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



F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei, Christine Stevens, Jennifer Reichert, Maureen S Mulhern, Mykyta Artomov, Sherif Gerges, Brooke Sheppard, Xinyi Xu, Aparna Bhaduri, Utku Norman, Harrison Brand, Grace Schwartz, Rachel Nguyen, Elizabeth E Guerrero, Caroline Dias, Catalina Betancur, Edwin H Cook, Louise Gallagher, Michael Gill, James S Sutcliffe, Audrey Thurm, Michael E Zwick, Anders D Børglum, Matthew W State, A Ercument Cicek, Michael E Talkowski, David J Cutler, Bernie Devlin, Stephan J Sanders, Kathryn Roeder, Mark J Daly, Joseph D Buxbaum. Cell 2020
Times Cited: 273




List of shared articles



Times cited

Role of Ash1l in Tourette syndrome and other neurodevelopmental disorders.
Cheng Zhang, Lulu Xu, Xueping Zheng, Shiguo Liu, Fengyuan Che. Dev Neurobiol 2021
2

Autism Spectrum Disorder Genetics and the Search for Pathological Mechanisms.
Devanand S Manoli, Matthew W State. Am J Psychiatry 2021
4

Molecular Pathways within Autism Spectrum Disorder Endophenotypes.
Silvana Briuglia, Marco Calabrò, Anna Paola Capra, Sara Briguori, Maria Angela La Rosa, Concetta Crisafulli. J Mol Neurosci 2021
1

Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience.
Helen Rankin Willsey, Cameron R T Exner, Yuxiao Xu, Amanda Everitt, Nawei Sun, Belinda Wang, Jeanselle Dea, Galina Schmunk, Yefim Zaltsman, Nia Teerikorpi,[...]. Neuron 2021
1

Cell Type-Specific Predictive Models Perform Prioritization of Genes and Gene Sets Associated With Autism.
Jinting Guan, Yang Wang, Yiping Lin, Qingyang Yin, Yibo Zhuang, Guoli Ji. Front Genet 2021
0

Defective AMPA-mediated synaptic transmission and morphology in human neurons with hemizygous SHANK3 deletion engrafted in mouse prefrontal cortex.
Simone Chiola, Kandy L Napan, Yueqi Wang, Roman M Lazarenko, Celeste J Armstrong, Jun Cui, Aleksandr Shcheglovitov. Mol Psychiatry 2021
0

Genetic contributions to autism spectrum disorder.
A Havdahl, M Niarchou, A Starnawska, M Uddin, C van der Merwe, V Warrier. Psychol Med 2021
0

Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review.
Lisa Pavinato, Slavica Trajkova, Enrico Grosso, Elisa Giorgio, Alessandro Bruselles, Francesca Clementina Radio, Tommaso Pippucci, Paola Dimartino, Marco Tartaglia, Aleksandar Petlichkovski,[...]. Am J Med Genet A 2021
0

Single-Cell Transcriptomics Supports a Role of CHD8 in Autism.
Anke Hoffmann, Dietmar Spengler. Int J Mol Sci 2021
0

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


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

Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.
Veronica B Searles Quick, Belinda Wang, Matthew W State. Neuropsychopharmacology 2021
6

Transcriptomic Insight Into the Polygenic Mechanisms Underlying Psychiatric Disorders.
Leanna M Hernandez, Minsoo Kim, Gil D Hoftman, Jillian R Haney, Luis de la Torre-Ubieta, Bogdan Pasaniuc, Michael J Gandal. Biol Psychiatry 2021
2

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

Gene variations in autism spectrum disorder are associated with alteration of gut microbiota, metabolites and cytokines.
Zhi Liu, Xuhua Mao, Zhou Dan, Yang Pei, Rui Xu, Mengchen Guo, Kangjian Liu, Faming Zhang, Junyu Chen, Chuan Su,[...]. Gut Microbes 2021
0

Exploring the biological role of postzygotic and germinal de novo mutations in ASD.
A Alonso-Gonzalez, M Calaza, J Amigo, J González-Peñas, R Martínez-Regueiro, M Fernández-Prieto, M Parellada, C Arango, Cristina Rodriguez-Fontenla, A Carracedo. Sci Rep 2021
0

Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis.
Joon-Yong An, Jae Ho Jung, Leejee Choi, Eric D Wieben, Brian G Mohney. Genes (Basel) 2021
0

CaMKII Phosphorylation Regulates Synaptic Enrichment of Shank3.
Jaehoon Jeong, Yan Li, Katherine W Roche. eNeuro 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



An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.
Cinzia Cameli, Marta Viggiano, Magali J Rochat, Alessandra Maresca, Leonardo Caporali, Claudio Fiorini, Flavia Palombo, Pamela Magini, Renée C Duardo, Fabiola Ceroni,[...]. J Cell Mol Med 2021
1

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