Marka van Blitterswijk

9.9k citations

47 papers · 2.8k indexed · 2 hit papers · h-index 24

Impact in

Neurology top 0.5%
- Amyotrophic Lateral Sclerosis Research
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
Genetics top 0.5%
- Neurogenetic and Muscular Disorders Research

Papers in

Neurology 37
- Amyotrophic Lateral Sclerosis Research 37
- Parkinson's Disease Mechanisms and Treatments 13
- Neurological diseases and metabolism 7
Genetics 25
- Neurogenetic and Muscular Disorders Research 25

Co-authors: Rosa Rademakers Mariely DeJesus‐Hernandez Dennis W. Dickson Leonard Petrucelli Tania F. Gendron Karen Jansen‐West Kevin F. Bieniek Khrista Boylan
Journals: Neurobiology of Aging (7 papers)Molecular Neurodegeneration (5 papers)Acta Neuropathologica (4 papers)Neurology (4 papers)Experimental Neurology (2 papers)
Partner nations: United States Netherlands Belgium

In The Last Decade

Marka van Blitterswijk

44 papers receiving 2.8k citations

Hit Papers

align trajectories log scale

Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS 2013 · 415 citations

Peers

Countries citing papers authored by Marka van Blitterswijk

Since Specialization

Citations

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

Fields of papers citing papers by Marka van Blitterswijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marka van Blitterswijk. 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 Marka van Blitterswijk. The network helps show where Marka van Blitterswijk may publish in the future.

