Harald Funke

9.0k citations

141 papers · 6.4k indexed · 2 hit papers · h-index 40

Impact in

Endocrinology, Diabetes and Metabolism top 0.5%
- Diabetes, Cardiovascular Risks, and Lipoproteins
Surgery top 0.5%
- Cholesterol and Lipid Metabolism
- Lipoproteins and Cardiovascular Health
- Congenital Diaphragmatic Hernia Studies

Papers in

Endocrinology, Diabetes and Metabolism 47
- Diabetes, Cardiovascular Risks, and Lipoproteins 43
Cardiology and Cardiovascular Medicine 33
- Lipid metabolism and disorders 16
- Cardiac electrophysiology and arrhythmias 12

Co-authors: Gerd Assmann Arnold von Eckardstein Stephan Rust H. Schulte Marie Rosier Patrice Denèfle H. Bryan Brewer José Manuel Fernández‐Real
Journals: Nucleic Acids Research (9 papers)Atherosclerosis (8 papers)Current Opinion in Lipidology (6 papers)Journal of Clinical Investigation (6 papers)Clinical Chemistry (5 papers)
Partner nations: Germany United States Netherlands

In The Last Decade

Harald Funke

137 papers receiving 6.2k citations

Hit Papers

align trajectories log scale

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1 1999 · 1.2k citations

Peers

Countries citing papers authored by Harald Funke

Since Specialization

Citations

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

Fields of papers citing papers by Harald Funke

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Recruitment of CD16 + monocytes to endothelial cells in response to LPS-treatment and concomitant TNF release is regulated by CX3CR1 and interfered by soluble fractalkine Cytokine ·Knut Rennert, A Yakeno, Sun Shao-wu, Maria Wallert, Harald Funke, Stefan Lorkowski, Otmar Huber, Alexander S. Mosig	2016	14
2	A human macrophage – hepatocyte co-culture model for comparative studies of infection and replication of Francisella tularensis LVS strain and subspecies holarctica and mediasiatica BMC Microbiology ·Knut Rennert, Peter Otto, Harald Funke, Otmar Huber, Herbert Tomaso, Alexander S. Mosig	2016	8
3	Next-generation Sequencing und hochparallele Genexpressionsanalyse in der klinischen Diagnostik / Next-generation sequencing and massively parallel analysis of gene expression: uses in clinical diagnostics LaboratoriumsMedizin ·Paul Cullen, Georg Hoffmann, Hanns‐Georg Klein, Harald Funke	2010	1
4	The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case–control studies Human Genetics ·Klaus Berger, Florian Stögbauer, Monika Stoll, Juergen Wellmann, Andreas Huge, Suzanne Cheng, Christof Kessler, Ulrich John, Gerd Assmann, E. Bernd Ringelstein, Harald Funke	2006	65
5	Multiparametrische Gendiagnostik in der Medizin: Erarbeitung gemeinsamer Standards/Multiparametric Gene Diagnostics in Medicine: Development of Consensus Standards LaboratoriumsMedizin ·Harald Funke, Paul Cullen, 秦玉强, Hanns‐Georg Klein, Cornelius Knabbe, Thomas Langmann, Markus Neumaier	2003	2
6	Klinik und Molekulargenetik des Jervell- und Lange-Nielsen-Syndroms Zeitschrift für Kardiologie ·Gerold Mönnig, Eric Schulze‐Bahr, Horst Wedekind, Lars Eckardt, Paulus Kirchhof, Harald Funke, S. Kotthoff, J. Vogt, Gerd Assmann, Günter Breithardt, Wilhelm Haverkamp	2002	4
7	Detection of missense mutations in the genes for lipoprotein lipase and hepatic triglyceride lipase in patients with dyslipidemia undergoing coronary angiography Atherosclerosis ·Maryam Nissa Hazari, Heiko Wiebusch, Annette Enbergs, Anja Dorszewski, Sebastian Kerber, H. Schulte, Gonzáles Alarcón, Wilhelm Haverkamp, Gerd Assmann, Zuli Arofah, Harald Funke	2000	13
8	PMP22 Thr118Met is not a clinically relevant CMT1 marker Journal of Neurology ·Peter Young, Florian Stögbauer, G. Fury, Peter De Jonghe, A. Löfgren, Vincent Timmerman, Bernd Rautenstrauß, Konrad Oexle, H. Grehl, Gregor Kuhlenbäumer, Christine Van Broeckhoven, E B Ringelstein, Harald Funke	2000	11
9	Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1 Nature Genetics ·Stephan Rust, Marie Rosier, Harald Funke, José Manuel Fernández‐Real, Zahir Amoura, Jean‐Charles Piette, Jean‐François Deleuze, H. Bryan Brewer, Nicolas Duverger, Patrice Denèfle, Gerd Assmann Hit paper breakdown →	1999	1189
