Stefan A. Haas

16.4k total citations · 2 hit papers
55 papers, 4.8k citations indexed

About

Stefan A. Haas is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Stefan A. Haas has authored 55 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 18 papers in Genetics and 4 papers in Immunology. Recurrent topics in Stefan A. Haas's work include RNA Research and Splicing (12 papers), Genomics and Phylogenetic Studies (10 papers) and RNA and protein synthesis mechanisms (9 papers). Stefan A. Haas is often cited by papers focused on RNA Research and Splicing (12 papers), Genomics and Phylogenetic Studies (10 papers) and RNA and protein synthesis mechanisms (9 papers). Stefan A. Haas collaborates with scholars based in Germany, United States and Netherlands. Stefan A. Haas's co-authors include Martin Vingron, Hans Lehrach, Sean O’Keeffe, Marc Hild, Britta Koch, Renato Paro, Marcel H. Schulz, Michael Boutros, Hugues Richard and Marie‐Laure Yaspo and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Stefan A. Haas

54 papers receiving 4.7k citations

Hit Papers

align trajectories sort by overperformance

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.

A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome

2008 949 citations Marc Sultan, Marcel H. Schulz et al. Science profile →
Genome-Wide RNAi Analysis of Growth and Viability in Drosophila Cells

2004 571 citations Michael Boutros, Amy A. Kiger et al. Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefan A. Haas Germany	34	3.5k	927	607	551	311	55	4.8k
A. Francis Stewart Germany	44	5.2k 1.5×	1.5k 1.6×	352 0.6×	384 0.7×	245 0.8×	98	6.2k
David Oxley United Kingdom	39	5.4k 1.5×	946 1.0×	843 1.4×	735 1.3×	350 1.1×	109	6.8k
Xiaosong Huang United States	15	4.3k 1.2×	881 1.0×	677 1.1×	765 1.4×	579 1.9×	34	6.7k
Gloria A. Brar United States	23	6.1k 1.7×	770 0.8×	587 1.0×	634 1.2×	242 0.8×	40	6.6k
Ping Liang United States	42	3.7k 1.1×	1.0k 1.1×	440 0.7×	898 1.6×	379 1.2×	151	5.5k
Jun Fu China	38	4.4k 1.2×	1.5k 1.6×	378 0.6×	478 0.9×	332 1.1×	115	5.9k
P. Julien Switzerland	7	2.7k 0.8×	790 0.9×	345 0.6×	422 0.8×	236 0.8×	8	3.7k
V Reinke United States	37	4.5k 1.3×	962 1.0×	351 0.6×	691 1.3×	137 0.4×	74	6.1k
Joseph White United States	24	3.3k 0.9×	730 0.8×	323 0.5×	1.6k 2.9×	467 1.5×	43	5.4k
Robert J. Shmookler Reis United States	39	2.7k 0.8×	511 0.6×	287 0.5×	300 0.5×	260 0.8×	134	4.4k

Countries citing papers authored by Stefan A. Haas

Since Specialization

Citations

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

Fields of papers citing papers by Stefan A. Haas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stefan A. Haas. 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 Stefan A. Haas. The network helps show where Stefan A. Haas may publish in the future.

Co-authorship network of co-authors of Stefan A. Haas

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

Paliou, Christina, Philine Guckelberger, Robert Schöpflin, et al.. (2019). Preformed chromatin topology assists transcriptional robustness of Shh during limb development. Proceedings of the National Academy of Sciences. 116(25). 12390–12399. 122 indexed citations

Andrey, Guillaume, Robert Schöpflin, Ivana Jerković, et al.. (2016). Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding. Genome Research. 27(2). 223–233. 96 indexed citations

Hackmann, Karl, Andreas Rump, Stefan A. Haas, et al.. (2015). Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?. American Journal of Medical Genetics Part A. 170(1). 94–102. 8 indexed citations

Lesca, Gaëtan, Marie‐Pierre Moizard, Gérald Bussy, et al.. (2013). Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. American Journal of Medical Genetics Part A. 161(12). 3063–3071. 30 indexed citations

Sun, Ruping, Michael I. Love, Tomasz Żemojtel, et al.. (2012). Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads. Bioinformatics. 28(7). 1024–1025. 15 indexed citations

Huppke, Peter, Cornelia Brendel, Vera M. Kalscheuer, et al.. (2012). Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin. The American Journal of Human Genetics. 90(1). 61–68. 68 indexed citations

Huang, Lingli, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, et al.. (2012). A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability. The American Journal of Human Genetics. 91(4). 694–702. 73 indexed citations

Lin, Shen, Stefan A. Haas, Tomasz Żemojtel, et al.. (2010). Genome-wide comparison of cyanobacterial transposable elements, potential genetic diversity indicators. Gene. 473(2). 139–149. 48 indexed citations

Haas, Stefan A., Holger Hackstein, Gregor Bein, et al.. (2009). Identification of novel transcriptional regulators involved in macrophage differentiation and activation in U937 cells. BMC Immunology. 10(1). 18–18. 98 indexed citations

10.

Hu, Hao, Klaus Wrogemann, Vera M. Kalscheuer, et al.. (2009). Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing. HAL (Le Centre pour la Communication Scientifique Directe). 3(1-4). 41–49. 35 indexed citations

11.

Sultan, Marc, Marcel H. Schulz, Hugues Richard, et al.. (2008). A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome. Science. 321(5891). 956–960. 949 indexed citations breakdown →

12.

Hecht, Jochen, Heiner Kuhl, Stefan A. Haas, et al.. (2006). Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep. BMC Genomics. 7(1). 172–172. 23 indexed citations

13.

Hui, Jingyi, Lee-Hsueh Hung, Monika Heiner, et al.. (2005). Intronic CA‐repeat and CA‐rich elements: a new class of regulators of mammalian alternative splicing. The EMBO Journal. 24(11). 1988–1998. 191 indexed citations

14.

Boutros, Michael, Amy A. Kiger, Susan Armknecht, et al.. (2004). Genome-Wide RNAi Analysis of Growth and Viability in Drosophila Cells. Science. 303(5659). 832–835. 571 indexed citations breakdown →

15.

Gupta, Shobhit, Dorothea Zink, Bernhard Korn, Martin Vingron, & Stefan A. Haas. (2004). Genome wide identification and classification of alternative splicing based on EST data. Bioinformatics. 20(16). 2579–2585. 70 indexed citations

16.

Haas, Stefan A.. (2003). Genome-scale design of PCR primers and long oligomers for DNA microarrays. Nucleic Acids Research. 31(19). 5576–5581. 27 indexed citations

17.

Coward, Eivind, Stefan A. Haas, & Martin Vingron. (2002). SpliceNest: visualizing gene structure and alternative splicing based on EST clusters. Trends in Genetics. 18(1). 53–55. 35 indexed citations

18.

Boer, Judith M., Wolfgang Huber, Holger Sültmann, et al.. (2001). Identification and Classification of Differentially Expressed Genes in Renal Cell Carcinoma by Expression Profiling on a Global Human 31,500-Element cDNA Array. Genome Research. 11(11). 1861–1870. 157 indexed citations

19.

Haas, Stefan A., Tim Beißbarth, Éric Rivals, Antje Krause, & Martin Vingron. (2000). GeneNest: automated generation and visualization of gene indices. Trends in Genetics. 16(11). 521–523. 34 indexed citations

20.

Haas, Stefan A., Martin Vingron, Annemarie Poustka, & Stefan Wiemann. (1998). Primer design for large scale sequencing. Nucleic Acids Research. 26(12). 3006–3012. 68 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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