The UK10K project identifies rare variants in health and disease

by Walter, Klaudia, Min, Josine L, Huang, Jie, Crooks, Lucy, Memari, Yasin, McCarthy, Shane, Perry, John R B, Xu, ChangJiang, Futema, Marta, Lawson, Daniel, Iotchkova, Valentina, Schiffels, Stephan, Hendricks, Audrey E, Danecek, Petr, Li, Rui, Floyd, James, Wain, Louise V, Barroso, Inês, Humphries, Steve E, Hurles, Matthew E, Zeggini, Eleftheria, Barrett, Jeffrey C, Plagnol, Vincent, Richards, J Brent, Greenwood, Celia M T, Timpson, Nicholas J, Durbin, Richard, Soranzo, Nicole
Published in Nature (London)

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

by Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.
Published in American journal of human genetics

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

by Huang, Jie, Howie, Bryan, McCarthy, Shane, Memari, Yasin, Walter, Klaudia, Min, Josine L, Danecek, Petr, Malerba, Giovanni, Trabetti, Elisabetta, Zheng, Hou-Feng, Gambaro, Giovanni, Richards, J Brent, Durbin, Richard, Timpson, Nicholas J, Marchini, Jonathan, Soranzo, Nicole
Published in Nature communications

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

by Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.
Published in Proceedings of the National Academy of Sciences - PNAS

Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

by Teh, Bin Tean, Stratton, Michael R, Futreal, P. Andrew, Dalgliesh, Gillian L, Furge, Kyle, Greenman, Chris, Chen, Lina, Bignell, Graham, Butler, Adam, Davies, Helen, Edkins, Sarah, Hardy, Claire, Latimer, Calli, Teague, Jon, Andrews, Jenny, Barthorpe, Syd, Beare, Dave, Buck, Gemma, Campbell, Peter J, Forbes, Simon, Jia, Mingming, Jones, David, Knott, Henry, Kok, Chai Yin, Lau, King Wai, Leroy, Catherine, Lin, Meng-Lay, McBride, David J, Maddison, Mark, Maguire, Simon, McLay, Kirsten, Menzies, Andrew, Mironenko, Tatiana, Mulderrig, Lee, Mudie, Laura, O'Meara, Sarah, Pleasance, Erin, Rajasingham, Arjunan, Shepherd, Rebecca, Smith, Raffaella, Stebbings, Lucy, Stephens, Philip, Tang, Gurpreet, Tarpey, Patrick S, Turrell, Kelly, Dykema, Karl J, Khoo, Sok Kean, Petillo, David, Wondergem, Bill, Anema, John, Kahnoski, Richard J
Published in Nature (London)

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

by Postmus, Iris, Trompet, Stella, Deshmukh, Harshal A, Barnes, Michael R, Li, Xiaohui, Warren, Helen R, Chasman, Daniel I, Zhou, Kaixin, Arsenault, Benoit J, Donnelly, Louise A, Wiggins, Kerri L, Avery, Christy L, Griffin, Paula, Feng, QiPing, Taylor, Kent D, Li, Guo, Evans, Daniel S, Smith, Albert V, de Keyser, Catherine E, Johnson, Andrew D, de Craen, Anton J M, Stott, David J, Buckley, Brendan M, Ford, Ian, Westendorp, Rudi G J, Slagboom, P Eline, Sattar, Naveed, Munroe, Patricia B, Sever, Peter, Poulter, Neil, Stanton, Alice, Shields, Denis C, O'Brien, Eoin, Shaw-Hawkins, Sue, Chen, Y-D Ida, Nickerson, Deborah A, Smith, Joshua D, Dubé, Marie Pierre, Boekholdt, S Matthijs, Hovingh, G Kees, Kastelein, John J P, McKeigue, Paul M, Betteridge, John, Neil, Andrew, Durrington, Paul N, Doney, Alex, Carr, Fiona, Morris, Andrew, McCarthy, Mark I, Groop, Leif, Ahlqvist, Emma, Bis, Joshua C, Rice, Kenneth, Smith, Nicholas L, Whitsel, Eric A, Stürmer, Til, Boerwinkle, Eric, Ngwa, Julius S, O'Donnell, Christopher J, Vasan, Ramachandran S, Wei, Wei-Qi, Wilke, Russell A, Liu, Ching-Ti, Sun, Fangui, Guo, Xiuqing, Heckbert, Susan R, Post, Wendy, Sotoodehnia, Nona, Arnold, Alice M, Stafford, Jeanette M, Ding, Jingzhong, Herrington, David M, Kritchevsky, Stephen B, Eiriksdottir, Gudny, Launer, Leonore J, Harris, Tamara B, Chu, Audrey Y, Giulianini, Franco, MacFadyen, Jean G, Barratt, Bryan J, Nyberg, Fredrik, Stricker, Bruno H, Uitterlinden, André G, Hofman, Albert, Rivadeneira, Fernando, Emilsson, Valur, Franco, Oscar H, Ridker, Paul M, Gudnason, Vilmundur, Liu, Yongmei, Denny, Joshua C, Ballantyne, Christie M, Rotter, Jerome I, Adrienne Cupples, L, Psaty, Bruce M, Palmer, Colin N A, Tardif, Jean-Claude, Hitman, Graham, Krauss, Ronald M, Caulfield, Mark J
Published in Nature communications

