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Stephen Mullin

University of Plymouth

21H指数
71论文数
1.9K被引数
收录论文 26
发表时间
Loss of serotonergic function in carriers of PRKN mutations: a [11C]DASB PET studyPRKN突变携带者的血清素能功能丧失: [11C]DASB PET研究
err2026-01-29
err0
errOAAI
errEdoardo Rosario de Natale; Heather Wilson; Joji P. Verghese; Eoin Mulroy; Savvas Antoniadis; Alana Terry; Francesco Cavallieri; Micol Avenali; Pasquale Nigro; Varvara Valotassiou; Eugenii A. Rabiner; Stephen Mullin; Nicola Tambasco; Maria Teresa Pellecchia; Georgia Xiromerisiou; Vicky L. Marshall; Esther Sammler; Enza Maria Valente; Franco Valzania; Kailash P. Bhatia; Marios Politis
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Machine learning to predict stroke risk from routine hospital data: A systematic review
err2025-04-01
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errOAAI
errHeseltine-Carp, William; Courtman, Megan; Browning, Daniel; Kasabe, Aishwarya; Allen, Michael; Streeter, Adam; Ifeachor, Emmanuel; James, Martin; Mullin, Stephen
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Improving recruitment and retention of people with Parkinson's disease to clinical studies: A scoping review
err2025-01-14
err0
errOAAI
errPetty, Rebecca; Agarwal, Veena; Allison, Jennifer; Bartolomeu-Pires, Sandra; Bartlett, Michele; Boey, Timothy; Croucher, Rebecca; Collins, Helen; Collins, Sally; Davies, Emma; Duffen, Joy; Ellis-Doyle, Romy; Gonzalez-Robles, Cristina; Inches, Jemma; Mills, Georgia; Wonnacott, Sheila; Foltynie, Thomas; Allgar, Victoria; Thompson, Tom; Carroll, Camille B.; Mullin, Stephen; Louise-Zeissler, Marie
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Consensus Guidance for Genetic Counseling in GBA1 Variants: A Focus on Parkinson's DiseaseGBA1变异基因咨询的共识指南: 帕金森病的焦点
err2024-09-11
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errOAAI
errVieira, Sophia R. L.; Mezabrovschi, Roxana; Toffoli, Marco; Del Pozo, Sara Lucas; Menozzi, Elisa; Mullin, Stephen; Yalkic, Selen; Limbachiya, Naomi; Koletsi, Sofia; Loefflad, Nadine; Lopez, Grisel J.; Gan-Or, Ziv; Alcalay, Roy N.; Sidransky, Ellen; Schapira, Anthony H. V.
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Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study基因靶向试验时代基因检测的相关性: 罗斯托克帕金森病研究
errBRAIN
IF11.7
err2024-08-01
err8
errOAAI
errWestenberger, Ana; Skrahina, Volha; Usnich, Tatiana; Beetz, Christian; Vollstedt, Eva-Juliane; Laabs, Bjoern-Hergen; Paul, Jefri J.; Curado, Filipa; Skobalj, Snezana; Gaber, Hanaa; Olmedillas, Maria; Bogdanovic, Xenia; Ameziane, Najim; Schell, Nathalie; Aasly, Jan Olav; Afshari, Mitra; Agarwal, Pinky; Aldred, Jason; Alonso-Frech, Fernando; Anderson, Roderick; Araujo, Rui; Arkadir, David; Avenali, Micol; Balal, Mehmet; Benizri, Sandra; Bette, Sagari; Bhatia, Perminder; Bonello, Michael; Braga-Neto, Pedro; Brauneis, Sarah; Cardoso, Francisco Eduardo Costa; Cavallieri, Francesco; Classen, Joseph; Cohen, Lisa; Coletta, Della; Crosiers, David; Cullufi, Paskal; Dashtipour, Khashayar; Demirkiran, Meltem; Aguiar, Patricia de Carvalho; De Rosa, Anna; Djaldetti, Ruth; Dogu, Okan; Ghilardi, Maria