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

Characterizing Rare DNA Copy-Number Variants in Pediatric Obsessive-Compulsive Disorder

儿童强迫症中罕见DNA拷贝数变异的特征分析

Abdallah, Sarah B; Olfson, Emily; Cappi, Carolina; Greenspun, Samantha; Zai, Gwyneth; Rosário, Maria C; Willsey, A Jeremy; Shavitt, Roseli G; Miguel, Euripedes C; Kennedy, James L; Richter, Margaret A; Fernandez, Thomas V

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

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

Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

全基因组关联研究揭示吉尔·德·拉·图雷特综合征的新基因位点

Tsetsos, Fotis; Topaloudi, Apostolia; Jain, Pritesh; Yang, Zhiyu; Yu, Dongmei; Kolovos, Petros; Tumer, Zeynep; Rizzo, Renata; Hartmann, Andreas; Depienne, Christel; Worbe, Yulia; Müller-Vahl, Kirsten R; Cath, Danielle C; Boomsma, Dorret I; Wolanczyk, Tomasz; Zekanowski, Cezary; Barta, Csaba; Nemoda, Zsofia; Tarnok, Zsanett; Padmanabhuni, Shanmukha S; Buxbaum, Joseph D; Grice, Dorothy; Glennon, Jeffrey; Stefansson, Hreinn; Hengerer, Bastian; Yannaki, Evangelia; Stamatoyannopoulos, John A; Benaroya-Milshtein, Noa; Cardona, Francesco; Hedderly, Tammy; Heyman, Isobel; Huyser, Chaim; Mir, Pablo; Morer, Astrid; Mueller, Norbert; Munchau, Alexander; Plessen, Kerstin J; Porcelli, Cesare; Roessner, Veit; Walitza, Susanne; Schrag, Anette; Martino, Davide; Tischfield, Jay A; Heiman, Gary A; Willsey, A Jeremy; Dietrich, Andrea; Davis, Lea K; Crowley, James J; Mathews, Carol A; Scharf, Jeremiah M; Georgitsi, Marianthi; Hoekstra, Pieter J; Paschou, Peristera

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

A foundational atlas of autism protein interactions reveals molecular convergence

自闭症蛋白质相互作用基础图谱揭示分子趋同性

Wang, Belinda; Vartak, Rasika; Zaltsman, Yefim; Naing, Zun Zar Chi; Hennick, Kelsey M; Polacco, Benjamin J; Bashir, Ali; Eckhardt, Manon; Bouhaddou, Mehdi; Xu, Jiewei; Sun, Nawei; Lasser, Micaela C; Zhou, Yuan; McKetney, Justin; Guiley, Keelan Z; Chan, Una; Kaye, Julia A; Chadha, Nishant; Cakir, Merve; Gordon, Martin; Khare, Prachi; Drake, Sam; Drury, Vanessa; Burke, David F; Gonzalez, Silvano; Alkhairy, Sahar; Thomas, Reuben; Lam, Stephanie; Morris, Montana; Bader, Ethel; Seyler, Meghan; Baum, Tierney; Krasnoff, Rebecca; Wang, Sheng; Pham, Presley; Arbalaez, Juan; Pratt, Dexter; Chag, Shivali; Mahmood, Nadir; Rolland, Thomas; Bourgeron, Thomas; Finkbeiner, Steven; Swaney, Danielle L; Bandyopadhay, Sourav; Ideker, Trey; Beltrao, Pedro; Willsey, Helen Rankin; Obernier, Kirsten; Nowakowski, Tomasz J; Hüttenhain, Ruth; State, Matthew W; Willsey, A Jeremy; Krogan, Nevan J

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

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

罕见的X染色体连锁变异主要导致男性患自闭症、图雷特综合征和注意力缺陷多动障碍的风险。

Wang, Sheng; Wang, Belinda; Drury, Vanessa; Drake, Sam; Sun, Nawei; Alkhairo, Hasan; Arbelaez, Juan; Duhn, Clif; Bal, Vanessa H; Langley, Kate; Martin, Joanna; Hoekstra, Pieter J; Dietrich, Andrea; Xing, Jinchuan; Heiman, Gary A; Tischfield, Jay A; Fernandez, Thomas V; Owen, Michael J; O'Donovan, Michael C; Thapar, Anita; State, Matthew W; Willsey, A Jeremy

Bypassing Formation of Oxide Intermediate via Chemical Vapor Deposition for the Synthesis of an Mn-N-C Catalyst with Improved ORR Activity

通过化学气相沉积法绕过氧化物中间体的形成,合成具有改进的氧还原反应活性的Mn-NC催化剂

Stracensky, Thomas; Jiao, Li; Sun, Qiang; Liu, Ershuai; Yang, Fan; Zhong, Sichen; Cullen, David A; Myers, Deborah J; Kropf, A Jeremy; Jia, Qingying; Mukerjee, Sanjeev; Xu, Hui