Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Carlos E. Arboleda-Bustos"'
Autor:
Ana Cecília Guimarães Alves, Natalie Mary Sukow, Gabriel Adelman Cipolla, Marla Mendes, Thiago P. Leal, Maria Luiza Petzl-Erler, Ricardo Lehtonen Rodrigues Souza, Ilíada Rainha de Souza, Cesar Sanchez, Meddly Santolalla, Douglas Loesch, Michael Dean, Moara Machado, Jee-Young Moon, Robert Kaplan, Kari E. North, Scott Weiss, Mauricio L. Barreto, M. Fernanda Lima-Costa, Heinner Guio, Omar Cáceres, Carlos Padilla, Eduardo Tarazona-Santos, Ignacio F. Mata, Elena Dieguez, Víctor Raggio, Andres Lescano, Vitor Tumas, Vanderci Borges, Henrique B. Ferraz, Carlos R. Rieder, Artur Schumacher-Schuh, Bruno L. Santos-Lobato, Pedro Chana-Cuevas, William Fernandez, Gonzalo Arboleda, Humberto Arboleda, Carlos E. Arboleda-Bustos, Timothy D. O’Connor, Marcia Holsbach Beltrame, Victor Borda
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
In adulthood, the ability to digest lactose, the main sugar present in milk of mammals, is a phenotype (lactase persistence) observed in historically herder populations, mainly Northern Europeans, Eastern Africans, and Middle Eastern nomads. As the
Externí odkaz:
https://doaj.org/article/83fade9eedf24b7d99f1452beb4bd4e7
Autor:
Juan David Caicedo, Alejandro Cáceres, Carlos E. Arboleda-Bustos, María Fernanda Mahecha, Jenny Ortega, Gonzalo Arboleda, Humberto Arboleda
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 39, Iss 3, Pp 595-600 (2019)
Introducción. Los proyectos del mapa de haplotipos (HapMap) y de los 1.000 genomas han sido fundamentales para la compresión del componente genético de las enfermedades comunes y los fenotipos normales. Sin embargo, la variabilidad genética colom
Externí odkaz:
https://doaj.org/article/f72fd7699dd24ddea735fa0eb8b3a046
Autor:
Orlando Ricaurte, Karina Neita, Danyela Valero, Jenny Ortega-Rojas, Carlos E. Arboleda-Bustos, Camilo Zubieta, José Penagos, Gonzalo Arboleda
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 38, Iss 0, Pp 86-92 (2018)
Introduction: Gliomas are the most common primary tumors of the central nervous system and, according to their malignancy, they are graded from I to IV. Recent studies have found that there is an association between gliomas and mutations in exon 4 of
Externí odkaz:
https://doaj.org/article/0007757794d842b49ab9c6b84ae9e4cf
Autor:
Carolina Andrea Infante Molina, Laura Marlen Mora Forero, Jenny C. Ortega Rojas, Carlos E. Arboleda-Bustos, William Fernández, Humberto Arboleda, Gonzalo Arboleda
Publikováno v:
NOVA, Vol 12, Iss 21 (2014)
La enfermedad de Parkinson es un desorden neurodegenerativo complejo, caracterizado por la pérdida progresiva de las neuronas dopaminérgicas de la sustancia nigra pars compacta. Fac-tores tanto ambientales como genéticos se ha determinado que cont
Externí odkaz:
https://doaj.org/article/6f4074d6aa164075bcc2f17bb5f6d11c
Autor:
Thiago P Leal, Jennifer N French-Kwawu, Mateus H Gouveia, Victor Borda, Miguel Inca-Martinez, Emily A Mason, Andrea RVR Horimoto, Douglas P Loesch, Elif I Sarihan, Mario R Cornejo-Olivas, Luis E Torres, Pilar E Mazzetti-Soler, Carlos Cosentino, Elison H Sarapura-Castro, Andrea Rivera-Valdivia, Angel C Medina, Elena M Dieguez, Víctor E Raggio, Andrés Lescano, Vitor Tumas, Vanderci Borges, Henrique B Ferraz, Carlos R Rieder, Artur Schumacher-Schuh, Bruno L Santos-Lobato, Carlos Velez-Pardo, Marlene Jimenez-Del-Rio, Francisco Lopera, Sonia Moreno, Pedro Chana-Cuevas, William Fernandez, Gonzalo Arboleda, Humberto Arboleda, Carlos E Arboleda Bustos, Dora Yearout, Maria F Lima-Costa, Eduardo Tarazona, Cyrus Zabetian, Timothy A Thornton, Timothy D O’Connor, Ignacio F Mata
Publikováno v:
medRxiv
Sex differences in Parkinson Disease (PD) risk are well-known. However, it is still unclear the role of sex chromosomes in the development and progression of PD. We performed the first X-chromosome Wide Association Study (XWAS) for PD risk in Latin A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611448199f677e7660d221b8a0d775d6
https://europepmc.org/articles/PMC9915833/
https://europepmc.org/articles/PMC9915833/
Autor:
Ignacio F. Mata, Artur F. Schumacher-Schuh, Carlos Velez-Pardo, Gonzalo Arboleda, Emily Mason, Andrea R. V. R. Horimoto, Elif Irem Sarihan, Bruno Lopes Santos-Lobato, Carlos Roberto de Mello Rieder, Dora Yearout, Angel C. Medina, Elison Sarapura-Castro, Pedro Chana-Cuevas, Andrea Rivera-Valdivia, Carlos Cosentino, Timothy D. O’Connor, Sonia Moreno, Víctor Raggio, Cyrus P. Zabetian, Timothy A. Thornton, Vitor Tumas, Mario Cornejo-Olivas, Marlene Jimenez-Del-Rio, Miguel Inca-Martinez, Vanderci Borges, Pilar Mazzetti, Carlos E. Arboleda-Bustos, Douglas Loesch, Francisco Lopera, Luis Torres, Humberto Arboleda, Henrique Ballalai Ferraz, Elena Dieguez, William Fernandez, Andres G. Lescano
