Hubert J.M. Smeets

7.8k citations

133 papers · 4.6k indexed · h-index 38

Molecular Biology top 2%
Clinical Biochemistry top 0.2%
Cardiology and Cardiovascular Medicine top 5%
Cellular and Molecular Neuroscience top 5%
Genetics top 5%

Co-authors: I.F.M. de Coo Mike Gerards Suzanne C.E.H. Sallevelt Bernard A. van Oost Pieter A. Doevendans Joep Geraedts Han G. Brunner Stephen T. Reeders
Topics: Mitochondrial Function and Pathology (64 papers)Metabolism and Genetic Disorders (31 papers)ATP Synthase and ATPases Research (21 papers)
Cited by: Clinical Biochemistry Immunology and Allergy Molecular Biology
Journals: Science New England Journal of Medicine Nucleic Acids Research
Partner nations: Netherlands Belgium United Kingdom

In The Last Decade

Hubert J.M. Smeets

132 papers receiving 4.5k citations

Peers

Countries citing papers authored by Hubert J.M. Smeets

Since Specialization

Citations

This map shows the geographic impact of Hubert 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 Hubert 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 Hubert J.M. Smeets more than expected).

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Hubert J.M. Smeets. A scholar is included among the top collaborators of Hubert 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 Hubert J.M. Smeets. Hubert J.M. Smeets 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	Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases 2024 ·International Journal of Molecular Sciences ·(unknown),(unknown),Silvia Santoro,Monique M. Gerrits,Elisabetta Mascia,Margherita Marchi,Erika Salvi,Hubert J.M. Smeets,Janneke G. J. Hoeijmakers,Filippo Martinelli Boneschi,Massimo Filippi,Giuseppe Lauria,Catharina G. Faber,Federica Esposito	2
2	Fusion of Wild-Type Mesoangioblasts with Myotubes of mtDNA Mutation Carriers Leads to a Proportional Reduction in mtDNA Mutation Load 2023 ·International Journal of Molecular Sciences ·(unknown),(unknown),(unknown),Erika Timmer,Monique Ummelen,Anton H. N. Hopman,Hubert J.M. Smeets,(unknown)	4
3	Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy 2022 ·International Journal of Molecular Sciences ·(unknown),Rowida Almomani,Margherita Marchi,Bianca T. A. de Greef,(unknown),Janneke G. J. Hoeijmakers,Patrick Lindsey,Erika Salvi,Gidon J. Bönhof,Dan Ziegler,Rayaz A. Malik,Stephen G. Waxman,Giuseppe Lauria,Catharina G. Faber,Hubert J.M. Smeets,Monique M. Gerrits	14
4	Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy 2022 ·International Journal of Molecular Sciences ·(unknown),Rowida Almomani,Margherita Marchi,Erika Salvi,Bianca T. A. de Greef,(unknown),Janneke G. J. Hoeijmakers,Patrick Lindsey,Stephen G. Waxman,Giuseppe Lauria,Catharina G. Faber,Hubert J.M. Smeets,Monique M. Gerrits	15
5	Plasma GDF-15 concentration is not elevated in open-angle glaucoma 2021 ·PLoS ONE ·(unknown),(unknown),Tos T. J. M. Berendschot,I.F.M. de Coo,Hubert J.M. Smeets,Carroll A.B. Webers,Theo G. M. F. Gorgels	7
6	Parental repeat length instability in myotonic dystrophy type 1 pre- and protomutations 2020 ·European Journal of Human Genetics ·(unknown),Debby M.E.I. Hellebrekers,Bianca T. A. de Greef,Hubert J.M. Smeets,Christine de Die‐Smulders,Catharina G. Faber,Monique M. Gerrits	17
7	Differential effect of lacosamide on Nav1.7 variants from responsive and non-responsive patients with small fibre neuropathy 2020 ·Brain ·(unknown),Mark Estación,Brian S. Tanaka,Bianca T. A. de Greef,Janneke G. J. Hoeijmakers,Margot Geerts,Monique M. Gerrits,Hubert J.M. Smeets,Catharina G. Faber,Ingemar S.J. Merkies,Giuseppe Lauria,Sulayman D. Dib‐Hajj,Stephen G. Waxman	32
8	Healthy, mtDNA-mutation free mesoangioblasts from mtDNA patients qualify for autologous therapy 2019 ·Stem Cell Research & Therapy ·(unknown),(unknown),Erika Timmer,(unknown),Patrick Lindsey,Mattia Quattrocelli,Maurilio Sampaolesi,(unknown),I.F.M. de Coo,Hubert J.M. Smeets	13
9	Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome Sequencing 2017 ·The Journal of Pediatrics ·Tom E. J. Theunissen,Suzanne C.E.H. Sallevelt,Debby M.E.I. Hellebrekers,Bart de Koning,Alexandra T.M. Hendrickx,B.J.C. van den Bosch,Rick Kamps,Kees Schoonderwoerd,Radek Szklarczyk,(unknown),I.F.M. de Coo,Hubert J.M. Smeets	6
