يعرض 1 - 10 نتائج من 582 نتيجة بحث عن '"Dalgard, Clifton L."', وقت الاستعلام: 1.16s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Investigation of the genetic aetiology of Lewy body diseases with and without dementia

    المؤلفون: Wu, Lesley Yue, Real, Raquel, Martinez-Carrasco, Alejandro, Chia, Ruth, Lawton, Michael A, Shoai, Maryam, Bresner, Catherine, Blauwendraat, Cornelis, Singleton, Andrew B, Ryten, Mina, 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, 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, Thomas, Alan J, Tilley, Bension S, Troakes, Claire, Brett, Francesca, Brice, Alexis, Duyckaerts, Charles

    المصدر: Brain Communications. 6(4)

    مصطلحات موضوعية: Biomedical and Clinical Sciences, Biological Psychology, Clinical Sciences, Neurosciences, Psychology, Neurodegenerative, Genetics, Prevention, Aging, Lewy Body Dementia, Brain Disorders, Dementia, Alzheimer's Disease Related Dementias (ADRD), Parkinson's Disease, Human Genome, Acquired Cognitive Impairment, Clinical Research, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), 2.1 Biological and endogenous factors, Neurological, International Lewy Body Dementia Genomics Consortium, APOE, Lewy body diseases, dementia, genome-wide association studies, Clinical sciences, Biological psychology

    وصف الملف: application/pdf

    URL الوصول: https://escholarship.org/uc/item/0r55t25b
    https://escholarship.org/content/qt0r55t25b/qt0r55t25b.pdf

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  2. 2
    دورية أكاديمية
    A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats

    المؤلفون: de Jong, Tristan V, Pan, Yanchao, Rastas, Pasi, Munro, Daniel, Tutaj, Monika, Akil, Huda, Benner, Chris, Chen, Denghui, Chitre, Apurva S, Chow, William, Colonna, Vincenza, Dalgard, Clifton L, Demos, Wendy M, Doris, Peter A, Garrison, Erik, Geurts, Aron M, Gunturkun, Hakan M, Guryev, Victor, Hourlier, Thibaut, Howe, Kerstin, Huang, Jun, Kalbfleisch, Ted, Kim, Panjun, Li, Ling, Mahaffey, Spencer, Martin, Fergal J, Mohammadi, Pejman, Ozel, Ayse Bilge, Polesskaya, Oksana, Pravenec, Michal, Prins, Pjotr, Sebat, Jonathan, Smith, Jennifer R, Woods, Leah C Solberg, Tabakoff, Boris, Tracey, Alan, Uliano-Silva, Marcela, Villani, Flavia, Wang, Hongyang, Sharp, Burt M, Telese, Francesca, Jiang, Zhihua, Saba, Laura, Wang, Xusheng, Murphy, Terence D, Palmer, Abraham A, Kwitek, Anne E, Dwinell, Melinda R, Williams, Robert W, Li, Jun Z, Chen, Hao

    المصدر: Cell Genomics. 4(4)

    مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Genetics, Human Genome, Biotechnology, Good Health and Well Being, Rats, Animals, Genome, Molecular Sequence Annotation, Genomics, Whole Genome Sequencing, Genetic Variation, Rnor_6.0, genetic map, heterogeneous stock, hybrid rat diversity panel, inbred strains, mRatBN7.2, phylogenetic tree, rat, recombinant inbred, reference genome

    وصف الملف: application/pdf

    URL الوصول: https://escholarship.org/uc/item/9p74s81d
    https://escholarship.org/content/qt9p74s81d/qt9p74s81d.pdf

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  3. 3
    دورية أكاديمية
    Author Correction: Proteogenomic analysis of enriched HGSOC tumor epithelium identifies prognostic signatures and therapeutic vulnerabilities

