Holistic Determination of Optoelectronic Properties using High-Throughput Spectroscopy of Surface-Guided CsPbBr3 Nanowires von Church, Stephen A., Choi, Hoyeon, Al-Amairi, Nawal, Al-Abri, Ruqaiya, Sanders, Ella, Oksenberg, Eitan, Joselevich, Ernesto, Parkinson, Patrick W.

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High-Throughput Spectroscopy of Geometry-Tunable Arrays of Axial InGaAs Nanowire Heterostructures with Twin-Induced Carrier Confinement von Jeong, Hyowon W., Church, Stephen A., Döblinger, Markus, Ajay, Akhil, Haubmann, Benjamin, Patel, Nikesh, Finley, Jonathan J., Parkinson, Patrick W., Koblmüller, Gregor

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Highly Strained III–V–V Coaxial Nanowire Quantum Wells with Strong Carrier Confinement von Zhang, Yunyan, Davis, George, Fonseka, H. Aruni, Velichko, Anton, Gustafsson, Anders, Godde, Tillmann, Saxena, Dhruv, Aagesen, Martin, Parkinson, Patrick W, Gott, James A, Huo, Suguo, Sanchez, Ana M, Mowbray, David J, Liu, Huiyun

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Two-Dimensional Diffusion of Excitons in a Perylene Diimide Monolayer Quenched by a Fullerene Heterojunction von Kerfoot, James, Korolkov, Vladimir V, Svatek, Simon A, Alkhamisi, Manal, Taniguchi, Takashi, Watanabe, Kenji, Parkinson, Patrick W, Beton, Peter H

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Holistic Determination of Optoelectronic Properties using High-Throughput Spectroscopy of Surface-Guided CsPbBr$_3$ Nanowires von Church, Stephen A, Choi, Hoyeon, Al-Amairi, Nawal, Al-Abri, Ruqaiya, Sanders, Ella, Oksenberg, Eitan, Joselevich, Ernesto, Parkinson, Patrick W

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Holistic Determination of Optoelectronic Properties using High-Throughput Spectroscopy of Surface-Guided CsPbBr\(_3\) Nanowires von Church, Stephen A, Choi, Hoyeon, Al-Amairi, Nawal, Al-Abri, Ruqaiya, Sanders, Ella, Oksenberg, Eitan, Joselevich, Ernesto, Parkinson, Patrick W

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Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study von Noyce, Alastair J, Kia, Demis A, Hemani, Gibran, Nicolas, Aude, Price, T Ryan, De Pablo-Fernandez, Eduardo, Haycock, Philip C, Lewis, Patrick A, Foltynie, Thomas, Davey Smith, George, Schrag, Anette, Lees, Andrew J, Hardy, John, Singleton, Andrew, Nalls, Mike A, Pearce, Neil, Lawlor, Debbie A, Wood, Nicholas W

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Chemogenetic Interrogation of a Brain-wide Fear Memory Network in Mice von Vetere, Gisella, Kenney, Justin W., Tran, Lina M., Xia, Frances, Steadman, Patrick E., Parkinson, John, Josselyn, Sheena A., Frankland, Paul W.

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Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study von Rizig, Mie, Bandres-Ciga, Sara, Levine, Kristin S, Adeniji, Olaleye Akinmola, Agabi, Osigwe Paul, Arigbodi, Ohwotemu Michael, Erameh, Cyril Oshomah, Okunoye, Olaitan, Komolafe, Morenikeji Adeyoyin, Odeniyi, Olanike Adedoyin, Ojini, Francis Ibe, D'Souza, Andrea M, Osemwegie, Nosakhare, Leonard, Hampton L, Ozomma, Simon Izuchukwu, Zubair, Yusuf Agboola, Abiodun, Oladunni, Akinyemi, Rufus, Ali, Mohammed, Bello, Abiodun, Erameh, Cyril, Farombi, Temitope, Imarhiagbe, Frank, Iwuozo, Emmanuel, Nwazor, Ernest, Ojini, Francis, Onwuegbuzie, Gerald, Ozomma, Simon, Zubair, Yusuf, Gueumekane Bila lamou, Eric, Shalash, Ali, Khedr, Eman, El-Jaafary, Shaimaa, Hamed, Sharifa, Melka Oda, Dereje, Debebe Gelan, Yohanesse, Charway-Felli, Augustina, Stephen Sarfo, Fred, Koita, Abdou, Bell, Abiodun, Adebowale, Akintunde A., Akpekpe, John, Agu, Christian, Agabi Osigwe, Paul, Balarabe, Salisu, Williams, Uduak, Hilaire Dominique, Ewodo Touna, Mochan, Andre, Ben Djebara, Mouna, Kacem, Imen, Mkada, Imen, Atadzhanov, Masharip, Jama, Fatumah, Hall, Deborah A., Warren, Natalie, Chauppeta, Brian, Rawls, Ashley, O'Grady, Alyssa, Sherer, Todd, Blauwendraat, Cornelis, Brice, Alexis, Illarionova, Anastasia, Quattrone, Andrea, Kishore, Asha, Ahmad-Annuar, Azlina, Mollenhauer, Brit, Carroll, Camille, Rieder, Carlos, KP, Divya, Fon, Edward A., Gatto, Emilia M, Xiromerisiou, Georgia, Hiu-Fai Chan, Germaine, Kaishibayeva, Gulnaz, Leonard, Hampton, Iwaki, Hirotaka, Chen, Honglei, F. Mata, Ignacio, Aasly, Jan O., Kim, Jonggeol Jeff, Lohmann, Katja, Kumar, Kishore, Shulman, Lisa, Parnetti, Lucilla, Periñan Tocino, Maria Teresa, Ibrahim Norlinah, Mohamed, Williams, Nigel, Kaiyrzhanov, Rauan, Krüger, Rejko, Wu, Ruey-Meei, Bandres-Ciga, Sara, Wu, Serena, Lim, Shen-Yang, Ertan, Sibel, Foroud, Tatiana, Pitcher, Toni, Tumas, Vitor, Luo, Wei, Zhou, Xiaopu, Tavadyan, Zaruhi

