Estudio de asociación genómica para resistencia a Cooperia punctata en bovinos cruzados en el trópico subhúmedo de México

Autor: Adriana García-Ruíz, Felipe de Jesús Ruíz-Lopez, Miguel Alonso-Díaz, Elke Von-Son-de-Fernex, Sara Olazarán-Jenkins, Vicente Eliezer Vega-Murillo, Maria Eugenia López-Arellano

Publikováno v: Revista Mexicana de Ciencias Pecuarias, Vol 10, Iss 2, Pp 482-489 (2019)

El objetivo del presente estudio fue evaluar la resistencia a la infección natural por Cooperia spp. en bovinos jóvenes cruzados Cebú x Holstein, en trópico. Catorce (14) becerros de cuatro meses de edad fueron tratados con desparasitante y trasl

Externí odkaz: https://doaj.org/article/f7130f57ea114c4eb44dcd242fe6bfd6

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Autor: Alexandra Barry, Michelle T. McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Debiec, Yang Luo, China Nagano, Tomoko Horinouchi, Seulgi Jung, Manuela Colucci, Dina F. Ahram, Adele Mitrotti, Aditi Sinha, Nynke Teeninga, Gina Jin, Shirlee Shril, Gianluca Caridi, Monica Bodria, Tze Y. Lim, Rik Westland, Francesca Zanoni, Maddalena Marasa, Daniel Turudic, Mario Giordano, Loreto Gesualdo, Riccardo Magistroni, Isabella Pisani, Enrico Fiaccadori, Jana Reiterova, Silvio Maringhini, William Morello, Giovanni Montini, Patricia L. Weng, Francesco Scolari, Marijan Saraga, Velibor Tasic, Domenica Santoro, Joanna A. E. van Wijk, Danko Milošević, Yosuke Kawai, Krzysztof Kiryluk, Martin R. Pollak, Ali Gharavi, Fangmin Lin, Ana Cristina Simœs e Silva, Ruth J. F. Loos, Eimear E. Kenny, Michiel F. Schreuder, Aleksandra Zurowska, Claire Dossier, Gema Ariceta, Magdalena Drozynska-Duklas, Julien Hogan, Augustina Jankauskiene, Friedhelm Hildebrandt, Larisa Prikhodina, Kyuyoung Song, Arvind Bagga, Hae Cheong, Gian Marco Ghiggeri, Prayong Vachvanichsanong, Kandai Nozu, Dongwon Lee, Marina Vivarelli, Soumya Raychaudhuri, Katsushi Tokunaga, Simone Sanna-Cherchi, Pierre Ronco, Kazumoto Iijima, Matthew G. Sampson

Publikováno v: Nature Communications, 14, 1
Nature communications, Berlin : Nature Research, 2023, vol. 14, no, 1, art. no. 2481, p. [1-13]
Nature Communications, 14(1):2481. Nature Publishing Group UK
Barry, A, McNulty, M T, Jia, X, Gupta, Y, Debiec, H, Luo, Y, Nagano, C, Horinouchi, T, Jung, S, Colucci, M, Ahram, D F, Mitrotti, A, Sinha, A, Teeninga, N, Jin, G, Shril, S, Caridi, G, Bodria, M, Lim, T Y, Westland, R, Zanoni, F, Marasa, M, Turudic, D, Giordano, M, Gesualdo, L, Magistroni, R, Pisani, I, Fiaccadori, E, Reiterova, J, Maringhini, S, Morello, W, Montini, G, Weng, P L, Scolari, F, Saraga, M, Tasic, V, Santoro, D, van Wijk, J A E, Milošević, D, Kawai, Y, Kiryluk, K, Pollak, M R, Gharavi, A, Lin, F, Simœs e Silva, A C, Loos, R J F, Kenny, E E, Schreuder, M F, Zurowska, A, Dossier, C, Ariceta, G, Drozynska-Duklas, M, Hogan, J, Jankauskiene, A, Hildebrandt, F, Prikhodina, L, Song, K, Bagga, A, Cheong, H, Ghiggeri, G M, Vachvanichsanong, P, Nozu, K, Lee, D, Vivarelli, M, Raychaudhuri, S, Tokunaga, K, Sanna-Cherchi, S, Ronco, P, Iijima, K & Sampson, M G 2023, ' Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome ', Nature Communications, vol. 14, no. 1, 2481 . https://doi.org/10.1038/s41467-023-37985-w
Nature Communications, 14
Scientia

