Marialuisa Quadri

3.6k citations

22 papers · 1.2k indexed · h-index 16

Neurology top 2%
Physiology top 10%
Cellular and Molecular Neuroscience top 10%
Molecular Biology
Nutrition and Dietetics top 5%

Co-authors: Vincenzo Bonifati Guido J. Breedveld Simone Olgiati Ben A. Oostra Giovanni Cossu Josja Graafland Mario Quarantelli Marina Picillo
Topics: Parkinson's Disease Mechanisms and Treatments (14 papers)Neurological diseases and metabolism (12 papers)Neurological disorders and treatments (4 papers)
Cited by: Neurology Nutrition and Dietetics
Journals: The American Journal of Human Genetics Neurobiology of Aging Movement Disorders
Partner nations: Netherlands Italy United States

In The Last Decade

Marialuisa Quadri

22 papers receiving 1.1k citations

Peers

Countries citing papers authored by Marialuisa Quadri

Since Specialization

Citations

This map shows the geographic impact of Marialuisa Quadri's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marialuisa Quadri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marialuisa Quadri more than expected).

Fields of papers citing papers by Marialuisa Quadri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marialuisa Quadri. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marialuisa Quadri. The network helps show where Marialuisa Quadri may publish in the future.

Co-authorship network of co-authors of Marialuisa Quadri

This figure shows the co-authorship network connecting the top 25 collaborators of Marialuisa Quadri. A scholar is included among the top collaborators of Marialuisa Quadri based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marialuisa Quadri. Marialuisa Quadri is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	LRP10 variants in progressive supranuclear palsy 2020 ·Neurobiology of Aging ·Leonie J.M. Vergouw,Shamiram Melhem,Laura Donker Kaat,Wang Zheng Chiu,(unknown),Guido J. Breedveld,Agnita J.W. Boon,Li-San Wang,Adam C. Naj,(unknown),Laura B. Cantwell,Marialuisa Quadri,Owen A. Ross,Dennis W. Dickson,Gerard D. Schellenberg,John C. van Swieten,Vincenzo Bonifati,Frank Jan de Jong	5
2	Clinical and Pathological Phenotypes of LRP10 Variant Carriers with Dementia 2020 ·Journal of Alzheimer s Disease ·Leonie J.M. Vergouw,Hanneke Geut,Guido J. Breedveld,(unknown),Marialuisa Quadri,(unknown),Annemieke J.M. Rozemüller,John C. van Swieten,Frank Jan de Jong,Wilma D. J. van de Berg,Vincenzo Bonifati	5
3	LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the Netherlands 2019 ·Parkinsonism & Related Disorders ·Leonie J.M. Vergouw,Annemieke Ruitenberg,Tsz Hang Wong,Shamiram Melhem,Guido J. Breedveld,Chiara Criscuolo,Giuseppe De Michele,Frank Jan de Jong,Vincenzo Bonifati,John C. van Swieten,Marialuisa Quadri	13
4	Characterization of Brain Lysosomal Activities in GBA-Related and Sporadic Parkinson’s Disease and Dementia with Lewy Bodies 2018 ·Molecular Neurobiology ·Tim E. Moors,Silvia Paciotti,Angela Ingrassia,Marialuisa Quadri,Guido J. Breedveld,Anna Tasegian,Davide Chiasserini,Paolo Eusebi,Gonzalo Durán-Pacheco,Thomas Kremer,Paolo Calabresi,Vincenzo Bonifati,Lucilla Parnetti,Tommaso Beccari,Wilma D. J. van de Berg	108
5	ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia 2018 ·Neurology Genetics ·Christian G. Bouwkamp,Zaid Afawi,Aviva Fattal‐Valevski,Inge E. Krabbendam,Stefano Rivetti,Rafik Masalha,Marialuisa Quadri,Guido J. Breedveld,(unknown),Muhammad Abu Tailakh,H. Berna Beverloo,Giovanni Stévanin,Alexis Brice,Wilfred F. J. van IJcken,Meike W. Vernooij,Amalia M. Dolga,Femke M.S. de Vrij,Vincenzo Bonifati,Steven A. Kushner	22
6	PTRHD1 Loss‐of‐function mutation in an african family with juvenile‐onset Parkinsonism and intellectual disability 2018 ·Movement Disorders ·(unknown),Jonathan Carr,Soraya Bardien,(unknown),(unknown),Guido J. Breedveld,Rick van Minkelen,Rutger W. W. Brouwer,Wilfred F. J. van IJcken,Marjon A. van Slegtenhorst,Vincenzo Bonifati,Marialuisa Quadri	17
7	The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPAN 2017 ·Parkinsonism & Related Disorders ·Simone Olgiati,Okan Doğu,Zeynep Tüfekçıoğlu,(unknown),Esen Saka,Murat Gültekin,Hakan Kaleağası,(unknown),Josja Graafland,Guido J. Breedveld,Marialuisa Quadri,(unknown),(unknown),(unknown),(unknown),Başar Bılgıç,Bülent Elibol,Murat Emre,Haşmet Hanağası,Vincenzo Bonifati	31
8	TMEM230: How does it fit in the etiology and pathogenesis of Parkinson's disease? 2017 ·Movement Disorders ·Wim Mandemakers,Marialuisa Quadri,María Stamelou,Vincenzo Bonifati	8