    المؤلفون: Bateman, Nicholas W.Aff1, Aff2, Aff3, IDs41698024005889_cor1, Abulez, TamaraAff1, Aff2, Soltis, Anthony R., McPherson, Andrew, Choi, Seongmin, Garsed, Dale W.Aff6, Aff7, Pandey, Ahwan, Tian, ChunqiaoAff1, Aff2, Hood, Brian L.Aff1, Aff2, Conrads, Kelly A.Aff1, Aff2, Teng, Pang-ningAff1, Aff2, Oliver, JulieAff1, Aff2, Gist, GlennAff1, Aff2, Mitchell, DaveAff1, Aff2, Litzi, Tracy J.Aff1, Aff2, Tarney, Christopher M., Crothers, Barbara A., Mhawech-Fauceglia, Paulette, Dalgard, Clifton L., Wilkerson, Matthew D., Pierobon, Mariaelena, Petricoin, Emanuel F., Yan, Chunhua, Meerzaman, Daoud, Bodelon, Clara, Wentzensen, Nicolas, Lee, Jerry S. H., Huntsman, David G., Shah, Sohrab, Shriver, Craig D., Phippen, Neil T., Darcy, Kathleen M.Aff1, Aff2, Aff3, Bowtell, David D. L.Aff6, Aff7, Conrads, Thomas P.Aff1, Aff3, Aff15, IDs41698024005889_cor35, Maxwell, G. LarryAff1, Aff3, Aff15, IDs41698024005889_cor36

    المصدر: npj Precision Oncology. 8(1)

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  4. 4
    دورية أكاديمية
    Proteogenomic analysis of enriched HGSOC tumor epithelium identifies prognostic signatures and therapeutic vulnerabilities

    المؤلفون: Bateman, Nicholas W.Aff1, Aff2, Aff3, IDs41698024005198_cor1, Abulez, TamaraAff1, Aff2, Soltis, Anthony R., McPherson, Andrew, Choi, Seongmin, Garsed, Dale W.Aff6, Aff7, Pandey, Ahwan, Tian, ChunqiaoAff1, Aff2, Hood, Brian L.Aff1, Aff2, Conrads, Kelly A.Aff1, Aff2, Teng, Pang-ningAff1, Aff2, Oliver, JulieAff1, Aff2, Gist, GlennAff1, Aff2, Mitchell, DaveAff1, Aff2, Litzi, Tracy J.Aff1, Aff2, Tarney, Christopher M., Crothers, Barbara A., Mhawech-Fauceglia, Paulette, Dalgard, Clifton L., Wilkerson, Matthew D., Pierobon, Mariaelena, Petricoin, Emanuel F., Yan, Chunhua, Meerzaman, Daoud, Bodelon, Clara, Wentzensen, Nicolas, Lee, Jerry S. H., Huntsman, David G., Shah, Sohrab, Shriver, Craig D., Phippen, Neil T., Darcy, Kathleen M.Aff1, Aff2, Aff3, Bowtell, David D. L.Aff6, Aff7, Conrads, Thomas P.Aff1, Aff3, Aff15, IDs41698024005198_cor35, Maxwell, G. LarryAff1, Aff3, Aff15, IDs41698024005198_cor36

    المصدر: npj Precision Oncology. 8(1)

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  5. 5
    دورية أكاديمية
    The influence of microbial colonization on inflammatory versus pro-healing trajectories in combat extremity wounds

    المؤلفون: Schobel, Seth A.Aff1, Aff2, Aff3, IDs41598024524795_cor1, Gann, Eric R.Aff1, Aff2, Aff3, Unselt, DesireeAff1, Aff2, Aff3, Aff13, Grey, Scott F.Aff1, Aff2, Aff3, Lisboa, Felipe A.Aff1, Aff2, Aff3, Upadhyay, Meenu M., Rouse, MichaelAff1, Aff2, Aff3, Tallowin, SimonAff1, Aff2, Aff4, Be, Nicholas A., Zhang, Xijun, Dalgard, Clifton L.Aff6, Aff7, Wilkerson, Matthew D.Aff6, Aff7, Hauskrecht, Milos, Badylak, Stephen F.Aff9, Aff11, Zamora, RubenAff9, Aff10, Vodovotz, YoramAff9, Aff10, Potter, Benjamin K.Aff1, Aff2, Aff12, Davis, Thomas A., Elster, Eric A.Aff1, Aff2, Aff12

    المصدر: Scientific Reports. 14(1)

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  6. 6
    دورية أكاديمية
    Genetic analysis of the X chromosome in people with Lewy body dementia nominates new risk loci

    المؤلفون: Bayram, Ece, Reho, Paolo, Litvan, Irene, Ding, Jinhui, Gibbs, J. Raphael, Dalgard, Clifton L.Aff4, Aff5, Traynor, Bryan J.Aff6, Aff7, Aff8, Scholz, Sonja W.Aff2, Aff6, Chia, RuthAff7, IDs41531024006497_cor10

