Bé Wieringa

15.6k citations

193 papers · 12.6k indexed · 4 hit papers · h-index 55

Cellular and Molecular Neuroscience top 0.2%
- Genetic Neurodegenerative Diseases 60
Molecular Biology top 0.5%
- Mitochondrial Function and Pathology 36
- Muscle Physiology and Disorders 30
- Ion channel regulation and function 16
- Protein Tyrosine Phosphatases 13
- Fungal and yeast genetics research 12
Neurology top 0.5%
Cell Biology top 0.5%
- Muscle metabolism and nutrition 24
Cardiology and Cardiovascular Medicine top 1%
- Cardiomyopathy and Myosin Studies 20

Co-authors: Gerard J.M. Martens Helena Xicoy Frank Oerlemans Robert G. Korneluk Gert Jansen Wiljan Hendriks Jack Fransen Bernard A. van Oost
Cited by: Cellular and Molecular Neuroscience Molecular Biology Neurology
Journals: Journal of Biological Chemistry (14 papers)Nucleic Acids Research (14 papers)Genomics (13 papers)
Partner nations: Netherlands United States Germany

In The Last Decade

Bé Wieringa

193 papers receiving 12.4k citations

Hit Papers

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Peers

Countries citing papers authored by Bé Wieringa

Since Specialization

Citations

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

Fields of papers citing papers by Bé Wieringa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Expanded CUG repeats in DMPK transcripts adopt diverse hairpin conformations without influencing the structure of the flanking sequences RNA ·María-José Conejero,Bé Wieringa,Derick G. Wansink	2019	12
2	Design and Analysis of Effects of Triplet Repeat Oligonucleotides in Cell Models for Myotonic Dystrophy Molecular Therapy — Nucleic Acids ·河込和作,Susan Mulders,E Teyssedou,阿部光延,Jesús Díaz Herrera,Eqbal Z. Darandari,Paola Dayana Cajas Chávez,Judith C. van Deutekom,Jack Fransen,Bé Wieringa,Derick G. Wansink	2013	36
3	TRPM7 Is Required for Breast Tumor Cell Metastasis Cancer Research ·Jeroen Middelbeek,Arthur J. Kuipers,Linda Henneman,Daan Visser,Ilse Eidhof,Remco van Horssen,Bé Wieringa,Sander Canisius,Wilbert Zwart,Lodewyk F.A. Wessels,Fred C.G.J. Sweep,Peter Bult,Paul N. Span,Frank N. van Leeuwen,Kees Jalink	2012	176
4	Gene duplication and conversion events shaped three homologous, differentially expressed myosin regulatory light chain (MLC2) genes European Journal of Cell Biology ·Katsumata Shizuo,Gijs J. Overheul,Ronny Derks,Bé Wieringa,Wiljan Hendriks,Derick G. Wansink	2012	11
5	Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Federica Valsecchi,Claire Monge,Marleen Forkink,Ad J.C. de Groof,Giovanni Bénard,Rodrigue Rossignol,Herman G.P. Swarts,Sjenet E. van Emst‐de Vries,Richard J. Rodenburg,Maria Antonietta Calvaruso,Leo Nijtmans,Bavo Heeman,Peggy Roestenberg,Bé Wieringa,Jan Smeıtınk,Werner J.H. Koopman,Peter H.G.M. Willems	2012	57
6	Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy Proceedings of the National Academy of Sciences ·Susan Mulders,Walther J. A. A. van den Broek,Thurman M. Wheeler,Huib J. E. Croes,Petra van Kuik‐Romeijn,Sjef J. de Kimpe,Denis Furling,Gerard Platenburg,Geneviève Gourdon,Charles A. Thornton,Bé Wieringa,Derick G. Wansink	2009	204
7	Activation of glucose transport and AMP‐activated protein kinase during muscle contraction in adenylate kinase‐1 knockout mice Acta Physiologica ·Fath El-Bab,Marie Sandström,Vahid T. Mustafayev,Håkan Westerblad,Bé Wieringa,Abram Katz	2007	15
8	Rab6 family proteins interact with the dynein light chain protein DYNLRB1 Cell Motility and the Cytoskeleton ·Bas F.J. Wanschers,Lars Riensche,Mietske Wijers,Bé Wieringa,Stephen M. King,Jack Fransen	2007	62
9	Neuroprotective mechanisms of creatine occur in the absence of mitochondrial creatine kinase Neurobiology of Disease ·Péter Klivènyi,Noel Y. Calingasan,Anatoly A. Starkov,Irina G. Stavrovskaya,Bruce S. Kristal,Lichuan Yang,Bé Wieringa,M. Flint Beal	2004	47
10	Cloning and characterization of mCRIP2, a mouse LIM‐only protein that interacts with PDZ domain IV of PTP‐BL Genes to Cells ·Marco van Ham,Huib J. E. Croes,Jan Schepens,Jack Fransen,Bé Wieringa,Wiljan Hendriks	2003	26
