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Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29].

Clinical immunology (Orlando, Fla.)

Harris VM, Sharma R, Cavett J, Kurien BT, Liu K, Koelsch KA, Rasmussen A, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Alarcon-Riquelme ME, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Xie G, Siminovitch KA, Ng WF, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Mariette X, Lessard CJ, Harley JB, Sivils KL, Scofield RH.
PMID: 29195081
Clin Immunol. 2018 Feb;187:137-138. doi: 10.1016/j.clim.2017.11.012. Epub 2017 Dec 07.

No abstract available.

Cite
Harris VM, Sharma R, Cavett J, et al. Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29]. Clin Immunol. 2017;187:137-138doi: 10.1016/j.clim.2017.11.012.
Harris, V. M., Sharma, R., Cavett, J., Kurien, B. T., Liu, K., Koelsch, K. A., Rasmussen, A., Radfar, L., Lewis, D., Stone, D. U., Kaufman, C. E., Li, S., Segal, B., Wallace, D. J., Weisman, M. H., Venuturupalli, S., Kelly, J. A., Alarcon-Riquelme, M. E., Pons-Estel, B., Jonsson, R., Lu, X., Gottenberg, J. E., Anaya, J. M., Cunninghame-Graham, D. S., Huang, A. J. W., Brennan, M. T., Hughes, P., Alevizos, I., Miceli-Richard, C., Keystone, E. C., Bykerk, V. P., Hirschfield, G., Xie, G., Siminovitch, K. A., Ng, W. F., Nordmark, G., Bucher, S. M., Eriksson, P., Omdal, R., Rhodus, N. L., Rischmueller, M., Rohrer, M., Wahren-Herlenius, M., Witte, T., Mariette, X., Lessard, C. J., Harley, J. B., Sivils, K. L., & Scofield, R. H. (2018). Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29]. Clinical immunology (Orlando, Fla.), 187137-138. https://doi.org/10.1016/j.clim.2017.11.012
Harris, Valerie M, et al. "Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29]." Clinical immunology (Orlando, Fla.) vol. 187 (2018): 137-138. doi: https://doi.org/10.1016/j.clim.2017.11.012
Harris VM, Sharma R, Cavett J, Kurien BT, Liu K, Koelsch KA, Rasmussen A, Radfar L, Lewis D, Stone DU, Kaufman CE, Li S, Segal B, Wallace DJ, Weisman MH, Venuturupalli S, Kelly JA, Alarcon-Riquelme ME, Pons-Estel B, Jonsson R, Lu X, Gottenberg JE, Anaya JM, Cunninghame-Graham DS, Huang AJW, Brennan MT, Hughes P, Alevizos I, Miceli-Richard C, Keystone EC, Bykerk VP, Hirschfield G, Xie G, Siminovitch KA, Ng WF, Nordmark G, Bucher SM, Eriksson P, Omdal R, Rhodus NL, Rischmueller M, Rohrer M, Wahren-Herlenius M, Witte T, Mariette X, Lessard CJ, Harley JB, Sivils KL, Scofield RH. Corrigendum to "Klinefelter's syndrome (47,XXY) is in excess among men with Sjögren's syndrome" [Clin. Immunol. 168 (2016) 25-29]. Clin Immunol. 2018 Feb;187:137-138. doi: 10.1016/j.clim.2017.11.012. Epub 2017 Dec 07. PMID: 29195081.
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Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality.

The Journal of clinical investigation

Nakanishi T, Pigazzini S, Degenhardt F, Cordioli M, Butler-Laporte G, Maya-Miles D, Bujanda L, Bouysran Y, Niemi ME, Palom A, Ellinghaus D, Khan A, Martínez-Bueno M, Rolker S, Amitrano S, Roade Tato L, Fava F, Spinner CD, Prati D, Bernardo D, Garcia F, Darcis G, Fernández-Cadenas I, Holter JC, Banales JM, Frithiof R, Kiryluk K, Duga S, Asselta R, Pereira AC, Romero-Gómez M, Nafría-Jiménez B, Hov JR, Migeotte I, Renieri A, Planas AM, Ludwig KU, Buti M, Rahmouni S, Alarcón-Riquelme ME, Schulte EC, Franke A, Karlsen TH, Valenti L, Zeberg H, Richards JB, Ganna A.
PMID: 34597274
J Clin Invest. 2021 Dec 01;131(23). doi: 10.1172/JCI152386.