    المصدر: npj Parkinson's Disease. 10(1)

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  7. 7
    دورية أكاديمية
    Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

    المؤلفون: Matuozzo, DanielaAff1, Aff2, Talouarn, EstelleAff1, Aff2, Marchal, AstridAff1, Aff2, Zhang, Peng, Manry, JeremyAff1, Aff2, Seeleuthner, YoannAff1, Aff2, Zhang, Yu, Bolze, Alexandre, Chaldebas, Matthieu, Milisavljevic, Baptiste, Gervais, AdrianAff1, Aff2, Bastard, PaulAff1, Aff2, Aff3, Asano, Takaki, Bizien, LucyAff1, Aff2, Barzaghi, Federica, Abolhassani, HassanAff7, Aff8, Tayoun, Ahmad AbouAff9, Aff10, Aiuti, AlessandroAff11, Aff12, Darazam, Ilad AlaviAff13, Aff14, Allende, Luis M., Alonso-Arias, Rebeca, Arias, Andrés AugustoAff3, Aff17, Aff18, Aytekin, Gokhan, Bergman, PeterAff20, Aff21, Bondesan, Simone, Bryceson, Yenan T., Bustos, Ingrid G., Cabrera-Marante, Oscar, Carcel, Sheila, Carrera, Paola, Casari, GiorgioAff27, Aff28, Chaïbi, KhalilAff29, Aff30, Colobran, RogerAff31, Aff32, Aff33, Condino-Neto, Antonio, Covill, Laura E., Delmonte, Ottavia M., Zein, Loubna El, Flores, CarlosAff36, Aff37, Aff38, Aff39, Gregersen, Peter K., Gut, Marta, Haerynck, Filomeen, Halwani, Rabih, Hancerli, Selda, Hammarström, Lennart, Hatipoğlu, Nevin, Karbuz, Adem, Keles, Sevgi, Kyheng, Christèle, Leon-Lopez, Rafael, Franco, Jose Luis, Mansouri, DavoodAff50, Aff51, Aff52, Martinez-Picado, JavierAff53, Aff54, Aff55, Aff56, Aff57, Akcan, Ozge Metin, Migeotte, Isabelle, Morange, Pierre-EmmanuelAff59, Aff60, Morelle, Guillaume, Martin-Nalda, AndreaAff31, Aff61, Aff62, Novelli, GiuseppeAff63, Aff64, Novelli, Antonio, Ozcelik, Tayfun, Palabiyik, Figen, Pan-Hammarström, Qiang, de Diego, Rebeca Pérez, Planas-Serra, LauraAff68, Aff69, Pleguezuelo, Daniel E., Prando, Carolina, Pujol, AuroraAff56, Aff68, Aff69, Reyes, Luis Felipe, Rivière, Jacques G.Aff31, Aff61, Aff62, Rodriguez-Gallego, CarlosAff72, Aff73, Rojas, Julian, Rovere-Querini, PatriziaAff12, Aff74, Schlüter, AgathaAff68, Aff69, Shahrooei, MohammadAff75, Aff76, Sobh, Ali, Soler-Palacin, PereAff31, Aff61, Aff62, Tandjaoui-Lambiotte, Yacine, Tipu, Imran, Tresoldi, Cristina, Troya, Jesus, van de Beek, Diederik, Zatz, Mayana, Zawadzki, PawelAff84, Aff85, Al-Muhsen, Saleh Zaid, Alosaimi, Mohammed Faraj, Alsohime, Fahad M., Baris-Feldman, HagitAff87, Aff88, Butte, Manish J., Constantinescu, Stefan N.Aff90, Aff91, Aff92, Aff93, Cooper, Megan A., Dalgard, Clifton L.Aff95, Aff96, Fellay, JacquesAff97, Aff98, Aff99, Heath, James R., Lau, Yu-Lung, Lifton, Richard P.Aff102, Aff103, Aff104, Maniatis, TomAff105, Aff106, Mogensen, Trine H.Aff107, Aff108, von Bernuth, Horst, Lermine, Alban, Vidaud, Michel, Boland, Anne, Deleuze, Jean-François, Nussbaum, Robert, Kahn-Kirby, Amanda, Mentre, France, Tubiana, Sarah, Gorochov, Guy, Tubach, Florence, Hausfater, PierreAff117, Aff118, Meyts, Isabelle, Zhang, Shen-YingAff1, Aff2, Aff3, Puel, AnneAff1, Aff2, Aff3, Notarangelo, Luigi D., Boisson-Dupuis, StephanieAff1, Aff2, Aff3, Su, Helen C., Boisson, BertrandAff1, Aff2, Aff3, Jouanguy, EmmanuelleAff1, Aff2, Aff3, Casanova, Jean-LaurentAff1, Aff2, Aff3, Aff121, IDs13073023012780_cor126, Zhang, QianAff1, Aff2, Aff3, Abel, LaurentAff1, Aff2, Aff3, Cobat, AurélieAff1, Aff2, Aff3, IDs13073023012780_cor129

