Holger Hummerich - Concepedia

Author

Holger Hummerich

University College London ORCID

Also Known As

H Hummerich, H. Hummerich, Holger Hummerich, Holger Hummerich (27634), Hummerich, H, Hummerich, Holger, Marc Hulsman

Publications

7.5K

Citations

H-Index

Concepts

All Affiliations

University College London MRC Prion Unit National Hospital for Neurology and Neurosurgery Medical Research Council Curtin University

About

Holger Hummerich is an author at University College London specializing in medicine, genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	22	6.1K
2	Natural Sciences	3	3	654
3	Public Health	3	3	162
4	Health Sciences	2	2	33
5	Engineering	1	1	33

Holger Hummerich

Publications

7.2K

Citations

H-Index

Page 1

	Year	Citations
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Manish A. Shah, Nicole A. Datson, Lakshmi Srinidhi, Cell Genetic DiseasesGenome InstabilityNovel GeneGenetic DisorderGenetics	1993	3.1K
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia Gaia Skibinski, Jeremy Brown, Lisa Chakrabarti, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceGenetic DisorderGeneticsDementia	2005	804
Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport Majid Hafezparast, Rainer Klocke, Christiana Ruhrberg, Science GeneticsRetrograde TransportCytoskeletonSocial SciencesDegenerative Disorders	2003	681
Genetic Analysis of the Cytoplasmic Dynein Subunit Families K. Kevin Pfister, Paresh Shah, Holger Hummerich, PLoS Genetics Dynein SubunitsGeneticsMolecular BiologyMolecular GeneticsCytoskeleton	2006	313
Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat Christine Ambrose, Mabel P. Duyao, Glenn Barnes, Somatic Cell and Molecular Genetics Genetic DisorderNatural SciencesGeneticsDisease GeneGenomic Mechanism	1994	272
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease Henne Holstege, Marc Hulsman, Camille Charbonnier, Nature Genetics	2022	206
Activation of nuclear factor-kappa B signalling promotes cellular senescence Emilie Marie Isabelle Rovillain, Lucielle Mansfield, Constantino Caetano, Oncogene Cell RegulationCell DeathCellular SenescenceMedicineCell Biology	2011	195
A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure Simon Mead, Jerome Whitfield, Mark Poulter, New England Journal of Medicine	2009	190
HTT-lowering reverses Huntington’s disease immune dysfunction caused by NFκB pathway dysregulation Ulrike Träger, Ralph André, Nayana Lahiri, Brain	2014	178
Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study Simon Mead, Mark Poulter, James Uphill, The Lancet Neurology	2008	153

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