Jonas Denecke

6.0k citations

82 papers · 2.1k indexed · h-index 27

Co-authors: Thorsten Marquardt Christian Kranz J. Weglage Reinhold Feldmann Hans-Georg Koch Jessika Johannsen Erik Harms Kurt Ullrich
Topics: Neurogenetic and Muscular Disorders Research (17 papers)Glycosylation and Glycoproteins Research (12 papers)Metabolism and Genetic Disorders (11 papers)
Cited by: Clinical Biochemistry Genetics Molecular Biology
Journals: Journal of Clinical Investigation Blood Brain
Partner nations: Germany United States Netherlands

In The Last Decade

Jonas Denecke

75 papers receiving 2.0k citations

Peers

Countries citing papers authored by Jonas Denecke

Since Specialization

Citations

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

Fields of papers citing papers by Jonas Denecke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonas Denecke

This figure shows the co-authorship network connecting the top 25 collaborators of Jonas Denecke. A scholar is included among the top collaborators of Jonas Denecke 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 Jonas Denecke. Jonas Denecke 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	Cognitive function in SMA patients with 2 or 3 SMN2 copies treated with SMN-modifying or gene addition therapy during the first year of life 2024 ·European Journal of Paediatric Neurology ·(unknown),Deike Weiss,Anna Perez,(unknown),P. Weber,Claudia Weiß,(unknown),(unknown),Maja von der Hagen,Jens Schallner,B Claussen,(unknown),Andreas Hahn,(unknown),(unknown),Andreas Ziegler,Jonas Denecke,Jessika Johannsen	12
2	Immunoadsorption is equally effective as plasma exchange in paediatric neuroimmunological disorders - A retrospective multicentre study 2024 ·European Journal of Paediatric Neurology ·(unknown),(unknown),Sebastian Loos,Jonas Denecke,Ellen Knierim,Dominik Müller,Lutz T. Weber,Christina Taylan,Julia Thumfart	0
3	Overview of Neuro-Ophthalmic Findings in Leukodystrophies 2024 ·Journal of Clinical Medicine ·(unknown),Simon Dulz,(unknown),(unknown),Gerhard Schön,(unknown),Sarah Maier,Jonas Denecke,Annette Bley	0
4	DySMA – an Instrument to Monitor Swallowing Function in Children with Spinal Muscular Atrophy ages 0 to 24 Months: Development, Consensus, and Pilot Testing 2024 ·Journal of Neuromuscular Diseases ·(unknown),Stefanie Witt,Jessika Johannsen,Deike Weiss,Jonas Denecke,(unknown),Almut Nießen,Julia Quitmann,Christina Pflug,(unknown)	2
5	Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males 2021 ·Human Genetics ·Hans‐Jürgen Kreienkamp,Matias Wagner,Heike Weigand,(unknown),Marie McDonald,Boris Keren,Cyril Mignot,Julie Gauthier,(unknown),Jacques L. Michaud,(unknown),Rosemarie Smith,Ulrike Löbel,Maja Hempel,Christian Kubisch,Jonas Denecke,Philippe M. Campeau,Jennifer Bain,Davor Lessel	13
6	ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants 2021 ·Neurogenetics ·Katja Kloth,Bernarda Lozić,(unknown),Mariëtte J.V. Hoffer,(unknown),Hölger Thiele,Janine Altmüller,Christian Kubisch,Ping Yee Billie Au,Jonas Denecke,Emilia K. Bijlsma,Davor Lessel	14
7	Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort 2021 ·Clinical Genetics ·Amelie T. van der Ven,Jessika Johannsen,Fanny Kortüm,Matias Wagner,Konstantinos Tsiakas,Tatjana Bierhals,Davor Lessel,Theresia Herget,Katja Kloth,Jasmin Lisfeld,(unknown),Nadia Obi,Saskia B. Wortmann,Holger Prokisch,Christian Kubisch,Jonas Denecke,René Santer,Maja Hempel	8
8	Dominant KPNA3 Mutations Cause Infantile‐Onset Hereditary Spastic Paraplegia 2021 ·Annals of Neurology ·Claudia Schob,Maja Hempel,Dana Šafka Brožková,(unknown),Soo Yeon Kim,Nurit Assia Batzir,Naama Orenstein,Tatjana Bierhals,Jessika Johannsen,(unknown),Jong‐Hee Chae,Pavel Seeman,(unknown),Fang Fang,Christian Kubisch,Stefan Kindler,Jonas Denecke	6
