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Building on the clinical applicability of ctDNA analysis in non-metastatic pancreatic ductal adenocarcinoma.
Labiano I, Huerta AE, Alsina M, Arasanz H, Castro N, Mendaza S, Lecumberri A, Gonzalez-Borja I, Guerrero-Setas D, Patiño-Garcia A, Alkorta-Aranburu G, Hernández-Garcia I, Arrazubi V, Mata E, Gomez D, Viudez A, Vera R
Sci Rep, 14(1):16203, 13 Jul 2024
Cited by: 0 articles | PMID: 39003322 | PMCID: PMC11246447
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Building on the clinical applicability of ctDNA analysis in non-metastatic pancreatic ductal adenocarcinoma
Labiano I, Huerta AE, Alsina M, Arasanz H, Castro N, Mendaza S, Lecumberri A, Gonzalez-Borja I, Guerrero-Setas D, Patiño-Garcia A, Alkorta-Aranburu G, Hernandez-Garcia I, Arrazubi V, Mata E, Gomez D, Viudez A, Vera R
Research Square, 02 May 2024
Cited by: 0 articles | PPR: PPR846884
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Gut microbiota produces biofilm-associated amyloids with potential for neurodegeneration.
Fernández-Calvet A, Matilla-Cuenca L, Izco M, Navarro S, Serrano M, Ventura S, Blesa J, Herráiz M, Alkorta-Aranburu G, Galera S, Ruiz de Los Mozos I, Mansego ML, Toledo-Arana A, Alvarez-Erviti L, Valle J
Nat Commun, 15(1):4150, 16 May 2024
Cited by: 1 article | PMID: 38755164 | PMCID: PMC11099085
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Whole exome sequencing and machine learning germline analysis of individuals presenting with extreme phenotypes of high and low risk of developing tobacco-associated lung adenocarcinoma.
Patiño-García A, Guruceaga E, Andueza MP, Ocón M, Fodop Sokoudjou JJ, de Villalonga Zornoza N, Alkorta-Aranburu G, Uria IT, Gurpide A, Camps C, Jantus-Lewintre E, Navamuel-Andueza M, Sanmamed MF, Melero I, Elgendy M, Fusco JP, Zulueta JJ, de-Torres JP, Bastarrika G, [...] Perez-Gracia JL
EBioMedicine, 102:105048, 13 Mar 2024
Cited by: 0 articles | PMID: 38484556 | PMCID: PMC10955643
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Next-generation sequencing improves precision medicine in hearing loss.
Imizcoz T, Prieto-Matos C, Manrique-Huarte R, Calavia D, Huarte A, Pruneda PC, Ordoñez GR, Cañada-Higueras E, Patiño-García A, Alkorta-Aranburu G, Manrique Rodríguez M
Front Genet, 14:1264899, 22 Sep 2023
Cited by: 0 articles | PMID: 37811145 | PMCID: PMC10557071
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Laboratory Cross-Comparison and Ring Test Trial for Tumor BRCA Testing in a Multicenter Epithelial Ovarian Cancer Series: The BORNEO GEICO 60-0 Study.
Garcia-Casado Z, Oaknin A, Mendiola M, Alkorta-Aranburu G, Antunez-Lopez JR, Moreno-Bueno G, Palacios J, Yubero A, Marquez R, Gallego A, Sanchez-Heras AB, Lopez-Guerrero JA, Lopez-Guerrero JA, Perez-Segura C, Barretina-Ginesta P, Alarcon J, Gaba L, Marquez A, Matito J, [...] Vivancos A
J Pers Med, 12(11):1842, 04 Nov 2022
Cited by: 1 article | PMID: 36579549 | PMCID: PMC9698073
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Primary trimethylaminuria syndrome: more than an unpleasant odor.
Antoñanzas J, Querol-Cisneros E, Alkorta-Aranburu G, Patiño-García A, España A
Int J Dermatol, 62(3):e176-e178, 17 Aug 2022
Cited by: 0 articles | PMID: 35975805
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NGS-Based Molecular Karyotyping of Multiple Myeloma: Results from the GEM12 Clinical Trial.
Rosa-Rosa JM, Cuenca I, Medina A, Vázquez I, Sánchez-delaCruz A, Buenache N, Sánchez R, Jiménez C, Rosiñol L, Gutiérrez NC, Ruiz-Heredia Y, Barrio S, Oriol A, Martin-Ramos ML, Blanchard MJ, Ayala R, Ríos-Tamayo R, Sureda A, Hernández MT, [...] Martínez-Lopez J
Cancers (Basel), 14(20):5169, 21 Oct 2022
Cited by: 1 article | PMID: 36291952 | PMCID: PMC9601262
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Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma.
Gállego Pérez-Larraya J, Garcia-Moure M, Labiano S, Patiño-García A, Dobbs J, Gonzalez-Huarriz M, Zalacain M, Marrodan L, Martinez-Velez N, Puigdelloses M, Laspidea V, Astigarraga I, Lopez-Ibor B, Cruz O, Oscoz Lizarbe M, Hervas-Stubbs S, Alkorta-Aranburu G, Tamayo I, Tavira B, [...] Alonso MM
N Engl J Med, 386(26):2471-2481, 01 Jun 2022
Cited by: 103 articles | PMID: 35767439
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Familial primary cutaneous amyloidosis: Caspase activation may be involved in amyloid formation.
Antoñanzas J, Pelacho-Samper B, Alkorta-Aranburu G, Echeveste JI, Alonso AE
Exp Dermatol, 31(10):1638-1640, 25 Jul 2022
Cited by: 0 articles | PMID: 35790029 | PMCID: PMC9796099
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Next-generation sequencing of bile cell-free DNA for the early detection of patients with malignant biliary strictures.
Arechederra M, Rullán M, Amat I, Oyon D, Zabalza L, Elizalde M, Latasa MU, Mercado MR, Ruiz-Clavijo D, Saldaña C, Fernández-Urién I, Carrascosa J, Jusué V, Guerrero-Setas D, Zazpe C, González-Borja I, Sangro B, Herranz JM, Purroy A, [...] Avila MA
Gut, 71(6):1141-1151, 20 Jul 2021
Cited by: 23 articles | PMID: 34285068 | PMCID: PMC9120390
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Machine Learning-Based Approach Highlights the Use of a Genomic Variant Profile for Precision Medicine in Ovarian Failure.
Henarejos-Castillo I, Aleman A, Martinez-Montoro B, Gracia-Aznárez FJ, Sebastian-Leon P, Romeu M, Remohi J, Patiño-Garcia A, Royo P, Alkorta-Aranburu G, Diaz-Gimeno P
