The practical use of genome sequencing data in the management of a feline colony pedigree

por Farias, Fabiana H. G., Tomlinson, Chad, Labuda, Jeffrey, Perez-Camargo, Gerardo, Middleton, Rondo, Warren, Wesley C.
Publicado 2017

Comparison of cellular location and expression of Plakophilin‐2 in epidermal cells from nonlesional atopic skin and healthy skin in German shepherd dogs

por Ardesjö‐Lundgren, Brita, Tengvall, Katarina, Bergvall, Kerstin, Farias, Fabiana H.G., Wang, Liya, Hedhammar, Åke, Lindblad‐Toh, Kerstin, Andersson, Göran
Publicado 2017

Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis

por Tengvall, Katarina, Kierczak, Marcin, Bergvall, Kerstin, Olsson, Mia, Frankowiack, Marcel, Farias, Fabiana H. G., Pielberg, Gerli, Carlborg, Örjan, Leeb, Tosso, Andersson, Göran, Hammarström, Lennart, Hedhammar, Åke, Lindblad-Toh, Kerstin
Publicado 2013

Correction: Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis

por Tengvall, Katarina, Kierczak, Marcin, Bergvall, Kerstin, Olsson, Mia, Frankowiack, Marcel, Farias, Fabiana H. G., Pielberg, Gerli, Carlborg, Örjan, Leeb, Tosso, Andersson, Göran, Hammarström, Lennart, Hedhammar, Åke, Lindblad-Toh, Kerstin
Publicado 2013

Correction: Genome-Wide Analysis in German Shepherd Dogs Reveals Association of a Locus on CFA 27 with Atopic Dermatitis

por Tengvall, Katarina, Kierczak, Marcin, Bergvall, Kerstin, Olsson, Mia, Frankowiack, Marcel, Farias, Fabiana H. G., Pielberg, Gerli, Carlborg, Örjan, Leeb, Tosso, Andersson, Göran, Hammarström, Lennart, Hedhammar, Åke, Lindblad-Toh, Kerstin
Publicado 2015

Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd...

por Tengvall, Katarina, Kozyrev, Sergey, Kierczak, Marcin, Bergvall, Kerstin, Farias, Fabiana H. G., Ardesjö-Lundgren, Brita, Olsson, Mia, Murén, Eva, Hagman, Ragnvi, Leeb, Tosso, Pielberg, Gerli, Hedhammar, Åke, Andersson, Göran, Lindblad-Toh, Kerstin
Publicado 2016

Multiple Changes of Gene Expression and Function Reveal Genomic and Phenotypic Complexity in SLE-like Disease

por Wilbe, Maria, Kozyrev, Sergey V., Farias, Fabiana H. G., Bremer, Hanna D., Hedlund, Anna, Pielberg, Gerli R., Seppälä, Eija H., Gustafson, Ulla, Lohi, Hannes, Carlborg, Örjan, Andersson, Göran, Hansson-Hamlin, Helene, Lindblad-Toh, Kerstin
Publicado 2015

TREM2 brain transcript-specific studies in AD and TREM2 mutation carriers

por Del-Aguila, Jorge L., Benitez, Bruno A., Li, Zeran, Dube, Umber, Mihindukulasuriya, Kathie A., Budde, John P., Farias, Fabiana H. G., Fernández, Maria Victoria, Ibanez, Laura, Jiang, Shan, Perrin, Richard J., Cairns, Nigel J., Morris, John C., Harari, Oscar, Cruchaga, Carlos
Publicado 2019

A new domestic cat genome assembly based on long sequence reads empowers feline genomic medicine and identifies a novel gene for dwarfism

por Buckley, Reuben M., Davis, Brian W., Brashear, Wesley A., Farias, Fabiana H. G., Kuroki, Kei, Graves, Tina, Hillier, LaDeana W., Kremitzki, Milinn, Li, Gang, Middleton, Rondo P., Minx, Patrick, Tomlinson, Chad, Lyons, Leslie A., Murphy, William J., Warren, Wesley C.
Publicado 2020

The Novel Evolution of the Sperm Whale Genome

por Warren, Wesley C, Kuderna, Lukas, Alexander, Alana, Catchen, Julian, Pérez-Silva, José G, López-Otín, Carlos, Quesada, Víctor, Minx, Patrick, Tomlinson, Chad, Montague, Michael J, Farias, Fabiana H G, Walter, Ronald B, Marques-Bonet, Tomas, Glenn, Travis, Kieran, Troy J, Wise, Sandra S, Wise, John Pierce, Waterhouse, Robert M, Wise, John Pierce
Publicado 2017

African Americans Have Differences in CSF Soluble TREM2 and Associated Genetic Variants

por Schindler, Suzanne E., Cruchaga, Carlos, Joseph, Amulya, McCue, Lena, Farias, Fabiana H.G., Wilkins, Consuelo H., Deming, Yuetiva, Henson, Rachel L., Mikesell, Robert J., Piccio, Laura, Llibre-Guerra, Jorge J., Moulder, Krista L., Fagan, Anne M., Ances, Beau M., Benzinger, Tammie L.S., Xiong, Chengjie, Holtzman, David M., Morris, John C.
Publicado 2021

