Sabina Liechti‐Gallati

4.7k total citations · 1 hit paper
59 papers, 2.8k citations indexed

About

Sabina Liechti‐Gallati is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Sabina Liechti‐Gallati has authored 59 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 13 papers in Cell Biology and 13 papers in Genetics. Recurrent topics in Sabina Liechti‐Gallati's work include Cystic Fibrosis Research Advances (11 papers), Metabolism and Genetic Disorders (10 papers) and Cellular transport and secretion (9 papers). Sabina Liechti‐Gallati is often cited by papers focused on Cystic Fibrosis Research Advances (11 papers), Metabolism and Genetic Disorders (10 papers) and Cellular transport and secretion (9 papers). Sabina Liechti‐Gallati collaborates with scholars based in Switzerland, Germany and France. Sabina Liechti‐Gallati's co-authors include Hans Moser, Louis M. Kunkel, Corlee J. Bertelson, Anthony P. Monaco, Richard Kraemer, P. Birrer, A Rüdeberg, Ronald G. Crystal, Richard C. Hubbard and Noel G. McElvaney and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and Blood.

In The Last Decade

Sabina Liechti‐Gallati

59 papers receiving 2.7k citations

Hit Papers

An explanation for the phenotypic differences between pat... 1988 2026 2000 2013 1988 250 500 750
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.

  1. An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
    1988 934 citations Anthony P. Monaco, Corlee J. Bertelson et al. Genomics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sabina Liechti‐Gallati Switzerland 23 1.8k 490 481 460 430 59 2.8k
Reed Hickey United States 17 1.6k 0.9× 561 1.1× 313 0.7× 135 0.3× 405 0.9× 19 2.7k
Børge Teisner Denmark 29 997 0.5× 197 0.4× 282 0.6× 256 0.6× 115 0.3× 63 2.4k
Anna Savoia Italy 38 1.7k 0.9× 193 0.4× 778 1.6× 737 1.6× 533 1.2× 121 4.1k
Steven Goossens Belgium 26 1.9k 1.0× 209 0.4× 242 0.5× 168 0.4× 121 0.3× 71 3.0k
Laurent Metzinger France 27 2.0k 1.1× 287 0.6× 284 0.6× 120 0.3× 123 0.3× 51 2.6k
Gilbert-André Keller United States 14 1.0k 0.6× 134 0.3× 144 0.3× 265 0.6× 143 0.3× 17 1.9k
Anne E. Hughes United Kingdom 26 1.0k 0.6× 243 0.5× 311 0.6× 215 0.5× 151 0.4× 59 3.0k
Jeffrey R. Crosby United States 21 915 0.5× 160 0.3× 171 0.4× 246 0.5× 399 0.9× 37 2.2k
Takashi Nakaoka Japan 22 1.6k 0.9× 302 0.6× 192 0.4× 221 0.5× 89 0.2× 47 2.2k
Scott Cooper United States 35 1.5k 0.8× 130 0.3× 376 0.8× 351 0.8× 996 2.3× 97 5.1k

Countries citing papers authored by Sabina Liechti‐Gallati

Since Specialization
Citations

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

Fields of papers citing papers by Sabina Liechti‐Gallati

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sabina Liechti‐Gallati. 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 Sabina Liechti‐Gallati. The network helps show where Sabina Liechti‐Gallati may publish in the future.

