greene, Jacek Gronwald, null null, null null, Eric Hahnen, Christopher A Haiman, Niclas Håkansson, Ute Hamann, Thomas V O Hansen, Holly R Harris, Mikael Hartman, Florian Heitz, Michelle A T Hildebrandt, Estrid Høgdall, Claus K Høgdall, John L Hopper, Ruea-Yea Huang, Chad Huff, Peter J Hulick, David G Huntsman, Evgeny N Imyanitov, null null, null null, Claudine Isaacs, Anna Jakubowska, Paul A James, Ramunas Janavicius, Allan Jensen, Oskar Th Johannsson, Esther M John, Michael E Jones, Daehee Kang, Beth Y Karlan, Anthony Karnezis, Linda E Kelemen, Elza Khusnutdinova, Lambertus A L M Kiemeney, Byoung-Gie Kim, Susanne K Kjaer, Ian Komenaka, Jolanta Kupryjanczyk, Allison W Kurian, Ava Kwong, Diether Lambrechts, Melissa C Larson, Conxi Lazaro Garcia, Nhu D Le, Goska Leslie, Jenny Lester, Fabienne Lesueur, Douglas A Levine, Lian Li, Jingmei Li, Jennifer T Loud, Karen H Lu, Jan Lubiński, Phuong L Mai, Siranoush Manoukian, Jeffrey R Marks, Rayna Kim Matsuno, Keitaro Matsuo, Taymaa May, Lesley McGuffog, John R McLaughlin, Iain A McNeish, Noura Mebirouk, Usha Menon, Austin Miller, Jonathan Beesley, Albina Minlikeeva, Francesmary Modugno, Marco Montagna, Kirsten B Moysich, Elizabeth Munro, Katherine L Nathanson, Susan L Neuhausen, Heli Nevanlinna, Joanne Ngeow Yuen Yie, Henriette Roed Nielsen, Finn C Nielsen, Liene Nikitina-Zake, Kunle Odunsi, Kenneth Offit, Edith Olah, Siel Olbrecht, Olufunmilayo I Olopade, Sara H Olson, Håkan Olsson, Ana Osorio, Laura Papi, Sue-Kyung Park, Michael T Parsons, Harsha Pathak, Inge Sokilde Pedersen, Ana Peixoto, Tanja Pejovic, Pedro Perez-Segura, Jennifer B Permuth, Beth N Peshkin, Paolo Peterlongo, Anna Piskorz, Darya Prokofyeva, Paolo Radice, Johanna Rantala, Marjorie J Riggan, Harvey A Risch, Cristina Rodriguez-Antona, Eric A Ross, Mary Anne Rossing, Ingo Runnebaum, Dale R Sandler, Marta Santamariña, Penny Soucy, Rita K Schmutzler, V Wendy Setiawan, Kang Shan, Weiva Sieh, Jacques Simard, Christian F Singer, Anna P Sokolenko, Honglin Song, Melissa C Southey, Helen Steed, Dominique Stoppat-Lyonnet, Rebecca Sutphen, Anthony J Swerdlow, Yen Yen Tan, Manuel R Teixeira, Soo-Hwang Teo, Kathryn L Terry, Mary Beth Terry, null null, null null, Mads Thomassen, Pamela J Thompson, Liv Cecilie Vestrheim Thomsen, Darcy L Thull, Marc Tischkowitz, Linda Titus, Amanda Ewart Toland, Diana Torres, Britton Trabert, Ruth C Travis, Nadine Tung, Shelley T Tworoger, Ellen Valen, Anne M van Altena, Annemieke H van der Hout, Els Van Nieuwenhuysen, Elizabeth J vanRensburg, Ana Vega, Digna Velez Edwards, Robert A Vierkant, Frances Wang, Barbara Wappenschmidt, Penelope M Webb, Clarice R Weinberg, Jeffrey N Weitzel, Nicolas Wentzensen, Emily White, Alice S Whittemore, Stacey J Winham, Alicja Wolk, Yin-Ling Woo, Anna H Wu, Li Yan, Drakoulis Yannoukakos, Katia M Zavaglia, Wei Zheng, Argyrios Ziogas, Kristin K Zorn, Zdenek Kleibl, Douglas F Easton, Kate Lawrenson, Anna De Fazio, Thomas A Sellers, Susan J Ramus, Celeste L Pearce, Alvaro N A Monteiro, Julie M Cunningham, Ellen L Goode, Joellen M Schildkraut, Andrew Berchuck, Georgia Chenevix-Trench, Simon A Gayther, Antonis C Antoniou, Paul David Peter Pharoah
Polygenic risk modeling for prediction of epithelial ovarian cancer risk. European journal of human genetics : EJHG 30 (3) (2022)
