المؤلفون: Bayram, Ece, Reho, Paolo, Litvan, Irene, International LBD Genomics, KRÜGER, Rejko, MAY, Patrick, Ding, Jinhui, Gibbs, J Raphael, Dalgard, Clifton L, Traynor, Bryan J, Scholz, Sonja W, Chia, Ruth

المساهمون: Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group), Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group), LIH - Luxembourg Institute of Health

المصدر: NPJ Parkinson's Disease, 10 (1), 39 (2024-02-20)

مصطلحات موضوعية: Lewy body dementia, X chromosome, GWAS, XWAS, Life sciences, Genetics & genetic processes, Human health sciences, Neurology, Sciences du vivant, Génétique & processus génétiques, Sciences de la santé humaine, Neurologie

العلاقة: FNR11264123 - Ncer-pd, 2015 (01/01/2015-30/11/2020) - Rejko Krüger; urn:issn:2373-8057; https://orbilu.uni.lu/handle/10993/60368Test; info:hdl:10993/60368; https://orbilu.uni.lu/bitstream/10993/60368/1/s41531-024-00649-7.pdfTest; scopus-id:2-s2.0-85185685644; info:pmid:38378815

الإتاحة: https://doi.org/10.1038/s41531-024-00649-7Test
https://orbilu.uni.lu/handle/10993/60368Test
https://orbilu.uni.lu/bitstream/10993/60368/1/s41531-024-00649-7.pdfTest

المؤلفون: Kaivola, Karri, Chia, Ruth, Ding, Jinhui, Rasheed, Memoona, Fujita, Masashi, Menon, Vilas, Walton, Ronald L, Collins, Ryan L, Billingsley, Kimberley, Brand, Harrison, Talkowski, Michael, Zhao, Xuefang, Dewan, Ramita, Stark, Ali, Ray, Anindita, Solaiman, Sultana, Alvarez Jerez, Pilar, Malik, Laksh, Dawson, Ted M, Rosenthal, Liana S, Albert, Marilyn S, Pletnikova, Olga, Troncoso, Juan C, Masellis, Mario, Keith, Julia, Black, Sandra E, Ferrucci, Luigi, Resnick, Susan M, Tanaka, Toshiko, Topol, Eric, Torkamani, Ali, Tienari, Pentti, Foroud, Tatiana M, Ghetti, Bernardino, Landers, John E, Ryten, Mina, Morris, Huw R, Hardy, John A, Mazzini, Letizia, D'Alfonso, Sandra, Moglia, Cristina, Calvo, Andrea, Serrano, Geidy E, Beach, Thomas G, Ferman, Tanis, Graff-Radford, Neill R, Boeve, Bradley F, Wszolek, Zbigniew K, Dickson, Dennis W, Chiò, Adriano, Bennett, David A, De Jager, Philip L, Ross, Owen A, Dalgard, Clifton L, Gibbs, J Raphael, Traynor, Bryan J, Scholz, Sonja W

المساهمون: Kaivola, Karri, Chia, Ruth, Ding, Jinhui, Rasheed, Memoona, Fujita, Masashi, Menon, Vila, Walton, Ronald L, Collins, Ryan L, Billingsley, Kimberley, Brand, Harrison, Talkowski, Michael, Zhao, Xuefang, Dewan, Ramita, Stark, Ali, Ray, Anindita, Solaiman, Sultana, Alvarez Jerez, Pilar, Malik, Laksh, Dawson, Ted M, Rosenthal, Liana S, Albert, Marilyn S, Pletnikova, Olga, Troncoso, Juan C, Masellis, Mario, Keith, Julia, Black, Sandra E, Ferrucci, Luigi, Resnick, Susan M, Tanaka, Toshiko, Topol, Eric, Torkamani, Ali, Tienari, Pentti, Foroud, Tatiana M, Ghetti, Bernardino, Landers, John E, Ryten, Mina, Morris, Huw R, Hardy, John A, Mazzini, Letizia, D'Alfonso, Sandra, Moglia, Cristina, Calvo, Andrea, Serrano, Geidy E, Beach, Thomas G, Ferman, Tani, Graff-Radford, Neill R, Boeve, Bradley F, Wszolek, Zbigniew K, Dickson, Dennis W, Chiò, Adriano, Bennett, David A, De Jager, Philip L, Ross, Owen A, Dalgard, Clifton L, Gibbs, J Raphael, Traynor, Bryan J, Scholz, Sonja W

