Results overview: Found 12 records in 0.03 seconds.
Articles, 8 records found
Research literature, 4 records found
Articles 8 records found  
1.
13 p, 2.4 MB Human-lineage-specific genomic elements are associated with neurodegenerative disease and APOE transcript usage / Chen, Zhongbo (Department of Genetics and Genomic Medicine. Great Ormond Street Institute of Child Health. University College London) ; Zhang, David (Department of Genetics and Genomic Medicine. Great Ormond Street Institute of Child Health. University College London) ; Reynolds, Regina H. (Department of Genetics and Genomic Medicine. Great Ormond Street Institute of Child Health. University College London) ; Gustavsson, Emil K. (Department of Genetics and Genomic Medicine. Great Ormond Street Institute of Child Health. University College London) ; García-Ruiz, Sonia (Department of Genetics and Genomic Medicine. Great Ormond Street Institute of Child Health. University College London) ; D'Sa, Karishma (Department of Genetics and Genomic Medicine. Great Ormond Street Institute of Child Health. University College London) ; Fairbrother-Browne, Aine (Department of Genetics and Genomic Medicine. Great Ormond Street Institute of Child Health. University College London) ; Vandrovcova, Jana (UCL Queen Square Institute of Neurology (Regne Unit)) ; Noyce, Alastair J. (UCL Queen Square Institute of Neurology (Regne Unit)) ; Kaiyrzhanov, Rauan (UCL Queen Square Institute of Neurology (Regne Unit)) ; Middlehurst, Ben (Institute of Translational Medicine. University of Liverpool) ; Kia, Demis A. (UCL Queen Square Institute of Neurology (Regne Unit)) ; Tan, Manuela (UCL Queen Square Institute of Neurology (Regne Unit)) ; Morris, Huw R. (UCL Queen Square Institute of Neurology (Regne Unit)) ; Plun-Favreau, Helen (UCL Queen Square Institute of Neurology (Regne Unit)) ; Holmans, Peter (MRC Centre for Neuropsychiatric Genetics & Genomics) ; Trabzuni, Daniah (Department of Genetics. King Faisal Specialist Hospital and Research Centre) ; Bras, Jose (UCL Queen Square Institute of Neurology (Regne Unit)) ; Quinn, John (Institute of Translational Medicine. University of Liverpool) ; Mok, Kin Y. (UCL Queen Square Institute of Neurology (Regne Unit)) ; Kinghorn, Kerri J. (Institute of Healthy Ageing. University College London (UCL)) ; Billingsley, Kimberley (Institute of Translational Medicine. University of Liverpool) ; Wood, Nicholas W.. (UCL Queen Square Institute of Neurology (Regne Unit)) ; Lewis, Patrick (University of Reading) ; Schreglmann, Sebastian (UCL Queen Square Institute of Neurology (Regne Unit)) ; Guerreiro, Rita (UK Dementia Research Institute. University College London (UCL)) ; Lovering, Ruth (Institute of Cardiovascular Science. University College London (UCL)) ; R'Bibo, Lea (UCL Queen Square Institute of Neurology (Regne Unit)) ; Manzoni, Claudia (University of Reading) ; Rizig, Mie (UCL Queen Square Institute of Neurology (Regne Unit)) ; Guelfi, Sebastian (Department of Neurodegenerative Disease. Queen Square Institute of Neurology. University College London (UCL)) ; Escott-Price, Valentina (Cardiff University School of Medicine) ; Chelban, Viorica (UCL Queen Square Institute of Neurology (Regne Unit)) ; Foltynie, Thomas (UCL Queen Square Institute of Neurology (Regne Unit)) ; Williams, Nigel (Cardiff University School of Medicine) ; Brice, Alexis (Institut du Cerveau et de la Moelle épinière (París, França)) ; Danjou, Fabrice (Institut du Cerveau et de la Moelle épinière (París, França)) ; Lesage, Suzanne (Institut du Cerveau et de la Moelle épinière (París, França)) ; Corvol, Jean-Christophe (Institut du Cerveau et de la Moelle épinière (París, França)) ; Martinez Rande, Maria (INSERM UMR 1220 and Paul Sabatier University) ; Schulte, Claudia (German Center for Neurodegenerative Diseases) ; Brockmann, Kathrin (German Center for Neurodegenerative Diseases) ; Simón-Sánchez, Javier (German Center for Neurodegenerative Diseases) ; Heutink, Peter (German Center for Neurodegenerative Diseases) ; Rizzu, Patrizia (German Center for Neurodegenerative Diseases) ; Sharma, Manu (Centre for Genetic Epidemiology. Institute for Clinical Epidemiology and Applied Biometry. University of Tubingen) ; Gasser, Thomas (German Center for Neurodegenerative Diseases) ; Nicolas, Aude (National Institute on Aging (Estats Units d'Amèrica)) ; Cookson, Mark R (National Institute on Aging (Estats Units d'Amèrica)) ; Bandres-Ciga, Sara (National Institute on Aging (Estats Units d'Amèrica)) ; Blauwendraat, Cornelis (National Institute of Neurological Disorders and Stroke) ; Craig, David W (Department of Translational Genomics. Keck School of Medicine. University of Southern California) ; Faghri, Faraz (Department of Computer Science. University of Illinois at Urbana-Champaign) ; Gibbs, J.Raphael (National Institute on Aging (Estats Units d'Amèrica)) ; Hernandez, Dena G. (National Institute on Aging (Estats Units d'Amèrica)) ; Van Keuren-Jensen, Kendall (Neurogenomics Division. TGen) ; Shulman, Joshua M. (Jan and Dan Duncan Neurological Research Institute. Texas Children's Hospital) ; Leonard, Hampton L. (Laboratory of Neurogenetics. National Institute on Aging) ; Nalls, Mike A. (Data Tecnica International) ; Robak, Laurie (Jan and Dan Duncan Neurological Research Institute. Texas Children's Hospital) ; Lubbe, Steven (Ken and Ruth Davee Department of Neurology. Northwestern University Feinberg School of Medicine) ; Finkbeiner, Steven (Taube/Koret Center for Neurodegenerative Disease Research) ; Mencacci, Niccolo E. (Northwestern University Feinberg School of Medicine) ; Lungu, Codrin (National Institutes of Health Division of Clinical Research. NINDS. National Institutes of Health) ; Singleton, Andrew B. (Laboratory of Neurogenetics. National Institute on Aging) ; Scholz, Sonja (Neurodegenerative Diseases Research Unit. National Institute of Neurological Disorders and Stroke) ; Reed, Xylena (Laboratory of Neurogenetics. National Institute on Aging) ; Alcalay, Roy N (Taub Institute for Research on Alzheimer's Disease and the Aging Brain. College of Physicians and Surgeons. Columbia University Medical Center) ; Gan-Or, Ziv (McGill University) ; Rouleau, Guy A. (McGill University) ; Krohn, Lynne (McGill University) ; van Hilten, Jacobus J. (Department of Neurology. Leiden University Medical Center) ; Marinus, Johan (Department of Neurology. Leiden University Medical Center) ; Adarmes-Gómez, A.D (Instituto de Biomedicina de Sevilla) ; Aguilar Barberà, Miquel (Fundacio per la Recerca Biomedica i Social Mutua Terrassa) ; Alvarez, Ignacio (Hospital Universitari MútuaTerrassa (Terrassa, Catalunya)) ; Alvarez, Victoria (Hospital Universitario Central de Asturias) ; Barrero, Francisco Javier (Hospital Universitario San Cecilio (Granada)) ; Bergareche Yarza, Jesús Alberto (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Bernal-Bernal, Inmaculada (Hospital Clínic i Provincial de Barcelona) ; Blázquez Estrada, Marta (Hospital Universitario Central de Asturias) ; Bonilla-Toribio, Marta (Hospital Clínic i Provincial de Barcelona) ; Botía, Juan (Universidad de Murcia. Departamento de Ingeniería de la Información y las Comunicaciones) ; Boungiorno, M. T (Fundacio per la Recerca Biomedica i Social Mutua Terrassa) ; Buiza-Rueda, Dolores (Instituto de Biomedicina de Sevilla) ; Cámara, Ana (Hospital Clínic i Provincial de Barcelona) ; Carrillo, Fátima (Instituto de Biomedicina de Sevilla) ; Carrión-Claro, M (Instituto de Biomedicina de Sevilla) ; Cerdan, Debora (Hospital General de Segovia) ; Clarimón, Jordi (Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas) ; Compta, Yaroslau (Hospital Clínic i Provincial de Barcelona) ; Diez-Fairen, Monica (Fundacio per la Recerca Biomedica i Social Mutua Terrassa) ; Dols Icardo, Oriol (Institut d'Investigació Biomèdica Sant Pau) ; Duarte, Jacinto (Hospital General de Segovia) ; Duran, Raquel (Centro de Investigacion Biomedica. Universidad de Granada) ; Escamilla-Sevilla, Francisco (Instituto de Investigación Sanitaria de Granada) ; Ezquerra, Mario (Hospital Clínic i Provincial de Barcelona) ; Feliz, Cici (Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz) ; Fernández, Manel (Hospital Clínic i Provincial de Barcelona) ; Fernández-Santiago, Rubén (Hospital Clínic i Provincial de Barcelona) ; Garcia, Ciara (Hospital Universitario Central de Asturias) ; García-Ruiz, Pedro (Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz) ; Gómez-Garre, Pilar (Instituto