Christine Makowski

1.9k total citations
18 papers, 480 citations indexed

About

Christine Makowski is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christine Makowski has authored 18 papers receiving a total of 480 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christine Makowski's work include Metabolism and Genetic Disorders (5 papers), Epilepsy research and treatment (3 papers) and Pharmacological Effects and Toxicity Studies (3 papers). Christine Makowski is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Epilepsy research and treatment (3 papers) and Pharmacological Effects and Toxicity Studies (3 papers). Christine Makowski collaborates with scholars based in Germany, Austria and United States. Christine Makowski's co-authors include Thomas Meitinger, Holger Prokisch, Johannes A. Mayr, Thomas Bast, Rainer Boor, Gerhard Kluger, Felix Schneider, Uwe Runge, Edda Haberlandt and Jan‐Peter Ernst and has published in prestigious journals such as Brain, The Journal of Pediatrics and Gene.

In The Last Decade

Christine Makowski

17 papers receiving 471 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Christine Makowski Germany 10 229 143 116 95 94 18 480
Léna Damaj France 11 186 0.8× 108 0.8× 38 0.3× 42 0.4× 80 0.9× 19 479
Dawn Cordeiro Canada 10 200 0.9× 173 1.2× 145 1.3× 18 0.2× 55 0.6× 15 484
Komudi Siriwardena Canada 13 279 1.2× 255 1.8× 114 1.0× 31 0.3× 83 0.9× 25 671
Anna Wedell Sweden 11 321 1.4× 220 1.5× 40 0.3× 23 0.2× 36 0.4× 28 498
Suzanne D. DeBrosse United States 12 246 1.1× 182 1.3× 55 0.5× 18 0.2× 22 0.2× 17 422
Merçè Pineda Spain 13 302 1.3× 300 2.1× 35 0.3× 29 0.3× 85 0.9× 19 562
Stephanie Kleinle Germany 17 587 2.6× 292 2.0× 31 0.3× 39 0.4× 51 0.5× 27 772
Keiko Ishigaki Japan 13 252 1.1× 46 0.3× 48 0.4× 68 0.7× 17 0.2× 58 476
Carlos E. Speck‐Martins Brazil 11 137 0.6× 66 0.5× 20 0.2× 27 0.3× 48 0.5× 23 314
Charlotte Thiels Germany 11 225 1.0× 40 0.3× 27 0.2× 56 0.6× 20 0.2× 25 399

Countries citing papers authored by Christine Makowski

Since Specialization
Citations

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

Fields of papers citing papers by Christine Makowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Makowski

This figure shows the co-authorship network connecting the top 25 collaborators of Christine Makowski. A scholar is included among the top collaborators of Christine Makowski 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 Christine Makowski. Christine Makowski is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Borggraefe, Ingo, et al.. (2025). Significance of Behavioural Problems on Family Impact in Angelman Syndrome: A Prospective Cross-Sectional Study. Journal of Autism and Developmental Disorders.
2.
Kobayashi, Erica Sanford, Yael Dinur Schejter, Christine Makowski, et al.. (2024). Biallelic Loss of Function Variants in SENP7 Cause Immunodeficiency with Neurologic and Muscular Phenotypes. The Journal of Pediatrics. 274. 114180–114180. 2 indexed citations
3.
Krey, Ilona, Janina Gburek‐Augustat, Johannes R. Lemke, et al.. (2024). Precision Medicine in Angelman Syndrome. Neuropediatrics. 56(2). 69–82. 2 indexed citations
4.
5.
Vermehren‐Schmaedick, Anke, Sarah C. Reed, Gary A. Bellus, et al.. (2021). Characterization of PARP6 Function in Knockout Mice and Patients with Developmental Delay. Cells. 10(6). 1289–1289. 9 indexed citations
6.
Krüger, Marcus, Theresa Brunet, Christine Makowski, et al.. (2020). Congenital lymphedema as a rare and first symptom of tuberous sclerosis complex. Gene. 753. 144815–144815. 6 indexed citations
7.
Westphal, Dominik S., et al.. (2018). MAP2 – A Candidate Gene for Epilepsy, Developmental Delay and Behavioral Abnormalities in a Patient With Microdeletion 2q34. Frontiers in Genetics. 9. 99–99. 11 indexed citations
8.
Feichtinger, René G., Michaela Brunner‐Krainz, Bader Alhaddad, et al.. (2017). Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. Oxidative Medicine and Cellular Longevity. 2017(1). 7202589–7202589. 33 indexed citations
9.
10.
Simons, Cas, David A. Dyment, Stephen J. Bent, et al.. (2017). A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy. Brain. 140(12). 3105–3111. 59 indexed citations
11.
Gušić, Mirjana, Roman Günthner, Bader Alhaddad, et al.. (2017). Biallelic Mutations in SLC1A2; an Additional Mode of Inheritance for SLC1A2-Related Epilepsy. Neuropediatrics. 49(1). 59–62. 14 indexed citations
12.
Steinborn, M., et al.. (2016). High resolution transbulbar sonography in children with suspicion of increased intracranial pressure. Child s Nervous System. 32(4). 655–660. 34 indexed citations
13.
Mayr, Johannes A., Tobias B. Haack, Peter Freisinger, et al.. (2015). Spectrum of combined respiratory chain defects. Journal of Inherited Metabolic Disease. 38(4). 629–640. 76 indexed citations
14.
Banka, Siddharth, Christian de Goede, Wyatt W. Yue, et al.. (2014). Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: A treatable neurological disorder caused by TPK1 mutations. Molecular Genetics and Metabolism. 113(4). 301–306. 43 indexed citations
15.
Makowski, Christine, M. Steinborn, Walter Bonfig, Bettina Sadowski, & Dorothea Besch. (2012). Visual Loss without Headache in Children with Pseudotumor Cerebri and Growth Hormone Treatment. Neuropediatrics. 44(4). 203–207. 9 indexed citations
16.
Haack, Tobias B., Christine Makowski, Elisabeth Graf, et al.. (2012). Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown‐Vialetto‐Van Laere syndrome. Journal of Inherited Metabolic Disease. 35(6). 943–948. 66 indexed citations
17.
Kluger, Gerhard, Edda Haberlandt, Gerhard Kurlemann, et al.. (2010). First European long-term experience with the orphan drug rufinamide in childhood-onset refractory epilepsy. Epilepsy & Behavior. 17(4). 546–548. 44 indexed citations
18.
Kluger, Gerhard, Gerhard Kurlemann, Edda Haberlandt, et al.. (2009). Effectiveness and tolerability of rufinamide in children and adults with refractory epilepsy: First European experience. Epilepsy & Behavior. 14(3). 491–495. 62 indexed citations

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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