Jana Ebler

6.3k total citations
13 papers, 420 citations indexed

About

Jana Ebler is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Jana Ebler has authored 13 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Plant Science. Recurrent topics in Jana Ebler's work include Genomics and Phylogenetic Studies (9 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Jana Ebler is often cited by papers focused on Genomics and Phylogenetic Studies (9 papers), Genomics and Rare Diseases (5 papers) and Genomic variations and chromosomal abnormalities (3 papers). Jana Ebler collaborates with scholars based in Germany, United States and Netherlands. Jana Ebler's co-authors include Tobias Marschall, Benedict Paten, Mikko Rautiainen, Evan E. Eichler, Jan O. Korbel, Peter Ebert, Peter A. Audano, Wayne E. Clarke, Yafei Mao and Glenn Hickey and has published in prestigious journals such as Nature Genetics, Bioinformatics and Genome Research.

In The Last Decade

Jana Ebler

13 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jana Ebler Germany	9	314	201	149	37	15	13	420
Liudmila S. Mainzer United States	6	139 0.4×	107 0.5×	49 0.3×	39 1.1×	12 0.8×	12	259
Snædís Kristmundsdóttir Iceland	7	212 0.7×	166 0.8×	81 0.5×	27 0.7×	9 0.6×	7	321
Marinus F. van Batenburg Netherlands	5	519 1.7×	121 0.6×	117 0.8×	55 1.5×	13 0.9×	6	582
Qiangwei Zhou China	12	443 1.4×	74 0.4×	294 2.0×	46 1.2×	13 0.9×	18	605
Yi-Fei Huang United States	15	502 1.6×	259 1.3×	46 0.3×	80 2.2×	16 1.1×	22	645
Xavi Guitart United States	4	244 0.8×	118 0.6×	111 0.7×	20 0.5×	8 0.5×	4	310
Marta Puig Spain	12	313 1.0×	274 1.4×	265 1.8×	8 0.2×	16 1.1×	15	454
Philip C. Dishuck United States	6	206 0.7×	130 0.6×	110 0.7×	15 0.4×	8 0.5×	9	281
Tarryn Porter United Kingdom	3	181 0.6×	69 0.3×	42 0.3×	38 1.0×	32 2.1×	4	289
Allison Regier United States	4	162 0.5×	165 0.8×	44 0.3×	44 1.2×	5 0.3×	6	275

Countries citing papers authored by Jana Ebler

Since Specialization

Citations

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

Fields of papers citing papers by Jana Ebler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jana Ebler

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

All Works

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13 of 13 papers shown

Ashraf, Hufsah, Jana Ebler, & Tobias Marschall. (2023). Allele detection using k-mer-based sequencing error profiles. Bioinformatics Advances. 3(1). vbad149–vbad149. 1 indexed citations

Harvey, William T., Peter Ebert, Jana Ebler, et al.. (2023). Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall. Genome Research. 33(12). 2029–2040. 14 indexed citations

Porubský, David, William T. Harvey, Allison N. Rozanski, et al.. (2023). Inversion polymorphism in a complete human genome assembly. Genome biology. 24(1). 100–100. 15 indexed citations

Nebral, Karin, Jana Ebler, Daniel Picard, et al.. (2023). Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia. HemaSphere. 7(8). e925–e925. 15 indexed citations

Liao, Wen‐Wei, Mobin Asri, Jana Ebler, et al.. (2023). A draft human pangenome reference. Yearbook of pediatric endocrinology. 11 indexed citations

Ebler, Jana, et al.. (2022). BubbleGun: enumerating bubbles and superbubbles in genome graphs. Bioinformatics. 38(17). 4217–4219. 7 indexed citations

Ebler, Jana, Peter Ebert, Wayne E. Clarke, et al.. (2022). Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes. Nature Genetics. 54(4). 518–525. 110 indexed citations

Valle-Inclán, Jose Espejo, Nicolle Besselink, Ewart de Bruijn, et al.. (2022). A multi-platform reference for somatic structural variation detection. Cell Genomics. 2(6). 100139–100139. 17 indexed citations

Mari, Rebecca Serra, Jana Ebler, Mikko Rautiainen, et al.. (2020). Haplotype threading: accurate polyploid phasing from long reads. Genome biology. 21(1). 252–252. 54 indexed citations

10.

Eizenga, Jordan M., Adam M. Novak, Jonas A. Sibbesen, et al.. (2020). Pangenome Graphs. Annual Review of Genomics and Human Genetics. 21(1). 139–162. 135 indexed citations

11.

Ebler, Jana, Marina Haukness, Trevor Pesout, Tobias Marschall, & Benedict Paten. (2019). Haplotype-aware diplotyping from noisy long reads. Genome biology. 20(1). 116–116. 33 indexed citations

12.

Ebler, Jana, Marina Haukness, Trevor Pesout, Benedict Paten, & Tobias Marschall. (2018). Haplotype-aware diplotyping from noisy long reads. Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations

13.

Ebler, Jana, Alexander Schönhuth, & Tobias Marschall. (2017). Genotyping inversions and tandem duplications. Bioinformatics. 33(24). 4015–4023. 7 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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