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National randomized controlled trial of virtual house calls for Parkinson disease von Beck, Christopher A, Beran, Denise B, Biglan, Kevin M, Boyd, Cynthia M, Dorsey, E Ray, Schmidt, Peter N, Simone, Richard, Willis, Allison W, Galifianakis, Nicholas B, Katz, Maya, Tanner, Caroline M, Dodenhoff, Kristen, Aldred, Jason, Carter, Julie, Fraser, Andrew, Jimenez-Shahed, Joohi, Hunter, Christine, Spindler, Meredith, Reichwein, Suzanne, Mari, Zoltan, Dunlop, Becky, Morgan, John C, McLane, Dedi, Hickey, Patrick, Gauger, Lisa, Richard, Irene Hegeman, Mejia, Nicte I, Bwala, Grace, Nance, Martha, Shih, Ludy C, Singer, Carlos, Vargas-Parra, Silvia, Zadikoff, Cindy, Okon, Natalia, Feigin, Andrew, Ayan, Jean, Vaughan, Christina, Pahwa, Rajesh, Dhall, Rohit, Hassan, Anhar, DeMello, Steven, Riggare, Sara S, Wicks, Paul, Achey, Meredith A, Elson, Molly J, Goldenthal, Steven, Keenan, H Tait, Korn, Ryan, Schwarz, Heidi, Sharma, Saloni, Stevenson, E Anna, Zhu, William

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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies von Nalls, Michael A, Plagnol, Vincent, Hernandez, Dena G, Sharma, Manu, Sheerin, Una-Marie, Saad, Mohamad, Simón-Sánchez, J, Schulte, Claudia, Lesage, Suzanne, Sveinbjörnsdóttir, Sigurlaug, Stefánsson, Kári, Martinez, Maria, Hardy, John, Heutink, Peter, Brice, Alexis, Gasser, Thomas, Singleton, Andrew B, Wood, Nicholas W

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A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity von van der Lee, Sven J., Conway, Olivia J., Jansen, Iris, Carrasquillo, Minerva M., Kleineidam, Luca, van den Akker, Erik, Hernández, Isabel, van Eijk, Kristel R., Stringa, Najada, Chen, Jason A., Zettergren, Anna, Andlauer, Till F. M., Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleó, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E., Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael, Fortea, Juan, Keogh, Michael J., Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A., Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M., Indakoetxea, Begoña, Collij, Lyduine E., Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W., van Berckel, Bart N. M., Wiendl, Heinz, Strickland, Samantha L., Pastor, Pau, Rodríguez Rodríguez, Eloy, Boeve, Bradley F., Petersen, Ronald C., Ferman, Tanis J., van Gerpen, Jay A., Reinders, Marcel J. T., Uitti, Ryan J., Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Mercè, Zettl, Uwe K., van Schoor, Natasja M., Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K., Ross, Owen A., Dickson, Dennis W., Graff-Radford, Neill R., Knopman, David, Rademakers, Rosa, Lemstra, Afina W., Pijnenburg, Yolande A. L., Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Huisman, Martijn A., Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A., Sørensen, Thorkild I. A., Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, Clarimón, Jordi, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W., Ramirez, Alfredo, Ruiz, Agustín, Slagboom, Eline, van der Flier, Wiesje M., Holstege, Henne