BackgroundThere is considerable variability in COVID-19 outcomes among younger adults, and some of this variation may be due to genetic predisposition.MethodsWe combined individual level data from 13,888 COVID-19 patients (n = 7185 hospitalized) from 17 cohorts in 9 countries...

Cite
Nakanishi T, Pigazzini S, Degenhardt F, et al. Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. J Clin Invest. 2021;131(23)doi: 10.1172/JCI152386.
Nakanishi, T., Pigazzini, S., Degenhardt, F., Cordioli, M., Butler-Laporte, G., Maya-Miles, D., Bujanda, L., Bouysran, Y., Niemi, M. E., Palom, A., Ellinghaus, D., Khan, A., Martínez-Bueno, M., Rolker, S., Amitrano, S., Roade Tato, L., Fava, F., Spinner, C. D., Prati, D., Bernardo, D., Garcia, F., Darcis, G., Fernández-Cadenas, I., Holter, J. C., Banales, J. M., Frithiof, R., Kiryluk, K., Duga, S., Asselta, R., Pereira, A. C., Romero-Gómez, M., Nafría-Jiménez, B., Hov, J. R., Migeotte, I., Renieri, A., Planas, A. M., Ludwig, K. U., Buti, M., Rahmouni, S., Alarcón-Riquelme, M. E., Schulte, E. C., Franke, A., Karlsen, T. H., Valenti, L., Zeberg, H., Richards, J. B., & Ganna, A. (2021). Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. The Journal of clinical investigation, 131(23), . https://doi.org/10.1172/JCI152386
Nakanishi, Tomoko, et al. "Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality." The Journal of clinical investigation vol. 131,23 (2021). doi: https://doi.org/10.1172/JCI152386
Nakanishi T, Pigazzini S, Degenhardt F, Cordioli M, Butler-Laporte G, Maya-Miles D, Bujanda L, Bouysran Y, Niemi ME, Palom A, Ellinghaus D, Khan A, Martínez-Bueno M, Rolker S, Amitrano S, Roade Tato L, Fava F, Spinner CD, Prati D, Bernardo D, Garcia F, Darcis G, Fernández-Cadenas I, Holter JC, Banales JM, Frithiof R, Kiryluk K, Duga S, Asselta R, Pereira AC, Romero-Gómez M, Nafría-Jiménez B, Hov JR, Migeotte I, Renieri A, Planas AM, Ludwig KU, Buti M, Rahmouni S, Alarcón-Riquelme ME, Schulte EC, Franke A, Karlsen TH, Valenti L, Zeberg H, Richards JB, Ganna A. Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality. J Clin Invest. 2021 Dec 01;131(23). doi: 10.1172/JCI152386. PMID: 34597274; PMCID: PMC8631592.
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Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data.

Genes

Ongaro L, Molinaro L, Flores R, Marnetto D, Capodiferro MR, Alarcón-Riquelme ME, Moreno-Estrada A, Mabunda N, Ventura M, Tambets K, Achilli A, Capelli C, Metspalu M, Pagani L, Montinaro F.
PMID: 34680976
Genes (Basel). 2021 Oct 07;12(10). doi: 10.3390/genes12101580.

A general imbalance in the proportion of disembarked males and females in the Americas has been documented during the Trans-Atlantic Slave Trade and the Colonial Era and, although less prominent, more recently. This imbalance may have left a signature...