Co-authors

The 25 scholars most cited alongside Marka van Blitterswijk, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Marka van Blitterswijk Line = papers co-authored together Marka van Blitterswijk links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Differential neuronal vulnerability to C9orf72 repeat expansion driven by Xbp1-induced endoplasmic reticulum-associated degradation Cell Reports ·Jacek Michna, Alec Vincent, David Boud, 井上周平, Wen Chen, Т.Н. Гавришова, 卢宪梅, Dongwei Xu, Carol J. Savage, David Osumi-Sutherland, Manuel Campello, S. S. R. M. D. H. R. Wijesekara, Nitzan Uri, Nathaniel S. Woodling, Rosa Rademakers, Adrian M. Isaacs, Carlo Sala Frigerio, Marka van Blitterswijk, Tammaryn Lashley, Teresa Niccoli	2025	1
2	Characterizing the expression profile of 3R tau pathology in Pick’s disease Science Advances ·Tomioka, Alexandra I. Soto‐Beasley, И Г Абрамов, Michael G. Heckman, Yingxue Ren, David Boud, Zachary Quicksall, W. J. Work, Monica Castanedes‐Casey, Zbigniew K. Wszołek, Bradley F. Boeve, Keith A. Josephs, Caroline Graff, Marka van Blitterswijk, Melissa E. Murray, Shanu F. Roemer, Dennis W. Dickson, Owen A. Ross	2025	1
3	Amyotrophic lateral sclerosis caused by hexanucleotide repeat expansions in C9orf72: from genetics to therapeutics The Lancet Neurology ·Sarah Mizielinska, Guillaume M. Hautbergue, Tania F. Gendron, Marka van Blitterswijk, Orla Hardiman, John Ravits, Adrian M. Isaacs, Rosa Rademakers	2025	9
4	Expanding the spectrum of annexin A11 proteinopathy in frontotemporal lobar degeneration and motor neuron disease Acta Neuropathologica ·Katie Madgett, Richard Crook, 张宗新, Rosi Novita, Peizhou Jiang, Shanu F. Roemer, Hiroaki Sekiya, Michael DeTure, Matthew Baker, Wouter De Coster, Björn Oskarsson, Keith A. Josephs, Z. R. Voznyak, Marka van Blitterswijk, Dennis W. Dickson	2025	0
5	P528: Utilizing long-read sequencing technologies to enable discovery of disease genes associated with complex neurological phenotypes Genetics in Medicine Open ·张宗新, 윤명애, Viviana Sarmiento Guzmán, P. Matet, BY CATHERINE C. MANZI, NiCole A. Finch, Richard Crook, Karthik Muthusamy, Ralitza H. Gavrilova, Marka van Blitterswijk, Eric W. Klee	2025	0
6	Targeted long-read sequencing to quantify methylation of the C9orf72 repeat expansion Molecular Neurodegeneration ·윤명애, NiCole A. Finch, Mariely DeJesus‐Hernandez, Jazmyne L. Jackson, Matthew Baker, Vinogradova Galina, Eric D. Wieben, Mark Ebbert, Jaimin Shah, Leonard Petrucelli, Rosa Rademakers, Björn Oskarsson, Marka van Blitterswijk	2024	4
7	Upper motor neuron‐predominant motor neuron disease presenting as atypical parkinsonism: A clinicopathological study Brain Pathology ·風雅池谷, Shunsuke Koga, Shinsuke Fujioka, C Vock, Kevin F. Bieniek, Hiroaki Sekiya, Mariely DeJesus‐Hernandez, NiCole A. Finch, Marka van Blitterswijk, Masataka Nakamura, Yoshio Tsuboi, Melissa E. Murray, Zbigniew K. Wszołek, Dennis W. Dickson	2024	1
8	Analysis of Structural Variants Previously Associated With ALS in Europeans Highlights Genomic Architectural Differences in Africans Neurology Genetics ·Soufiane Elmejdoub, DANYANG GE, Jeannine M. Heckmann, Gerrit Botha, Nicola Mulder, Gang Wu, Evadnie Rampersaud, Jason R. Myers, Marka van Blitterswijk, Rosa Rademakers, J. Paul Taylor, Joanne Wuu, Michael Benatar, 惠桂木	2023	1
9	Elevated methylation levels, reduced expression levels, and frequent contractions in a clinical cohort of C9orf72 expansion carriers Molecular Neurodegeneration ·Jazmyne L. Jackson, NiCole A. Finch, Matthew Baker, Jennifer M. Kachergus, Mariely DeJesus‐Hernandez, 優人渡辺, Elizabeth Christopher, Mercedes Prudencio, Michael G. Heckman, E. Aubrey Thompson, Dennis W. Dickson, Jaimin Shah, Björn Oskarsson, Leonard Petrucelli, Rosa Rademakers, Marka van Blitterswijk	2020	31
10	Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations Annals of Clinical and Translational Neurology ·Nobutaka Sakae, Shanu F. Roemer, Kevin F. Bieniek, Melissa E. Murray, Matthew Baker, Koji Kasanuki, Neill R. Graff‐Radford, Leonard Petrucelli, Marka van Blitterswijk, Rosa Rademakers, Dennis W. Dickson	2019	20
11	TMEM106B haplotypes have distinct gene expression patterns in aged brain Molecular Neurodegeneration ·Yingxue Ren, Marka van Blitterswijk, Mariet Allen, Minerva M. Carrasquillo, Joseph S. Reddy, Xue Wang, Thomas G. Beach, Dennis W. Dickson, Nilüfer Ertekin‐Taner, Yan W. Asmann, Rosa Rademakers	2018	25
12	Transthyretin as Potential Biomarker for C9ORF72 -related Diseases (I8-2A) Neurology ·Marka van Blitterswijk, NiCole A. Finch, Matthew Baker, Xue Wang, Kevin F. Bieniek, Mariely DeJesus‐Hernandez, Bianca A. Duah, Yan W. Asmann, Michael G. Heckman, Patricia E. Brown, Keith A. Josephs, Ana Claudia Alves Sene, David S. Knopman, Ronald C. Petersen, Leonard Petrucelli, Bradley Boeve, Neill R. Graff‐Radford, Khrista Boylan, Dennis W. Dickson, Rosa Rademakers	2015	1
13	Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS Neuron ·Peter E.A. Ash, Kevin F. Bieniek, Tania F. Gendron, Thomas R. Caulfield, Wen-Lang Lin, Mariely DeJesus‐Hernandez, Marka van Blitterswijk, Karen Jansen‐West, Joseph W. Paul, Rosa Rademakers, Khrista Boylan, Dennis W. Dickson, Leonard Petrucelli Hit paper breakdown →	2013	804
14	Profilin-1 mutations are rare in patients with amyotrophic lateral sclerosis and frontotemporal dementia Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·Marka van Blitterswijk, Matthew Baker, Kevin F. Bieniek, David S. Knopman, Keith A. Josephs, Bradley F. Boeve, Richard J. Caselli, Zbigniew K. Wszołek, Ronald C. Petersen, Neill R. Graff‐Radford, Khrista Boylan, Dennis W. Dickson, Rosa Rademakers	2013	23
15	How do C9ORF72 repeat expansions cause amyotrophic lateral sclerosis and frontotemporal dementia Current Opinion in Neurology ·Marka van Blitterswijk, Mariely DeJesus‐Hernandez, Rosa Rademakers	2012	136
16	Genetic Overlap between Apparently Sporadic Motor Neuron Diseases PLoS ONE ·Marka van Blitterswijk, Lotte Vlam, Michael A. van Es, W. Ludo van der Pol, Eric A. M. Hennekam, Dennis Dooijes, Helenius J. Schelhaas, Anneke J. van der Kooi, Marianne de Visser, Jan H. Veldink, Leonard H. van den Berg	2012	51
17	VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient Neurobiology of Aging ·Marka van Blitterswijk, Michael A. van Es, Max Koppers, Wouter van Rheenen, Jelena Medic, Helenius J. Schelhaas, Anneke J. van der Kooi, Marianne de Visser, Jan H. Veldink, Leonard H. van den Berg	2012	67
18	Mutational analysis of TARDBP in Parkinson's disease Neurobiology of Aging ·Marka van Blitterswijk, Michael A. van Es, Dagmar Verbaan, Jacobus J. van Hilten, Hans Scheffer, Bart P.C. van de Warrenburg, Jan H. Veldink, Leonard H. van den Berg	2012	5
19	Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients Neurobiology of Aging ·Marka van Blitterswijk, Anna M. Blokhuis, Michael A. van Es, Paul W.J. van Vught, Gezahagn Bekele Teshebo, Helenius J. Schelhaas, Anneke J. van der Kooi, Marianne de Visser, Jan H. Veldink, Leonard H. van den Berg	2012	11
20	Mutational analysis of TARDBP in neurodegenerative diseases Neurobiology of Aging ·Nicola Ticozzi, Ashley LeClerc, Marka van Blitterswijk, Pamela Keagle, Diane McKenna‐Yasek, Peter C. Sapp, Vincenzo Silani, Anne‐Marie Wills, Robert H. Brown, John E. Landers	2009	52

