H. Smeets

1.5k citations

21 papers · 1.1k indexed · h-index 11

Impact in

Cellular and Molecular Neuroscience top 5%
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Parkinson's Disease Mechanisms and Treatments

Papers in

Cellular and Molecular Neuroscience 9
- Genetic Neurodegenerative Diseases 8
- Hereditary Neurological Disorders 2
Molecular Biology 17
- Mitochondrial Function and Pathology 6
- Fungal and yeast genetics research 4
- DNA Repair Mechanisms 3
- Epigenetics and DNA Methylation 3

Co-authors: Bé Wieringa Gert Jansen Hans‐Hilger Ropers Catherine Tsilfidis Robert G. Korneluk Gary Shutler Charalampos Aslanidis Mani S. Mahadevan
Journals: Nucleic Acids Research (5 papers)Neurology (2 papers)Journal of Neurology Neurosurgery & Psychiatry (2 papers)Journal of Cachexia Sarcopenia and Muscle (1 paper)New England Journal of Medicine (1 paper)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

H. Smeets

21 papers receiving 1.1k citations

Peers

Countries citing papers authored by H. Smeets

Since Specialization

Citations

This map shows the geographic impact of H. 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. 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. Smeets more than expected).

Fields of papers citing papers by H. Smeets

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	A novel orthotopic mouse model replicates human lung cancer cachexia Journal of Cachexia Sarcopenia and Muscle ·Wouter R. P. H. van de Worp, Jan Theys, Tatyana Vladimirovna Utyanskaya, Brent van der Heyden, Frank Verhaegen, Duncan Hauser, Florian Caiment, H. Smeets, Annemie M.W.J. Schols, Ardy van Helvoort, Ramon Langen	2023	9
2	Yield of peripheral sodium channels gene screening in pure small fibre neuropathy Journal of Neurology Neurosurgery & Psychiatry ·Vinicius Santos Moura, 朱国鑫, Janneke G. J. Hoeijmakers, Bianca T. A. de Greef, Patrick Lindsey, Rowida Almomani, Margherita Marchi, Jo Vanoevelen, H. Smeets, Stephen G. Waxman, Giuseppe Lauria, Ingemar S.J. Merkies, Catharina G. Faber, Monique M. Gerrits	2018	52
3	No Fabry Disease in Patients Presenting with Isolated Small Fiber Neuropathy PLoS ONE ·Bianca T. A. de Greef, Janneke G. J. Hoeijmakers, Emma E. Wolters, H. Smeets, Arthur van den Wijngaard, Ingemar S. J. Merkies, Catharina G. Faber, Monique M. Gerrits	2016	30
4	PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring Human Reproduction Update ·Debby M.E.I. Hellebrekers, Rory Wolfe, Alexandra T.M. Hendrickx, I.F.M. de Coo, Dana Wu, Joep Geraedts, Patrick F. Chinnery, H. Smeets	2012	67
5	Encephalopathic attacks in a family co-segregating myotonic dystrophy type 1, an intermediate Charcot-Marie-Tooth neuropathy and early hearing loss Journal of Neurology Neurosurgery & Psychiatry ·Frank Spaans, Catharina G. Faber, H. Smeets, Paul A.M. Hofman, 卢湧湧, Darren G. Monckton, Christine de Die‐Smulders	2009	7
6	Genetische identificatie van patiënten en families met lange-QT-syndroom: Grote regionale verschillen in de resultaten van 10 jaar Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank ·Luo Wei, Pieter G. Postema, Irene M. van Langen, Eline A. Nannenberg, Mariëlle Alders, Roselie Jongbloed, H. Smeets, Arthur A.M. Wilde	2007	3
7	Rett syndrome in females with CTS hot spot deletions: A disorder profile American Journal of Medical Genetics Part A ·William Catanzaro, Leonor Rosa Rojas Marmolejo, Paul Casaer, A.A.W. Peters, Alina T. Midro, Els Schollen, Kees van Roozendaal, Ute Moog, Gert Matthijs, J. Herbergs, H. Smeets, Leopold Curfs, C. T. R. M. Schrander‐Stumpel, J. P. Fryns	2004	57
8	Rett syndrome in adolescent and adult females: Clinical and molecular genetic findings American Journal of Medical Genetics Part A ·Eric Smeets, Els Schollen, Ute Moog, Gert Matthijs, J. Herbergs, H. Smeets, Leopold Curfs, C. T. R. M. Schrander‐Stumpel, J. P. Fryns	2003	44
9	Autosomal dominant Alport syndrome linked to the type IV collage 3 and 4 genes (COL4A3 and COL4A4) Nephrology Dialysis Transplantation ·J. Ashley Jefferson, Henny H. Lemmink, Bojan Anand, Claire Hill, H. Smeets, C. Doherty, Alexander P. Maxwell	1997	89