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Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus von Trabzuni, Daniah, Ryten, Mina, Emmett, Warren, Ramasamy, Adaikalavan, Lackner, Karl J, Zeller, Tanja, Walker, Robert, Smith, Colin, Lewis, Patrick A, Mamais, Adamantios, de Silva, Rohan, Vandrovcova, Jana, Hernandez, Dena, Nalls, Michael A, Sharma, Manu, Garnier, Sophie, Lesage, Suzanne, Simon-Sanchez, Javier, Gasser, Thomas, Heutink, Peter, Brice, Alexis, Singleton, Andrew, Cai, Huaibin, Schadt, Eric, Wood, Nicholas W, Bandopadhyay, Rina, Weale, Michael E, Hardy, John, Plagnol, Vincent

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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study von Ross, Owen A, Dr, Soto-Ortolaza, Alexandra I, BSc, Heckman, Michael G, MS, Aasly, Jan O, Prof, Abahuni, Nadine, MD, Annesi, Grazia, Prof, Bacon, Justin A, BSc, Bardien, Soraya, PhD, Bozi, Maria, MD, Brice, Alexis, Prof, Brighina, Laura, MD, Van Broeckhoven, Christine, Prof, Carr, Jonathan, Prof, Chartier-Harlin, Marie-Christine, Prof, Dardiotis, Efthimios, MD, Dickson, Dennis W, Prof, Diehl, Nancy N, BS, Elbaz, Alexis, Prof, Ferrarese, Carlo, Prof, Ferraris, Alessandro, MD, Fiske, Brian, PhD, Gibson, J Mark, Prof, Gibson, Rachel, PhD, Hadjigeorgiou, Georgios M, MD, Hattori, Nobutaka, Prof, Ioannidis, John PA, Prof, Jasinska-Myga, Barbara, MD, Jeon, Beom S, Prof, Kim, Yun Joong, Prof, Klein, Christine, Prof, Kruger, Rejko, MD, Kyratzi, Elli, MD, Lesage, Suzanne, PhD, Lin, Chin-Hsien, MD, Lynch, Timothy, Prof, Maraganore, Demetrius M, Prof, Mellick, George D, PhD, Mutez, Eugénie, MD, Nilsson, Christer, Prof, Opala, Grzegorz, Prof, Park, Sung Sup, Prof, Puschmann, Andreas, MD, Quattrone, Aldo, Prof, Sharma, Manu, PhD, Silburn, Peter A, Prof, Sohn, Young Ho, Prof, Stefanis, Leonidas, MD, Tadic, Vera, MD, Theuns, Jessie, PhD, Tomiyama, Hiroyuki, MD, Uitti, Ryan J, Prof, Valente, Enza Maria, Prof, van de Loo, Simone, PhD, Vassilatis, Demetrios K, PhD, Vilariño-Güell, Carles, PhD, White, Linda R, Prof, Wirdefeldt, Karin, MD, Wszolek, Zbigniew K, Prof, Wu, Ruey-Meei, Prof, Farrer, Matthew J, Prof

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Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease von Blauwendraat, Cornelis, Reed, Xylena, Kia, Demis A, Gan-Or, Ziv, Lesage, Suzanne, Pihlstrøm, Lasse, Guerreiro, Rita, Gibbs, J. Raphael, Sabir, Marya, Ahmed, Sarah, Ding, Jinhui, Alcalay, Roy N, Hassin-Baer, Sharon, Pittman, Alan M, Brooks, Janet, Edsall, Connor, Hernandez, Dena G, Chung, Sun Ju, Goldwurm, Stefano, Toft, Mathias, Schulte, Claudia, Bras, Jose, Wood, Nicholas W, Brice, Alexis, Morris, Huw R, Scholz, Sonja W, Nalls, Mike A, Singleton, Andrew B, Cookson, Mark R

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

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Graphene-silicon-on-insulator (GSOI) Schottky diode photodetectors von Selvi, Hakan, Hill, Ernie W, Parkinson, Patrick, Echtermeyer, Tim J

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

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Adaptive Global Innovative Learning Environment for Glioblastoma: GBM AGILE von Alexander, Brian M, Ba, Sujuan, Berger, Mitchel S, Berry, Donald A, Cavenee, Webster K, Chang, Susan M, Cloughesy, Timothy F, Jiang, Tao, Khasraw, Mustafa, Li, Wenbin, Mittman, Robert, Poste, George H, Wen, Patrick Y, Yung, W K Alfred, Barker, Anna D

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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease von Holmans, Peter, Moskvina, Valentina, Jones, Lesley, Sharma, Manu, Vedernikov, Alexey, Buchel, Finja, Saad, Mohamad, Sadd, Mohamad, Bras, Jose M, Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W, Martinez, Maria, Singleton, Andrew B, Nalls, Michael A, Hardy, John, Morris, Huw R, Williams, Nigel M

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