Reema Paudel

2.2k citations

20 papers · 1.4k indexed · 1 hit paper · h-index 16

Neurology top 1%
Cellular and Molecular Neuroscience top 5%
Physiology top 5%
Molecular Biology
Neurology top 2%

Co-authors: Henry Houlden John Hardy Janice L. Holton Tamás Révész Nicholas Wood Andrew J. Lees Abi Li Kailash P. Bhatia
Topics: Neurological disorders and treatments (9 papers)Neurological diseases and metabolism (8 papers)Genetic Neurodegenerative Diseases (7 papers)
Cited by: Neurology Sensory Systems
Journals: Nature Genetics Brain Neurology
Partner nations: United Kingdom United States India

In The Last Decade

Reema Paudel

20 papers receiving 1.4k 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 Reema Paudel

Since Specialization

Citations

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

Fields of papers citing papers by Reema Paudel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Reema Paudel

This figure shows the co-authorship network connecting the top 25 collaborators of Reema Paudel. A scholar is included among the top collaborators of Reema Paudel 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 Reema Paudel. Reema Paudel 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	Pure Cerebellar Ataxia with Homozygous Mutations in the PNPLA6 Gene 2016 ·The Cerebellum ·Sarah Wiethoff,Conceição Bettencourt,Reema Paudel,Prochi F. Madon,Yo‐Tsen Liu,Joshua Hersheson,Noshir Wadia,Joy Desai,Henry Houlden	20
2	Neuropathology of Beta-propeller protein associated neurodegeneration (BPAN): a new tauopathy 2015 ·Acta Neuropathologica Communications ·Reema Paudel,(unknown),Sarah Wiethoff,Rina Bandopadhyay,Kailash P. Bhatia,(unknown),Henry Houlden,Janice L. Holton	36
3	DYT6 Dystonia: A Neuropathological Study 2015 ·Neurodegenerative Diseases ·Reema Paudel,Abi Li,John Hardy,Kailash P. Bhatia,Henry Houlden,Janice L. Holton	16
4	Forebrain deletion of the dystonia protein torsinA causes dystonic-like movements and loss of striatal cholinergic neurons 2015 ·eLife ·Samuel S. Pappas,(unknown),Sandra M. Holley,Carlos Cepeda,Omar S. Mabrouk,Jenny-Marie T. Wong,(unknown),Reema Paudel,Henry Houlden,Robert T. Kennedy,Michael S. Levine,William T. Dauer	104
5	Neuropathological features of genetically confirmed DYT1 dystonia: investigating disease-specific inclusions 2014 ·Acta Neuropathologica Communications ·Reema Paudel,Aoife P. Kiely,Abi Li,Tammaryn Lashley,Rina Bandopadhyay,John Hardy,Hyder A. Jinnah,Kailash P. Bhatia,Henry Houlden,Janice L. Holton	18
6	C19orf12 mutation leads to a pallido-pyramidal syndrome 2013 ·Gene ·Michael C. Kruer,Mustafa A. Salih,Catherine Mooney,(unknown),Salah A. Elmalik,Mohammad M. Kabiraj,Arif O. Khan,Reema Paudel,Henry Houlden,Hamid Azzedine,Fowzan S. Alkuraya	22
7	Pantothenate kinase‐associated neurodegeneration is not a synucleinopathy 2012 ·Neuropathology and Applied Neurobiology ·(unknown),Reema Paudel,Robert M. Johnson,Robert J. Courtney,Andrew J. Lees,Janice L. Holton,John Hardy,Tamás Révész,Henry Houlden	37
8	Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia 2012 ·Journal of the Neurological Sciences ·Georgios Koutsis,Sally Pemble,Mary G. Sweeney,Reema Paudel,Nicholas Wood,Μάριος Πάνας,Athina Kladi,Henry Houlden	7
9	Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia 2012 ·Annals of Neurology ·Joshua Hersheson,Niccolò E. Mencacci,Mary B. Davis,Nicola MacDonald,Daniah Trabzuni,Mina Ryten,Alan Pittman,Reema Paudel,Eleanna Kara,Katherine A. Fawcett,Vincent Plagnol,Kailash P. Bhatia,Alan Medlar,Horia Stanescu,John Hardy,Robert Kleta,Nicholas Wood,Henry Houlden	120
