Transcription factor and chromatin features predict genes associated with eQTLs

por Wang, Dennis, Rendon, Augusto, Wernisch, Lorenz
Publicado 2013

Treatment planning using tailored and standard cylindrical light diffusers for Photodynamic therapy of the prostate

por Rendon, Augusto, Beck, J. Christopher, Lilge, Lothar
Publicado 2008

Transcription factor co-localization patterns affect human cell type-specific gene expression

por Wang, Dennis, Rendon, Augusto, Ouwehand, Willem, Wernisch, Lorenz
Publicado 2012

Comparison of Methods for Competitive Tests of Pathway Analysis

por Evangelou, Marina, Rendon, Augusto, Ouwehand, Willem H., Wernisch, Lorenz, Dudbridge, Frank
Publicado 2012

PyCellBase, an efficient python package for easy retrieval of biological data from heterogeneous sources

por Perez-Gil, Daniel, Lopez, Francisco J., Dopazo, Joaquin, Marin-Garcia, Pablo, Rendon, Augusto, Medina, Ignacio
Publicado en BMC Bioinformatics (2019)

Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci

por Paul, Dirk S., Albers, Cornelis A., Rendon, Augusto, Voss, Katrin, Stephens, Jonathan, van der Harst, Pim, Chambers, John C., Soranzo, Nicole, Ouwehand, Willem H., Deloukas, Panos
Publicado 2013

HGVA: the Human Genome Variation Archive

por Lopez, Javier, Coll, Jacobo, Haimel, Matthias, Kandasamy, Swaathi, Tarraga, Joaquin, Furio-Tari, Pedro, Bari, Wasim, Bleda, Marta, Rueda, Antonio, Gräf, Stefan, Rendon, Augusto, Dopazo, Joaquin, Medina, Ignacio
Publicado en Nucleic Acids Res (2017)

A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site

por Nürnberg, Sylvia T., Rendon, Augusto, Smethurst, Peter A., Paul, Dirk S., Voss, Katrin, Thon, Jonathan N., Lloyd-Jones, Heather, Sambrook, Jennifer G., Tijssen, Marloes R., Italiano, Joseph E., Deloukas, Panos, Gottgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H.
Publicado 2012

Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits

por Paul, Dirk S., Nisbet, James P., Yang, Tsun-Po, Meacham, Stuart, Rendon, Augusto, Hautaviita, Katta, Tallila, Jonna, White, Jacqui, Tijssen, Marloes R., Sivapalaratnam, Suthesh, Basart, Hanneke, Trip, Mieke D., Göttgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H., Deloukas, Panos
Publicado 2011

Correction: Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits

por Paul, Dirk S., Nisbet, James P., Yang, Tsun-Po, Meacham, Stuart, Rendon, Augusto, Hautaviita, Katta, Tallila, Jonna, White, Jacqui, Tijssen, Marloes R., Sivapalaratnam, Suthesh, Basart, Hanneke, Trip, Mieke D., Göttgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H., Deloukas, Panos
Publicado 2011

Monocyte Gene Expression Signature of Patients with Early Onset Coronary Artery Disease

por Sivapalaratnam, Suthesh, Basart, Hanneke, Watkins, Nicholas A., Maiwald, Stepanie, Rendon, Augusto, Krishnan, Unni, Sondermeijer, Brigitte M., Creemers, Esther E., Pinto-Sietsma, Sara J., Hovingh, Kees, Ouwehand, Willem H., Kastelein, John J. P., Goodall, Alison H., Trip, Mieke D.
Publicado 2012

Canonical Wnt signaling in megakaryocytes regulates proplatelet formation

por Macaulay, Iain C., Thon, Jonathan N., Tijssen, Marloes R., Steele, Brian M., MacDonald, Bryan T., Meade, Gerardene, Burns, Philippa, Rendon, Augusto, Salunkhe, Vishal, Murphy, Ronan P., Bennett, Cavan, Watkins, Nicholas A., He, Xi, Fitzgerald, Desmond J., Italiano, Joseph E., Maguire, Patricia B.
Publicado 2013

Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome

por Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H
Publicado 2011

A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function

por Soranzo, Nicole, Rendon, Augusto, Gieger, Christian, Jones, Chris I., Watkins, Nicholas A., Menzel, Stephan, Döring, Angela, Stephens, Jonathan, Prokisch, Holger, Erber, Wendy, Potter, Simon C., Bray, Sarah L., Burns, Philippa, Jolley, Jennifer, Falchi, Mario, Kühnel, Brigitte, Erdmann, Jeanette, Schunkert, Heribert, Samani, Nilesh J., Illig, Thomas, Garner, Stephen F., Rankin, Angela, Meisinger, Christa, Bradley, John R., Thein, Swee Lay, Goodall, Alison H., Spector, Tim D., Deloukas, Panos, Ouwehand, Willem H.
Publicado 2009

Integrating Genome-Wide Genetic Variations and Monocyte Expression Data Reveals Trans-Regulated Gene Modules in Humans

por Rotival, Maxime, Zeller, Tanja, Wild, Philipp S., Maouche, Seraya, Szymczak, Silke, Schillert, Arne, Castagné, Raphaele, Deiseroth, Arne, Proust, Carole, Brocheton, Jessy, Godefroy, Tiphaine, Perret, Claire, Germain, Marine, Eleftheriadis, Medea, Sinning, Christoph R., Schnabel, Renate B., Lubos, Edith, Lackner, Karl J., Rossmann, Heidi, Münzel, Thomas, Rendon, Augusto, Consortium, Cardiogenics, Erdmann, Jeanette, Deloukas, Panos, Hengstenberg, Christian, Diemert, Patrick, Montalescot, Gilles, Ouwehand, Willem H., Samani, Nilesh J., Schunkert, Heribert, Tregouet, David-Alexandre, Ziegler, Andreas, Goodall, Alison H., Cambien, François, Tiret, Laurence, Blankenberg, Stefan
Publicado 2011

A HaemAtlas: characterizing gene expression in differentiated human blood cells

por Watkins, Nicholas A., Gusnanto, Arief, de Bono, Bernard, De, Subhajyoti, Miranda-Saavedra, Diego, Hardie, Debbie L., Angenent, Will G. J., Attwood, Antony P., Ellis, Peter D., Erber, Wendy, Foad, Nicola S., Garner, Stephen F., Isacke, Clare M., Jolley, Jennifer, Koch, Kerstin, Macaulay, Iain C., Morley, Sarah L., Rendon, Augusto, Rice, Kate M., Taylor, Niall, Thijssen-Timmer, Daphne C., Tijssen, Marloes R., van der Schoot, C. Ellen, Wernisch, Lorenz, Winzer, Thilo, Dudbridge, Frank, Buckley, Christopher D., Langford, Cordelia F., Teichmann, Sarah, Göttgens, Berthold, Ouwehand, Willem H.
Publicado 2009

Human phenotype ontology annotation and cluster analysis to unravel genetic defects in 707 cases with unexplained bleeding and platelet disorders

por Westbury, Sarah K, Turro, Ernest, Greene, Daniel, Lentaigne, Claire, Kelly, Anne M, Bariana, Tadbir K, Simeoni, Ilenia, Pillois, Xavier, Attwood, Antony, Austin, Steve, Jansen, Sjoert BG, Bakchoul, Tamam, Crisp-Hihn, Abi, Erber, Wendy N, Favier, Rémi, Foad, Nicola, Gattens, Michael, Jolley, Jennifer D, Liesner, Ri, Meacham, Stuart, Millar, Carolyn M, Nurden, Alan T, Peerlinck, Kathelijne, Perry, David J, Poudel, Pawan, Schulman, Sol, Schulze, Harald, Stephens, Jonathan C, Furie, Bruce, Robinson, Peter N, van Geet, Chris, Rendon, Augusto, Gomez, Keith, Laffan, Michael A, Lambert, Michele P, Nurden, Paquita, Ouwehand, Willem H, Richardson, Sylvia, Mumford, Andrew D, Freson, Kathleen
Publicado en Genome Med (2015)