Cite
Ongaro L, Molinaro L, Flores R, et al. Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. Genes (Basel). 2021;12(10)doi: 10.3390/genes12101580.
Ongaro, L., Molinaro, L., Flores, R., Marnetto, D., Capodiferro, M. R., Alarcón-Riquelme, M. E., Moreno-Estrada, A., Mabunda, N., Ventura, M., Tambets, K., Achilli, A., Capelli, C., Metspalu, M., Pagani, L., & Montinaro, F. (2021). Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. Genes, 12(10), . https://doi.org/10.3390/genes12101580
Ongaro, Linda, et al. "Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data." Genes vol. 12,10 (2021). doi: https://doi.org/10.3390/genes12101580
Ongaro L, Molinaro L, Flores R, Marnetto D, Capodiferro MR, Alarcón-Riquelme ME, Moreno-Estrada A, Mabunda N, Ventura M, Tambets K, Achilli A, Capelli C, Metspalu M, Pagani L, Montinaro F. Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. Genes (Basel). 2021 Oct 07;12(10). doi: 10.3390/genes12101580. PMID: 34680976; PMCID: PMC8535939.
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Cytotoxic lymphocytes are dysregulated in multisystem inflammatory syndrome in children.

medRxiv : the preprint server for health sciences

Beckmann ND, Comella PH, Cheng E, Lepow L, Beckmann AG, Mouskas K, Simons NW, Hoffman GE, Francoeur NJ, Del Valle DM, Kang G, Moya E, Wilkins L, Le Berichel J, Chang C, Marvin R, Calorossi S, Lansky A, Walker L, Yi N, Yu A, Harnett M, Eaton M, Hatem S, Jamal H, Akyatan A, Tabachnikova A, Liharska LE, Cotter L, Fennessey B, Vaid A, Barturen G, Tyler SR, Shah H, Wang YC, Hara Sridhar S, Soto J, Bose S, Madrid K, Ellis E, Merzier E, Vlachos K, Fishman N, Tin M, Smith M, Xie H, Patel M, Argueta K, Harris J, Karekar N, Batchelor C, Lacunza J, Yishak M, Tuballes K, Scott L, Kumar A, Jaladanki S, Thompson R, Clark E, Losic B, Zhu J, Wang W, Kasarskis A, Glicksberg BS, Nadkarni G, Bogunovic D, Elaiho C, Gangadharan S, Ofori-Amanfo G, Alesso-Carra K, Onel K, Wilson KM, Argmann C, Alarcón-Riquelme ME, Marron TU, Rahman A, Kim-Schulze S, Gnjatic S, Gelb BD, Merad M, Sebra R, Schadt EE, Charney AW.
PMID: 32909006
medRxiv. 2020 Sep 02; doi: 10.1101/2020.08.29.20182899.

Multisystem inflammatory syndrome in children (MIS-C) presents with fever, inflammation and multiple organ involvement in individuals under 21 years following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. To identify genes, pathways and cell types driving MIS-C, we sequenced...

