Long-lasting transcription in hippocampal area CA1 after contextual fear conditioning

von Mizuno, Keiko, Jeffries, Aaron R., Abel, Ted, Giese, K. Peter
Veröffentlicht in Neurobiol Learn Mem (2020)

The role of omega-3 fatty acids in preventing glucocorticoid-induced reduction in human hippocampal neurogenesis and increase in apoptosis

von Borsini, Alessandra, Stangl, Doris, Jeffries, Aaron R., Pariante, Carmine M., Thuret, Sandrine
Veröffentlicht in Transl Psychiatry (2020)

Characterization of Six Bacteriophages of Serratia liquefaciens CP6 Isolated from the Sugar Beet Phytosphere

von Ashelford, Kevin E., Fry, John C., Bailey, Mark J., Jeffries, Aaron R., Day, Martin J.
Veröffentlicht 1999

Random or Stochastic Monoallelic Expressed Genes Are Enriched for Neurodevelopmental Disorder Candidate Genes

von Jeffries, Aaron R., Collier, David A., Vassos, Evangelos, Curran, Sarah, Ogilvie, Caroline M., Price, Jack
Veröffentlicht 2013

Whole transcriptome in silico screening implicates cardiovascular and infectious disease in the mechanism of action underlying atypical antipsychotic side effects

von Malekizadeh, Yasaman, Williams, Gareth, Kelson, Mark, Whitfield, David, Mill, Jonathan, Collier, David A., Ballard, Clive, Jeffries, Aaron R., Creese, Byron
Veröffentlicht in Alzheimers Dement (N Y) (2020)

Allelic Skewing of DNA Methylation Is Widespread across the Genome

von Schalkwyk, Leonard C., Meaburn, Emma L., Smith, Rebecca, Dempster, Emma L., Jeffries, Aaron R., Davies, Matthew N., Plomin, Robert, Mill, Jonathan
Veröffentlicht 2010

Attenuated Induction of the Unfolded Protein Response in Adult Human Primary Astrocytes in Response to Recurrent Low Glucose

von Weightman Potter, Paul G., Washer, Sam J., Jeffries, Aaron R., Holley, Janet E., Gutowski, Nick J., Dempster, Emma L., Beall, Craig
Veröffentlicht in Front Endocrinol (Lausanne) (2021)

Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons

von Cocks, Graham, Romanyuk, Nataliya, Amemori, Takashi, Jendelova, Pavla, Forostyak, Oksana, Jeffries, Aaron R, Perfect, Leo, Thuret, Sandrine, Dayanithi, Govindan, Sykova, Eva, Price, Jack
Veröffentlicht 2013

No Effect of Genome-Wide Significant Schizophrenia Risk Variation at the DRD2 Locus on the Allelic Expression of DRD2 in Postmortem Striatum

von Toste, Carolina C., Duarte, Rodrigo R.R., Jeffries, Aaron R., Selvackadunco, Sashika, Troakes, Claire, O'Donovan, Michael C., Hill, Matthew J., Bray, Nicholas J.
Veröffentlicht in Mol Neuropsychiatry (2019)

The utility of patient specific induced pluripotent stem cells for the modelling of Autistic Spectrum Disorders

von Cocks, Graham, Curran, Sarah, Gami, Priya, Uwanogho, Dafe, Jeffries, Aaron R., Kathuria, Annie, Lucchesi, Walter, Wood, Victoria, Dixon, Rosemary, Ogilvie, Caroline, Steckler, Thomas, Price, Jack
Veröffentlicht 2013

Effects of cis-regulatory variation differ across regions of the adult human brain

von Buonocore, Federica, Hill, Matthew J., Campbell, Colin D., Oladimeji, Paul B., Jeffries, Aaron R., Troakes, Claire, Hortobagyi, Tibor, Williams, Brenda P., Cooper, Jonathan D., Bray, Nicholas J.
Veröffentlicht 2010

Differential aging‐related changes in neurophysiology and gene expression in IB4‐positive and IB4‐negative nociceptive neurons

von Mis, Malgorzata A., Rogers, Mark F., Jeffries, Aaron R., Wilbrey, Anna L., Chen, Lubin, Yang, Yang, Dib‐Hajj, Sulayman, Waxman, Stephen G., Stevens, Edward B., Randall, Andrew D.
Veröffentlicht in Aging Cell (2018)

