المؤلفون: Manzoni, Claudia, Kia, Demis A., Ferrari, Raffaele, Leonenko, Ganna, Costa, Beatrice, Saba, Valentina, Jabbari, Edwin, Tan, Manuela MX, Albani, Diego, Alvarez, Victoria, Alvarez, Ignacio, Andreassen, Ole A., Angiolillo, Antonella, Arighi, Andrea, Baker, Matt, Benussi, Luisa, Bessi, Valentina, Binetti, Giuliano, Blackburn, Daniel J., Boada, Merce, Boeve, Bradley F., Borrego-Ecija, Sergi, Borroni, Barbara, Bråthen, Geir, Brooks, William S., Bruni, Amalia C., Caroppo, Paola, Bandres-Ciga, Sara, Clarimon, Jordi, Colao, Rosanna, Cruchaga, Carlos, Danek, Adrian, de Boer, Sterre CM, de Rojas, Itziar, di Costanzo, Alfonso, Dickson, Dennis W., Diehl-Schmid, Janine, Dobson-Stone, Carol, Dols-Icardo, Oriol, Donizetti, Aldo, Dopper, Elise, Durante, Elisabetta, Ferrari, Camilla, Forloni, Gianluigi, Frangipane, Francesca, Fratiglioni, Laura, Kramberger, Milica G., Galimberti, Daniela, Gallucci, Maurizio, García-González, Pablo, Ghidoni, Roberta, Giaccone, Giorgio, Graff, Caroline, Graff-Radford, Neill R., Grafman, Jordan, Halliday, Glenda M., Hernandez, Dena G., Hjermind, Lena E., Hodges, John R., Holloway, Guy, Huey, Edward D., Illán-Gala, Ignacio, Josephs, Keith A., Knopman, David S., Kristiansen, Mark, Kwok, John B., Leber, Isabelle, Leonard, Hampton L., Libri, Ilenia, Lleo, Alberto, Mackenzie, Ian R., Madhan, Gaganjit K., Maletta, Raffaele, Marquié, Marta, Maver, Ales, Menendez-Gonzalez, Manuel, Milan, Graziella, Miller, Bruce L., Morris, Christopher M., Morris, Huw R., Nacmias, Benedetta, Newton, Judith, Nielsen, Jørgen E., Nilsson, Christer, Novelli, Valeria, Padovani, Alessandro, Pal, Suvankar, Pasquier, Florence, Pastor, Pau, Perneczky, Robert, Peterlin, Borut, Petersen, Ronald C., Piguet, Olivier, Pijnenburg, Yolande AL, Puca, Annibale A., Rademakers, Rosa, Rainero, Innocenzo, Reus, Lianne M., Richardson, Anna MT, Riemenschneider, Matthias, Rogaeva, Ekaterina, Rogelj, Boris, Rollinson, Sara, Rosen, Howard, Rossi, Giacomina, Rowe, James B., Rubino, Elisa, Ruiz, Agustin, Salvi, Erika, Sanchez-Valle, Raquel, Sando, Sigrid Botne, Santillo, Alexander F., Saxon, Jennifer A., Schlachetzki, Johannes CM, Scholz, Sonja W., Seelaar, Harro, Seeley, William W., Serpente, Maria, Sorbi, Sandro, Sordon, Sabrina, St George-Hyslop, Peter, Thompson, Jennifer C., Van Broeckhoven, Christine, Van Deerlin, Vivianna M., Van der Lee, Sven J., Van Swieten, John, Tagliavini, Fabrizio, van der Zee, Julie, Veronesi, Arianna, Vitale, Emilia, Waldo, Maria Landqvist, Yokoyama, Jennifer S., Nalls, Mike A., Momeni, Parastoo, Singleton, Andrew B., Hardy, John, Escott-Price, Valentina

المصدر: American Journal of Human Genetics MultiPark: Multidisciplinary research focused on Parkinson´s disease. 111(7):1316-1329

مصطلحات موضوعية: Medicin och hälsovetenskap, Klinisk medicin, Neurologi, Medical and Health Sciences, Clinical Medicine, Neurology

URL الوصول: https://lup.lub.lu.se/record/c85863e6-3c3b-4645-80f8-238c58f493f6
http://dx.doi.org/10.1016/j.ajhg.2024.05.017

المؤلفون: Brolin, Kajsa, Bandres-Ciga, Sara, Leonard, Hampton, Makarious, Mary B., Blauwendraat, Cornelis, Mata, Ignacio F., Foo, Jia Nee, Pihlstrøm, Lasse, Swanberg, Maria, Gan-Or, Ziv, Tan, Manuela MX

المصدر: Neurobiology of Aging EpiHealth: Epidemiology for Health MultiPark: Multidisciplinary research focused on Parkinson´s disease. 109:264-268

مصطلحات موضوعية: Genetics, Parkinson's disease, RIC3, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

