Cinzia Lavarino

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 21

Top Topics

Advanced Non Small Cell Lung Cancer

Sentinel Lymph Node

Tyrosine Kinase

Top Venues

Cancer discovery

American journal of medical genetics. Part A

Orphanet journal of rare diseases

JCO precision oncology

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

Publications

Nicole Revencu, Astrid Eijkelenboom, Claire Bracquemart, Pia Alhopuro, Judith Armstrong, Eulalia Baselga, Claudia Cesario, Maria Lisa Dentici, Melanie Eyries, Sofia Frisk, Helena Gásdal Karstensen, Nagore Gene-Olaciregui, Sirpa Kivirikko, Cinzia Lavarino, Inger-Lise Mero, Rodolphe Michiels, Elisa Pisaneschi, Bitten Schönewolf-Greulich, Ilse Wieland, Martin Zenker, Miikka Vikkula
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA. Orphanet journal of rare diseases 19 (1) (2024)
Mònica Sánchez-Guixé, Ferran Muinos, Morena Pinheiro-Santin, Victor Gonzalez-Huici, Carlos J Rodriguez-Hernandez, Alexandra Avgustinova, Cinzia Lavarino, Nuria Lopez-Bigas, Jaume Catala-Mora, Núria López-Bigas
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues. Cancer discovery 14 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Mònica Sánchez-Guixé, Ferran Muinos, Morena Pinheiro-Santin, Victor Gonzalez-Huici, Carlos J Rodriguez-Hernandez, Alexandra Avgustinova, Cinzia Lavarino, Nuria Lopez-Bigas, Jaume Catala-Mora, Núria López-Bigas
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues. Cancer discovery (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Mònica Sánchez-Guixé, Ferran Muinos, Morena Pinheiro-Santin, Victor Gonzalez-Huici, Carlos J Rodriguez-Hernandez, Alexandra Avgustinova, Cinzia Lavarino, Nuria Lopez-Bigas, Jaume Catala-Mora, Núria López-Bigas
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues. Cancer discovery 14 (6) (2024)
Mònica Sánchez-Guixé, Ferran Muinos, Morena Pinheiro-Santin, Victor Gonzalez-Huici, Carlos J Rodriguez-Hernandez, Alexandra Avgustinova, Cinzia Lavarino, Nuria Lopez-Bigas, Jaume Catala-Mora, Núria López-Bigas
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues. Cancer discovery (2024)
Mònica Sánchez-Guixé, Ferran Muinos, Morena Pinheiro-Santin, Victor Gonzalez-Huici, Carlos J Rodriguez-Hernandez, Alexandra Avgustinova, Cinzia Lavarino, Nuria Lopez-Bigas, Jaume Catala-Mora, Núria López-Bigas
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues. Cancer discovery 14 (6) (2024)
Mònica Sánchez-Guixé, Ferran Muinos, Morena Pinheiro-Santin, Victor Gonzalez-Huici, Carlos J Rodriguez-Hernandez, Alexandra Avgustinova, Cinzia Lavarino, Nuria Lopez-Bigas, Jaume Catala-Mora, Núria López-Bigas
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues. Cancer discovery 14 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A 194 (6) (2024)
Nicole Revencu, Astrid Eijkelenboom, Claire Bracquemart, Pia Alhopuro, Judith Armstrong, Eulalia Baselga, Claudia Cesario, Maria Lisa Dentici, Melanie Eyries, Sofia Frisk, Helena Gásdal Karstensen, Nagore Gene-Olaciregui, Sirpa Kivirikko, Cinzia Lavarino, Inger-Lise Mero, Rodolphe Michiels, Elisa Pisaneschi, Bitten Schönewolf-Greulich, Ilse Wieland, Martin Zenker, Miikka Vikkula
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA. Orphanet journal of rare diseases 19 (1) (2024)
Mònica Sánchez-Guixé, Ferran Muinos, Morena Pinheiro-Santin, Victor Gonzalez-Huici, Carlos J Rodriguez-Hernandez, Alexandra Avgustinova, Cinzia Lavarino, Nuria Lopez-Bigas, Jaume Catala-Mora, Núria López-Bigas
Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues. Cancer discovery 14 (6) (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Martina De Bortoli, Marta Ivars, Nicole Revencu, Marie-Cécile Nassogne, Cinzia Lavarino, Sonia Paco, Martin M Y Lammens, Anne Renders, Dana Dumitriu, Raphaël Helaers, Laurence M Boon, Eulalia Baselga, Miikka Vikkula
