Mads E. Hauberg

15.3k total citations
16 papers, 1000 citations indexed

About

Mads E. Hauberg is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Mads E. Hauberg has authored 16 papers receiving a total of 1000 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Mads E. Hauberg's work include Epigenetics and DNA Methylation (6 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic Associations and Epidemiology (3 papers). Mads E. Hauberg is often cited by papers focused on Epigenetics and DNA Methylation (6 papers), Genomics and Chromatin Dynamics (4 papers) and Genetic Associations and Epidemiology (3 papers). Mads E. Hauberg collaborates with scholars based in Denmark, United States and Germany. Mads E. Hauberg's co-authors include Panos Roussos, John F. Fullard, Yasmin L. Hurd, Bin Zhang, Alexey Kozlenkov, Stella Dracheva, Minghui Wang, Andrew McKenzie, Patrizia Casaccia and Alexandra Keenan and has published in prestigious journals such as Science, Nature Communications and Nature Genetics.

In The Last Decade

Mads E. Hauberg

15 papers receiving 996 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mads E. Hauberg Denmark	13	644	368	119	114	108	16	1000
Ilaria Guella Canada	20	454 0.7×	274 0.7×	126 1.1×	127 1.1×	152 1.4×	45	1.3k
Marc P. Forrest United States	17	676 1.0×	465 1.3×	186 1.6×	63 0.6×	74 0.7×	28	1.1k
Yonatan Perez Israel	14	728 1.1×	248 0.7×	155 1.3×	73 0.6×	146 1.4×	27	1.1k
Michael P. Starkey United Kingdom	7	629 1.0×	305 0.8×	143 1.2×	67 0.6×	70 0.6×	11	1.2k
Brandon C. Sos United States	9	773 1.2×	139 0.4×	71 0.6×	152 1.3×	137 1.3×	13	1.1k
Gwendolyn E. Kaeser United States	9	863 1.3×	168 0.5×	73 0.6×	175 1.5×	178 1.6×	11	1.2k
Xihui Liu China	15	736 1.1×	123 0.3×	81 0.7×	158 1.4×	91 0.8×	30	1.2k
Sebastian Guelfi United Kingdom	9	529 0.8×	283 0.8×	64 0.5×	96 0.8×	246 2.3×	12	1.1k
Mari Kondo Japan	15	351 0.5×	169 0.5×	126 1.1×	42 0.4×	71 0.7×	41	726
Song Chen China	8	452 0.7×	75 0.2×	116 1.0×	81 0.7×	127 1.2×	18	704

Countries citing papers authored by Mads E. Hauberg

Since Specialization

Citations

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

Fields of papers citing papers by Mads E. Hauberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mads E. Hauberg. 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 Mads E. Hauberg. The network helps show where Mads E. Hauberg may publish in the future.

Co-authorship network of co-authors of Mads E. Hauberg

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

All Works

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16 of 16 papers shown

Hauberg, Mads E., Aia Elise Jønch, & Christina Fagerberg. (2025). Partial 3q tetrasomy: Defining the syndrome, neocentromeres, and an additional case report. European Journal of Medical Genetics. 76. 105021–105021.

Bendl, Jaroslav, Kiran Girdhar, Mads E. Hauberg, et al.. (2023). Neuronal, glial and microglial maps of epigenetic and transcriptomics dysregulations in Alzheimer’s disease. Alzheimer s & Dementia. 19(S1). 1 indexed citations

Zhao, Bingxin, Tengfei Li, Stephen M. Smith, et al.. (2022). Common variants contribute to intrinsic human brain functional networks. Nature Genetics. 54(4). 508–517. 69 indexed citations

Zhao, Bingxin, Tengfei Li, Yue Yang, et al.. (2021). Common genetic variation influencing human white matter microstructure. Science. 372(6548). 107 indexed citations

McKenzie, Andrew, Minghui Wang, Mads E. Hauberg, et al.. (2021). Author Correction: Brain Cell Type Specific Gene Expression and Co-expression Network Architectures. Scientific Reports. 11(1). 19430–19430. 8 indexed citations

Egervári, Gabor, John F. Fullard, Joseph A. Landry, et al.. (2020). Chromatin accessibility mapping of the striatum identifies tyrosine kinase FYN as a therapeutic target for heroin use disorder. Nature Communications. 11(1). 4634–4634. 20 indexed citations

Hauberg, Mads E., Jordi Creus‐Muncunill, Jaroslav Bendl, et al.. (2020). Common schizophrenia risk variants are enriched in open chromatin regions of human glutamatergic neurons. Nature Communications. 11(1). 5581–5581. 45 indexed citations

Fullard, John F., Mads E. Hauberg, Jaroslav Bendl, et al.. (2018). An atlas of chromatin accessibility in the adult human brain. Genome Research. 28(8). 1243–1252. 108 indexed citations

McKenzie, Andrew, Minghui Wang, Mads E. Hauberg, et al.. (2018). Brain Cell Type Specific Gene Expression and Co-expression Network Architectures. Scientific Reports. 8(1). 8868–8868. 271 indexed citations

10.

Hauberg, Mads E., John F. Fullard, Lingxue Zhu, et al.. (2018). Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls. Molecular Psychiatry. 24(11). 1685–1695. 29 indexed citations

11.

Giambartolomei, Claudia, Wen Zhang, Mads E. Hauberg, et al.. (2018). A Bayesian framework for multiple trait colocalization from summary association statistics. Bioinformatics. 34(15). 2538–2545. 159 indexed citations

12.

Fullard, John F., Claudia Giambartolomei, Mads E. Hauberg, et al.. (2017). Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci. Human Molecular Genetics. 26(10). 1942–1951. 49 indexed citations

13.

Hauberg, Mads E., Panos Roussos, Jakob Grove, Anders D. Børglum, & Manuel Mattheisen. (2016). Analyzing the Role of MicroRNAs in Schizophrenia in the Context of Common Genetic Risk Variants. JAMA Psychiatry. 73(4). 369–369. 67 indexed citations

14.

Qvist, Per, Jane Christensen, Irina Vardya, et al.. (2016). The Schizophrenia-Associated BRD1 Gene Regulates Behavior, Neurotransmission, and Expression of Schizophrenia Risk Enriched Gene Sets in Mice. Biological Psychiatry. 82(1). 62–76. 19 indexed citations

15.

Christensen, Jane, Jonatan Pallesen, Manuel Mattheisen, et al.. (2016). Identification of the BRD1 interaction network and its impact on mental disorder risk. Genome Medicine. 8(1). 53–53. 24 indexed citations

16.

Hauberg, Mads E., Manuel Mattheisen, Anne Louise Askou, et al.. (2016). Schizophrenia risk variants affecting microRNA function and site-specific regulation of NT5C2 by miR-206. European Neuropsychopharmacology. 26(9). 1522–1526. 24 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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