Armengol L - Search Results

1

Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis.

de Cid R, Riveira-Munoz E, Zeeuwen PL, Robarge J, Liao W, Dannhauser EN, Giardina E, Stuart PE, Nair R, Helms C, Escaramís G, Ballana E, Martín-Ezquerra G, den Heijer M, Kamsteeg M, Joosten I, Eichler EE, Lázaro C, Pujol RM, Armengol L, Abecasis G, Elder JT, Novelli G, Armour JA, Kwok PY, Bowcock A, Schalkwijk J, Estivill X. de Cid R, et al. Among authors: armengol l. Nat Genet. 2009 Feb;41(2):211-5. doi: 10.1038/ng.313. Epub 2009 Jan 25. Nat Genet. 2009. PMID: 19169253 Free PMC article.

2

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.

Estivill X, Armengol L. Estivill X, et al. Among authors: armengol l. PLoS Genet. 2007 Oct;3(10):1787-99. doi: 10.1371/journal.pgen.0030190. PLoS Genet. 2007. PMID: 17953491 Free PMC article.

3

Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events.

Bosch N, Cáceres M, Cardone MF, Carreras A, Ballana E, Rocchi M, Armengol L, Estivill X. Bosch N, et al. Among authors: armengol l. Hum Mol Genet. 2007 Nov 1;16(21):2572-82. doi: 10.1093/hmg/ddm209. Epub 2007 Aug 7. Hum Mol Genet. 2007. PMID: 17684299

4

Analysis of the multi-copy gene family FAM90A as a copy number variant in different ethnic backgrounds.

Bosch N, Escaramís G, Mercader JM, Armengol L, Estivill X. Bosch N, et al. Among authors: armengol l. Gene. 2008 Sep 1;420(2):113-7. doi: 10.1016/j.gene.2008.05.003. Epub 2008 May 13. Gene. 2008. PMID: 18602769

5

Worldwide population distribution of the common LCE3C-LCE3B deletion associated with psoriasis and other autoimmune disorders.

Bassaganyas L, Riveira-Muñoz E, García-Aragonés M, González JR, Cáceres M, Armengol L, Estivill X. Bassaganyas L, et al. Among authors: armengol l. BMC Genomics. 2013 Apr 17;14:261. doi: 10.1186/1471-2164-14-261. BMC Genomics. 2013. PMID: 23594316 Free PMC article.

6

Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements.

Armengol L, Pujana MA, Cheung J, Scherer SW, Estivill X. Armengol L, et al. Hum Mol Genet. 2003 Sep 1;12(17):2201-8. doi: 10.1093/hmg/ddg223. Epub 2003 Jul 8. Hum Mol Genet. 2003. PMID: 12915466

7

Identification of copy number variants defining genomic differences among major human groups.

Armengol L, Villatoro S, González JR, Pantano L, García-Aragonés M, Rabionet R, Cáceres M, Estivill X. Armengol L, et al. PLoS One. 2009 Sep 30;4(9):e7230. doi: 10.1371/journal.pone.0007230. PLoS One. 2009. PMID: 19789632 Free PMC article.

8

Accurate molecular diagnosis of phenylketonuria and tetrahydrobiopterin-deficient hyperphenylalaninemias using high-throughput targeted sequencing.

Trujillano D, Perez B, González J, Tornador C, Navarrete R, Escaramis G, Ossowski S, Armengol L, Cornejo V, Desviat LR, Ugarte M, Estivill X. Trujillano D, et al. Among authors: armengol l. Eur J Hum Genet. 2014 Apr;22(4):528-34. doi: 10.1038/ejhg.2013.175. Epub 2013 Aug 14. Eur J Hum Genet. 2014. PMID: 23942198 Free PMC article.

9

ProSeeK: a web server for MLPA probe design.

Pantano L, Armengol L, Villatoro S, Estivill X. Pantano L, et al. Among authors: armengol l. BMC Genomics. 2008 Nov 28;9:573. doi: 10.1186/1471-2164-9-573. BMC Genomics. 2008. PMID: 19040730 Free PMC article.

10

Accounting for uncertainty when assessing association between copy number and disease: a latent class model.

González JR, Subirana I, Escaramís G, Peraza S, Cáceres A, Estivill X, Armengol L. González JR, et al. Among authors: armengol l. BMC Bioinformatics. 2009 Jun 6;10:172. doi: 10.1186/1471-2105-10-172. BMC Bioinformatics. 2009. PMID: 19500389 Free PMC article.

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