M
Murray J. Cairns
Researcher at University of Newcastle
Publications - 201
Citations - 14007
Murray J. Cairns is an academic researcher from University of Newcastle. The author has contributed to research in topics: microRNA & Gene. The author has an hindex of 45, co-authored 175 publications receiving 10172 citations. Previous affiliations of Murray J. Cairns include Harvard University & Johnson & Johnson.
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Journal ArticleDOI
124. A comparative examination of the anti-inflammatory effects of SSRI and SNRI antidepressants on microglia
TL;DR: Evidence is found to suggest that cAMP signalling may be partially involved in regulating the anti-inflammatory response of SSRIs, which could suggest that antidepressants may owe at least some of their therapeutic effectiveness to their anti- inflammatory properties.
Journal ArticleDOI
Evidence of genetic overlap and causal relationships between blood-based biochemical traits and human cortical anatomy
TL;DR: In this article , the authors explored shared genetic architecture and evidence for causal relationships between a panel of 50 biochemical traits and measures of cortical thickness and surface area, and found strong evidence suggesting CRP and vitamin D exert causal effects on region-specific cortical thickness, with univariable and multivariable Mendelian randomization further supporting a negative causal relationship between serum CRP levels and thickness of the lingual region.
Journal ArticleDOI
RNA modulators of complex phenotypes in mammalian cells
TL;DR: The construction and application of a random small RNA expression library is reported on, which identifies a range of small RNA-encoding gene inserts that overcome resistance to 5-fluorouracil or tumour necrosis factor alpha- induced cell death in colorectal cancer cells.
Book ChapterDOI
Nucleic acid sequence analysis using DNAzymes.
Murray J. Cairns,Lun-Quan Sun +1 more
TL;DR: The sequence specificity of the "10-23" RNA-cleaving DNA enzyme can be utilized to discriminate between subtle differences in nucleic acid sequence to examine the HPV status of genomic DNA derived from Caski cells, which are known to be positive for HPV16.
Journal ArticleDOI
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations
Dongjing Liu,Dara Meyer,Brian Kenneth Fennessy,Claudia Feng,Esther Cheng,Jessica S. Johnson,Youngbin Park,Marysia-Kolbe Rieder,S. Ascolillo,A. de Pins,Amanda Dobbyn,Dannielle Lebovitch,Emily Moya,Tan Hoang Nguyen,Lillian Wilkins,Arsalan Hassan,Henry S. Aghanwa,M. Ansari,Aftab Asif,Rubina Aslam,J. L. Ayuso,Tim B. Bigdeli,Stefano Bignotti,Julio Bobes,Bekh Bradley,Peter F. Buckley,Murray J. Cairns,Stanley V. Catts,Abdul Rashid Chaudhry,David Cohen,Brett Collins,Angèle Consoli,Javier Costas,Benedicto Crespo-Facorro,Nikolaos P. Daskalakis,Michael H. Davidson,Kenneth L. Davis,Faith Dickerson,Imtiaz Ahmad Dogar,Elodie Drapeau,Lourdes Fañanás,Ayman H. Fanous,Warda Fatima,M Fatjo,C. Filippich,Joseph H. Friedman,John F. Fullard,Penelope Georgakopoulos,Marianna Giannitelli,Ina Giegling,Melissa J. Green,Olivier Guillin,Blanca Gutiérrez,Herlina Y. Handoko,Stella Kim Hansen,Maryam Haroon,Vahram Haroutunian,Frans Henskens,Fahad Abdulwahed Hussain,Assen Jablensky,Jamil Junejo,Brian Kelly,Shams ud Din Elias Khan,Muhammad Nasar Sayeed Khan,Anisuzzaman Khan,Hamid R. Khawaja,Bakht Khizar,Steven P. Kleopoulos,James Knowles,Bettina Konte,Agung A.A.A Kusumawardhani,Naeem Leghari,Xudong Liu,Adriana Lori,Carmel M. Loughland,Khalid Mahmood,Saqib Mahmood,Dolores Malaspina,Danish Malik,Amy J. M. McNaughton,Patricia T. Michie,Vasiliki Michopolous,Esther Molina,María Dolores Moltó,Asim Munir,Gerard Muntané,Farooq Naeem,Derek J. Nancarrow,Amina Nasar,Tanvir Nasr,Jude U. Ohaeri,Jurg Ott,Christos Pantelis,Sathish Periyasamy,Ana G. Pinto,Abigail Powers,Belén Ramos,Nusrat Rana,M Rapaport,Abraham Reichenberg,Safaa Saker-Delye,Ulrich Schall,Peter R. Schofield,Rodney J. Scott,Megan Shanahan,Cynthia Shannon Weickert,Calvin Sjaarda,Heather Smith,Jose Javier Suárez-Rama,Muhammad Assad Tariq,Florence Thibaut,Paul A. Tooney,Muhammad Umar,Elisabeth Vilella,Mark Weiser,Jinxian Wu,R.T Yolken,Katherine E. Burdick,Joseph D. Buxbaum,Enrico Domenici,Sophia Frangou,T. Hartmann,Claudine Laurent-Levinson,Dheeraj Malhotra,Carlos N. Pato,Michele T. Pato,Kerry J. Ressler,Panos Roussos,Dan Rujescu,Celso Arango,Alessandro Bertolini,Giuseppe Blasi,Luisella Bocchio-Chiavetto,Dominique Campion,Vaughan J. Carr,Janice M. Fullerton,Massimo Gennarelli,Javier González-Peñas,Douglas F. Levinson,Bryan J. Mowry,Vishwajit L. Nimgaokar,Giulio Pergola,Antonio Rampino,Jorge A. Cervilla,Margarita Rivera,Sibylle G. Schwab,Dieter B. Wildenauer,Mark J. Daly,Benjamin M. Neale,Tarjinder Singh,Michael Conlon O'Donovan,Michael John Owen,James T.R. Walters,Muhammad Ayub,Anil K. Malhotra,Todd Lencz,Patrick F. Sullivan,Pamela Sklar,Eli A. Stahl,Laura M. Huckins,Alexander W. Charney +160 more
TL;DR: In this article , the authors designed a custom sequencing panel of 161 genes selected based on the current knowledge of SCZ genetics and sequenced a new cohort of 11,580 SCZ cases and 10,555 controls of diverse ancestries.