Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sandra Catalina Mesa"'
Autor:
Juliana Trujillo Gómez, Sandra Milena Tobón Carvajal, Blair Ortiz Giraldo, Sandra Catalina Mesa Restrepo, Gabriel Jaime Vélez Rengifo, José William Cornejo Ochoa
Publikováno v:
Acta Neurológica Colombiana, Vol 31, Iss 4 (2023)
Introducción: La hiperglicinemia no cetósica (HGNC) es un error innato del metabolismo del grupo de las aminoacidopatías, de carácter autosómico recesivo, causado por un defecto en el sistema de clivaje de la glicina. Es una entidad rara y no se
Externí odkaz:
https://doaj.org/article/ef4373b45e024996be42acdccdb26535
Autor:
Ana Carolina Sierra Montoya, Sandra Catalina Mesa Restrepo, Jorge Mauricio Cuartas Arias, William Cornejo Ochoa
Publikováno v:
International Journal of Psychological Research, Vol 11, Iss 1, Pp 58-69 (2018)
Introduction: Attention Deficit Hyperactivity Disorder (ADHD) is the most common behavioral issue for children. One of the sleeping disorders most frequently related to ADHD is the Restless Legs Syndrome (RLS), characterized by an irresistible urge t
Externí odkaz:
https://doaj.org/article/cbbb41664c7a4d799464a4c6ff01077f
Autor:
Laura Fernanda Niño Serna, Tatiana Guerrero Molina, María Clara Velásquez González, Verónica Ramírez, Sandra Catalina Mesa Restrepo, Carlos Chinchilla Mejía, José William Cornejo Ochoa
Publikováno v:
Acta Neurológica Colombiana, Vol 30, Iss 3 (2015)
Introduccion: Las enfermedades alérgicas y el trastorno por déficit de atención son entidades frecuentes en la niñez. Alguno autores han sugerido una asociación entre estas. Objetivos: Establecer la prevalencia de alergias en niños con déficit
Externí odkaz:
https://doaj.org/article/69f2228ffa244cfebb0466cb56ad8616
Autor:
Ana Carolina Sierra Montoya, Jorge Mauricio Cuartas Arias, William Cornejo Ochoa, Sandra Catalina Mesa Restrepo
Publikováno v:
International Journal of Psychological Research
International Journal of Psychological Research, Vol 11, Iss 1 (2018)
Universidad de San Buenaventura-Medellín
Biblioteca Digital Universidad de San Buenaventura
Repositorio USB
Universidad de San Buenaventura
instacron:Universidad de San Buenaventura
International Journal of Psychological Research, Vol 11, Iss 1, Pp 58-69 (2018)
International Journal of Psychological Research, Vol 11, Iss 1 (2018)
Universidad de San Buenaventura-Medellín
Biblioteca Digital Universidad de San Buenaventura
Repositorio USB
Universidad de San Buenaventura
instacron:Universidad de San Buenaventura
International Journal of Psychological Research, Vol 11, Iss 1, Pp 58-69 (2018)
Introduction: Attention Deficit Hyperactivity Disorder (ADHD) is the most common behavioral issue for children. One of the sleeping disorders most frequently related to ADHD is the Restless Legs Syndrome (RLS), characterized by an irresistible urge t
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
Autor:
