Rita Guerreiro

42.3k citations

130 papers · 5.6k indexed · 1 hit paper · h-index 40

Physiology top 0.5%
Neurology top 0.5%
Molecular Biology top 5%
Neurology top 0.2%
Genetics top 2%

Co-authors: José Brás John Hardy Andrew Singleton Catarina R. Oliveira Deborah Gustafson Susana Carmona Tamás Révész Janice L. Holton
Topics: Alzheimer's disease research and treatments (36 papers)Parkinson's Disease Mechanisms and Treatments (20 papers)Genomics and Rare Diseases (17 papers)
Cited by: Neurology Physiology
Journals: Cell Proceedings of the National Academy of SciencesSHILAP Revista de lepidopterología
Partner nations: United Kingdom United States Portugal

In The Last Decade

Rita Guerreiro

126 papers receiving 5.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

2009 509 citations José Brás, Emma Deas et al. Brain profile →

Peers

Countries citing papers authored by Rita Guerreiro

Since Specialization

Citations

This map shows the geographic impact of Rita Guerreiro'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 Rita Guerreiro with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Rita Guerreiro more than expected).

Fields of papers citing papers by Rita Guerreiro

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rita Guerreiro. 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 Rita Guerreiro. The network helps show where Rita Guerreiro may publish in the future.

