Lopez-Bigas N - Search Results

1

Author Correction: High p16 expression and heterozygous RB1 loss are biomarkers for CDK4/6 inhibitor resistance in ER⁺ breast cancer.

Palafox M, Monserrat L, Bellet M, Villacampa G, Gonzalez-Perez A, Oliveira M, Brasó-Maristany F, Ibrahimi N, Kannan S, Mina L, Herrera-Abreu MT, Òdena A, Sánchez-Guixé M, Capelán M, Azaro A, Bruna A, Rodríguez O, Guzmán M, Grueso J, Viaplana C, Hernández J, Su F, Lin K, Clarke RB, Caldas C, Arribas J, Michiels S, García-Sanz A, Turner NC, Prat A, Nuciforo P, Dienstmann R, Verma CS, Lopez-Bigas N, Scaltriti M, Arnedos M, Saura C, Serra V. Palafox M, et al. Nat Commun. 2022 Nov 14;13(1):6928. doi: 10.1038/s41467-022-34580-3. Nat Commun. 2022. PMID: 36376284 Free PMC article. No abstract available.

2

Expansion of the BioCyc collection of pathway/genome databases to 160 genomes.

Karp PD, Ouzounis CA, Moore-Kochlacs C, Goldovsky L, Kaipa P, Ahrén D, Tsoka S, Darzentas N, Kunin V, López-Bigas N. Karp PD, et al. Nucleic Acids Res. 2005 Oct 24;33(19):6083-9. doi: 10.1093/nar/gki892. Print 2005. Nucleic Acids Res. 2005. PMID: 16246909 Free PMC article.

3

Structural and functional properties of genes involved in human cancer.

Furney SJ, Higgins DG, Ouzounis CA, López-Bigas N. Furney SJ, et al. BMC Genomics. 2006 Jan 11;7:3. doi: 10.1186/1471-2164-7-3. BMC Genomics. 2006. PMID: 16405732 Free PMC article.

4

On the association between chromosomal rearrangements and genic evolution in humans and chimpanzees.

Marques-Bonet T, Sànchez-Ruiz J, Armengol L, Khaja R, Bertranpetit J, Lopez-Bigas N, Rocchi M, Gazave E, Navarro A. Marques-Bonet T, et al. Genome Biol. 2007;8(10):R230. doi: 10.1186/gb-2007-8-10-r230. Genome Biol. 2007. PMID: 17971225 Free PMC article.

5

Beyond 100 genomes.

Janssen P, Audit B, Cases I, Darzentas N, Goldovsky L, Kunin V, Lopez-Bigas N, Peregrin-Alvarez JM, Pereira-Leal JB, Tsoka S, Ouzounis CA. Janssen P, et al. Genome Biol. 2003;4(5):402. doi: 10.1186/gb-2003-4-5-402. Epub 2003 Apr 28. Genome Biol. 2003. PMID: 12734008 Free PMC article.

6

Are splicing mutations the most frequent cause of hereditary disease?

López-Bigas N, Audit B, Ouzounis C, Parra G, Guigó R. López-Bigas N, et al. FEBS Lett. 2005 Mar 28;579(9):1900-3. doi: 10.1016/j.febslet.2005.02.047. FEBS Lett. 2005. PMID: 15792793 Free article.

7

A partially supervised classification approach to dominant and recessive human disease gene prediction.

Calvo B, López-Bigas N, Furney SJ, Larrañaga P, Lozano JA. Calvo B, et al. Comput Methods Programs Biomed. 2007 Mar;85(3):229-37. doi: 10.1016/j.cmpb.2006.12.003. Epub 2007 Jan 26. Comput Methods Programs Biomed. 2007. PMID: 17258838

8

Genome-wide identification of genes likely to be involved in human genetic disease.

López-Bigas N, Ouzounis CA. López-Bigas N, et al. Nucleic Acids Res. 2004 Jun 4;32(10):3108-14. doi: 10.1093/nar/gkh605. Print 2004. Nucleic Acids Res. 2004. PMID: 15181176 Free PMC article.

9

Highly consistent patterns for inherited human diseases at the molecular level.

López-Bigas N, Blencowe BJ, Ouzounis CA. López-Bigas N, et al. Bioinformatics. 2006 Feb 1;22(3):269-77. doi: 10.1093/bioinformatics/bti781. Epub 2005 Nov 15. Bioinformatics. 2006. PMID: 16287936

10

Loss of dE2F compromises mitochondrial function.

Ambrus AM, Islam AB, Holmes KB, Moon NS, Lopez-Bigas N, Benevolenskaya EV, Frolov MV. Ambrus AM, et al. Dev Cell. 2013 Nov 25;27(4):438-51. doi: 10.1016/j.devcel.2013.10.002. Dev Cell. 2013. PMID: 24286825 Free PMC article.

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