Linkage Analysis with Dense SNP Maps in Isolated Populations

ανά Bellenguez, Céline, Ober, Carole, Bourgain, Catherine
Έκδοση 2009

A Multiple Splitting Approach to Linkage Analysis in Large Pedigrees Identifies a Linkage to Asthma on Chromosome 12

ανά Bellenguez, Céline, Ober, Carole, Bourgain, Catherine
Τόπος έκδοσης Genet Epidemiol (2009)

A robust clustering algorithm for identifying problematic samples in genome-wide association studies

ανά Bellenguez, Céline, Strange, Amy, Freeman, Colin, Donnelly, Peter, Spencer, Chris C.A.
Έκδοση 2012

Accuracy of heritability estimations in presence of hidden population stratification

ανά Dandine-Roulland, Claire, Bellenguez, Céline, Debette, Stéphanie, Amouyel, Philippe, Génin, Emmanuelle, Perdry, Hervé
Τόπος έκδοσης Sci Rep (2016)

Genetic Variants Modulating CRIPTO Serum Levels Identified by Genome-Wide Association Study in Cilento Isolates

ανά Ruggiero, Daniela, Nappo, Stefania, Nutile, Teresa, Sorice, Rossella, Talotta, Francesco, Giorgio, Emilia, Bellenguez, Celine, Leutenegger, Anne-Louise, Liguori, Giovanna L., Ciullo, Marina
Τόπος έκδοσης PLoS Genet (2015)

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

ανά Polašek, Ozren, Hayward, Caroline, Bellenguez, Celine, Vitart, Veronique, Kolčić, Ivana, McQuillan, Ruth, Saftić, Vanja, Gyllensten, Ulf, Wilson, James F, Rudan, Igor, Wright, Alan F, Campbell, Harry, Leutenegger, Anne-Louise
Έκδοση 2010

Genome-wide association interaction analysis for Alzheimer's disease

ανά Gusareva, Elena S., Carrasquillo, Minerva M., Bellenguez, Céline, Cuyvers, Elise, Colon, Samuel, Graff-Radford, Neill R., Petersen, Ronald C., Dickson, Dennis W., Mahachie Johna, Jestinah M., Bessonov, Kyrylo, Van Broeckhoven, Christine, Williams, Julie, Amouyel, Philippe, Sleegers, Kristel, Ertekin-Taner, Nilüfer, Lambert, Jean-Charles, Van Steen, Kristel
Τόπος έκδοσης Neurobiol Aging (2014)

Genome-wide association study of rate of cognitive decline in Alzheimer’s Disease patients identifies novel genes and pathways

ανά Sherva, Richard, Gross, Alden, Mukherjee, Shubhabrata, Koesterer, Ryan, Amouyel, Philippe, Bellenguez, Celine, Dufouil, Carole, Bennett, David A., Chibnik, Lori, Cruchaga, Carlos, del-Aguila, Jorge, Farrer, Lindsay A., Mayeux, Richard, Munsie, Leanne, Winslow, Ashley, Newhouse, Stephen, Saykin, Andrew J., Kauwe, John S.K., Crane, Paul K., Green, Robert C.
Τόπος έκδοσης Alzheimers Dement (2020)

ABCA7 rare variants and Alzheimer disease risk

ανά Le Guennec, Kilan, Nicolas, Gaël, Quenez, Olivier, Charbonnier, Camille, Wallon, David, Bellenguez, Céline, Grenier-Boley, Benjamin, Rousseau, Stéphane, Richard, Anne-Claire, Rovelet-Lecrux, Anne, Bacq, Delphine, Garnier, Jean-Guillaume, Olaso, Robert, Boland, Anne, Meyer, Vincent, Deleuze, Jean-François, Amouyel, Philippe, Munter, Hans Markus, Bourque, Guillaume, Lathrop, Mark, Frebourg, Thierry, Redon, Richard, Letenneur, Luc, Dartigues, Jean-François, Pasquier, Florence, Rollin-Sillaire, Adeline, Génin, Emmanuelle, Lambert, Jean-Charles, Hannequin, Didier, Campion, Dominique
Τόπος έκδοσης Neurology (2016)

Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype

ανά Ma, Yiyi, Jun, Gyungah R., Zhang, Xiaoling, Chung, Jaeyoon, Naj, Adam C., Chen, Yuning, Bellenguez, Celine, Hamilton-Nelson, Kara, Martin, Eden R., Kunkle, Brian W., Bis, Joshua C., Debette, Stéphanie, DeStefano, Anita L., Fornage, Myriam, Nicolas, Gaël, van Duijn, Cornelia, Bennett, David A., De Jager, Philip L., Mayeux, Richard, Haines, Jonathan L, Pericak-Vance, Margaret A., Seshadri, Sudha, Lambert, Jean-Charles, Schellenberg, Gerard D., Lunetta, Kathryn L., Farrer, Lindsay A.
Τόπος έκδοσης JAMA Neurol (2019)

Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies

ανά Choi, Seung Hoan, Ruggiero, Daniela, Sorice, Rossella, Song, Ci, Nutile, Teresa, Vernon Smith, Albert, Concas, Maria Pina, Traglia, Michela, Barbieri, Caterina, Ndiaye, Ndeye Coumba, Stathopoulou, Maria G., Lagou, Vasiliki, Maestrale, Giovanni Battista, Sala, Cinzia, Debette, Stephanie, Kovacs, Peter, Lind, Lars, Lamont, John, Fitzgerald, Peter, Tönjes, Anke, Gudnason, Vilmundur, Toniolo, Daniela, Pirastu, Mario, Bellenguez, Celine, Vasan, Ramachandran S., Ingelsson, Erik, Leutenegger, Anne-Louise, Johnson, Andrew D., DeStefano, Anita L., Visvikis-Siest, Sophie, Seshadri, Sudha, Ciullo, Marina
Τόπος έκδοσης PLoS Genet (2016)

Association of variants in HTRA1 and NOTCH3 with MRI-defined extremes of cerebral small vessel disease in older subjects

ανά Mishra, Aniket, Chauhan, Ganesh, Violleau, Marie-Helene, Vojinovic, Dina, Jian, Xueqiu, Bis, Joshua C, Li, Shuo, Saba, Yasaman, Grenier-Boley, Benjamin, Yang, Qiong, Bartz, Traci M, Hofer, Edith, Soumaré, Aïcha, Peng, Fen, Duperron, Marie-Gabrielle, Foglio, Mario, Mosley, Thomas H, Schmidt, Reinhold, Psaty, Bruce M, Launer, Lenore J, Boerwinkle, Eric, Zhu, Yicheng, Mazoyer, Bernard, Lathrop, Mark, Bellenguez, Celine, Van Duijn, Cornelia M, Ikram, M Arfan, Schmidt, Helena, Longstreth, W T, Fornage, Myriam, Seshadri, Sudha, Joutel, Anne, Tzourio, Christophe, Debette, Stephanie
Τόπος έκδοσης Brain (2019)

SUCLG2 identified as both a determinator of CSF Aβ(1–42) levels and an attenuator of cognitive decline in Alzheimer's disease

ανά Ramirez, Alfredo, van der Flier, Wiesje M., Herold, Christine, Ramonet, David, Heilmann, Stefanie, Lewczuk, Piotr, Popp, Julius, Lacour, André, Drichel, Dmitriy, Louwersheimer, Eva, Kummer, Markus P., Cruchaga, Carlos, Hoffmann, Per, Teunissen, Charlotte, Holstege, Henne, Kornhuber, Johannes, Peters, Oliver, Naj, Adam C., Chouraki, Vincent, Bellenguez, Céline, Gerrish, Amy, Heun, Reiner, Frölich, Lutz, Hüll, Michael, Buscemi, Lara, Herms, Stefan, Kölsch, Heike, Scheltens, Philip, Breteler, Monique M., Rüther, Eckart, Wiltfang, Jens, Goate, Alison, Jessen, Frank, Maier, Wolfgang, Heneka, Michael T., Becker, Tim, Nöthen, Markus M.
Τόπος έκδοσης Hum Mol Genet (2014)

Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer’s Disease

ανά Chouraki, Vincent, Reitz, Christiane, Maury, Fleur, Bis, Joshua C., Bellenguez, Celine, Yu, Lei, Jakobsdottir, Johanna, Mukherjee, Shubhabrata, Adams, Hieab H., Choi, Seung Hoan, Larson, Eric B., Fitzpatrick, Annette, Uitterlinden, Andre G., de Jager, Philip L., Hofman, Albert, Gudnason, Vilmundur, Vardarajan, Badri, Ibrahim-Verbaas, Carla, van der Lee, Sven J., Lopez, Oscar, Dartigues, Jean-François, Berr, Claudine, Amouyel, Philippe, Bennett, David A., van Duijn, Cornelia, DeStefano, Anita L., Launer, Lenore J., Ikram, M. Arfan, Crane, Paul K., Lambert, Jean-Charles, Mayeux, Richard, Seshadri, Sudha
Τόπος έκδοσης J Alzheimers Dis (2016)

Multiomics integrative analysis identifies APOE allele-specific blood biomarkers associated to Alzheimer’s disease etiopathogenesis

ανά Madrid, Laura, Moreno-Grau, Sonia, Ahmad, Shahzad, González-Pérez, Antonio, de Rojas, Itziar, Xia, Rui, Martino Adami, Pamela V., García-González, Pablo, Kleineidam, Luca, Yang, Qiong, Damotte, Vincent, Bis, Joshua C., Noguera-Perea, Fuensanta, Bellenguez, Céline, Jian, Xueqiu, Marín-Muñoz, Juan, Grenier-Boley, Benjamin, Orellana, Adela, Ikram, M. Arfan, Amouyel, Philippe, Satizabal, Claudia L., Real, Luis Miguel, Antúnez-Almagro, Carmen, DeStefano, Anita, Cabrera-Socorro, Alfredo, Sims, Rebecca, Van Duijn, Cornelia M., Boerwinkle, Eric, Ramírez, Alfredo, Fornage, Myriam, Lambert, Jean-Charles, Williams, Julie, Seshadri, Sudha, Ried, Janina S., Ruiz, Agustín, Saez, Maria Eugenia
Τόπος έκδοσης Aging (Albany NY) (2021)

Missense variant in TREML2 protects against Alzheimer's disease

ανά Benitez, Bruno A., Jin, Sheng Chih, Guerreiro, Rita, Graham, Rob, Lord, Jenny, Harold, Denise, Sims, Rebecca, Lambert, Jean-Charles, Gibbs, J. Raphael, Bras, Jose, Sassi, Celeste, Harari, Oscar, Bertelsen, Sarah, Lupton, Michelle K., Powell, John, Bellenguez, Celine, Brown, Kristelle, Medway, Christopher, Haddick, Patrick CG., van der Brug, Marcel P., Bhangale, Tushar, Ortmann, Ward, Behrens, Tim, Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Schellenberg, Gerard D., Haines, Jonathan L., Turton, Jim, Braae, Anne, Barber, Imelda, Fagan, Anne M., Holtzman, David M., Morris, John C., Williams, Julie, Kauwe, John S.K., Amouyel, Philippe, Morgan, Kevin, Singleton, Andy, Hardy, John, Goate, Alison M., Cruchaga, Carlos
Έκδοση 2014

Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes

ανά Zhou, Kaixin, Bellenguez, Celine, Spencer, Chris CA, Bennett, Amanda J, Coleman, Ruth L, Tavendale, Roger, Hawley, Simon A., Donnelly, Louise A, Schofield, Chris, Groves, Christopher J, Burch, Lindsay, Carr, Fiona, Strange, Amy, Freeman, Colin, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Dronov, Serge, Duncanson, Audrey, Edkins, Sarah, Gray, Emma, Hunt, Sarah, Jankowski, Janusz, Langford, Cordelia, Markus, Hugh S, Mathew, Christopher G, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Samani, Nilesh J, Trembath, Richard, Viswanathan, Ananth C, Wood, Nicholas W, Harries, Lorna W, Hattersley, Andrew T, Doney, Alex SF, Colhoun, Helen, Morris, Andrew D, Sutherland, Calum, Hardie, D. Grahame, Peltonen, Leena, McCarthy, Mark I, Holman, Rury R., Palmer, Colin N.A., Donnelly, Peter, Pearson, Ewan R
Έκδοση 2010

Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21

ανά Spencer, Chris C.A., Plagnol, Vincent, Strange, Amy, Gardner, Michelle, Paisan-Ruiz, Coro, Band, Gavin, Barker, Roger A., Bellenguez, Celine, Bhatia, Kailash, Blackburn, Hannah, Blackwell, Jennie M., Bramon, Elvira, Brown, Martin A., Brown, Matthew A., Burn, David, Casas, Juan-Pablo, Chinnery, Patrick F., Clarke, Carl E., Corvin, Aiden, Craddock, Nicholas, Deloukas, Panos, Edkins, Sarah, Evans, Jonathan, Freeman, Colin, Gray, Emma, Hardy, John, Hudson, Gavin, Hunt, Sarah, Jankowski, Janusz, Langford, Cordelia, Lees, Andrew J., Markus, Hugh S., Mathew, Christopher G., McCarthy, Mark I., Morrison, Karen E., Palmer, Colin N.A., Pearson, Justin P., Peltonen, Leena, Pirinen, Matti, Plomin, Robert, Potter, Simon, Rautanen, Anna, Sawcer, Stephen J., Su, Zhan, Trembath, Richard C., Viswanathan, Ananth C., Williams, Nigel W., Morris, Huw R., Donnelly, Peter, Wood, Nicholas W.
Έκδοση 2011

Common variants in the HLA-DRB1-HLA-DQA1 Class II region are associated with susceptibility to visceral leishmaniasis

ανά Fakiola, Michaela, Strange, Amy, Cordell, Heather J., Miller, E. Nancy, Pirinen, Matti, Su, Zhan, Mishra, Anshuman, Mehrotra, Sanjana, Monteiro, Gloria R., Band, Gavin, Bellenguez, Céline, Dronov, Serge, Edkins, Sarah, Freeman, Colin, Giannoulatou, Eleni, Gray, Emma, Hunt, Sarah E., Lacerda, Henio G., Langford, Cordelia, Pearson, Richard, Pontes, Núbia N., Rai, Madhukar, Singh, S.P., Smith, Linda, Sousa, Olivia, Vukcevic, Damjan, Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S., Mathew, Christopher G., Palmer, Colin N.A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Wilson, Mary E., Deloukas, Panos, Peltonen, Leena, Christiansen, Frank, Witt, Campbell, Jeronimo, Selma M.B., Sundar, Shyam, Spencer, Chris C.A., Blackwell, Jenefer M., Donnelly, Peter
Έκδοση 2013

A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer’s disease

ανά Huang, Kuan-lin, Marcora, Edoardo, Pimenova, Anna A, Di Narzo, Antonio F, Kapoor, Manav, Jin, Sheng Chih, Harari, Oscar, Bertelsen, Sarah, Fairfax, Benjamin P, Czajkowski, Jake, Chouraki, Vincent, Grenier-Boley, Benjamin, Bellenguez, Céline, Deming, Yuetiva, McKenzie, Andrew, Raj, Towfique, Renton, Alan E, Budde, John, Smith, Albert, Fitzpatrick, Annette, Bis, Joshua C, DeStefano, Anita, Adams, Hieab HH, Ikram, M Arfan, van der Lee, Sven, Del-Aguila, Jorge L., Fernandez, Maria Victoria, Ibañez, Laura, Sims, Rebecca, Escott-Price, Valentina, Mayeux, Richard, Haines, Jonathan L, Farrer, Lindsay A, Pericak-Vance, Margaret A., Lambert, Jean Charles, van Duijn, Cornelia, Launer, Lenore, Seshadri, Sudha, Williams, Julie, Amouyel, Philippe, Schellenberg, Gerard D, Zhang, Bin, Borecki, Ingrid, Kauwe, John S K, Cruchaga, Carlos, Hao, Ke, Goate, Alison M
Τόπος έκδοσης Nat Neurosci (2017)