Tissue-biased expansion of DNMT3A-mutant clones in a mosaic individual is associated with conserved epigenetic erosion

von Tovy, Ayala, Reyes, Jaime M., Gundry, Michael C., Brunetti, Lorenzo, Lee-Six, Henry, Petljak, Mia, Park, Hyun Jung, Guzman, Anna G., Rosas, Carina, Jeffries, Aaron R, Baple, Emma, Mill, Jonathan, Crosby, Andrew H., Sency, Valerie, Xin, Baozhong, Machado, Heather E., Castillo, Danielle, Weitzel, Jeffrey N., Li, Wei, Stratton, Michael R., Campbell, Peter J., Wang, Heng, Sanders, Mathijs A., Goodell, Margaret A.
Veröffentlicht in Cell Stem Cell (2020)

Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging

von Jeffries, Aaron R., Maroofian, Reza, Salter, Claire G., Chioza, Barry A., Cross, Harold E., Patton, Michael A., Dempster, Emma, Temple, I. Karen, Mackay, Deborah J.G., Rezwan, Faisal I., Aksglaede, Lise, Baralle, Diana, Dabir, Tabib, Hunter, Matthew F., Kamath, Arveen, Kumar, Ajith, Newbury-Ecob, Ruth, Selicorni, Angelo, Springer, Amanda, Van Maldergem, Lionel, Varghese, Vinod, Yachelevich, Naomi, Tatton-Brown, Katrina, Mill, Jonathan, Crosby, Andrew H., Baple, Emma L.
Veröffentlicht in Genome Res (2019)

Novel epigenetic clock for fetal brain development predicts prenatal age for cellular stem cell models and derived neurons

von Steg, Leonard C., Shireby, Gemma L., Imm, Jennifer, Davies, Jonathan P., Franklin, Alice, Flynn, Robert, Namboori, Seema C., Bhinge, Akshay, Jeffries, Aaron R., Burrage, Joe, Neilson, Grant W. A., Walker, Emma M., Perfect, Leo W., Price, Jack, McAlonan, Grainne, Srivastava, Deepak P., Bray, Nicholas J., Cope, Emma L., Jones, Kimberley M., Allen, Nicholas D., Pishva, Ehsan, Dempster, Emma L., Lunnon, Katie, Mill, Jonathan, Hannon, Eilis
Veröffentlicht in Mol Brain (2021)

Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration

von Muto, Valentina, Flex, Elisabetta, Kupchinsky, Zachary, Primiano, Guido, Galehdari, Hamid, Dehghani, Mohammadreza, Cecchetti, Serena, Carpentieri, Giovanna, Rizza, Teresa, Mazaheri, Neda, Sedaghat, Alireza, Vahidi Mehrjardi, Mohammad Yahya, Traversa, Alice, Di Nottia, Michela, Kousi, Maria M., Jamshidi, Yalda, Ciolfi, Andrea, Caputo, Viviana, Malamiri, Reza Azizi, Pantaleoni, Francesca, Martinelli, Simone, Jeffries, Aaron R., Zeighami, Jawaher, Sherafat, Amir, Di Giuda, Daniela, Shariati, Gholam Reza, Carrozzo, Rosalba, Katsanis, Nicholas, Maroofian, Reza, Servidei, Serenella, Tartaglia, Marco
Veröffentlicht in Neurology (2018)

Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms

von Jones, Samuel E., Lane, Jacqueline M., Wood, Andrew R., van Hees, Vincent T., Tyrrell, Jessica, Beaumont, Robin N., Jeffries, Aaron R., Dashti, Hassan S., Hillsdon, Melvyn, Ruth, Katherine S., Tuke, Marcus A., Yaghootkar, Hanieh, Sharp, Seth A., Jie, Yingjie, Thompson, William D., Harrison, Jamie W., Dawes, Amy, Byrne, Enda M., Tiemeier, Henning, Allebrandt, Karla V., Bowden, Jack, Ray, David W., Freathy, Rachel M., Murray, Anna, Mazzotti, Diego R., Gehrman, Philip R., Lawlor, Debbie A., Frayling, Timothy M., Rutter, Martin K., Hinds, David A., Saxena, Richa, Weedon, Michael N.
Veröffentlicht in Nat Commun (2019)