Hubert Pausch

5.9k total citations
92 papers, 2.3k citations indexed

About

Hubert Pausch is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Hubert Pausch has authored 92 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Genetics, 29 papers in Molecular Biology and 21 papers in Cancer Research. Recurrent topics in Hubert Pausch's work include Genetic and phenotypic traits in livestock (65 papers), Genetic Mapping and Diversity in Plants and Animals (49 papers) and Cancer-related molecular mechanisms research (21 papers). Hubert Pausch is often cited by papers focused on Genetic and phenotypic traits in livestock (65 papers), Genetic Mapping and Diversity in Plants and Animals (49 papers) and Cancer-related molecular mechanisms research (21 papers). Hubert Pausch collaborates with scholars based in Switzerland, Germany and Finland. Hubert Pausch's co-authors include Ruedi Fries, Reiner Emmerling, Danang Crysnanto, Christine Wurmser, Kay‐Uwe Götz, Hermann Schwarzenbacher, Simone Jung, Tim M. Strom, Sandra Jansen and Christian Edel and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Communications.

In The Last Decade

Hubert Pausch

88 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hubert Pausch Switzerland 28 1.9k 573 511 461 408 92 2.3k
Gwenola Tosser‐Klopp France 27 1.3k 0.7× 176 0.3× 609 1.2× 370 0.8× 413 1.0× 58 2.0k
Rachel Hawken Australia 32 2.4k 1.2× 426 0.7× 726 1.4× 403 0.9× 554 1.4× 92 3.1k
A. Eggen France 24 1.4k 0.7× 459 0.8× 386 0.8× 153 0.3× 231 0.6× 79 1.7k
Laurent Schibler France 30 1.7k 0.9× 442 0.8× 997 2.0× 257 0.6× 326 0.8× 96 2.6k
B. Harlizius Netherlands 27 1.7k 0.9× 395 0.7× 403 0.8× 289 0.6× 119 0.3× 72 2.0k
Stephanie McKay United States 25 1.7k 0.9× 461 0.8× 584 1.1× 430 0.9× 327 0.8× 55 2.4k
D. Di Berardino Italy 23 1.4k 0.7× 847 1.5× 528 1.0× 201 0.4× 248 0.6× 94 2.0k
Marina R. S. Fortes Australia 28 1.9k 1.0× 175 0.3× 400 0.8× 508 1.1× 860 2.1× 113 2.5k
Jonathan E. Beever United States 25 1.2k 0.6× 398 0.7× 705 1.4× 213 0.5× 165 0.4× 86 2.0k
B. A. Freking United States 30 1.5k 0.8× 184 0.3× 983 1.9× 204 0.4× 476 1.2× 91 2.5k

Countries citing papers authored by Hubert Pausch

Since Specialization
Citations

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

Fields of papers citing papers by Hubert Pausch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hubert Pausch

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

All Works

20 of 20 papers shown
1.
Leonard, Alexander S., Xena Marie Mapel, & Hubert Pausch. (2024). RNA-DNA differences in variant calls from cattle tissues result in erroneous eQTLs. BMC Genomics. 25(1). 750–750.
2.
Leonard, Alexander S., Xena Marie Mapel, & Hubert Pausch. (2024). Pangenome-genotyped structural variation improves molecular phenotype mapping in cattle. Genome Research. 34(2). 300–309. 20 indexed citations
3.
Leonard, Alexander S., et al.. (2024). Taurine pangenome uncovers a segmental duplication upstream of KIT associated with depigmentation in white-headed cattle. Genome Research. 35(4). 1041–1052. 6 indexed citations
4.
5.
Leonard, Alexander S., et al.. (2023). Graph construction method impacts variation representation and analyses in a bovine super-pangenome. Genome biology. 24(1). 124–124. 29 indexed citations
6.
Mapel, Xena Marie, et al.. (2023). Structural variants and short tandem repeats impact gene expression and splicing in bovine testis tissue. Genetics. 225(3). 6 indexed citations
7.
Mapel, Xena Marie, et al.. (2022). Bull fertility and semen quality are not correlated with dairy and production traits in Brown Swiss cattle. SHILAP Revista de lepidopterología. 3(2). 120–125. 15 indexed citations
8.
Crysnanto, Danang, Alexander S. Leonard, Zih‐Hua Fang, & Hubert Pausch. (2021). Novel functional sequences uncovered through a bovine multiassembly graph. Proceedings of the National Academy of Sciences. 118(20). 48 indexed citations
9.
Kadri, Naveen Kumar, et al.. (2021). Autosomal recessive loci contribute significantly to quantitative variation of male fertility in a dairy cattle population. BMC Genomics. 22(1). 225–225. 15 indexed citations
10.
Wurmser, Christine, et al.. (2021). A nonsense mutation of bone morphogenetic protein-15 (BMP15) causes both infertility and increased litter size in pigs. BMC Genomics. 22(1). 38–38. 6 indexed citations
11.
Kadri, Naveen Kumar, et al.. (2021). Characterization of a haplotype-reference panel for genotyping by low-pass sequencing in Swiss Large White pigs. BMC Genomics. 22(1). 290–290. 21 indexed citations
12.
Janett, Fredi, Zih‐Hua Fang, Xaver Sidler, et al.. (2020). Infertility due to defective sperm flagella caused by an intronic deletion in DNAH17 that perturbs splicing. Genetics. 217(2). 11 indexed citations
13.
Wurmser, Christine, Danang Crysnanto, Anu Sironen, et al.. (2020). Deletion of porcine BOLL is associated with defective acrosomes and subfertility in Yorkshire boars. Animal Genetics. 51(6). 945–949. 5 indexed citations
14.
Fang, Zih‐Hua, et al.. (2020). A 63‐bp insertion in exon 2 of the porcine KIF21A gene is associated with arthrogryposis multiplex congenita. Animal Genetics. 51(5). 820–823. 2 indexed citations
15.
Berg, Irene van den, Ruidong Xiang, Janez Jenko, et al.. (2020). Meta-analysis for milk fat and protein percentage using imputed sequence variant genotypes in 94,321 cattle from eight cattle breeds. Genetics Selection Evolution. 52(1). 37–37. 50 indexed citations
16.
Pausch, Hubert, Hermann Schwarzenbacher, Johann Burgstaller, et al.. (2015). Homozygous haplotype deficiency reveals deleterious mutations compromising reproductive and rearing success in cattle. BMC Genomics. 16(1). 312–312. 58 indexed citations
17.
Pausch, Hubert, Christine Wurmser, Christian Edel, et al.. (2014). Exploiting Whole Genome Sequence Data for the Identification of Causal Trait Variants in Cattle. Proceedings of the World Congress on Genetics Applied to Livestock Production. 191. 4 indexed citations
18.
Segelke, Dierck, Helge Täubert, Sandra Jansen, et al.. (2014). Management of Genetic Characteristics. Bulletin - International Bull Evaluation Service/Interbull bulletin. 85–88. 3 indexed citations
19.
Schwarzenbacher, Hermann & Hubert Pausch. (2014). Bovine Spastic Paresis: A Genome-Wide Study in Fleckvieh. Proceedings of the World Congress on Genetics Applied to Livestock Production. 497. 1 indexed citations
20.
Fries, Ruedi & Hubert Pausch. (2011). Individuelle Genomsequenzierung von Nutztieren – auf dem Weg zur genomischen Selektion 2.0. Züchtungskunde. 83. 371–381. 1 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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