André Reis

37.1k total citations · 2 hit papers
320 papers, 13.6k citations indexed

About

André Reis is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, André Reis has authored 320 papers receiving a total of 13.6k indexed citations (citations by other indexed papers that have themselves been cited), including 192 papers in Molecular Biology, 118 papers in Genetics and 44 papers in Cell Biology. Recurrent topics in André Reis's work include Genetics and Neurodevelopmental Disorders (43 papers), Genomic variations and chromosomal abnormalities (28 papers) and Skin and Cellular Biology Research (21 papers). André Reis is often cited by papers focused on Genetics and Neurodevelopmental Disorders (43 papers), Genomic variations and chromosomal abnormalities (28 papers) and Skin and Cellular Biology Research (21 papers). André Reis collaborates with scholars based in Germany, United States and United Kingdom. André Reis's co-authors include Anita Rauch, Arif B. Ekici, Kathrin Saar, Karl Sperling, Christiane Zweier, Ulrike Hüffmeier, Christian T. Thiel, Franz Rüschendorf, Heiko Traupe and Cornelia Kraus and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

André Reis

313 papers receiving 13.2k 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.

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

1998 811 citations André Reis et al. profile →
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

1998 783 citations André Reis et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
André Reis	7.7k	4.4k	1.8k	1.6k	1.4k	320	13.6k
Fowzan S. Alkuraya	6.8k 0.9×	4.6k 1.0×	1.3k 0.7×	1.0k 0.6×	635 0.5×	385	11.5k
David Bick	10.4k 1.4×	10.3k 2.3×	1.1k 0.6×	1.1k 0.7×	1.2k 0.9×	83	22.0k
G.M. Lathrop	6.7k 0.9×	7.1k 1.6×	1.2k 0.7×	1.9k 1.2×	1.1k 0.8×	235	16.2k
Tim M. Strom	8.0k 1.0×	6.0k 1.4×	1.2k 0.7×	472 0.3×	1.5k 1.1×	216	16.6k
Paul A. Overbeek	9.6k 1.2×	3.2k 0.7×	1.8k 1.0×	609 0.4×	555 0.4×	166	13.0k
Thomas L. Saunders	7.8k 1.0×	2.2k 0.5×	3.1k 1.8×	2.7k 1.6×	1.2k 0.9×	160	15.3k
En Li	17.0k 2.2×	4.7k 1.1×	2.5k 1.4×	1.6k 1.0×	1.7k 1.2×	119	22.4k
Debra J. Gilbert	10.8k 1.4×	3.0k 0.7×	1.7k 1.0×	3.6k 2.2×	2.7k 2.0×	256	17.7k
Niklas Dahl	5.9k 0.8×	2.9k 0.6×	1.3k 0.8×	675 0.4×	658 0.5×	245	9.8k
Christine M. Distèche	10.6k 1.4×	6.9k 1.6×	621 0.4×	2.3k 1.4×	925 0.7×	226	17.3k

Countries citing papers authored by André Reis

Since Specialization

Citations

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

Fields of papers citing papers by André Reis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of André Reis

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

Fröb, Franziska, Margherita Alfonsetti, Mandy Krumbiegel, et al.. (2025). A novel human organoid model system reveals requirement of TCF4 for oligodendroglial differentiation. Life Science Alliance. 8(6). e202403102–e202403102. 1 indexed citations

Krumbiegel, Mandy, Thomas Rupprecht, Cornelia Kraus, et al.. (2024). Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2 . Clinical Genetics. 106(2). 180–186.

