A Meta-Analysis of Alzheimer’s Disease Brain Transcriptomic Data

Bằng Patel, Hamel, Dobson, Richard J.B., Newhouse, Stephen J.
Xuất bản năm J Alzheimers Dis (2019)

Working Towards a Blood-Derived Gene Expression Biomarker Specific for Alzheimer’s Disease

Bằng Patel, Hamel, Iniesta, Raquel, Stahl, Daniel, Dobson, Richard J.B., Newhouse, Stephen J.
Xuất bản năm J Alzheimers Dis (2020)

The effects of genotype on inflammatory response in hippocampal progenitor cells: A computational approach

Bằng Lee, Hyunah, Metz, Amelie, McDiarmid, Amina, Palmos, Alish, Lee, Sang H., Curtis, Charles J., Patel, Hamel, Newhouse, Stephen J., Thuret, Sandrine
Xuất bản năm Brain Behav Immun Health (2021)

Genome-Wide Association of Heroin Dependence in Han Chinese

Bằng Kalsi, Gursharan, Euesden, Jack, Coleman, Jonathan R. I., Ducci, Francesca, Aliev, Fazil, Newhouse, Stephen J., Liu, Xiehe, Ma, Xiaohong, Wang, Yingcheng, Collier, David A., Asherson, Philip, Li, Tao, Breen, Gerome
Xuất bản năm PLoS One (2016)

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA sequencing data of ALS patients

Bằng Iacoangeli, Alfredo, Al Khleifat, Ahmad, Sproviero, William, Shatunov, Aleksey, Jones, Ashley R., Opie-Martin, Sarah, Naselli, Ersilia, Topp, Simon D., Fogh, Isabella, Hodges, Angela, Dobson, Richard J., Newhouse, Stephen J., Al-Chalabi, Ammar
Xuất bản năm Amyotroph Lateral Scler Frontotemporal Degener (2019)

Loss of Trem2 in microglia leads to widespread disruption of cell coexpression networks in mouse brain

Bằng Carbajosa, Guillermo, Malki, Karim, Lawless, Nathan, Wang, Hong, Ryder, John W., Wozniak, Eva, Wood, Kristie, Mein, Charles A., Dobson, Richard J.B., Collier, David A., O'Neill, Michael J., Hodges, Angela K., Newhouse, Stephen J.
Xuất bản năm Neurobiol Aging (2018)

C9orf72 intermediate expansions of 24–30 repeats are associated with ALS

Bằng Iacoangeli, Alfredo, Al Khleifat, Ahmad, Jones, Ashley R., Sproviero, William, Shatunov, Aleksey, Opie-Martin, Sarah, Morrison, Karen E., Shaw, Pamela J., Shaw, Christopher E., Fogh, Isabella, Dobson, Richard J., Newhouse, Stephen J., Al-Chalabi, Ammar
Xuất bản năm Acta Neuropathol Commun (2019)

Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer

Bằng Traylor, Matthew, Walker, Jemma L., Corrigan, Adele A., Hernandez, Monica A., Newhouse, Stephen J., Folarin, Amos A., Patel, Hamel, Ross, Paul J., Sanderson, Jeremy D., Spicer, James, Prescott, Natalie J., Mathew, Christopher G., Marinaki, Anthony M., Lewis, Cathryn M.
Xuất bản năm PLoS One (2018)

Applying polygenic risk scoring for psychiatric disorders to a large family with bipolar disorder and major depressive disorder

Bằng de Jong, Simone, Diniz, Mateus Jose Abdalla, Saloma, Andiara, Gadelha, Ary, Santoro, Marcos L., Ota, Vanessa K., Noto, Cristiano, Curtis, Charles, Newhouse, Stephen J., Patel, Hamel, Hall, Lynsey S., O`Reilly, Paul F., Belangero, Sintia I., Bressan, Rodrigo A., Breen, Gerome
Xuất bản năm Commun Biol (2018)

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

Bằng Addis, Laura, Sproviero, William, Thomas, Sanjeev V, Caraballo, Roberto H, Newhouse, Stephen J, Gomez, Kumudini, Hughes, Elaine, Kinali, Maria, McCormick, David, Hannan, Siobhan, Cossu, Silvia, Taylor, Jacqueline, Akman, Cigdem I, Wolf, Steven M, Mandelbaum, David E, Gupta, Rajesh, van der Spek, Rick A, Pruna, Dario, Pal, Deb K
Xuất bản năm J Med Genet (2018)