Co-authorship network of co-authors of Sabina Liechti‐Gallati

This figure shows the co-authorship network connecting the top 25 collaborators of Sabina Liechti‐Gallati. A scholar is included among the top collaborators of Sabina Liechti‐Gallati 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 Sabina Liechti‐Gallati. Sabina Liechti‐Gallati 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.
Laporte, Jocelyn, Stephan M. Tanner, Wolfram Kreß, et al.. (2000). MTM1 mutations in X-linked myotubular myopathy. Human Mutation. 15(5). 393–409. 164 indexed citations
2.
Liechti‐Gallati, Sabina, et al.. (1999). Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease. European Journal of Human Genetics. 7(5). 590–598. 74 indexed citations
3.
Rohrbach, Marianne, Richard Kraemer, & Sabina Liechti‐Gallati. (1998). Screening of the FcεRI‐β‐Gene in a Swiss Population of Asthmatic Children: No Association with E237G and Identification of New Sequence Variations. Disease Markers. 14(3). 177–186. 17 indexed citations
4.
5.
Laporte, Jocelyn, Stephan M. Tanner, F Blondeau, et al.. (1998). Genomic organization of the MTM1 gene implicated in X-linked myotubular myopathy. European Journal of Human Genetics. 6(4). 325–330. 21 indexed citations
6.
Leibundgut, Elisabeth Oppliger, Bendicht Wermuth, Jean‐Pierre Colombo, & Sabina Liechti‐Gallati. (1996). Ornithine transcarbamylase deficiency: Characterization of gene mutations and polymorphisms. Human Mutation. 8(4). 333–339. 18 indexed citations
7.
Kioschis, Petra, Ute C. Rogner, Sabine M. Klauck, et al.. (1996). A 900-kb Cosmid Contig and 10 New Transcripts within the Candidate Region for Myotubular Myopathy (MTM1). Genomics. 33(3). 365–373. 22 indexed citations
8.
Marti, Ulrich, Christoph Elsing, Eberhard L. Renner, Sabina Liechti‐Gallati, & Jürg Reichen. (1996). Differential expression of Na+,H+-antiporter mRNA in biliary epithelial cells and in hepatocytes. Journal of Hepatology. 24(4). 498–502. 21 indexed citations
9.
10.
Laporte, Jocelyn, et al.. (1996). X-linked myotubular myopathy: Refinement of the critical gene region. Neuromuscular Disorders. 6(4). 275–281. 7 indexed citations
11.
Liechti‐Gallati, Sabina & Richard Kraemer. (1995). Cystic fibrosis mutations and immotile cilia syndrome. Clinical Genetics. 47(6). 328–329. 3 indexed citations
12.
Liechti‐Gallati, Sabina, et al.. (1995). Chronic Metabolic Alkalosis: Not Uncommon in Young Children with Severe Cystic Fibrosis. American Journal of Nephrology. 15(3). 245–250. 13 indexed citations
13.
Aebi, Christoph, et al.. (1995). The age at onset of chronicPseudomonas aeruginosa colonization in cystic fibrosis —prognostic significance. European Journal of Pediatrics. 154(S4). S69–S73. 34 indexed citations
14.
Birrer, P., Noel G. McElvaney, A Rüdeberg, et al.. (1994). Protease-Antiprotease Imbalance in the Lungs of Children with Cystic Fibrosis. American Journal of Respiratory and Critical Care Medicine. 150(1). 207–213. 315 indexed citations
15.
Grimm, T., Gerhard Meng, Sabina Liechti‐Gallati, et al.. (1994). On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.. Journal of Medical Genetics. 31(3). 183–186. 84 indexed citations
16.
Mullis, Primus E., et al.. (1991). Short Stature in a Patient with Cystic Fibrosis Caused by a 6.7-kb Human Growth Hormone Gene Deletion. Hormone Research. 36(1-2). 4–8. 7 indexed citations
17.
Liechti‐Gallati, Sabina, Naseem Malik, M. Alkan, et al.. (1991). Association between Haplotypes and Specific Mutations in Swiss Cystic Fibrosis Families. Pediatric Research. 30(4). 304–308. 8 indexed citations
18.
Liechti‐Gallati, Sabina, Volker Schneider, P E Mullis, & Hans Moser. (1990). RFLPs for Duchenne muscular dystrophy cDNA clones 9 and 10.. Europe PMC (PubMed Central). 46(6). 1090–4. 2 indexed citations
19.
Liechti‐Gallati, Sabina, Volker Schneider, Marco Mächler, et al.. (1990). Haplotype analysis for CF‐linked DNA polymorphisms in Switzerland. Clinical Genetics. 37(6). 442–449. 3 indexed citations
20.
Monaco, Anthony P., Corlee J. Bertelson, Sabina Liechti‐Gallati, Hans Moser, & Louis M. Kunkel. (1988). An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. Genomics. 2(1). 90–95. 934 indexed citations breakdown →

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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