H. ter Laak

1.3k citations

37 papers · 934 indexed · h-index 19

Co-authors: P. H. K. Jap Jan van Deursen Bé Wieringa A. Heerschap Frank Oerlemans W. Ruitenbeek R. C. A. Sengers F.J.M. Gabreëls
Topics: Mitochondrial Function and Pathology (14 papers)Metabolism and Genetic Disorders (13 papers)Muscle Physiology and Disorders (8 papers)
Cited by: Clinical Biochemistry Cell Biology Molecular Biology
Journals: Cell Proceedings of the National Academy of Sciences Brain
Partner nations: Netherlands Germany Italy

In The Last Decade

H. ter Laak

36 papers receiving 909 citations

Peers

Countries citing papers authored by H. ter Laak

Since Specialization

Citations

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

Fields of papers citing papers by H. ter Laak

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. ter Laak

This figure shows the co-authorship network connecting the top 25 collaborators of H. ter Laak. A scholar is included among the top collaborators of H. ter Laak 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. ter Laak. H. ter Laak 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

#	Work	Indexed citations
1	Dystrophic Myopathy of the Diaphragm with Recurrent Severe Respiratory Failure is Congenital Myasthenic Syndrome 11 2022 ·Journal of Neuromuscular Diseases ·(unknown),(unknown),(unknown),H. ter Laak,(unknown),Benno Küsters,(unknown),Erik‐Jan Kamsteeg,B. Eymard,Jonne Doorduin,Nicol C. Voermans	2
2	Muscle 3243A→G mutation load and capacity of the mitochondrial energy‐generating system 2008 ·Annals of Neurology ·A.J.M. Janssen,Markus Schuelke,Jan Smeıtınk,Frans J.M. Trijbels,R. C. A. Sengers,Barbara Lucke,Liesbeth T. Wintjes,Éva Morava,Baziel G.M. van Engelen,(unknown),Frans A. Hol,(unknown),H. ter Laak,Marjo S. van der Knaap,Francjan J. van Spronsen,Richard J. Rodenburg,Lambert P. van den Heuvel	20
3	Severe Congenital Muscular Dystrophy in a LAMA2-Mutated Case 2007 ·Pediatric Neurology ·Claudia Di Blasi,Nens van Alfen,(unknown),H. ter Laak,Marina Mora	0
4	Neuromuscular Abnormalities in Ataxia Telangiectasia: A Clinical, Electrophysiological and Muscle Ultrasound Study 2007 ·Neuropediatrics ·M.M.M. Verhagen,Nens van Alfen,Sigrid Pillen,Corry M.R. Weemaes,(unknown),J.A.P. Hiel,H. ter Laak,Marcel van Deuren,Annegien Broeks,Michèl A.A.P. Willemsen	17
5	A case of neuromuscular mimicry 2006 ·Neuromuscular Disorders ·(unknown),Sebastiaan Overeem,Baziel G.M. van Engelen,Hans Scheffer,Christa van den Elzen,H. ter Laak,Martin Lammens,H. Jurgen Schelhaas,Machiel J. Zwarts	7
6	Skeletal Muscle Ultrasonography in Children with a Dysfunction in the Oxidative Phosphorylation System 2006 ·Neuropediatrics ·Sigrid Pillen,Éva Morava,(unknown),H. ter Laak,Maaike de Vries,Richard J. Rodenburg,Machiel J. Zwarts	27
7	Investigation of a Family Following Fulminant Malignant Hyperthermia 2004 ·Journal of Clinical Neuromuscular Disease ·Marc Snoeck,R. C. A. Sengers,David Iles,H. ter Laak,Rachel Robinson,George W. Padberg	2
8	Congenital hypertrophic cardiomyopathy, cataract, mitochondrial myopathy and defective oxidative phosphorylation in two siblings with Sengers-like syndrome 2004 ·European Journal of Pediatrics ·Éva Morava,R. C. A. Sengers,H. ter Laak,Lambert van den Heuvel,A.J.M. Janssen,Frans J.M. Trijbels,(unknown),C Boelen,Jan Smeıtınk	29
9	Scheie Syndrome Presenting as Myopathy 2001 ·Neuropediatrics ·Aad Verrips,Baziel G.M. van Engelen,H. ter Laak,Pieter Wesseling,Jeroen de Jong,F.J.M. Gabreëls	1
