Michaela Jaksch

3.0k citations

40 papers · 1.9k indexed · h-index 24

Molecular Biology top 5%
Clinical Biochemistry top 0.5%
Physiology top 10%
Cellular and Molecular Neuroscience top 10%
Nutrition and Dietetics top 5%

Co-authors: Klaus-Dieter Gerbitz Sabine Hofmann Rita Horváth Hanns Lochmüller J. A. Maassen Johannes M.W. van den Ouweland Peter Freisinger Josef Müller‐Höcker
Topics: Mitochondrial Function and Pathology (27 papers)ATP Synthase and ATPases Research (17 papers)Metabolism and Genetic Disorders (15 papers)
Cited by: Clinical Biochemistry Molecular Biology Nutrition and Dietetics
Journals: The Lancet Nucleic Acids Research Neurology
Partner nations: Germany Austria United Kingdom

In The Last Decade

Michaela Jaksch

40 papers receiving 1.9k citations

Peers

Countries citing papers authored by Michaela Jaksch

Since Specialization

Citations

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

Fields of papers citing papers by Michaela Jaksch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michaela Jaksch

This figure shows the co-authorship network connecting the top 25 collaborators of Michaela Jaksch. A scholar is included among the top collaborators of Michaela Jaksch 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 Michaela Jaksch. Michaela Jaksch 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	Mitochondrial Phosphate–Carrier Deficiency: A Novel Disorder of Oxidative Phosphorylation 2007 ·The American Journal of Human Genetics ·Johannes A. Mayr,Olaf Merkel,Sepp D. Kohlwein,Boris Gebhardt,Hansjosef Böhles,(unknown),Johannes Koch,Michaela Jaksch,Hanns Lochmüller,Rita Horváth,Peter Freisinger,Wolfgang Sperl	120
2	Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy 2005 ·Neuromuscular Disorders ·Rita Horváth,Benedikt Schoser,Josef Müller‐Höcker,(unknown),Michaela Jaksch,Hanns Lochmüller	44
3	Expression profiling in patients with complex IV respiratory chain deficiencies 2002 ·European Journal of Human Genetics ·Konstanze Hörtnagel,Michaela Jaksch,Jobst Landgrebe,(unknown),Thomas Meitinger	3
4	Familial left ventricular hypertrabeculation in two blind brothers 2002 ·Cardiovascular Pathology ·Josef Finsterer,Claudia Stöllberger,Michaela Jaksch	10
5	A novel mutation in the deoxyguanosine kinase gene causing depletion of mitochondrial DNA 2002 ·Annals of Neurology ·Jan‐Willem Taanman,(unknown),Ania C. Muntau,Michaela Jaksch,Nadine Cohen,Hanna Mandel	38
6	Depletion of mitochondrial DNA in the liver of an infant with neonatal giant cell hepatitis 2002 ·Human Pathology ·Josef Müller‐Höcker,(unknown),Sebastian Daniel Schäfer,Michaela Jaksch,(unknown),D. Pongratz,Jan‐Willem Taanman	24
7	Wolff-Parkinson-White syndrome and isolated left ventricular abnormal trabeculation as a manifestation of Leber's hereditary optic neuropathy. 2001 ·PubMed ·Josef Finsterer,Claudia Stöllberger,(unknown),Michaela Jaksch	19
8	Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies 2001 ·Journal of Medical Genetics ·Michaela Jaksch,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	16
9	Cytochrome c oxidase deficiency due to mutations in SCO2, encoding a mitochondrial copper-binding protein, is rescued by copper in human myoblasts 2001 ·Human Molecular Genetics ·Michaela Jaksch	99
10	Characterization of human muscle type cofilin (CFL2) in normal and regenerating muscle 2001 ·European Journal of Biochemistry ·Christian Thirion,Rolf Stucka,(unknown),Albrecht Gruhler,Michaela Jaksch,Kristen L. Nowak,N. Binz,Nigel G. Laing,Hanns Lochmüller	57
11	Multiple origins of the mtDNA 7472insC mutation associated with hearing loss and neurological dysfunction 2001 ·European Journal of Human Genetics ·Tim Hutchin,Nuria Navarro-Coy,Guy Van Camp,Valeria Tiranti,Massimo Zeviani,Markus Schuelke,Michaela Jaksch,Valerie Newton,Robert F. Mueller	20
12	Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency 2000 ·Human Molecular Genetics ·Michaela Jaksch	190
13	Characterization of Human SCO1 and COX17 Genes in Mitochondrial Cytochrome-c-Oxidase Deficiency 2000 ·Biochemical and Biophysical Research Communications ·Rita Horváth,Hanns Lochmüller,Rolf Stucka,Jianbo Yao,Eric A. Shoubridge,Sangho Kim,Klaus-Dieter Gerbitz,Michaela Jaksch	26
14	Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochromec oxidase deficiency 1999 ·Annals of Neurology ·Valeria Tiranti,Michaela Jaksch,Sabine Hofmann,(unknown),Konstanze Hoertnagel,(unknown),Peter Freisinger,Laurence A. Bindoff,Klaus-Dieter Gerbitz,Giacomo P. Comi,Graziella Uziel,Massimo Zeviani,Thomas Meitinger	85
15	Population Genetics and Disease Susceptibility: Characterization of Central European Haplogroups By mtDNA Gene Mutations, Correlation with D Loop Variants and Association With Disease 1997 ·Human Molecular Genetics ·Sabine Hofmann,Michaela Jaksch,(unknown),Stijn F. L. Mertens,(unknown),(unknown),Klaus-Dieter Gerbitz	135
16	A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus 1996 ·Human Mutation ·Michaela Jaksch,Sabine Hofmann,(unknown),B. Obermaier–Kusser,Stephan Zierz,Klaus-Dieter Gerbitz	19
17	Mitochondrial diabetes mellitus: a review 1995 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Klaus-Dieter Gerbitz,Johannes M.W. van den Ouweland,J. A. Maassen,Michaela Jaksch	160
18	Screening for mitochondrial DNA (mtDNA) point mutations using nonradioactive single strand conformation polymorphism (SSCP) analysis 1995 ·Clinical Biochemistry ·Michaela Jaksch,Klaus-Dieter Gerbitz,Christian Kilger	24
19	Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNA^Leu(UUR) gene 1993 ·FEBS Letters ·Klaus-Dieter Gerbitz,(unknown),Michaela Jaksch,S. Zierz,(unknown)	45
20	Nerve growth factor and choline acetyltransferase activity levels in the rat brain following experimental impairment of cerebral glucose and energy metabolism 1992 ·Journal of Neuroscience Research ·Rainer Hellweg,Roger M. Nitsch,C. Hock,Michaela Jaksch,S. Høyer	76

About Michaela Jaksch

Michaela Jaksch is a scholar working on Clinical Biochemistry, Molecular Biology and Cardiology and Cardiovascular Medicine, having authored 40 papers that have together received 1.9k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (27 papers), ATP Synthase and ATPases Research (17 papers) and Metabolism and Genetic Disorders (15 papers). The work is most often cited by research in Clinical Biochemistry (768 citations), Molecular Biology (1.5k citations) and Nutrition and Dietetics (177 citations). Michaela Jaksch has collaborated with scholars based in Germany, Austria and United Kingdom. Frequent co-authors include Klaus-Dieter Gerbitz, Sabine Hofmann, Rita Horváth, Hanns Lochmüller, J. A. Maassen, Johannes M.W. van den Ouweland, Peter Freisinger, Josef Müller‐Höcker, Thomas Klopstock and D. Pongratz. Their work appears in journals such as The Lancet, Nucleic Acids Research 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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