Signatures of mutation and selection in the cancer genome

by Edkins, Sarah, Deloukas, Panos, Widaa, Sara, Dalgliesh, Gillian L, Bignell, Graham R, Davies, Helen, Swamy, Sajani, Chen, Lina, Stratton, Michael R, Futreal, P. Andrew, Teh, Bin T, Greenman, Chris D, Yang, Fengtang, Butler, Adam P, Campbell, Peter J, Andrews, Jenny M, Buck, Gemma, Hinton, Jonathon, Fu, Beiyuan, Fahey, Ciara, Beare, David, Latimer, Calli
Published in Nature (London)

Gene filtering strategies for machine learning guided biomarker discovery using neonatal sepsis RNA-seq data

by Parkinson, Edward, Liberatore, Federico, Watkins, W John, Andrews, Robert, Edkins, Sarah, Hibbert, Julie, Strunk, Tobias, Currie, Andrew, Ghazal, Peter
Published in Frontiers in genetics

Patterns of somatic mutation in human cancer genomes

by Futreal, P. Andrew, Stratton, Michael R, Greenman, Christopher, Stephens, Philip, Smith, Raffaella, Dalgliesh, Gillian L, Hunter, Christopher, Bignell, Graham, Davies, Helen, Teague, Jon, Butler, Adam, Stevens, Claire, Edkins, Sarah, O'Meara, Sarah, Vastrik, Imre, Schmidt, Esther E, Avis, Tim, Barthorpe, Syd, Bhamra, Gurpreet, Buck, Gemma, Choudhury, Bhudipa, Clements, Jody, Cole, Jennifer, Dicks, Ed, Forbes, Simon, Gray, Kris, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jon, Jenkinson, Andy, Jones, David, Menzies, Andy, Mironenko, Tatiana, Perry, Janet, Raine, Keiran, Richardson, Dave, Shepherd, Rebecca, Small, Alexandra, Tofts, Calli, Varian, Jennifer, Webb, Tony, West, Sofie, Widaa, Sara, Yates, Andy, Cahill, Daniel P, Louis, David N, Goldstraw, Peter, Nicholson, Andrew G, Brasseur, Francis, Looijenga, Leendert, Weber, Barbara L, Chiew, Yoke-Eng, deFazio, Anna, Greaves, Mel F, Green, Anthony R, Campbell, Peter, Birney, Ewan, Easton, Douglas F, Chenevix-Trench, Georgia, Tan, Min-Han, Khoo, Sok Kean, Teh, Bin Tean, Yuen, Siu Tsan, Leung, Suet Yi, Wooster, Richard
Published in Nature