de Biomedicina de Sevilla) ; Gomez Heredia, Maria Jose (Hospital Universitario Virgen de la Victoria (Màlaga, Andalusia)) ; Gonzalez-Aramburu, Isabel (Instituto de Investigación Sanitaria Valdecilla (Santander, Cantàbria)) ; Gorostidi Pagola, Ana (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Hoenicka, Janet (Institut de Recerca Sant Joan de Déu) ; Infante, Jon (Hospital Universitario Ramón y Cajal (Madrid)) ; Jesús, Silvia (Instituto de Biomedicina de Sevilla) ; Jimenez-Escrig, Adriano (Hospital Universitario Ramón y Cajal (Madrid)) ; Kulisevsky, Jaime (Institut d'Investigació Biomèdica Sant Pau) ; Labrador-Espinosa, Miguel A (Instituto de Biomedicina de Sevilla) ; Lopez-Sendon, Jose Luis (Hospital Universitario Ramón y Cajal (Madrid)) ; López de Munain Arregui, Adolfo (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Macias, Daniel (Instituto de Biomedicina de Sevilla) ; Martínez Torres, Irene (Hospital Universitari i Politècnic La Fe (València)) ; Marín, Juan (Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas) ; Marti, Maria Jose (Hospital Clínic i Provincial de Barcelona) ; Martínez-Castrillo, Juan Carlos (Hospital Universitario Ramón y Cajal (Madrid)) ; Méndez-del-Barrio, Carlota (Instituto de Biomedicina de Sevilla) ; Menéndez González, Manuel (Hospital Universitario Central de Asturias) ; Mata, Marina (Hospital Universitario Infanta Sofía (San Sebastián de los Reyes)) ; Mínguez, Adolfo (Instituto de Investigación Sanitaria de Granada) ; Mir, Pablo (Instituto de Biomedicina de Sevilla) ; Mondragon Rezola, Elisabet (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Muñoz, Esteban (Instituto de Biomedicina de Sevilla) ; Pagonabarraga Mora, Javier (Institut d'Investigació Biomèdica Sant Pau) ; Pastor, Pau (Hospital Universitari MútuaTerrassa (Terrassa, Catalunya)) ; Perez Errazquin, Francisco (Hospital Universitario Virgen de la Victoria (Màlaga, Andalusia)) ; Periñán-Tocino, Teresa (Instituto de Biomedicina de Sevilla) ; Ruiz-Martínez, Javier (Hospital Universitario Donostia. Instituto de Investigación Sanitaria Biodonostia) ; Ruz, Clara (Centro de Investigacion Biomedica. Universidad de Granada) ; Sanchez Rodriguez, Antonio (Instituto de Investigación Sanitaria Valdecilla (Santander, Cantàbria)) ; Sierra, María (Instituto de Investigación Sanitaria Valdecilla (Santander, Cantàbria)) ; Suarez-Sanmartin, Esther (Hospital Universitario Central de Asturias) ; Tabernero, Cesar (Hospital General de Segovia) ; Tartari, Juan Pablo (Hospital Universitari MútuaTerrassa (Terrassa, Catalunya)) ; Tejera-Parrado, Cristina (Instituto de Biomedicina de Sevilla) ; Tolosa, Eduard (Hospital Clínic i Provincial de Barcelona) ; Valldeoriola, Francesc (Hospital Clínic i Provincial de Barcelona) ; Vargas-González, Laura (Instituto de Biomedicina de Sevilla) ; Vela, Lydia (Hospital Universitario Fundación Alcorcón) ; Vives, Francisco (Centro de Investigacion Biomedica. Universidad de Granada) ; Zimprich, Alexander (Department of Neurology. Medical University of Vienna) ; Pihlstrom, Lasse (Oslo University Hospital (Oslo, Noruega)) ; Toft, Mathias (Oslo University Hospital (Oslo, Noruega)) ; Koks, Sulev (Department of Reproductive Biology. Estonian University of Life Sciences) ; Taba, Pille (Department of Neurology and Neurosurgery. University of Tartu) ; Hassin-Baer, Sharon (Sackler Faculty of Medicine. Tel Aviv University) ; Hardy, John (Institute for Advanced Study. The Hong Kong University of Science and Technology. The Hong Kong University of Science and Technology) ; Houlden, Henry (Department of Neuromuscular Disease. Queen Square Institute of Neurology. UCL) ; Gagliano Taliun, Sarah A. (Montréal Heart Institute) ; Botía, Juan (Universidad de Murcia. Departamento de Ingeniería de la Información y las Comunicaciones) ; Ryten, Mina (Great Ormond Street Institute of Child Health (Londres, Regne Unit)) ; Universitat Autònoma de Barcelona
Knowledge of genomic features specific to the human lineage may provide insights into brain-related diseases. We leverage high-depth whole genome sequencing data to generate a combined annotation identifying regions simultaneously depleted for genetic variation (constrained regions) and poorly conserved across primates. [...]