Co-authorship network of co-authors of Rita Guerreiro

This figure shows the co-authorship network connecting the top 25 collaborators of Rita Guerreiro. A scholar is included among the top collaborators of Rita Guerreiro 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 Rita Guerreiro. Rita Guerreiro 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	Exploring first-degree family history in a cohort of Portuguese Alzheimer’s disease patients: population evidence for X-chromosome linked and recessive inheritance of risk factors 2024 ·Journal of Neurology ·Miguel Tábuas‐Pereira,(unknown),João Durães,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Célia Kun‐Rodrigues,Maria Rosário Almeida,Inês Baldeiras,José Brás,Rita Guerreiro,(unknown)	1
2	Molecular Characterization of Portuguese Patients with Hereditary Cerebellar Ataxia 2022 ·Cells ·Mariana Santos,Joana Damásio,Susana Carmona,(unknown),(unknown),(unknown),Clara Barbot,José Barros,José Brás,Jorge Sequeiros,Rita Guerreiro	5
3	Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype–phenotype correlation 2022 ·Neurogenetics ·Miguel Tábuas‐Pereira,Rita Guerreiro,Célia Kun‐Rodrigues,Maria Rosário Almeida,José Brás,Isabel Santana	2
4	Rare variants in TP73 in a frontotemporal dementia cohort link this gene with primary progressive aphasia phenotypes 2022 ·European Journal of Neurology ·Miguel Tábuas‐Pereira,Isabel Santana,Maria Rosário Almeida,João Durães,(unknown),Diana Duro,Célia Kun‐Rodrigues,José Brás,Rita Guerreiro	2
5	Congenital ataxia due to novel variant in ATP8A2 2021 ·Clinical Genetics ·Joana Damásio,Diana Santos,Sara Morais,José Brás,Rita Guerreiro,(unknown),Sara Cavaco,Inês Carrilho,Clara Barbot,José Barros,Jorge Sequeiros	6
6	Alzheimer’s Disease Genetics: Review of Novel Loci Associated with Disease 2020 ·Miguel Tábuas‐Pereira,Isabel Santana,Rita Guerreiro,José Brás	20
7	Psychiatric Manifestations of ATP13A2 Mutations 2020 ·Movement Disorders Clinical Practice ·Bettina Balint,Joana Damásio,Francesca Magrinelli,Rita Guerreiro,José Brás,Kailash P. Bhatia	4
8	A deletion of IDUA exon 10 in a family of Golden Retriever dogs with an attenuated form of mucopolysaccharidosis type I 2020 ·Journal of Veterinary Internal Medicine ·Kiterie M. E. Faller,Alison E. Ridyard,Rodrigo Gutierrez‐Quintana,(unknown),Célia Kun‐Rodrigues,Tatiana Orme,Karen Tylee,Heather J. Church,Rita Guerreiro,José Brás	3
9	PCN136 Cost-Effectiveness Analysis of Dacomitinib Versus Gefitinib for the First-line Treatment of Locally Advanced or Metastatic Non-Small Cell Lung Cancer with Epidermal Growth Factor Receptor (EGFR)-Activating Mutations in Portugal 2020 ·Value in Health ·L. Silva Miguel,(unknown),Joana Alarcão,Rita Guerreiro,(unknown),Margarida Borges	2
10	The Genetics of Dementia with Lewy Bodies: Current Understanding and Future Directions 2018 ·Current Neurology and Neuroscience Reports ·Tatiana Orme,Rita Guerreiro,José Brás	72
11	PCN107 - BURDEN AND COSTS OF ACUTE MYELOID LEUKAEMIA IN PORTUGAL 2018 ·Value in Health ·Rita Guerreiro,(unknown),João Costa,(unknown),Joana Alarcão,(unknown),(unknown)	1
12	PCN112 - BURDEN AND COSTS OF ACUTE LYMPHOBLASTIC LEUKAEMIA IN PORTUGAL 2018 ·Value in Health ·(unknown),L. Silva Miguel,João Costa,Joana Alarcão,(unknown),Rita Guerreiro,(unknown)	1
13	Acute Lymphoblastic Leukaemia’s Burden Of Disease In Portugal 2017 ·Value in Health ·(unknown),Joana Alarcão,(unknown),Rita Guerreiro,L. Silva Miguel,(unknown)	1
14	Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutation 2016 ·Neurobiology of Aging ·José Brás,Ruth Djaldetti,(unknown),Simon Mead,Lee Darwent,Alberto Lleó,José Luís Molinuevo,Rafael Blesa,Andrew Singleton,John Hardy,Jordi Clarimón,Rita Guerreiro	18
15	Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement 2013 ·JAMA Neurology ·Rita Guerreiro,Ebba Lohmann,José Brás,J. Raphael Gibbs,Jonathan D. Rohrer,Nicole Gurunlian,(unknown),Başar Bılgıç,Haşmet Hanağası,Hakan Gürvıt,Murat Emre,Andrew Singleton,John Hardy	262
16	Insights into TREM2 biology by network analysis of human brain gene expression data 2013 ·Neurobiology of Aging ·Paola Forabosco,Adaikalavan Ramasamy,Daniah Trabzuni,Robert Walker,Colin Smith,José Brás,Adam P. Levine,John Hardy,Jennifer M. Pocock,Rita Guerreiro,Michael E. Weale,Mina Ryten	138
17	Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease 2012 ·Nature reviews. Neuroscience ·José Brás,Rita Guerreiro,John Hardy	78
18	PRNP allelic series from 19 years of prion protein gene sequencing at the MRC Prion Unit 2010 ·Human Mutation ·(unknown),Mark Poulter,Tracy Campbell,Gary Adamson,(unknown),Rita Guerreiro,Graham S. Jackson,James C. Stevens,Hadi Manji,John Collinge,Simon Mead	65
19	Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's diseasebreakdown → 2009 ·Brain ·(unknown),José Brás,Emma Deas,Sean S. O’Sullivan,Laura Parkkinen,Robin Lachmann,Abi Li,Janice L. Holton,Rita Guerreiro,Reema Paudel,(unknown),Andrew Singleton,Andrew J. Lees,John Hardy,Henry Houlden,Tamás Révész,Nicholas Wood	509
20	G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort 2005 ·Movement Disorders ·José Brás,Rita Guerreiro,Maria Helena Ribeiro,Cristina Januário,Ana Morgadinho,Catarina R. Oliveira,Luı́s Cunha,John Hardy,(unknown)	83

About Rita Guerreiro

Rita Guerreiro is a scholar working on Neurology, Neurology and Physiology, having authored 130 papers that have together received 5.6k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (36 papers), Parkinson's Disease Mechanisms and Treatments (20 papers) and Genomics and Rare Diseases (17 papers). The work is most often cited by research in Neurology (1.7k citations), Neurology (1.9k citations) and Physiology (2.6k citations). Rita Guerreiro has collaborated with scholars based in United Kingdom, United States and Portugal. Frequent co-authors include José Brás, John Hardy, Andrew Singleton, Catarina R. Oliveira, Deborah Gustafson, Susana Carmona, Tamás Révész, Janice L. Holton, Jonathan D. Rohrer and Isabel Santana. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and SHILAP Revista de lepidopterología.

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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