A citation-based method for searching scientific literature

Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker, Tarinder Singh, Lambertus Klei, Jack Kosmicki, Fu Shih-Chen, Branko Aleksic, Monica Biscaldi, Patrick F Bolton, Jessica M Brownfeld, Jinlu Cai, Nicholas G Campbell, Angel Carracedo, Maria H Chahrour, Andreas G Chiocchetti, Hilary Coon, Emily L Crawford, Sarah R Curran, Geraldine Dawson, Eftichia Duketis, Bridget A Fernandez, Louise Gallagher, Evan Geller, Stephen J Guter, R Sean Hill, Juliana Ionita-Laza, Patricia Jimenz Gonzalez, Helena Kilpinen, Sabine M Klauck, Alexander Kolevzon, Irene Lee, Irene Lei, Jing Lei, Terho Lehtimäki, Chiao-Feng Lin, Avi Ma'ayan, Christian R Marshall, Alison L McInnes, Benjamin Neale, Michael J Owen, Noriio Ozaki, Mara Parellada, Jeremy R Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Sachse, Stephan J Sanders, Chad Schafer, Martin Schulte-Rüther, David Skuse, Christine Stevens, Peter Szatmari, Kristiina Tammimies, Otto Valladares, Annette Voran, Wang Li-San, Lauren A Weiss, A Jeremy Willsey, Timothy W Yu, Ryan K C Yuen, Edwin H Cook, Christine M Freitag, Michael Gill, Christina M Hultman, Thomas Lehner, Aaarno Palotie, Gerard D Schellenberg, Pamela Sklar, Matthew W State, James S Sutcliffe, Christiopher A Walsh, Stephen W Scherer, Michael E Zwick, Jeffrey C Barett, David J Cutler, Kathryn Roeder, Bernie Devlin, Mark J Daly, Joseph D Buxbaum. Nature 2014
Times Cited: 1246







List of shared articles



Times cited


Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth.
Médéric Jeanne, Marie-Laure Vuillaume, Dévina C Ung, Valerie E Vancollie, Christel Wagner, Stephan C Collins, Sandrine Vonwill, Damien Haye, Nora Chelloug, Rolph Pfundt,[...]. Hum Genet 2021
1

Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes.
Kuokuo Li, Zhengbao Ling, Tengfei Luo, Guihu Zhao, Qiao Zhou, Xiaomeng Wang, Kun Xia, Jinchen Li, Bin Li. Life (Basel) 2021
0

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Madelyn A Gillentine, Tianyun Wang, Kendra Hoekzema, Jill Rosenfeld, Pengfei Liu, Hui Guo, Chang N Kim, Bert B A De Vries, Lisenka E L M Vissers, Magnus Nordenskjold,[...]. Genome Med 2021
0

Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities.
Médéric Jeanne, Hélène Demory, Aubin Moutal, Marie-Laure Vuillaume, Sophie Blesson, Rose-Anne Thépault, Sylviane Marouillat, Judith Halewa, Saskia M Maas, M Mahdi Motazacker,[...]. Am J Hum Genet 2021
0

Targeted sequencing and integrative analysis of 3195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genes.
Tao Wang, Yi Zhang, Liqui Liu, Yan Wang, Huiqian Chen, Tianda Fan, Jinchen Li, Kun Xia, Zhongsheng Sun. J Genet Genomics 2021
0

Distinct genetic patterns of shared and unique genes across four neurodevelopmental disorders.
Yijia Zhang, Ruochen Wang, Zhenwei Liu, Shan Jiang, Lifeng Du, Kairui Qiu, Fengxia Li, Qiongdan Wang, Jing Jin, Xiaomin Chen,[...]. Am J Med Genet B Neuropsychiatr Genet 2021
0

The emerging role of chromatin remodelers in neurodevelopmental disorders: a developmental perspective.
Britt Mossink, Moritz Negwer, Dirk Schubert, Nael Nadif Kasri. Cell Mol Life Sci 2021
2

YWHAG Mutations Cause Childhood Myoclonic Epilepsy and Febrile Seizures: Molecular Sub-regional Effect and Mechanism.
Xing-Guang Ye, Zhi-Gang Liu, Jie Wang, Jie-Min Dai, Pei-Xiu Qiao, Ping-Ming Gao, Wei-Ping Liao. Front Genet 2021
0

Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Yi Zhang, Tao Wang, Yan Wang, Kun Xia, Jinchen Li, Zhongsheng Sun. Mol Neurobiol 2021
0

De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.
Caroline Dias, Rolph Pfundt, Tjitske Kleefstra, Janneke Shuurs-Hoeijmakers, Elles M J Boon, Johanna M van Hagen, Petra Zwijnenburg, Marjan M Weiss, Boris Keren, Cyril Mignot,[...]. Am J Med Genet A 2021
0

Multi-parametric analysis of 57 SYNGAP1 variants reveal impacts on GTPase signaling, localization, and protein stability.
Fabian Meili, William J Wei, Wun-Chey Sin, Warren M Meyers, Iulia Dascalu, Daniel B Callaghan, Sanja Rogic, Paul Pavlidis, Kurt Haas. Am J Hum Genet 2021
0

MVP predicts the pathogenicity of missense variants by deep learning.
Hongjian Qi, Haicang Zhang, Yige Zhao, Chen Chen, John J Long, Wendy K Chung, Yongtao Guan, Yufeng Shen. Nat Commun 2021
0

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
Chloe X Yap, Gail A Alvares, Anjali K Henders, Tian Lin, Leanne Wallace, Alaina Farrelly, Tiana McLaren, Jolene Berry, Anna A E Vinkhuyzen, Maciej Trzaskowski,[...]. Mol Autism 2021
0