A citation-based method for searching scientific literature

M G Butler. J Intellect Disabil Res 2017
Times Cited: 39



Michiala Cafferkey, Joo Wook Ahn, Frances Flinter, Caroline Ogilvie. Am J Med Genet A 2014
Times Cited: 35




List of shared articles



Times cited

Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.
Chih-Ping Chen, Shu-Yuan Chang, Liang-Kai Wang, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang,[...]. Taiwan J Obstet Gynecol 2018
8

Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities.
Renee Bend, Lior Cohen, Melissa T Carter, Michael J Lyons, Dmitriy Niyazov, Mohamad A Mikati, Samantha K Rojas, Richard E Person, Yue Si, Ingrid M Wentzensen,[...]. Eur J Hum Genet 2020
6

A Rare Case of Concomitant Deletions in 15q11.2 and 19p13.3.
Ilária C Sgardioli, Elaine Lustosa-Mendes, Ana P Dos Santos, Társis P Vieira, Vera L Gil-da-Silva-Lopes. Cytogenet Genome Res 2018
1

Modelling Learning and Memory in Drosophila to Understand Intellectual Disabilities.
Vittoria Mariano, Tilmann Achsel, Claudia Bagni, Alexandros K Kanellopoulos. Neuroscience 2020
2

Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.
A M Manzardo, N Weisensel, S Ayala, W Hossain, M G Butler. Clin Genet 2018
12