A citation-based method for searching scientific literature

George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll, Michael C O'Donovan, Michael J Owen. Biol Psychiatry 2014
Times Cited: 191



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




List of shared articles



Times cited

A cross-comparison of cognitive ability across 8 genomic disorders.
Michael Mortillo, Jennifer G Mulle. Curr Opin Genet Dev 2021
0

Genetic Advances in Autism.
Anita Thapar, Michael Rutter. J Autism Dev Disord 2020
5

Genetic mechanisms of neurodevelopmental disorders.
P Y Billie Au, Alison Eaton, David A Dyment. Handb Clin Neurol 2020
0

Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4-BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature.
Natália Oliva-Teles, Maria Chiara de Stefano, Louise Gallagher, Severin Rakic, Paula Jorge, Goran Cuturilo, Silvana Markovska-Simoska, Isabella Borg, Jeanne Wolstencroft, Zeynep Tümer,[...]. Int J Environ Res Public Health 2020
0

Experience of chromosomal microarray applied in prenatal and postnatal settings in Hong Kong.
Shirley S W Cheng, Kelvin Y K Chan, Kelphen K P Leung, Patrick K C Au, Wai-Keung Tam, Samuel K M Li, Ho-Ming Luk, Anita S Y Kan, Brian H Y Chung, Ivan F M Lo,[...]. Am J Med Genet C Semin Med Genet 2019
12


Submicroscopic aberrations of chromosome 16 in prenatal diagnosis.
Xiaoqing Wu, Liangpu Xu, Ying Li, Na Lin, Linjuan Su, Meiying Cai, Xiaorui Xie, Lin Zheng, Hailong Huang, Yuan Lin. Mol Cytogenet 2019
1

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders.
L D'Abate, S Walker, R K C Yuen, K Tammimies, J A Buchanan, R W Davies, B Thiruvahindrapuram, J Wei, J Brian, S E Bryson,[...]. Nat Commun 2019
9

Increased Ca2+ signaling in NRXN1α +/- neurons derived from ASD induced pluripotent stem cells.
Sahar Avazzadeh, Katya McDonagh, Jamie Reilly, Yanqin Wang, Stephanie D Boomkamp, Veronica McInerney, Janusz Krawczyk, Jacqueline Fitzgerald, Niamh Feerick, Matthew O'Sullivan,[...]. Mol Autism 2019
11

Progress in the genetics of autism spectrum disorder.
Marc Woodbury-Smith, Stephen W Scherer. Dev Med Child Neurol 2018
49