Epilepsy with faint capillary malformation or reticulated telangiectasia associated with mosaic AKT3 pathogenic variants. American journal of medical genetics. Part A (2024)
Nagore Gene-Olaciregui, Marta Perez-Somarriba, Vicente Santa-Maria, Ofelia Cruz, Soledad Gómez-González, Alicia Castañeda, Mariona Suñol, Carlota Rovira, Jordi Muchart, José Hinojosa, Andrés Morales La Madrid, Cinzia Lavarino
Clinical and Molecular Evolution of an ALK -Driven Infant-Type Hemispheric Glioma Treated Sequentially With Second- and Third-Generation Anaplastic Lymphoma Kinase Inhibitors. JCO precision oncology 7 (2023)
Eshini Panditharatna, Joana G Marques, Tingjian Wang, Maria C Trissal, Ilon Liu, Li Jiang, Alexander Beck, Andrew Groves, Neekesh V Dharia, Deyao Li, Samantha E Hoffman, Guillaume Kugener, McKenzie L Shaw, Hafsa M Mire, Olivia A Hack, Joshua M Dempster, Caleb A Lareau, Lingling Dai, Logan H Sigua, Michael A Quezada, Ann-Catherine J Stanton, Meghan Wyatt, Zohra Kalani, Amy Goodale, Francisca Vazquez, Frederica Piccioni, John G Doench, David E Root, Jamie N Anastas, Kristen L Jones, Amy Saur Conway, Sylwia A Stopka, Michael S Regan, Yu Liang, Hyuk-Soo Seo, Kijun Song, Puspalata Bashyal, William P Jerome, Nathan D Mathewson, Sirano Dhe-Paganon, Mario L Suvà, Angel Montero Carcaboso, Cinzia Lavarino, Jaume Catala-Mora, Quang-De Nguyen, Keith L Ligon, Yang Shi, Sameer Agnihotri, Nathalie Y R Agar, Kimberly Stegmaier, Charles D Stiles, Michelle Monje, Todd R Golub, Jun Qi, Mariella G Filbin
BAF Complex Maintains Glioma Stem Cells in Pediatric H3K27M Glioma. Cancer discovery 12 (12) (2022)
Diana M Carvalho, Peter J Richardson, Nagore Olaciregui, Reda Stankunaite, Cinzia Lavarino, Valeria Molinari, Elizabeth A Corley, Daniel P Smith, Ruth Ruddle, Adam Donovan, Akos Pal, Florence I Raynaud, Sara Temelso, Alan Mackay, John P Overington, Anne Phelan, David Sheppard, Andrew Mackinnon, Bassel Zebian, Safa Al-Sarraj, Ashirwad Merve, Jeremy Pryce, Jacques Grill, Michael Hubank, Ofelia Cruz Martinez, Andres Morales La Madrid, Sabine Mueller, Angel Montero Carcaboso, Fernando Carceller, Chris Jones
Repurposing vandetanib plus everolimus for the treatment of ACVR1-mutant diffuse intrinsic pontine glioma. Cancer discovery (2021)
Riyue Bao, Anita Ng, Mark Sasaki, Myvizhi Esai Selvan, Alyna Katti, Hyesan Lee, Lei Huang, Andrew D Skol, Cinzia Lavarino, Hector Salvador, Robert J Klein, Zeynep Hülya Gümüş, Jaume Mora, Kenan Onel
Functional Common and Rare ERBB2 Germline Variants Cooperate in Familial and Sporadic Cancer Susceptibility. Cancer prevention research (Philadelphia, Pa.) 14 (4) (2021)
Mar Petit-Pedrol, Mar Guasp, Thaís Armangue, Cinzia Lavarino, Andrés Morales La Madrid, Albert Saiz, Francesc Graus, Josep O Dalmau
Absence of GluD2 Antibodies in Patients With Opsoclonus-Myoclonus Syndrome. Neurology 96 (7) (2020)
Santiago Zugbi, Daiana Ganiewich, Arpita Bhattacharyya, Rosario Aschero, Daniela Ottaviani, Claudia Sampor, Eduardo G Cafferata, Marcela Mena, Mariana Sgroi, Ursula Winter, Gabriela Lamas, Mariona Suñol, Manuel Daroqui, Edgardo Baialardo, Beatriz Salas, Anirban Das, Adriana Fandiño, Jasmine H Francis, Fabiana Lubieniecki, Cinzia Lavarino, Ralph Garippa, Osvaldo L Podhajcer, David H Abramson, François Radvanyi, Guillermo Chantada, Andrea Sabina Llera, Paula S Schaiquevich
Clinical, Genomic, and Pharmacological Study of MYCN-Amplified RB1 Wild-Type Metastatic Retinoblastoma. Cancers 12 (9) (2020)
Sara Sánchez-Molina, Elisabet Figuerola-Bou, Enrique Blanco, María Sánchez-Jiménez, Pablo Táboas, Soledad Gómez-González, Cecilia Ballaré, Daniel José García-Domínguez, Estela Prada, Lourdes Hontecillas-Prieto, Angel Montero Carcaboso, Òscar Martínez Tirado, Inmaculada Hernández-Muñoz, Enrique de Álava, Cinzia Lavarino, Luciano Di Croce, Jaume Mora
RING1B recruits EWSR1-FLI1 and cooperates in the remodeling of chromatin necessary for Ewing sarcoma tumorigenesis. Science advances 6 (43) (2020)