Henry Houlden

64.7k citations

512 papers · 20.7k indexed · 5 hit papers · h-index 70

Molecular Biology top 0.5%
Cellular and Molecular Neuroscience top 0.1%
Neurology top 0.05%
Physiology top 0.1%
Neurology top 0.05%

Co-authors: John Hardy Mary M. Reilly Andrew Singleton Michael Mullan Fiona Crawford Nicholas Wood Janice L. Holton Kailash P. Bhatia
Topics: Genetic Neurodegenerative Diseases (117 papers)Neurological diseases and metabolism (102 papers)Hereditary Neurological Disorders (101 papers)
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Nature Proceedings of the National Academy of Sciences Journal of Biological Chemistry
Partner nations: United Kingdom United States Italy

In The Last Decade

Henry Houlden

479 papers receiving 20.2k citations

Hit Papers

5 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.

A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N–terminus of β–amyloid

1992 1.1k citations Henry Houlden et al. profile →
Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene

1991 913 citations Henry Houlden, Liana Fidani et al. profile →
Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy

1999 600 citations Henry Houlden, John Hardy et al. profile →
A common polymorphism in the brain‐derived neurotrophic factor gene ( BDNF ) modulates human cortical plasticity and the response to rTMS

2008 539 citations Mark J. Edwards, Henry Houlden et al. profile →
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