    المصدر: Genome Medicine. 16(1)

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  8. 8
    دورية أكاديمية
    Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer’s disease

    المؤلفون: Bhattarai, PrabeshAff1, Aff2, Gunasekaran, Tamil IniyanAff1, Aff3, Belloy, Michael E.Aff4, Aff5, Aff6, Reyes-Dumeyer, DollyAff1, Aff3, Jülich, Dörthe, Tayran, HüseyinAff1, Aff2, Yilmaz, ElanurAff1, Aff2, Flaherty, DelaneyAff2, Aff8, Turgutalp, BengisuAff1, Aff2, Sukumar, Gauthaman, Alba, Camille, McGrath, Elisa Martinez, Hupalo, Daniel N., Bacikova, Dagmar, Le Guen, YannAff4, Aff10, Lantigua, RafaelAff1, Aff2, Aff11, Medrano, Martin, Rivera, DionesAff13, Aff14, Recio, Patricia, Nuriel, TalAff2, Aff8, Ertekin-Taner, NilüferAff15, Aff16, Teich, Andrew F.Aff1, Aff2, Aff8, Dickson, Dennis W., Holley, Scott, Greicius, Michael, Dalgard, Clifton L.Aff17, Aff18, Zody, Michael, Mayeux, RichardAff1, Aff2, Aff3, Aff20, Aff21, Kizil, CaghanAff1, Aff2, Aff3, IDs00401024027211_cor29, Vardarajan, Badri N.Aff1, Aff2, Aff3, IDs00401024027211_cor30

    المصدر: Acta Neuropathologica: Pathology and Mechanisms of Neurological Disease. 147(1)

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  9. 9
    دورية أكاديمية
    Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias

    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, Jerez, Pilar Alvarez, 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, Soltis, Anthony R, Viollet, Coralie, Sukumar, Gauthaman, Alba, Camille, Lott, Nathaniel, Martinez, Elisa McGrath, Tuck, Meila, Singh, Jatinder, Bacikova, Dagmar, Zhang, Xijun, Hupalo, Daniel N, Adeleye, Adelani, Wilkerson, Matthew D, Pollard, Harvey B, Dalgard, Clifton L, Gan-Or, Ziv, Rogaeva, Ekaterina, Brice, Alexis, Lesage, Suzanne, Xiromerisiou, Georgia, Calvo, Andrea, Canosa, Antonio, Chio, Adriano, Logroscino, Giancarlo, Mora, Gabriele, Krüger, Reijko, 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, Hardy, John A, Hodges, Angela K, Love, Seth, McKeith, Ian G, Morris, Christopher M, Morris, Huw R, Palmer, Laura, Pickering-Brown, Stuart, Ryten, Mina, Thomas, Alan J, Troakes, Claire, Barrett, Matthew J, Beach, Thomas G, Bekris, Lynn M, Bennett, David A, Boeve, Bradley F, Dickson, Dennis W, Faber, Kelley, Ferman, Tanis, Flanagan, Margaret E, Foroud, Tatiana M, Ghetti, Bernardino, Gibbs, J Raphael

    المصدر: Cell Genomics. 3(6)

    مصطلحات موضوعية: Biological Sciences, Genetics, Brain Disorders, Dementia, ALS, Rare Diseases, Neurodegenerative, Neurosciences, Human Genome, Frontotemporal Dementia (FTD), Alzheimer's Disease, Alzheimer's Disease Related Dementias (ADRD), Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Acquired Cognitive Impairment, Aging, Aetiology, 2.1 Biological and endogenous factors, Neurological, American Genome Center, International LBD Genomics Consortium, International ALS/FTD Consortium, PROSPECT Consortium, Lewy body dementia, amyotrophic lateral sclerosis, case-control study, frontotemporal dementia, genome-wide association study, non–Alzheimer's dementia, resource, structural variant