مصطلحات موضوعية: Lewy body dementia, amyotrophic lateral sclerosi, case-control study, frontotemporal dementia, genome-wide association study, non–Alzheimer's dementia, resource, structural variant

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37388914; volume:3; issue:6; firstpage:100316; lastpage:100326; numberofpages:11; journal:CELL GENOMICS; https://hdl.handle.net/2318/1919190Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85161957826

الإتاحة: https://doi.org/10.1016Test/j.xgen.2023.100316
https://hdl.handle.net/2318/1919190Test

المؤلفون: Zanovello, Matteo, Ibáñez, Kristina, Brown, Anna-Leigh, Sivakumar, Prasanth, Bombaci, Alessandro, Santos, Liana, van Vugt, Joke J F A, Narzisi, Giuseppe, Karra, Ramita, Scholz, Sonja, Ding, Jinhui, Gibbs, J Raphael, Chiò, Adriano, Dalgard, Clifton, Weisburd, Ben, Hanna, Michael G, Greensmith, Linda, Phatnani, Hemali, Veldink, Jan H, Traynor, Bryan J, Polke, James, Houlden, Henry, Fratta, Pietro, Tucci, Arianna

المساهمون: Zanovello, Matteo, Ibáñez, Kristina, Brown, Anna-Leigh, Sivakumar, Prasanth, Bombaci, Alessandro, Santos, Liana, van Vugt, Joke J F A, Narzisi, Giuseppe, Karra, Ramita, Scholz, Sonja, Ding, Jinhui, Gibbs, J Raphael, Chiò, Adriano, Dalgard, Clifton, Weisburd, Ben, Hanna, Michael G, Greensmith, Linda, Phatnani, Hemali, Veldink, Jan H, Traynor, Bryan J, Polke, Jame, Houlden, Henry, Fratta, Pietro, Tucci, Arianna

مصطلحات موضوعية: androgen receptor, bioinformatics, population genetics, spinal and bulbar muscular atrophy, whole-genome sequencing

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36797998; info:eu-repo/semantics/altIdentifier/wos/WOS:000980256600001; volume:146; issue:7; firstpage:2723; lastpage:2729; numberofpages:7; journal:BRAIN; https://hdl.handle.net/20.500.11768/159116Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85164209619; https://academic.oup.com/brain/article/146/7/2723/7043521?login=trueTest

الإتاحة: https://doi.org/20.500.11768/159116Test
https://doi.org/10.1093/brain/awad050Test
https://hdl.handle.net/20.500.11768/159116Test
https://academic.oup.com/brain/article/146/7/2723/7043521?login=trueTest