URL الوصول: https://lup.lub.lu.se/record/d88f01a8-9f86-4f7c-becb-3e7e36aaf438
http://dx.doi.org/10.1016/j.neurobiolaging.2021.08.009

المؤلفون: Lawton, Michael, Tan, Manuela Mx, Ben-Shlomo, Yoav, Baig, Fahd, Barber, Thomas, Klein, Johannes C, Evetts, Samuel G, Millin, Stephanie, Malek, Naveed, Grosset, Katherine, Barker, Roger A, Williams, Nigel, Burn, David J, Foltynie, Thomas, Morris, Huw R, Wood, Nicholas, Grosset, Donald G, Hu, Michele Tao-Ming

المساهمون: Lawton, Michael [0000-0002-3419-0354], Tan, Manuela Mx [0000-0001-5835-669X], Klein, Johannes C [0000-0002-8553-2801], Foltynie, Thomas [0000-0003-0752-1813], Morris, Huw R [0000-0002-5473-3774], Hu, Michele Tao-Ming [0000-0001-6382-5841], Apollo - University of Cambridge Repository

مصطلحات موضوعية: GENETICS, PARKINSON'S DISEASE

وصف الملف: application/pdf; text/xml

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de35023a94eda9939419c0a3419f087e
https://www.repository.cam.ac.uk/handle/1810/338592

المؤلفون: Tan, Manuela MX, Malek, Naveed, Lawton, Michael A, Hubbard, Leon, Pittman, Alan M, Joseph, Theresita, Hehir, Jason, Swallow, Diane MA, Grosset, Katherine A, Marrinan, Sarah L, Bajaj, Nin, Barker, Roger A, Burn, David J, Bresner, Catherine, Foltynie, Thomas, Hardy, John, Wood, Nicholas, Ben-Shlomo, Yoav, Grosset, Donald G, Williams, Nigel M, Morris, Huw R

المساهمون: Barker, Roger [0000-0001-8843-7730], Apollo - University of Cambridge Repository

المصدر: Brain

مصطلحات موضوعية: Adult, Aged, 80 and over, Male, Genotype, phenotype, prevalence, Parkinson Disease, Original Articles, Mendelian Randomization Analysis, Middle Aged, United Kingdom, nervous system diseases, Cohort Studies, Population Surveillance, Mutation, Parkinson’s disease, Humans, Female, genetics, Genetic Testing, Prospective Studies, heterogeneity, Aged

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::740488f08ea587cfa7e9e1bde7807d23
https://openaccess.sgul.ac.uk/id/eprint/111060/1/awz191.pdf

المؤلفون: Tan, Manuela MX, Malek, Naveed, Lawton, Michael A, Hubbard, Leon, Pittman, Alan M, Joseph, Theresita, Hehir, Jason, Swallow, Diane MA, Grosset, Katherine A, Marrinan, Sarah L, Bajaj, Nin, Barker, Roger A, Burn, David J, Bresner, Catherine, Foltynie, Thomas, Hardy, John, Wood, Nicholas, Ben-Shlomo, Yoav, Grosset, Donald G, Williams, Nigel M, Morris, Huw R

مصطلحات موضوعية: Adult, Aged, 80 and over, Male, Genotype, phenotype, prevalence, Parkinson Disease, Mendelian Randomization Analysis, Middle Aged, United Kingdom, nervous system diseases, 3. Good health, Cohort Studies, Population Surveillance, Mutation, Parkinson’s disease, Humans, genetics, Female, Genetic Testing, Prospective Studies, heterogeneity, Aged

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::8dcaf4e622bd78c1123ec14ab417c607

المؤلفون: Tan, Manuela MX, Lawton, Michael A, Jabbari, Edwin, Reynolds, Regina H, Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Pollard, Miriam I, Hubbard, Leon, Malek, Naveed, Grosset, Katherine A, Marrinan, Sarah L, Bajaj, Nin, Barker, Roger A, Burn, David J, Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W, Williams-Gray, Caroline H, Hardy, John, Nalls, Michael A, Singleton, Andrew B, Williams, Nigel M, Ben-Shlomo, Yoav, Hu, Michele TM, Grosset, Donald G, Shoai, Maryam, Morris, Huw R

مصطلحات موضوعية: genome-wide association study, Cognition, Parkinson's disease, Disease Progression, Humans, genetics, Parkinson Disease, progression, Biomarkers, 3. Good health

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::419f777324a7304a256312e2eae0cd68

المؤلفون: Tan, Manuela MX, Hong, James S, Bras, Jose, Lubbe, Steven J, Grosset, Donald G, Wood, Nick W, Schapira, Anthony H, Hardy, John, Houlden, Henry, Morris, Huw R

المصدر: Journal of Neurology, Neurosurgery, & Psychiatry (JNNP); 2017, Vol. 88 Issue: Supplement 1 pA60-A61, 2p