10	Cerebrotendinous xanthomatosis 2000 ·Neuromuscular Disorders ·Aad Verrips,Baziel G.M. van Engelen,H. ter Laak,A.A.W.M. Gabreëls‐Festen,Anjo J.W.M. Janssen,Machiel J. Zwarts,Ron A. Wevers,F.J.M. Gabreëls	25
11	Early-Onset Sensorineural Hearing Loss and Late-Onset Neurologic Complaints Caused by a Mitochondrial Mutation at Position 7472 1998 ·Archives of Otolaryngology - Head and Neck Surgery ·R.J.H. Ensink,Kristien Verhoeven,Henri A. M. Marres,P.L.M. Huygen,G.W. Padberg,H. ter Laak,Guy Van Camp,Patrick J. Willems,C. W. R. J. Cremers	10
12	Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status 1996 ·Brain ·Peter Henricus Maria Franciscus van Domburg,A.A.W.M. Gabreëls‐Festen,F.J.M. Gabreëls,I.F.M. de Coo,W. Ruitenbeek,Pieter Wesseling,H. ter Laak	25
13	Association of Congenital Muscular Dystrophy with Hypoplasia of the Lateral Abdominal Wall Musculature and Hypoplasia of the External Genitalia 1996 ·Neuropediatrics ·(unknown),W.O. Renier,F. Gabreëls,(unknown),H. ter Laak,R.A. Mullaart	2
14	Human Diseases with Defects in Oxidative Phosphorylation. 1. Decreased Amounts of Assembled Oxidative Phosphorylation Complexes in Mitochondrial Encephalomyopathies 1995 ·European Journal of Biochemistry ·Herman Bentlage,I.F.M. de Coo,H. ter Laak,R. C. A. Sengers,F. Trijbels,W. Ruitenbeek,W. Schlote,Kathy Pfeiffer,Simonida Gencic,Gebhard von Jagow,(unknown)	33
15	Effects of the creatine analogue β-guanidinopropionic acid on skeletal muscles of mice deficient in muscle creatine kinase 1994 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Jan van Deursen,P. H. K. Jap,A. Heerschap,H. ter Laak,W. Ruitenbeek,B. Wieringa	35
16	Skeletal muscles of mice deficient in muscle creatine kinase lack burst activity 1993 ·Cell ·Jan van Deursen,A. Heerschap,Frank Oerlemans,(unknown),P. H. K. Jap,H. ter Laak,Bé Wieringa	280
17	Postnatal Development of Pyruvate Oxidation in Quadriceps Muscle of the Rat 1992 ·Neonatology ·Wolfgang Sperl,(unknown),J. M. F. Trijbels,W. Ruitenbeek,Robin de Graaf,H. ter Laak,(unknown),(unknown),A.J.M. Janssen	5
18	MELAS Syndrome - Report of Two Patients, and Comparison with Data of 24 Patients Derived from the Literature* 1991 ·Neuropediatrics ·(unknown),F.J.M. Gabreëls,W. Ruitenbeek,R. C. A. Sengers,W.O. Renier,H.O.M. Thijssen,H. ter Laak	11
19	An autosomal dominant type of congenital muscular dystrophy 1985 ·Clinical Neurology and Neurosurgery ·(unknown),F. Gabreëls,W. O. Renier,(unknown),Elbert A.J. Joosten,A. M. Stadhouders,H. ter Laak	1
20	Neuroaxonal pathology of central and peripheral nervous systems in cerebrotendinous xanthomatosis (CTX) 1984 ·Acta Neuropathologica ·(unknown),E.M.G. Joosten,(unknown),A.A.W.M. Gabreëls‐Festen,H. H. J. Jaspar,H. ter Laak,(unknown)	27

About H. ter Laak

H. ter Laak is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology, having authored 37 papers that have together received 934 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (14 papers), Metabolism and Genetic Disorders (13 papers) and Muscle Physiology and Disorders (8 papers). The work is most often cited by research in Clinical Biochemistry (184 citations), Cell Biology (187 citations) and Molecular Biology (634 citations). H. ter Laak has collaborated with scholars based in Netherlands, Germany and Italy. Frequent co-authors include P. H. K. Jap, Jan van Deursen, Bé Wieringa, A. Heerschap, Frank Oerlemans, W. Ruitenbeek, R. C. A. Sengers, F.J.M. Gabreëls, Jan Smeıtınk and Éva Morava. Their work appears in journals such as Cell, Proceedings of the National Academy of Sciences and Brain.

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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