Christopher Hakkaart, John F Pearson, Louise Marquart, Joe G Dennis, George A R Wiggins, Daniel R Barnes, Bridget A Robinson, Peter D Mace, Kristiina Aittomäki, Irene L Andrulis, Banu K Arun, Jacopo Azzollini, Judith Balmaña, Rosa B Barkardottir, Sami Belhadj, Lieke Berger, Marinus J Blok, Susanne E Boonen, Julika Borde, Angela R Bradbury, Joan Brunet, Saundra S Buys, Maria A Caligo, Ian G Campbell, Wendy K Chung, Kathleen B M Claes, null null, null null, Marie-Agnès Collonge-Rame, Jackie Cook, Casey Cosgrove, Fergus J Couch, Mary B Daly, Sita Dandiker, Rosemarie Davidson, Miguel de la Hoya, Robin de Putter, Capucine Delnatte, Mallika Dhawan, Orland Diez, Yuan Chun Ding, Susan M Domchek, Alan Donaldson, Jacqueline Eason, Douglas F Easton, Hans Ehrencrona, Christoph Engel, D Gareth Evans, Ulrike Faust, Lidia Feliubadaló, Florentia Fostira, Eitan Friedman, Megan Frone, Debra Frost, Judy Garber, Simon A Gayther, Andrea Gehrig, Paul Gesta, Andrew K Godwin, David E Goldgar, Mark H Greene, Eric Hahnen, Christopher R Hake, Ute Hamann, Thomas V O Hansen, Jan Hauke, Julia Hentschel, Natalie Herold, Ellen Honisch, Peter J Hulick, Evgeny N Imyanitov, null null, null null, null null, Claudine Isaacs, Louise Izatt, Angel Izquierdo, Anna Jakubowska, Paul A James, Ramunas Janavicius, Esther M John, Joseph Vijai, Beth Y Karlan, Zoe Kemp, Judy Kirk, Irene Konstantopoulou, Marco Koudijs, Ava Kwong, Yael Laitman, Fiona Lalloo, Christine Lasset, Charlotte Lautrup, Conxi Lazaro Garcia, Clémentine Legrand, Goska Leslie, Fabienne Lesueur, Phuong L Mai, Siranoush Manoukian, Véronique Mari, John W M Martens, Lesley McGuffog, Noura Mebirouk, Alfons Meindl, Austin Miller, Marco Montagna, Lidia Moserle, Emmanuelle Mouret-Fourme, Hannah Musgrave, Sophie Nambot, Katherine L Nathanson, Susan L Neuhausen, Heli Nevanlinna, Joanne Ngeow Yuen Yie, Tu Nguyen-Dumont, Liene Nikitina-Zake, Kenneth Offit, Edith Olah, Olufunmilayo I Olopade, Ana Osorio, Claus-Eric Ott, Sue-Kyung Park, Michael T Parsons, Inge Sokilde Pedersen, Ana Peixoto, Pedro Perez-Segura, Paolo Peterlongo, Timea Pocza, Paolo Radice, Juliane Ramser, Johanna Rantala, Gustavo C Rodriguez, Karina Rønlund, Efraim H Rosenberg, Maria Rossing, Rita K Schmutzler, Payal D Shah, Saba Sharif, Priyanka Sharma, Lucy E Side, Jacques Simard, Christian F Singer, Katie Snape, Doris Steinemann, Dominique Stoppa-Lyonnet, Christian Sutter, Yen Yen Tan, Manuel R Teixeira, Soo-Hwang Teo, Mads Thomassen, Darcy L Thull, Marc Tischkowitz, Amanda Ewart Toland, Alison H Trainer, Vishakha Tripathi, Nadine Tung, Klaartje van Engelen, Elizabeth J vanRensburg, Ana Vega, Alessandra Viel, Lisa Walker, Jeffrey N Weitzel, Marijke R Wevers, Georgia Chenevix-Trench, Amanda B Spurdle, Antonis C Antoniou, Logan C Walker
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers. Communications biology 5 (1) (2022)
Paula Rofes, Álex Teulé, Lidia Feliubadaló, Mònica Salinas, Raquel Cuesta, Sílvia Iglesias, Olga Campos, Sara González, Gabriel Capellá, Joan Brunet, Jesús Del Valle, Conxi Lazaro Garcia
Mosaicism in PTEN-new case and comment on the literature. European journal of human genetics : EJHG 30 (6) (2022)
Pilar Mur, Lorena Magraner-Pardo, Sandra García-Mulero, Anna Díez-Villanueva, Jesús Del Valle, Elsa Ezquerro, Conxi Lazaro Garcia, Gabriel Capellá Munar, Victor Moreno, Rebeca Sanz-Pamplona, Tirso Pons, Laura Valle
Solving the enigma of POLD1 p.V295M as a potential cause of increased cancer risk. European journal of human genetics : EJHG (2021)