Gabriela dos Santos; Eggers, Carsten; Elibol, Bulent; Ellenbogen, Aaron; Ertan, Sibel; Fabiani, Giorgio; Falkenburger, Bjoern H.; Farrow, Simon; Fay-Karmon, Tsviya; Ferencz, Gerald J.; Fonoff, Erich Talamoni; Fragoso, Yara Dadalti; Genc, Gencer; Gorospe, Arantza; Grandas, Francisco; Gruber, Doreen; Gudesblatt, Mark; Gurevich, Tanya; Hagenah, Johann; Hanagasi, Hasmet A.; Hassin-Baer, Sharon; Hauser, Robert A.; Hernandez-Vara, Jorge; Herting, Birgit; Hinson, Vanessa K.; Hogg, Elliot; Hu, Michele T.; Hummelgen, Eduardo; Hussey, Kelly; Infante, Jon; Isaacson, Stuart H.; Jauma, Serge; Koleva-Alazeh, Natalia; Kuhlenbaeumer, Gregor; Kuehn, Andrea; Litvan, Irene; Lopez-Manzanares, Lydia; Luxmore, McKenzie; Manandhar, Sujeena; Marcaud, Veronique; Markopoulou, Katerina; Marras, Connie; McKenzie, Mark; Matarazzo, Michele; Merello, Marcelo; Mollenhauer, Brit; Morgan, John C.; Mullin, Stephen; Musacchio, Thomas; Myers, Bennett; Negrotti, Anna; Nieves, Anette; Nitsan, Zeev; Oskooilar, Nader; Oztop-Cakmak, Ozgur; Pal, Gian; Pavese, Nicola; Percesepe, Antonio; Piccoli, Tommaso; de Souza, Carolina Pinto; Prell, Tino; Pulera, Mark; Raw, Jason; Reetz, Kathrin; Reiner, Johnathan; Rosenberg, David; Ruiz-Lopez, Marta; Martinez, Javier Ruiz; Sammler, Esther; Santos-Lobato, Bruno Lopes; Saunders-Pullman, Rachel; Schlesinger, Ilana; Schofield, Christine M.; Schumacher-Schuh, Artur F.; Scott, Burton; Sesar, ngel; Shafer, Stuart J.; Sheridan, Ray; Silverdale, Monty; Sophia, Rani; Spitz, Mariana; Stathis, Pantelis; Stocchi, Fabrizio; Tagliati, Michele; Tai, Yen F.; Terwecoren, Annelies; Thonke, Sven; Toenges, Lars; Toschi, Giulia; Tumas, Vitor; Urban, Peter Paul; Vacca, Laura; Vandenberghe, Wim; Valente, Enza Maria; Valzania, Franco; Vela-Desojo, Lydia; Weill, Caroline; Weise, David; Wojcieszek, Joanne; Wolz, Martin; Yahalom, Gilad; Yalcin-Cakmakli, Gul; Zittel, Simone; Zlotnik, Yair; Kandaswamy, Krishna K.; Balck, Alexander; Hanssen, Henrike; Borsche, Max; Lange, Lara M.; Csoti, Ilona; Lohmann, Katja; Kasten, Meike; Brueggemann, Norbert; Rolfs, Arndt; Klein, Christine; Bauer, Peter
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Whole genome sequencing for copy number variant detection to improve diagnosis and management of rare diseases
err2024-06-05
err2
errOAAI
errBowman, Pamela; Grimes, Hannah; Dallosso, Anthony R.; Berry, Ian; Mullin, Stephen; Rankin, Julia; Low, Karen J.
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Phenotypic effect of GBA1 variants in individuals with and without Parkinson's disease: The RAPSODI study
err2023-11-01
err6
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errToffoli, Marco; Chohan, Harneek; Mullin, Stephen; Jesuthasan, Aaron; Yalkic, Selen; Koletsi, Sofia; Menozzi, Elisa; Rahall, Soraya; Limbachiya, Naomi; Loefflad, Nadine; Higgins, Abigail; Bestwick, Jonathan; Lucas-Del-Pozo, Sara; Fierli, Federico; Farbos, Audrey; Mezabrovschi, Roxana; Lee-Yin, Chiao; Schrag, Anette; Moreno-Martinez, David; Hughes, Derralynn; Noyce, Alastair; Colclough, Kevin; Jeffries, Aaron R.; Proukakis, Christos; Schapira, Anthony H. V.
