| TP53 mutations in human cancers: functional selection and impact on cancer prognosis and outcomes A Petitjean, MIW Achatz, AL Borresen-Dale, P Hainaut, M Olivier Oncogene 26 (15), 2157-2165, 2007 | 1168 | 2007 |
| Cancer screening recommendations for individuals with Li-Fraumeni syndrome CP Kratz, MI Achatz, L Brugieres, T Frebourg, JE Garber, MLC Greer, ... Clinical Cancer Research 23 (11), e38-e45, 2017 | 507 | 2017 |
| Clinical management and tumor surveillance recommendations of inherited mismatch repair deficiency in childhood U Tabori, JR Hansford, MI Achatz, CP Kratz, SE Plon, T Frebourg, ... Clinical Cancer Research 23 (11), e32-e37, 2017 | 241 | 2017 |
| The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families MIW Achatz, M Olivier, F Le Calvez, G Martel-Planche, A Lopes, BM Rossi, ... Cancer letters 245 (1-2), 96-102, 2007 | 241 | 2007 |
| Baseline surveillance in Li-Fraumeni syndrome using whole-body magnetic resonance imaging: a meta-analysis ML Ballinger, A Best, PL Mai, PP Khincha, JT Loud, JA Peters, MI Achatz, ... JAMA oncology 3 (12), 1634-1639, 2017 | 192 | 2017 |
| PTEN, DICER1, FH, and Their Associated Tumor Susceptibility Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood KAP Schultz, SP Rednam, J Kamihara, L Doros, MI Achatz, ... Clinical Cancer Research 23 (12), e76-e82, 2017 | 186 | 2017 |
| Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect S Garritano, F Gemignani, EI Palmero, M Olivier, G Martel‐Planche, ... Human mutation 31 (2), 143-150, 2010 | 182 | 2010 |
| Gastric cancer in individuals with Li-Fraumeni syndrome S Masciari, A Dewanwala, EM Stoffel, GY Lauwers, H Zheng, MI Achatz, ... Genetics in Medicine 13 (7), 651-657, 2011 | 175 | 2011 |
| Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil EI Palmero, L Schüler-Faccini, M Caleffi, MIW Achatz, M Olivier, ... Cancer letters 261 (1), 21-25, 2008 | 144 | 2008 |
| Germline DNA copy number variation in familial and early-onset breast cancer ACV Krepischi, MIW Achatz, EMM Santos, SS Costa, BCG Lisboa, ... Breast Cancer Research 14, 1-8, 2012 | 136 | 2012 |
| Cancer screening recommendations and clinical management of inherited gastrointestinal cancer syndromes in childhood MI Achatz, CC Porter, L Brugières, H Druker, T Frebourg, WD Foulkes, ... Clinical Cancer Research 23 (13), e107-e114, 2017 | 134 | 2017 |
| Tumor protein 53 mutations and inherited cancer: beyond Li-Fraumeni syndrome EI Palmero, MIW Achatz, P Ashton-Prolla, M Olivier, P Hainaut Current Opinion in Oncology 22 (1), 64, 2010 | 132 | 2010 |
| Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortium PL Mai, D Malkin, JE Garber, JD Schiffman, JN Weitzel, LC Strong, ... Cancer genetics 205 (10), 479-487, 2012 | 117 | 2012 |
| Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients FC Silva, BCG Lisboa, MCP Figueiredo, GT Torrezan, ÉMM Santos, ... BMC medical genetics 15, 1-11, 2014 | 109 | 2014 |
| Variable population prevalence estimates of germline TP53 variants: A gnomAD‐based analysis KC de Andrade, MN Frone, T Wegman‐Ostrosky, PP Khincha, J Kim, ... Human mutation 40 (1), 97-105, 2019 | 104 | 2019 |
| Molecular characterization of choroid plexus tumors reveals novel clinically relevant subgroups DM Merino, A Shlien, A Villani, M Pienkowska, S Mack, V Ramaswamy, ... Clinical Cancer Research 21 (1), 184-192, 2015 | 103 | 2015 |
| Analysis of the Li-Fraumeni spectrum based on an international germline TP53 variant data set: an international agency for research on cancer TP53 database analysis CP Kratz, C Freycon, KN Maxwell, KE Nichols, JD Schiffman, DG Evans, ... JAMA oncology 7 (12), 1800-1805, 2021 | 98 | 2021 |
| The germline mutational landscape of BRCA1 and BRCA2 in Brazil EI Palmero, DM Carraro, B Alemar, MAM Moreira, A Ribeiro-dos-Santos, ... Scientific reports 8 (1), 9188, 2018 | 86 | 2018 |
| TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li–Fraumeni syndrome: impact on age at first diagnosis V Marcel, EI Palmero, P Falagan-Lotsch, G Martel-Planche, ... Journal of medical genetics 46 (11), 766-772, 2009 | 84 | 2009 |
| Highly prevalent TP53 mutation predisposing to many cancers in the Brazilian population: a case for newborn screening? MIW Achatz, P Hainaut, P Ashton-Prolla The lancet oncology 10 (9), 920-925, 2009 | 83 | 2009 |
Pierre HainautProfessor, Cancer Biology, University Grenoble Alpes and Director, Institute for Advanceduniv-grenoble-alpes.fr의 이메일 확인됨