BackgroundLarge-scale Parkinson’s disease (PD) genome-wide association studies (GWAS) and meta-analyses have, until recently, only been conducted on subjects with European-ancestry. Consequently, polygenic risk scores (PRS) constructed using PD GWA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::901d5d3a600be69a23d909c2aaeca919
https://doi.org/10.1101/2021.11.09.21265082
https://doi.org/10.1101/2021.11.09.21265082
Autor:
Carlos E. Arboleda-Bustos, Douglas Loesch, Paul Cannon, Francisco Lopera, Carlos Cosentino, Andrea Rivera-Valdivia, Carlos Velez-Pardo, Cyrus P. Zabetian, Mario Cornejo-Olivas, Ignacio F. Mata, Sonia Moreno, Karl Heilbron, Carlos Roberto de Mello Rieder, Miguel Inca-Martinez, Andrea R. V. R. Horimoto, Pilar Mazzetti, Luis Torres, Vanderci Borges, Dora Yearout, Elison Sarapura-Castro, Gonzalo Arboleda, Timothy D. O’Connor, Artur F. Schumacher-Schuh, Elif Irem Sarihan, Bruno Lopes Santos-Lobato, Vitor Tumas, Marlene Jimenez-Del-Rio, Pedro Chana-Cuevas, William Fernandez, Emily Mason, Andres G. Lescano, Humberto Arboleda, Elena Dieguez, Henrique Ballalai Ferraz, Angel C. Medina, Timothy A. Thornton, Víctor Raggio
Publikováno v:
Ann Neurol
OBJECTIVE This work was undertaken in order to identify Parkinson's disease (PD) risk variants in a Latino cohort, to describe the overlap in the genetic architecture of PD in Latinos compared to European-ancestry subjects, and to increase the divers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c7df57c1d86c1d1326a1208b2e1c60d
https://pubmed.ncbi.nlm.nih.gov/34476843
https://pubmed.ncbi.nlm.nih.gov/34476843
Autor:
Alejandro Cáceres, Juan David Caicedo, Carlos E. Arboleda-Bustos, Humberto Arboleda, María Fernanda Mahecha, Gonzalo Arboleda, Jenny Ortega
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 39, Iss 3, Pp 595-600 (2019)
Biomédica : Revista del Instituto Nacional de Salud
Biomédica, Volume: 39, Issue: 3, Pages: 595-600, Published: 30 SEP 2019
Biomédica : Revista del Instituto Nacional de Salud
Biomédica, Volume: 39, Issue: 3, Pages: 595-600, Published: 30 SEP 2019
Resumen Introducción. Los proyectos del mapa de haplotipos (HapMap) y de los 1.000 genomas han sido fundamentales para la compresión del componente genético de las enfermedades comunes y los fenotipos normales. Sin embargo, la variabilidad genéti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7448cdc67abdb294d9ef5751d8b1b67
https://revistabiomedica.org/index.php/biomedica/article/view/4753
https://revistabiomedica.org/index.php/biomedica/article/view/4753
Autor:
Andrea Rivera-Valdivia, Carlos Roberto de Mello Rieder, Víctor Raggio, Emily Mason, Miguel Inca-Martinez, William Fernandez, Angel C. Medina, Paul Cannon, Henrique Ballalai Ferraz, Andres G. Lescano, Pilar Mazzetti, Karl Heilbron, Sonia Moreno, Gonzalo Arboleda, Humberto Arboleda, Timothy D. O’Connor, Carlos E. Arboleda-Bustos, Vanderci Borges, Timothy A. Thornton, Ignacio F. Mata, Bruno Lopes Santos-Lobato, Pedro Chana-Cuevas, Carlos Velez-Pardo, Vitor Tumas, Elena Dieguez, Cyrus P. Zabetian, Douglas Loesch, Francisco Lopera, Marlene Jimenez-Del-Rio, Luis Torres, Dora Yearout, Mario Cornejo-Olivas, Elif Irem Sarihan, Carlos Cosentino, Andrea R. V. R. Horimoto, Elison Sarapura-Castro, Artur F. Schumacher-Schuh
To date, over 90 Parkinson’s disease (PD) risk variants have been reported from genome-wide association studies (GWAS). However, these GWAS efforts have been limited to individuals of European and East Asian ancestry. We performed the first GWAS of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::474c573306004b2a7bda8c26bacfcc29
https://doi.org/10.1101/2020.11.09.20227124
https://doi.org/10.1101/2020.11.09.20227124
Autor:
Jenny Ortega-Rojas, Carlos E. Arboleda-Bustos, Esneyder Guerrero, Juan Neira, Humberto Arboleda
Publikováno v:
Alzheimer disease and associated disorders. 36(1)
The Apolipoprotein E (APOE) gene is the main risk factor for late-onset Alzheimer disease (LOAD). Genetic variants and haplotypes in regions near the APOE locus may be associated with LOAD in the Colombian population.We evaluated frequencies and risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b00ff98fb2e2d45b854d8cb05d6da73a
https://pubmed.ncbi.nlm.nih.gov/35149606
https://pubmed.ncbi.nlm.nih.gov/35149606