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Towards a multi-arm multi-stage platform trial of disease modifying approaches in Parkinson's disease迈向帕金森氏病疾病改善方法的多臂多阶段平台试验
errBRAIN
IF11.7
err2023-02-28
err16
errOAAI
errFoltynie, Tom; Gandhi, Sonia; Gonzalez-Robles, Cristina; Zeissler, Marie-Louise; Mills, Georgia; Barker, Roger; Carpenter, James; Schrag, Anette; Schapira, Anthony; Bandmann, Oliver; Mullin, Stephen; Duffen, Joy; McFarthing, Kevin; Chataway, Jeremy; Parmar, Mahesh; Carroll, Camille
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ARTIFICIAL INTELLIGENCE BASED DETECTION OF PARKINSON'S DISEASE IN MAGNETIC RESONANCE IMAGING BRAIN SCANS
err2022-08-12
err1
PREAI
errCourtman, Megan; Thurston, Mark; McGavin, Lucy; Caroll, Camille; Sun, Lingfen; Ifeachor, Emmanuel; Mullin, Stephen
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Comprehensive short and long read sequencing analysis for the Gaucher and Parkinson's disease-associated GBA gene
err2022-07-06
err23
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errToffoli, Marco; Chen, Xiao; Sedlazeck, Fritz J.; Lee, Chiao-Yin; Mullin, Stephen; Higgins, Abigail; Koletsi, Sofia; Garcia-Segura, Monica Emili; Sammler, Esther; Scholz, Sonja W.; Schapira, Anthony H. V.; Eberle, Michael A.; Proukakis, Christos
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Combined GCASE/ALPHA-synuclein pattern may identify specific prodomal PD patterns in GBA carriers: A cluster analysis study
err2021-10-01
err0
PREAI
errAvenali, Micol; Cerri, Silvia; Cerami, Chiara; Crespi, Chiara; Gegg, Matthew; Mullin, Stephen; Toffoli, Marco; Hughes, Derralyn; Valente, Enza; Tassorelli, Cristina; Schapira, Anthony; Blandini, Fabio
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Intronic Haplotypes in the GBA Gene Do Not Predict Age at Diagnosis of Parkinson's Disease
err2021-05-19
err4
errOAAI
errToffoli, Marco; Higgins, Abigail; Lee, Chiao; Koletsi, Sofia; Chen, Xiao; Eberle, Michael; Sedlazeck, Fritz J.; Mullin, Stephen; Proukakis, Christos; Schapira, Anthony H., V
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Brain Microglial Activation Increased in Glucocerebrosidase (GBA) Mutation Carriers without Parkinson's disease
err2020-12-05
err49
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errMullin, Stephen; Stokholm, Morten Gersel; Hughes, Derralyn; Mehta, Atul; Parbo, Peter; Hinz, Rainer; Pavese, Nicola; Brooks, David J.; Schapira, Anthony H., V
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USABILITY TESTING OF A NON-MOTOR SYMPTOM APP IN PD
err2019-11-14
err0
PREAI
errDominey, Thea; Mullin, Stephen; Edwards, Emma; Whipps, John; Whipps, Sue; Carroll, Camille
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Evolution and clustering of prodromal parkinsonian features in GBA1 carriers
err2019-06-28
err38
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errMullin, Stephen; Beavan, Michelle; Bestwick, Jonathan; McNeill, Alisdair; Proukakis, Christos; Cox, Timothy; Hughes, Derralynn; Mehta, Atul; Zetterberg, Henrik; Schapira, Anthony H. V.
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Evolution of prodromal parkinsonian features in a cohort of GBA mutation-positive individuals: a 6-year longitudinal study
err2019-06-20
err48
PREAI
errAvenali, Micol; Toffoli, Marco; Mullin, Stephen; McNeil, Alisdair; Hughes, Derralynn A.; Mehta, A.; Blandini, Fabio; Schapira, Anthony H. V.
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Glucocerebrosidase mutations and synucleinopathies: Toward a model of precision medicine
err2018-12-27
err74
PREAI
errBlandini, Fabio; Cilia, Roberto; Cerri, Silvia; Pezzoli, Gianni; Schapira, Anthony H. V.; Mullin, Stephen; Lanciego, Jose L.
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