Sarah Wiethoff

5.8k total citations · 1 hit paper
38 papers, 1.9k citations indexed

About

Sarah Wiethoff is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Sarah Wiethoff has authored 38 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 13 papers in Neurology. Recurrent topics in Sarah Wiethoff's work include Neurological diseases and metabolism (10 papers), Genetic Neurodegenerative Diseases (8 papers) and Hereditary Neurological Disorders (7 papers). Sarah Wiethoff is often cited by papers focused on Neurological diseases and metabolism (10 papers), Genetic Neurodegenerative Diseases (8 papers) and Hereditary Neurological Disorders (7 papers). Sarah Wiethoff collaborates with scholars based in Germany, United Kingdom and United States. Sarah Wiethoff's co-authors include John C. Rothwell, Masashi Hamada, Dirk Wildgruber, Wolfgang Grodd, Henry Houlden, Thomas Ethofer, Cornelia Herbert, Benjamin Kreifelts, Silke Anders and Thomas Ethofer and has published in prestigious journals such as PLoS ONE, NeuroImage and Neurology.

In The Last Decade

Sarah Wiethoff

34 papers receiving 1.9k 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.

Variability in Response to Transcranial Direct Current Stimulation of the Motor Cortex

2014 615 citations Sarah Wiethoff, Masashi Hamada et al. Brain stimulation profile →

Peers

Countries citing papers authored by Sarah Wiethoff

Since Specialization

Citations

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

Fields of papers citing papers by Sarah Wiethoff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Wiethoff

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Wiethoff. A scholar is included among the top collaborators of Sarah Wiethoff 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 Sarah Wiethoff. Sarah Wiethoff is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Case report: Clinical, genetic and immunological characterization of a novel XK variant in a patient with McLeod syndrome 2024 ·Frontiers in Genetics ·(unknown), (unknown), Michael Heming, (unknown), (unknown), (unknown), Christian Thomas, Heinz Wiendl, Gerd Meyer zu Hörste, Sarah Wiethoff	0
2	Microglia contribute to the production of the amyloidogenic ABri peptide in familial British dementia 2024 ·Acta Neuropathologica ·Charles Arber, Jackie M. Casey, (unknown), (unknown), (unknown), Sarah Wiethoff, (unknown), Thomas M. Piers, Matthew J. Price, Agueda Rostagno, Jorge Ghiso, Patrick A. Lewis, Tamas Revesz, John Hardy, Jennifer M. Pocock, Henry Houlden, Jonathan M. Schott, Derviş A. Salih, Tammaryn Lashley, Selina Wray	3
3	Allelic and phenotypic heterogeneity in Junctophillin-3 related neurodevelopmental and movement disorders 2021 ·European Journal of Human Genetics ·Thomas Bourinaris, (unknown), Stéphanie Efthymiou, Sarah Wiethoff, Vincenzo Salpietro, Henry Houlden	3
4	CSF NFL in a Longitudinally Assessed PD Cohort: Age Effects and Cognitive Trajectories 2020 ·Movement Disorders ·Stefanie Lerche, Isabel Wurster, (unknown), Milan Zimmermann, Gerrit Machetanz, Sarah Wiethoff, (unknown), (unknown), (unknown), Christian Deuschle, Elke Stransky, (unknown), Thomas Gasser, Kathrin Brockmann	35
5	Revising a diagnosis of functional neurological disorder—a case report 2020 ·Oxford Medical Case Reports ·Alex J. Berry, Sarah Wiethoff	0
6	Defining diagnostic cutoffs in neurological patients for serum very long chain fatty acids (VLCFA) in genetically confirmed X-Adrenoleukodystrophy 2020 ·Scientific Reports ·Tim W. Rattay, Maren Rautenberg, (unknown), Holger Hengel, Andreas Traschütz, (unknown), Stefanie N. Hayer, Rebecca Schüle, Sarah Wiethoff, Lena Zeltner, Tobias B. Haack, Alexander Čegan, Lüdger Schöls, Erwin Schleicher, Andreas Peter	42
7	Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4) 2019 ·Journal of Neurology ·Tim W. Rattay, Andreas Boldt, (unknown), Sarah Wiethoff, Holger Hengel, Rebecca Schüle, Lüdger Schöls	16
8	Quick Flicks: Association of Paroxysmal Kinesigenic Dyskinesia and Tics 2018 ·Movement Disorders Clinical Practice ·Bettina Balint, Sarah Wiethoff, Davide Martino, (unknown), Anna Latorre, Christos Ganos, Henry Houlden, Kailash P. Bhatia	4
9	Genetics of neurodegenerative diseases: an overview 2017 ·Handbook of clinical neurology ·Lasse Pihlstrøm, Sarah Wiethoff, Henry Houlden	71
10	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
11	Gene co-expression networks shed light into diseases of brain iron accumulation 2015 ·Neurobiology of Disease ·Conceição Bettencourt, Paola Forabosco, Sarah Wiethoff, Moones Heidari, Daniel M. Johnstone, Juan A. Botía, Joanna F. Collingwood, John Hardy, Elizabeth A. Milward, Mina Ryten, Henry Houlden	22
12	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
13	Using human induced pluripotent stem cells to model cerebellar disease: Hope and hype 2015 ·Journal of Neurogenetics ·Sarah Wiethoff, Charles Arber, Abi Li, Selina Wray, Henry Houlden, Rickie Patani	8
14	Variability in Response to Transcranial Direct Current Stimulation of the Motor Cortex breakdown → 2014 ·Brain stimulation ·Sarah Wiethoff, Masashi Hamada, John C. Rothwell	615
15	Assessment of functional and morphometric endpoints in patients with non-arteritic anterior ischemic optic neuropathy (NAION) 2014 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·Christoph Kernstock, Flemming Beisse, Sarah Wiethoff, Andrea Mast, E. Krapp, (unknown), Janko Dietzsch, Wolf A. Lagrèze, Dominik Fischer, Ulrich Schiefer	24
16	Novel single base-pair deletion in exon 1 of XK gene leading to McLeod syndrome with chorea, muscle wasting, peripheral neuropathy, acanthocytosis and haemolysis 2014 ·Journal of the Neurological Sciences ·Sarah Wiethoff, Georgia Xiromerisiou, Conceição Bettencourt, Anna Kioumi, (unknown), (unknown), (unknown), (unknown), (unknown), John Hardy, Henry Houlden	3
17	Functional responses and structural connections of cortical areas for processing faces and voices in the superior temporal sulcus 2013 ·NeuroImage ·Thomas Ethofer, (unknown), Sarah Wiethoff, (unknown), (unknown), Dirk Wildgruber, Benjamin Kreifelts	66
18	Retinal nerve fibre layer loss in hereditary spastic paraplegias is restricted to complex phenotypes 2012 ·BMC Neurology ·Sarah Wiethoff, (unknown), Lüdger Schöls, Manuel Fischer	15
19	Decreased retinal sensitivity and loss of retinal nerve fibers in multiple system atrophy 2012 ·Graefe s Archive for Clinical and Experimental Ophthalmology ·Manuel Fischer, Matthis Synofzik, Christoph Kernstock, Janko Dietzsch, (unknown), Julia Schicks, Karin Srulijes, Sarah Wiethoff, Oliver Menn, Daniela Berg, Lüdger Schöls, Ulrich Schiefer	18
20	Response and habituation of the amygdala during processing of emotional prosody 2009 ·Neuroreport ·Sarah Wiethoff, Dirk Wildgruber, Wolfgang Grodd, Thomas Ethofer	59

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.

Explore authors with similar magnitude of impact