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



Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson, Joshua D Smith, Bryan Paeper, Deborah A Nickerson, Jeanselle Dea, Shan Dong, Luis E Gonzalez, Jeffrey D Mandell, Shrikant M Mane, Michael T Murtha, Catherine A Sullivan, Michael F Walker, Zainulabedin Waqar, Liping Wei, A Jeremy Willsey, Boris Yamrom, Yoon-ha Lee, Ewa Grabowska, Ertugrul Dalkic, Zihua Wang, Steven Marks, Peter Andrews, Anthony Leotta, Jude Kendall, Inessa Hakker, Julie Rosenbaum, Beicong Ma, Linda Rodgers, Jennifer Troge, Giuseppe Narzisi, Seungtai Yoon, Michael C Schatz, Kenny Ye, W Richard McCombie, Jay Shendure, Evan E Eichler, Matthew W State, Michael Wigler. Nature 2014
Times Cited: 1119




List of shared articles



Times cited

COMPASS and SWI/SNF complexes in development and disease.
Bercin K Cenik, Ali Shilatifard. Nat Rev Genet 2021
5

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

Large mosaic copy number variations confer autism risk.
Maxwell A Sherman, Rachel E Rodin, Giulio Genovese, Caroline Dias, Alison R Barton, Ronen E Mukamel, Bonnie Berger, Peter J Park, Christopher A Walsh, Po-Ru Loh. Nat Neurosci 2021
3

Chromatin Remodeler CHD8 in Autism and Brain Development.
Anke Hoffmann, Dietmar Spengler. J Clin Med 2021
2

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

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

Kinase Signaling in Dendritic Development and Disease.
Kimya Nourbakhsh, Smita Yadav. Front Cell Neurosci 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


A white paper on a neurodevelopmental framework for drug discovery in autism and other neurodevelopmental disorders.
C M Díaz-Caneja, M W State, R J Hagerman, S Jacquemont, O Marín, C Bagni, D Umbricht, E Simonoff, F de Andrés-Trelles, A Kaale,[...]. Eur Neuropsychopharmacol 2021
1

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

Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders.
E El Khouri, J Ghoumid, D Haye, F Giuliano, L Drevillon, A Briand-Suleau, P De La Grange, V Nau, T Gaillon, T Bienvenu,[...]. Mol Psychiatry 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

Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.
Maya Chopra, Meriel McEntagart, Jill Clayton-Smith, Konrad Platzer, Anju Shukla, Katta M Girisha, Anupriya Kaur, Parneet Kaur, Rolph Pfundt, Hermine Veenstra-Knol,[...]. 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

Cul3 regulates cytoskeleton protein homeostasis and cell migration during a critical window of brain development.
Jasmin Morandell, Lena A Schwarz, Bernadette Basilico, Saren Tasciyan, Georgi Dimchev, Armel Nicolas, Christoph Sommer, Caroline Kreuzinger, Christoph P Dotter, Lisa S Knaus,[...]. Nat Commun 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


Expression Changes in Epigenetic Gene Pathways Associated With One-Carbon Nutritional Metabolites in Maternal Blood From Pregnancies Resulting in Autism and Non-Typical Neurodevelopment.
Yihui Zhu, Charles E Mordaunt, Blythe P Durbin-Johnson, Marie A Caudill, Olga V Malysheva, Joshua W Miller, Ralph Green, S Jill James, Stepan B Melnyk, M Daniele Fallin,[...]. Autism Res 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

Origin of Sex-Biased Mental Disorders: An Evolutionary Perspective.
Rama S Singh, Karun K Singh, Shiva M Singh. J Mol Evol 2021
0

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


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