Frank Baas

35.1k citations

361 papers · 21.7k indexed · 5 hit papers · h-index 79

Neurology top 0.2%
- Neurological diseases and metabolism 28
- Peripheral Neuropathies and Disorders 18
Cellular and Molecular Neuroscience top 0.2%
- Hereditary Neurological Disorders 56
- Genetic Neurodegenerative Diseases 25
- Nerve injury and regeneration 17
Neurology top 0.2%
- Neurological diseases and metabolism 28
- Peripheral Neuropathies and Disorders 18
Oncology top 0.2%
- Drug Transport and Resistance Mechanisms 26
Molecular Biology top 0.5%
- RNA modifications and cancer 30
- RNA Research and Splicing 25

Co-authors: Piet Borst Marcel Kool Marcel de Haas Rik J. Scheper George L. Scheffer Pieter A. Bolhuis Wiep Scheper Marianne de Visser
Cited by: Neurology Cellular and Molecular Neuroscience Oncology
Journals: Human Molecular Genetics (12 papers)PLoS ONE (11 papers)Neurology (10 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Frank Baas

356 papers receiving 21.2k citations

Hit Papers

5 papers align trajectories log scale

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.

2001 Science
1999 Proceedings of the National Academy of Sciences
1998 Journal of Clinical Investigation
1997 PubMed
1994 Proceedings of the National Academy of Sciences

