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

Deleterious coding variation associated with autism is shared across ancestries

与自闭症相关的有害编码变异在不同祖先群体中是共通的。

Natividad Avila, Marina; Jung, Seulgi; Satterstrom, F Kyle; Fu, Jack M; Levy, Tess; Sloofman, Laura G; Klei, Lambertus; Pichardo, Thariana; Marquez, Dalia; Stevens, Christine R; Cusick, Caroline M; Ames, Jennifer L; Campos, Gabriele S; Cerros, Hilda; Chaskel, Roberto; Costa, Claudia I S; Cuccaro, Michael L; Lopez, Andrea Del Pilar; Fernandez, Magdalena; Ferro, Eugenio; Galeano, Liliana; Girardi, Ana Cristina D E S; Griswold, Anthony J; Hernandez, Luis C; Lourenço, Naila; Ludena, Yunin; Núñez-Ríos, Diana; Oyama, Rosa; Peña, Katherine P; Pessah, Isaac; Schmidt, Rebecca; Sweeney, Holly M; Tolentino, Lizbeth; Wang, Jaqueline Y T; Albores-Gallo, Lilia; Croen, Lisa A; Cruz-Fuentes, Carlos S; Hertz-Picciotto, Irva; Kolevzon, Alexander; Lattig, Maria Claudia; Mayo, Liliana; Passos-Bueno, Maria Rita; Pericak-Vance, Margaret A; Siper, Paige M; Tassone, Flora; Trelles, M Pilar; Talkowski, Michael E; Daly, Mark J; Mahjani, Behrang; De Rubeis, Silvia; Cook, Edwin H; Roeder, Kathryn; Betancur, Catalina; Devlin, Bernie; Buxbaum, Joseph D

Maternal body mass index in early pregnancy and autism in offspring: a population-based cohort study in Sweden and Denmark

孕早期母亲体重指数与后代自闭症:一项基于瑞典和丹麦人群的队列研究

Morin, Matilda; Yin, Weiyao; MacLean, Heidi; Devlin, Bernie; Reichenberg, Abraham; Swan, Shanna H; Buxbaum, Joseph D; Schendel, Diana; Persson, Martina; Laursen, Thomas Munk; Kolevzon, Alexander; Grove, Jakob; Klei, Lambertus; Roeder, Kathryn; Sandin, Sven

A framework to infer de novo exonic variants when parental genotypes are missing enhances association studies of autism

当父母基因型缺失时,推断新生外显子变异的框架可以增强自闭症关联研究。

Moon, Haeun; Sloofman, Laura; Avila, Marina Natividad; Klei, Lambertus; Devlin, Bernie; Buxbaum, Joseph D; Roeder, Kathryn

PACS1 syndrome variant alters proteomic landscape of developing cortical organoids

PACS1综合征变异体改变了发育中皮质类器官的蛋白质组图谱

Gomez-Maqueo, Ximena; Rylaarsdam, Lauren E; Woo, Ashley; Schroder, Annika L; Rakotomamonjy, Jennifer; Bossert, Clare L; Smith, Tess A; Ruiz, Shelby; Gilardi, Jordan; Klei, Lambertus; Devlin, Bernie; MacDonald, Matthew L; Guemez-Gamboa, Alicia

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

与自闭症相关的有害编码变异在不同人群中具有一致性,例如拉丁美洲混血人群就体现了这一点。

Avila, Marina Natividad; Jung, Seulgi; Satterstrom, F Kyle; Fu, Jack M; Levy, Tess; Sloofman, Laura G; Klei, Lambertus; Pichardo, Thariana; Stevens, Christine R; Cusick, Caroline M; Ames, Jennifer L; Campos, Gabriele S; Cerros, Hilda; Chaskel, Roberto; Costa, Claudia I S; Cuccaro, Michael L; Del Pilar Lopez, Andrea; Fernandez, Magdalena; Ferro, Eugenio; Galeano, Liliana; Girardi, Ana Cristina D E S; Griswold, Anthony J; Hernandez, Luis C; Lourenço, Naila; Ludena, Yunin; Nuñez, Diana L; Oyama, Rosa; Peña, Katherine P; Pessah, Isaac; Schmidt, Rebecca; Sweeney, Holly M; Tolentino, Lizbeth; Wang, Jaqueline Y T; Albores-Gallo, Lilia; Croen, Lisa A; Cruz-Fuentes, Carlos S; Hertz-Picciotto, Irva; Kolevzon, Alexander; Lattig, Maria C; Mayo, Liliana; Passos-Bueno, Maria Rita; Pericak-Vance, Margaret A; Siper, Paige M; Tassone, Flora; Trelles, M Pilar; Talkowski, Michael E; Daly, Mark J; Mahjani, Behrang; De Rubeis, Silvia; Cook, Edwin H; Roeder, Kathryn; Betancur, Catalina; Devlin, Bernie; Buxbaum, Joseph D

