Associated Papers
Steroid hormone receptors, exome sequencing and treatment responsiveness of breast cancer patient-derived xenografts originated in a South American country.
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Scientific Reports, 2025
39827242 (PubMed )
Supplement: 41598_2025_86389_MOESM2_ESM.xlsx › Sheet1
Burden of Mendelian disorders in a large Middle Eastern biobank.
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Genome Medicine, 2024
38584274 (PubMed )
Supplement: 13073_2024_1307_MOESM1_ESM.xlsx › Table_S3
NTHL1 is a recessive cancer susceptibility gene.
Nurmi AK et al.
Scientific Reports, 2023
38036545 (PubMed )
Supplement: 41598_2023_47441_MOESM1_ESM.pdf
Genetic control of meiosis surveillance mechanisms in mammals.
Huang Y et al.
Frontiers in Cell and Developmental Biology, 2023
36910159 (PubMed )
Supplement: DataSheet2.PDF
Sequence analysis of 37 candidate genes for male infertility: challenges in variant assessment and validating genes.
Araujo TF et al.
Andrology, 2020
Insights Into the Somatic Mutation Burden of Hepatoblastomas From Brazilian Patients.
Aguiar TFM et al.
Frontiers in Oncology, 2020
32432034 (PubMed )
Supplement: Table_6.XLSX › HB46
iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors.
Melguizo-Sanchis D et al.
Cell Death & Disease, 2018
29374141 (PubMed )
Supplement: 41419_2017_141_MOESM8_ESM.xlsx › SAA3_Deleterious_Hits
Analysis of the meiotic recombination gene REC8 for sequence variations in a population with severe male factor infertility.
Griffin J et al.
Systems Biology in Reproductive Medicine, 0
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