Birgit Czermin

3.9k citations

27 papers · 2.3k indexed · 1 hit paper · h-index 19

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Molecular Biology top 5%
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- Cancer-related gene regulation
- Mitochondrial Function and Pathology
- RNA modifications and cancer
- ATP Synthase and ATPases Research

Papers in ⓘ

Clinical Biochemistry 9
- Metabolism and Genetic Disorders 9
Molecular Biology 26
- Mitochondrial Function and Pathology 17
- ATP Synthase and ATPases Research 8
- Genomics and Chromatin Dynamics 5
- Epigenetics and DNA Methylation 5
- RNA modifications and cancer 4
- Cancer-related gene regulation 3

Co-authors: Axel Imhof (5 shared papers)Donna McCabe (2 shared papers)Vincenzo Pirrotta (2 shared papers)Raffaella Melfi (1 shared paper)Rita Horváth (18 shared papers)Elke Holinski‐Feder (12 shared papers)Günter Reuter (1 shared paper)Alexander Brehm (1 shared paper)
Journals: Journal of Neurology (3 papers)Neuromuscular Disorders (3 papers)Neurology (2 papers)Journal of Neurology Neurosurgery & Psychiatry (2 papers)Journal of Inherited Metabolic Disease (1 paper)
Partner nations: Germany United Kingdom United States

In The Last Decade

Birgit Czermin

27 papers receiving 2.2k citations

Hit Papers

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Drosophila Enhancer of Zeste/ESC Complexes Have a Histone H3 Methyltransferase Activity that Marks Chromosomal Polycomb Sites 2002 · 1.2k citations