المؤلفون: Yu, Eric, Krohn, Lynne, Ruskey, Jennifer, A, Asayesh, Farnaz, Spiegelman, Dan, Shah, Zalak, Chia, Ruth, Arnulf, Isabelle, Hu, Michele, T M, Montplaisir, Jacques, Y, Gagnon, Jean‐françois, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Ibrahim, Abubaker, Heidbreder, Anna, Sonka, Karel, Dusek, Petr, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel‐döring, Friederike, Cochen de Cock, Valérie, Ferini‐strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley, F, Rouleau, Guy, A, Postuma, Ronald, B, Scholz, Sonja, W, Gan‐or, Ziv, Sixel-Döring, Friederike, Abramzon, Yevgeniya, Ahmed, Sarah, Alba, Camille, Albert, Marilyn S., Bacikova, Dagmar, Barrett, Matthew J., Beach, Thomas G., Bennett, David A., Besser, Lilah M., Bigio, Eileen H., Boeve, Bradley F., Bohannan, Ryan C., Caraway, Chad A., Palma, Jose-Alberto, Dalgard, Clifton L., Dickson, Dennis, Ding, Jinhui, Faber, Kelley, Ferman, Tanis, Ferrucci, Luigi, Flanagan, Margaret E., Foroud, Tatiana M., Ghetti, Bernardino, Gibbs, J. Raphael, Goate, Alison, Goldstein, David, Graff-Radford, Neill R., Hu, Heng-Chen, Hupalo, Daniel, Kaiser, Scott M., Kaufmann, Horacio, Kim, Ronald C., Klein, Gregory, Kukull, Walter, Kuzma, Amanda, Leverenz, James, Lopez, Grisel, Mao, Qinwen, Martinez-Mcgrath, Elisa, Masliah, Eliezer, Monuki, Ed, Newell, Kathy L., Norcliffe-Kaufmann, Lucy, Perkins, Matthew, Pletnikova, Olga, Renton, Alan E., Resnick, Susan M., Ross, Owen A., Sabir, Marya S., Scherzer, Clemens R., Scholz, Sonja W., Serrano, Geidy, Shakkotai, Vikram, Sidransky, Ellen, Singleton, Andrew B., Tanaka, Toshiko, Tayebi, Nahid, Traynor, Bryan J., Troncoso, Juan C., Viollet, Coralie, Walton, Ronald L., Woltjer, Randy, Wszolek, Zbigniew K., Black, Sandra E., Gan-Or, Ziv, Keith, Julia, Masellis, Mario, Rogaeva, Ekaterina, Aarsland, Dag, Al-Sarraj, Safa, Attems, Johannes, Ferrari, Raffaele, Gentleman, Steve, Hardy, John A., Hodges, Angela K., Love, Seth, Mckeith, Ian, Morris, Christopher M., Morris, Huw R., Palmer, Laura, Pickering-Brown, Stuart, Reynolds, Regina H., Ryten, Mina, Thomas, Alan J., Tilley, Bension S., Troakes, Claire, Brett, Francesca, Brice, Alexis, Duyckaerts, Charles, Lesage, Suzanne, Brunetti, Maura, Calvo, Andrea, Canosa, Antonio, Chiò, Adriano, Floris, Gianluca, Logroscino, Giancarlo, Zecca, Chiara, Clarimon, Jordi, Diez-Fairen, Monica, Fortea, Juan, González-Aramburu, Isabel, Infante, Jon, Lage, Carmen, Lleó, Alberto, Pastor, Pau, Porcel-Molina, Laura, Rodríguez-Rodríguez, Eloy, Sanchez-Juan, Pascual, Krüger, Rejko, May, Patrick, Xiromerisiou, Georgia

المساهمون: Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), EuroMov - Digital Health in Motion (Euromov DHM), IMT - MINES ALES (IMT - MINES ALES), Institut Mines-Télécom Paris (IMT)-Institut Mines-Télécom Paris (IMT)-Université de Montpellier (UM), Clinique Médicale Beausoleil

المصدر: EISSN: 2328-9503 ; Annals of Clinical and Translational Neurology ; https://hal.science/hal-04505868Test ; Annals of Clinical and Translational Neurology, 2023, 10 (9), pp.1682-1687. ⟨10.1002/acn3.51841⟩

مصطلحات موضوعية: MESH: Humans, MESH: Lewy Body Disease, MESH: REM Sleep Behavior Disorder, MESH: Synucleinopathies, MESH: HLA-DRB1 Chains, MESH: HLA Antigens, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37401389; hal-04505868; https://hal.science/hal-04505868Test; https://hal.science/hal-04505868/documentTest; https://hal.science/hal-04505868/file/Ann%20Clin%20Transl%20Neurol%20-%202023%20-%20Yu%20-%20HLA%20in%20isolated%20REM%20sleep%20behavior%20disorder%20and%20Lewy%20body%20dementia.pdfTest; PUBMED: 37401389; PUBMEDCENTRAL: PMC10502660

الإتاحة: https://doi.org/10.1002/acn3.51841Test
https://hal.science/hal-04505868Test
https://hal.science/hal-04505868/documentTest
https://hal.science/hal-04505868/file/Ann%20Clin%20Transl%20Neurol%20-%202023%20-%20Yu%20-%20HLA%20in%20isolated%20REM%20sleep%20behavior%20disorder%20and%20Lewy%20body%20dementia.pdfTest