11	Two structurally distinct and spatially compartmentalized adenylate kinases are expressed from the AK1 gene in mouse brain Molecular and Cellular Biochemistry ·Edwin Janssen,J. W. Kuiper,Denice M. Hodgson,Leonid V. Zingman,Alexey E. Alekseev,André Terzic,Bé Wieringa	2003	23
12	Developmental expression of the cell adhesion molecule-like protein tyrosine phosphatases LAR, RPTPδ and RPTPσ in the mouse Mechanisms of Development ·Roel Q.J. Schaapveld,Jan Schepens,Dietmar Bächner,Joline Attema,Bé Wieringa,Liana Ramos Mendes,Wiljan Hendriks	1998	60
13	Mouse Choroideremia Gene Mutation Causes Photoreceptor Cell Degeneration and is not Transmitted through the Female Germline Human Molecular Genetics ·José A. J. M. van den Hurk,Wiljan Hendriks,Dorien J.R. van de Pol,Frank Oerlemans,Gesine B. Jaissle,Klaus Rüther,Konrad Köhler,Jens Hartmann,Eberhart Zrenner,Hans van Bokhoven,Bé Wieringa,Hans‐Hilger Ropers,Frans P.M. Cremers	1997	57
14	Impaired Mammary Gland Development and Function in Mice Lacking LAR Receptor-like Tyrosine Phosphatase Activity Developmental Biology ·Roel Q.J. Schaapveld,Jan Schepens,Gertraud W. Robinson,Joline Attema,Frank Oerlemans,Jack Fransen,Michel Streuli,Bé Wieringa,Lothar Hennighausen,Wiljan Hendriks	1997	114
15	Abnormal myotonic dystrophy protein kinase levels produce only mild myopathy in mice Nature Genetics ·Gert Jansen,Patricia J.T.A. Groenen,Dietmar Bächner,P. H. K. Jap,M. Coerwinkel,Frank Oerlemans,Paul Ngugi,Bärbel Gohlsch,Dirk Pette,Jaap J. Plomp,Peter Molenaar,Marcel G.J. Nederhoff,Cees J. A. van Echteld,Marleen Dekker,Anton Berns,H. Hameister,Bé Wieringa	1996	250
16	Mice deficient in ubiquitous mitochondrial creatine kinase are viable and fertile Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Karen Steeghs,Frank Oerlemans,Bé Wieringa	1995	40
17	Approaching the multifaceted nature of energy metabolism: inactivation of the cytosolic creatine kinases via homologous recombination in mouse embryonic stem cells Molecular and Cellular Biochemistry ·Jan van Deursen,Bé Wieringa	1994	7
18	Expression of the gene encoding human brain creatine kinase depends on sequences immediately following the transcription start point Gene ·Edwin C.M. Mariman,Bé Wieringa	1991	20
19	Physical fine-mapping of a deletion spanning the Norrie gene Human Genetics ·P.J. Diergaarde,Bé Wieringa,E. M. Bleeker‐Wagemakers,Katherine B. Sims,Xandra O. Breakefield,Hans‐Hilger Ropers	1989	13
20	Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q Genomics ·G. McCan,Chuman Achumani,Aaron McCauley,Frank Oerlemans,H.J.M. Smeets,Jan Schepens,Theo J.M. Hulsebos,D.J. Cockburn,Yvonne Boyd,Mary B. Davis,Wolfgang Rettig,Duncan Shaw,A.D. Roses,Hilger H. Ropers,Bé Wieringa	1989	67

About Bé Wieringa

Bé Wieringa is a scholar working on Cellular and Molecular Neuroscience, Cell Biology, Molecular Biology, Clinical Biochemistry and Cardiology and Cardiovascular Medicine, having authored 193 papers that have together received 12.6k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (60 papers), Mitochondrial Function and Pathology (36 papers), Muscle Physiology and Disorders (30 papers), Muscle metabolism and nutrition (24 papers), Cardiomyopathy and Myosin Studies (20 papers), Ion channel regulation and function (16 papers), Protein Tyrosine Phosphatases (13 papers) and Fungal and yeast genetics research (12 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (4.9k citations), Molecular Biology (9.3k citations), Neurology (1.6k citations), Cell Biology (1.7k citations) and Cardiology and Cardiovascular Medicine (1.4k citations). Bé Wieringa has collaborated with scholars based in Netherlands, United States and Germany. Frequent co-authors include Gerard J.M. Martens, Helena Xicoy, Frank Oerlemans, Robert G. Korneluk, Gert Jansen, Wiljan Hendriks, Jack Fransen, Bernard A. van Oost, Mani S. Mahadevan and Chris T. Amemiya. Their work appears in journals such as Journal of Biological Chemistry, Nucleic Acids Research, Genomics, Human Molecular Genetics and Human Genetics.

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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