H.J.M. Smeets

3.7k citations

63 papers · 2.4k indexed · h-index 30

Molecular Biology top 5%
Genetics top 5%
Immunology and Allergy top 1%
Clinical Biochemistry top 1%
Cellular and Molecular Neuroscience top 5%

Co-authors: Henny H. Lemmink Bernard A. van Oost Toshio Mochizuki I.F.M. de Coo Corinne Antignac Patrick Lindsey Auke B.C. Otten Mariko Mariyama
Topics: Mitochondrial Function and Pathology (16 papers)Metabolism and Genetic Disorders (8 papers)Cell Adhesion Molecules Research (7 papers)
Cited by: Immunology and Allergy Clinical Biochemistry Nephrology
Journals: Journal of Clinical Investigation Nature GeneticsSHILAP Revista de lepidopterología
Partner nations: Netherlands United States Belgium

In The Last Decade

H.J.M. Smeets

62 papers receiving 2.4k citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Non-extensitivity and criticality of atomic hydropathicity around a voltage-gated sodium channel’s pore: a modeling study 2021 ·Journal of Biological Physics ·Markos Xenakis,Dimos Kapetis,Yang Yang,Jordi Heijman,Stephen G. Waxman,Giuseppe Lauria,Catharina G. Faber,H.J.M. Smeets,Patrick Lindsey,Ronald Westra	3
2	Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing 2020 ·PLoS ONE ·Rowida Almomani,Margherita Marchi,(unknown),Patrick Lindsey,Erika Salvi,Bart de Koning,Silvia Santoro,Stefania Magri,H.J.M. Smeets,Filippo Martinelli Boneschi,(unknown),Dan Ziegler,Janneke G. J. Hoeijmakers,Gidon J. Bönhof,Sulayman D. Dib‐Hajj,Stephen G. Waxman,Ingemar S.J. Merkies,Giuseppe Lauria,Catharina G. Faber,Monique M. Gerrits,(unknown)	13
3	Expression of pathogenic SCN9A mutations in the zebrafish: A model to study small-fiber neuropathy 2018 ·Experimental Neurology ·(unknown),(unknown),Auke B.C. Otten,Monique M. Gerrits,Janneke G. J. Hoeijmakers,Stephen G. Waxman,Raffaella Lombardi,Giuseppe Lauria,Ingemar S.J. Merkies,H.J.M. Smeets,Catharina G. Faber,Jo Vanoevelen	17
4	Evidence of digenic inheritance in Alport syndrome 2015 ·Journal of Medical Genetics ·Maria Antonietta Mencarelli,Laurence Heidet,Helen Storey,Michel van Geel,Bertrand Knebelmann,Chiara Fallerini,Nunzia Miglietti,(unknown),Francesco Cetta,John A. Sayer,Arthur van den Wijngaard,Shu Yau,Francesca Mari,Mirella Bruttini,Francesca Ariani,Karin Dahan,H.J.M. Smeets,Corinne Antignac,Frances Flinter,Alessandra Renieri	107
5	Epidermal Cyst Formation and Hyperkeratosis in a Patient Treated with Vismodegib for Locally Advanced Basal Cell Carcinoma 2015 ·Acta Dermato Venereologica ·(unknown),Tjinta Brinkhuizen,Patricia M.M.B. Soetekouw,H.J.M. Smeets,Myrurgia Abdul Hamid,Klara Mosterd	3
6	TGF-β stimulation in human and murine cells reveals commonly affected biological processes and pathways at transcription level 2014 ·BMC Systems Biology ·(unknown),(unknown),Gudrun Walenda,Steffen K. Meurer,Kristin Seré,Qiong Lin,H.J.M. Smeets,Kurt Hoffmann,Wolfgang Wagner,Martin Zenke,Ralf Weiskirchen,Holger Fröhlich	34
7	ProlongedNrf1overexpression triggers adipocyte inflammation and insulin resistance 2010 ·Journal of Cellular Biochemistry ·(unknown),Patrick Lindsey,Carla Kallen,H.J.M. Smeets	16
8	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 2010 ·Human Molecular Genetics ·(unknown),Rhoda Stefanatos,Berit Adam,(unknown),H.J.M. Smeets,Florence Niel,Cyril Goizet,Benoı̂t Arveiler,Michel Kœnig,Clotilde Lagier‐Tourenne,Jean‐Louis Mandel,Catharina G. Faber,Christine de Die‐Smulders,Frank Spaans,Darren G. Monckton	120