Hirbo, Jibril, Francesca Pasutto, Eric R. Gamazon, et al.. (2023). Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome. BMC Genomics. 24(1). 75–75. 6 indexed citations

Schwarz, Sigrid C., Thomas W. Rösler, Thomas Arzberger, et al.. (2023). Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue. Acta Neuropathologica Communications. 11(1). 40–40. 9 indexed citations

Wunderle, Marius, Matthias Ruebner, Hanna Huebner, et al.. (2023). Ex Vivo Chromosomal Radiosensitivity Testing in Patients with Pathological Germline Variants in Breast Cancer High-Susceptibility Genes BReast CAncer 1 and BReast CAncer 2. Current Issues in Molecular Biology. 45(8). 6618–6633. 2 indexed citations

Wittmann, Marie‐Theres, Sayako Katada, Elisabeth Sock, et al.. (2021). scRNA sequencing uncovers a TCF4-dependent transcription factor network regulating commissure development in mouse. Development. 148(14). 11 indexed citations

Fröb, Franziska, et al.. (2020). Transcription factor Tcf4 is the preferred heterodimerization partner for Olig2 in oligodendrocytes and required for differentiation. Nucleic Acids Research. 48(9). 4839–4857. 43 indexed citations

Pinto, Pedro, et al.. (2017). “Fatuk-Kuak Hosi Timor Lorosa’e”:Caves of Timor-Leste. Research at the University of Copenhagen (University of Copenhagen). 1 indexed citations

Rech, Jürgen, Axel J. Hueber, Norbert Blank, et al.. (2017). Evidence for genetic overlap between adult onset Still’s disease and hereditary periodic fever syndromes. Rheumatology International. 38(1). 111–120. 21 indexed citations

10.

Popp, Bernt, Arif B. Ekici, Christian T. Thiel, et al.. (2017). Exome Pool-Seq in neurodevelopmental disorders. European Journal of Human Genetics. 25(12). 1364–1376. 59 indexed citations

11.

Berner, Daniel, Matthias Zenkel, Francesca Pasutto, et al.. (2017). Alternative splicing and nonsense-mediated mRNA decay contribute to regulation of LOXL1 expression in response to cellular stress in pseudoexfoliation. Investigative Ophthalmology & Visual Science. 58(8). 4909–4909. 1 indexed citations

12.

Zenkel, Matthias, Ursula Schlötzer‐Schrehardt, Daniel Berner, et al.. (2017). Dysregulated expression of POMP and TMEM136 may contribute to impaired proteasome function and endothelial dysfunction in eyes with pseudoexfoliation syndrome/glaucoma. Investigative Ophthalmology & Visual Science. 58(8). 4902–4902. 1 indexed citations

13.

Schlötzer‐Schrehardt, Ursula, Matthias Zenkel, Ursula Hoja, et al.. (2016). LOXL1 intronic variants influence LOXL1 expression through differential transcription factor binding in pseudoexfoliation syndrome/glaucoma. Investigative Ophthalmology & Visual Science. 57(12). 789–789. 1 indexed citations

14.

Pasutto, Francesca, Lucia Mauri, Bernt Popp, et al.. (2015). Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma. Gene. 568(1). 76–80. 7 indexed citations

15.

Zweier, Christiane, Cornelia Kraus, Louise Brueton, et al.. (2013). A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype. Journal of Medical Genetics. 50(12). 838–847. 32 indexed citations

16.

Huehne, Kathrin, Stefan Leis, Tino Muenster, et al.. (2009). High post surgical opioid requirements in Crohn's disease are not due to a general change in pain sensitivity. European Journal of Pain. 13(10). 1036–1042. 19 indexed citations

17.

Rauch, Anita, Juliane Hoyer, Sabine Guth, et al.. (2006). Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. American Journal of Medical Genetics Part A. 140A(19). 2063–2074. 288 indexed citations

18.

Küster, Wolfgang, et al.. (1995). Keratosis palmoplantaris striata Brünauer-Fuhs-Siemens: klinische, lipidbiochemische und molekularbiologische Untersuchungen. 70(4). 63–268. 1 indexed citations

19.

Reis, André, et al.. (1994). Molecular and clinical heterogeneity in palmoplantar keratoderma (PPK). The American Journal of Human Genetics. 55. 1 indexed citations

20.

Maçek, Milan, Milan Maçek, Milan Maçek, et al.. (1991). The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy. Clinical Genetics. 39(3). 219–222. 6 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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