المؤلفون: Kaivola, Karri, Chia, Ruth, Ding, Jinhui, Rasheed, Memoona, Fujita, Masashi, Menon, Vilas, Walton, Ronald L., Collins, Ryan L., Billingsley, Kimberley, Brand, Harrison, Talkowski, Michael, Zhao, Xuefang, Dewan, Ramita, Stark, Ali, Ray, Anindita, Solaiman, Sultana, Alvarez Jerez, Pilar, Malik, Laksh, Dawson, Ted M., Rosenthal, Liana S., Albert, Marilyn S., Pletnikova, Olga, Troncoso, Juan C., Masellis, Mario, Keith, Julia, Black, Sandra E., Ferrucci, Luigi, Resnick, Susan M., Tanaka, Toshiko, Topol, Eric, Torkamani, Ali, Tienari, Pentti, Foroud, Tatiana M., Ghetti, Bernardino, Landers, John E., Ryten, Mina, Morris, Huw R., Hardy, John A., Mazzini, Letizia, D'Alfonso, Sandra, Moglia, Cristina, Calvo, Andrea, Serrano, Geidy E., Beach, Thomas G., Ferman, Tanis, Graff-Radford, Neill R., Boeve, Bradley F., Wszolek, Zbigniew K., Dickson, Dennis W., Chiò, Adriano, Bennett, David A., De Jager, Philip L., Ross, Owen A., Dalgard, Clifton L., Gibbs, J. Raphael, Traynor, Bryan J., Scholz, Sonja W., Soltis, Anthony R., Viollet, Coralie, Sukumar, Gauthaman, Alba, Camille, Lott, Nathaniel, McGrath Martinez, Elisa, Tuck, Meila, Singh, Jatinder, Bacikova, Dagmar, Zhang, Xijun, Hupalo, Daniel N., Adeleye, Adelani, Wilkerson, Matthew D., Pollard, Harvey B., Gan-Or, Ziv, Rogaeva, Ekaterina, Brice, Alexis, Lesage, Suzanne, Xiromerisiou, Georgia, Canosa, Antonio, Chio, Adriano, Logroscino, Giancarlo, Mora, Gabriele, Krüger, Rejko, May, Patrick, Alcolea, Daniel, Clarimon, Jordi, Fortea, Juan, Gonzalez-Aramburu, Isabel, Infante, Jon, Lage, Carmen, Lleó, Alberto, Pastor, Pau, Sanchez-Juan, Pascual, Brett, Francesca, Aarsland, Dag, Al-Sarraj, Safa, Attems, Johannes, Gentleman, Steve, Hodges, Angela K., Love, Seth, McKeith, Ian G., Morris, Christopher M., Palmer, Laura, Pickering-Brown, Stuart, Thomas, Alan J., Troakes, Claire, Barrett, Matthew J., Bekris, Lynn M., Faber, Kelley, Flanagan, Margaret E., Goate, Alison, Goldstein, David S., Kaufmann, Horacio, Kukull, Walter A., Leverenz, James B., Lopez, Grisel, Mao, Qinwen, Masliah, Eliezer, Monuki, Edwin, Newell, Kathy L., Palma, Jose-Alberto, Perkins, Matthew, Renton, Alan E., Scherzer, Clemens R., Shakkottai, Vikram G., Sidransky, Ellen, Tayebi, Nahid, Woltjer, Randy, Baloh, Robert H., Bowser, Robert, Broach, James, Camu, William, Cooper-Knock, John, Drepper, Carsten, Drory, Vivian E., Dunckley, Travis L., Feldman, Eva, Fratta, Pietro, Gerhard, Glenn, Gibson, Summer B., Glass, Jonathan D., Harms, Matthew B., Heiman-Patterson, Terry D., Jansson, Lilja, Kirby, Janine, Kwan, Justin, Laaksovirta, Hannu, Landi, Francesco, Le Ber, Isabelle, Lumbroso, Serge, MacGowan, Daniel J. L., Maragakis, Nicholas J., Mouzat, Kevin, Myllykangas, Liisa, Orrell, Richard W., Ostrow, Lyle W., Pamphlett, Roger, Pioro, Erik, Pulst, Stefan M., Ravits, John M., Robberecht, Wim, Rothstein, Jeffrey D., Sendtner, Michael, Shaw, Pamela J., Sidle, Katie C., Simmons, Zachary, Stein, Thor, Stone, David J., Tienari, Pentti J., Valori, Miko, Van Damme, Philip, Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Zinman, Lorne

المساهمون: Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group), Luxembourg Centre for Systems Biomedicine (LCSB): Clinical & Experimental Neuroscience (Krüger Group), LIH - Luxembourg Institute of Health

المصدر: Cell Genomics, 100316 (2023-05-04)

مصطلحات موضوعية: Structural variants, Non-Alzheimer dementia, Lewy body dementia, frontotemporal dementia, amyotrophic lateral sclerosis, Human health sciences, Neurology, Life sciences, Genetics & genetic processes, Sciences de la santé humaine, Neurologie, Sciences du vivant, Génétique & processus génétiques

