Concepedia

Author

Andrea H. Németh

University of OxfordORCID

Also Known As

A H Nemeth, A H Németh, A NEMETH, A Nemeth, A Németh, A. H. Nemeth, A. Nemeth, A. Németh, A.H. Németh, AH Nemeth

213

Publications

11.9K

Citations

55

H-Index

186

Concepts

All Affiliations

University of OxfordOxford University Hospitals NHS TrustChurchill HospitalUniversity College LondonJohn Radcliffe Hospital
AH

About

Andrea H. Németh is an author at University of Oxford specializing in medicine, genetics, and neurology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

31

46

5K

2

Natural Sciences

4

4

772

3

Public Health

3

3

205

4

Engineering

2

2

71

5

Health Sciences

2

2

63

Andrea H. Németh

×

95

Publications

8.2K

Citations

47

H-Index

YearCitations

EV-TRACK: transparent reporting and centralizing knowledge in extracellular vesicle research

Jan Van Deun, Pieter Mestdagh, Patrizia Agostinis,

Nature Methods

2017

1.2K

Low-density lipoprotein mimics blood plasma-derived exosomes and microvesicles during isolation and detection

Barbara W. Sódar, Ágnes Kittel, Krisztina Pálóczi,

Scientific Reports

2016

521

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2

Maria-Ceù Moreira, Sandra Klur, Andrea H. Németh,

Nature Genetics

2004

518

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders

Jenny C. Taylor, Hilary C. Martin, Stefano Lise,

Nature Genetics

2015

378

A conserved sorting-associated protein is mutant in chorea-acanthocytosis

Luca Rampoldi, Carol Dobson‐Stone, Justin P. Rubio,

Nature Genetics

2001

353

Differential detergent sensitivity of extracellular vesicle subpopulations

Xabier Osteikoetxea, Barbara W. Sódar, Andrea H. Németh,

Organic & Biomolecular Chemistry

2015

247

Improved Characterization of EV Preparations Based on Protein to Lipid Ratio and Lipid Properties

Xabier Osteikoetxea, Andrea Balogh, Katalin Szabó-Taylor,

PLoS ONE

2015

207

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Alexander J. Abrams, Robert B. Hufnagel, Adriana Rebelo,

Nature Genetics

2015

200

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model

Andrea H. Németh, Alexandra Kwasniewska, Stefano Lise,

Brain

2013

171

Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease

Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar,

Ophthalmology

2016

164

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