α1-A680T Variant in GUCY1A3 as a Candidate Conferring Protection From Pulmonary Hypertension Among Kyrgyz Highlanders von Wilkins, Martin R, Aldashev, Almaz A, Wharton, John, Rhodes, Christopher J, Vandrovcova, Jana, Kasperaviciute, Dalia, Bhosle, Shriram G, Mueller, Michael, Geschka, Sandra, Rison, Stuart, Kojonazarov, Baktybek, Morrell, Nicholas W, Neidhardt, Inga, Surmeli, Nur Basek, Aitman, Tim J, Stasch, Johannes-Peter, Behrends, Soenke, Marletta, Michael A

Volltext

Association of variation in Fcγ receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples von McKinney, Cushla, Fanciulli, Manuela, Merriman, Marilyn E, Phipps-Green, Amanda, Alizadeh, Behrooz Z, Koeleman, Bobby P C, Dalbeth, Nicola, Gow, Peter J, Harrison, Andrew A, Highton, John, Jones, Peter B, Stamp, Lisa K, Steer, Sophia, Barrera, Pilar, Coenen, Marieke J H, Franke, Barbara, van Riel, Piet L C M, Vyse, Tim J, Aitman, Tim J, Radstake, Timothy R D J, Merriman, Tony R

Volltext

FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans von Molokhia, Mariam, Fanciulli, Manuela, Petretto, Enrico, Patrick, Alan Leslie, McKeigue, Paul, Roberts, Amy L., Vyse, Tim J., Aitman, Tim J.

Volltext

Ancient DNA at the edge of the world: Continental immigration and the persistence of Neolithic male lineages in Bronze Age Orkney von Dulias, Katharina, Foody, M George B, Justeau, Pierre, Silva, Marina, Martiniano, Rui, Oteo-García, Gonzalo, Fichera, Alessandro, Rodrigues, Simão, Gandini, Francesca, Meynert, Alison, Donnelly, Kevin, Aitman, Timothy J, Chamberlain, Andrew, Lelong, Olivia, Kozikowski, George, Powlesland, Dominic, Waddington, Clive, Mattiangeli, Valeria, Bradley, Daniel G, Bryk, Jaroslaw, Soares, Pedro, Wilson, James F, Wilson, Graeme, Moore, Hazel, Pala, Maria, Edwards, Ceiridwen J, Richards, Martin B

Volltext

Genetic basis of transcriptome differences between the founder strains of the rat HXB/BXH recombinant inbred panel von Simonis, Marieke, Atanur, Santosh S, Linsen, Sam, Guryev, Victor, Ruzius, Frans-Paul, Game, Laurence, Lansu, Nico, de Bruijn, Ewart, van Heesch, Sebastiaan, Jones, Steven JM, Pravenec, Michal, Aitman, Tim J, Cuppen, Edwin

Volltext

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats von Baud, Amelie, Hermsen, Roel, Guryev, Victor, Stridh, Pernilla, Graham, Delyth, McBride, Martin W, Foroud, Tatiana, Calderari, Sophie, Diez, Margarita, Ockinger, Johan, Beyeen, Amennai D, Gillett, Alan, Abdelmagid, Nada, Guerreiro-Cacais, Andre Ortlieb, Jagodic, Maja, Tuncel, Jonatan, Norin, Ulrika, Beattie, Elisabeth, Huynh, Ngan, Miller, William H, Koller, Daniel L, Alam, Imranul, Falak, Samreen, Osborne-Pellegrin, Mary, Martinez-Membrives, Esther, Canete, Toni, Blazquez, Gloria, Vicens-Costa, Elia, Mont-Cardona, Carme, Diaz-Moran, Sira, Tobena, Adolf, Hummel, Oliver, Zelenika, Diana, Saar, Kathrin, Patone, Giannino, Bauerfeind, Anja, Bihoreau, Marie-Therese, Heinig, Matthias, Lee, Young-Ae, Rintisch, Carola, Schulz, Herbert, Wheeler, David A, Worley, Kim C, Muzny, Donna M, Gibbs, Richard A, Lathrop, Mark, Lansu, Nico, Toonen, Pim, Ruzius, Frans Paul, de Bruijn, Ewart, Hauser, Heidi, Adams, David J, Keane, Thomas, Atanur, Santosh S, Aitman, Tim J, Flicek, Paul, Malinauskas, Tomas, Jones, E Yvonne, Ekman, Diana, Lopez-Aumatell, Regina, Dominiczak, Anna F, Johannesson, Martina, Holmdahl, Rikard, Olsson, Tomas, Gauguier, Dominique, Hubner, Norbert, Fernandez-Teruel, Alberto, Cuppen, Edwin, Mott, Richard, Flint, Jonathan

Volltext

FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans von Molokhia, Mariam, Fanciulli, Manuela, Petretto, Enrico, Patrick, Alan Leslie, McKeigue, Paul, Roberts, Amy L, Vyse, Tim J, Aitman, Tim J

Volltext

Genomes and phenomes of a population of outbred rats and its progenitors von Baud, Amelie, Guryev, Victor, Hummel, Oliver, Johannesson, Martina, Flint, Jonathan

Volltext

Association of variation in Fc  receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples von McKinney, C., Fanciulli, M., Merriman, M. E., Phipps-Green, A., Alizadeh, B. Z., Koeleman, B. P. C., Dalbeth, N., Gow, P. J., Harrison, A. A., Highton, J., Jones, P. B., Stamp, L. K., Steer, S., Barrera, P., Coenen, M. J. H., Franke, B., van Riel, P. L. C. M., Vyse, T. J., Aitman, T. J., Radstake, T. R. D. J., Merriman, T. R.

