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Maria Isabel Achatz

Showing results (61-70 of 71) with videos related to

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Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 12, 2020
Li-Fraumeni Exploration Consortium Data Coordinating Center: Building an Interactive Web-Based Resource for Collaborative International Cancer Epidemiology Research for a Rare ConditionPhuong L Mai, Sharon R Sand, Neiladri Saha, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 12, 2025
Update on Cancer Screening Recommendations for Individuals with Li-Fraumeni SyndromeMaria Isabel Achatz, Anita Villani, Alison A Bertuch, et al.
Cancer Genetics|September 4, 2012
Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortiumPhuong L Mai, David Malkin, Judy E Garber, et al.
JAMA Oncology|August 4, 2017
Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysisMandy L Ballinger, Ana Best, Phuong L Mai, et al.
Genome Medicine|October 23, 2025
A quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndromeCristina Fortuno, Megan N Frone, Jessica Mester, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 19, 2015
Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanomaSusana Puig, Miriam Potrony, Francisco Cuellar, et al.
Scientific Reports|June 17, 2018
The germline mutational landscape of BRCA1 and BRCA2 in BrazilEdenir Inêz Palmero, Dirce Maria Carraro, Barbara Alemar, et al.
Science Advances|July 9, 2020
XAF1 as a modifier of p53 function and cancer susceptibilityEmilia M Pinto, Bonald C Figueiredo, Wenan Chen, et al.
Endocrine-Related Cancer|April 9, 2025
Genotype-specific neoplastic risk profiles in patients with VHL diseaseAthina Ganner, Alfonso Massimiliano Ferrara, Peggy Sekula, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 14, 2023
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer RiskLenka Stolarova, Petra Kleiblova, Petra Zemankova, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 12, 2020
Li-Fraumeni Exploration Consortium Data Coordinating Center: Building an Interactive Web-Based Resource for Collaborative International Cancer Epidemiology Research for a Rare ConditionPhuong L Mai, Sharon R Sand, Neiladri Saha, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 12, 2025
Update on Cancer Screening Recommendations for Individuals with Li-Fraumeni SyndromeMaria Isabel Achatz, Anita Villani, Alison A Bertuch, et al.
Cancer Genetics|September 4, 2012
Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortiumPhuong L Mai, David Malkin, Judy E Garber, et al.
JAMA Oncology|August 4, 2017
Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysisMandy L Ballinger, Ana Best, Phuong L Mai, et al.
Genome Medicine|October 23, 2025
A quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndromeCristina Fortuno, Megan N Frone, Jessica Mester, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 19, 2015
Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanomaSusana Puig, Miriam Potrony, Francisco Cuellar, et al.
Scientific Reports|June 17, 2018
The germline mutational landscape of BRCA1 and BRCA2 in BrazilEdenir Inêz Palmero, Dirce Maria Carraro, Barbara Alemar, et al.
Science Advances|July 9, 2020
XAF1 as a modifier of p53 function and cancer susceptibilityEmilia M Pinto, Bonald C Figueiredo, Wenan Chen, et al.
Endocrine-Related Cancer|April 9, 2025
Genotype-specific neoplastic risk profiles in patients with VHL diseaseAthina Ganner, Alfonso Massimiliano Ferrara, Peggy Sekula, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 14, 2023
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer RiskLenka Stolarova, Petra Kleiblova, Petra Zemankova, et al.
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