HuGE Literature Finder
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| Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia. Annals of human genetics 2017 Nov . Al Eissa Mariam M, Fiorentino Alessia, Sharp Sally I, O'Brien Niamh L, Wolfe Kate, Giaroli Giovanni, Curtis David, Bass Nicholas J, McQuillin Andr |
| Inhibition of the Schizophrenia-Associated MicroRNA miR-137 Disrupts Nrg1a Neurodevelopmental Signal Transduction. Cell reports 2017 Jul 20 (1): 1-12. Thomas Kristen Therese, Anderson Bart Russell, Shah Niraj, Zimmer Stephanie Elaine, Hawkins Daniel, Valdez Arielle Nicole, Gu Qiaochu, Bassell Gary Jonath |
| Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports. American journal of medical genetics. Part A 2016 Feb . Brownstein Catherine A, Kleiman Robin J, Engle Elizabeth C, Towne Meghan C, D'Angelo Eugene J, Yu Timothy W, Beggs Alan H, Picker Jonathan, Fogler Jason M, Carroll Devon, Schmitt Rachel C O, Wolff Robert R, Shen Yiping, Lip Va, Bilguvar Kaya, Kim April, Tembulkar Sahil, O'Donnell Kyle, Gonzalez-Heydrich Jose |
| Analysis of t(9;17)(q33.2;q25.3) chromosomal breakpoint regions and genetic association reveals novel candidate genes for bipolar disorder. Bipolar disorders 2015 Mar 17 (2): 205-11. Rajkumar Anto P, Christensen Jane H, Mattheisen Manuel, Jacobsen Iben, Bache Iben, Pallesen Jonatan, Grove Jakob, Qvist Per, McQuillin Andrew, Gurling Hugh M, Tümer Zeynep, Mors Ole, Børglum Anders |
| Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling. G3 (Bethesda, Md.) 2014 Jan 5 (1): 61-72. Liu Yaping, Pham Xuan, Zhang Lilei, Chen Pei-Lung, Burzynski Grzegorz, McGaughey David M, He Shan, McGrath John A, Wolyniec Paula, Fallin Margaret D, Pierce Megan S, McCallion Andrew S, Pulver Ann E, Avramopoulos Dimitrios, Valle Dav |
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