Complex landscapes of somatic rearrangement in human breast cancer genomes

by Lau, King Wai, Mudie, Laura J, Churcher, Carol, Stratton, Michael R, Silver, Daniel P, van 't Veer, Laura, Børresen-Dale, Anne-Lise, Stebbings, Lucy A, McBride, David J, Martens, John W. M, Simpson, Jared T, Leroy, Catherine, Russnes, Hege E. G, Latimer, Calli, Jia, Mingming, Edkins, Sarah, Natrajan, Rachael, Reis-Filho, Jorge S, Varela, Ignacio, Swerdlow, Harold, Lin, Meng-Lay, Richardson, Andrea L, Pleasance, Erin D, Sieuwerts, Anieta M, Stephens, Philip J, Futreal, P. Andrew, Greenman, Chris D, Burton, John, Langerød, Anita, Quail, Michael A, Foekens, John A, Campbell, Peter J, Teague, Jon W
Published in Nature (London)

Gata2 as a Crucial Regulator of Stem Cells in Adult Hematopoiesis and Acute Myeloid Leukemia

by Menendez-Gonzalez, Juan Bautista, Vukovic, Milica, Abdelfattah, Ali, Saleh, Lubaid, Almotiri, Alhomidi, Thomas, Leigh-anne, Agirre-Lizaso, Aloña, Azevedo, Aleksandra, Menezes, Ana Catarina, Tornillo, Giusy, Edkins, Sarah, Kong, Kay, Giles, Peter, Anjos-Afonso, Fernando, Tonks, Alex, Boyd, Ashleigh S., Kranc, Kamil R., Rodrigues, Neil P.
Published in Stem cell reports

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

by Iglesias, Adriana I, Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N Cooke, Willoughby, Colin E, Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P, Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L, Kearns, Lisa S, Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M, Taylor, Kent D, Bonnemaijer, Pieter, Rotter, Jerome I, Martin, Nicholas G, Zeller, Tanja, Mills, Richard A, Souzeau, Emmanuelle, Staffieri, Sandra E, Jonas, Jost B, Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H, Lucas, Sionne E M, Wong, Tien Yin, Beutel, Manfred E, Wilson, James F, Uitterlinden, André G, Vithana, Eranga N, Foster, Paul J, Hysi, Pirro G, Hewitt, Alex W, Khor, Chiea Chuen, Pasquale, Louis R, Montgomery, Grant W, Klaver, Caroline C W, Aung, Tin, Pfeiffer, Norbert, Mackey, David A, Hammond, Christopher J, Cheng, Ching-Yu, Craig, Jamie E, Rabinowitz, Yaron S, Wiggs, Janey L, Burdon, Kathryn P, van Duijn, Cornelia M, MacGregor, Stuart
Published in Nature communications

Whole-genome sequence-based analysis of thyroid function

by Taylor, Peter N, Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J, Traglia, Michela, Brown, Suzanne J, Mullin, Benjamin H, Shihab, Hashem A, Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R, Beilby, John P, Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D, Hui, Jennie, Lim, Ee M, McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R B, Bell, Jordana T, Yuan, Wei, Relton, Caroline, Gaunt, Tom, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L, Woltersdorf, Wolfram, Zeggini, Eleftheria, Zheng, Hou-Feng, Toniolo, Daniela, Dayan, Colin M, Naitza, Silvia, Walsh, John P, Spector, Tim, Davey Smith, George, Durbin, Richard, Richards, J Brent, Sanna, Serena, Soranzo, Nicole, Timpson, Nicholas J, Wilson, Scott G
Published in Nature communications

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

by HUNTER, Chris, SMITH, Raffaella, O'MEARA, Sarah, PARKER, Adrian, AVIS, Tim, BARTHORPE, Syd, BRACKENBURY, Lisa, BUCK, Gemma, BUTLER, Adam, CLEMENTS, Jody, COLE, Jennifer, DICKS, Ed, CAHILL, Daniel P, FORBES, Simon, GORTON, Matthew, GRAY, Kristian, HALLIDAY, Kelly, HARRISON, Rachel, HILLS, Katy, HINTON, Jonathon, JENKINSON, Andy, JONES, David, KOSMIDOU, Vivienne, STEPHENS, Philip, LAMAN, Ross, LUGG, Richard, MENZIES, Andrew, PERRY, Janet, PETTY, Robert, RAINE, Keiran, RICHARDSON, David, SHEPHERD, Rebecca, SMALL, Alexandra, SOLOMON, Helen, STEVENS, Claire, TOFTS, Calli, VARIAN, Jennifer, WEST, Sofie, WIDAA, Sara, YATES, Andy, EASTON, Douglas F, RIGGINS, Gregory, ROY, Jennifer E, LEVINE, Kymberly K, MUELLER, Wolf, TEAGUE, Jon, BATCHELOR, Tracy T, LOUIS, David N, STRATTON, Michael R, FUTREAL, P. Andrew, WOOSTER, Richard, GREENMAN, Chris, EDKINS, Sarah, BIGNELL, Graham, DAVIES, Helen
Published in Cancer research (Chicago, Ill.)