2021 - 10.1038/s41467-021-22262-5
Nature communications, Vol. 12 Núm. 1 (january 2021) , p. 2076  
2.
15 p, 3.4 MB Disruption of NIPBL/Scc2 in Cornelia de Lange Syndrome provokes cohesin genome-wide redistribution with an impact in the transcriptome / Garcia, Patricia (Universidad de Salamanca) ; Fernández Hernández, Rita (Institut d'Investigació Biomèdica de Bellvitge) ; Cuadrado, Ana (Centro Nacional de Investigaciones Oncológicas) ; Coca, Ignacio (Genomics Laboratory (Barcelona)) ; Gómez, Antonio (Parc Científic de Barcelona) ; Maqueda, Maria (Institut d'Investigació Biomèdica de Bellvitge) ; Latorre Pellicer, Ana (Universidad de Zaragoza) ; Puisac, Beatriz (Universidad de Zaragoza) ; Ramos, Feliciano J. (Universidad de Zaragoza) ; Sandoval, Juan (Instituto de Investigación Sanitaria La Fe) ; Esteller, M (Institut Germans Trias i Pujol. Institut de Recerca contra la Leucèmia Josep Carreras) ; Mosquera, José Luis (Institut d'Investigació Biomèdica de Bellvitge) ; Rodríguez, Jairo (Genomics Laboratory (Barcelona)) ; Pié, J. (Universidad de Zaragoza) ; Losada, Ana (Centro Nacional de Investigaciones Oncológicas) ; Queralt, Ethel (Instituto de Biomedicina de Valencia (IBV-CSIC)) ; Universitat Autònoma de Barcelona
Cornelia de Lange syndrome (CdLS) is a rare disease affecting multiple organs and systems during development. Mutations in the cohesin loader, NIPBL/Scc2, were first described and are the most frequent in clinically diagnosed CdLS patients. [...]
2021 - 10.1038/s41467-021-24808-z
Nature communications, Vol. 12 Núm. 1 (january 2021) , p. 4551  
3.
14 p, 1.2 MB Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome / Storm, Catherine S. (University College London) ; Kia, Demis A. (University College London) ; Almramhi, Mona M. (King Abdulaziz University) ; Bandres-Ciga, Sara (National Institute on Aging (Estats Units d'Amèrica)) ; Finan, Chris (University Medical Center Utrecht) ; Noyce, A. J. (UCL Institute of Neurology (Regne Unit)) ; Kaiyrzhanov, R. (UCL Institute of Neurology (Regne Unit)) ; Middlehurst, B. (University of Liverpool) ; Tan, M. (University College London) ; Houlden, Henry (UCL Institute of Neurology (Regne Unit)) ; Morris, H. R. (University College London) ; Plun-Favreau, H. (UCL Institute of Neurology (Regne Unit)) ; Holmans, Peter (MRC Centre for Neuropsychiatric Genetics & Genomics) ; Hardy, J. (UCL Institute of Neurology (Regne Unit)) ; Trabzuni, D. (UCL Institute of Neurology (Regne Unit)) ; Quinn, J. (Institute of Translational Medicine. University of Liverpool) ; Bubb, Vivien (Institute of Translational Medicine. University of Liverpool) ; Mok, K. Y. (UCL Institute of Neurology (Regne Unit)) ; Kinghorn, K. J. (University College London) ; Lewis, P. (University of Reading) ; Schreglmann, S. R. (UCL Institute of Neurology (Regne Unit)) ; Lovering, R. (University College London) ; R'Bibo, L. (UCL Institute of Neurology (Regne Unit)) ; Manzoni, C. (University of Reading) ; Rizig, M. (UCL Institute of Neurology (Regne Unit)) ; Ryten, Mina (UCL Institute of Neurology (Regne Unit)) ; Guelfi, S. (UCL Institute of Neurology (Regne Unit)) ; Escott-Price, Valentina (MRC Centre for Neuropsychiatric Genetics and Genomics. Cardiff University School of Medicine) ; Chelban, Viorica (UCL Institute of Neurology (Regne Unit)) ; Foltynie, T. (UCL Institute of Neurology (Regne Unit)) ; Williams, N. (MRC Centre for Neuropsychiatric Genetics and Genomics) ; Morrison, K. E. (Faculty of Medicine. University of Southampton) ; Clarke, C. (Sandwell and West Birmingham Hospitals NHS Trust) ; Harvey, K. (UCL School of Pharmacy) ; Jacobs, B. M. (Wolfson Institute of Preventive Medicine. QMUL) ; Brice, Alexis (Sorbonne Université) ; Danjou, Fabrice (Sorbonne Université) ; Lesage, S. (Sorbonne Universités) ; Corvol, Jean-Christophe (Sorbonne Universités) ; Martinez, M. (Paul Sabatier University) ; Schulte, C. (DZNE. German Center for Neurodegenerative Diseases) ; Brockmann, Kathrin (DZNE. German