Thomas Leis

702 total citations
14 papers, 583 citations indexed

About

Thomas Leis is a scholar working on Molecular Biology, Genetics and General Health Professions. According to data from OpenAlex, Thomas Leis has authored 14 papers receiving a total of 583 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Genetics and 3 papers in General Health Professions. Recurrent topics in Thomas Leis's work include Advanced biosensing and bioanalysis techniques (3 papers), Genomics and Rare Diseases (2 papers) and RNA Interference and Gene Delivery (2 papers). Thomas Leis is often cited by papers focused on Advanced biosensing and bioanalysis techniques (3 papers), Genomics and Rare Diseases (2 papers) and RNA Interference and Gene Delivery (2 papers). Thomas Leis collaborates with scholars based in Germany, Austria and United States. Thomas Leis's co-authors include Reinald Repp, Arndt Borkhardt, Jochen Harbott, Fritz Lampert, Oskar A. Haas, Joachim Kreuder, Traudl Henn, J. Hammermann, Wolfgang Rascher and Martin Reichel and has published in prestigious journals such as Oncogene, Leukemia and International Journal of Gynecology & Obstetrics.

In The Last Decade

Thomas Leis

14 papers receiving 572 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thomas Leis Germany	9	386	146	113	83	57	14	583
Jian‐Pei Fang China	14	269 0.7×	301 2.1×	118 1.0×	99 1.2×	93 1.6×	87	733
Casey Dagnall United States	15	308 0.8×	29 0.2×	31 0.3×	39 0.5×	55 1.0×	43	573
Maurien Pruis Netherlands	11	225 0.6×	99 0.7×	36 0.3×	115 1.4×	22 0.4×	15	423
Thomas R. Hickernell United States	10	468 1.2×	20 0.1×	71 0.6×	23 0.3×	37 0.6×	25	785
Elizabeth Yang United States	11	294 0.8×	149 1.0×	47 0.4×	68 0.8×	45 0.8×	33	495
Ioanna Bouba Greece	13	147 0.4×	25 0.2×	90 0.8×	122 1.5×	202 3.5×	31	561
Silvia Mangioni Italy	12	128 0.3×	210 1.4×	327 2.9×	93 1.1×	58 1.0×	17	742
Hui-liang Xue China	10	138 0.4×	158 1.1×	184 1.6×	122 1.5×	14 0.2×	54	395
P.R.L.C. Lam-Po-Tang Australia	14	193 0.5×	155 1.1×	111 1.0×	192 2.3×	219 3.8×	44	642

Countries citing papers authored by Thomas Leis

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Leis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Leis

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

All Works

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14 of 14 papers shown

Kraus, Cornelia, et al.. (2019). Severe Epileptic Encephalopathy in Siblings due to a Novel Heterozygous CACNA1A Gene Mutation. Neuropediatrics. 1 indexed citations

Gusek-Schneider, Gabriele C., et al.. (2015). Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report. Neuropediatrics. 46(S 01). 2 indexed citations

Reuter, Miriam S., Jörn Oliver Sass, Thomas Leis, et al.. (2014). HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disorders. American Journal of Medical Genetics Part A. 164(12). 3162–3169. 28 indexed citations

Nkenke, Emeka, E Vairaktaris, Christian Knipfer, et al.. (2011). Prospective assessment of complications associated with ultrasound activated resorbable pin osteosynthesis in pediatric craniofacial surgery: preliminary results. Neurocirugía. 22(6). 498–506. 12 indexed citations

Nkenke, Emeka, Eleftherios Vairaktaris, S. Schwarz, et al.. (2011). Prospective assessment of complications associated with ultrasound activated resorbable pin osteosynthesis in pediatric craniofacial surgery: preliminary results. Neurocirugía. 22(6). 498–506. 1 indexed citations

Neubert, Antje, et al.. (2009). Drug utilisation on a preterm and neonatal intensive care unit in Germany: a prospective, cohort-based analysis. European Journal of Clinical Pharmacology. 66(1). 87–95. 75 indexed citations

Langer, Thorsten, Markus Metzler, Dirk Reinhardt, et al.. (2003). Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: Almost identical MLL breakpoints in therapy‐related AML after treatment without etoposides. Genes Chromosomes and Cancer. 36(4). 393–401. 61 indexed citations

Reichel, Martin, Esther Gillert, Sieglinde Angermüller, et al.. (2001). Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL. Oncogene. 20(23). 2900–2907. 68 indexed citations

Gillert, Esther, Thomas Leis, Reinald Repp, et al.. (1999). A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells. Oncogene. 18(33). 4663–4671. 95 indexed citations

10.

Leis, Thomas, Reinald Repp, Arndt Borkhardt, et al.. (1998). A new fingerprint method for sequence analysis of chromosomal translocations at the genomic DNA level. Leukemia. 12(5). 758–763. 8 indexed citations

11.

Borkhardt, Arndt, Reinald Repp, Oskar A. Haas, et al.. (1997). Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11)(q13;q23). Oncogene. 14(2). 195–202. 212 indexed citations

12.

Villar, José, Ubaldo Farnot, Fernando C. Barros, et al.. (1993). A randomized trial of psychosocial support during high‐risk pregnancies. International Journal of Gynecology & Obstetrics. 41(3). 339–339. 3 indexed citations

13.

Langer, Ana, et al.. (1993). [Psychosocial support in pregnancy as a strategy to promote the newborn's health].. PubMed. 45(4). 317–28. 9 indexed citations

14.

McGavin, Μ. D. & Thomas Leis. (1968). MULTIPLE CUTANEOUS MASTOCYTOMAS IN A BULL. Australian Veterinary Journal. 44(1). 20–22. 8 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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