Mutation analysis of 24 known cancer genes in the NCI-60 cell line set

by Ikediobi, Ogechi N, Davies, Helen, Bignell, Graham, Edkins, Sarah, Stevens, Claire, O'Meara, Sarah, Santarius, Thomas, Avis, Tim, Barthorpe, Syd, Brackenbury, Lisa, Buck, Gemma, Butler, Adam, Clements, Jody, Cole, Jennifer, Dicks, Ed, Forbes, Simon, Gray, Kristian, Halliday, Kelly, Harrison, Rachel, Hills, Katy, Hinton, Jonathan, Hunter, Chris, Jenkinson, Andy, Jones, David, Kosmidou, Vivienne, Lugg, Richard, Menzies, Andrew, Mironenko, Tatiana, Parker, Adrian, Perry, Janet, Raine, Keiran, Richardson, David, Shepherd, Rebecca, Small, Alex, Smith, Raffaella, Solomon, Helen, Stephens, Philip, Teague, Jon, Tofts, Calli, Varian, Jennifer, Webb, Tony, West, Sofie, Widaa, Sara, Yates, Andy, Reinhold, William, Weinstein, John N, Stratton, Michael R, Futreal, P Andrew, Wooster, Richard
Published in Molecular cancer therapeutics

Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

by van Rooij, Jeroen, Uitterlinden, André G, Kraaij, Robert, Heutink, Peter, Nalls, Mike A, Plagnol, Vincent, Sharma, Manu, Saad, Mohamad, Simón-Sánchez, Javier, Schulte, Claudia, Lesage, Suzanne, Arepalli, Sampath, Barker, Roger, Ben, Yoav, Berendse, Henk W, Berg, Daniela, Bhatia, Kailash, de Bie, Rob M A, Bloem, Bas, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M, Brockmann, Kathrin, Brooks, Janet, Burn, David J, Majounie, Elisa, Charlesworth, Gavin, Lungu, Codrin, Chen, Honglei, Chong, Sean, Clarke, Carl E, Mark Cooper, J, Corvol, Jean Christophe, Counsell, Carl, Damier, Philippe, Dartigues, Jean-François, Deloukas, Panos, Dexter, David T, van Dijk, Karin D, Durif, Frank, Dürr, Alexandra, Evans, Jonathan R, Foltynie, Thomas, Gardner, Michelle, Raphael Gibbs, J, Gray, Emma, Guerreiro, Rita, Harris, Clare, van Hilten, Jacobus J, Hofman, Albert, Hollenbeck, Albert, Holton, Janice, Hu, Michele, Huang, Xuemei, Wurster, Isabel, Hudson, Gavin, Hunt, Sarah E, Lees, Andrew, Lichtner, Peter, Lopez, Grisel, Lorenz, Delia, McNeill, Alisdair, Moorby, Catriona, Moore, Matthew, Morris, Huw R, Morrison, Karen E, Pearson, Justin, Perlmutter, Joel S, Pétursson, Hjörvar, Pollak, Pierre, Riess, Olaf, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Scheffer, Hans, Shaw, Karen, Shoulson, Ira, Shulman, Joshua, Sidransky, Ellen, Smith, Colin, Spencer, Chris C A, Stefánsson, Hreinn, Bettella, Francesco, Stockton, Joanna D, Strange, Amy, Talbot, Kevin, Tanner, Carlie M, Tashakkori-Ghanbaria, Avazeh, Trabzuni, Daniah, Uitterlinden, André G, Walker, Robert, van de Warrenburg, Bart, Wickremaratchi, Mirdhu, Williams, Nigel, Williams-Gray, Caroline H, Winder-Rhodes, Sophie, Martinez, Maria, Wood, Nicholas W, Brice, Alexis, Gasser, Thomas
Published in Brain (London, England : 1878)