J Pers Med, 11(7):609, 27 Jun 2021
Cited by: 2 articles | PMID: 34199109 | PMCID: PMC8305607
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Performance comparison of two next-generation sequencing panels to detect actionable mutations in cell-free DNA in cancer patients.
Macías M, Cañada-Higueras E, Alegre E, Bielsa A, Gracia J, Patiño-García A, Ferrer-Costa R, Sendino T, Andueza MP, Mateos B, Rodríguez J, Corral J, Gúrpide A, Lopez-Picazo JM, Perez-Gracia JL, Gil-Bazo I, Alkorta-Aranburu G, González Á
Clin Chem Lab Med, 58(8):1341-1348, 01 Jul 2020
Cited by: 6 articles | PMID: 32623849
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The Dynamic Use of EGFR Mutation Analysis in Cell-Free DNA as a Follow-Up Biomarker during Different Treatment Lines in Non-Small-Cell Lung Cancer Patients.
Macías M, Alegre E, Alkorta-Aranburu G, Patiño-García A, Mateos B, Andueza MP, Gúrpide A, Lopez-Picazo JM, Gil-Bazo I, Perez-Gracia JL, González Á
Dis Markers, 2019:7954921, 23 Jan 2019
Cited by: 7 articles | PMID: 30809319 | PMCID: PMC6364099
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Reprogramming human T cell function and specificity with non-viral genome targeting.
Roth TL, Puig-Saus C, Yu R, Shifrut E, Carnevale J, Li PJ, Hiatt J, Saco J, Krystofinski P, Li H, Tobin V, Nguyen DN, Lee MR, Putnam AL, Ferris AL, Chen JW, Schickel JN, Pellerin L, Carmody D, [...] Marson A
Nature, 559(7714):405-409, 11 Jul 2018
Cited by: 422 articles | PMID: 29995861 | PMCID: PMC6239417
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Does arterial hypertension influence the onset of Huntington's disease?
Valcárcel-Ocete L, Fullaondo A, Alkorta-Aranburu G, García-Barcina M, Roos RAC, Hjermind LE, Saft C, Frontali M, Reilmann R, Rickards H, REGISTRY investigators of the European Huntington’s Disease Network (EHDN), Zubiaga AM, Aguirre A
PLoS One, 13(5):e0197975, 23 May 2018
Cited by: 7 articles | PMID: 29791508 | PMCID: PMC5965871
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Reprogramming human T cell function and specificity with non-viral genome targeting
Roth TL, Puig-Saus C, Yu R, Shifrut E, Carnevale J, Hiatt J, Saco J, Li H, Li J, Tobin V, Nguyen D, Ferris AM, Chen J, Schickel J, Pellerin L, Carmody D, Alkorta-Aranburu G, Del Gaudio D, Matsumoto H, [...] Marson A
bioRxiv, 31 Aug 2017
Cited by: 1 article | PPR: PPR21494
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Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA.
Sanyoura M, Jacobsen L, Carmody D, Del Gaudio D, Alkorta-Aranburu G, Arndt K, Hu Y, Kobiernicki F, Kusmartseva I, Atkinson MA, Philipson LH, Schatz D, Campbell-Thompson M, Greeley SAW
J Clin Endocrinol Metab, 103(1):35-45, 01 Jan 2018
Cited by: 16 articles | PMID: 28938416 | PMCID: PMC5761488
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Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes.
Guidugli L, Johnson AK, Alkorta-Aranburu G, Nelakuditi V, Arndt K, Churpek JE, Godley LA, Townsley D, Young NS, Fitzpatrick C, Del Gaudio D, Das S, Li Z
Leukemia, 31(5):1226-1229, 20 Jan 2017
Cited by: 29 articles | PMID: 28104920 | PMCID: PMC5420790
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Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3.
Infante E, Alkorta-Aranburu G, El-Gharbawy A
Clin Case Rep, 5(8):1277-1283, 28 Jun 2017
Cited by: 4 articles | PMID: 28781842 | PMCID: PMC5538066
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Olfactory Dysfunction in Older Adults is Associated with Feelings of Depression and Loneliness.
Sivam A, Wroblewski KE, Alkorta-Aranburu G, Barnes LL, Wilson RS, Bennett DA, Pinto JM
Chem Senses, 41(4):293-299, 24 Jan 2016
Cited by: 26 articles | PMID: 26809485 | PMCID: PMC5006107
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Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults.
Dong J, Yang J, Tranah G, Franceschini N, Parimi N, Alkorta-Aranburu G, Xu Z, Alonso A, Cummings SR, Fornage M, Huang X, Kritchevsky S, Liu Y, London S, Niu L, Wilson RS, De Jager PL, Yu L, Singleton AB, [...] Chen H
Medicine (Baltimore), 94(47):e1892, 01 Nov 2015
Cited by: 10 articles | PMID: 26632684 | PMCID: PMC5058953
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Improved molecular diagnosis of patients with neonatal diabetes using a combined next-generation sequencing and MS-MLPA approach.
Alkorta-Aranburu G, Sukhanova M, Carmody D, Hoffman T, Wysinger L, Keller-Ramey J, Li Z, Johnson AK, Kobiernicki F, Botes S, Fitzpatrick C, Das S, Del Gaudio D
J Pediatr Endocrinol Metab, 29(5):523-531, 01 May 2016
Cited by: 12 articles | PMID: 26894574
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PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population.
Livne OE, Han L, Alkorta-Aranburu G, Wentworth-Sheilds W, Abney M, Ober C, Nicolae DL
PLoS Comput Biol, 11(3):e1004139, 03 Mar 2015
Cited by: 24 articles | PMID: 25735005 | PMCID: PMC4348507
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Estimating the Ages of Selection Signals from Different Epochs in Human History.
Nakagome S, Alkorta-Aranburu G, Amato R, Howie B, Peter BM, Hudson RR, Di Rienzo A
Mol Biol Evol, 33(3):657-669, 05 Nov 2015
Cited by: 20 articles | PMID: 26545921 | PMCID: PMC5009997
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1-25 of 38 results