10	Rare novel variants in the ZIC3 gene cause X-linked heterotaxy 2016 ·European Journal of Human Genetics ·Aimée Paulussen,Anja Steyls,Jo Vanoevelen,(unknown),Ingrid P.C. Krapels,Godelieve R.F. Claes,Sonja Chocron,(unknown),Gita Tan-Sindhunata,Catarina Lundin,Irene Valenzuela,Bálint Nagy,Iben Bache,Lisa Leth Maroun,Kristiina Avela,Han G. Brunner,Hubert J.M. Smeets,Jeroen Bakkers,Arthur van den Wijngaard	16
11	Preventing the transmission of mitochondrial DNA disorders: selecting the good guys or kicking out the bad guys 2013 ·Reproductive BioMedicine Online ·Hubert J.M. Smeets	25
12	Defective NDUFA9 as a novel cause of neonatally fatal complex I disease 2011 ·Journal of Medical Genetics ·B.J.C. van den Bosch,Mike Gerards,Wim J. Sluiter,Alexander P.A. Stegmann,(unknown),Debby M.E.I. Hellebrekers,Renske Oegema,(unknown),Holger Prokisch,Katharina Danhauser,Kees Schoonderwoerd,I.F.M. de Coo,Hubert J.M. Smeets	46
13	Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation 2009 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·(unknown),I.F.M. de Coo,Liesbeth Spruijt,L. Elly A. de Wit,Hubert J.M. Smeets,Wim J. Sluiter	19
14	Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Geert Poelmans,J.J.M. Engelen,(unknown),Hubert J.M. Smeets,Eric Schoenmakers,Barbara Franke,Jan K. Buitelaar,(unknown),(unknown),Jean Steyaert,C. T. R. M. Schrander‐Stumpel	63
15	Altered myocardial gene expression reveals possible maladaptive processes in heterozygous and homozygous cardiac myosin-binding protein C knockout mice 2007 ·Genomics ·Lars Eijssen,B.J.C. van den Bosch,Nicolas Vignier,Patrick Lindsey,(unknown),Lucie Carrier,Pieter A. Doevendans,Ger J. Vusse,Hubert J.M. Smeets	11
16	Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients 2006 ·Genetics in Medicine ·(unknown),Mike Gerards,Lars Eijssen,Alexandra T.M. Hendrickx,Roselie Jongbloed,John H. J. Wokke,Rogier Q. Hintzen,(unknown),I.F.M. de Coo,Egill Briem,Valeria Tiranti,Hubert J.M. Smeets	28
17	Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation 2004 ·Molecular Human Reproduction ·L.J.A.M. Jacobs,I.F.M. de Coo,Jeroen G. Nijland,R. J. H. Galjaard,Frans J. Los,Kees Schoonderwoerd,Martinus F. Niermeijer,Joep Geraedts,H.R. Scholte,Hubert J.M. Smeets	31
18	Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation 2000 ·Kidney International ·(unknown),Laurence Heidet,Erika Timmer,B.J.C. van den Bosch,Anu Leinonen,Corinne Antignac,J. Ashley Jefferson,Alexander P. Maxwell,L.A.H. Monnens,(unknown),Hubert J.M. Smeets	104
19	Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation 2000 ·Kidney International ·(unknown),Laurence Heidet,Erika Timmer,B.J.C. van den Bosch,Anu Leinonen,Corinne Antignac,J. Ashley Jefferson,Alexander P. Maxwell,L.A.H. Monnens,Cornelis H. Schröder,Hubert J.M. Smeets	1
20	Identification of Four Novel Mutations in the COL4A5 Gene of Patients with Alport Syndrome 1993 ·Genomics ·Henny H. Lemmink,Cornelis H. Schröder,Han G. Brunner,Marcel Nelen,Jing Zhou,Karl Tryggvason,(unknown),(unknown),Wolfgang Rascher,Bernard A. van Oost,Hubert J.M. Smeets	20

About Hubert J.M. Smeets

Hubert J.M. Smeets is a scholar working on Clinical Biochemistry, Molecular Biology and Immunology and Allergy, having authored 133 papers that have together received 4.6k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (64 papers), Metabolism and Genetic Disorders (31 papers) and ATP Synthase and ATPases Research (21 papers). The work is most often cited by research in Clinical Biochemistry (926 citations), Immunology and Allergy (396 citations) and Molecular Biology (3.0k citations). Hubert J.M. Smeets has collaborated with scholars based in Netherlands, Belgium and United Kingdom. Frequent co-authors include I.F.M. de Coo, Mike Gerards, Suzanne C.E.H. Sallevelt, Bernard A. van Oost, Pieter A. Doevendans, Joep Geraedts, Han G. Brunner, Stephen T. Reeders, B.J.C. van den Bosch and Florence H. J. van Tienen. Their work appears in journals such as Science, New England Journal of Medicine and Nucleic Acids Research.

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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