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Beckmann ND, Comella PH, Cheng E, et al. Cytotoxic lymphocytes are dysregulated in multisystem inflammatory syndrome in children. medRxiv. 2020;doi: 10.1101/2020.08.29.20182899.
Beckmann, N. D., Comella, P. H., Cheng, E., Lepow, L., Beckmann, A. G., Mouskas, K., Simons, N. W., Hoffman, G. E., Francoeur, N. J., Del Valle, D. M., Kang, G., Moya, E., Wilkins, L., Le Berichel, J., Chang, C., Marvin, R., Calorossi, S., Lansky, A., Walker, L., Yi, N., Yu, A., Harnett, M., Eaton, M., Hatem, S., Jamal, H., Akyatan, A., Tabachnikova, A., Liharska, L. E., Cotter, L., Fennessey, B., Vaid, A., Barturen, G., Tyler, S. R., Shah, H., Wang, Y. C., Hara Sridhar, S., Soto, J., Bose, S., Madrid, K., Ellis, E., Merzier, E., Vlachos, K., Fishman, N., Tin, M., Smith, M., Xie, H., Patel, M., Argueta, K., Harris, J., Karekar, N., Batchelor, C., Lacunza, J., Yishak, M., Tuballes, K., Scott, L., Kumar, A., Jaladanki, S., Thompson, R., Clark, E., Losic, B., Zhu, J., Wang, W., Kasarskis, A., Glicksberg, B. S., Nadkarni, G., Bogunovic, D., Elaiho, C., Gangadharan, S., Ofori-Amanfo, G., Alesso-Carra, K., Onel, K., Wilson, K. M., Argmann, C., Alarcón-Riquelme, M. E., Marron, T. U., Rahman, A., Kim-Schulze, S., Gnjatic, S., Gelb, B. D., Merad, M., Sebra, R., Schadt, E. E., & Charney, A. W. (2020). Cytotoxic lymphocytes are dysregulated in multisystem inflammatory syndrome in children. medRxiv : the preprint server for health sciences, . https://doi.org/10.1101/2020.08.29.20182899
Beckmann, Noam D, et al. "Cytotoxic lymphocytes are dysregulated in multisystem inflammatory syndrome in children." medRxiv : the preprint server for health sciences vol. (2020). doi: https://doi.org/10.1101/2020.08.29.20182899
Beckmann ND, Comella PH, Cheng E, Lepow L, Beckmann AG, Mouskas K, Simons NW, Hoffman GE, Francoeur NJ, Del Valle DM, Kang G, Moya E, Wilkins L, Le Berichel J, Chang C, Marvin R, Calorossi S, Lansky A, Walker L, Yi N, Yu A, Harnett M, Eaton M, Hatem S, Jamal H, Akyatan A, Tabachnikova A, Liharska LE, Cotter L, Fennessey B, Vaid A, Barturen G, Tyler SR, Shah H, Wang YC, Hara Sridhar S, Soto J, Bose S, Madrid K, Ellis E, Merzier E, Vlachos K, Fishman N, Tin M, Smith M, Xie H, Patel M, Argueta K, Harris J, Karekar N, Batchelor C, Lacunza J, Yishak M, Tuballes K, Scott L, Kumar A, Jaladanki S, Thompson R, Clark E, Losic B, Zhu J, Wang W, Kasarskis A, Glicksberg BS, Nadkarni G, Bogunovic D, Elaiho C, Gangadharan S, Ofori-Amanfo G, Alesso-Carra K, Onel K, Wilson KM, Argmann C, Alarcón-Riquelme ME, Marron TU, Rahman A, Kim-Schulze S, Gnjatic S, Gelb BD, Merad M, Sebra R, Schadt EE, Charney AW. Cytotoxic lymphocytes are dysregulated in multisystem inflammatory syndrome in children. medRxiv. 2020 Sep 02; doi: 10.1101/2020.08.29.20182899. PMID: 32909006; PMCID: PMC7480058.
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PeacoQC: Peak-based selection of high quality cytometry data.

Cytometry. Part A : the journal of the International Society for Analytical Cytology

Emmaneel A, Quintelier K, Sichien D, Rybakowska P, Marañón C, Alarcón-Riquelme ME, Van Isterdael G, Van Gassen S, Saeys Y.
PMID: 34549881
Cytometry A. 2021 Sep 22; doi: 10.1002/cyto.a.24501. Epub 2021 Sep 22.

In cytometry analysis, a large number of markers is measured for thousands or millions of cells, resulting in high-dimensional datasets. During the measurement of these samples, erroneous events can occur such as clogs, speed changes, slow uptake of the...

