日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study protocol

拉丁美洲强迫症基因组学跨种族研究计划 (LATINO):研究方案

Crowley, James J; Cappi, Carolina; Ochoa-Panaifo, Marcos E; Frederick, Renee M; Kook, Minjee; Wiese, Andrew D; Rancourt, Diana; Atkinson, Elizabeth G; Giusti-Rodriguez, Paola; Anderberg, Jacey L; Abramowitz, Jonathan S; Adorno, Victor R; Aguirre, Cinthia; Alves, Gilberto S; Alves, Gustavo S; Ancalade, NaEshia; Arellano Espinosa, Alejandro A; Arnold, Paul D; Ayton, Daphne M; Barbosa, Izabela G; Castano, Laura Marcela Barón; Barrera, Cynthia N; Berardo, María Celeste; Berrones, Dayan; Best, John R; Bigdeli, Tim B; Burton, Christie L; Buxbaum, Joseph D; Callahan, Jennifer L; Carneiro, Maria Cecília B; Cepeda, Sandra L; Chazelle, Evelyn; Chire, Jessica M; Munoz, Macarena Churruca; Quiroz, Pamela Claisse; Cobite, Journa; Comer, Jonathan S; Costa, Daniel L; Crosbie, Jennifer; Cruz, Victor O; Dager, Guillermo; Daza, Luisa F; de la Rosa-Gómez, Anabel; Del Río, Daniela; Delage, Fernanda Z; Dreher, Carolina B; Fay, Lucila; Fazio, Tomas; Ferrão, Ygor A; Ferreira, Gabriela M; Figueroa, Edith G; Fontenelle, Leonardo F; Forero, Diego A; Fragoso, Daniele T H; Gadad, Bharathi S; Garrison, Sheldon R; González, Andres; Gonzalez, Laura D; González, Marco A; Gonzalez-Barrios, Polaris; Goodman, Wayne K; Grice, Dorothy E; Guintivano, Jerry; Guttfreund, Daniel G; Guzick, Andrew G; Halvorsen, Matthew W; Hovey, Joseph D; Huang, Hailiang; Irreño-Sotomonte, Jonathan; Janssen-Aguilar, Reinhard; Jensen, Matias; Jimenez Reynolds, Alexandra Z; Lujambio, Joali Alexandra Juárez; Khalfe, Nasim; Knutsen, Madison A; Lack, Caleb; Lanzagorta, Nuria; Lima, Monicke O; Longhurst, Melanie O; Lozada Martinez, David A; Luna, Elba S; Marques, Andrea H; Martinez, Molly S; de Los Angeles Matos, Maria; Maye, Caitlyn E; McGuire, Joseph F; Menezes, Gabriela; Minaya, Charlene; Miño, Tomás; Mithani, Sara M; de Oca, Circe Montes; Morales-Rivero, Alonso; Moreira-de-Oliveira, Maria E; Morris, Olivia J; Muñoz, Sandra I; Naqqash, Zainab; Núñez Bracho, Ambar A; Núñez Bracho, Belinda E; Rojas, Maria Corina Ochoa; Olavarria Castaman, Luis A; Balmaceda, Trinidad Olivos; Ortega, Iliana; Patel, Darpan I; Patrick, Ainsley K; Paz Y Mino, Mariel; Perales Orellana, Jose L; Stumpf, Bárbara Perdigão; Peregrina, Tamara; Duarte, Tania Pérez; Piacsek, Kelly L; Placencia, Maritza; Prieto, María Belén; Quarantini, Lucas C; Quarantini-Alvim, Yana; Ramos, Renato T; Ramos, Iaroslava C; Ramos, Vanessa R; Ramsey, Kesley A; Ray, Elise V; Richter, Margaret A; Riemann, Bradley C; Rivas, Juan C; Rosario, Maria C; Ruggero, Camilo J; Ruiz-Chow, Angel A; Ruiz-Velasco, Alejandra; Sagarnaga, Melisa N; Sampaio, Aline S; Saraiva, Leonardo C; Schachar, Russell J; Schneider, Sophie C; Schweissing, Ethan J; Seligman, Laura D; Shavitt, Roseli G; Soileau, Keaton J; Stewart, S Evelyn; Storch, Shaina B; Strouphauer, Emily R; Cuevas, Vissente Tapia; Timpano, Kiara R; la Garza, Beatriz Treviño-de; Vallejo-Silva, Alexie; Vargas-Medrano, Javier; Vásquez, María I; Martinez, Guadalupe Vidal; Weinzimmer, Saira A; Yanez, Mauricio A; Zai, Gwyneth; Zapata-Restrepo, Lina M; Zappa, Luz M; Zepeda-Burgos, Raquel M; Zoghbi, Anthony W; Miguel, Euripedes C; Rodriguez, Carolyn I; Martinez Mallen, Mayra C; Moya, Pablo R; Borda, Tania; Moyano, María Beatriz; Mattheisen, Manuel; Pereira, Stacey; Lázaro-Muñoz, Gabriel; Martinez-Gonzalez, Karen G; Pato, Michele T; Nicolini, Humberto; Storch, Eric A

Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia

罕见的串联重复序列扩增与精神分裂症中参与突触和神经元信号传导功能的基因相关

Wen, Jia; Trost, Brett; Engchuan, Worrawat; Halvorsen, Matthew; Pallotto, Linda M; Mitina, Aleksandra; Ancalade, NaEshia; Farrell, Martilias; Backstrom, Ian; Guo, Keyi; Pellecchia, Giovanna; Thiruvahindrapuram, Bhooma; Giusti-Rodriguez, Paola; Rosen, Jonathan David; Li, Yun; Won, Hyejung; Magnusson, Patrik K E; Gyllensten, Ulf; Bassett, Anne S; Hultman, Christina M; Sullivan, Patrick F; Yuen, Ryan K C; Szatkiewicz, Jin P

Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study Protocol

拉丁美洲强迫症基因组学跨种族研究计划(LATINO):研究方案

Crowley, James J; Cappi, Carolina; Ochoa-Panaifo, Marcos E; Frederick, Renee M; Kook, Minjee; Wiese, Andrew D; Rancourt, Diana; Atkinson, Elizabeth G; Giusti-Rodriguez, Paola; Anderberg, Jacey L; Abramowitz, Jonathan S; Adorno, Victor R; Aguirre, Cinthia; Alves, Gustavo S; Alves, Gilberto S; Ancalade, NaEshia; Espinosa, Alejandro A Arellano; Arnold, Paul D; Ayton, Daphne M; Barbosa, Izabela G; Castano, Laura Marcela Barón; Barrera, Cynthia N; Prieto, María Belén; Berardo, María Celeste; Berrones, Dayan; Best, John R; Bigdeli, Tim B; Burton, Christie L; Callahan, Jennifer L; Carneiro, Maria Cecília B; Cepeda, Sandra L; Chazelle, Evelyn; Chire, Jessica M; Munoz, Macarena Churruca; Quiroz, Pamela Claisse; Cobite, Journa; Comer, Jonathan S; Costa, Daniel L; Crosbie, Jennifer; Cruz, Victor O; Dager, Guillermo; Daza, Luisa F; de la Rosa-Gómez, Anabel; Del Río, Daniela; Delage, Fernanda Z; Dreher, Carolina B; Fay, Lucila; Fazio, Tomas; Ferrão, Ygor A; Ferreira, Gabriela M; Figueroa, Edith G; Fontenelle, Leonardo F; Forero, Diego A; Fragoso, Daniele Th; Gadad, Bharathi S; Garrison, Sheldon R; González, Andres; Gonzalez, Laura D; González, Marco A; Gonzalez-Barrios, Polaris; Goodman, Wayne; Guintivano, Jerry; Guttfreund, Daniel G; Guzick, Andrew G; Halvorsen, Matthew W; Hovey, Joseph D; Janssen-Aguilar, Reinhard; Jensen, Matias; Reynolds, Alexandra Z Jimenez; Lujambio, Joali Alexandra Juárez; Khalfe, Nasim; Knutsen, Madison A; Lack, Caleb; Lanzagorta, Nuria; Lima, Monicke O; Longhurst, Melanie O; Martinez, David A Lozada; Luna, Elba S; Marques, Andrea H; Martinez, Molly; de Los Angeles Matos, Maria; Maye, Caitlyn E; McGuire, Joseph F; Menezes, Gabriela; Minaya, Charlene; Miño, Tomás; Mithani, Sara M; de Oca, Circe Montes; Morales-Rivero, Alonso; Moreira-de-Oliveira, Maria E; Morris, Olivia J; Muñoz, Sandra I; Naqqash, Zainab; Bracho, Ambar A Núñez; Bracho, Belinda E Núñez; Rojas, Maria Corina Ochoa; Castaman, Luis A Olavarria; Ortega, Iliana; Patel, Darpan I; Patrick, Ainsley K; Mino, Mariel Paz Y; Orellana, Jose L Perales; Stumpf, Bárbara Perdigão; Peregrina, Tamara; Duarte, Tania Pérez; Piacsek, Kelly L; Placencia, Maritza; Quarantini, Lucas C; Quarantini-Alvim, Yana; Ramos, Renato T; Ramos, Iaroslava C; Ramos, Vanessa R; Ramsey, Kesley A; Ray, Elise V; Richter, Margaret A; Riemann, Bradley C; Rivas, Juan C; Rosario, Maria C; Ruggero, Camilo J; Ruiz-Chow, Angel A; Ruiz-Velasco, Alejandra; Sampaio, Aline S; Saraiva, Leonardo C; Schachar, Russell J; Schneider, Sophie C; Schweissing, Ethan J; Seligman, Laura D; Shavitt, Roseli G; Soileau, Keaton J; Stewart, S Evelyn; Storch, Shaina B; Strouphauer, Emily R; Timpano, Kiara R; Treviño-de la Garza, Beatriz; Vargas-Medrano, Javier; Vásquez, María I; Martinez, Guadalupe Vidal; Weinzimmer, Saira A; Yanez, Mauricio A; Zai, Gwyneth; Zapata-Restrepo, Lina M; Zappa, Luz M; Zepeda-Burgos, Raquel M; Zoghbi, Anthony W; Miguel, Euripedes C; Rodriguez, Carolyn I; Mallen, Mayra C Martinez; Moya, Pablo R; Borda, Tania; Moyano, María Beatriz; Mattheisen, Manuel; Pereira, Stacey; Lázaro-Muñoz, Gabriel; Martinez-Gonzalez, Karen G; Pato, Michele T; Nicolini, Humberto; Storch, Eric A