Mary M. Robertson, Peter Heutink, Leonhard Lennertz, Victor I. Reus, John Hardy, Mark A. Riddle, Beatriz Camarena, Helena Garrido, Robert A. King, Simon Girard, Christine Lochner, Michael H. Bloch, Patrick Evans, Anuar Konkashbaev, Jack Samuels, Priya Moorjani, Chiara Sabatti, Andrew J. Pakstis, Ying Wang, O. Joseph Bienvenu, Richard Delorme, David L. Pauls, Rainald Moessner, Gary A. Heiman, Daniel A. Geller, Marco A. Grados, Eric R. Gamazon, John Piacentini, Dan J. Stein, William Cornejo Ochoa, Maria Conceição do Rosário, Karin Egberts, Thomas L. Lowe, Christopher K. Edlund, Jan Smit, Christopher Pittenger, Denise A. Chavira, Marion Leboyer, Homero Vallada, Sandra Catalina Mesa Restrepo, Jacquelyn Crane, Donald W. Black, David V. Conti, Paul Sandor, Humberto Nicolini, Lisa Osiecki, Jeremy Veenstra-VanderWeele, Catherine Mayerfeld, Danielle Posthuma, Edna Grünblatt, Carolina Cappi, Robert B. Weiss, Cristina Barlassina, Sara Lupoli, Chunyu Liu, Sian M. J. Hemmings, Ben A. Oostra, D. Denys, Susanne Walitza, Lea K. Davis, Stephen A. Haddad, Luis Diego Herrera, Jubel Morgan, Hans Joergen Grabe, Benjamin M. Neale, Thomas V. Fernandez, Yehuda Pollak, Roel A. Ophoff, Gerald Nestadt, Harvey S. Singer, Stephan Ruhrmann, Bernadette Cullen, Michael Wagner, Nuria Lanzagorta, Jeremiah M. Scharf, Cathy L. Budman, Ruth D. Bruun, R. Kurlan, Valsama Eapen, Jesen Fagerness, Desmond Campbell, James L. Kennedy, Carlos N. Pato, Nancy J. Cox, Pieter J. Hoekstra, Joseph Jankovic, Cathy L. Barr, Peter Falkai, Donald L. Gilbert, Fortu Benarroch, Dianne M. Hezel, Maria Cristina Cavallini, Brooke Sheppard, Fabio Macciardi, William M. McMahon, Laura Bellodi, Maurizio Turiel, Wolfgang Maier, Varda Gross-Tsur, Helena Brentani, Dongmei Yu, Danielle C. Cath, Ana V. Valencia Duarte, Eduardo Fournier, James A. Knowles, Tobias J. Renner, Erika L. Nurmi, Guy A. Rouleau, Benjamin D. Greenberg, Nelson B. Freimer, Shaun Purcell, Patience J. Gallagher, Roxana Romero, Gregory L. Hanna, Paolo Manunta, Edwin H. Cook, Michele T. Pato, Sylvain Chouinard, Scott L. Rauch, James T. McCracken, Gloria Gerber, Carol A. Mathews, Jens R. Wendland, Sampath Arepalli, Dennis L. Murphy, Daniele Cusi, Barbara Kremeyer, Vladimir Coric, Aline S. Sampaio, Erika Salvi, Julio C. Cardona Silgado, Cornelia Illmann, James F. Leckman, Euripedes Constantino Miguel, H. Müller, Yin Yao Shugart, Eric Strengman, Ana Gabriela Hounie, Michael E. Weale, Gabriel Bedoya Berrió, Margaret A. Richter, Maurizio Marconi, Allan L. Naarden, Michael A. Jenike, M.R. Cookson, David R. Rosenberg, Andres Ruiz-Linares, S. Evelyn Stewart, Paul D. Arnold, H.G.M. Westenberg, Yves Dion, Jay A. Tischfield, Eske M. Derks, Lauren M. McGrath
Publikováno v:
American Journal of Psychiatry, 172(1), 82-93. American Psychiatric Association
The American Journal of Psychiatry, 172(1), 82-93. American Psychiatric Association
The American journal of psychiatry 172(1), 82-93 (2015). doi:10.1176/appi.ajp.2014.13101306
Yu, D M, Mathews, C A, Scharf, J M, Neale, B M, Davis, L K, Gamazon, E R, Derks, E M, Evans, P, Edlund, C K, Crane, J, Osiecki, L, Gallagher, P, Gerber, G, Haddad, S, Illmann, C, McGrath, L M, Mayerfeld, C, Arepalli, S, Barlassina, C, Barr, C L, Bellodi, L, Benarroch, F, Berrio, G B, Bienvenu, O J, Black, D W, Bloch, M H, Brentani, H, Bruun, R D, Budman, C L, Camarena, B, Campbell, D D, Cappi, C, Silgado, J C C, Cavallini, M C, Chavira, D A, Chouinard, S, Cook, E H, Cookson, M