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Emmaneel A, Quintelier K, Sichien D, et al. PeacoQC: Peak-based selection of high quality cytometry data. Cytometry A. 2021;doi: 10.1002/cyto.a.24501.
Emmaneel, A., Quintelier, K., Sichien, D., Rybakowska, P., Marañón, C., Alarcón-Riquelme, M. E., Van Isterdael, G., Van Gassen, S., & Saeys, Y. (2021). PeacoQC: Peak-based selection of high quality cytometry data. Cytometry. Part A : the journal of the International Society for Analytical Cytology, . https://doi.org/10.1002/cyto.a.24501
Emmaneel, Annelies, et al. "PeacoQC: Peak-based selection of high quality cytometry data." Cytometry. Part A : the journal of the International Society for Analytical Cytology vol. (2021). doi: https://doi.org/10.1002/cyto.a.24501
Emmaneel A, Quintelier K, Sichien D, Rybakowska P, Marañón C, Alarcón-Riquelme ME, Van Isterdael G, Van Gassen S, Saeys Y. PeacoQC: Peak-based selection of high quality cytometry data. Cytometry A. 2021 Sep 22; doi: 10.1002/cyto.a.24501. Epub 2021 Sep 22. PMID: 34549881.
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Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature.

Scientific reports

Teruel M, Barturen G, Martínez-Bueno M, Castellini-Pérez O, Barroso-Gil M, Povedano E, Kerick M, Català-Moll F, Makowska Z, Buttgereit A, Pers JO, Marañón C, Ballestar E, Martin J, Carnero-Montoro E, Alarcón-Riquelme ME.
PMID: 34857786
Sci Rep. 2021 Dec 02;11(1):23292. doi: 10.1038/s41598-021-01324-0.

Primary Sjögren's syndrome (SS) is a systemic autoimmune disease characterized by lymphocytic infiltration and damage of exocrine salivary and lacrimal glands. The etiology of SS is complex with environmental triggers and genetic factors involved. By conducting an integrated multi-omics...

Cite
Teruel M, Barturen G, Martínez-Bueno M, et al. Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature. Sci Rep. 2021;11(1):23292doi: 10.1038/s41598-021-01324-0.
Teruel, M., Barturen, G., Martínez-Bueno, M., Castellini-Pérez, O., Barroso-Gil, M., Povedano, E., Kerick, M., Català-Moll, F., Makowska, Z., Buttgereit, A., Pers, J. O., Marañón, C., Ballestar, E., Martin, J., Carnero-Montoro, E., & Alarcón-Riquelme, M. E. (2021). Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature. Scientific reports, 11(1), 23292. https://doi.org/10.1038/s41598-021-01324-0
Teruel, María, et al. "Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature." Scientific reports vol. 11,1 (2021): 23292. doi: https://doi.org/10.1038/s41598-021-01324-0
Teruel M, Barturen G, Martínez-Bueno M, Castellini-Pérez O, Barroso-Gil M, Povedano E, Kerick M, Català-Moll F, Makowska Z, Buttgereit A, Pers JO, Marañón C, Ballestar E, Martin J, Carnero-Montoro E, Alarcón-Riquelme ME. Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature. Sci Rep. 2021 Dec 02;11(1):23292. doi: 10.1038/s41598-021-01324-0. PMID: 34857786; PMCID: PMC8640069.
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Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas.

Human molecular genetics

Ongaro L, Mondal M, Flores R, Marnetto D, Molinaro L, Alarcón-Riquelme ME, Moreno-Estrada A, Mabunda N, Ventura M, Tambets K, Hellenthal G, Capelli C, Kivisild T, Metspalu M, Pagani L, Montinaro F.
PMID: 34196708
Hum Mol Genet. 2021 Nov 01;30(22):2123-2134. doi: 10.1093/hmg/ddab177.

American populations are one of the most interesting examples of recently admixed groups, where ancestral components from three major continental human groups (Africans, Eurasians and Native Americans) have admixed within the last 15 generations. Recently, several genetic surveys focusing...