Oligosaccharyltransferase-Subunit Mutations in Nonsyndromic Mental Retardation

by Molinari, Florence, Foulquier, François, Tarpey, Patrick S., Morelle, Willy, Boissel, Sarah, Teague, Jon, Edkins, Sarah, Futreal, P. Andrew, Stratton, Michael R., Turner, Gillian, Matthijs, Gert, Gecz, Jozef, Munnich, Arnold, Colleaux, Laurence
Published in American journal of human genetics

Imputation-based meta-analysis of severe malaria in three African populations

by Band, Gavin, Le, Quang Si, Jostins, Luke, Pirinen, Matti, Kivinen, Katja, Jallow, Muminatou, Sisay-Joof, Fatoumatta, Bojang, Kalifa, Pinder, Margaret, Sirugo, Giorgio, Conway, David J, Nyirongo, Vysaul, Kachala, David, Molyneux, Malcolm, Taylor, Terrie, Ndila, Carolyne, Peshu, Norbert, Marsh, Kevin, Williams, Thomas N, Alcock, Daniel, Andrews, Robert, Edkins, Sarah, Gray, Emma, Hubbart, Christina, Jeffreys, Anna, Rowlands, Kate, Schuldt, Kathrin, Clark, Taane G, Small, Kerrin S, Teo, Yik Ying, Kwiatkowski, Dominic P, Rockett, Kirk A, Barrett, Jeffrey C, Spencer, Chris C A
Published in PLoS genetics

Somatic mutations of the protein kinase gene family in human lung cancer

by DAVIES, Helen, HUNTER, Chris, PARKER, Adrian, O'MEARA, Sarah, AVIS, Tim, BARTHORPE, Syd, BRACKENBURY, Lisa, BUCK, Gemma, CLEMENTS, Jody, COLE, Jennifer, DICKS, Ed, EDWARDS, Ken, SMITH, Raffaella, FORBES, Simon, GORTON, Matthew, GRAY, Kristian, HALLIDAY, Kelly, HARRISON, Rachel, HILLS, Katy, HINTON, Jonathon, JONES, David, KOSMIDOU, Vivienne, LAMAN, Ross, STEPHENS, Philip, LUGG, Richard, MENZIES, Andrew, PERRY, Janet, PETTY, Robert, RAINE, Keiran, SHEPHERD, Rebecca, SMALL, Alexandra, SOLOMON, Helen, STEPHENS, Yvonne, TOFTS, Calli, GREENMAN, Chris, VARIAN, Jennifer, WEBB, Anthony, WEST, Sofie, WIDAA, Sara, YATES, Andrew, BRASSEUR, Francis, COOPER, Colin S, FLANAGAN, Adrienne M, GREEN, Anthony, KNOWLES, Maggie, BIGNELL, Graham, LEUNG, Suet Y, LOOIJENGA, Leendert H. J, MALKOWICZ, Bruce, PIEROTTI, Marco A, TEH, Bin T, YUEN, Siu T, LAKHANI, Sunil R, EASTON, Douglas F, WEBER, Barbara L, GOLDSTRAW, Peter, TEAGUE, Jon, BUTLER, Adam, EDKINS, Sarah, STEVENS, Claire
Published in Cancer research (Chicago, Ill.)

Distinctive Features of Orbital Adipose Tissue (OAT) in Graves' Orbitopathy

by Zhang, Lei, Evans, Anna, von Ruhland, Chris, Draman, Mohd Shazli, Edkins, Sarah, Vincent, Amy E, Berlinguer-Palmini, Rolando, Rees, D Aled, Haridas, Anjana S, Morris, Dan, Tee, Andrew R, Ludgate, Marian, Turnbull, Doug M, Karpe, Fredrik, Dayan, Colin M
Published in International journal of molecular sciences