About Marka van Blitterswijk

Marka van Blitterswijk is a scholar working on Neurology, Genetics, Neurology, Cellular and Molecular Neuroscience and Physiology, having authored 47 papers that have together received 2.8k indexed citations. Recurring topics across this work include Amyotrophic Lateral Sclerosis Research (37 papers), Neurogenetic and Muscular Disorders Research (25 papers), Parkinson's Disease Mechanisms and Treatments (13 papers), Genetic Neurodegenerative Diseases (10 papers), Neurological diseases and metabolism (7 papers), Alzheimer's disease research and treatments (7 papers), Mitochondrial Function and Pathology (4 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Neurology (2.2k citations), Genetics (1.3k citations), Neurology (492 citations), Cellular and Molecular Neuroscience (525 citations) and Molecular Biology (1.3k citations). Marka van Blitterswijk has collaborated with scholars based in United States, Netherlands and Belgium. Frequent co-authors include Rosa Rademakers, Mariely DeJesus‐Hernandez, Dennis W. Dickson, Leonard Petrucelli, Tania F. Gendron, Karen Jansen‐West, Kevin F. Bieniek, Khrista Boylan, Peter E.A. Ash and Thomas R. Caulfield. Their work appears in journals such as Neurobiology of Aging, Molecular Neurodegeneration, Acta Neuropathologica, Neurology and Experimental Neurology.

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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