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The Lancet. Respiratory Medicine|January 17, 2014
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association studyImre Noth, Yingze Zhang, Shwu-Fan Ma, et al.
Elife|April 19, 2021
DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formationLaura Morcom, Ilan Gobius, Ashley Pl Marsh, et al.
Human Molecular Genetics|April 16, 2013
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachmentMirna Kirin, Aman Chandra, David G Charteris, et al.
Bioorganic & Medicinal Chemistry Letters|February 25, 2006
N-Alkyl-N-arylmethylpiperidin-4-amines: novel dual inhibitors of serotonin and norepinephrine reuptakeJ R Boot, S L Boulet, B P Clark, et al.
Genes|August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous DisorderThuong T Ha, Rosemary Burgess, Morgan Newman, et al.
Nature Genetics|November 14, 2018
Subtype-specific regulatory network rewiring in acute myeloid leukemiaSalam A Assi, Maria Rosaria Imperato, Daniel J L Coleman, et al.
JAMA|May 23, 2013
Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosisAnna L Peljto, Yingze Zhang, Tasha E Fingerlin, et al.
Journal of Alzheimer'S Disease : JAD|November 14, 2022
Differentiation of Subjective Cognitive Decline, Mild Cognitive Impairment, and Dementia Using qEEG/ERP-Based Cognitive Testing and Volumetric MRI in an Outpatient Specialty Memory ClinicAarthi S Ganapathi, Ryan M Glatt, Tess H Bookheimer, et al.
Bioorganic & Medicinal Chemistry Letters|October 5, 2010
Discovery of 2-substituted benzoxazole carboxamides as 5-HT3 receptor antagonistsZhicai Yang, David J Fairfax, Jun-Ho Maeng, et al.
Human Mutation|October 26, 2017
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndromeAshley P L Marsh, Timothy J Edwards, Charles Galea, et al.
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