R, Coric, V, Cullen, B, Cusi, D, Delorme, R, Denys, D, Dion, Y, Eapen, V, Egberts, K, Falkai, P, Fernandez, T, Fournier, E, Garrido, H, Geller, D, Gilbert, D L, Girard, S L, Grabe, H J, Grados, M A, Greenberg, B D, Gross-Tsur, V, Grunblatt, E, Hardy, J, Heiman, G A, Hemmings, S M J, Herrera, L D, Hezel, D M, Hoekstra, P J, Jankovic, J, Kennedy, J L, King, R A, Konkashbaev, A I, Kremeyer, B, Kurlan, R, Lanzagorta, N, Leboyer, M, Leckman, J F, Lennertz, L, Liu, C Y, Lochner, C, Lowe, T L, Lupoli, S, Macciardi, F, Maier, W, Manunta, P, Marconi, M, McCracken, J T, Restrepo, S C M, Moessner, R, Moorjani, P, Morgan, J, Muller, H, Murphy, D L, Naarden, A L, Nurmi, E, Ochoa, W C, Ophoff, R A, Pakstis, A J, Pato, M T, Pato, C N, Piacentini, J, Pittenger, C, Pollak, Y, Smit, J H, Posthuma, D, Cox, N J & Pauls, D L 2015, ' Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD ', American Journal of Psychiatry, vol. 172, no. 1, pp. 82-93 . https://doi.org/10.1176/appi.ajp.2014.13101306
American Journal of Psychiatry, 172(1), 82-93. AMER PSYCHIATRIC PUBLISHING, INC
American Journal of Psychiatry, 172(1), 82. American Psychiatric Association
American journal of psychiatry, 172(1), 82-93. American Psychiatric Association
The American Journal of Psychiatry, 172(1), 82-93. American Psychiatric Association
The American journal of psychiatry 172(1), 82-93 (2015). doi:10.1176/appi.ajp.2014.13101306
Yu, D M, Mathews, C A, Scharf, J M, Neale, B M, Davis, L K, Gamazon, E R, Derks, E M, Evans, P, Edlund, C K, Crane, J, Osiecki, L, Gallagher, P, Gerber, G, Haddad, S, Illmann, C, McGrath, L M, Mayerfeld, C, Arepalli, S, Barlassina, C, Barr, C L, Bellodi, L, Benarroch, F, Berrio, G B, Bienvenu, O J, Black, D W, Bloch, M H, Brentani, H, Bruun, R D, Budman, C L, Camarena, B, Campbell, D D, Cappi, C, Silgado, J C C, Cavallini, M C, Chavira, D A, Chouinard, S, Cook, E H, Cookson, M R, Coric, V, Cullen, B, Cusi, D, Delorme, R, Denys, D, Dion, Y, Eapen, V, Egberts, K, Falkai, P, Fernandez, T, Fournier, E, Garrido, H, Geller, D, Gilbert, D L, Girard, S L, Grabe, H J, Grados, M A, Greenberg, B D, Gross-Tsur, V, Grunblatt, E, Hardy, J, Heiman, G A, Hemmings, S M J, Herrera, L D, Hezel, D M, Hoekstra, P J, Jankovic, J, Kennedy, J L, King, R A, Konkashbaev, A I, Kremeyer, B, Kurlan, R, Lanzagorta, N, Leboyer, M, Leckman, J F, Lennertz, L, Liu, C Y, Lochner, C, Lowe, T L, Lupoli, S, Macciardi, F, Maier, W, Manunta, P, Marconi, M, McCracken, J T, Restrepo, S C M, Moessner, R, Moorjani, P, Morgan, J, Muller, H, Murphy, D L, Naarden, A L, Nurmi, E, Ochoa, W C, Ophoff, R A, Pakstis, A J, Pato, M T, Pato, C N, Piacentini, J, Pittenger, C, Pollak, Y, Smit, J H, Posthuma, D, Cox, N J & Pauls, D L 2015, ' Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD ', American Journal of Psychiatry, vol. 172, no. 1, pp. 82-93 . https://doi.org/10.1176/appi.ajp.2014.13101306
American Journal of Psychiatry, 172(1), 82-93. AMER PSYCHIATRIC PUBLISHING, INC
American Journal of Psychiatry, 172(1), 82. American Psychiatric Association
American journal of psychiatry, 172(1), 82-93. American Psychiatric Association