Center for Neurodegenerative Diseases) ; Simón-Sánchez, J. (DZNE. German Center for Neurodegenerative Diseases) ; Heutink, Peter (University of Tübingen) ; Rizzu, P. (DZNE. German Center for Neurodegenerative Diseases) ; Sharma, M. (University of Tubingen) ; Gasser, T. (DZNE. German Center for Neurodegenerative Diseases) ; Schneider, S. A. (udwig-Maximilians-University Munich) ; Cookson, Mark R (Laboratory of Neurogenetics. National Institute on Aging) ; Blauwendraat, Cornelis (Laboratory of Neurogenetics. National Institute on Aging) ; Craig, David W (University of Southern California) ; Billingsley, K. (National Institute on Aging (Estats Units d'Amèrica)) ; Makarious, M. B. (National Institute on Aging (Estats Units d'Amèrica)) ; Narendra, D. P. (National Institute of Neurological Disorders and Stroke) ; Faghri, F. (University of Illinois at Urbana-Champaign) ; Gibbs, J. R. (National Institute on Aging (Bethesda, Estats Units d'Amèrica)) ; Hernandez, D. G. (National Institute on Aging (Estats Units d'Amèrica)) ; Van Keuren-Jensen, K. (Neurogenomics Division. TGen) ; Shulman, J. M. (Texas Children's Hospital) ; Iwaki, H. (Laboratory of Neurogenetics. National Institute on Aging) ; Leonard, H. L. (Laboratory of Neurogenetics. National Institute on Aging) ; Nalls, M. A. (CEO/Consultant Data Tecnica International) ; Robak, L. (Baylor College of Medicine) ; Bras, Jose (Van Andel Research Institute) ; Guerreiro, Rita (Van Andel Research Institute) ; Lubbe, S. (Northwestern University Feinberg School of Medicine) ; Troycoco, T. (National Institutes of Health (Bethesda, Estats Units d'Amèrica)) ; Finkbeiner, S. (Taube/Koret Center for Neurodegenerative Disease Research) ; Mencacci, N. E. (Northwestern University Feinberg School of Medicine) ; Lungu, C. (National Institutes of Health Division of Clinical Research. NINDS. National Institutes of Health) ; Singleton, A. B. (Laboratory of Neurogenetics. National Institute on Aging) ; Scholz, S. W. (National Institute of Neurological Disorders and Stroke) ; Reed, X. (Laboratory of Neurogenetics. National Institute on Aging) ; Uitti, R. J. (Mayo Clinic) ; Ross, O. A. (Mayo Clinic) ; Grenn, F. P. (National Institute on Aging (Estats Units d'Amèrica)) ; Moore, A. (National Institute on Aging (Estats Units d'Amèrica)) ; Alcalay, Roy N (Columbia University Medical Center) ; Wszolek, Z. K. (Mayo Clinic) ; Gan-Or, Z. (McGill University) ; Rouleau, G. A. (McGill University) ; Krohn, L. (McGill University) ; Mufti, K. (McGill University) ; van Hilten, J. J. (Leiden University Medical Center) ; Marinus, J. (Leiden University Medical Center) ; Adarmes-Gómez, A.D (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Aguilar Barberà, Miquel (Mútua de Terrassa) ; Alvarez, Ignacio (Mútua de Terrassa) ; Alvarez, Victoria (Hospital Universitario Central de Asturias) ; Barrero, F. J. (Universidad de Granada) ; Yarza, J. A. B. (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Bernal-Bernal, I. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Blázquez Estrada, Marta (Hospital Universitario Central de Asturias) ; Bonilla-Toribio, Marta (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Botía, J. A. (Universidad de Murcia) ; Boungiorno, M. T. (Mútua de Terrassa) ; Buiza-Rueda, Dolores (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Cámara, Ana (Hospital Clínic i Provincial de Barcelona) ; Carrillo, F. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Carrión-Claro, M. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Cerdan, Debora (Hospital General de Segovia) ; Clarimón, Jordi (Institut d'Investigació Biomèdica Sant Pau) ; Compta, Yaroslau (Hospital Clínic i Provincial de Barcelona) ; Diez-Fairen, M. (Mútua de Terrassa) ; Dols Icardo, Oriol (Institut d'Investigació Biomèdica Sant Pau) ; Duarte, Jacinto (Hospital General de Segovia) ; Duran, Raquel (Universidad de Granada) ; Escamilla-Sevilla, Francisco (Instituto de Investigación Sanitaria de Granada) ; Ezquerra, Mario (Hospital Clínic i Provincial de Barcelona) ; Feliz, Cici (Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz) ; Fernández, Manel (Hospital Clínic i Provincial de Barcelona) ; Fernández-Santiago, Rubén (Hospital Clínic i Provincial de Barcelona) ; Garcia, C.. (Hospital Universitario Central de Asturias) ; García-Ruiz, Pedro (Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz) ; Gómez-Garre, P. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Gomez Heredia, Maria Jose (Hospital Universitario Virgen de la Victoria (Màlaga, Andalusia)) ; Gonzalez-Aramburu, Isabel (Instituto de Investigación Sanitaria Valdecilla (Santander, Cantàbria)) ; Pagola, A. G. (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Hoenicka, Janet (Institut de Recerca Sant Joan de Déu) ; Infante, Jon (Hospital Universitario Marqués de Valdecilla (Santander, Cantabria)) ; Jesús, S. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Jiménez-Escrig, Adriano (Hospital Universitario Ramón y Cajal (Madrid)) ; Kulisevsky, Jaime (Institut d'Investigació Biomèdica Sant Pau) ; Labrador-Espinosa, Miguel A (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Lopez-Sendon, Jose Luis (Hospital Universitario Ramón y Cajal (Madrid)) ; de Munain Arregui, A. L. (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Macías-García, Daniel (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Torres, I. M. (Hospital Universitari i Politècnic La Fe (València)) ; Marín, Juan (Institut d'Investigació Biomèdica Sant Pau) ; Marti, Maria Jose (Hospital Clínic i Provincial de Barcelona) ; Martínez-Castrillo, Juan Carlos (Instituto Ramón y Cajal de Investigación Sanitaria (Madrid)) ; Méndez-del-Barrio, C. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; González, M. M. (Hospital Universitario Central de Asturias) ; Mata, Marina (Hospital Universitario Virgen de las Nieves (Granada)) ; Mínguez, A. (Hospital Universitario Virgen de las Nieves (Granada)) ; Mir, P. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Rezola, E. M. (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Muñoz, Esteban (Hospital Clínic i Provincial de Barcelona) ; Pagonabarraga Mora, Javier (Hospital Universitario Infanta Sofía (San Sebastián de los Reyes)) ; Pastor, Pau (Hospital Universitari MútuaTerrassa (Terrassa, Catalunya)) ; Perez-Errazquin, Francisco (Hospital Universitario Virgen de la Victoria (Màlaga, Andalusia)) ; Periñán-Tocino, T. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Ruiz-Martínez, J. (Biodonostia Osasun Ikerketako Institutura (País Basc)) ; Ruz, Clara (Universidad de Granada) ; Rodriguez, A. S. (Instituto de Investigación Sanitaria Valdecilla (Santander, Cantàbria)) ; Sierra, Maria (Instituto de Investigación Sanitaria Valdecilla (Santander, Cantàbria)) ; Suarez-Sanmartin, E. (Hospital Universitario Central de Asturias) ; Tabernero, Cesar (Hospital General de Segovia) ; Tartari, J. P. (Mútua de Terrassa) ; Tejera-Parrado, C. (v) ; Tolosa, Eduard (Hospital Clínic i Provincial de Barcelona) ; Valldeoriola, Francesc (Hospital Clínic i Provincial de Barcelona) ; Vargas-González, L. (Hospital Universitario Virgen del Rocío (Sevilla, Andalusia)) ; Vela, Lydia (Hospital Universitario Fundación Alcorcón) ; Vives, Francisco (Universidad de Granada) ; Zimprich, Alexander (Medical University of Vienna) ; Pihlstrom, L. (Oslo University Hospital (Oslo)) ; Toft, M. (Oslo University Hospital (Oslo, Noruega)) ; Taba, P. (University of Tartu) ; Koks, S. (The Perron Institute for Neurological and Translational Science) ; Hassin-Baer, S. (Sackler Faculty of Medicine. Tel Aviv University) ; Majamaa, K. (Oulu University Hospital (Finlàndia)) ; Siitonen, A. (Oulu University Hospital (Finlàndia)) ; Tienari, P. (Helsinki University Hospital (Finlàndia)) ; Okubadejo, N. U. (University of Lagos) ; Ojo, O. O. (University of Lagos) ; Shashkin, C. (Kazakh National Medical University named after Asfendiyarov) ; Zharkinbekova, N. (South Kazakhstan Medical Academy) ; Akhmetzhanov, Vadim (Astana Medical University) ; Kaishybayeva, G. (Scientific and Practical Center "Institute of Neurology named after Smagul Kaishibayev") ; Karimova, A. (Scientific and Practical Center "Institute of Neurology named after Smagul Kaishibayev") ; Khaibullin, T. (Semey Medical University) ; Lynch, T. L. (The Dublin Neurological Institute at the Mater Misericordiae University Hospital) ; Hingorani, Aroon (Health Data Research UK) ; Wood, Nicholas W.. (University College London) ; Universitat Autònoma de Barcelona
