An I. Jonckheere

1.5k citations

24 papers · 986 indexed · h-index 14

Molecular Biology top 10%
Clinical Biochemistry top 1%
Physiology
Pediatrics, Perinatology and Child Health
Epidemiology

Co-authors: Richard J. Rodenburg Jan Smeıtınk Lambert P. van den Heuvel Martijn A. Huynen Leo Nijtmans A.J.M. Janssen Maaike C. de Vries Mariël A.M. van den Brand
Topics: Mitochondrial Function and Pathology (13 papers)Metabolism and Genetic Disorders (10 papers)ATP Synthase and ATPases Research (8 papers)
Cited by: Clinical Biochemistry Molecular Biology Biochemistry
Journals: PLoS ONE Brain Scientific Reports
Partner nations: Belgium Netherlands Germany

In The Last Decade

An I. Jonckheere

22 papers receiving 971 citations

Peers

Countries citing papers authored by An I. Jonckheere

Since Specialization

Citations

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

Fields of papers citing papers by An I. Jonckheere

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by An I. Jonckheere. 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 An I. Jonckheere. The network helps show where An I. Jonckheere may publish in the future.

Co-authorship network of co-authors of An I. Jonckheere

This figure shows the co-authorship network connecting the top 25 collaborators of An I. Jonckheere. A scholar is included among the top collaborators of An I. Jonckheere 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 An I. Jonckheere. An I. Jonckheere 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	Natural history of three late-diagnosed classic Galactosemia patients 2024 ·Molecular Genetics and Metabolism Reports ·Dulce Quelhas,Sandra D.K. Kingma,An I. Jonckheere,(unknown),(unknown),(unknown),(unknown),Gert Matthijs,Laura K.M. Steinbusch,Jaak Jaeken,Isabel Rivera,M. Estela Rubio‐Gozalbo	0
2	The Impact of Intraventricular Hemorrhage and Periventricular Leukomalacia on Mortality and Neurodevelopmental Outcome in Very Preterm and Very Low Birthweight Infants: A Prospective Population-based Cohort Study 2023 ·The Journal of Pediatrics ·Aurelie Pascal,Nele De Bruyn,Gunnar Naulaers,Els Ortibus,Britta Hanssen,Ann Oostra,(unknown),(unknown),(unknown),Alexandra Casaer,(unknown),Sabine Laroche,An I. Jonckheere,Katleen Plaskie,(unknown),Els Bruneel,(unknown),(unknown),Paul Govaert,Christine Van den Broeck	13
3	Metachromatic leukodystrophy: To screen or not to screen? 2023 ·European Journal of Paediatric Neurology ·An I. Jonckheere,Sandra D.K. Kingma,François Eyskens,Victoria Bordon,Anna Jansen	1
4	Clinical Investigation of French Maritime Pine Bark Extract on Attention-Deficit Hyperactivity Disorder as compared to Methylphenidate and Placebo: Part 1: Efficacy in a Randomised Trial 2022 ·Journal of Functional Foods ·(unknown),Annelies Verlaet,Annelies Breynaert,Tania Naessens,Erik Fransén,Hélène Verhelst,Dirk Van West,(unknown),An I. Jonckheere,Diane Beysen,(unknown),(unknown),(unknown),Huub F. J. Savelkoul,Tess De Bruyne,Luc Pieters,Berten Ceulemans,Nina Hermans	4
5	MPS I: Early diagnosis, bone disease and treatment, where are we now? 2021 ·Journal of Inherited Metabolic Disease ·Sandra D.K. Kingma,An I. Jonckheere	8
6	Neurodevelopmental outcomes of very preterm and very-low-birthweight infants in a population-based clinical cohort with a definite perinatal treatment policy 2020 ·European Journal of Paediatric Neurology ·Aurelie Pascal,Gunnar Naulaers,Els Ortibus,Ann Oostra,(unknown),(unknown),(unknown),Alexandra Casaer,(unknown),Sabrina Laroche,An I. Jonckheere,Katleen Plaskie,(unknown),(unknown),Els Bruneel,(unknown),(unknown),Paul Govaert,Christine Van den Broeck	18
7	Primary skeletal muscle myoblasts from chronic heart failure patients exhibit loss of anti-inflammatory and proliferative activity 2016 ·BMC Cardiovascular Disorders ·(unknown),An M. Van Berendoncks,An I. Jonckheere,Richard J. Rodenburg,Patrick Lauwers,Viviane Van Hoof,An Wouters,Filip Lardon,Vicky Y. Hoymans,Christiaan Vrints	12
8	Quantifying small molecule phenotypic effects using mitochondrial morpho-functional fingerprinting and machine learning 2015 ·Scientific Reports ·Lionel Blanchet,Jan Smeıtınk,(unknown),(unknown),Mina Pellegrini,An I. Jonckheere,Richard J. Rodenburg,L.M.C. Buydens,Julien Beyrath,Peter H.G.M. Willems,Werner J.H. Koopman	39