المؤلفون: Rees, Richard N, Tan, Manuela MX, Pittman, Alan M, Ben-Shlomo, Yoav, Williams, Nigel M, Grosset, Donald G, Morris, Huw R

المصدر: Journal of Neurology, Neurosurgery, & Psychiatry (JNNP); 2017, Vol. 88 Issue: Supplement 1 pA38-A38, 1p

المؤلفون: Naveed Malek, Michele T.M. Hu, Miriam I Pollard, Hirotaka Iwaki, Mike A. Nalls, Sofia Kanavou, Caroline H. Williams-Gray, Catherine Bresner, Cornelis Blauwendraat, Yoav Ben-Shlomo, Roger A. Barker, John Hardy, Sarah L Marrinan, Manuela Tan, Donald G. Grosset, Katherine A Grosset, David J. Burn, Michael A Lawton, Leon Hubbard, Edwin Jabbari, Nin Bajaj, Andrew B. Singleton, Huw R. Morris, Nigel Williams, Thomas Foltynie, Maryam Shoai, Regina H. Reynolds, Nicholas W. Wood

المساهمون: Tan, Manuela MX [0000-0001-5835-669X], Jabbari, Edwin [0000-0001-6844-882X], Iwaki, Hirotaka [0000-0002-8982-7885], Foltynie, Thomas [0000-0003-0752-1813], Williams-Gray, Caroline H [0000-0002-2648-9743], Morris, Huw R [0000-0002-5473-3774], Apollo - University of Cambridge Repository

المصدر: Tan, M M X, Lawton, M A, Jabbari, E, Reynolds, R H, Iwaki, H, Blauwendraat, C, Kanavou, S, Pollard, M I, Hubbard, L, Malek, N, Grosset, K A, Marrinan, S L, Bajaj, N, Barker, R A, Burn, D J, Bresner, C, Foltynie, T, Wood, N W, Williams-Gray, C H, Hardy, J, Nalls, M A, Singleton, A B, Williams, N M, Ben-Shlomo, Y, Hu, M T M, Grosset, D G, Shoai, M & Morris, H R 2020, ' Genome-wide association studies of cognitive and motor progression in Parkinson's disease ', Movement Disorders, vol. 36, no. 2, pp. 424-433 . https://doi.org/10.1002/mds.28342

مصطلحات موضوعية: 0301 basic medicine, Apolipoprotein E, Oncology, medicine.medical_specialty, Movement disorders, Parkinson's disease, Genome-wide association study, Disease, 03 medical and health sciences, Cognition, 0302 clinical medicine, Internal medicine, Humans, Medicine, genetics, Allele, Cognitive impairment, 030304 developmental biology, Genetic association, 0303 health sciences, genome-wide association study, business.industry, Parkinson Disease, medicine.disease, 3. Good health, 030104 developmental biology, Neurology, Disease Progression, Disease risk, progression, Neurology (clinical), medicine.symptom, business, Biomarkers, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbef07c1d8dea584285b7afd5951e034

المؤلفون: Lawton M; Population Health Sciences, University of Bristol Medical School, Bristol, UK Michael.Lawton@bristol.ac.uk., Tan MM; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.; UCL Movement Disorders Centre, University College London, London, UK., Ben-Shlomo Y; Population Health Sciences, University of Bristol Medical School, Bristol, UK., Baig F; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Molecular and Clinical Sciences Institute, St. George's University of London, London, UK., Barber T; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Oxford Parkinson's Disease Centre, University of Oxford, Oxford, UK., Klein JC; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Oxford Parkinson's Disease Centre, University of Oxford, Oxford, UK., Evetts SG; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Oxford Parkinson's Disease Centre, University of Oxford, Oxford, UK., Millin S; Oxford Parkinson's Disease Centre, University of Oxford, Oxford, UK.; Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, UK., Malek N; Department of Neurology, Queen's Hospital, Romford, Essex, UK., Grosset K; Department of Neurology, Institute of Neurological Sciences, Queen Elizabeth University Hospital and University of Glasgow, Glasgow, UK., Barker RA; Cambridge Centre for Brain Repair, University of Cambridge, Cambridge, UK., Williams N; Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK., Burn DJ; Faculty of Medical Sciences, Newcastle University, Newcastle, UK., Foltynie T; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK., Morris HR; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK.; UCL Movement Disorders Centre, University College London, London, UK., Wood N; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, UK., Grosset DG; Department of Neurology, Institute of Neurological Sciences, Queen Elizabeth University Hospital and University of Glasgow, Glasgow, UK., Hu MT; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.; Oxford Parkinson's Disease Centre, University of Oxford, Oxford, UK.

المصدر: Journal of neurology, neurosurgery, and psychiatry [J Neurol Neurosurg Psychiatry] 2022 Jun 22. Date of Electronic Publication: 2022 Jun 22.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 2985191R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-330X (Electronic) Linking ISSN: 00223050 NLM ISO Abbreviation: J Neurol Neurosurg Psychiatry Subsets: MEDLINE