Elisabeth Graf

11.9k total citations · 2 hit papers
45 papers, 2.8k citations indexed

About

Elisabeth Graf is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Elisabeth Graf has authored 45 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 16 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Elisabeth Graf's work include Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Metabolism and Genetic Disorders (6 papers). Elisabeth Graf is often cited by papers focused on Genomics and Rare Diseases (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Metabolism and Genetic Disorders (6 papers). Elisabeth Graf collaborates with scholars based in Germany, Austria and Switzerland. Elisabeth Graf's co-authors include Tim M. Strom, Thomas Meitinger, Thomas Wieland, Tobias B. Haack, Holger Prokisch, Thomas Schwarzmayr, Maja Mockenhaupt, Claudia de Toma, Alain Hovnanian and Christine Lonjou and has published in prestigious journals such as Nature Communications, Nature Genetics and PLoS ONE.

In The Last Decade

Elisabeth Graf

39 papers receiving 2.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the deubiquitinase gene USP8 cause Cushing's disease

2014 405 citations Martín Reincke, Silviu Sbiera et al. Nature Genetics profile →
An atlas of the aging lung mapped by single cell transcriptomics and deep tissue proteomics

2019 390 citations Ilias Angelidis, Lukas M. Simon et al. Nature Communications profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elisabeth Graf Germany	25	1.2k	411	411	340	316	45	2.8k
Sarah K. Bronson United States	26	1.8k 1.5×	428 1.0×	370 0.9×	178 0.5×	214 0.7×	44	3.2k
Brian T. Scott United States	27	1.7k 1.4×	655 1.6×	109 0.3×	284 0.8×	319 1.0×	40	3.0k
Annie Laquerrière France	32	1.4k 1.1×	842 2.0×	584 1.4×	84 0.2×	204 0.6×	109	3.3k
Aqeela Afzal United States	27	1.1k 0.9×	328 0.8×	80 0.2×	259 0.8×	190 0.6×	54	2.6k
Masashi Tanaka Japan	17	1.6k 1.3×	583 1.4×	607 1.5×	134 0.4×	189 0.6×	43	3.2k
Pentti J. Tienari Finland	37	1.9k 1.6×	1.7k 4.1×	583 1.4×	104 0.3×	169 0.5×	143	5.5k
Junji Ishida Japan	31	1.5k 1.2×	315 0.8×	222 0.5×	620 1.8×	962 3.0×	68	3.7k
Nobuyuki Murakami Japan	27	1.2k 0.9×	501 1.2×	628 1.5×	77 0.2×	231 0.7×	112	2.8k
Hiroki Aoki Japan	33	1.9k 1.6×	262 0.6×	273 0.7×	107 0.3×	821 2.6×	114	4.3k
Leonardo Guasti United Kingdom	32	1.7k 1.4×	211 0.5×	407 1.0×	583 1.7×	313 1.0×	66	2.9k

Countries citing papers authored by Elisabeth Graf

Since Specialization

Citations

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

Fields of papers citing papers by Elisabeth Graf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabeth Graf

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabeth Graf. A scholar is included among the top collaborators of Elisabeth Graf 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 Elisabeth Graf. Elisabeth Graf 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

Krenn, Martin, Axel Schmidt, Matias Wagner, et al.. (2025). AlphaMissense prediction for the evaluation of missense variants in the diagnostic setting of neuromuscular disorders. Journal of Neuromuscular Diseases. 708678093–708678093.

Krenn, Martin, Matias Wagner, Karin Trimmel, et al.. (2025). Holistic Exome-Based Genetic Testing in Adults With Epilepsy. Neurology Genetics. 11(3). e200260–e200260. 1 indexed citations

Stangner, Konstanze, Chris H. Wendt, Elisabeth Graf, et al.. (2025). Apremilast improves cardiomyocyte cohesion and arrhythmia in different models for arrhythmogenic cardiomyopathy. Stem Cell Research & Therapy. 16(1). 609–609.

