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

Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility

自闭症基因变异会破坏肠道神经元迁移并导致胃肠道运动障碍

Kate E McCluskey, Katherine M Stovell, Karen Law, Elina Kostyanovskaya, James D Schmidt, Cameron R T Exner, Jeanselle Dea, Elise Brimble, Matthew W State, A Jeremy Willsey, Helen Rankin Willsey

Ciliary biology intersects autism and congenital heart disease.

纤毛生物学与自闭症和先天性心脏病有关联

Teerikorpi Nia, McCluskey Kate E, Bader Ethel, Lasser Micaela C, Wang Sheng, Nguyen Catherine H, Schmidt James D, Kostyanovskaya Elina, Sun Nawei, Dea Jeanselle, Nowakowski Tomasz J, Willsey A Jeremy, Willsey Helen Rankin

Convergence of autism proteins at the cilium

自闭症蛋白质在纤毛处的汇聚

Elina Kostyanovskaya, Micaela C Lasser, Belinda Wang, James Schmidt, Ethel Bader, Chad Buteo, Juan Arbelaez, Aria Rani Sindledecker, Kate E McCluskey, Octavio Castillo, Sheng Wang, Jeanselle Dea, Kathryn A Helde, J Michael Graglia, Elise Brimble, David B Kastner, Aliza T Ehrlich, Matthew W State, A

Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disorders

罕见编码突变鉴定出36个与强迫症和慢性抽动障碍相关的大效应风险基因

Wang, Belinda; Tran, Matthew N; Wang, Sheng; Liu, Yuting; Olfson, Emily; Wang, George; Sun, Nawei; Dea, Jeanselle; Olwal, Charles Ochieng'; Bertolace, Lyvia; Bloch, Michael H; Cappi, Carolina; Chang, Yi-Chieh; Chavira, Denise; Coffey, Barbara J; Falkenstein, Martha J; Frank, Adam C; Franklin, Martin E; Garayalde, Stephanie; Garrido, Helena; Grados, Marco; Hatem, Rami; Howell, Allyna-London; Khim, Starlette; Kuckertz, Jennie M; Le, Mindy M; Libby, Allison; McCarty, Ryan J; McNamara, Mary E; McNeil, Daniel; Miguel, Euripedes C; Nasello, Cara; Nguyen, Binh; Norbu, Tenzin; Oh, Lauren; Ordway, Ashley; Paciotti, Catherine; Peskin, Viviana A; Pittenger, Christopher; Simpson, Helen Blair; Martin, Heather Simpson; Tischfield, Max A; Xing, Jinchuan; Zakrzewski, Jessica J; Dietrich, Andrea; Gilbert, Donald L; Hoekstra, Pieter J; Kim, Young Shin; Kuperman, Samuel; Rosen, Alyssa; Zinner, Samuel H; Bouhaddou, Mehdi; King, Robert A; Rouleau, Guy; Ressler, Kerry J; Mathews, Carol A; Krogan, Nevan J; Sestan, Nenad; Tischfield, Jay A; Lee, A Moses; Heiman, Gary A; Fernandez, Thomas V; Willsey, A Jeremy; State, Matthew W

Ciliary biology intersects autism and congenital heart disease

纤毛生物学与自闭症和先天性心脏病相关

Nia Teerikorpi, Micaela C Lasser, Sheng Wang, Elina Kostyanovskaya, Ethel Bader, Nawei Sun, Jeanselle Dea, Tomasz J Nowakowski, A Jeremy Willsey, Helen Rankin Willsey

Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility

自闭症基因变异会扰乱肠神经元迁移,导致胃肠动力障碍。

McCluskey, Kate E; Stovell, Katherine M; Law, Karen; Kostyanovskaya, Elina; Schmidt, James; Exner, Cameron R T; Dea, Jeanselle; Brimble, Elise; State, Matthew W; Willsey, A Jeremy; Willsey, Helen Rankin

Pleiotropy of autism-associated chromatin regulators

自闭症相关染色质调节剂的多效性

Micaela Lasser, Nawei Sun, Yuxiao Xu, Sheng Wang, Sam Drake, Karen Law, Silvano Gonzalez, Belinda Wang, Vanessa Drury, Octavio Castillo, Yefim Zaltsman, Jeanselle Dea, Ethel Bader, Kate E McCluskey, Matthew W State, A Jeremy Willsey, Helen Rankin Willsey

Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience

大型自闭症基因的平行体内分析表明皮质神经发生和雌激素与风险和恢复力有关

Helen Rankin Willsey, Cameron R T Exner, Yuxiao Xu, Amanda Everitt, Nawei Sun, Belinda Wang, Jeanselle Dea, Galina Schmunk, Yefim Zaltsman, Nia Teerikorpi, Albert Kim, Aoife S Anderson, David Shin, Meghan Seyler, Tomasz J Nowakowski, Richard M Harland, A Jeremy Willsey, Matthew W State

A convergent molecular network underlying autism and congenital heart disease

自闭症和先天性心脏病背后的趋同分子网络

Rosenthal, Sara Brin; Willsey, Helen Rankin; Xu, Yuxiao; Mei, Yuan; Dea, Jeanselle; Wang, Sheng; Curtis, Charlotte; Sempou, Emily; Khokha, Mustafa K; Chi, Neil C; Willsey, Arthur Jeremy; Fisch, Kathleen M; Ideker, Trey

The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos

神经发育障碍风险基因 DYRK1A 是非洲爪蟾胚胎纤毛发生和大脑大小控制所必需的

Helen Rankin Willsey, Yuxiao Xu, Amanda Everitt, Jeanselle Dea, Cameron R T Exner, A Jeremy Willsey, Matthew W State, Richard M Harland