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Patrizia Rizzu
Researcher at German Center for Neurodegenerative Diseases
Publications - 101
Citations - 17635
Patrizia Rizzu is an academic researcher from German Center for Neurodegenerative Diseases. The author has contributed to research in topics: Frontotemporal dementia & Gene. The author has an hindex of 44, co-authored 92 publications receiving 15304 citations. Previous affiliations of Patrizia Rizzu include Erasmus University Medical Center & VU University Amsterdam.
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Journal ArticleDOI
Functional annotation of human long noncoding RNAs via molecular phenotyping
Jordan A. Ramilowski,Chi Wai Yip,Saumya Agrawal,Jen-Chien Chang,Yari Ciani,Ivan V. Kulakovskiy,Mickaël Mendez,Jasmine Li Ching Ooi,John F. Ouyang,Nicholas J. Parkinson,Andreas Petri,Leonie Roos,Jessica Severin,Kayoko Yasuzawa,Imad Abugessaisa,Altuna Akalin,Ivan Antonov,Erik Arner,Alessandro Bonetti,Hidemasa Bono,Beatrice Borsari,Frank Brombacher,Christopher J. F. Cameron,Carlo Vittorio Cannistraci,Ryan Cardenas,Melissa Cardon,Howard Y. Chang,Josée Dostie,Luca Ducoli,Alexander V. Favorov,Alexandre Fort,Diego Garrido,Noa Gil,Juliette Gimenez,Reto Guler,Lusy Handoko,Jayson Harshbarger,Akira Hasegawa,Yuki Hasegawa,Kosuke Hashimoto,Norihito Hayatsu,Peter Heutink,Tetsuro Hirose,Eddie Luidy Imada,Masayoshi Itoh,Bogumil Kaczkowski,Aditi Kanhere,Emily Kawabata,Hideya Kawaji,Tsugumi Kawashima,S. Thomas Kelly,Miki Kojima,Naoto Kondo,Haruhiko Koseki,Tsukasa Kouno,Anton Kratz,Mariola Kurowska-Stolarska,Andrew T. Kwon,Jeffrey T. Leek,Andreas Lennartsson,Marina Lizio,Fernando López-Redondo,Joachim Luginbühl,Shiori Maeda,Vsevolod J. Makeev,Vsevolod J. Makeev,Luigi Marchionni,Yulia A. Medvedeva,Yulia A. Medvedeva,Aki Minoda,Ferenc Müller,Manuel Muñoz-Aguirre,Mitsuyoshi Murata,Hiromi Nishiyori,Kazuhiro R. Nitta,Shuhei Noguchi,Yukihiko Noro,Ramil N. Nurtdinov,Yasushi Okazaki,Valerio Orlando,Denis Paquette,Callum J.C. Parr,Owen J. L. Rackham,Patrizia Rizzu,Diego Fernando Sánchez Martinez,Albin Sandelin,Pillay Sanjana,Colin A. Semple,Youtaro Shibayama,Divya M. Sivaraman,Takahiro Suzuki,Suzannah C. Szumowski,Michihira Tagami,Martin S. Taylor,Chikashi Terao,Malte Thodberg,Supat Thongjuea,Vidisha Tripathi,Igor Ulitsky,Roberto Verardo,Ilya E. Vorontsov,Chinatsu Yamamoto,Robert Young,J Kenneth Baillie,Alistair R. R. Forrest,Roderic Guigó,Michael M. Hoffman,Chung-Chau Hon,Takeya Kasukawa,Sakari Kauppinen,Juha Kere,Boris Lenhard,Claudio Schneider,Harukazu Suzuki,Ken Yagi,Michiel J. L. de Hoon,Jay W. Shin,Piero Carninci +117 more
TL;DR: The largest-to-date lncRNA knockdown data set with molecular phenotyping is disseminated for further exploration and functional roles for ZNF213-AS1 and lnc-KHDC3L-2 are highlighted.
Journal ArticleDOI
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Iris E. Jansen,Iris E. Jansen,Hui Ye,Sasja Heetveld,Marie C. Lechler,Helen Michels,Renée I. Seinstra,Steven J. Lubbe,Steven J. Lubbe,Valérie Drouet,Suzanne Lesage,Elisa Majounie,J. Raphael Gibbs,Mike A. Nalls,Mina Ryten,Mina Ryten,Juan A. Botía,Jana Vandrovcova,Javier Simón-Sánchez,Javier Simón-Sánchez,Melissa Castillo-Lizardo,Patrizia Rizzu,Cornelis Blauwendraat,Amit K. Chouhan,Yarong Li,Puja Yogi,Najaf Amin,Cornelia M. van Duijn,Huw R. Morris,Alexis Brice,Andrew B. Singleton,Della C. David,Ellen A. A. Nollen,Shushant Jain,Joshua M. Shulman,Peter Heutink,Peter Heutink,Peter Heutink +37 more
TL;DR: By integrating human genetic and functional evidence, this work identifies several PD susceptibility gene candidates for further investigation and highlights a powerful experimental strategy with broad applicability for future studies of disorders with complex genetic etiologies.
Journal ArticleDOI
Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease
Maria G. Macedo,Dagmar Verbaan,Y. Fang,Stephanie M. van Rooden,Martine Visser,Burcu Anar,Antonella Uras,Justus L. Groen,Patrizia Rizzu,Jacobus J. van Hilten,Peter Heutink +10 more
TL;DR: Parkin is the most frequently mutated gene in this EOPD cohort, followed by DJ‐1, PINK1 and LRRK2, and the low overall mutation frequency indicates that the extrapolation of mutation frequencies from other populations should be applied with caution.
Journal ArticleDOI
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.
Vincenzo Bonifati,Vincenzo Bonifati,Guido J. Breedveld,Ferdinando Squitieri,Nicola Vanacore,Pierluigi Brustenghi,Biswadjiet S. Harhangi,Pasquale Montagna,Milena Cannella,Giovanni Fabbrini,Patrizia Rizzu,Cornelia M. van Duijn,Ben A. Oostra,Giuseppe Meco,Peter Heutink +14 more
TL;DR: Location of autosomal recessive early‐onset parkinsonism to PARK7 is confirmed, suggesting it to be a frequent locus, and assignment of families to either PARK6 or PARK7 might be difficult because of the proximity of the two loci on chromosome 1p.
Journal ArticleDOI
Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric disease.
Xianjun Dong,Zhixiang Liao,David Gritsch,Yavor Hadzhiev,Yunfei Bai,Yunfei Bai,Joseph J. Locascio,Joseph J. Locascio,Boris Guennewig,Boris Guennewig,Boris Guennewig,Ganqiang Liu,Cornelis Blauwendraat,Tao Wang,Charles H. Adler,John C. Hedreen,Richard L.M. Faull,Matthew P. Frosch,Peter T. Nelson,Patrizia Rizzu,Antony A. Cooper,Antony A. Cooper,Peter Heutink,Thomas G. Beach,John S. Mattick,John S. Mattick,Ferenc Müller,Clemens R. Scherzer +27 more
TL;DR: This study shows that enhancers in dopamine neurons link genetic variation to neuropsychiatric traits, and expresses quantitative trait locus analysis revealed that Parkinson’s disease-associated variants on chromosome 17q21 cis-regulate the expression of an enhancer RNA in dopamine cells.