Genetics; Minimal change disease; Paediatric kidney disease Genética; Enfermedad de cambios mínimos; Enfermedad renal pediátrica Genètica; Malaltia de canvis mínims; Malaltia renal pediàtrica Pediatric steroid-sensitive nephrotic syndrome (pSSN

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::247e30d3fe784484e81581f8b3b90843

Evidence for shared genetic risk factors between lymphangioleiomyomatosis and pulmonary function

Autor: Mireia Tena-Garitaonaindia, Berta Sáez, Wonji Kim, Álvaro Casanova, Coline H.M. van Moorsel, José Antonio Rodríguez-Portal, Rosalía Laporta, Eline Blommaert, Krinio Giannikou, Julio Ancochea, Antonio Roman, Fermín Sánchez de Medina, Miquel Angel Pujana, Rafael de Cid, Maria Molina-Molina, Carmen Herranz, Piedad Ussetti, Claudia Valenzuela, Francesca Mateo, Roderic Espín, Alexandra Baiges, Marian J.R. Quanjel, Xavier Farré, David J. Kwiatkowski, Sungho Won, Joanne J. van der Vis

Publikováno v: Scientia
Digibug. Repositorio Institucional de la Universidad de Granada
instname
ERJ Open Research
article-version (VoR) Version of Record

This research was supported by Asociacion Espanola de LAM; The LAM Foundation Seed Grant 2019; Carlos III Institute of Health grants PI18/01029, PI21/01306 and ICI19/00047 (co-funded by European Regional Development Fund (ERDF), "A way to build Europ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1ba02be19ce5a0317c6f1f8e03bdc65
https://hdl.handle.net/10641/3291

Functional rare variants influence the clinical response to anti-TNF therapy in Crohn’s disease

Autor: [Chaparro M] Gastroenterology Unit. Hospital Universitario de La Princesa, Madrid, Spain. Instituto de Investigación Sanitaria Princesa (IIS-IP), Madrid, Spain. Universidad Autónoma de Madrid, Madrid, Spain. [Aterido A, Marsal S, Julia A] Grup de Recerca en Reumatologia, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Guerra I] Gastroenterology Unit, Hospital Universitario de Fuenlabrada, Madrid, Spain. Instituto de Investigación de Hospital La Paz (IdiPaz), Madrid, Spain. [Iborra M] Gastroenterology Unit, Hospital Universitario de La Fe, Valencia, Spain. [Cabriada JL] Gastroenterology Unit, Hospital Universitario de Galdakano, Vizcaya, Spain. [Bujanda L] Gastroenterology Unit, Hospital Universitario de Donostia, San Sebastián, Spain. Instituto Biodonostia, San Sebastián, Spain. UPV/EHU, Bilbao, Spain. Ikerbasque, Bilbao, Spain, Hospital Universitari Vall d'Hebron

Publikováno v: Scientia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______272::4709c48a568bdfdfa4b0aef116a02a96
https://hdl.handle.net/2072/433736

