Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Isabel C. Rivas"'
Autor:
Abhishek Nag, Elena G Bochukova, Barbara Kremeyer, Desmond D Campbell, Heike Muller, Ana V Valencia-Duarte, Julio Cardona, Isabel C Rivas, Sandra C Mesa, Mauricio Cuartas, Jharley Garcia, Gabriel Bedoya, William Cornejo, Luis D Herrera, Roxana Romero, Eduardo Fournier, Victor I Reus, Thomas L Lowe, I Sadaf Farooqi, Tourette Syndrome Association International Consortium for Genetics, Carol A Mathews, Lauren M McGrath, Dongmei Yu, Ed Cook, Kai Wang, Jeremiah M Scharf, David L Pauls, Nelson B Freimer, Vincent Plagnol, Andrés Ruiz-Linares
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59061 (2013)
Tourette syndrome (TS) is a neuropsychiatric disorder with a strong genetic component. However, the genetic architecture of TS remains uncertain. Copy number variation (CNV) has been shown to contribute to the genetic make-up of several neurodevelopm
Externí odkaz:
https://doaj.org/article/eafb2194ce3c4fd685929f44b9c67258
Autor:
Andres Ruiz-Linares, Isabel C. Rivas, Barbara Kremeyer, Ana Victoria Valencia-Duarte, Daniel J. White, Ibi Herzberg, J. García, Victoria Kay, M. Cuartas, Sandra Catalina Mesa, Gabriel Bedoya, William Cornejo, H. Müller
Publikováno v:
Psychiatric Genetics. 20:179-183
Gilles de la Tourette Syndrome (GTS) is a chronic neuropsychiatric disorder characterized by motor and vocal tics. Epidemiological evidence supports the importance of genetic factors in disease susceptibility, whereas pharmacological and neuroimaging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::787cf631d12d42f0e907285ec547d00b
https://doi.org/10.1097/ypg.0b013e32833a215a
https://doi.org/10.1097/ypg.0b013e32833a215a
Autor:
Barbara Kremeyer, Roxana Romero, Nelson B. Freimer, H. Müller, Thomas L. Lowe, Ana Victoria Valencia-Duarte, Lauren M. McGrath, Abhishek Nag, Kai Wang, David L. Pauls, Gabriel Bedoya, J. García, Carol A. Mathews, Desmond Campbell, Jeremiah M. Scharf, M. Cuartas, Luis Diego Herrera, Vincent Plagnol, Dongmei Yu, I. Sadaf Farooqi, Julio César Cardona, Sandra Catalina Mesa, Eduardo Fournier, Elena G. Bochukova, Victor I. Reus, Isabel C. Rivas, Ed Cook, William Cornejo, Andres Ruiz-Linares
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e59061 (2013)
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
PLoS ONE
PloS one, vol 8, iss 3
Nag, A; Bochukova, EG; Kremeyer, B; Campbell, DD; Muller, H; Valencia-Duarte, AV; et al.(2013). CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1. PLoS ONE, 8(3). doi: 10.1371/journal.pone.0059061. UCSF: Retrieved from: http://www.escholarship.org/uc/item/1z76j84n
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
PLoS ONE
PloS one, vol 8, iss 3
Nag, A; Bochukova, EG; Kremeyer, B; Campbell, DD; Muller, H; Valencia-Duarte, AV; et al.(2013). CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1. PLoS ONE, 8(3). doi: 10.1371/journal.pone.0059061. UCSF: Retrieved from: http://www.escholarship.org/uc/item/1z76j84n
Tourette syndrome (TS) is a neuropsychiatric disorder with a strong genetic component. However, the genetic architecture of TS remains uncertain. Copy number variation (CNV) has been shown to contribute to the genetic make-up of several neurodevelopm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dcc87add691eab2583d72048407a49a
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23533600/pdf/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23533600/pdf/?tool=EBI