9	Genetics of movement disorders in the next‐generation sequencing era 2016 ·Movement Disorders ·Simone Olgiati,Marialuisa Quadri,Vincenzo Bonifati	22
10	Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's disease 2015 ·Parkinsonism & Related Disorders ·(unknown),(unknown),E B Rolfe,Simone Olgiati,Marialuisa Quadri,Erik Simons,Karen Morrison,Vincenzo Bonifati,David Nicholl	22
11	Early-onset parkinsonism caused by alpha-synuclein gene triplication: Clinical and genetic findings in a novel family 2015 ·Parkinsonism & Related Disorders ·Simone Olgiati,Astrid Thomas,Marialuisa Quadri,Guido J. Breedveld,Josja Graafland,(unknown),Hannie Douben,Annelies de Klein,Marco Onofrj,Vincenzo Bonifati	47
12	Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes 2015 ·Movement Disorders ·Marialuisa Quadri,(unknown),Suvasini Sharma,Simone Olgiati,Josja Graafland,Guido J. Breedveld,(unknown),(unknown),Puneet Jain,Satinder Aneja,Atin Kumar,(unknown),(unknown),Bibek Talukdar,Vincenzo Bonifati	49
13	A new Turkish family with homozygous FBXO7 truncating mutation and juvenile atypical parkinsonism 2014 ·Parkinsonism & Related Disorders ·Gül Yalçın Çakmaklı,Simone Olgiati,Marialuisa Quadri,Guido J. Breedveld,Pietro Cortelli,Vincenzo Bonifati,Bülent Elibol	34
14	APC rearrangements in familial adenomatous polyposis: heterogeneity of deletion lengths and breakpoint sequences underlies similar phenotypes 2014 ·Familial Cancer ·Marialuisa Quadri,Annalisa Vetro,Viviana Gismondi,Monica Marabelli,Lucio Bertario,Paola Sala,Liliana Varesco,Orsetta Zuffardi,Guglielmina Nadia Ranzani	12
15	PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian family 2014 ·Neurogenetics ·Simone Olgiati,Anna De Rosa,Marialuisa Quadri,Chiara Criscuolo,Guido J. Breedveld,Marina Picillo,Sabina Pappatà,Mario Quarantelli,Paolo Barone,Giuseppe De Michele,Vincenzo Bonifati	87
16	Comprehensive LRRK2 and GBA screening in Portuguese patients with Parkinson's disease: Identification of a new family with the LRRK2 p.Arg1441His mutation and novel missense variants 2013 ·Parkinsonism & Related Disorders ·Lei Zhang,Marialuisa Quadri,Leonor Correia Guedes,Miguel Coelho,Anabela Valadas,Tiago Mestre,Patrícia Pita Lobo,Mário Miguel Rosa,Erik Simons,Ben A. Oostra,Joaquim J. Ferreira,Vincenzo Bonifati	8
17	Mutation in theSYNJ1Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism 2013 ·Human Mutation ·Marialuisa Quadri,Mingyan Fang,Marina Picillo,Simone Olgiati,Guido J. Breedveld,Josja Graafland,Bin Wu,Fengping Xu,Roberto Erro,Marianna Amboni,(unknown),Mario Quarantelli,Grazia Annesi,Aldo Quattrone,Hsin Fen Chien,Egberto Reis Barbosa,(unknown),Ben A. Oostra,Paolo Barone,Jun Wang,Vincenzo Bonifati	231
18	Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease 2012 ·Parkinsonism & Related Disorders ·Ekaterina Yonova‐Doing,Masharip Atadzhanov,Marialuisa Quadri,Paul Kelly,(unknown),(unknown),Erik Simons,Guido J. Breedveld,Ben A. Oostra,Vincenzo Bonifati	40
19	Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease 2012 ·The American Journal of Human Genetics ·Marialuisa Quadri,Antonio Federico,Tianna Zhao,Guido J. Breedveld,Carla Battisti,Cathérine C.S. Delnooz,Lies-Anne Severijnen,(unknown),Andrea Mignarri,Lucia Monti,Antioco Sanna,Peng Lü,Francesca Punzo,Giovanni Cossu,Rob Willemsen,(unknown),Ben A. Oostra,Bart P. van de Warrenburg,Vincenzo Bonifati	291
20	Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia 2011 ·Neurogenetics ·Marialuisa Quadri,Giovanni Cossu,Valeria Saddi,Erik Simons,Daniela Murgia,Maurizio Melis,Anna Ticca,Ben A. Oostra,Vincenzo Bonifati	68

About Marialuisa Quadri

Marialuisa Quadri is a scholar working on Neurology, Neurology and Cellular and Molecular Neuroscience, having authored 22 papers that have together received 1.2k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (14 papers), Neurological diseases and metabolism (12 papers) and Neurological disorders and treatments (4 papers). The work is most often cited by research in Neurology (605 citations), Neurology (241 citations) and Nutrition and Dietetics (252 citations). Marialuisa Quadri has collaborated with scholars based in Netherlands, Italy and United States. Frequent co-authors include Vincenzo Bonifati, Guido J. Breedveld, Simone Olgiati, Ben A. Oostra, Giovanni Cossu, Josja Graafland, Mario Quarantelli, Marina Picillo, Paolo Barone and Carla Battisti. Their work appears in journals such as The American Journal of Human Genetics, Neurobiology of Aging and Movement Disorders.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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