A citation-based method for searching scientific literature

Maryam Al Shehhi, Eva B Forman, Jacqueline E Fitzgerald, Veronica McInerney, Janusz Krawczyk, Sanbing Shen, David R Betts, Linda Mc Ardle, Kathleen M Gorman, Mary D King, Andrew Green, Louise Gallagher, Sally A Lynch. Eur J Med Genet 2019
Times Cited: 24



Christian P Schaaf, Philip M Boone, Srirangan Sampath, Charles Williams, Patricia I Bader, Jennifer M Mueller, Oleg A Shchelochkov, Chester W Brown, Heather P Crawford, James A Phalen, Nicole R Tartaglia, Patricia Evans, William M Campbell, Anne Chun-Hui Tsai, Lea Parsley, Stephanie W Grayson, Angela Scheuerle, Carol D Luzzi, Sandra K Thomas, Patricia A Eng, Sung-Hae L Kang, Ankita Patel, Pawel Stankiewicz, Sau W Cheung. Eur J Hum Genet 2012
Times Cited: 70




List of shared articles



Times cited

Genetic mechanisms of regression in autism spectrum disorder.
Kristiina Tammimies. Neurosci Biobehav Rev 2019
8

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

Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases.
Paolo Alfieri, Francesco Scibelli, Lorenzo Sinibaldi, Giovanni Valeri, Cristina Caciolo, Roberta Lucia Novello, Antonio Novelli, Maria Cristina Digilio, Marco Tartaglia, Stefano Vicari. Genes Brain Behav 2020
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