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Author Details
Full Name
Rafael Vald??s-Mas
Affiliation
Weizmann Institute of Science
ORCID
Career Start Year
2012
Papers
40
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36191844
Microbiome-phage interactions in inflammatory bowel disease.
Clin Microbiol Infect
2023
37499275
The microbial genotoxin colibactin exacerbates mismatch repair mutations in colorectal tumors.
Neoplasia
2023
37207358
The Role of Artificial Intelligence in Deciphering Diet-Disease Relationships: Case Studies.
Annu Rev Nutr
2023
36941399
Epithelial Nlrp10 inflammasome mediates protection against intestinal autoinflammation.
Nat Immunol
2023
35293392
Publisher Correction: Gut microbiota modulates weight gain in mice after discontinued smoke exposure.
Nature
2022
35839259
Dimensionality reduction of longitudinal 'omics data using modern tensor factorizations.
PLoS Comput Biol
2022
35931020
Targeted suppression of human IBD-associated gut microbiota commensals by phage consortia for treatment of intestinal inflammation.
Cell
2022
35987213
Personalized microbiome-driven effects of non-nutritive sweeteners on human glucose tolerance.
Cell
2022
34226711
Probiotics impact the antibiotic resistance gene reservoir along the human GI tract in a person-specific and antibiotic-dependent manner.
Nat Microbiol
2021
34880502
Gut microbiota modulates weight gain in mice after discontinued smoke exposure.
Nature
2021
34016160
Immunological and genetic kinetics from diagnosis to clinical progression in chronic lymphocytic leukemia.
Biomark Res
2021
32299093
Biological and clinical significance of dysplastic hematopoiesis in patients with newly diagnosed multiple myeloma.
Blood
2020
32653496
High-Throughput Screen Identifies Host and Microbiota Regulators of Intestinal Barrier Function.
Gastroenterology
2020
32584970
Genomic and epigenomic insights into the origin, pathogenesis, and clinical behavior of mantle cell lymphoma subtypes.
Blood
2020
32475991
Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma.
Leukemia
2020
30538135
<i>CCND2</i> and <i>CCND3</i> hijack immunoglobulin light-chain enhancers in cyclin D1<sup>-</sup> mantle cell lymphoma.
Blood
2019
31221673
Natural history and cell of origin of <i>TC</i> <i>F3</i>-<i>ZN</i> <i>F384</i> and <i>PTPN11</i> mutations in monozygotic twins with concordant BCP-ALL.
Blood
2019
31332389
Healthspan and lifespan extension by fecal microbiota transplantation into progeroid mice.
Nat Med
2019
30679325
Enhanced hemato-endothelial specification during human embryonic differentiation through developmental cooperation between <i>AF4-MLL</i> and <i>MLL-AF4</i> fusions.
Haematologica
2019
28912018
Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer.
Gastroenterology
2018
30181176
Altered patterns of global protein synthesis and translational fidelity in RPS15-mutated chronic lymphocytic leukemia.
Blood
2018
29900613
Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis.
Hum Mutat
2018
29448935
Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis.
Mol Cancer
2018
29666142
Tumor xenograft modeling identifies an association between TCF4 loss and breast cancer chemoresistance.
Dis Model Mech
2018
27991928
Stem cell-like transcriptional reprogramming mediates metastatic resistance to mTOR inhibition.
Oncogene
2017
26133394
POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance.
Genet Med
2016
26611460
Chronic lymphocytic leukemia: looking into the dark side of the genome.
Cell Death Differ
2016
27512155
Transplacental transfer of essential thrombocythemia in monozygotic twins.
Blood
2016
27096942
Erratum: Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
Sci Rep
2016
26852919
Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
Sci Rep
2016
24691292
Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype.
Gut
2015
26647970
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.
Nat Commun
2015
26052075
Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.
Gastroenterology
2015
26200345
Non-coding recurrent mutations in chronic lymphocytic leukaemia.
Nature
2015
25903372
Common and rare variants of microRNA genes in autism spectrum disorders.
World J Biol Psychiatry
2015
25810463
Comprehensive establishment and characterization of orthoxenograft mouse models of malignant peripheral nerve sheath tumors for personalized medicine.
EMBO Mol Med
2015
23999528
Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations.
Mol Psychiatry
2014
25351925
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy.
Nat Commun
2014
24145436
Landscape of somatic mutations and clonal evolution in mantle cell lymphoma.
Proc Natl Acad Sci U S A
2013
23284693
Estimation of copy number alterations from exome sequencing data.
PLoS One
2012
1 - 40 of 40
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