Peers

Countries citing papers authored by Frank Baas

Since Specialization

Citations

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

Fields of papers citing papers by Frank Baas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Frank Baas, 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 Frank Baas Line = papers co-authored together Frank Baas links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Loss-of-Function Variants in SUPT5H as Modifying Factors in Beta-Thalassemia International Journal of Molecular Sciences ·Cornelis L. Harteveld,Anton Edwards,Naufal Dekananda Anggara Putra,昆仑雪,Shaswat Pattnaik,J. Klemm-Toole,Y. Li,Mahdi Namazifar,Tablo Abdulrahim Ahmed,Linda Vijfhuizen,Sociedade Brasileira de Pediatria – Sbp,Christian Babbs,Douglas R. Higgs,J.F.M. Helming,Christina Vrettou,Joanne Traeger‐Synodinos,Frank Baas	2024	4
2	Bi-allelic NIT1 variants cause a brain small vessel disease characterized by movement disorders, massively dilated perivascular spaces, and intracerebral hemorrhage Genetics in Medicine ·Julie W. Rutten,Lori A. Isaacs,Beatriz Fileme,Aat A. Mulder,Jeroen Vreijling,Mark C. Kruit,Roman I. Koning,Susanne T. de Bot,Koen M. van Nieuwenhuizen,Hans J. Baelde,Henk W. Berendse,Laura Guarin,George J. G. Ruijter,Frank Baas,Carolina R. Jost,Sjoerd G. van Duinen,Esther Nibbeling,Gido Gravesteijn,Saskia A.J. Lesnik Oberstein	2024	2
3	Ankle-Foot-Orthosis “Hermes” Compensates Pathological Ankle Stiffness of Chronic Stroke—A Proof of Concept IEEE Transactions on Neural Systems and Rehabilitation Engineering ·Michael C Aaronoff,Jurriaan H. de Groot,Frank Baas,Marjon Stijntjes,F. M. Shvedsky,Sven K. Schiemanck,F.C.T. van der Helm,Herman van der Kooij,Winfred Mugge	2023	2
4	Effect of NOTCH3 EGFr Group, Sex, and Cardiovascular Risk Factors on CADASIL Clinical and Neuroimaging Outcomes Stroke ·英紀前田,Lori A. Isaacs,Gido Gravesteijn,Ricardo L. Álvarez Escobar,Anne Hafkemeijer,Jeroen van der Grond,Marie‐Noëlle W. Witjes‐Ané,Frank Baas,Julie W. Rutten,Saskia A.J. Lesnik Oberstein	2022	20
5	Therapeutic Intervention with Anti-Complement Component 5 Antibody Does Not Reduce NASH but Does Attenuate Atherosclerosis and MIF Concentrations in Ldlr-/-.Leiden Mice International Journal of Molecular Sciences ·Maria Kikkawa,Robert Kleemann,Wim van Duyvenvoorde,Irfan Nofri,Nanda Keijzer,سید محسن علوی پور,Cees van Kooten,Lars Verschuren,Aswin Menke,Amanda J. Kiliaan,Pripachkina Gn,Timothy R. Hughes,B. Paul Morgan,Frank Baas,Kees Fluiter,Martine C. Morrison	2022	9
6	Assembly defects of human tRNA splicing endonuclease contribute to impaired pre-tRNA processing in pontocerebellar hypoplasia Nature Communications ·Xiaoqin Lu,Pascal Devant,Silvia Panizza,Tasos Gogakos,Brooke L. Horning,Xiangmin Li,照喜鵜飼,MIRCEA FLONTA,Carla Schmidt,Thomas Tuschl,Frank Baas,Stefan Weitzer,Javier Martı̂nez,Simon Trowitzsch	2021	29
7	Genetic biomarkers for intravenous immunoglobulin response in chronic inflammatory demyelinating polyradiculoneuropathy European Journal of Neurology ·Krista Kuitwaard,Pieter A. van Doorn,V.K. Kozakevych,Wouter van Rijs,Frank Baas,Sietse Q. Nagelkerke,Taco W. Kuijpers,Departamento de Investigación IMA,Carina Bunschoten,Luis Ernesto Urrutia Martínez,Sten P. Willemsen,Bart C. Jacobs,Ruth Huizinga	2021	8
8	Naturally occurring NOTCH3 exon skipping attenuates NOTCH3 protein aggregation and disease severity in CADASIL patients Human Molecular Genetics ·Gido Gravesteijn,Johannes G. Dauwerse,Maurice Overzier,Ruth Calderón-Hernáiz,Ingrid M. Hegeman,Aat A. Mulder,Frank Baas,Mark C. Kruit,Gisela M. Terwindt,Sjoerd G. van Duinen,Carolina R. Jost,Annemieke Aartsma‐Rus,Saskia A.J. Lesnik Oberstein,Julie W. Rutten	2019	14
9	In Rheumatoid Arthritis, Synovitis at Different Inflammatory Sites Is Dominated by Shared but Patient-Specific T Cell Clones The Journal of Immunology ·Anne Musters,Paul L. Klarenbeek,Marieke E. Doorenspleet,伴幸高橋,R. E. Esveldt,Barbera D. C. van Schaik,Aldo Jongejan,Sander W. Tas,Antoine H. C. van Kampen,Frank Baas,Niek de Vries	2018	27
10	DRD1 rare variants associated with tardive-like dystonia: A pilot pathway sequencing study in dystonia Parkinsonism & Related Disorders ·J Groen,Katja Ritz,Thomas T. Warner,Frank Baas,Marina A.J. Tijssen	2014	7