Parkinson's disease is a neurodegenerative movement disorder that currently has no disease-modifying treatment, partly owing to inefficiencies in drug target identification and validation. We use Mendelian randomization to investigate over 3,000 genes that encode druggable proteins and predict their efficacy as drug targets for Parkinson's disease. [...]
2021 - 10.1038/s41467-021-26280-1
Nature communications, Vol. 12 Núm. 1 (december 2021) , p. 7342  
4.
26 p, 17.4 MB High-depth African genomes inform human migration and health / Choudhury, Ananyo (University of the Witwatersrand) ; Aron, S. (University of the Witwatersrand) ; Botigué, Laura (Centre de Recerca en Agrigenòmica) ; Sengupta, D. (University of the Witwatersrand) ; Botha, G. (University of Cape Town) ; Bensellak, T. (Abdelmalek Essaadi University) ; Wells, G. (University of the Western Cape) ; Kumuthini, J. (University of the Western Cape) ; Shriner, Daniel (National Institutes of Health (USA)) ; Fakim, Y. J. (University of Mauritius) ; Ghoorah, A. W. (University of Mauritius) ; Dareng, E. (Institute of Human Virology Nigeria) ; Odia, T. (Covenant University) ; Falola, O. (Covenant University) ; Adebiyi, E. (Covenant University) ; Hazelhurst, S. (University of the Witwatersrand) ; Mazandu, G. (University of Cape Town) ; Nyangiri, O. A. (Makerere University) ; Mbiyavanga, M. (University of Cape Town) ; Benkahla, A. (Institute Pasteur of Tunis) ; Kassim, S. K. (Ain Shams University (El Caire, Egipte)) ; Mulder, N. (University of Cape Town) ; Adebamowo, S. N. (University of Maryland Baltimore) ; Chimusa, E. R. (University of Cape Town) ; Muzny, D. (Baylor College of Medicine) ; Metcalf, G. (Baylor College of Medicine) ; Gibbs, R. A. (Baylor College of Medicine) ; Rotimi, C. (National Institutes of Health (USA)) ; Ramsay, M. (University of the Witwatersrand) ; Adeyemo, Adebowale A (National Institutes of Health (USA)) ; Lombard, Z. (University of the Witwatersrand) ; Hanchard, N. A. (Baylor College of Medicine) ; TrypanoGEN Research Group ; H3Africa Consortium
The African continent is regarded as the cradle of modern humans and African genomes contain more genetic variation than those from any other continent, yet only a fraction of the genetic diversity among African individuals has been surveyed. [...]
2020 - 10.1038/s41586-020-2859-7
Nature, Vol. 586 (October 2020) , p. 741-748  
5.
14 p, 2.3 MB Delayed γH2AX foci disappearance in mammary epithelial cells from aged women reveals an age-associated DNA repair defect / Anglada Pons, Teresa (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia) ; Repullés Fernández, Joan (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia) ; Espinal Berenguer, Anna (Universitat Autònoma de Barcelona. Servei d'Estadística Aplicada) ; LaBarge, Mark A. (Lawrence Berkeley National Laboratory) ; Stampfer, Martha R. (Lawrence Berkeley National Laboratory) ; Genescà, Anna (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia) ; Martín Flix, Marta (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia) ; Institut d'Investigació Biomèdica Sant Pau
Aging is a degenerative process in which genome instability plays a crucial role. To gain insight into the link between organismal aging and DNA repair capacity, we analyzed DNA double-strand break (DSB) resolution efficiency in human mammary epithelial cells from 12 healthy donors of young and old ages. [...]