Genetic associations with psychosis and affective disturbance in Alzheimer's disease

阿尔茨海默病中精神病和情感障碍的遗传关联

Antonsdottir, Inga Margret; Creese, Byron; Klei, Lambertus; DeMichele-Sweet, Mary Ann A; Weamer, Elise A; Garcia-Gonzalez, Pablo; Marquie, Marta; Boada, Mercè; Alarcón-Martín, Emilio; Valero, Sergi; Liu, Yushi; Hooli, Basavaraj; Aarsland, Dag; Selbaek, Geir; Bergh, Sverre; Rongve, Arvid; Saltvedt, Ingvild; Skjellegrind, Håvard K; Engdahl, Bo; Andreassen, Ole A; Borroni, Barbara; Mecocci, Patrizia; Wedatilake, Yehani; Mayeux, Richard; Foroud, Tatiana; Ruiz, Agustín; Lopez, Oscar L; Kamboh, M Ilyas; Ballard, Clive; Devlin, Bernie; Lyketsos, Constantine; Sweet, Robert A

Heritable Composite Phenotypes Defined by Combinations of Conduct Problem, Depression, and Temperament Features: Contributions to risk for Alcohol Problems

由行为问题、抑郁和气质特征组合定义的遗传复合表型:对酒精问题风险的贡献

Wang, Frances L; Klei, Lambertus; Devlin, Bernie; Molina, Brooke S G; Chassin, Laurie

Direct additive genetics and maternal effect contribute to the risk of Tourette disorder

直接累加遗传和母体效应均会增加患图雷特综合征的风险。

Mahjani, Behrang; Klei, Lambertus; Buxbaum Grice, Ariela S; Larsson, Henrik; Hultman, Christina M; Sandin, Sven; Devlin, Bernie; Buxbaum, Joseph D; Grice, Dorothy E

Comparison of gene expression in living and postmortem human brain

比较活体和死后人脑中的基因表达

Collado-Torres, Leonardo; Klei, Lambertus; Liu, Chunyu; Kleinman, Joel E; Hyde, Thomas M; Geschwind, Daniel H; Gandal, Michael J; Devlin, Bernie; Weinberger, Daniel R

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

罕见的编码变异有助于深入了解自闭症的遗传结构和表型背景。

Fu, Jack M; Satterstrom, F Kyle; Peng, Minshi; Brand, Harrison; Collins, Ryan L; Dong, Shan; Wamsley, Brie; Klei, Lambertus; Wang, Lily; Hao, Stephanie P; Stevens, Christine R; Cusick, Caroline; Babadi, Mehrtash; Banks, Eric; Collins, Brett; Dodge, Sheila; Gabriel, Stacey B; Gauthier, Laura; Lee, Samuel K; Liang, Lindsay; Ljungdahl, Alicia; Mahjani, Behrang; Sloofman, Laura; Smirnov, Andrey N; Barbosa, Mafalda; Betancur, Catalina; Brusco, Alfredo; Chung, Brian H Y; Cook, Edwin H; Cuccaro, Michael L; Domenici, Enrico; Ferrero, Giovanni Battista; Gargus, J Jay; Herman, Gail E; Hertz-Picciotto, Irva; Maciel, Patricia; Manoach, Dara S; Passos-Bueno, Maria Rita; Persico, Antonio M; Renieri, Alessandra; Sutcliffe, James S; Tassone, Flora; Trabetti, Elisabetta; Campos, Gabriele; Cardaropoli, Simona; Carli, Diana; Chan, Marcus C Y; Fallerini, Chiara; Giorgio, Elisa; Girardi, Ana Cristina; Hansen-Kiss, Emily; Lee, So Lun; Lintas, Carla; Ludena, Yunin; Nguyen, Rachel; Pavinato, Lisa; Pericak-Vance, Margaret; Pessah, Isaac N; Schmidt, Rebecca J; Smith, Moyra; Costa, Claudia I S; Trajkova, Slavica; Wang, Jaqueline Y T; Yu, Mullin H C; Cutler, David J; De Rubeis, Silvia; Buxbaum, Joseph D; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn; Sanders, Stephan J; Talkowski, Michael E