Peers

Countries citing papers authored by Birgit Czermin

Since Specialization

Citations

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

Fields of papers citing papers by Birgit Czermin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Birgit Czermin, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Birgit Czermin Line = papers co-authored together Birgit Czermin links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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#	Work
1	Drosophila Enhancer of Zeste/ESC Complexes Have a Histone H3 Methyltransferase Activity that Marks Chromosomal Polycomb Sites Cell ·Birgit Czermin, Raffaella Melfi, Donna McCabe, Volker Seitz, Axel Imhof, Vincenzo Pirrotta Hit paper breakdown →	2002	1238
2	Physical and functional association of SU(VAR)3‐9 and HDAC1 in Drosophila EMBO Reports ·Birgit Czermin, Gunnar Schotta, Bastian B. Hülsmann, Alexander Brehm, Peter B. Becker, Günter Reuter, Axel Imhof	2001	216
3	The Prevalence and Natural History of Dominant Optic Atrophy Due to OPA1 Mutations Ophthalmology ·Patrick Yu‐Wai‐Man, Philip G. Griffiths, Ailbhe Burke, P W Sellar, Michael W. Clarke, Lawrence Gnanaraj, Desiree Ah-Kine, Gavin Hudson, Birgit Czermin, Robert W. Taylor, Rita Horváth, Patrick F. Chinnery	2010	137
4	Adult-onset cerebellar ataxia due to mutations inCABC1/ADCK3 Journal of Neurology Neurosurgery & Psychiatry ·Rita Horváth, Birgit Czermin, Sweena Gulati, Stephanie Demuth, Gunnar Houge, Angela Pyle, Christine Dineiger, Emma L. Blakely, Adam Hassani, Charlotte Foley, Michael Brodhun, Karin Storm, Janbernd Kirschner, Gráinne S. Gorman, Hanns Lochmüller, Elke Holinski‐Feder, Robert W. Taylor, Patrick F. Chinnery	2011	79
5	The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene Journal of Neurology ·Peter Reilich, Rita Horváth, Sabine Krause, Nicolai Schramm, Douglass M. Turnbull, Michael I. Trenell, Kieren G. Hollingsworth, Gráinne S. Gorman, Volkmar Hans, Jens Reimann, Andrée MacMillan, Lesley Turner, Annette Schollen, Gregor Witte, Birgit Czermin, Elke Holinski‐Feder, Maggie C. Walter, Benedikt Schoser, Hanns Lochmüller	2011	71
6	Deficiency of the mitochondrial phosphate carrier presenting as myopathy and cardiomyopathy in a family with three affected children Neuromuscular Disorders ·Johannes A. Mayr, Franz Zimmermann, Rita Horváth, H.-C. Schneider, Benedikt Schoser, Elke Holinski‐Feder, Birgit Czermin, Peter Freisinger, Wolfgang Sperl	2011	60
7	Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency Brain ·John P. Kemp, Paul Smith, Angela Pyle, Vivienne C. M. Neeve, Helen Tuppen, Ulrike Schara, Beril Talim, Haluk Topaloğlu, Elke Holinski‐Feder, Angela Abicht, Birgit Czermin, Hanns Lochmüller, Robert McFarland, Patrick F. Chinnery, Zofia M. Chrzanowska‐Lightowlers, Robert N. Lightowlers, Robert W. Taylor, Rita Horváth	2010	55
8	Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutations Journal of Inherited Metabolic Disease ·Ulrike Schara, Jürgen‐Christoph von Kleist-Retzow, Elke Lainka, Patrick Gerner, Angela Pyle, Paul Smith, Hanns Lochmüller, Birgit Czermin, Angela Abicht, Elke Holinski‐Feder, Rita Horváth	2010	50
9	RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions Neurology ·Carl Fratter, Pravrutha Raman, Charlotte L. Alston, Emma L. Blakely, Kelly Jean Thomas Craig, Conrad Smith, Julie Evans, A Seller, Birgit Czermin, Michael G. Hanna, Joanna Poulton, Charlotte Brierley, T.G. Staunton, Peter D. Turnpenny, Andrew M. Schaefer, Patrick F. Chinnery, Rita Horváth, Douglass M. Turnbull, Gráinne S. Gorman, Rachael W. Taylor	2011	45
10	The N-Terminus of Drosophila SU(VAR)3−9 Mediates Dimerization and Regulates Its Methyltransferase Activity Biochemistry ·Ragnhild Eskeland, Birgit Czermin, Jörn Boeke, Tiziana Bonaldi, Jörg T. Regula, Axel Imhof	2004	43
11	Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2 Journal of Neurology ·Maggie C. Walter, Birgit Czermin, Solvig Müller-Ziermann, Stefanie Bulst, Joanna D. Stewart, Gavin Hudson, Peter Schneiderat, Angela Abicht, Elke Holinski‐Feder, Hanns Lochmüller, Patrick F. Chinnery, Thomas Klopstock, Rita Horváth	2010	35
12	Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1) Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Joanna Poulton, Michio Hirano, Antonella Spinazzola, Mónica Hernández, Claude Jardel, Anne Lombès, Birgit Czermin, Rita Horváth, Jan‐Willem Taanman, Agnès Rötig, Massimo Zeviani, Carl Fratter	2009	33
13	ESC, ESCL and their roles in Polycomb Group mechanisms Mechanisms of Development ·Katsuhito Ohno, Donna McCabe, Birgit Czermin, Axel Imhof, Vincenzo Pirrotta	2008	29
14	Clinical and neuropathological findings in patients with TACO1 mutations Neuromuscular Disorders ·Jürgen Seeger, Bertold Schrank, Angela Pyle, Rolf Stucka, U Lörcher, Solvig Müller-Ziermann, Angela Abicht, Birgit Czermin, Elke Holinski‐Feder, Hanns Lochmüller, Rita Horváth	2010	26
15	Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation Molecular Genetics and Metabolism ·Helen Tuppen, Janev Fehmi, Birgit Czermin, P Goffrini, Francesca Meloni, Iliana Ferrero, Langping He, Emma L. Blakely, Robert McFarland, Rita Horváth, Douglass M. Turnbull, Robert W. Taylor	2010	24
16	Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita Acta Neurologica Scandinavica ·Cornelia Kornblum, G Lutterbey, Birgit Czermin, Jens Reimann, J.-C. von Kleist-Retzow, Karin Jurkat‐Rott, Mike P. Wattjes	2009	24
17	Heteroplasmic mutation in the anticodon-stem of mitochondrial tRNAVal causing MNGIE-like gastrointestinal dysmotility and cachexia Journal of Neurology ·Rita Horváth, Andreas Bender, Angela Abicht, Elke Holinski‐Feder, Birgit Czermin, Tobias Trips, Peter Schneiderat, Hanns Lochmüller, Thomas Klopstock	2009	23
18	Predicting the contribution of novel POLG mutations to human disease through analysis in yeast model Mitochondrion ·Enrico Baruffini, Rita Horváth, Cristina Dallabona, Birgit Czermin, Eleonora Lamantea, Laurence A. Bindoff, Federica Invernizzi, Iliana Ferrero, Massimo Zeviani, Tiziana Lodi	2010	22
19	Respiratory chain deficiency in nonmitochondrial disease Neurology Genetics ·Angela Pyle, Helen Nightingale, Helen Griffin, Angela Abicht, Janbernd Kirschner, Ivo Barić, Mario Ćuk, Konstantinos Douroudis, L. Feder, Markus Kratz, Birgit Czermin, Stephanie Kleinle, Mauro Santibanez‐Koref, Veronika Karcagi, Elke Holinski‐Feder, Patrick F. Chinnery, Rita Horváth	2015	18
20	The Sounds of Silence – Histone Deacetylation Meets hisTone Methylation Genetica ·Birgit Czermin, Axel Imhof	2003	16

About Birgit Czermin

Birgit Czermin is a scholar working on Clinical Biochemistry, Molecular Biology, Biochemistry, Cellular and Molecular Neuroscience and Genetics, having authored 27 papers that have together received 2.3k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (17 papers), Metabolism and Genetic Disorders (9 papers), ATP Synthase and ATPases Research (8 papers), Genomics and Chromatin Dynamics (5 papers), Epigenetics and DNA Methylation (5 papers), Genetic Neurodegenerative Diseases (4 papers), RNA modifications and cancer (4 papers) and Cancer-related gene regulation (3 papers). The work is most often cited by research in Clinical Biochemistry (292 citations), Molecular Biology (2.1k citations), Aging (30 citations), Biochemistry (84 citations) and Genetics (248 citations). Birgit Czermin has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Axel Imhof, Donna McCabe, Vincenzo Pirrotta, Raffaella Melfi, Rita Horváth, Elke Holinski‐Feder, Günter Reuter, Alexander Brehm, Peter B. Becker and Gunnar Schotta. Their work appears in journals such as Journal of Neurology, Neuromuscular Disorders, Neurology, Journal of Neurology Neurosurgery & Psychiatry and Journal of Inherited Metabolic Disease.

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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