Volltext

Association of variation in Fcg receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples von McKinney, Cushla, Fanciulli, Manuela, Merriman, Marilyn E, Phipps-Green, Amanda, Alizadeh, Behrooz Z, Koeleman, Bobby P C, Dalbeth, Nicola, Gow, Peter J, Harrison, Andrew A, Highton, John, Jones, Peter B, Stamp, Lisa K, Steer, Sophia, Barrera, Pilar, Coenen, Marieke J H, Franke, Barbara, van Riel, Piet L C M, Vyse, Tim J, Aitman, Tim J, Radstake, Timothy R D J, Merriman, Tony R

Volltext

Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples von McKinney, Cushla, Fanciulli, Manuela, Merriman, Marilyn E, Phipps-Green, Amanda, Alizadeh, Behrooz Z, Koeleman, Bobby P C, Dalbeth, Nicola, Gow, Peter J, Harrison, Andrew A, Highton, John, Jones, Peter B, Stamp, Lisa K, Steer, Sophia, Barrera, Pilar, Coenen, Marieke J H, Franke, Barbara, van Riel, Piet L C M, Vyse, Tim J, Aitman, Tim J, Radstake, Timothy R D J, Merriman, Tony R

Volltext

Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta von Weerakkody, Ruwan, Ross, David, Parry, David A, Ziganshin, Bulat, Vandrovcova, Jana, Gampawar, Piyush, Abdullah, Abdulshakur, Biggs, Jennifer, Dumfarth, Julia, Ibrahim, Yousef, Bicknell, Colin, Field, Mark, Elefteriades, John, Cheshire, Nick, Aitman, Timothy J

Volltext

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency von Logan, Clare V., Murray, Jennie E., Parry, David A., Robertson, Andrea, Bellelli, Roberto, Tarnauskaitė, Žygimantė, Challis, Rachel, Cleal, Louise, Borel, Valerie, Fluteau, Adeline, Santoyo-Lopez, Javier, Aitman, Timothy J., Biankin, Andrew V., Cooke, Susanna L., Humphrey, Wendy Inglis, Martin, Sancha, Mennie, Lynne, Meynert, Alison, Miedzybrodzka, Zosia, Murphy, Fiona, Nourse, Craig, Santoyo-Lopez, Javier, Semple, Colin A., Williams, Nicola, Aitman, Tim, Barroso, Inês, Basel, Donald, Bicknell, Louise S., Goel, Himanshu, Hu, Hao, Huff, Chad, Hutchison, Michele, Joyce, Caroline, Knox, Rachel, Lacroix, Amy E., Langlois, Sylvie, McCandless, Shawn, McCarrier, Julie, Metcalfe, Kay A., Morrissey, Rose, Murphy, Nuala, Netchine, Irène, O’Connell, Susan M., Olney, Ann Haskins, Paria, Nandina, Rosenfeld, Jill A., Sherlock, Mark, Syverson, Erin, White, Perrin C., Wise, Carol, Yu, Yao, Zacharin, Margaret, Banerjee, Indraneel, Reijns, Martin, Bober, Michael B., Semple, Robert K., Boulton, Simon J., Rios, Jonathan J., Jackson, Andrew P.

Volltext

Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions von Halachev, Mihail, Meynert, Alison, Taylor, Martin S, Vitart, Veronique, Kerr, Shona M, Klaric, Lucija, Aitman, Timothy J, Haley, Chris S, Prendergast, James G, Pugh, Carys, Hume, David A, Harris, Sarah E, Liewald, David C, Deary, Ian J, Semple, Colin A, Wilson, James F

Volltext

GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements von Dixon, Peter H., Levine, Adam P., Cebola, Inês, Chan, Melanie M. Y., Amin, Aliya S., Aich, Anshul, Mozere, Monika, Maude, Hannah, Mitchell, Alice L., Zhang, Jun, Chambers, Jenny, Syngelaki, Argyro, Donnelly, Jennifer, Cooley, Sharon, Geary, Michael, Nicolaides, Kypros, Thorsell, Malin, Hague, William M., Estiu, Maria Cecilia, Marschall, Hanns-Ulrich, Gale, Daniel P., Williamson, Catherine

Volltext

Characterization of the macrophage transcriptome in glomerulonephritis-susceptible and -resistant rat strains von Maratou, K, Behmoaras, J, Fewings, C, Srivastava, P, D'Souza, Z, Smith, J, Game, L, Cook, T, Aitman, T

Volltext

DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency von Logan, Clare V, Murray, Jennie E, Parry, David A, Robertson, Andrea, Bellelli, Roberto, Tarnauskaitė, Žygimantė, Challis, Rachel, Cleal, Louise, Borel, Valerie, Fluteau, Adeline, Santoyo-Lopez, Javier, SGP Consortium, Aitman, Tim, Barroso, Inês, Basel, Donald, Bicknell, Louise S, Goel, Himanshu, Hu, Hao, Huff, Chad, Hutchison, Michele, Joyce, Caroline, Knox, Rachel, Lacroix, Amy E, Langlois, Sylvie, McCandless, Shawn, McCarrier, Julie, Metcalfe, Kay A, Morrissey, Rose, Murphy, Nuala, Netchine, Irène, O'Connell, Susan M, Olney, Ann Haskins, Paria, Nandina, Rosenfeld, Jill A, Sherlock, Mark, Syverson, Erin, White, Perrin C, Wise, Carol, Yu, Yao, Zacharin, Margaret, Banerjee, Indraneel, Reijns, Martin, Bober, Michael B, Semple, Robert K, Boulton, Simon J, Rios, Jonathan J, Jackson, Andrew P

Volltext bestellen