Differential gene expression analysis in blood of first episode psychosis patients

Bằng Leirer, Daniel J., Iyegbe, Conrad O., Di Forti, Marta, Patel, Hamel, Carra, Elena, Fraietta, Sara, Colizzi, Marco, Mondelli, Valeria, Quattrone, Diego, Lally, John, Ajnakina, Olesya, Lee, Sang Hyuck, Curtis, Charles J., Breen, Gerome, Pariante, Carmine, Aitchison, Katherine, Dazzan, Paola, Murray, Robin M., Dobson, Richard J.B., Newhouse, Stephen J.
Xuất bản năm Schizophr Res (2019)

Linkage Analysis Using Co-Phenotypes in the BRIGHT Study Reveals Novel Potential Susceptibility Loci for Hypertension

Bằng Wallace, Chris, Xue, Ming-Zhan, Newhouse, Stephen J., Marçano, Ana Carolina B., Onipinla, Abiodun K., Burke, Beverley, Gungadoo, Johannie, Dobson, Richard J., Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Mein, Charles, Samani, Nilesh J., Caulfield, Mark J., Clayton, David G., Munroe, Patricia B.
Được phát hành 2006

Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia

Bằng Wallace, Chris, Newhouse, Stephen J., Braund, Peter, Zhang, Feng, Tobin, Martin, Falchi, Mario, Ahmadi, Kourosh, Dobson, Richard J., Marçano, Ana Carolina B., Hajat, Cother, Burton, Paul, Deloukas, Panagiotis, Brown, Morris, Connell, John M., Dominiczak, Anna, Lathrop, G. Mark, Webster, John, Farrall, Martin, Spector, Tim, Samani, Nilesh J., Caulfield, Mark J., Munroe, Patricia B.
Được phát hành 2008

Immune signatures and disorder-specific patterns in a cross-disorder gene expression analysis

Bằng de Jong, Simone, Newhouse, Stephen J., Patel, Hamel, Lee, Sanghyuck, Dempster, David, Curtis, Charles, Paya-Cano, Jose, Murphy, Declan, Wilson, C. Ellie, Horder, Jamie, Mendez, M. Andreina, Asherson, Philip, Rivera, Margarita, Costello, Helen, Maltezos, Stefanos, Whitwell, Susannah, Pitts, Mark, Tye, Charlotte, Ashwood, Karen L., Bolton, Patrick, Curran, Sarah, McGuffin, Peter, Dobson, Richard, Breen, Gerome
Xuất bản năm Br J Psychiatry (2016)

An epigenome-wide association study of Alzheimer's disease blood highlights robust DNA hypermethylation in the HOXB6 gene

Bằng Roubroeks, Janou A.Y., Smith, Adam R., Smith, Rebecca G., Pishva, Ehsan, Ibrahim, Zina, Sattlecker, Martina, Hannon, Eilis J., Kłoszewska, Iwona, Mecocci, Patrizia, Soininen, Hilkka, Tsolaki, Magda, Vellas, Bruno, Wahlund, Lars-Olof, Aarsland, Dag, Proitsi, Petroula, Hodges, Angela, Lovestone, Simon, Newhouse, Stephen J., Dobson, Richard J.B., Mill, Jonathan, van den Hove, Daniël L.A., Lunnon, Katie
Xuất bản năm Neurobiol Aging (2020)

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

Bằng Org, Elin, Eyheramendy, Susana, Juhanson, Peeter, Gieger, Christian, Lichtner, Peter, Klopp, Norman, Veldre, Gudrun, Döring, Angela, Viigimaa, Margus, Sõber, Siim, Tomberg, Kärt, Eckstein, Gertrud, Kelgo, Piret, Rebane, Tiina, Shaw-Hawkins, Sue, Howard, Philip, Onipinla, Abiodun, Dobson, Richard J., Newhouse, Stephen J., Brown, Morris, Dominiczak, Anna, Connell, John, Samani, Nilesh, Farrall, Martin, Caulfield, Mark J., Munroe, Patricia B., Illig, Thomas, Wichmann, H.-Erich, Meitinger, Thomas, Laan, Maris
Được phát hành 2009