Brügger, Melanie, Matias Wagner, Elisabeth Graf, et al.. (2024). Genome Sequencing for Cases Unsolved by Exome Sequencing: Identifying a Single-Exon Deletion in TBCK in a Case from 30 Years Ago. Neuropediatrics. 55(4). 260–264. 1 indexed citations

Witzel, Simon, Matias Wagner, Chen Zhao, et al.. (2022). Fast versus slow disease progression in amyotrophic lateral sclerosis–clinical and genetic factors at the edges of the survival spectrum. Neurobiology of Aging. 119. 117–126. 6 indexed citations

Popp, Bernt, Melanie Brügger, Tobias Bartolomaeus, et al.. (2022). The constitutional gain‐of‐function variant p. Glu1099Lys in NSD2 is associated with a novel syndrome. Clinical Genetics. 103(2). 226–230. 2 indexed citations

Brunet, Theresa, Riccardo Berutti, Veronika Dill, et al.. (2022). Clonal hematopoiesis as a pitfall in germline variant interpretation in the context of Mendelian disorders. Human Molecular Genetics. 31(14). 2386–2395. 4 indexed citations

Vogel, Florian, Martin Krenn, Dominik S. Westphal, et al.. (2022). A de novo missense variant in GABRA4 alters receptor function in an epileptic and neurodevelopmental phenotype. Epilepsia. 63(4). e35–e41. 8 indexed citations

Keipert, Susanne, Dominik Lutter, Bjoern O. Schroeder, et al.. (2021). Author Correction: Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice. Nature Communications. 12(1). 1804–1804. 1 indexed citations

10.

Keipert, Susanne, Dominik Lutter, Bjoern O. Schroeder, et al.. (2020). Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice. Nature Communications. 11(1). 624–624. 62 indexed citations

11.

Westphal, Dominik S., Gloria Leszinski, Esther Rieger‐Fackeldey, et al.. (2019). Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing. Clinical Genetics. 95(5). 582–589. 22 indexed citations

12.

Angelidis, Ilias, Lukas M. Simon, Isis E. Fernandez, et al.. (2019). An atlas of the aging lung mapped by single cell transcriptomics and deep tissue proteomics. Nature Communications. 10(1). 963–963. 390 indexed citations breakdown →

13.

Cheng, Yiming, Jiang Li, Susanne Keipert, et al.. (2018). Prediction of Adipose Browning Capacity by Systematic Integration of Transcriptional Profiles. Cell Reports. 23(10). 3112–3125. 40 indexed citations

14.

Iuso, Arcangela, Bader Alhaddad, Urania Kotzaeridou, et al.. (2018). A Homozygous Splice Site Mutation in SLC25A42, Encoding the Mitochondrial Transporter of Coenzyme A, Causes Metabolic Crises and Epileptic Encephalopathy. JIMD Reports. 44. 1–7. 19 indexed citations

15.

Hadchouel, Alice, Thomas Wieland, Matthias Griese, et al.. (2015). Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island. The American Journal of Human Genetics. 96(5). 826–831. 76 indexed citations

16.

Reincke, Martín, Silviu Sbiera, Akira Hayakawa, et al.. (2014). Mutations in the deubiquitinase gene USP8 cause Cushing's disease. Nature Genetics. 47(1). 31–38. 405 indexed citations breakdown →

17.

Giehl, Kathrin, Gertrud Eckstein, Sandra M. Pasternack, et al.. (2012). Nonsense Mutations in AAGAB Cause Punctate Palmoplantar Keratoderma Type Buschke-Fischer-Brauer. The American Journal of Human Genetics. 91(4). 754–759. 41 indexed citations

18.

Beetz, Christian, Thomas R. Pieber, Nicole Hertel, et al.. (2012). Exome Sequencing Identifies a REEP1 Mutation Involved in Distal Hereditary Motor Neuropathy Type V. The American Journal of Human Genetics. 91(1). 139–145. 69 indexed citations

19.

Jamra, Rami Abou, Annick Raas‐Rothschild, Sebastian Eck, et al.. (2011). Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature. The American Journal of Human Genetics. 88(6). 788–795. 167 indexed citations

20.

Graf, Elisabeth, et al.. (1995). Das Lied von der Glocke : op. 45.

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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