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







List of shared articles



Times cited


Clinical evaluation of patients with a neuropsychiatric risk copy number variant.
Samuel Jra Chawner, Cameron J Watson, Michael J Owen. Curr Opin Genet Dev 2021
0

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

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