Targeting 160 Candidate Genes for Blood Pressure Regulation with a Genome-Wide Genotyping Array

Bằng Sõber, Siim, Org, Elin, Kepp, Katrin, Juhanson, Peeter, Eyheramendy, Susana, Gieger, Christian, Lichtner, Peter, Klopp, Norman, Veldre, Gudrun, Viigimaa, Margus, Döring, Angela, Putku, Margus, Kelgo, Piret, Shaw-Hawkins, Sue, Howard, Philip, Onipinla, Abiodun, Dobson, Richard J., Newhouse, Stephen J., Brown, Morris, Dominiczak, Anna, Connell, John, Samani, Nilesh, Farrall, Martin, Caulfield, Mark J., Munroe, Patricia B., Illig, Thomas, Wichmann, H.-Erich, Meitinger, Thomas, Laan, Maris
Được phát hành 2009

Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics

Bằng Iacoangeli, Alfredo, Lin, Tian, Al Khleifat, Ahmad, Jones, Ashley R., Opie-Martin, Sarah, Coleman, Jonathan R.I., Shatunov, Aleksey, Sproviero, William, Williams, Kelly L., Garton, Fleur, Restuadi, Restuadi, Henders, Anjali K., Mather, Karen A., Needham, Merilee, Mathers, Susan, Nicholson, Garth A., Rowe, Dominic B., Henderson, Robert, McCombe, Pamela A., Pamphlett, Roger, Blair, Ian P., Schultz, David, Sachdev, Perminder S., Newhouse, Stephen J., Proitsi, Petroula, Fogh, Isabella, Ngo, Shyuan T., Dobson, Richard J.B., Wray, Naomi R., Steyn, Frederik J., Al-Chalabi, Ammar
Xuất bản năm Cell Rep (2020)

SLC2A9 Is a High-Capacity Urate Transporter in Humans

Bằng Caulfield, Mark J, Munroe, Patricia B, O'Neill, Deb, Witkowska, Kate, Charchar, Fadi J, Doblado, Manuel, Evans, Sarah, Eyheramendy, Susana, Onipinla, Abiodun, Howard, Philip, Shaw-Hawkins, Sue, Dobson, Richard J, Wallace, Chris, Newhouse, Stephen J, Brown, Morris, Connell, John M, Dominiczak, Anna, Farrall, Martin, Lathrop, G. Mark, Samani, Nilesh J, Kumari, Meena, Marmot, Michael, Brunner, Eric, Chambers, John, Elliott, Paul, Kooner, Jaspal, Laan, Maris, Org, Elin, Veldre, Gudrun, Viigimaa, Margus, Cappuccio, Francesco P, Ji, Chen, Iacone, Roberto, Strazzullo, Pasquale, Moley, Kelle H, Cheeseman, Chris
Được phát hành 2008

Common Genetic Variation Near the Phospholamban Gene Is Associated with Cardiac Repolarisation: Meta-Analysis of Three Genome-Wide Association Studies

Bằng Nolte, Ilja M., Wallace, Chris, Newhouse, Stephen J., Waggott, Daryl, Fu, Jingyuan, Soranzo, Nicole, Gwilliam, Rhian, Deloukas, Panos, Savelieva, Irina, Zheng, Dongling, Dalageorgou, Chrysoula, Farrall, Martin, Samani, Nilesh J., Connell, John, Brown, Morris, Dominiczak, Anna, Lathrop, Mark, Zeggini, Eleftheria, Wain, Louise V., Newton-Cheh, Christopher, Eijgelsheim, Mark, Rice, Kenneth, de Bakker, Paul I. W., Pfeufer, Arne, Sanna, Serena, Arking, Dan E., Asselbergs, Folkert W., Spector, Tim D., Carter, Nicholas D., Jeffery, Steve, Tobin, Martin, Caulfield, Mark, Snieder, Harold, Paterson, Andrew D., Munroe, Patricia B., Jamshidi, Yalda
Được phát hành 2009