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Author Details
Full Name
Ana Pati??o-Garc??a
Affiliation
Center for Applied Medical Research.
ORCID
Career Start Year
1995
Papers
154
H Index
39
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35975805
Primary trimethylaminuria syndrome: more than an unpleasant odor.
Int J Dermatol
2023
35975805
Primary trimethylaminuria syndrome: more than an unpleasant odor.
Int J Dermatol
2023
36436516
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Lancet Oncol
2023
37596165
Genetically inferred birthweight, height, and puberty timing and risk of osteosarcoma.
Cancer Epidemiol
2023
37820087
Promises of oncolytic viral therapy for adult and children with brain glioma.
Curr Opin Oncol
2023
37802053
TIM-3 blockade in diffuse intrinsic pontine glioma models promotes tumor regression and antitumor immune memory.
Cancer Cell
2023
37566035
Intermediate Molecular Phenotypes to Identify Genetic Markers of Anthracycline-Induced Cardiotoxicity Risk.
Cells
2023
36712139
Intermediate molecular phenotypes to identify genetic markers of anthracycline-induced cardiotoxicity risk.
bioRxiv
2023
36805510
Identification of germline cancer predisposition variants in pediatric sarcoma patients from somatic tumor testing.
Sci Rep
2023
37596165
Genetically inferred birthweight, height, and puberty timing and risk of osteosarcoma.
Cancer Epidemiol
2023
37802053
TIM-3 blockade in diffuse intrinsic pontine glioma models promotes tumor regression and antitumor immune memory.
Cancer Cell
2023
37820087
Promises of oncolytic viral therapy for adult and children with brain glioma.
Curr Opin Oncol
2023
37566035
Intermediate Molecular Phenotypes to Identify Genetic Markers of Anthracycline-Induced Cardiotoxicity Risk.
Cells
2023
36712139
Intermediate molecular phenotypes to identify genetic markers of anthracycline-induced cardiotoxicity risk.
bioRxiv
2023
36436516
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
Lancet Oncol
2023
36805510
Identification of germline cancer predisposition variants in pediatric sarcoma patients from somatic tumor testing.
Sci Rep
2023
34965961
Local Treatment of a Pediatric Osteosarcoma Model with a 4-1BBL Armed Oncolytic Adenovirus Results in an Antitumor Effect and Leads to Immune Memory.
Mol Cancer Ther
2022
35844738
Case Report: The Value of Genomic Analysis in a Case of Megakaryoblastic Leukemia With Atypical Initial Manifestation.
Front Pediatr
2022
35393952
Exploiting 4-1BB immune checkpoint to enhance the efficacy of oncolytic virotherapy for diffuse intrinsic pontine gliomas.
JCI Insight
2022
35767439
Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma.
N Engl J Med
2022
35949950
Galectin-3 inhibition boosts the therapeutic efficacy of Semliki Forest virus in pediatric osteosarcoma.
Mol Ther Oncolytics
2022
36438828
<i>SLC7A8</i> coding for LAT2 is associated with early disease progression in osteosarcoma and transports doxorubicin.
Front Pharmacol
2022
35267543
The BRCA Gene in Epithelial Ovarian Cancer.
Cancers (Basel)
2022
34965961
Local Treatment of a Pediatric Osteosarcoma Model with a 4-1BBL Armed Oncolytic Adenovirus Results in an Antitumor Effect and Leads to Immune Memory.
Mol Cancer Ther
2022
35152364
Current status of precision medicine in pediatric oncology in Spain: a consensus report by the Spanish Society of Paediatric Haematology and Oncology (SEHOP).
Clin Transl Oncol
2022
35844738
Case Report: The Value of Genomic Analysis in a Case of Megakaryoblastic Leukemia With Atypical Initial Manifestation.
Front Pediatr
2022
35767439
Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma.