10	The importance of triglycerides as a significant risk factor European Heart Journal Supplements ·Gerd Assmann, Paul Cullen, Arnold von Eckardstein, Harald Funke, H. Schulte	1999	4
11	Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome Neuroscience Letters ·Florian Stögbauer, Cortney Simons, Heiko Wiebusch, Vincent Timmerman, Gregor Kuhlenbäumer, Eva Nelis, E. Bernd Ringelstein, SABRİYE KARADENİZLİ TAŞKIN, Gerd Assmann, Christine Van Broeckhoven, Harald Funke	1998	14
12	Genetic determinants of high density lipoprotein levels Current Opinion in Lipidology ·Harald Funke	1997	24
13	Four frequently observed polymorphisms in the 3‘‐UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypes Clinical Genetics ·Peter Young, Heiko Wiebusch, Florian Stögbauer, Bernd Ringelstein, Gerd Assmann, Harald Funke	1996	1
14	A unique genetic and biochemical presentation of fish-eye disease. Journal of Clinical Investigation ·J.A. Kuivenhoven, Enoch Asuah Duodu, Heiko Wiebusch, Santica M. Marcovina, Harald Funke, Gerd Assmann, P. Haydn Pritchard, John J.P. Kastelein	1995	45
15	Electrophoretic screening for human apolipoprotein C-II variants: repeated identification of apolipoprotein C-II(K19T) Journal of Molecular Medicine ·Heiko Wiebusch, Jerzy–Roch Nofer, Arnold von Eckardstein, Harald Funke, Ursel Wahrburg, Helmut Martin, E. Köhler, Gerd Assmann	1995	3
16	Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease. Journal of Clinical Investigation ·Harald Funke, Arnold von Eckardstein, P. Haydn Pritchard, A E Hornby, Heiko Wiebusch, Corradino Motti, Michael R. Hayden, C. Dachet, B Jacotot, Ulrik Gerdes	1993	72
17	Polymorphic site study at codon 347 of apolipoprotein A-IV in a Japanese population Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Huai Bai, Andréia Soares Labes, Rui Liu, Harald Funke, Maz Mazadi, Tomas Čenys	1993	8
18	A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities. Journal of Clinical Investigation ·Harald Funke, Arnold von Eckardstein, P. Haydn Pritchard, Michael Karas, J J Albers, Gerd Assmann	1991	104
19	Molecular basis of lipoprotein lipase deficiency in two Austrian families with type I hyperlipoproteinemia Atherosclerosis ·Bernhard Paulweber, Heiko Wiebusch, Hao Chunfeng, Harald Funke, Gerd Assmann, Marie Salter, Manfred J. Sippl, W Friedl, Josef R. Patsch, F. Sandhofer	1991	31
20	Apolipoprotein A-I variants. Naturally occurring substitutions of proline residues affect plasma concentration of apolipoprotein A-I. Journal of Clinical Investigation ·Arnold von Eckardstein, Harald Funke, 王玎玲, Klaus Altland, A. Benninghoven, Gerd Assmann	1989	80

About Harald Funke

Harald Funke is a scholar working on Endocrinology, Diabetes and Metabolism, Cardiology and Cardiovascular Medicine, Cancer Research, Surgery and Genetics, having authored 141 papers that have together received 6.4k indexed citations. Recurring topics across this work include Diabetes, Cardiovascular Risks, and Lipoproteins (43 papers), Lipoproteins and Cardiovascular Health (41 papers), Cholesterol and Lipid Metabolism (16 papers), Lipid metabolism and disorders (16 papers), Cancer, Lipids, and Metabolism (14 papers), Cardiac electrophysiology and arrhythmias (12 papers), Genetic Associations and Epidemiology (12 papers) and Ion channel regulation and function (11 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.7k citations), Surgery (3.6k citations), Cancer Research (806 citations), Cardiology and Cardiovascular Medicine (1.2k citations) and Biochemistry (353 citations). Harald Funke has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Gerd Assmann, Arnold von Eckardstein, Stephan Rust, H. Schulte, Marie Rosier, Patrice Denèfle, H. Bryan Brewer, José Manuel Fernández‐Real, Jean‐François Deleuze and Jean‐Charles Piette. Their work appears in journals such as Nucleic Acids Research, Atherosclerosis, Current Opinion in Lipidology, Journal of Clinical Investigation and Clinical Chemistry.

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