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Ongaro L, Mondal M, Flores R, et al. Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas. Hum Mol Genet. 2021;30(22):2123-2134doi: 10.1093/hmg/ddab177.
Ongaro, L., Mondal, M., Flores, R., Marnetto, D., Molinaro, L., Alarcón-Riquelme, M. E., Moreno-Estrada, A., Mabunda, N., Ventura, M., Tambets, K., Hellenthal, G., Capelli, C., Kivisild, T., Metspalu, M., Pagani, L., & Montinaro, F. (2021). Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas. Human molecular genetics, 30(22), 2123-2134. https://doi.org/10.1093/hmg/ddab177
Ongaro, Linda, et al. "Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas." Human molecular genetics vol. 30,22 (2021): 2123-2134. doi: https://doi.org/10.1093/hmg/ddab177
Ongaro L, Mondal M, Flores R, Marnetto D, Molinaro L, Alarcón-Riquelme ME, Moreno-Estrada A, Mabunda N, Ventura M, Tambets K, Hellenthal G, Capelli C, Kivisild T, Metspalu M, Pagani L, Montinaro F. Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas. Hum Mol Genet. 2021 Nov 01;30(22):2123-2134. doi: 10.1093/hmg/ddab177. PMID: 34196708; PMCID: PMC8561420.
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Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature.

Scientific reports

Teruel M, Barturen G, Martínez-Bueno M, Castellini-Pérez O, Barroso-Gil M, Povedano E, Kerick M, Català-Moll F, Makowska Z, Buttgereit A, Pers JO, Marañón C, Ballestar E, Martin J, Carnero-Montoro E, Alarcón-Riquelme ME.
PMID: 34857786
Sci Rep. 2021 Dec 02;11(1):23292. doi: 10.1038/s41598-021-01324-0.

Primary Sjögren's syndrome (SS) is a systemic autoimmune disease characterized by lymphocytic infiltration and damage of exocrine salivary and lacrimal glands. The etiology of SS is complex with environmental triggers and genetic factors involved. By conducting an integrated multi-omics...

Cite
Teruel M, Barturen G, Martínez-Bueno M, et al. Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature. Sci Rep. 2021;11(1):23292doi: 10.1038/s41598-021-01324-0.
Teruel, M., Barturen, G., Martínez-Bueno, M., Castellini-Pérez, O., Barroso-Gil, M., Povedano, E., Kerick, M., Català-Moll, F., Makowska, Z., Buttgereit, A., Pers, J. O., Marañón, C., Ballestar, E., Martin, J., Carnero-Montoro, E., & Alarcón-Riquelme, M. E. (2021). Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature. Scientific reports, 11(1), 23292. https://doi.org/10.1038/s41598-021-01324-0
Teruel, María, et al. "Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature." Scientific reports vol. 11,1 (2021): 23292. doi: https://doi.org/10.1038/s41598-021-01324-0
Teruel M, Barturen G, Martínez-Bueno M, Castellini-Pérez O, Barroso-Gil M, Povedano E, Kerick M, Català-Moll F, Makowska Z, Buttgereit A, Pers JO, Marañón C, Ballestar E, Martin J, Carnero-Montoro E, Alarcón-Riquelme ME. Integrative epigenomics in Sjögren´s syndrome reveals novel pathways and a strong interaction between the HLA, autoantibodies and the interferon signature. Sci Rep. 2021 Dec 02;11(1):23292. doi: 10.1038/s41598-021-01324-0. PMID: 34857786; PMCID: PMC8640069.
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Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data.

Genes

Ongaro L, Molinaro L, Flores R, Marnetto D, Capodiferro MR, Alarcón-Riquelme ME, Moreno-Estrada A, Mabunda N, Ventura M, Tambets K, Achilli A, Capelli C, Metspalu M, Pagani L, Montinaro F.
PMID: 34680976
Genes (Basel). 2021 Oct 07;12(10). doi: 10.3390/genes12101580.

A general imbalance in the proportion of disembarked males and females in the Americas has been documented during the Trans-Atlantic Slave Trade and the Colonial Era and, although less prominent, more recently. This imbalance may have left a signature...

