Marco Henneke

1.9k citations

35 papers · 1.1k indexed · h-index 19

Co-authors: Jutta Gärtner J.A. Berden Knut Brockmann Franz Rüschendorf Peter Nürnberg Bernhard Weschke Fuat Aksu Haluk Topaloğlu
Topics: RNA regulation and disease (16 papers)Metabolism and Genetic Disorders (8 papers)RNA Research and Splicing (5 papers)
Cited by: Clinical Biochemistry Neurology Molecular Biology
Journals: Proceedings of the National Academy of Sciences Nature Genetics Neurology
Partner nations: Germany Netherlands United States

In The Last Decade

Marco Henneke

34 papers receiving 1.0k citations

Peers

Countries citing papers authored by Marco Henneke

Since Specialization

Citations

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

Fields of papers citing papers by Marco Henneke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marco Henneke

This figure shows the co-authorship network connecting the top 25 collaborators of Marco Henneke. A scholar is included among the top collaborators of Marco Henneke 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 Marco Henneke. Marco Henneke 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	A novel remitting leukodystrophy associated with a variant in FBP2 2021 ·Brain Communications ·Agnieszka Gizak,(unknown),Steffi Dreha‐Kulaczewski,Janusz Wiśniewski,Przemysław Duda,Andreas Ohlenbusch,Brenda Huppke,Marco Henneke,Wolfgang Höhne,Janine Altmüller,Holger Thiele,Peter Nürnberg,Dariusz Rakus,Jutta Gärtner,Peter Huppke	2
2	Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both? 2020 ·Journal of Medical Genetics ·(unknown),Agnès Rötig,Charles‐Joris Roux,R. Lévy,Marco Henneke,Jutta Gärtner,(unknown),(unknown),Uluç Yiş,Laura Konczal,(unknown),(unknown),Pauline Gaignard,Claude Besmond,Laurence Hubert,Marlène Rio,Giulia Barcia,Arnold Münnich,Nathalie Boddaert,Manuel Schiff	5
3	Zebrafish disease model of human RNASET2 deficient cystic leukoencephalopathy displays abnormalities in early microglia 2020 ·Biology Open ·Thomas Weber,Lars Schlotawa,Roland Dosch,Noémie Hamilton,(unknown),(unknown),(unknown),Jutta Gärtner,Marco Henneke	6
4	Einseitige Optikusatrophie bei einem 9-jährigen Patienten 2020 ·Der Ophthalmologe ·(unknown),(unknown),Marco Henneke,Nicolas Feltgen,Hans Hoerauf,(unknown)	0
5	Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutières syndrome 2016 ·European Journal of Paediatric Neurology ·Davide Tonduti,Simona Orcesi,Emma M. Jenkinson,Imen Dorboz,Florence Renaldo,Celeste Panteghini,Gillian Rice,Marco Henneke,John H. Livingston,Monique Elmaleh,Lydie Bürglen,Michèl A.A.P. Willemsen,Luisa Chiapparini,Barbara Garavaglia,Diana Rodriguez,Odile Boespflug‐Tanguy,Isabella Moroni,Yanick J. Crow	24
6	Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review 2016 ·BMC Neurology ·Matthias Kettwig,Orly Elpeleg,Eike Wegener,Steffi Dreha‐Kulaczewski,Marco Henneke,Jutta Gärtner,Peter Huppke	17
7	Phenotypic and molecular insights into CASK-related disorders in males 2015 ·Orphanet Journal of Rare Diseases ·Ute Moog,Tatjana Bierhals,K. Gerhard Brand,(unknown),Saskia Biskup,Thomas Brune,Jonas Denecke,C E de Die-Smulders,Christina Evers,Maja Hempel,Marco Henneke,Helger G. Yntema,Björn Menten,Joachim Pietz,Rolph Pfundt,Jörg Schmidtke,Doris Steinemann,Constance T. R. M. Stumpel,Lionel Van Maldergem,Kerstin Kutsche	59
8	Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder 2014 ·European Journal of Paediatric Neurology ·(unknown),Simon Edvardson,Dorit Lev,Esther Leshinsky‐Silver,Liat Ben‐Sira,Marco Henneke,Tally Lerman‐Sagie,Lubov Blumkin	7
9	Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation 2013 ·European Journal of Medical Genetics ·Rebecca Buchert,Steffen Uebe,(unknown),Hasan Tawamie,(unknown),Haruo Shimazaki,Marco Henneke,Arif B. Ekici,André Reis,Rami Abou Jamra	16
