Ximena Bonilla
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Explore the profile of Ximena Bonilla including associated specialties, affiliations and a list of published articles.
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22
Citations
814
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Recent Articles
1.
Wegmann R, Bonilla X, Casanova R, Chevrier S, Coelho R, Esposito C, et al.
Nat Commun
. 2024 Oct;
15(1):9402.
PMID: 39477946
Deep single-cell multi-omic profiling offers a promising approach to understand and overcome drug resistance in relapsed or refractory (rr) acute myeloid leukemia (AML). Here, we combine single-cell ex vivo drug...
2.
Immer A, Stark S, Jacob F, Bonilla X, Thomas T, Kahles A, et al.
Bioinformatics
. 2024 Jun;
40(Suppl 1):i189-i198.
PMID: 38940152
Motivation: Multimodal profiling strategies promise to produce more informative insights into biomedical cohorts via the integration of the information each modality contributes. To perform this integration, however, the development of...
3.
Bonilla X, Lara A, Llano-Leon M, Lopez-Gonzalez D, Hernandez-Mejia D, Bustos R, et al.
Int J Mol Sci
. 2023 Nov;
24(21).
PMID: 37958529
Umbilical cord blood (UCB) serves as a source of hematopoietic stem and progenitor cells (HSPCs) utilized in the regeneration of hematopoietic and immune systems, forming a crucial part of the...
4.
Forny P, Bonilla X, Lamparter D, Shao W, Plessl T, Frei C, et al.
Nat Metab
. 2023 Jan;
5(1):80-95.
PMID: 36717752
Methylmalonic aciduria (MMA) is an inborn error of metabolism with multiple monogenic causes and a poorly understood pathogenesis, leading to the absence of effective causal treatments. Here we employ multi-layered...
5.
Ma C, Chen N, Jolly A, Zhao S, Coban-Akdemir Z, Tian W, et al.
Genet Med
. 2022 Sep;
24(11):2262-2273.
PMID: 36112137
Purpose: Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) is characterized by congenital absence of the uterus, cervix, and the upper part of the vagina in females. Whole-gene deletion and loss-of-function variants in TBX6 have...
6.
Irmisch A, Bonilla X, Chevrier S, Lehmann K, Singer F, Toussaint N, et al.
Cancer Cell
. 2021 Jan;
39(3):288-293.
PMID: 33482122
The application and integration of molecular profiling technologies create novel opportunities for personalized medicine. Here, we introduce the Tumor Profiler Study, an observational trial combining a prospective diagnostic approach to...
7.
Chen N, Zhao S, Jolly A, Wang L, Pan H, Yuan J, et al.
Am J Hum Genet
. 2021 Jan;
108(2):337-345.
PMID: 33434492
Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS) is associated with congenital absence of the uterus, cervix, and the upper part of the vagina; it is a sex-limited trait. Disrupted development of the Müllerian ducts...
8.
Robles-Espinoza C, Mohammadi P, Bonilla X, Gutierrez-Arcelus M
Curr Opin Genet Dev
. 2020 Dec;
66:10-19.
PMID: 33383480
Allele-specific gene expression can influence disease traits. Non-coding germline genetic variants that alter regulatory elements can cause allele-specific gene expression and contribute to cancer susceptibility. In tumors, both somatic copy...
9.
Stark S, Ficek J, Locatello F, Bonilla X, Chevrier S, Singer F, et al.
Bioinformatics
. 2020 Dec;
36(Suppl_2):i919-i927.
PMID: 33381818
Motivation: Recent technological advances have led to an increase in the production and availability of single-cell data. The ability to integrate a set of multi-technology measurements would allow the identification...
10.
Segal E, Zhang F, Lin X, King G, Shalem O, Shilo S, et al.
Nat Med
. 2020 Jun;
26(8):1309.
PMID: 32591764
An amendment to this paper has been published and can be accessed via a link at the top of the paper.