Cite
Ongaro L, Molinaro L, Flores R, et al. Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. Genes (Basel). 2021;12(10)doi: 10.3390/genes12101580.
Ongaro, L., Molinaro, L., Flores, R., Marnetto, D., Capodiferro, M. R., Alarcón-Riquelme, M. E., Moreno-Estrada, A., Mabunda, N., Ventura, M., Tambets, K., Achilli, A., Capelli, C., Metspalu, M., Pagani, L., & Montinaro, F. (2021). Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. Genes, 12(10), . https://doi.org/10.3390/genes12101580
Ongaro, Linda, et al. "Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data." Genes vol. 12,10 (2021). doi: https://doi.org/10.3390/genes12101580
Ongaro L, Molinaro L, Flores R, Marnetto D, Capodiferro MR, Alarcón-Riquelme ME, Moreno-Estrada A, Mabunda N, Ventura M, Tambets K, Achilli A, Capelli C, Metspalu M, Pagani L, Montinaro F. Evaluating the Impact of Sex-Biased Genetic Admixture in the Americas through the Analysis of Haplotype Data. Genes (Basel). 2021 Oct 07;12(10). doi: 10.3390/genes12101580. PMID: 34680976; PMCID: PMC8535939.
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[Systemic lupus erythematosus. «What do we know and where are we heading?»].

Reumatologia clinica

Alarcón Riquelme ME.
PMID: 21794669
Reumatol Clin. 2010 Jan-Feb;6(1):1-2. doi: 10.1016/j.reuma.2009.01.002. Epub 2009 May 28.

No abstract available.

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Alarcón Riquelme ME. Genética del lupus eritematoso generalizado. ¿Qué se sabe y a dónde se va? [Systemic lupus erythematosus. «What do we know and where are we heading?»]. Reumatol Clin. 2009;6(1):1-2doi: 10.1016/j.reuma.2009.01.002.
Alarcón Riquelme, M. E. (2010). Genética del lupus eritematoso generalizado. ¿Qué se sabe y a dónde se va? [Systemic lupus erythematosus. «What do we know and where are we heading?»]. Reumatologia clinica, 6(1), 1-2. https://doi.org/10.1016/j.reuma.2009.01.002
Alarcón Riquelme, Marta Eugenia. "Genética del lupus eritematoso generalizado. ¿Qué se sabe y a dónde se va?" [Systemic lupus erythematosus. «What do we know and where are we heading?»]. Reumatologia clinica vol. 6,1 (2010): 1-2. doi: https://doi.org/10.1016/j.reuma.2009.01.002
Alarcón Riquelme ME. Genética del lupus eritematoso generalizado. ¿Qué se sabe y a dónde se va? [Systemic lupus erythematosus. «What do we know and where are we heading?»]. Reumatol Clin. 2010 Jan-Feb;6(1):1-2. doi: 10.1016/j.reuma.2009.01.002. Epub 2009 May 28. Spanish. PMID: 21794669.
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Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease.

Frontiers in immunology

Frejo L, Requena T, Okawa S, Gallego-Martinez A, Martinez-Bueno M, Aran I, Batuecas-Caletrio A, Benitez-Rosario J, Espinosa-Sanchez JM, Fraile-Rodrigo JJ, García-Arumi AM, González-Aguado R, Marques P, Martin-Sanz E, Perez-Fernandez N, Pérez-Vázquez P, Perez-Garrigues H, Santos-Perez S, Soto-Varela A, Tapia MC, Trinidad-Ruiz G, Del Sol A, Alarcon Riquelme ME, Lopez-Escamez JA.
PMID: 29326686
Front Immunol. 2017 Dec 13;8:1739. doi: 10.3389/fimmu.2017.01739. eCollection 2017.

Meniere's disease (MD) is a rare disorder characterized by episodic vertigo, sensorineural hearing loss, tinnitus, and aural fullness. It is associated with a fluid imbalance between the secretion of endolymph in the cochlear duct and its reabsorption into the...

