Rieder C.R.M.
154
Coauthors
5
Documentos
Volumen de publicaciones por año
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| Año de publicación | Num. Publicaciones |
|---|---|
| 2013 | 1 |
| 2017 | 1 |
| 2018 | 1 |
| 2021 | 2 |
Publicaciones por áreas de conocimiento
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| Área de conocimiento | Num. Publicaciones |
|---|---|
| Genética | 8 |
| Neurología | 1 |
| Salud pública | 1 |
| Ciencias naturales | 1 |
Publicaciones por áreas temáticas
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| Área temática | Num. Publicaciones |
|---|---|
| Enfermedades | 4 |
| Medicina y salud | 2 |
| Artes | 1 |
| Fisiología humana | 1 |
| Grupos de personas | 1 |
| Mammalia | 1 |
| Historia de América del Norte | 1 |
| Farmacología y terapéutica | 1 |
Principales fuentes de datos
| Origen | Num. Publicaciones |
|---|---|
| Scopus | 5 |
| Google Scholar | 1 |
| RRAAE | 0 |
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Coautores destacados por número de publicaciones
| Coautor | Num. Publicaciones |
|---|---|
| Cosentino C. | 5 |
| Borges V. | 5 |
| Shumacher-Schuh A. | 5 |
| Mata I.F. | 4 |
| Mazzetti P. | 4 |
| Ferraz H.B. | 4 |
| Raggio V. | 4 |
| Dieguez E. | 4 |
| Torres L. | 4 |
| Lopera F. | 4 |
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Top Keywords
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Publicaciones del autor
Care of patients with Huntington's disease in South America: A survey
ArticleAbstract: Huntington's disease (HD) is a rare neurodegenerative disease with a multitude of symptoms, which rePalabras claves:Comprehensive health care, Genetic counseling, Huntington DiseaseAutores:Chaná-Cuevas P., Cosentino C., Costa Cardoso F.E., Fernandez W., Horta Maciel R.O., Rieder C.R.M., Serrano Dueñas Marcos, Weiser R.Fuentes:googlescopusErratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry (npj Parkinson's Disease, (2017), 3, 1, (19), 10.1038/s41531-017-0020-6)
OtherAbstract: The original version of this article contained an error in the name of gene LRRK2, which was incorrePalabras claves:Autores:Andree-Muñoz B., Borges V., Cornejo-Olivas M., Cosentino C., Dieguez E., Ferraz H.B., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lopera F., Mata I.F., Mazzetti P., Micheli F., Perandones C., Raggio V., Rieder C.R.M., Shumacher-Schuh A., Torres L., Tumas V., Velez-Pardo C., Velit-Salazar M.R., Waldherr S., Yearout D., Zabetian C.P.Fuentes:scopusVariable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry /692/617/375/1718 /631/208/1516 article
ArticleAbstract: Genetic risk: Uncovering ethnic-specific mutations: A new study reveals the frequency of Leucine RepPalabras claves:Autores:Andree-Muñoz B., Borges V., Cornejo-Olivas M., Cosentino C., Dieguez E., Ferraz H.B., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lopera F., Mata I.F., Mazzetti P., Micheli F., Perandones C., Raggio V., Rieder C.R.M., Shumacher-Schuh A., Torres L., Tumas V., Velez-Pardo C., Velit-Salazar M.R., Waldherr S., Yearout D., Zabetian C.P.Fuentes:scopusTracing the Distribution of European Lactase Persistence Genotypes Along the Americas
ArticleAbstract: In adulthood, the ability to digest lactose, the main sugar present in milk of mammals, is a phenotyPalabras claves:dairy consumption, lactose intolerance, Latin America, MCM6 gene, nutrition policies, Population genetics, –13910C > TAutores:Adelman Cipolla G., Arboleda G., Arboleda H., Arboleda-Bustos C.E., Beltrame M.H., Borda V., Borges V., Cáceres O., Chana-Cuevas P., Dean M., Dieguez E., Fernandez W., Ferraz H.B., Guimarães Alves A.C., Guio H., Kaplan R., Leal T.P., Lehtonen Rodrigues Souza R., Lescano A.G., Lima-Costa M.F., Loesch D., Machado M., Mata I.F., Mauricio L. Barreto, Mendes M., Moon J.Y., North K.E., O’Connor T.D., Padilla C., Petzl-Erler M.L., Raggio V., Rainha de Souza I., Rieder C.R.M., Sanchez C., Santolalla M.L., Santos-Lobato B.L., Shumacher-Schuh A., Sukow N.M., Tarazona-Santos E.M., Tumas V., Weiss S.T.Fuentes:scopusGenome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients
ArticleAbstract: Background: Parkinson's disease is the second most common neurodegenerative disorder and affects peoPalabras claves:copy number variants, Genetics, Latin America, Parkinson's DiseaseAutores:Acosta G.T., Amorin I., Arboleda G., Arboleda H., Arboleda-Bustos C.E., Borges V., Chana-Cuevas P., Cornejo-Olivas M., Cosentino C., Dieguez E., Fernandez W., Ferraz H.B., Ferrera A., Fornaguera J., Gatto E.M., Guillén A.H., Horimoto A.V.R., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lal D., Lescano A.G., Loesch D., Lopera F., Martinez-Ramirez D., Mata I.F., Mazzetti P., Medina A., Micheli F., Moreno S., Muñoz B.A., Niestroj L.M., Orozco J.L., O´Connor T.D., Pérez-Palma E., Raggio V., Rieder C.R.M., Rivera A., Rivera-Valdivia A., Rodriguez M., Santos-Lobato B.L., Sarapura H., Sarapura-Castro E., Sarihan E.I., Shumacher-Schuh A., Thornton T.A., Torres L., Tumas V., Velez-Pardo C., Viñuela A., Yearout D., Zabetian C.P.Fuentes:scopus