Birgit Haberberger

1.4k total citations
5 papers, 504 citations indexed

About

Birgit Haberberger is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Birgit Haberberger has authored 5 papers receiving a total of 504 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 1 paper in Surgery. Recurrent topics in Birgit Haberberger's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (3 papers) and Autophagy in Disease and Therapy (1 paper). Birgit Haberberger is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (3 papers) and Autophagy in Disease and Therapy (1 paper). Birgit Haberberger collaborates with scholars based in Germany, Austria and Switzerland. Birgit Haberberger's co-authors include Holger Prokisch, Tobias B. Haack, Thomas Meitinger, Massimo Zeviani, Eleonora Lamantea, Valentina Strecker, Ilka Wittig, Boris Rolinski, Elisabeth Graf and Johannes A. Mayr and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Birgit Haberberger

5 papers receiving 497 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Birgit Haberberger Germany	5	432	243	64	42	39	5	504
Sze Chern Lim Australia	11	766 1.8×	355 1.5×	97 1.5×	72 1.7×	56 1.4×	13	899
Nevena MacKay Canada	9	388 0.9×	152 0.6×	23 0.4×	28 0.7×	123 3.2×	9	514
N. MacKay Canada	13	373 0.9×	315 1.3×	28 0.4×	15 0.4×	6 0.2×	15	552
Leslie Matalonga Spain	11	219 0.5×	49 0.2×	35 0.5×	20 0.5×	22 0.6×	23	334
Patrick Nitschké France	5	200 0.5×	72 0.3×	69 1.1×	31 0.7×	6 0.2×	7	296
Nanna Cornelius Denmark	8	423 1.0×	341 1.4×	32 0.5×	22 0.5×	2 0.1×	10	551
Matteo Granatiero Italy	6	420 1.0×	206 0.8×	46 0.7×	9 0.2×	3 0.1×	8	541
Asmaa Mamoune France	8	197 0.5×	44 0.2×	55 0.9×	40 1.0×	2 0.1×	10	361
Michela Ranieri Italy	8	209 0.5×	74 0.3×	11 0.2×	12 0.3×	10 0.3×	8	350
Justine E. Marum Australia	8	152 0.4×	59 0.2×	101 1.6×	26 0.6×	38 1.0×	14	302

Countries citing papers authored by Birgit Haberberger

Since Specialization

Citations

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

Fields of papers citing papers by Birgit Haberberger

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgit Haberberger

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

All Works

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5 of 5 papers shown

1.

Collet, Marie Oxenbøll, Zahra Assouline, Damien Bonnet, et al.. (2015). High incidence and variable clinical outcome of cardiac hypertrophy due to ACAD9 mutations in childhood. European Journal of Human Genetics. 24(8). 1112–1116. 26 indexed citations

2.

Jackson, Christopher B., Jean‐Marc Nuoffer, Dagmar Hahn, et al.. (2013). Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency. Journal of Medical Genetics. 51(3). 170–175. 67 indexed citations

3.

Mayr, Johannes A., Tobias B. Haack, Elisabeth Graf, et al.. (2012). Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome. The American Journal of Human Genetics. 90(2). 314–320. 165 indexed citations

4.

Haack, Tobias B., Boris Rolinski, Birgit Haberberger, et al.. (2012). Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings. Journal of Inherited Metabolic Disease. 36(1). 55–62. 67 indexed citations

5.

Haack, Tobias B., Katharina Danhauser, Birgit Haberberger, et al.. (2010). Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. Nature Genetics. 42(12). 1131–1134. 179 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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