العلاقة: https://linkinghub.elsevier.com/retrieve/pii/S2666979X23000848Test; FNR11264123 - Ncer-pd, 2015 (01/01/2015-30/11/2020) - Rejko Krüger; urn:issn:2666-979X; https://orbilu.uni.lu/handle/10993/55292Test; info:hdl:10993/55292; https://orbilu.uni.lu/bitstream/10993/55292/1/Kaivola2023.CellGenomics.pdfTest; scopus-id:2-s2.0-85161957826

الإتاحة: https://doi.org/10.1016Test/j.xgen.2023.100316
https://orbilu.uni.lu/handle/10993/55292Test
https://orbilu.uni.lu/bitstream/10993/55292/1/Kaivola2023.CellGenomics.pdfTest

المؤلفون: Makarious, Mary B, Lake, Julie, Pitz, Vanessa, Fu, Allen Ye, Guidubaldi, Joseph L, Solsberg, Caroline Warly, Bandres-Ciga, Sara, Leonard, Hampton L, Kim, Jonggeol Jeffrey, Billingsley, Kimberley J, Grenn, Francis P, Alvarez Jerez, Pilar, Alvarado, Chelsea, Iwaki, Hirotaka, Ta, Michael, Vitale, Dan, Hernandez, Dena, Torkamani, Ali, Ryten, Mina, Hardy, John, UK Brain Expression Consortium, (UKBEC), Scholz, Sonja W, Traynor, Bryan J, Dalgard, Clifton L, Ehrlich, Debra J, Tanaka, Toshiko, Ferrucci, Luigi, Beach, Thomas G, Serrano, Geidy E, Real, Raquel, Morris, Huw R, Ding, Jinhui, Gibbs, J Raphael, Singleton, Andrew B, Nalls, Mike A, Bhangale, Tushar, Blauwendraat, Cornelis

المصدر: Brain , 146 (11) pp. 4622-4632. (2023)

مصطلحات موضوعية: Parkinson’s disease, burden, GBA1, LRRK2, genetics, rare variant

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10172879/1/awad214.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10172879Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10172879/1/awad214.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10172879Test/

المؤلفون: Zanovello, Matteo, Ibáñez, Kristina, Brown, Anna-Leigh, Sivakumar, Prasanth, Bombaci, Alessandro, Santos, Liana, van Vugt, Joke JFA, Narzisi, Giuseppe, Karra, Ramita, Scholz, Sonja, Ding, Jinhui, Gibbs, J Raphael, Chiò, Adriano, Dalgard, Clifton, Weisburd, Ben, American Genome Center (TAGC) consortium, Genomics England Resea, ., Project MinE ALS Sequencing Consortium, ., NYGC ALS Consortium, ., Hanna, Michael G, Greensmith, Linda, Phatnani, Hemali, Veldink, Jan H, Traynor, Bryan J, Polke, James, Houlden, Henry, Fratta, Pietro, Tucci, Arianna

المصدر: Brain , 146 (7) pp. 2723-2729. (2023)

مصطلحات موضوعية: androgen receptor, bioinformatics, population genetics, spinal and bulbar muscular atrophy, whole-genome sequencing

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10165321/7/Zanovello_awad050.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10165321Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10165321/7/Zanovello_awad050.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10165321Test/