10	Genetic screening of Greek patients with Huntington's disease phenocopies identifies an SCA8 expansion 2012 ·Journal of Neurology ·Georgios Koutsis,Georgia Karadima,Amelie Pandraud,Mary G. Sweeney,Reema Paudel,Henry Houlden,Nicholas Wood,Μάριος Πάνας	13
11	Review: Genetics and neuropathology of primary pure dystonia 2012 ·Neuropathology and Applied Neurobiology ·Reema Paudel,John Hardy,Tamás Révész,Janice L. Holton,Henry Houlden	28
12	THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations 2012 ·Movement Disorders ·Georgia Xiromerisiou,Henry Houlden,Nikolaos Scarmeas,María Stamelou,Eleanna Kara,John Hardy,Andrew J. Lees,Prasad Korlipara,Patricia Limousin,Reema Paudel,Georgios M. Hadjigeorgiou,Kailash P. Bhatia	46
13	Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts 2012 ·Neuroscience Letters ·Michael C. Kruer,Reema Paudel,Wendy Wagoner,Lynn Sanford,Eleanna Kara,Allison Gregory,Thomas Foltynie,Andrew J. Lees,Kailash P. Bhatia,John Hardy,Susan J. Hayflick,Henry Houlden	10
14	THAP1 mutations (DYT6) are an additional cause of early-onset dystonia 2010 ·Neurology ·Henry Houlden,Susanne A. Schneider,Reema Paudel,Anna Melchers,Petra Schwingenschuh,Mark J. Edwards,John Hardy,Kailash P. Bhatia	68
15	Indian‐subcontinent NBIA: Unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms 2010 ·Movement Disorders ·Annu Aggarwal,Susanne A. Schneider,Henry Houlden,Monty Silverdale,Reema Paudel,Coro Paisán‐Ruíz,(unknown),(unknown),Darshana Sanghvi,John Hardy,Kailash P. Bhatia,Mohit Bhatt	33
16	Mutational analysis of parkin and PINK1 in multiple system atrophy 2010 ·Neurobiology of Aging ·Janet Brooks,Henry Houlden,Anna Melchers,(unknown),Jinhui Ding,Abi Li,Reema Paudel,Tamás Révész,Janice L. Holton,Nicholas Wood,Andrew J. Lees,Andrew Singleton,Sonja W. Scholz	19
17	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
18	Mutations in TRPV4 cause Charcot-Marie-Tooth disease type 2C 2009 ·Nature Genetics ·Guida Landouré,Anselm A. Zdebik,Tara Martinez,Barrington G. Burnett,Horia Stanescu,Hitoshi Inada,Yijun Shi,(unknown),Lingling Kong,Clare H. Munns,(unknown),Christopher B. Phelps,Reema Paudel,Henry Houlden,Christy L. Ludlow,Michael J. Caterina,Rachelle Gaudet,Robert Kleta,Kenneth H. Fischbeck,Charlotte J. Sumner	236
19	GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY 2009 ·Neurology ·(unknown),(unknown),Reema Paudel,Sonja W. Scholz,(unknown),Andrew J. Lees,Tamás Révész,John Hardy,C.J. Mathias,Nicholas Wood,JL Holton,Henry Houlden	51
20	Molecular identification, distribution and ecology of larval malaria mosquitoes in Carrasco/Chapare Valleys, Bolivia 2005 ·The Keep (Eastern Illinois University) ·Reema Paudel	1

About Reema Paudel

Reema Paudel is a scholar working on Neurology, Neurology and Cellular and Molecular Neuroscience, having authored 20 papers that have together received 1.4k indexed citations. Recurring topics across this work include Neurological disorders and treatments (9 papers), Neurological diseases and metabolism (8 papers) and Genetic Neurodegenerative Diseases (7 papers). The work is most often cited by research in Neurology (785 citations), Neurology (320 citations) and Sensory Systems (140 citations). Reema Paudel has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Henry Houlden, John Hardy, Janice L. Holton, Tamás Révész, Nicholas Wood, Andrew J. Lees, Abi Li, Kailash P. Bhatia, Andrew Singleton and Rita Guerreiro. Their work appears in journals such as Nature Genetics, Brain and Neurology.

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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