2009 509 citations Janice L. Holton, Reema Paudel et al. profile →

Peers

Countries citing papers authored by Henry Houlden

Since Specialization

Citations

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

Fields of papers citing papers by Henry Houlden

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Henry Houlden

This figure shows the co-authorship network connecting the top 25 collaborators of Henry Houlden. A scholar is included among the top collaborators of Henry Houlden 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 Henry Houlden. Henry Houlden 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	CSF1R -Related Disorder 2024 ·Neurology Genetics ·(unknown),(unknown),Jeremy Chataway,Henry Houlden,David S. Lynch	5
2	Clinical and molecular heterogeneity of VPS13D-related neurodevelopmental and movement disorders 2023 ·Gene ·Tipu Sultan,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Stéphanie Efthymiou,Vincenzo Salpietro,Henry Houlden	4
3	Pure cerebellar ataxia due to bi‐allelic PRDX3 variants including recurring p.Asp202Asn 2023 ·Annals of Clinical and Translational Neurology ·Stéphanie Efthymiou,(unknown),Georgios Koutsis,(unknown),Reza Maroofian,(unknown),Georgios Velonakis,Luiz Felipe Vasconcellos,Salmo Raskin,Varunvenkat M. Srinivasan,Alistair T. Pagnamenta,(unknown),(unknown),(unknown),Hélio Afonso Ghizoni Teive,Henry Houlden	2
4	Intronic enhancers of the human SNCA gene predominantly regulate its expression in brain in vivo 2022 ·Science Advances ·Fubo Cheng,(unknown),Chang Liu,Peter A. Barbuti,Libo Yu-Taeger,Nicolas Casadei,Jeannette Hübener‐Schmid,Jakob Admard,Karsten Boldt,Katrin Junger,Marius Ueffing,Henry Houlden,Manu Sharma,Rejko Krüger,(unknown),Thomas Ott,Olaf Rieß	6
5	Small vessel disease burden and intracerebral haemorrhage in patients taking oral anticoagulants 2021 ·Journal of Neurology Neurosurgery & Psychiatry ·David Seiffge,Duncan Wilson,Gareth Ambler,Gargi Banerjee,Isabel C. Hostettler,Henry Houlden,Clare Shakeshaft,Hannah Cohen,Tarek Yousry,Rustam Al‐Shahi Salman,Gregory Y.H. Lip,Martin M. Brown,Keith W. Muir,Hans Rolf Jäger,David J. Werring	26
6	SORL1 mutation in a Greek family with Parkinson's disease and dementia 2021 ·Annals of Clinical and Translational Neurology ·Georgia Xiromerisiou,Thomas Bourinaris,Henry Houlden,Patrick A. Lewis,Konstantin Senkevich,Monia Hammer,Monica Federoff,(unknown),Cleanthe Spanaki,Georgios M. Hadjigeorgiou,(unknown),Liana Fidani,(unknown),Ziv Gan‐Or,Andrew Singleton,Jana Vandrovcová,John Hardy	4
7	Longer term stroke risk in intracerebral haemorrhage survivors 2020 ·Journal of Neurology Neurosurgery & Psychiatry ·Gargi Banerjee,Duncan Wilson,Gareth Ambler,Isabel C. Hostettler,Clare Shakeshaft,Hannah Cohen,Tarek Yousry,Rustam Al‐Shahi Salman,Gregory Y.H. Lip,Henry Houlden,Keith W. Muir,Martin M. Brown,Hans Rolf Jäger,David J. Werring	14
8	Expanding the molecular and phenotypic spectrum of truncating MT-ATP6 mutations 2020 ·Neurology Genetics ·Enrico Bugiardini,Emanuela Bottani,Silvia Marchet,(unknown),Cristiane Benincá,Alejandro Horga,Cathy E. Woodward,Amanda Lam,Iain P. Hargreaves,Annapurna Chalasani,Alessandra Valerio,Eleonora Lamantea,Kerrie Venner,Janice L. Holton,Massimo Zeviani,Henry Houlden,Rosaline C. M. Quinlivan,Costanza Lamperti,Michael G. Hanna,Robert D. S. Pitceathly	25
9	Genetic testing in dementia — utility and clinical strategies 2020 ·Nature Reviews Neurology ·(unknown),Janna Kenny,Natalie S. Ryan,Jonathan D. Rohrer,Jonathan M. Schott,Henry Houlden,Nick C. Fox,Sarah J. Tabrizi,Simon Mead	25
10	A de novo truncating mutation in ASXL1 associated with segmental overgrowth 2019 ·UCL Discovery (University College London) ·Stéphanie Efthymiou,Vincenzo Salpietro,(unknown),Maria R. Bonsignore,(unknown),Gabriella Di Rosa,Henry Houlden	2
11	Further supporting evidence for REEP1 phenotypic and allelic heterogeneity 2019 ·Neurology Genetics ·Reza Maroofian,Mahdiyeh Behnam,Rauan Kaiyrzhanov,Vincenzo Salpietro,(unknown),Henry Houlden	3
12	Phenotypes, genotypes, and the management of paroxysmal movement disorders 2018 ·Developmental Medicine & Child Neurology ·Laura Silveira‐Moriyama,Stjepana Kovac,Manju A. Kurian,Henry Houlden,Andrew Lees,Matthew C. Walker,Emmanuel Roze,Alex R. Paciorkowski,Jonathan W. Mink,Thomas T. Warner	26
13	A COMPOUND HETEROZYGOUS MUTATION IN THE VACCINIA RELATED KINASE-1 GENE IS A CAUSE OF HEREDITARY MOTOR NEUROPATHY WITH UPPER MOTOR NEURON SIGNS 2016 ·UCL Discovery (University College London) ·(unknown),Alexander M. Rossor,Alejandro Horga,(unknown),Henry Houlden,Mary M. Reilly	4
14	C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies 2013 ·Neurology ·Davina J. Hensman Moss,Mark Poulter,Jon Beck,Jason Hehir,James M. Polke,Tracy Campbell,(unknown),Ese Mudanohwo,Peter McColgan,Andrea Haworth,Edward J. Wild,Mary G. Sweeney,Henry Houlden,Simon Mead,Sarah J. Tabrizi	137
15	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
16	Characterisation of PLA2G6 as a locus for dystonia-parkinsonism 2008 ·UCL Discovery (University College London) ·Coro Paisán‐Ruiz,Kailash P. Bhatia,(unknown),Dena Hernandez,(unknown),Nicholas Wood,J Hardy,Henry Houlden,Andrew Singleton,(unknown)	3
17	Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11 (vol 39, pg 1434, 2007) 2008 ·UCL Discovery (University College London) ·Henry Houlden,J J Johnson,Christopher Gardner‐Thorpe,Tammaryn Lashley,Dena Hernández,Paul Worth,A. B. Singleton,(unknown),JL Holton,Tom Révész,(unknown),Paola Giunti,Nicholas Wood	18
18	Early onset familial Alzheimer's disease - Mutation frequency in 31 families 2002 ·Deakin Research Online (Deakin University) ·(unknown),J. A. Beck,(unknown),Andrew Dickinson,Nick C. Fox,Richard J. Harvey,Henry Houlden,(unknown),John Collinge	77
19	Clinical and genetic characterisation of families with triple a (Allgrove) syndrome 2002 ·UCL Discovery (University College London) ·Henry Houlden,(unknown),(unknown),C.J. Mathias,(unknown),Nicholas Wood,Mary M. Reilly	1
20	Familial cerebral amyloid angiopathy related to stroke and dementia. 2001 ·PubMed ·B Frangione,T Révész,Rubén Vidal,Janice L. Holton,Tammaryn Lashley,Henry Houlden,Nicholas Wood,Agueda Rostagno,Gordon T. Plant,Jorge Ghiso	23

About Henry Houlden

Henry Houlden is a scholar working on Neurology, Neurology and Cellular and Molecular Neuroscience, having authored 512 papers that have together received 20.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (117 papers), Neurological diseases and metabolism (102 papers) and Hereditary Neurological Disorders (101 papers). The work is most often cited by research in Neurology (5.1k citations), Neurology (7.0k citations) and Cellular and Molecular Neuroscience (7.0k citations). Henry Houlden has collaborated with scholars based in United Kingdom, United States and Italy. Frequent co-authors include John Hardy, Mary M. Reilly, Andrew Singleton, Michael Mullan, Fiona Crawford, Nicholas Wood, Janice L. Holton, Kailash P. Bhatia, Tamás Révész and Andrew J. Lees. Their work appears in journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

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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