المؤلفون: Yu, Eric, Krohn, Lynne, Ruskey, Jennifer, A, Asayesh, Farnaz, Spiegelman, Dan, Shah, Zalak, Chia, Ruth, Arnulf, Isabelle, Hu, Michele, T M, Montplaisir, Jacques, Y, Gagnon, Jean‐françois, Desautels, Alex, Dauvilliers, Yves, Gigli, Gian Luigi, Valente, Mariarosaria, Janes, Francesco, Bernardini, Andrea, Högl, Birgit, Stefani, Ambra, Ibrahim, Abubaker, Heidbreder, Anna, Sonka, Karel, Dusek, Petr, Kemlink, David, Oertel, Wolfgang, Janzen, Annette, Plazzi, Giuseppe, Antelmi, Elena, Figorilli, Michela, Puligheddu, Monica, Mollenhauer, Brit, Trenkwalder, Claudia, Sixel‐döring, Friederike, Cochen de Cock, Valérie, Ferini‐strambi, Luigi, Dijkstra, Femke, Viaene, Mineke, Abril, Beatriz, Boeve, Bradley, F, Rouleau, Guy, A, Postuma, Ronald, B, Scholz, Sonja, W, Gan‐or, Ziv, Sixel-Döring, Friederike, Abramzon, Yevgeniya, Ahmed, Sarah, Alba, Camille, Albert, Marilyn S., Bacikova, Dagmar, Barrett, Matthew J., Beach, Thomas G., Bennett, David A., Besser, Lilah M., Bigio, Eileen H., Boeve, Bradley F., Bohannan, Ryan C., Caraway, Chad A., Palma, Jose-Alberto, Dalgard, Clifton L., Dickson, Dennis, Ding, Jinhui, Faber, Kelley, Ferman, Tanis, Ferrucci, Luigi, Flanagan, Margaret E., Foroud, Tatiana M., Ghetti, Bernardino, Gibbs, J. Raphael, Goate, Alison, Goldstein, David, Graff-Radford, Neill R., Hu, Heng-Chen, Hupalo, Daniel, Kaiser, Scott M., Kaufmann, Horacio, Kim, Ronald C., Klein, Gregory, Kukull, Walter, Kuzma, Amanda, Leverenz, James, Lopez, Grisel, Mao, Qinwen, Martinez-Mcgrath, Elisa, Masliah, Eliezer, Monuki, Ed, Newell, Kathy L., Norcliffe-Kaufmann, Lucy, Perkins, Matthew, Pletnikova, Olga, Renton, Alan E., Resnick, Susan M., Ross, Owen A., Sabir, Marya S., Scherzer, Clemens R., Scholz, Sonja W., Serrano, Geidy, Shakkotai, Vikram, Sidransky, Ellen, Singleton, Andrew B., Tanaka, Toshiko, Tayebi, Nahid, Traynor, Bryan J., Troncoso, Juan C., Viollet, Coralie, Walton, Ronald L., Woltjer, Randy, Wszolek, Zbigniew K., Black, Sandra E., Gan-Or, Ziv, Keith, Julia, Masellis, Mario, Rogaeva, Ekaterina, Aarsland, Dag, Al-Sarraj, Safa, Attems, Johannes, Ferrari, Raffaele, Gentleman, Steve, Hardy, John A., Hodges, Angela K., Love, Seth, Mckeith, Ian, Morris, Christopher M., Morris, Huw R., Palmer, Laura, Pickering-Brown, Stuart, Reynolds, Regina H., Ryten, Mina, Thomas, Alan J., Tilley, Bension S., Troakes, Claire, Brett, Francesca, Brice, Alexis, Duyckaerts, Charles, Lesage, Suzanne, Brunetti, Maura, Calvo, Andrea, Canosa, Antonio, Chiò, Adriano, Floris, Gianluca, Logroscino, Giancarlo, Zecca, Chiara, Clarimon, Jordi, Diez-Fairen, Monica, Fortea, Juan, González-Aramburu, Isabel, Infante, Jon, Lage, Carmen, Lleó, Alberto, Pastor, Pau, Porcel-Molina, Laura, Rodríguez-Rodríguez, Eloy, Sanchez-Juan, Pascual, Krüger, Rejko, May, Patrick, Xiromerisiou, Georgia

المساهمون: Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), EuroMov - Digital Health in Motion (Euromov DHM), IMT - MINES ALES (IMT - MINES ALES), Institut Mines-Télécom Paris (IMT)-Institut Mines-Télécom Paris (IMT)-Université de Montpellier (UM), Clinique Médicale Beausoleil

المصدر: EISSN: 2328-9503 ; Annals of Clinical and Translational Neurology ; https://hal.science/hal-04505868Test ; Annals of Clinical and Translational Neurology, 2023, 10 (9), pp.1682-1687. ⟨10.1002/acn3.51841⟩

مصطلحات موضوعية: MESH: Humans, MESH: Lewy Body Disease, MESH: REM Sleep Behavior Disorder, MESH: Synucleinopathies, MESH: HLA-DRB1 Chains, MESH: HLA Antigens, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37401389; hal-04505868; https://hal.science/hal-04505868Test; https://hal.science/hal-04505868/documentTest; https://hal.science/hal-04505868/file/Ann%20Clin%20Transl%20Neurol%20-%202023%20-%20Yu%20-%20HLA%20in%20isolated%20REM%20sleep%20behavior%20disorder%20and%20Lewy%20body%20dementia.pdfTest; PUBMED: 37401389; PUBMEDCENTRAL: PMC10502660