A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations

por Palmer, Elizabeth E., Kumar, Raman, Gordon, Christopher T., Shaw, Marie, Hubert, Laurence, Carroll, Renee, Rio, Marlène, Murray, Lucinda, Leffler, Melanie, Dudding-Byth, Tracy, Oufadem, Myriam, Lalani, Seema R., Lewis, Andrea M., Xia, Fan, Tam, Allison, Webster, Richard, Brammah, Susan, Filippini, Francesca, Pollard, John, Spies, Judy, Minoche, Andre E., Cowley, Mark J., Risen, Sarah, Powell-Hamilton, Nina N., Tusi, Jessica E., Immken, LaDonna, Nagakura, Honey, Bole-Feysot, Christine, Nitschké, Patrick, Garrigue, Alexandrine, de Saint Basile, Geneviève, Kivuva, Emma, Scott, Richard H., Rendon, Augusto, Munnich, Arnold, Newman, William, Kerr, Bronwyn, Besmond, Claude, Rosenfeld, Jill A., Amiel, Jeanne, Field, Michael, Gecz, Jozef
Publicado en Am J Hum Genet (2017)

Development and validation of a universal blood donor genotyping platform: a multinational prospective study

por Gleadall, Nicholas S., Veldhuisen, Barbera, Gollub, Jeremy, Butterworth, Adam S., Ord, John, Penkett, Christopher J., Timmer, Tiffany C., Sauer, Carolin M., van der Bolt, Nieke, Brown, Colin, Brugger, Kim, Dilthey, Alexander T., Duarte, Daniel, Grimsley, Shane, van den Hurk, Katja, Jongerius, John M., Luken, Jessie, Megy, Karyn, Miflin, Gail, Nelson, Christopher S., Prinsze, Femmeke J., Sambrook, Jennifer, Simeoni, Ilenia, Sweeting, Michael, Thornton, Nicole, Trompeter, Sara, Tuna, Salih, Varma, Ram, Walker, Matthew R., Danesh, John, Roberts, David J., Ouwehand, Willem H., Stirrups, Kathleen E., Rendon, Augusto, Westhoff, Connie M., Di Angelantonio, Emanuele, van der Schoot, C. Ellen, Astle, William J., Watkins, Nicholas A., Lane, William J.
Publicado en Blood Adv (2020)

SMIM1 underlies the Vel blood group and influences red blood cell traits

por Cvejic, Ana, Haer-Wigman, Lonneke, Stephens, Jonathan C, Kostadima, Myrto, Smethurst, Peter A, Frontini, Mattia, van den Akker, Emile, Bertone, Paul, Bielczyk-Maczyńska, Ewa, Farrow, Samantha, Fehrmann, Rudolf SN, Gray, Alan, de Haas, Masja, Haver, Vincent G, Jordan, Gregory, Karjalainen, Juha, Kerstens, Hindrik HD, Kiddle, Graham, Lloyd-Jones, Heather, Needs, Malcolm, Poole, Joyce, Soussan, Aicha Ait, Rendon, Augusto, Rieneck, Klaus, Sambrook, Jennifer G, Schepers, Hein, Silljé, Herman H W, Sipos, Botond, Swinkels, Dorine, Tamuri, Asif U, Verweij, Niek, Watkins, Nicholas A, Westra, Harm-Jan, Stemple, Derek, Franke, Lude, Soranzo, Nicole, Stunnenberg, Hendrik G, Goldman, Nick, van der Harst, Pim, van der Schoot, C Ellen, Ouwehand, Willem H, Albers, Cornelis A
Publicado 2013