    وصف الملف: application/pdf

    URL الوصول: https://escholarship.org/uc/item/93p4m5vv

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  10. 10
    دورية أكاديمية
    Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

    المؤلفون: Matuozzo, Daniela, Talouarn, Estelle, Marchal, Astrid, Zhang, Peng, Manry, Jeremy, Seeleuthner, Yoann, Zhang, Yu, Bolze, Alexandre, Chaldebas, Matthieu, Milisavljevic, Baptiste, Gervais, Adrian, Bastard, Paul, Asano, Takaki, Bizien, Lucy, Barzaghi, Federica, Abolhassani, Hassan, Abou Tayoun, Ahmad, Aiuti, Alessandro, Alavi Darazam, Ilad, Allende, Luis M, Alonso-Arias, Rebeca, Arias, Andrés Augusto, Aytekin, Gokhan, Bergman, Peter, Bondesan, Simone, Bryceson, Yenan T, Bustos, Ingrid G, Cabrera-Marante, Oscar, Carcel, Sheila, Carrera, Paola, Casari, Giorgio, Chaïbi, Khalil, Colobran, Roger, Condino-Neto, Antonio, Covill, Laura E, Delmonte, Ottavia M, El Zein, Loubna, Flores, Carlos, Gregersen, Peter K, Gut, Marta, Haerynck, Filomeen, Halwani, Rabih, Hancerli, Selda, Hammarström, Lennart, Hatipoğlu, Nevin, Karbuz, Adem, Keles, Sevgi, Kyheng, Christèle, Leon-Lopez, Rafael, Franco, Jose Luis, Mansouri, Davood, Martinez-Picado, Javier, Metin Akcan, Ozge, Migeotte, Isabelle, Morange, Pierre-Emmanuel, Morelle, Guillaume, Martin-Nalda, Andrea, Novelli, Giuseppe, Novelli, Antonio, Ozcelik, Tayfun, Palabiyik, Figen, Pan-Hammarström, Qiang, de Diego, Rebeca Pérez, Planas-Serra, Laura, Pleguezuelo, Daniel E, Prando, Carolina, Pujol, Aurora, Reyes, Luis Felipe, Rivière, Jacques G, Rodriguez-Gallego, Carlos, Rojas, Julian, Rovere-Querini, Patrizia, Schlüter, Agatha, Shahrooei, Mohammad, Sobh, Ali, Soler-Palacin, Pere, Tandjaoui-Lambiotte, Yacine, Tipu, Imran, Tresoldi, Cristina, Troya, Jesus, van de Beek, Diederik, Zatz, Mayana, Zawadzki, Pawel, Al-Muhsen, Saleh Zaid, Alosaimi, Mohammed Faraj, Alsohime, Fahad M, Baris-Feldman, Hagit, Butte, Manish J, Constantinescu, Stefan N, Cooper, Megan A, Dalgard, Clifton L, Fellay, Jacques, Heath, James R, Lau, Yu-Lung, Lifton, Richard P, Maniatis, Tom, Mogensen, Trine H, von Bernuth, Horst, Lermine, Alban, Vidaud, Michel

    المصدر: Genome Medicine. 15(1)

    مصطلحات موضوعية: Clinical Research, Infectious Diseases, Pneumonia & Influenza, Genetics, Human Genome, Prevention, 2.1 Biological and endogenous factors, Aetiology, Humans, Young Adult, Adult, Middle Aged, COVID-19, SARS-CoV-2, Toll-Like Receptor 3, Toll-Like Receptor 7, Interferon Type I, Autoantibodies, COVID Human Genetic Effort, COVIDeF Study Group, French COVID Cohort Study Group, CoV-Contact Cohort, COVID-STORM Clinicians, COVID Clinicians, Orchestra Working Group, Amsterdam UMC Covid-19 Biobank, NIAID-USUHS COVID Study Group, Immunity, Rare variants, Type I interferon, Clinical Sciences

    وصف الملف: application/pdf

    URL الوصول: https://escholarship.org/uc/item/922199h2

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