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

Autor: Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasas, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, (PGC), ADHD Working Group of the Psychiatric Genomics Consortium, Andreassen, Ole A., Arranz, Maria Jesús, Banaschewski, Tobias, Bau, Claiton, Bellgrove, Mark, Biederman, Joseph, Brikell, Isabell, Buitelaar, Jan K., Burton, Christie L., Casas, Miguel, Crosbie, Jennifer, Doyle, Alysa E., Ebstein, Richard P., Elia, Josephine, Elizabeth, Corfield C., Grevet, Eugenio, Grizenko, Natalie, Havdahl, Alexandra, Hawi, Ziarih, Hebebrand, Johannes, Hervas, Amaia, Hohmann, Sarah, Haavik, Jan, Joober, Ridha, Kent, Lindsey, Kuntsi, Jonna, Langley, Kate, Larsson, Henrik, Lesch, Klaus-Peter, Leung, Patrick W. L., Liao, Calwing, Loo, Sandra K., Martin, Joanna, Martin, Nicholas G., Medland, Sarah E., Miranda, Ana, Mota, Nina Roth, Oades, Robert D., Ramos-Quiroga, Josep Antoni, Reif, Andreas, Rietschel, Marcella, Roeyers, Herbert, Rohde, Luis Augusto, Rothenberger, Aribert, Rovira, Paula, Sánchez-Mora, Cristina, Schachar, Russell James, Sengupta, Sarojini, Artigas, Maria Soler, Steinhausen, Hans-Christoph, Thapar, Anita, Witt, Stephanie H., Yang, Li, Zayats, Tetyana, Zhang-James, Yanli, Cormand, Bru, Hougaard, David M., Neale, Benjamin M., Franke, Barbara, Faraone, Stephen V., Børglum, Anders D.

Publikováno v: Dipòsit Digital de la UB
Universidad de Barcelona
NATURE COMMUNICATIONS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
ADHD Working Group of the Psychiatric Genomics Consortium (PGC) 2021, ' Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder ', Nature Communications, vol. 12, no. 1, pp. 576 . https://doi.org/10.1038/s41467-020-20443-2
Nature Communications
Nature Communications, 12, 1
Demontis, D, Walters, R K, Rajagopal, V M, Waldman, I D, Grove, J, Als, T D, Dalsgaard, S, Ribasas, M, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Werge, T, Nordentoft, M, Mors, O, Mortensen, P B, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Cormand, B, Hougaard, D M, Neale, B M, Franke, B, Faraone, S V & Børglum, A D 2021, ' Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder ', Nature Communications, vol. 12, 576 . https://doi.org/10.1038/s41467-020-20443-2
Nature Communications, 12
Nature Communications, Vol 12, Iss 1, Pp 1-12 (2021)
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Nature communications, vol 12, iss 1
Demontis, D, Walters, R K, Rajagopal, V M, Waldman, I D, Grove, J, Als, T D, Dalsgaard, S, Ribasas, M, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Werge, T, Nordentoft, M, Mors, O, Mortensen, P B, Andreassen, O A, Arranz, M J, Banaschewski, T, Bau, C, Bellgrove, M, Biederman, J, Brikell, I, Buitelaar, J K, Burton, C L, Casas, M, Crosbie, J, Doyle, A E, Ebstein, R P, Elia, J, Elizabeth, C C, Grevet, E, Grizenko, N, Havdahl, A, Hawi, Z, Hebebrand, J, Hervas, A, Hohmann, S, Haavik, J, Joober, R, Kent, L, Kuntsi, J, Langley, K, Larsson, H, Lesch, K P, Leung, P W L, Liao, C, Loo, S K, Martin, J, Martin, N G, Medland, S E, Miranda, A & ADHD Working Group of the Psychiatric Genomics Consortium (PGC) 2021, ' Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder ', Nature Communications, vol. 12, 576 . https://doi.org/10.1038/s41467-020-20443-2
Scientia
Demontis, D, Walters, R K, Rajagopal, V M, Waldman, I D, Grove, J, Als, T D, Dalsgaard, S, Ribasas, M, Bybjerg-Grauholm, J, Bækvad-Hansen, M, Werge, T, Nordentoft, M, Mors, O, Mortensen, P B, ADHD Working Group of the Psychiatric Genomics Consortium (PGC), Cormand, B, Hougaard, D M, Neale, B M, Franke, B, Faraone, S V & Børglum, A D 2021, ' Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder ', Nature Communications, vol. 12, no. 1, 576 . https://doi.org/10.1038/s41467-020-20443-2

Attention-Deficit/Hyperactivity Disorder (ADHD) is a childhood psychiatric disorder often comorbid with disruptive behavior disorders (DBDs). Here, we report a GWAS meta-analysis of ADHD comorbid with DBDs (ADHD + DBDs) including 3802 cases and 31,30

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85769f5200da08265c94e873fc58e414
http://hdl.handle.net/2445/173506