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

精神分裂症中位于拓扑关联域边界的超罕见结构变异负担增加

Halvorsen, Matthew; Huh, Ruth; Oskolkov, Nikolay; Wen, Jia; Netotea, Sergiu; Giusti-Rodriguez, Paola; Karlsson, Robert; Bryois, Julien; Nystedt, Björn; Ameur, Adam; Kähler, Anna K; Ancalade, NaEshia; Farrell, Martilias; Crowley, James J; Li, Yun; Magnusson, Patrik K E; Gyllensten, Ulf; Hultman, Christina M; Sullivan, Patrick F; Szatkiewicz, Jin P

Characterization of Single Gene Copy Number Variants in Schizophrenia

精神分裂症中单基因拷贝数变异的特征分析

Szatkiewicz, Jin P; Fromer, Menachem; Nonneman, Randal J; Ancalade, NaEshia; Johnson, Jessica S; Stahl, Eli A; Rees, Elliott; Bergen, Sarah E; Hultman, Christina M; Kirov, George; O'Donovan, Michael; Owen, Michael; Holmans, Peter; Sklar, Pamela; Sullivan, Patrick F; Purcell, Shaun M; Crowley, James J; Ruderfer, Douglas M

Common-variant associations with fragile X syndrome

常见变异与脆性X综合征的关联

Crowley, James J; Szatkiewicz, Jin; Kähler, Anna K; Giusti-Rodriguez, Paola; Ancalade, NaEshia; Booker, Jessica K; Carr, Jennifer L; Crawford, Greg E; Losh, Molly; Stockmeier, Craig A; Taylor, Annette K; Piven, Joseph; Sullivan, Patrick F

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa

探索与神经性厌食症患者的精神和神经发育障碍相关的大型、罕见拷贝数变异

Yilmaz, Zeynep; Szatkiewicz, Jin P; Crowley, James J; Ancalade, NaEshia; Brandys, Marek K; van Elburg, Annemarie; de Kovel, Carolien G F; Adan, Roger A H; Hinney, Anke; Hebebrand, Johannes; Gratacos, Monica; Fernandez-Aranda, Fernando; Escaramis, Georgia; Gonzalez, Juan R; Estivill, Xavier; Zeggini, Eleftheria; Sullivan, Patrick F; Bulik, Cynthia M

Disruption of the microRNA 137 primary transcript results in early embryonic lethality in mice

microRNA 137 初级转录本的破坏会导致小鼠早期胚胎致死。

Crowley, James J; Collins, Ann L; Lee, Rebecca J; Nonneman, Randal J; Farrell, Martilias S; Ancalade, NaEshia; Mugford, Joshua W; Agster, Kara L; Nikolova, Viktoriya D; Moy, Sheryl S; Sullivan, Patrick F