9	A Bumpy Ride on the Diagnostic Bench of Massive Parallel Sequencing, the Case of the Mitochondrial Genome 2014 ·PLoS ONE ·(unknown),(unknown),Claudia Spits,Katrien Stouffs,An I. Jonckheere,Linda De Meırleır,Willy Lissens,Arnaud Vanlander,Joél Smet,Boél De Paepe,Rudy Van Coster,Sara Seneca	13
10	Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench? 2014 ·European Journal of Human Genetics ·Sara Seneca,(unknown),Rudy Van Coster,Joél Smet,Willy Lissens,Arnaud Vanlander,Boél De Paepe,An I. Jonckheere,Katrien Stouffs,Linda De Meırleır	31
11	A mutation in the human CBP4 ortholog UQCC3 impairs complex III assembly, activity and cytochrome b stability 2014 ·Human Molecular Genetics ·Bas F.J. Wanschers,Radek Szklarczyk,Mariël A.M. van den Brand,An I. Jonckheere,(unknown),Roel Smeets,Richard J. Rodenburg,(unknown),Ingrid B. Helland,(unknown),Terje Rootwelt,Martin Ott,Lambert van den Heuvel,Leo Nijtmans,Martijn A. Huynen	55
12	A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathy 2013 ·Brain ·An I. Jonckheere,G. Herma Renkema,(unknown),Lambert P. van den Heuvel,Alexander Hoischen,Christian Gilissen,Sander B. Nabuurs,Martijn A. Huynen,Maaike C. de Vries,Jan Smeıtınk,Richard J. Rodenburg	73
13	Early treatment of a child with NAGS deficiency using N-carbamyl glutamate results in a normal neurological outcome 2013 ·European Journal of Pediatrics ·(unknown),Anna Jansen,Philippe Goyens,Geert A. Martens,Stefaan Peeters,An I. Jonckheere,Linda De Meırleır	14
14	Developing outcome measures for pediatric mitochondrial disorders: Which complaints and limitations are most burdensome to patients and their parents? 2012 ·Mitochondrion ·Saskia Koene,Saskia B. Wortmann,Maaike C. de Vries,An I. Jonckheere,Éva Morava,Imelda J. M. de Groot,Jan Smeıtınk	32
15	Restoration of complex V deficiency caused by a novel deletion in the human TMEM70 gene normalizes mitochondrial morphology 2011 ·Mitochondrion ·An I. Jonckheere,Merei Huigsloot,Martin Lammens,Jitske Jansen,Lambert P. van den Heuvel,Ute Spiekerkoetter,Jürgen‐Christoph von Kleist-Retzow,Marleen Forkink,Werner J.H. Koopman,Radek Szklarczyk,Martijn A. Huynen,Jack Fransen,Jan Smeıtınk,Richard J. Rodenburg	35
16	Mitochondrial ATP synthase: architecture, function and pathology 2011 ·Journal of Inherited Metabolic Disease ·An I. Jonckheere,Jan Smeıtınk,Richard J. Rodenburg	438
17	High-Throughput Assay to Measure Oxygen Consumption in Digitonin-Permeabilized Cells of Patients with Mitochondrial Disorders 2009 ·Clinical Chemistry ·An I. Jonckheere,Merei Huigsloot,A.J.M. Janssen,(unknown),Jan Smeıtınk,Richard J. Rodenburg	21
18	Biochemical and genetic analysis of 3-methylglutaconic aciduria type IV: a diagnostic strategy 2008 ·Brain ·Saskia B. Wortmann,Richard J. Rodenburg,An I. Jonckheere,Maaike C. de Vries,Marjan Huizing,Katrin Heldt,Lambert P. van den Heuvel,U. Wendel,Leo A. J. Kluijtmans,Udo F. H. Engelke,Ron A. Wevers,Jan Smeıtınk,Éva Morava	58
19	A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy 2007 ·Journal of Medical Genetics ·An I. Jonckheere,Marije Hogeveen,Leo Nijtmans,Mariël A.M. van den Brand,A.J.M. Janssen,J H S Diepstra,(unknown),Lambertus P. van den Heuvel,Frans A. Hol,Tom Hofste,Livia Kapusta,Ulrich Dillmann,Mohammed Ghiath Shamdeen,Jan Smeıtınk,Richard J. Rodenburg	88
20	Successful liver transplantation for argininosuccinate lyase deficiency (ASLD) 2006 ·Journal of Inherited Metabolic Disease ·Eddy Robberecht,(unknown),An I. Jonckheere,Stéphanie Van Biervliet,D. Carton	10

About An I. Jonckheere

An I. Jonckheere is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology, having authored 24 papers that have together received 986 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (13 papers), Metabolism and Genetic Disorders (10 papers) and ATP Synthase and ATPases Research (8 papers). The work is most often cited by research in Clinical Biochemistry (319 citations), Molecular Biology (762 citations) and Biochemistry (35 citations). An I. Jonckheere has collaborated with scholars based in Belgium, Netherlands and Germany. Frequent co-authors include Richard J. Rodenburg, Jan Smeıtınk, Lambert P. van den Heuvel, Martijn A. Huynen, Leo Nijtmans, A.J.M. Janssen, Maaike C. de Vries, Mariël A.M. van den Brand, Éva Morava and Saskia B. Wortmann. Their work appears in journals such as PLoS ONE, Brain and Scientific Reports.

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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