2019 - 10.18632/aging.101849
Aging (Albany NY), Vol. 11, Num. 5 (March 2019) , p. 1510-1523  
6.
11 p, 625.0 KB Human inversions and their functional consequences / Puig Font, Marta (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Casillas Viladerrams, Sònia (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Villatoro, Sergi (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Cáceres Aguilar, Mario (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí")
Polymorphic inversions are a type of structural variants that are difficult to analyze owing to their balanced nature and the location of breakpoints within complex repeated regions. So far, only a handful of inversions have been studied in detail in humans and current knowledge about their possible functional effects is still limited. [...]
2015 - 10.1093/bfgp/elv020
Briefings in Functional Genomics, Vol. 14, issue 5 (2015) , p. 369-379  
7.
10 p, 596.5 KB PeSV-fisher : identification of somatic and non-somatic structural variants using next generation sequencing data / Escaramís, Georgina (Centre de Regulació Genòmica) ; Tornador, Cristian (Centre de Regulació Genòmica) ; Bassaganyas, Laia (Centre de Regulació Genòmica) ; Rabionet, Raquel (Centre de Regulació Genòmica) ; Tubio, Jose M. C. (Centre de Regulació Genòmica) ; Martínez-Fundichely, Alexander (Centre de Regulació Genòmica) ; Cáceres Aguilar, Mario (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Gut, Marta (Centre Nacional d'Anàlisi Genòmica) ; Ossowski, Stephan (Centre de Regulació Genòmica) ; Estivill, Xavier (Centre de Regulació Genòmica)
Next-generation sequencing technologies expedited research to develop efficient computational tools for the identification of structural variants (SVs) and their use to study human diseases. As deeper data is obtained, the existence of higher complexity SVs in some genomes becomes more evident, but the detection and definition of most of these complex rearrangements is still in its infancy. [...]
2013 - 10.1371/journal.pone.0063377
PloS one, Vol. 8 issue 5 (2013) , art. e63377  
8.
10 p, 3.7 MB PopHumanScan : the online catalog of human genome adaptation / Murga-Moreno, Jesus (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Coronado-Zamora, Marta (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Bodelon de Frutos, Alejandra (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí") ; Barbadilla Prados, Antonio (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Casillas Viladerrams, Sònia (Universitat Autònoma de Barcelona. Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí")
Since the migrations that led humans to colonize Earth, our species has faced frequent adaptive challenges that have left signatures in the landscape of genetic variation and that we can identify in our today-s genomes. [...]
2019 - 10.1093/nar/gky959
Nucleic acids research, Vol. 47, issue D1 (Jan 2019) , p. D1080-D1089  

Research literature 4 records found  
1.
1 p, 978.9 KB Predicting human intelligence. Is it a near future? / Casas Cascante, Clara ; Gutiérrez García, José Manuel, dir. (Universitat Autònoma de Barcelona. Departament de Filosofia) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2016
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234 p, 3.4 MB Análisis, validación y estudio poblacional de las inversiones entre dos genomas humanos / Vicente Salvador, David ; Cáceres Aguilar, Mario, dir. (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia
Las inversiones fueron las primeras variantes estructurales detectadas y asociadas a efectos fenotípicos en varias especies. Sin embargo, la dificultad de su estudio las ha llevado a ser las peor caracterizadas en genomas complejos como el humano. [...]
Inversions were the first type of structural variants to be detected and associated to phenotypic effects in different species. However, studying them was difficult and they have become one of the less characterized variants in complex genomes such as the human. [...]

[Barcelona] : Universitat Autònoma de Barcelona, 2014  
3.
1 p, 243.2 KB The impact of Alu elements on human genome and its role in hereditary breast and ovarian cancer(HBOC) syndrome / Muyas, Francesc ; García Guerreiro, María Pilar, dir. (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2014
Grau en Genètica [833]  
4.
1 p, 6.2 MB LINE-1 retrotransposons and their impact on the human genome and in disease-causing mutations / Corrales Lorite, S. ; García Guerreiro, María Pilar, dir. (Universitat Autònoma de Barcelona. Departament de Genètica i de Microbiologia) ; Universitat Autònoma de Barcelona. Facultat de Biociències
2013
Grau en Genètica [833]  

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