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Search life-sciences literature (45,100,050 articles, preprints and more)

Search results

Building on the clinical applicability of ctDNA analysis in non-metastatic pancreatic ductal adenocarcinoma.

Building on the clinical applicability of ctDNA analysis in non-metastatic pancreatic ductal adenocarcinoma

Gut microbiota produces biofilm-associated amyloids with potential for neurodegeneration.

Whole exome sequencing and machine learning germline analysis of individuals presenting with extreme phenotypes of high and low risk of developing tobacco-associated lung adenocarcinoma.

Next-generation sequencing improves precision medicine in hearing loss.

Laboratory Cross-Comparison and Ring Test Trial for Tumor BRCA Testing in a Multicenter Epithelial Ovarian Cancer Series: The BORNEO GEICO 60-0 Study.

Primary trimethylaminuria syndrome: more than an unpleasant odor.

NGS-Based Molecular Karyotyping of Multiple Myeloma: Results from the GEM12 Clinical Trial.

Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma.

Familial primary cutaneous amyloidosis: Caspase activation may be involved in amyloid formation.

Next-generation sequencing of bile cell-free DNA for the early detection of patients with malignant biliary strictures.

Machine Learning-Based Approach Highlights the Use of a Genomic Variant Profile for Precision Medicine in Ovarian Failure.

Performance comparison of two next-generation sequencing panels to detect actionable mutations in cell-free DNA in cancer patients.

The Dynamic Use of EGFR Mutation Analysis in Cell-Free DNA as a Follow-Up Biomarker during Different Treatment Lines in Non-Small-Cell Lung Cancer Patients.

Reprogramming human T cell function and specificity with non-viral genome targeting.

Does arterial hypertension influence the onset of Huntington's disease?

Reprogramming human T cell function and specificity with non-viral genome targeting

Pancreatic Histopathology of Human Monogenic Diabetes Due to Causal Variants in KCNJ11, HNF1A, GATA6, and LMNA.

Clinical utility of gene panel-based testing for hereditary myelodysplastic syndrome/acute leukemia predisposition syndromes.

Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3.

Olfactory Dysfunction in Older Adults is Associated with Feelings of Depression and Loneliness.

Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults.

Improved molecular diagnosis of patients with neonatal diabetes using a combined next-generation sequencing and MS-MLPA approach.

PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population.

Estimating the Ages of Selection Signals from Different Epochs in Human History.

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