H.J.M. Smeets

3.7k total citations
63 papers, 2.4k citations indexed

About

H.J.M. Smeets is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, H.J.M. Smeets has authored 63 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 16 papers in Genetics and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in H.J.M. Smeets's work include Mitochondrial Function and Pathology (16 papers), Metabolism and Genetic Disorders (8 papers) and Cell Adhesion Molecules Research (7 papers). H.J.M. Smeets is often cited by papers focused on Mitochondrial Function and Pathology (16 papers), Metabolism and Genetic Disorders (8 papers) and Cell Adhesion Molecules Research (7 papers). H.J.M. Smeets collaborates with scholars based in Netherlands, United States and Belgium. H.J.M. Smeets's co-authors include Henny H. Lemmink, Bernard A. van Oost, Toshio Mochizuki, I.F.M. de Coo, Corinne Antignac, Patrick Lindsey, Auke B.C. Otten, Mariko Mariyama, Christine Verellen‐Dumoulin and Marie-Claire Gübler and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

H.J.M. Smeets

62 papers receiving 2.4k citations

Peers

H.J.M. Smeets

GENET

CMN

Alfredo Brusco Italy

Jeanette M. Cunningham United States

Juha Saharinen Finland

Elisabet Wallgard Sweden

Gwenaëlle Collod‐Béroud France

Stanley A. Vinores United States

Rosanna Dono France

Mordechai Shohat Israel

Alessandro Malandrini Italy

Graciela B. Sala‐Newby United Kingdom

Alfredo Brusco Italy

H.J.M. Smeets

2.2k ×1.5

799 ×1.6

GENET

135 ×0.3

109 ×0.4

859 ×3.0

CMN

Citations per year, relative to H.J.M. Smeets H.J.M. Smeets (= 1×) peers Alfredo Brusco

Countries citing papers authored by H.J.M. Smeets

Since Specialization

Citations

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

Fields of papers citing papers by H.J.M. Smeets

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H.J.M. Smeets. 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 H.J.M. Smeets. The network helps show where H.J.M. Smeets may publish in the future.

Co-authorship network of co-authors of H.J.M. Smeets

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

All Works

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20 of 20 papers shown

Xenakis, Markos, Dimos Kapetis, Yang Yang, et al.. (2021). Non-extensitivity and criticality of atomic hydropathicity around a voltage-gated sodium channel’s pore: a modeling study. Journal of Biological Physics. 47(1). 61–77. 3 indexed citations

Almomani, Rowida, Margherita Marchi, Patrick Lindsey, et al.. (2020). Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing. PLoS ONE. 15(9). e0238467–e0238467. 13 indexed citations

Otten, Auke B.C., Monique M. Gerrits, Janneke G. J. Hoeijmakers, et al.. (2018). Expression of pathogenic SCN9A mutations in the zebrafish: A model to study small-fiber neuropathy. Experimental Neurology. 311. 257–264. 17 indexed citations

Mencarelli, Maria Antonietta, Laurence Heidet, Helen Storey, et al.. (2015). Evidence of digenic inheritance in Alport syndrome. Journal of Medical Genetics. 52(3). 163–174. 107 indexed citations

Brinkhuizen, Tjinta, et al.. (2015). Epidermal Cyst Formation and Hyperkeratosis in a Patient Treated with Vismodegib for Locally Advanced Basal Cell Carcinoma. Acta Dermato Venereologica. 95(5). 618–619. 3 indexed citations

Walenda, Gudrun, Steffen K. Meurer, Kristin Seré, et al.. (2014). TGF-β stimulation in human and murine cells reveals commonly affected biological processes and pathways at transcription level. BMC Systems Biology. 8(1). 55–55. 34 indexed citations

Lindsey, Patrick, et al.. (2010). ProlongedNrf1overexpression triggers adipocyte inflammation and insulin resistance. Journal of Cellular Biochemistry. 111(6). 1575–1585. 16 indexed citations

Stefanatos, Rhoda, Berit Adam, H.J.M. Smeets, et al.. (2010). Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients. Human Molecular Genetics. 19(8). 1399–1412. 120 indexed citations

Bredenoord, Annelien L., Wybo Dondorp, Guido Pennings, et al.. (2009). Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practice. European Journal of Human Genetics. 17(12). 1550–1559. 29 indexed citations

10.

Steensel, Maurice A. M. Van, Maaike Vreeburg, Jan Engelen, et al.. (2008). Contiguous gene syndrome due to a maternally inherited 8.41 Mb distal deletion of chromosome band Xp22.3 in a boy with short stature, ichthyosis, epilepsy, mental retardation, cerebral cortical heterotopias and Dandy–Walker malformation. American Journal of Medical Genetics Part A. 146A(22). 2944–2949. 21 indexed citations

11.

Pennings, Guido, et al.. (2007). Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders. Human Reproduction Update. 14(1). 83–94. 41 indexed citations

12.

Steensel, Maurice A. M. Van, Valerie L. R. M. Verstraeten, Jorge Frank, et al.. (2006). Novel Mutations in the BHD Gene and Absence of Loss of Heterozygosity in Fibrofolliculomas of Birt-Hogg-Dubé Patients. Journal of Investigative Dermatology. 127(3). 588–593. 52 indexed citations

13.

Paulussen, Aimée, Ann Raes, R. J. E. Jongbloed, et al.. (2005). HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency. Cardiovascular Research. 67(3). 467–475. 18 indexed citations

14.

Coo, I.F.M. de, W.O. Renier, W. Ruitenbeek, et al.. (1999). A 4-base pair deletion in the mitochondrial cytochromeb gene associated with parkinsonism/MELAS overlap syndrome. Annals of Neurology. 45(1). 130–133. 107 indexed citations

15.

Monnens, L.A.H., et al.. (1999). Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin. Kidney International. 55(4). 1217–1224. 43 indexed citations

16.

Jefferson, J. Ashley, et al.. (1997). Autosomal dominant Alport syndrome linked to the type IV collagen alpha3 and alpha4 genes. Nephrology Dialysis Transplantation. 1595–1599. 1 indexed citations

17.

Jongmans, Wim, M Vuillaume, Krystyńa Chrzańowska, et al.. (1997). Nijmegen Breakage Syndrome Cells Fail To Induce the p53-Mediated DNA Damage Response following Exposure to Ionizing Radiation. Molecular and Cellular Biology. 17(9). 5016–5022. 99 indexed citations

18.

Smeets, H.J.M., Rosella Hermens, Han G. Brunner, Hans‐Hilger Ropers, & B. Wieringa. (1991). Identification of variable simple sequence motifs in 19q13.2-qter: Markers for the myotonic dystrophy locus. Genomics. 9(2). 257–263. 30 indexed citations

19.

Oerlemans, Frank, H.J.M. Smeets, Jan Schepens, et al.. (1989). Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q. Genomics. 4(3). 384–396. 67 indexed citations

20.

Smeets, H.J.M., et al.. (1988). Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides. Human Genetics. 80(1). 49–52. 11 indexed citations

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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