Núria Catasús, Belen Garcia, Iván Galván-Femenía, Adrià Plana, Alejandro Negro, Inma Rosas, Andrea Ros, Emilio Amilibia, Juan Luis Becerra, Cristina Hostalot, Francesc Rocaribas, Isabel Bielsa, Conxi Lazaro Garcia, Rafael de Cid, Eduard Serra, Ignacio Blanco, Elisabeth Castellanos, null null
Revisiting the UK Genetic Severity Score for NF2: a proposal for the addition of a functional genetic component. Journal of medical genetics (2021)
Jacopo Boni, Aida Idani, Carla Roca, Lidia Feliubadaló, Eva Tomiak, Evan Weber, William D Foulkes, Alexandre Orthwein, Zaki El Haffaf, Conxi Lazaro Garcia, Barbara Rivera
A decade of RAD51C and RAD51D germline variants in cancer. Human mutation 43 (3) (2021)
Mariona Terradas, Pilar Mur, Sami Belhadj, Emma Roisin Woodward, George Joseph Burghel, Pau M Muñoz-Torres, Isabel Quintana, Matilde Navarro, Joan Brunet, Conxi Lazaro Garcia, Marta Pineda, Victor Moreno, Gabriel Capellá Munar, Dafydd Gareth Evans, Laura Valle
TP53, a gene for colorectal cancer predisposition in the absence of Li-Fraumeni-associated phenotypes. Gut 70 (6) (2020)
Taru A Muranen, Sofia Khan, Rainer Fagerholm, Kristiina Aittomäki, Julie M Cunningham, Joe G Dennis, Goska Leslie, Lesley McGuffog, Michael T Parsons, Jacques Simard, Susan Slager, Penny Soucy, Douglas F Easton, Marc Tischkowitz, Amanda B Spurdle, null null, Rita K Schmutzler, Barbara Wappenschmidt, Eric Hahnen, Maartje J Hooning, null null, Christian F Singer, Gabriel Wagner, Mads Thomassen, Inge Sokilde Pedersen, Susan M Domchek, Katherine L Nathanson, Conxi Lazaro Garcia, Caroline Maria Rossing, Irene L Andrulis, Manuel R Teixeira, Paul A James, Judy Garber, Jeffrey N Weitzel, null null, Anna Jakubowska, Drakoulis Yannoukakos, Esther M John, Melissa C Southey, Marjanka K Schmidt, Antonis C Antoniou, Georgia Chenevix-Trench, Carl Blomqvist, Heli Nevanlinna
Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer. NPJ breast cancer 6 (2020)
José Marcos Moreno-Cabrera, Jesús Del Valle, Lidia Feliubadaló, Marta Pineda, Sara González, Olga Campos, Raquel Cuesta, Joan Brunet, Eduard Serra, Gabriel Capellà, Bernat Gel, Conxi Lazaro Garcia
Screening of CNVs using NGS data improves mutation detection yield and decreases costs in genetic testing for hereditary cancer. Journal of medical genetics (2020)
José Marcos Moreno-Cabrera, Jesús Del Valle, Elisabeth Castellanos, Lidia Feliubadaló, Marta Pineda, Joan Brunet, Eduard Serra, Gabriel Capellà, Conxi Lazaro Garcia, Bernat Gel
Evaluation of CNV detection tools for NGS panel data in genetic diagnostics. European journal of human genetics : EJHG 28 (12) (2020)
Juana Fernández-Rodríguez, Andrés Morales La Madrid, Bernat Gel, Alicia Castañeda Heredia, Héctor Salvador, María Martínez-Iniesta, Catia Moutinho, Jordi Morata, Holger Heyn, Ignacio Blanco, Edgar Creus-Bachiller, Gabriel Capella, Lourdes Farré, August Vidal, Francisco Soldado, Lucas Krauel, Mariona Suñol, Eduard Serra, Alberto Villanueva, Conxi Lazaro Garcia
Use of patient derived orthotopic xenograft models for real-time therapy guidance in a pediatric sporadic malignant peripheral nerve sheath tumor. Therapeutic advances in medical oncology 12 (2020)
Pilar Mur, Ann-Sofie Jemth, Luka Bevc, Nuno Amaral, Matilde Navarro, Rafael Valdés-Mas, Tirso Pons, Gemma Aiza, Miguel Urioste, Alfonso Valencia, Conxi Lazaro Garcia, Victor Moreno, Xose S Puente, Pål Stenmark, Ulrika Warpman-Berglund, Gabriel Capellá Munar, Thomas Helleday, Laura Valle
Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis. Human mutation 39 (9) (2018)