الإتاحة: https://doi.org/10.1002/acn3.51841Test
https://hal.science/hal-04505868Test
https://hal.science/hal-04505868/documentTest
https://hal.science/hal-04505868/file/Ann%20Clin%20Transl%20Neurol%20-%202023%20-%20Yu%20-%20HLA%20in%20isolated%20REM%20sleep%20behavior%20disorder%20and%20Lewy%20body%20dementia.pdfTest

المؤلفون: Billingsley, Kimberley J., Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P., Makarious, Mary B., Moore, Anni, Vitale, Daniel, Reed, Xylena, Hernandez, Dena, Torkamani, Ali, Ryten, Mina, Hardy, John, Consortium (UKBEC), UK Brain Expression, Chia, Ruth, Scholz, Sonja W., Traynor, Bryan J., Dalgard, Clifton L., Ehrlich, Debra J., Tanaka, Toshiko, Ferrucci, Luigi, Beach, Thomas G., Serrano, Geidy E., Quinn, John P., Bubb, Vivien J., Collins, Ryan L, Zhao, Xuefang, Walker, Mark, Pierce-Hoffman, Emma, Brand, Harrison, Talkowski, Michael E., Casey, Bradford, Cookson, Mark R, Markham, Androo, Nalls, Mike A., Mahmoud, Medhat, Sedlazeck, Fritz J, Blauwendraat, Cornelis, Gibbs, J. Raphael, Singleton, Andrew B.

وصف الملف: application/pdf

العلاقة: Billingsley, Kimberley J., Ding, Jinhui, Jerez, Pilar Alvarez, et al. "Genome-Wide Analysis of Structural Variants in Parkinson Disease." Annals of Neurology, 93, no. 5 (2023) Wiley: 1012-1022. https://doi.org/10.1002/ana.26608Test.; https://hdl.handle.net/1911/114860Test; 2023-Billingsley; https://doi.org/10.1002/ana.26608Test

الإتاحة: https://doi.org/10.1002/ana.26608Test
https://hdl.handle.net/1911/114860Test

المؤلفون: Kaivola, Karri, Chia, Ruth, Ding, Jinhui, Rasheed, Memoona, Fujita, Masashi, Menon, Vilas, Walton, Ronald L., Collins, Ryan L., Billingsley, Kimberley, Brand, Harrison, Talkowski, Michael, Zhao, Xuefang, Dewan, Ramita, Stark, Ali, Ray, Anindita, Solaiman, Sultana, Alvarez Jerez, Pilar, Malik, Laksh, Dawson, Ted M., Rosenthal, Liana S., Albert, Marilyn S., Pletnikova, Olga, Troncoso, Juan C., Masellis, Mario, Keith, Julia, Black, Sandra E., Ferrucci, Luigi, Resnick, Susan M., Tanaka, Toshiko, American Genome Center, International LBD Genomics Consortium, International ALS/FTD Consortium, PROSPECT Consortium, Topol, Eric, Torkamani, Ali, Tienari, Pentti, Foroud, Tatiana M., Ghetti, Bernardino, Landers, John E., Ryten, Mina, Morris, Huw R., Hardy, John A., Mazzini, Letizia, D'Alfonso, Sandra, Moglia, Cristina, Calvo, Andrea, Serrano, Geidy E., Beach, Thomas G., Ferman, Tanis, Graff-Radford, Neill R., Boeve, Bradley F., Wszolek, Zbigniew K., Dickson, Dennis W., Chiò, Adriano, Bennett, David A., De Jager, Philip L., Ross, Owen A., Dalgard, Clifton L., Gibbs, J. Raphael, Traynor, Bryan J., Scholz, Sonja W.

المساهمون: Medical and Molecular Genetics, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Lewy body dementia, Frontotemporal dementia, Amyotrophic lateral sclerosis, Structural variant, Genome-wide association study, Non–Alzheimer's dementia

وصف الملف: application/pdf

العلاقة: Cell Genomics; Kaivola K, Chia R, Ding J, et al. Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias. Cell Genom. 2023;3(6):100316. Published 2023 May 4. doi:10.1016/j.xgen.2023.100316; https://hdl.handle.net/1805/38097Test

الإتاحة: https://doi.org/10.1016Test/j.xgen.2023.100316
https://hdl.handle.net/1805/38097Test