10	Assessment of myelination in hypomyelinating disorders by quantitative MRI 2012 ·Journal of Magnetic Resonance Imaging ·Steffi Dreha‐Kulaczewski,Knut Brockmann,Marco Henneke,Peter Dechent,Bernd Wilken,Jutta Gärtner,Gunther Helms	2
11	Assessment of myelination in hypomyelinating disorders by quantitative MRI 2012 ·Journal of Magnetic Resonance Imaging ·Steffi Dreha‐Kulaczewski,Knut Brockmann,Marco Henneke,Peter Dechent,Bernd Wilken,Jutta Gärtner,Gunther Helms	19
12	rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA 2011 ·Proceedings of the National Academy of Sciences ·(unknown),Firat Kara,(unknown),Marco Henneke,Jason R. Willer,Melissa S. Hillwig,Ronald G. Gregg,Gustavo C. MacIntosh,Jutta Gärtner,A. Alia,Adam Hurlstone	81
13	Pelizaeus–Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction 2010 ·European Journal of Human Genetics ·(unknown),Marco Henneke,Birgitta C. Burckhardt,Jutta Gärtner	25
14	In vivo proton MR spectroscopy findings specific for adenylosuccinate lyase deficiency 2010 ·NMR in Biomedicine ·Marco Henneke,Steffi Dreha‐Kulaczewski,Knut Brockmann,Marinette van der Graaf,Michèl A.A.P. Willemsen,Udo F. H. Engelke,Peter Dechent,Arend Heerschap,Gunther Helms,Ron A. Wevers,Jutta Gärtner	7
15	GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease 2007 ·Neurology ·Marco Henneke,Patricia Combes,(unknown),Enrico Bertini,Knut Brockmann,Alessandro P. Burlina,(unknown),Andreas Ohlenbusch,Barbara Plecko,Diana Rodriguez,Odile Boespflug‐Tanguy,Jutta Gärtner	59
16	Pitfall in Metabolic Screening in a Patient with Fatal Peroxisomal β-Oxidation Defect 2006 ·Neuropediatrics ·Hendrik Rosewich,H. R. Waterham,(unknown),Sacha Ferdinandusse,Marco Henneke,D. H. Hunneman,Jutta Gärtner	33
17	Identification of ten novel mutations in patients with eIF2B-related disorders 2005 ·Human Mutation ·Andreas Ohlenbusch,Marco Henneke,Knut Brockmann,(unknown),F. Hanefeld,Alfried Kohlschütter,Jutta Gärtner	37
18	Cystic leukoencephalopathy without megalencephaly 2005 ·Neurology ·Marco Henneke,(unknown),V. Engelbrecht,Fuat Aksu,Enrico Bertini,Genila Bibat,Knut Brockmann,(unknown),M. Mayer,Vlatka Mejaški‐Bošnjak,S. Naidu,Eva Neumaier‐Probst,Diana Rodriguez,(unknown),Alfried Kohlschütter,Jutta Gärtner	20
19	Mutation analysis of the M6b gene in patients with Pelizaeus–Merzbacher‐like syndrome 2004 ·American Journal of Medical Genetics Part A ·Marco Henneke,(unknown),Hans Christian Hennies,(unknown),Jutta Gärtner	7
20	Identification of twelve novel mutations in patients with classic and variant forms of maple syrup urine disease 2003 ·Human Mutation ·Marco Henneke,(unknown),(unknown),Martina Müller‐Nurasyid,Peter Schadewaldt,Jutta Gärtner,U. Wendel	39

About Marco Henneke

Marco Henneke is a scholar working on Clinical Biochemistry, Neurology and Molecular Biology, having authored 35 papers that have together received 1.1k indexed citations. Recurring topics across this work include RNA regulation and disease (16 papers), Metabolism and Genetic Disorders (8 papers) and RNA Research and Splicing (5 papers). The work is most often cited by research in Clinical Biochemistry (109 citations), Neurology (115 citations) and Molecular Biology (834 citations). Marco Henneke has collaborated with scholars based in Germany, Netherlands and United States. Frequent co-authors include Jutta Gärtner, J.A. Berden, Knut Brockmann, Franz Rüschendorf, Peter Nürnberg, Bernhard Weschke, Fuat Aksu, Haluk Topaloğlu, Andreas Ohlenbusch and Birgit Uhlenberg. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Neurology.

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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