10	Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm. PubMed ·Gert Jansen, Patrick J. Willems, M. Coerwinkel, G. Bevilacqua, H. Smeets, Lieve Vits, C Höweler, J.B. Higgins, Bé Wieringa	1994	134
11	Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 New England Journal of Medicine ·Dominique Smeets, Ben C.J. Hamel, Marcel Nelen, H. Smeets, J. Bollen, Arie P.T. Smits, Hans‐Hilger Ropers, Bernard A. van Oost	1992	105
12	Cloning of the essential myotonic dystrophy region and mapping of the putative defect Nature ·Charalampos Aslanidis, Gert Jansen, Chris T. Amemiya, Gary Shutler, Mani S. Mahadevan, Catherine Tsilfidis, Kristoffer Sakseide, Jennifer Alleman, Ranjamin Amin, J. Beiler, Jessica L. Buxton, Keith Johnson, H. Smeets, Gregory G. Lennon, A.V. Carrano, Robert G. Korneluk, Bé Wieringa, Pieter J. de Jong	1992	405
13	Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region Genomics ·Gary Shutler, Robert G. Korneluk, Catherine Tsilfidis, Mani S. Mahadevan, J Bailly, H. Smeets, Gert Jansen, Bé Wieringa, Frans P. Lohman, Charalampos Aslanidis, Pieter J. de Jong	1992	19
14	Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy Neurology ·Han G. Brunner, Frank Spaans, H. Smeets, Chuman Achumani, Theo J.M. Hulsebos, Bé Wieringa, H.-H. Ropers	1991	10
15	MspI RFLP at 19cen–q12 identified by the anonymous DNA sequence pPM17.4 [D19S29] Nucleic Acids Research ·H. Smeets, Michael Smolle, Theo J.M. Hulsebos, HG Brunner, G. McCan, Hans‐Hilger Ropers, Bé Wieringa	1989	2
16	TaqI RFLP at 19q13.1 identified by the anonymous DNA sequence p5B18 [D19S28] Nucleic Acids Research ·H. Smeets, Jan Schepens, M. Coerwinkel, HG Brunner, G. McCan, H.-H. Ropers, Bé Wieringa	1989	3
17	Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy Human Genetics ·H. Smeets, Han G. Brunner, Hans‐Hilger Ropers, Юсупов Руслан Равильевич	1989	64
18	EcoRI RFLP at 19 cen-q13.2 identified by the anoymous DNA sequence pPM6.7 (D19S18) Nucleic Acids Research ·H. Smeets, Michael Smolle, Michela Marafini, Theo J.M. Hulsebos, Han G. Brunner, G. McCan, Hans‐Hilger Ropers, Bé Wieringa	1987	6
19	A locus at 19cen-19q13.2 (D19S15) containing three RFLPs linked to myotonic dystrophy (DM) is recognized by probe pJSB6 Nucleic Acids Research ·Jan Schepens, Theo J.M. Hulsebos, H. Smeets, M. Coerwinkel, Han G. Brunner, Hans‐Hilger Ropers, Bé Wieringa	1987	5
20	Isolation of a polymorphic DNA sequence pJSB11 (D19S16) from the human chromosome 19cen-q13.2 region linked to the myotonic dystrophy (DM) gene Nucleic Acids Research ·Jan Schepens, H. Smeets, Theo J.M. Hulsebos, Han G. Brunner, Bé Wieringa	1987	9

About H. Smeets

H. Smeets is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Neurology and Immunology and Allergy, having authored 21 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (8 papers), Mitochondrial Function and Pathology (6 papers), Fungal and yeast genetics research (4 papers), DNA Repair Mechanisms (3 papers), Epigenetics and DNA Methylation (3 papers), Genomics and Rare Diseases (2 papers), Hereditary Neurological Disorders (2 papers) and Parkinson's Disease Mechanisms and Treatments (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (571 citations), Neurology (247 citations), Genetics (360 citations), Molecular Biology (785 citations) and Immunology and Allergy (65 citations). H. Smeets has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Bé Wieringa, Gert Jansen, Hans‐Hilger Ropers, Catherine Tsilfidis, Robert G. Korneluk, Gary Shutler, Charalampos Aslanidis, Mani S. Mahadevan, Pieter J. de Jong and Chris T. Amemiya. Their work appears in journals such as Nucleic Acids Research, Neurology, Journal of Neurology Neurosurgery & Psychiatry, Journal of Cachexia Sarcopenia and Muscle and New England Journal of Medicine.

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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