Objective: Obsessive-compulsive disorder (OCD) and Tourette's syndrome are highly heritable neurodevelopmental disorders that are thought to share genetic risk factors. However, the identification of definitive susceptibility genes for these etiologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79e11312ccf27a5c74965ba6942d3999
https://pure.eur.nl/en/publications/c4492f78-db9b-4995-8b7c-16801f9e814c
https://pure.eur.nl/en/publications/c4492f78-db9b-4995-8b7c-16801f9e814c
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
Autor:
Patrick Evans, Jay A. Tischfield, Anuar Konkashbaev, Richard Delorme, Sandra Catalina Mesa Restrepo, Margaret A. Richter, Gregory L. Hanna, Allan L. Naarden, Michele T. Pato, Jian Yang, Denise A. Chavira, Damiaan Denys, Paul Sandor, Michael A. Jenike, Sian M. J. Hemmings, Paul D. Arnold, Stephan Ruhrmann, H.G.M. Westenberg, Yves Dion, Cathy L. Barr, Andres Ruiz-Linares, Brooke Sheppard, Leonhard Lennertz, Eske M. Derks, Lauren M. McGrath, Barbara Kremeyer, Marion Leboyer, Victor I. Reus, Cornelia Illmann, S. Evelyn Stewart, Dan J. Stein, Ana Gabriela Hounie, James T. McCracken, R. Kurlan, Chunyu Liu, Aline S. Sampaio, Thomas L. Lowe, Benjamin M. Neale, Yehuda Pollak, Desmond Campbell, Fabio Macciardi, Mary M. Robertson, Benjamin D. Greenberg, Ben A. Oostra, Rainald Moessner, Gary A. Heiman, Nuria Lanzagorta, Sylvain Chouinard, Rianne M. Blom, Karin Egberts, Carlos N. Pato, David V. Conti, Carol A. Mathews, Ying Wang, Marco A. Grados, Julio C. Cardona Silgado, S. Hong Lee, H. Müller, Eric R. Gamazon, Humberto Nicolini, Jan Smit, Euripedes Constantino Miguel, Jens R. Wendland, Cathy L. Budman, Laura Bellodi, Danielle Posthuma, Jubel Morgan, David R. Rosenberg, John Piacentini, Hans J. Grabe, Mark A. Riddle, Beatriz Camarena, Naomi R. Wray, Eric Strengman, Dennis L. Murphy, Simon Girard, Christine Lochner, Ruth D. Bruun, Joseph Jankovic, Edwin H. Cook, William M. McMahon, Scott L. Rauch, James F. Leckman, Peter Falkai, Fortu Benarroch, Christopher K. Edlund, Gabriel Bedoya Berrío, Homero Vallada, Susanne Walitza, Nelson B. Freimer, Stephen A. Haddad, Yin Yao Shugart, Danielle C. Cath, Nancy J. Cox, Varda Gross-Tsur, Guy A. Rouleau, Bernadette Cullen, Michael H. Bloch, Dieter Deforce, David L. Pauls, Thomas V. Fernandez, Roel A. Ophoff, Filip Van Nieuwerburgh, Gerald Nestadt, Dongmei Yu, Helena Garrido, Robert A. King, James L. Kennedy, Clare L. Keenan, Lisa Osiecki, Jack Samuels, Jeremy Veenstra-VanderWeele, Ana V. Valencia Duarte, James A. Knowles, Patience J. Gallagher, Carolina Cappi, Maria Conceição do Rosário, Andrew J. Pakstis, Christopher Pittenger, Michael Wagner, Jeremiah M. Scharf, Daniel A. Geller, Vladimir Coric, Tobias J. Renner, Oscar J. Bienvenu, Roxana Romero, William Cornejo Ochoa, Peter Heutink, Lea K. Davis, Harvey S. Singer, Maria Cristina Cavallini
Publikováno v:
Davis, L K, Yu, D, Keenan, C L, Gamazon, E R, Konkashbaev, A I, Derks, E M, Neale, B M, Yang, J, Lee, S H, Evans, P, Barr, C L, Bellodi, L, Benarroch, F, Berrio, G B, Bienvenu, O J, Bloch, M H, Blom, R M, Bruun, R D, Budman, C L, Camarena, B, Campbell, D, Cappi, C, Cardona Silgado, J C, Cath, D C, Cavallini, M C, Chavira, D A, Chouinard, S, Conti, D V, Cook, E H, Coric, V, Cullen, B A, Deforce, D, Delorme, R, Dion, Y, Edlund, C K, Egberts, K, Falkai, P, Fernandez, T V, Gallagher, P J, Garrido, H, Geller, D, Girard, S L, Grabe, H J, Grados, M A, Greenberg, B D, Gross-Tsur, V, Haddad, S, Heiman, G A, Hemmings, S M, Hounie, A G, Illmann, C, Jankovic, J, Jenike, M A, Kennedy, J L, King, R A, Kremeyer, B, Kurlan, R, Lanzagorta, N, Leboyer, M, Leckman, J F, Lennertz, L, Liu, C, Lochner, C, Lowe, T L, Macciardi, F, McCracken, J T, McGrath, L M, Mesa Restrepo, S C, Moessner, R, Morgan, J, Muller, H, Murphy, D L, Naarden, A L, Ochoa, W C, Ophoff, R A, Osiecki, L, Pakstis, A J, Pato, M T, Piacentini, J, Pittenger, C, Pollak, Y, Rauch, S L, Renner, T J, Reus, V I, Richter, M A, Riddle, M A, Robertson, M M, Romero, R, Rosàrio, M C, Rosenberg, D, Rouleau, G A, Ruhrmann, S, Ruiz-Linares, A, Sampaio, A S, Samuels, J, Sandor, P, Sheppard, B, Singer, H S, Smit, J H, Stein, D J, Strengman, E, Tischfield, J A, Valencia Duarte, A V, Vallada, H, van Nieuwerburgh, F, Veenstra-Vanderweele, J, Walitza, S, Wang, Y, Wendland, J R, Westenberg, H G, Shugart, Y Y, Miguel, E C, McMahon, W, Wagner, M, Nicolini, H, Posthuma, D, Hanna, G L, Heutink, P, Denys, D, Arnold, P D, Oostra, B A, Nestadt, G, Freimer, N B, Pauls, D L, Wray, N R, Stewart, S E, Mathews, C A, Knowles, J A, Cox, N J & Scharf, J M 2013, ' Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture ', PLoS Genetics, vol. 9, no. 10, e1003864, pp. e1003864 . https://doi.org/10.1371/journal.pgen.1003864
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS Genetics
PLoS Genetics, Vol 9, Iss 10, p e1003864 (2013)
PLoS Genetics 9(10), e1003864 (2013). doi:10.1371/journal.pgen.1003864
PLoS Genetics, 9(10):e1003864. Public Library of Science
PLOS Genetics
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
PLOS GENETICS
PLoS Genetics (print), 9(10). Public Library of Science
PLoS genetics, 9(10). Public Library of Science
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
PLoS Genetics
PLoS Genetics, Vol 9, Iss 10, p e1003864 (2013)
PLoS Genetics 9(10), e1003864 (2013). doi:10.1371/journal.pgen.1003864
PLoS Genetics, 9(10):e1003864. Public Library of Science
PLOS Genetics
Repositório Institucional da UNIFESP
Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
PLOS GENETICS
PLoS Genetics (print), 9(10). Public Library of Science
PLoS genetics, 9(10). Public Library of Science
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
The direct estimation of heritability from genome-wide common variant data as implemented in the program Genome-wide Complex Trait Analysis (GCTA) has provided a means to quantify heritability attributable to all interrogated variants. We have quanti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::686a4341f35ee18e526d61a0482fccdd
https://research.vumc.nl/en/publications/c9466bc4-c7d4-4632-bd50-3178b290bbeb
https://research.vumc.nl/en/publications/c9466bc4-c7d4-4632-bd50-3178b290bbeb
Autor:
Sierra Montoya, Ana Carolina1, Mesa Restrepo, Sandra Catalina1, Cuartas Arias, Jorge Mauricio2,3, Cornejo Ochoa, William4 jose.cornejo@udea.edu.co
Publikováno v:
International Journal of Psychological Research. 2018, Vol. 11 Issue 1, p58-69. 12p.
Publikováno v:
Journal of Inherited Metabolic Disease; Nov2021 Supplement S1, Vol. 44, p1-461, 461p