A citation-based method for searching scientific literature

Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren, Bhooma Thiruvahindrapduram, Andreas Fiebig, Stefan Schreiber, Jan Friedman, Cees E J Ketelaars, Yvonne J Vos, Can Ficicioglu, Susan Kirkpatrick, Rob Nicolson, Leon Sloman, Anne Summers, Clare A Gibbons, Ahmad Teebi, David Chitayat, Rosanna Weksberg, Ann Thompson, Cathy Vardy, Vicki Crosbie, Sandra Luscombe, Rebecca Baatjes, Lonnie Zwaigenbaum, Wendy Roberts, Bridget Fernandez, Peter Szatmari, Stephen W Scherer. Am J Hum Genet 2008
Times Cited: 1173



Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield, Marcin Imielinski, Edward C Frackelton, Jennifer Reichert, Emily L Crawford, Jeffrey Munson, Patrick M A Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James Flory, Frederick Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J Meyer, Evdokia Anagnostou, Takeshi Sakurai, Rachel M Game, Danielle S Rudd, Danielle Zurawiecki, Christopher J McDougle, Lea K Davis, Judith Miller, David J Posey, Shana Michaels, Alexander Kolevzon, Jeremy M Silverman, Raphael Bernier, Susan E Levy, Robert T Schultz, Geraldine Dawson, Thomas Owley, William M McMahon, Thomas H Wassink, John A Sweeney, John I Nurnberger, Hilary Coon, James S Sutcliffe, Nancy J Minshew, Struan F A Grant, Maja Bucan, Edwin H Cook, Joseph D Buxbaum, Bernie Devlin, Gerard D Schellenberg, Hakon Hakonarson. Nature 2009
Times Cited: 919




List of shared articles



Times cited

Cell Adhesion Molecules Involved in Neurodevelopmental Pathways Implicated in 3p-Deletion Syndrome and Autism Spectrum Disorder.
Josan Gandawijaya, Rosemary A Bamford, J Peter H Burbach, Asami Oguro-Ando. Front Cell Neurosci 2021
0

Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review.
Paola Castronovo, Marco Baccarin, Arianna Ricciardello, Chiara Picinelli, Pasquale Tomaiuolo, Francesca Cucinotta, Myriam Frittoli, Carla Lintas, Roberto Sacco, Antonio M Persico. Clin Genet 2020
13


Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
Lin Wang, Yi Zhang, Kuokuo Li, Zheng Wang, Xiaomeng Wang, Bin Li, Guihu Zhao, Zhenghuan Fang, Zhengbao Ling, Tengfei Luo,[...]. Mol Autism 2020
1

Linking Autism Risk Genes to Disruption of Cortical Development.
Marta Garcia-Forn, Andrea Boitnott, Zeynep Akpinar, Silvia De Rubeis. Cells 2020
2

The Role of Alpha-Synuclein and Other Parkinson's Genes in Neurodevelopmental and Neurodegenerative Disorders.
C Alejandra Morato Torres, Zinah Wassouf, Faria Zafar, Danuta Sastre, Tiago Fleming Outeiro, Birgitt Schüle. Int J Mol Sci 2020
4

The Gut-Brain Axis in Autism Spectrum Disorder: A Focus on the Metalloproteases ADAM10 and ADAM17.
Yuanpeng Zheng, Tessa A Verhoeff, Paula Perez Pardo, Johan Garssen, Aletta D Kraneveld. Int J Mol Sci 2020
1

A comparative study of the genetic components of three subcategories of autism spectrum disorder.
Jinchen Li, Shanshan Hu, Kun Zhang, Leisheng Shi, Yi Zhang, Tingting Zhao, Lin Wang, Xin He, Kun Xia, Chunyu Liu,[...]. Mol Psychiatry 2019
16

Psychiatric disorders in children with 16p11.2 deletion and duplication.
Maria Niarchou, Samuel J R A Chawner, Joanne L Doherty, Anne M Maillard, Sébastien Jacquemont, Wendy K Chung, LeeAnne Green-Snyder, Raphael A Bernier, Robin P Goin-Kochel, Ellen Hanson,[...]. Transl Psychiatry 2019
42

Genetic insights and neurobiological implications from NRXN1 in neuropsychiatric disorders.
Zhonghua Hu, Xiao Xiao, Zhuohua Zhang, Ming Li. Mol Psychiatry 2019
24