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Author: Henry Houlden

  • ORCiD: http://orcid.org/0000-0002-2866-7777
  • Most recently observed institution: Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK

Rankings

  • All-time downloads: 9,213 (rank: 20,932 (tie) )
  • Categories:
    • genetic and genomic medicine: 236 (rank: 6,862 (tie) )
    • genetics: 4,162 (rank: 4,214 (tie) )
    • genomics: 1,690 (rank: 13,567 )
    • neuroscience: 2,896 (rank: 7,158 (tie) )
    • systems biology: 229 (rank: 12,174 (tie) )

Downloads per author, site-wide

Preprints

G2P: Using machine learning to understand and predict genes causing rare neurological disorders

genetics more details view paper
  • Downloaded 1,980 times
  • Download rankings, all-time:
    • Site-wide: 7,575
    • In genetics: 355
  • Year to date:
    • Site-wide: 30,618
  • Since beginning of last month:
    • Site-wide: 27,997

Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at Chr16q11.2 and on the MAPT H1 allele.

neuroscience more details view paper
  • Downloaded 940 times
  • Download rankings, all-time:
    • Site-wide: 22,949
    • In neuroscience: 2,966
  • Year to date:
    • Site-wide: 21,046
  • Since beginning of last month:
    • Site-wide: 16,328

A genome-wide genetic pleiotropy approach identified shared loci between multiple system atrophy and inflammatory bowel disease

genetics more details view paper
  • Downloaded 920 times
  • Download rankings, all-time:
    • Site-wide: 23,689
    • In genetics: 1,147
  • Year to date:
    • Site-wide: 70,517
  • Since beginning of last month:
    • Site-wide: 58,151

Mitochondrial impairment and rescue in riboflavin responsive neuropathy

neuroscience more details view paper
  • Downloaded 792 times
  • Download rankings, all-time:
    • Site-wide: 29,224
    • In neuroscience: 3,942
  • Year to date:
    • Site-wide: 55,968
  • Since beginning of last month:
    • Site-wide: 39,619

Whole genome sequencing for diagnosis of neurological repeat expansion disorders

genomics more details view paper
  • Downloaded 757 times
  • Download rankings, all-time:
    • Site-wide: 31,176
    • In genomics: 2,790
  • Year to date:
    • Site-wide: 9,085
  • Since beginning of last month:
    • Site-wide: 12,602

DNA isolation protocol effects on nuclear DNA analysis by microarrays, droplet digital PCR, and whole genome sequencing, and on mitochondrial DNA copy number estimation

genomics more details view paper
  • Downloaded 565 times
  • Download rankings, all-time:
    • Site-wide: 45,693
    • In genomics: 3,662
  • Year to date:
    • Site-wide: 57,452
  • Since beginning of last month:
    • Site-wide: 41,129

Mutations In Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands Of Dendritic Growth And Synaptic Integrity

neuroscience more details view paper
  • Downloaded 523 times
  • Download rankings, all-time:
    • Site-wide: 50,125
    • In neuroscience: 7,365
  • Year to date:
    • Site-wide: 81,441
  • Since beginning of last month:
    • Site-wide: 83,645

Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform specific start-loss mutations of essential genes can cause genetic diseases

genetics more details view paper
  • Downloaded 476 times
  • Download rankings, all-time:
    • Site-wide: 55,778
    • In genetics: 2,598
  • Year to date:
    • Site-wide: 70,836
  • Since beginning of last month:
    • Site-wide: 75,908

Human-lineage-specific genomic elements: relevance to neurodegenerative disease and APOE transcript usage

neuroscience more details view paper
  • Downloaded 382 times
  • Download rankings, all-time:
    • Site-wide: 69,626
    • In neuroscience: 10,585
  • Year to date:
    • Site-wide: 59,809
  • Since beginning of last month:
    • Site-wide: 60,561

Genetic variants for head size share genes and pathways with cancer

genomics more details view paper
  • Downloaded 368 times
  • Download rankings, all-time:
    • Site-wide: 72,099
    • In genomics: 4,962
  • Year to date:
    • Site-wide: 41,817
  • Since beginning of last month:
    • Site-wide: 34,337

Human patient SFPQ homozygous mutation is found deleterious for brain and motor development in a zebrafish model

neuroscience more details view paper
  • Downloaded 259 times
  • Download rankings, all-time:
    • Site-wide: 94,043
    • In neuroscience: 14,597
  • Year to date:
    • Site-wide: 58,219
  • Since beginning of last month:
    • Site-wide: 51,978

Clinical, neuroimaging and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability

genetic and genomic medicine more details view paper
  • Downloaded 236 times
  • Download rankings, all-time:
    • Site-wide: 99,226
    • In genetic and genomic medicine: 396
  • Year to date:
    • Site-wide: 21,599
  • Since beginning of last month:
    • Site-wide: 22,125

Integrating protein networks and machine learning for disease stratification in the Hereditary Spastic Paraplegias

systems biology more details view paper
  • Downloaded 229 times
  • Download rankings, all-time:
    • Site-wide: 100,511
    • In systems biology: 2,338
  • Year to date:
    • Site-wide: 9,124
  • Since beginning of last month:
    • Site-wide: 56,754

Biallelic mutation of CLRN2 causes non-syndromic hearing loss in humans

genetics more details view paper
  • Downloaded 229 times
  • Download rankings, all-time:
    • Site-wide: 100,607
    • In genetics: 4,481
  • Year to date:
    • Site-wide: 60,591
  • Since beginning of last month:
    • Site-wide: 70,952

Leucine Rich Repeat Kinase 2 (LRRK2) Gly2019Ser Mutation Is Absent In A Second Cohort Of Nigerian Africans With Parkinson Disease.

genetics more details view paper
  • Downloaded 204 times
  • Download rankings, all-time:
    • Site-wide: 106,165
    • In genetics: 4,667
  • Year to date:
    • Site-wide: 133,282
  • Since beginning of last month:
    • Site-wide: 124,460

Delineating the molecular and phenotypic spectrum of the SETD1B-related syndrome

genetics more details view paper
  • Downloaded 195 times
  • Download rankings, all-time:
    • Site-wide: 108,174
    • In genetics: 4,739
  • Year to date:
    • Site-wide: 11,301
  • Since beginning of last month:
    • Site-wide: 9,298

Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy

genetics more details view paper
  • Downloaded 158 times
  • Download rankings, all-time:
    • Site-wide: 116,077
    • In genetics: 5,009
  • Year to date:
    • Site-wide: 125,212
  • Since beginning of last month:
    • Site-wide: 128,940

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