9	Preimplantation genetic diagnosis for mitochondrial DNA disorders: ethical guidance for clinical practice 2009 ·European Journal of Human Genetics ·Annelien L. Bredenoord,Wybo Dondorp,Guido Pennings,Christine de Die‐Smulders,H.J.M. Smeets,G. de Wert	29
10	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 2008 ·American Journal of Medical Genetics Part A ·Maurice A. M. Van Steensel,Maaike Vreeburg,Jan Engelen,(unknown),Alexander P.A. Stegmann,J. Herbergs,J.W.M. van Lent,H.J.M. Smeets,(unknown)	21
11	Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders 2007 ·Human Reproduction Update ·(unknown),Guido Pennings,H.J.M. Smeets,Guido de Wert	41
12	Novel Mutations in the BHD Gene and Absence of Loss of Heterozygosity in Fibrofolliculomas of Birt-Hogg-Dubé Patients 2006 ·Journal of Investigative Dermatology ·Maurice A. M. Van Steensel,Valerie L. R. M. Verstraeten,Jorge Frank,H.J.M. Smeets,Pamela Poblete‐Gutiérrez,(unknown),Reno S. Bladergroen,Peter M. Steijlen,Michel van Geel	52
13	HERG mutation predicts short QT based on channel kinetics but causes long QT by heterotetrameric trafficking deficiency 2005 ·Cardiovascular Research ·Aimée Paulussen,Ann Raes,R. J. E. Jongbloed,(unknown),A WILDE,Dirk J. Snyders,H.J.M. Smeets,Jeroen Aerssens	18
14	A 4-base pair deletion in the mitochondrial cytochromeb gene associated with parkinsonism/MELAS overlap syndrome 1999 ·Annals of Neurology ·I.F.M. de Coo,W.O. Renier,W. Ruitenbeek,H. J. ter Laak,M. Bakker,(unknown),Bernard A. van Oost,H.J.M. Smeets	107
15	Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skin 1999 ·Kidney International ·(unknown),L.A.H. Monnens,(unknown),Henny H. Lemmink,M.H. Breuning,Erika Timmer,H.J.M. Smeets	43
16	Autosomal dominant Alport syndrome linked to the type IV collagen alpha3 and alpha4 genes 1997 ·Nephrology Dialysis Transplantation ·J. Ashley Jefferson,(unknown),Alison Hughes,(unknown),H.J.M. Smeets,Cathal Doherty,Alexander P. Maxwell	1
17	Nijmegen Breakage Syndrome Cells Fail To Induce the p53-Mediated DNA Damage Response following Exposure to Ionizing Radiation 1997 ·Molecular and Cellular Biology ·Wim Jongmans,M Vuillaume,Krystyńa Chrzańowska,H.J.M. Smeets,Karl Sperling,Janet E. Hall	99
18	Identification of variable simple sequence motifs in 19q13.2-qter: Markers for the myotonic dystrophy locus 1991 ·Genomics ·H.J.M. Smeets,Rosella Hermens,Han G. Brunner,Hans‐Hilger Ropers,B. Wieringa	30
19	Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q 1989 ·Genomics ·(unknown),(unknown),(unknown),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	67
20	Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides 1988 ·Human Genetics ·H.J.M. Smeets,(unknown),Han G. Brunner,Hans‐Hilger Ropers,(unknown)	11

About H.J.M. Smeets

H.J.M. Smeets is a scholar working on Clinical Biochemistry, Immunology and Allergy and Structural Biology, having authored 63 papers that have together received 2.4k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (16 papers), Metabolism and Genetic Disorders (8 papers) and Cell Adhesion Molecules Research (7 papers). The work is most often cited by research in Immunology and Allergy (501 citations), Clinical Biochemistry (301 citations) and Nephrology (228 citations). H.J.M. Smeets has collaborated with scholars based in Netherlands, United States and Belgium. Frequent 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. Their work appears in journals such as Journal of Clinical Investigation, Nature Genetics and SHILAP Revista de lepidopterología.

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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