N Engl J Med
2022
35393952
Exploiting 4-1BB immune checkpoint to enhance the efficacy of oncolytic virotherapy for diffuse intrinsic pontine gliomas.
JCI Insight
2022
36438828
<i>SLC7A8</i> coding for LAT2 is associated with early disease progression in osteosarcoma and transports doxorubicin.
Front Pharmacol
2022
35949950
Galectin-3 inhibition boosts the therapeutic efficacy of Semliki Forest virus in pediatric osteosarcoma.
Mol Ther Oncolytics
2022
35152364
Current status of precision medicine in pediatric oncology in Spain: a consensus report by the Spanish Society of Paediatric Haematology and Oncology (SEHOP).
Clin Transl Oncol
2022
35267543
The BRCA Gene in Epithelial Ovarian Cancer.
Cancers (Basel)
2022
33376098
Delta-24-RGD, an Oncolytic Adenovirus, Increases Survival and Promotes Proinflammatory Immune Landscape Remodeling in Models of AT/RT and CNS-PNET.
Clin Cancer Res
2021
34076861
The paediatric cancer clinical research landscape in Spain: a 13-year multicentre experience of the new agents group of the Spanish Society of Paediatric Haematology and Oncology (SEHOP).
Clin Transl Oncol
2021
34281988
CD137 and PD-L1 targeting with immunovirotherapy induces a potent and durable antitumor immune response in glioblastoma models.
J Immunother Cancer
2021
33792916
Additional causal SNRPE mutations in hereditary hypotrichosis simplex.
Br J Dermatol
2021
33889513
Whole exome sequencing characterization of individuals presenting extreme phenotypes of high and low risk of developing tobacco-induced lung adenocarcinoma.
Transl Lung Cancer Res
2021
34199109
Machine Learning-Based Approach Highlights the Use of a Genomic Variant Profile for Precision Medicine in Ovarian Failure.
J Pers Med
2021
33919355
RGB-Marking to Identify Patterns of Selection and Neutral Evolution in Human Osteosarcoma Models.
Cancers (Basel)
2021
33376098
Delta-24-RGD, an Oncolytic Adenovirus, Increases Survival and Promotes Proinflammatory Immune Landscape Remodeling in Models of AT/RT and CNS-PNET.
Clin Cancer Res
2021
34771600
Clinical Value of NGS Genomic Studies for Clinical Management of Pediatric and Young Adult Bone Sarcomas.
Cancers (Basel)
2021
33792916
Additional causal SNRPE mutations in hereditary hypotrichosis simplex.
Br J Dermatol
2021
33919355
RGB-Marking to Identify Patterns of Selection and Neutral Evolution in Human Osteosarcoma Models.
Cancers (Basel)
2021
33889513
Whole exome sequencing characterization of individuals presenting extreme phenotypes of high and low risk of developing tobacco-induced lung adenocarcinoma.
Transl Lung Cancer Res
2021
34771600
Clinical Value of NGS Genomic Studies for Clinical Management of Pediatric and Young Adult Bone Sarcomas.
Cancers (Basel)
2021
34076861
The paediatric cancer clinical research landscape in Spain: a 13-year multicentre experience of the new agents group of the Spanish Society of Paediatric Haematology and Oncology (SEHOP).
Clin Transl Oncol
2021
34199109
Machine Learning-Based Approach Highlights the Use of a Genomic Variant Profile for Precision Medicine in Ovarian Failure.
J Pers Med
2021
34281988
CD137 and PD-L1 targeting with immunovirotherapy induces a potent and durable antitumor immune response in glioblastoma models.
J Immunother Cancer
2021
32191290
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.
JAMA Oncol
2020
32191290
Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma.
JAMA Oncol
2020
1 - 50 of 308
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The University of Texas M.D. Anderson Cancer Center
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Robert N Hoover
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Co-authored papers
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Richard Gorlick
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Massimo Serra
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Irene L Andrulis
University of Toronto
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Donald A Barkauskas
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