A rare regulatory variant in the MEF2D gene affects gene regulation and splicing and is associated with a SLE sub-phenotype in Swedish cohorts

por Farias, Fabiana H. G., Dahlqvist, Johanna, Kozyrev, Sergey V., Leonard, Dag, Wilbe, Maria, Abramov, Sergei N., Alexsson, Andrei, Pielberg, Gerli R., Hansson-Hamlin, Helene, Andersson, Göran, Tandre, Karolina, Bengtsson, Anders A., Sjöwall, Christopher, Svenungsson, Elisabet, Gunnarsson, Iva, Rantapää-Dahlqvist, Solbritt, Syvänen, Ann-Christine, Sandling, Johanna K., Eloranta, Maija-Leena, Rönnblom, Lars, Lindblad-Toh, Kerstin
Publicado 2018

Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders

por Yang, Chengran, Farias, Fabiana H.G., Ibanez, Laura, Suhy, Adam, Sadler, Brooke, Fernandez, Maria Victoria, Wang, Fengxian, Bradley, Joseph L., Eiffert, Brett, Bahena, Jorge A., Budde, John P., Li, Zeran, Dube, Umber, Sung, Yun Ju, Mihindukulasuriya, Kathie A., Morris, John C., Fagan, Anne M., Perrin, Richard J., Benitez, Bruno A., Rhinn, Herve, Harari, Oscar, Cruchaga, Carlos
Publicado 2021

Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease

por Ibanez, Laura, Bahena, Jorge A., Yang, Chengran, Dube, Umber, Farias, Fabiana H. G., Budde, John P., Bergmann, Kristy, Brenner-Webster, Carol, Morris, John C., Perrin, Richard J., Cairns, Nigel J., O’Donnell, John, Álvarez, Ignacio, Diez-Fairen, Monica, Aguilar, Miquel, Miller, Rebecca, Davis, Albert A., Pastor, Pau, Kotzbauer, Paul, Campbell, Meghan C., Perlmutter, Joel S., Rhinn, Herve, Harari, Oscar, Cruchaga, Carlos, Benitez, Bruno A.
Publicado 2020

Molecular pathways in patients with systemic lupus erythematosus revealed by gene-centred DNA sequencing

por Sandling, Johanna K, Pucholt, Pascal, Hultin Rosenberg, Lina, Farias, Fabiana H G, Kozyrev, Sergey V, Eloranta, Maija-Leena, Alexsson, Andrei, Bianchi, Matteo, Padyukov, Leonid, Bengtsson, Christine, Jonsson, Roland, Omdal, Roald, Lie, Benedicte A, Massarenti, Laura, Steffensen, Rudi, Jakobsen, Marianne A, Lillevang, Søren T, Lerang, Karoline, Molberg, Øyvind, Voss, Anne, Troldborg, Anne, Jacobsen, Søren, Syvänen, Ann-Christine, Jönsen, Andreas, Gunnarsson, Iva, Svenungsson, Elisabet, Rantapää-Dahlqvist, Solbritt, Bengtsson, Anders A, Sjöwall, Christopher, Leonard, Dag, Lindblad-Toh, Kerstin, Rönnblom, Lars
Publicado 2021

MULTI-ANCESTRY GENETIC STUDY IN 5,876 PATIENTS IDENTIFIES AN ASSOCIATION BETWEEN EXCITOTOXIC GENES AND EARLY OUTCOMES AFTER ACUTE ISCHEMIC STROKE.

por Ibanez, Laura, Heitsch, Laura, Carrera, Caty, Farias, Fabiana H.G., Dhar, Rajat, Budde, John, Bergmann, Kristy, Bradley, Joseph, Harari, Oscar, Phuah, Chia-Ling, Lemmens, Robin, Souza, Alessandro A. Viana Oliveira, Moniche, Francisco, Cabezas-Juan, Antonio, Arenillas, Juan Francisco, Krupinksi, Jerzy, Cullell, Natalia, Torres-Aguila, Nuria, Muiño, Elena, Cárcel-Márquez, Jara, Marti-Fabregas, Joan, Delgado-Mederos, Raquel, Marin-Bueno, Rebeca, Hornick, Alejandro, Vives-Bauza, Cristofol, Navarro, Rosa Diaz, Tur, Silvia, Jimenez, Carmen, Obach, Victor, Segura, Tomas, Serrano-Heras, Gemma, Chung, Jong-Won, Roquer, Jaume, Soriano-Tarraga, Carol, Giralt-Steinhauer, Eva, Mola-Caminal, Marina, Pera, Joanna, Lapicka-Bodzioch, Katarzyna, Derbisz, Justyna, Davalos, Antoni, Lopez-Cancio, Elena, Muñoz, Lucia, Tatlisumak, Turgut, Molina, Carlos, Ribo, Marc, Bustamante, Alejandro, Sobrino, Tomas, Castillo-Sanchez, Jose, Campos, Francisco, Rodriguez-Castro, Emilio, Arias-Rivas, Susana, Rodríguez-Yáñez, Manuel, Herbosa, Christina, Ford, Andria L., Arauz, Antonio, Lopes-Cendes, Iscia, Lowenkopf, Theodore, Barboza, Miguel A., Amini, Hajar, Stamova, Boryana, Ander, Bradley P., Sharp, Frank R, Kim, Gyeong Moon, Bang, Oh Young, Jimenez-Conde, Jordi, Slowik, Agnieszka, Stribian, Daniel, Tsai, Ellen A., Burkly, Linda C., Montaner, Joan, Fernandez-Cadenas, Israel, Lee, Jin-Moo, Cruchaga, Carlos
Publicado 2020