Knut Brockmann

10.5k citations

139 papers · 4.2k · 1 hit paper · h-index 35

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Endocrinology, Diabetes and Metabolism top 2%
- Thyroid Disorders and Treatments
- Growth Hormone and Insulin-like Growth Factors

Papers in

Molecular Biology 58
- RNA regulation and disease 23
Genetics 30
- Genetics and Neurodevelopmental Disorders 14
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 7

Co-authors: F. Hanefeld (33 shared papers)Alexandra M. Dumitrescu (2 shared papers)Samuel Refetoff (2 shared papers)Jutta Gärtner (31 shared papers)Xiao-Hui Liao (1 shared paper)Jens Frahm (17 shared papers)Petra J. W. Pouwels (8 shared papers)Peter Dechent (19 shared papers)
Journals: Neuropediatrics (15 papers)Neurology (9 papers)Orphanet Journal of Rare Diseases (5 papers)Journal of Clinical Medicine (5 papers)Journal of Medical Genetics (4 papers)
Partner nations: Germany United States Austria

In The Last Decade

Knut Brockmann

130 papers receiving 4.0k citations

Knut Brockmann's Hit Papers

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A Novel Syndrome Combining Thyroid and Neurological Abnormalities Is Associated with Mutations in a Monocarboxylate Transporter Gene 2004 · 568 citations