9	Evaluation of two family-based intervention programs for children affected by rare disease and their families – research network (CARE-FAM-NET): study protocol for a rater-blinded, randomized, controlled, multicenter trial in a 2x2 factorial design 2020 ·BMC Family Practice ·Johannes Boettcher,(unknown),Jonas Denecke,(unknown),Anne Daubmann,Antonia Zapf,Karl Wegscheider,Jan Zeidler,Johann‐Matthias Graf von der Schulenburg,Monika Bullinger,Miriam Rassenhofer,Michael Schulte‐Markwort,Silke Wiegand‐Grefe	21
10	A novel missense variant in the SDR domain of the WWOX gene leads to complete loss of WWOX protein with early-onset epileptic encephalopathy and severe developmental delay 2018 ·Neurogenetics ·Jessika Johannsen,Fanny Kortüm,Georg Rosenberger,(unknown),Markus Schirmer,Jonas Denecke,René Santer	18
11	Evaluation of Children with SMA Type 1 Under Treatment with Nusinersen within the Expanded Access Program in Germany 2018 ·Journal of Neuromuscular Diseases ·Astrid Pechmann,Thorsten Langer,David Schorling,Sabine Stein,Sibylle Emilie Vogt,Ulrike Schara,Heike Kölbel,Oliver Schwartz,Andreas Hahn,(unknown),Jessika Johannsen,Jonas Denecke,Claudia Weiß,Manuela Theophil,Janbernd Kirschner	104
12	Survival beyond the perinatal period expands the phenotypes caused by mutations in GLE1 2017 ·American Journal of Medical Genetics Part A ·Edith Said,Jessica X. Chong,Maja Hempel,Jonas Denecke,P Soler,Tim M. Strom,Deborah A. Nickerson,Christian Kubisch,Michael J. Bamshad,Davor Lessel	8
13	Epilepsy in neuronal ceroid lipofuscinoses 2015 ·Angela Schulz,Jonas Denecke,Alfried Kohlschütter	6
14	Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih 2009 ·Molecular Genetics and Metabolism ·(unknown),Heymut Omran,(unknown),Jonas Denecke,Janine Reunert,Thorsten Marquardt	19
15	Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): Where are we now? 2008 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jonas Denecke,Thorsten Marquardt	18
16	A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy 2007 ·The American Journal of Human Genetics ·Christian Kranz,(unknown),Jonas Denecke,(unknown),(unknown),Volker Debus,Hans-Gerd Kehl,Erik Harms,A. D. Reith,(unknown),H Gröbe,G. Hammersen,(unknown),Thorsten Marquardt	72
17	An activated 5? cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id) 2004 ·Human Mutation ·Jonas Denecke,Christian Kranz,Dirk Kemming,Hans-Georg Koch,Thorsten Marquardt	48
18	Congenital Disorder of Glycosylation Type Ik (CDG-Ik): A Defect of Mannosyltransferase I 2004 ·The American Journal of Human Genetics ·Christian Kranz,Jonas Denecke,Ludwig Lehle,Kristina Sohlbach,(unknown),Friedhelm Meinhardt,Rainer Rossi,Sonja Gudowius,Thorsten Marquardt	62
19	Phenylketonuria: No Specific Frontal Lobe-Dependent Neuropsychological Deficits of Early-Treated Patients in Comparison with Diabetics 2002 ·Pediatric Research ·Reinhold Feldmann,Jonas Denecke,Michael Pietsch,(unknown),J. Weglage	29
20	A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If) 2001 ·Journal of Clinical Investigation ·Christian Kranz,Jonas Denecke,Mark A. Lehrman,Sutapa Ray,(unknown),(unknown),Dijana Šagi,Jasna Peter‐Katalinić,Hudson H. Freeze,Thomas Schmid,(unknown),Erik Harms,Thorsten Marquardt	104

About Jonas Denecke

Jonas Denecke is a scholar working on Genetics, Clinical Biochemistry and Physiology, having authored 82 papers that have together received 2.1k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (17 papers), Glycosylation and Glycoproteins Research (12 papers) and Metabolism and Genetic Disorders (11 papers). The work is most often cited by research in Clinical Biochemistry (320 citations), Genetics (252 citations) and Molecular Biology (1.3k citations). Jonas Denecke has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Thorsten Marquardt, Christian Kranz, J. Weglage, Reinhold Feldmann, Hans-Georg Koch, Jessika Johannsen, Erik Harms, Kurt Ullrich, Michael Pietsch and Maja Hempel. Their work appears in journals such as Journal of Clinical Investigation, Blood 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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