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Frejo L, Requena T, Okawa S, et al. Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease. Front Immunol. 2017;8:1739doi: 10.3389/fimmu.2017.01739.
Frejo, L., Requena, T., Okawa, S., Gallego-Martinez, A., Martinez-Bueno, M., Aran, I., Batuecas-Caletrio, A., Benitez-Rosario, J., Espinosa-Sanchez, J. M., Fraile-Rodrigo, J. J., García-Arumi, A. M., González-Aguado, R., Marques, P., Martin-Sanz, E., Perez-Fernandez, N., Pérez-Vázquez, P., Perez-Garrigues, H., Santos-Perez, S., Soto-Varela, A., Tapia, M. C., Trinidad-Ruiz, G., Del Sol, A., Alarcon Riquelme, M. E., & Lopez-Escamez, J. A. (2017). Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease. Frontiers in immunology, 81739. https://doi.org/10.3389/fimmu.2017.01739
Frejo, Lidia, et al. "Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease." Frontiers in immunology vol. 8 (2017): 1739. doi: https://doi.org/10.3389/fimmu.2017.01739
Frejo L, Requena T, Okawa S, Gallego-Martinez A, Martinez-Bueno M, Aran I, Batuecas-Caletrio A, Benitez-Rosario J, Espinosa-Sanchez JM, Fraile-Rodrigo JJ, García-Arumi AM, González-Aguado R, Marques P, Martin-Sanz E, Perez-Fernandez N, Pérez-Vázquez P, Perez-Garrigues H, Santos-Perez S, Soto-Varela A, Tapia MC, Trinidad-Ruiz G, Del Sol A, Alarcon Riquelme ME, Lopez-Escamez JA. Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere's Disease. Front Immunol. 2017 Dec 13;8:1739. doi: 10.3389/fimmu.2017.01739. eCollection 2017. PMID: 29326686; PMCID: PMC5733484.
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Identification of a Shared Microbiomic and Metabolomic Profile in Systemic Autoimmune Diseases.

Journal of clinical medicine

Bellocchi C, Fernández-Ochoa Á, Montanelli G, Vigone B, Santaniello A, Quirantes-Piné R, Borrás-Linares I, Gerosa M, Artusi C, Gualtierotti R, Segura-Carrettero A, Alarcón-Riquelme ME, Beretta L.
PMID: 31450824
J Clin Med. 2019 Aug 23;8(9). doi: 10.3390/jcm8091291.

Dysbiosis has been described in systemic autoimmune diseases (SADs), including systemic lupus erythematosus (SLE), Sjögren's syndrome (SjS), and primary anti-phosholipid syndrome (PAPS), however the biological implications of these associations are often elusive. Stool and plasma samples from 114 subjects,...

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Bellocchi C, Fernández-Ochoa Á, Montanelli G, et al. Identification of a Shared Microbiomic and Metabolomic Profile in Systemic Autoimmune Diseases. J Clin Med. 2019;8(9)doi: 10.3390/jcm8091291.
Bellocchi, C., Fernández-Ochoa, �. �., Montanelli, G., Vigone, B., Santaniello, A., Quirantes-Piné, R., Borrás-Linares, I., Gerosa, M., Artusi, C., Gualtierotti, R., Segura-Carrettero, A., Alarcón-Riquelme, M. E., & Beretta, L. (2019). Identification of a Shared Microbiomic and Metabolomic Profile in Systemic Autoimmune Diseases. Journal of clinical medicine, 8(9), . https://doi.org/10.3390/jcm8091291
Bellocchi, Chiara, et al. "Identification of a Shared Microbiomic and Metabolomic Profile in Systemic Autoimmune Diseases." Journal of clinical medicine vol. 8,9 (2019). doi: https://doi.org/10.3390/jcm8091291
Bellocchi C, Fernández-Ochoa Á, Montanelli G, Vigone B, Santaniello A, Quirantes-Piné R, Borrás-Linares I, Gerosa M, Artusi C, Gualtierotti R, Segura-Carrettero A, Alarcón-Riquelme ME, Beretta L. Identification of a Shared Microbiomic and Metabolomic Profile in Systemic Autoimmune Diseases. J Clin Med. 2019 Aug 23;8(9). doi: 10.3390/jcm8091291. PMID: 31450824; PMCID: PMC6780636.
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