Peers

Countries citing papers authored by Knut Brockmann

Since Specialization

Citations

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

Fields of papers citing papers by Knut Brockmann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Knut Brockmann, 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 Knut Brockmann Line = papers co-authored together Knut Brockmann links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 139 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Novel Syndrome Combining Thyroid and Neurological Abnormalities Is Associated with Mutations in a Monocarboxylate Transporter Gene The American Journal of Human Genetics ·Alexandra M. Dumitrescu, Xiao-Hui Liao, Thomas B. Best, Knut Brockmann, Samuel Refetoff Hit paper breakdown →	2004	568
2	Regional Age Dependence of Human Brain Metabolites from Infancy to Adulthood as Detected by Quantitative Localized Proton MRS Pediatric Research ·Petra J. W. Pouwels, Knut Brockmann, Bernd Kruse, Bernd Wilken, Markus Wick, F. Hanefeld, Jens Frahm	1999	260
3	The expanding phenotype of GLUT1-deficiency syndrome Brain and Development ·Knut Brockmann	2009	185
4	Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study The Lancet Neurology ·Hendrik Rosewich, Hölger Thiele, Andreas Ohlenbusch, Ulrike Maschke, Janine Altmüller, Peter Frommolt, Birgit Zirn, Friedrich Ebinger, H. Siemes, Peter Nürnberg, Knut Brockmann, Jutta Gärtner	2012	181
5	Autosomal dominant Glut‐1 deficiency syndrome and familial epilepsy Annals of Neurology ·Knut Brockmann, Dong Wang, Christoph Korenke, Arpad von Moers, Yuan‐Yuan Ho, Juan M. Pascual, Kunyan Kuang, Hong Yang, Li Ma, Pamela Kranz‐Eble, Jorge Fischbarg, F. Hanefeld, Darryl C. De Vivo	2001	134
6	Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice Human Molecular Genetics ·Yaqun Zou, Daniela Zwolanek, Yayoi Izu, Shreya Gandhy, Gudrun Schreiber, Knut Brockmann, Marcella Devoto, Zuozhen Tian, Ying Hu, Guido Veit, Markus Meier, Jörg Stetefeld, Debbie Hicks, Volker Straub, Nicol C. Voermans, David E. Birk, Elisabeth R. Barton, Manuel Koch, Carsten G. Bönnemann	2013	106
7	Recessive Mutations in the Gene Encoding the Tight Junction Protein Occludin Cause Band-like Calcification with Simplified Gyration and Polymicrogyria The American Journal of Human Genetics ·Mary O’Driscoll, Sarah B. Daly, Jill Urquhart, Graeme C. Black, Daniela T. Pilz, Knut Brockmann, Meriel McEntagart, Ghada M. H. Abdel‐Salam, Maha S. Zaki, Nicole I. Wolf, Roger L. Ladda, Susan L. Sell, Stefano D’Arrigo, Waney Squier, William B. Dobyns, John H. Livingston, Yanick J. Crow	2010	99
8	The LYR Factors SDHAF1 and SDHAF3 Mediate Maturation of the Iron-Sulfur Subunit of Succinate Dehydrogenase Cell Metabolism ·Un Na, Wendou Yu, James E. Cox, Daniel K. Bricker, Knut Brockmann, Jared Rutter, Carl S. Thummel, Dennis R. Winge	2014	98
9	X–linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene Journal of Neurology ·Knut Brockmann, Alexandra M. Dumitrescu, Th. T. Best, F. Hanefeld, Samuel Refetoff	2005	86
10	The expanding clinical and genetic spectrum of ATP1A3-related disorders Neurology ·Hendrik Rosewich, Andreas Ohlenbusch, Peter Huppke, Lars Schlotawa, Martina Baethmann, Inês Carrilho, Simona Fiori, Charles Marques Lourenço, Sarah L. Sawyer, Robert Steinfeld, Jutta Gärtner, Knut Brockmann	2014	85
11	Valproic acid-induced pancreatitis: 16 new cases and a review of the literature Journal of Gastroenterology ·Thorsten Gerstner, D Büsing, Nellie Bell, Elke Longin, Johannes‐Martin Kasper, W.E.M. Klostermann, B. Hebing, F. Hanefeld, U. Eckel, Reiner Hoffmann, U Bettendorf, Birgit Weidner, Adelheid Wiemer‐Kruel, Knut Brockmann, Fritz-Wilhelm Neumann, T Sandrieser, Markus Wolff, Stephan König	2007	81
12	Tandem Mass Spectrometry for the Direct Assay of Enzymes in Dried Blood Spots: Application to Newborn Screening for Krabbe Disease Clinical Chemistry ·Yijun Li, Knut Brockmann, František Tureček, C. Ronald Scott, Michael H. Gelb	2004	67
13	GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease Neurology ·Marco Henneke, Patricia Combes, Simone Diekmann, Enrico Bertini, Knut Brockmann, Alessandro P. Burlina, Jens Kaiser, Andreas Ohlenbusch, Barbara Plecko, Diana Rodriguez, Odile Boespflug‐Tanguy, Jutta Gärtner	2007	66
14	Succinate in dystrophic white matter: A proton magnetic resonance spectroscopy finding characteristic for complex II deficiency Annals of Neurology ·Knut Brockmann, Alf Bjørnstad, Peter Dechent, Christoph Korenke, Jan Smeıtınk, J. M. F. Trijbels, Sabine Athanassopoulos, Rafael Villagrán, Ola H. Skjeldal, Ekkehard Wilichowski, Jens Frahm, F. Hanefeld	2002	63
15	Proton MRS profile of cerebral metabolic abnormalities in Krabbe disease Neurology ·Knut Brockmann, Peter Dechent, B. Wilken, Oliver Rusch, Jens Frahm, F. Hanefeld	2003	62
16	Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood Neuromuscular Disorders ·Knut Brockmann, P. E. Becker, Gudrun Schreiber, Karin Neubert, Edgar Brunner, Carsten G. Bönnemann	2007	60
17	Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations Journal of Neurology ·Knut Brockmann, Steffi Dreha‐Kulaczewski, Peter Dechent, Carsten G. Bönnemann, Gunther Helms, Mårten Kyllerman, Wolfgang Brück, Jens Frahm, Kathrin Huehne, Jutta Gärtner, Bernd Rautenstrauß	2008	60
18	Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy Brain ·Sebahattin Çırak, Florian von Deimling, Shrikesh Sachdev, Wesley J. Errington, Ralf Herrmann, Carsten G. Bönnemann, Knut Brockmann, Stephan Hinderlich, Tom H. Lindner, Alice Steinbrecher, Katrin Hoffmann, Gilbert G. Privé, Mark Hannink, Peter Nürnberg, Thomas Voït	2010	56
19	Quantitative proton MRS of Pelizaeus–Merzbacher disease Neurology ·F. Hanefeld, Knut Brockmann, Petra J. W. Pouwels, B. Wilken, Jens Frahm, Peter Dechent	2005	56
20	Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants? Clinical Genetics ·Moneef Shoukier, Nina Klein, Bernd Auber, Julia Wickert, Julia Schröder, Barbara Zoll, Peter Burfeind, Iris Bartels, EA Alsat, Michael Lingen, Paweł Grzmil, Susann Schulze, J. S. Keyser, Dagmar Weise, Matthew Borchers, Elke Hobbiebrunken, M Röbl, Jutta Gärtner, Knut Brockmann, Birgit Zirn	2012	55

About Knut Brockmann

Knut Brockmann is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Epidemiology and Physiology, having authored 139 papers that have together received 4.2k indexed citations. Recurring topics across this work include RNA regulation and disease (23 papers), Genetics and Neurodevelopmental Disorders (14 papers), Metabolism and Genetic Disorders (10 papers), Traumatic Brain Injury Research (10 papers), Epilepsy research and treatment (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Genomics and Rare Diseases (7 papers) and Hereditary Neurological Disorders (7 papers). The work is most often cited by research in Clinical Biochemistry (496 citations), Endocrinology, Diabetes and Metabolism (641 citations), Genetics (799 citations), Neurology (217 citations) and Molecular Biology (1.7k citations). Knut Brockmann has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include F. Hanefeld, Alexandra M. Dumitrescu, Samuel Refetoff, Jutta Gärtner, Xiao-Hui Liao, Jens Frahm, Petra J. W. Pouwels, Peter Dechent, Andreas Ohlenbusch and Bernd Wilken. Their work appears in journals such as Neuropediatrics, Neurology, Orphanet Journal of Rare Diseases, Journal of Clinical Medicine and Journal of Medical Genetics.

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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