11	Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia Human Molecular Genetics ·Sander M. Houten,Simone Denis,Heleen te Brinke,Aldo Jongejan,Antoine H. C. van Kampen,Eddie Bradley,Frank Baas,Raoul C. M. Hennekam,David S. Millington,Sarah P. Young,Dianne M. Frazier,Müge Güçsavaş‐Çalıkoğlu,Ronald J. A. Wanders	2014	54
12	Transcriptome sequencing (RNA-Seq) of human endobronchial biopsies: asthmaversuscontrols European Respiratory Journal ·Ching Yong Yick,Aeilko H. Zwinderman,Peter W.A. Kunst,Katrien Grünberg,Thaís Mauad,Annemiek Dijkhuis,Elisabeth H. Bel,Frank Baas,René Lutter,Peter J. Sterk	2013	65
13	COMT Val¹⁵⁸met genotype and striatal D_2/3 receptor binding in adults with 22q11 deletion syndrome Synapse ·Erik Boot,Jan Booij,Janneke Zinkstok,Frank Baas,Ann Swillen,Michael J. Owen,Declan Murphy,Kieran C. Murphy,Don Linszen,Thérèse A. van Amelsvoort	2011	16
14	Endoplasmic reticulum stress activates autophagy but not the proteasome in neuronal cells: implications for Alzheimer's disease Cell Death and Differentiation ·Diana A.T. Nijholt,Berlin (Germany) Institut fuer Sozialforschung und Betriebspaedagogik e.V.,LE ROUX,Ana Osório Oliveira,Celia R. Berkers,Rob Zwart,Huib Ovaa,Frank Baas,Jeroen J.M. Hoozemans,Wiep Scheper	2011	110
15	Utilization of unlocked nucleic acid (UNA) to enhance siRNA performance in vitro and in vivo Molecular BioSystems ·Maria Bach Laursen,Malgorzata Maria Pakula,Shan Gao,Kees Fluiter,Olaf R.F. Mook,Frank Baas,Daniela dos Santos Anjos,Χρήστος Ζυγογιάννης,Jesper Wengel,Jørgen Kjems,Jesper B. Bramsen	2010	93
16	Filling the gap in LNAantisense oligo gapmers: the effects of unlocked nucleic acid (UNA) and 4′- C -hydroxymethyl-DNA modifications on RNase H recruitment and efficacy of an LNA gapmer Molecular BioSystems ·Kees Fluiter,Olaf R.F. Mook,Jeroen Vreijling,Niels Langkjær,Torben Højland,Jesper Wengel,Frank Baas	2009	36
17	LAD-1/variant syndrome is caused by mutations in FERMT3 Blood ·Taco W. Kuijpers,Edith van de Vijver,Marian A. J. Weterman,Martin de Boer,Anton T. J. Tool,Timo K. van den Berg,Markus Moser,Marja E. Jakobs,Karl Seeger,Özden Sanal,Şule Ünal,Mualla Çetin,Dirk Roos,Arthur J. Verhoeven,Frank Baas	2008	160
18	Molecular Risk Stratification of Medulloblastoma Patients Based on Immunohistochemical Analysis of MYC, LDHB, and CCNB1 Expression Clinical Cancer Research ·Pradeep Padmanabhan,Nancy E. Hasselt,Dirk Troost,Huib N. Caron,Mara Popović,Lorna Zadravec Zaletel,Wiesława Grajkowska,Marta Perek‐Polnik,Maria‐Chiara Osterheld,David W. Ellison,Frank Baas,Rogier Versteeg,Marcel Kool	2008	41
19	Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines.breakdown → PubMed ·Marcel Kool,Marcel de Haas,George L. Scheffer,Rik J. Scheper,Ema S. Dreseris,Jenneke A. Juijn,Frank Baas,Byung-Jin CH이	1997	746
20	Altered MRP is associated with multidrug resistance and reduced drug accumulation in human SW-1573 cells British Journal of Cancer ·Pauline Birot,G J Zaman,Marcel de Haas,C. H. M. Versantvoort,M J Flens,Víctor Vilanova Pi,J. C. Aurich,Piet Borst,Frank Baas	1995	19

About Frank Baas

Frank Baas is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Genetics and Immunology, having authored 361 papers that have together received 21.7k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (56 papers), RNA modifications and cancer (30 papers), Neurological diseases and metabolism (28 papers), Drug Transport and Resistance Mechanisms (26 papers), RNA Research and Splicing (25 papers), Genetic Neurodegenerative Diseases (25 papers), Peripheral Neuropathies and Disorders (18 papers) and Nerve injury and regeneration (17 papers). The work is most often cited by research in Neurology (2.1k citations), Cellular and Molecular Neuroscience (3.9k citations), Neurology (3.2k citations), Oncology (5.4k citations) and Molecular Biology (9.4k citations). Frank Baas has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Piet Borst, Marcel Kool, Marcel de Haas, Rik J. Scheper, George L. Scheffer, Pieter A. Bolhuis, Wiep Scheper, Marianne de Visser, Antoine H. C. van Kampen and Jan J. M. de Vijlder. Their work appears in journals such as Human Molecular Genetics, PLoS ONE, Neurology, European Journal of Human Genetics and Annals of the Rheumatic Diseases.

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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