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 Netherlands. 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

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 Raymonda Varon, Christine Vissinga et al. Cell profile →
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

1998 783 citations Kathrin Saar, André Reis et al. profile →

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Severe manifestation of Rauch‐Azzarello syndrome associated with biallelic deletion of CTNND2 2024 ·Clinical Genetics ·(unknown), Mandy Krumbiegel, (unknown), (unknown), Thomas Rupprecht, Cornelia Kraus, Steffen Uebe, André Reis, Georgia Vasileiou	0
2	Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome 2023 ·BMC Genomics ·Jibril Hirbo, Francesca Pasutto, Eric R. Gamazon, Patrick Evans, (unknown), Daniel Berner, Julia Sealock, Ran Tao, Péter Straub, Anuar Konkashbaev, (unknown), Ursula Schlötzer‐Schrehardt, André Reis, Milam A. Brantley, Chiea Chuen Khor, Karen M. Joos, Nancy J. Cox	6
3	Different MAPT haplotypes influence expression of total MAPT in postmortem brain tissue 2023 ·Acta Neuropathologica Communications ·(unknown), Sigrid C. Schwarz, Thomas W. Rösler, Thomas Arzberger, Steve Gentleman, Otto Windl, Mandy Krumbiegel, André Reis, Viktoria Ruf, Jochen Herms, Günter U. Höglinger	9
4	Ex Vivo Chromosomal Radiosensitivity Testing in Patients with Pathological Germline Variants in Breast Cancer High-Susceptibility Genes BReast CAncer 1 and BReast CAncer 2 2023 ·Current Issues in Molecular Biology ·(unknown), Marius Wunderle, (unknown), Matthias Ruebner, Hanna Huebner, Juliane Hoyer, André Reis, Peter A. Fasching, Matthias W. Beckmann, Carolin C. Hack, Rainer Fietkau, Luitpold Distel	2
5	Transcription factor Tcf4 is the preferred heterodimerization partner for Olig2 in oligodendrocytes and required for differentiation 2020 ·Nucleic Acids Research ·(unknown), Franziska Fröb, (unknown), Marie‐Theres Wittmann, D. Chichung Lie, André Reis, Michael Wegner	43
6	“Fatuk-Kuak Hosi Timor Lorosa’e”:Caves of Timor-Leste 2017 ·Research at the University of Copenhagen (University of Copenhagen) ·(unknown), Pedro Pinto, M. Soares, Аnа Sofiа P. S. Reboleirа, André Reis, (unknown)	1
7	Exome Pool-Seq in neurodevelopmental disorders 2017 ·European Journal of Human Genetics ·Bernt Popp, Arif B. Ekici, Christian T. Thiel, Juliane Hoyer, Antje Wiesener, Cornelia Kraus, André Reis, Christiane Zweier	59
8	Evidence for genetic overlap between adult onset Still’s disease and hereditary periodic fever syndromes 2017 ·Rheumatology International ·(unknown), Jürgen Rech, Axel J. Hueber, Norbert Blank, Sabine Löhr, André Reis, Heinrich Sticht, Ulrike Hüffmeier	21
9	Dysregulated expression of POMP and TMEM136 may contribute to impaired proteasome function and endothelial dysfunction in eyes with pseudoexfoliation syndrome/glaucoma 2017 ·Investigative Ophthalmology & Visual Science ·Matthias Zenkel, Ursula Schlötzer‐Schrehardt, Daniel Berner, Friedrich E. Kruse, André Reis, Chiea Chuen Khor, (unknown), Francesca Pasutto	1
10	LOXL1 intronic variants influence LOXL1 expression through differential transcription factor binding in pseudoexfoliation syndrome/glaucoma 2016 ·Investigative Ophthalmology & Visual Science ·Ursula Schlötzer‐Schrehardt, Matthias Zenkel, Ursula Hoja, Mineo Ozaki, Tin Aung, Chiea Chuen Khor, Friedrich E. Kruse, André Reis, Francesca Pasutto	1
11	Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld–Rieger syndrome and glaucoma 2015 ·Gene ·Francesca Pasutto, Lucia Mauri, Bernt Popp, Heinrich Sticht, Arif B. Ekici, Elena Piozzi, Aldo Bonfante, Silvana Penco, Ursula Schlötzer‐Schrehardt, André Reis	7
12	Biallelic SEMA3A defects cause a novel type of syndromic short stature 2013 ·American Journal of Medical Genetics Part A ·(unknown), Markus Zweier, Heinrich Sticht, Christiane Zweier, (unknown), Juliane Hoyer, Steffen Uebe, Arie van Haeringen, Christian T. Thiel, Arif B. Ekici, André Reis, Anita Rauch	9
13	A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype 2013 ·Journal of Medical Genetics ·Christiane Zweier, Cornelia Kraus, Louise Brueton, Trevor Cole, Franziska Degenhardt, Hartmut Engels, Gabriele Gillessen‐Kaesbach, Luitgard Graul‐Neumann, Denise Horn, Juliane Hoyer, Walter Just, Anita Rauch, André Reis, Bernd Wollnik, Michael Zeschnigk, Hermann‐Josef Lüdecke, Dagmar Wieczorek	32
14	Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature 2011 ·The American Journal of Human Genetics ·Rami Abou Jamra, (unknown), Annick Raas‐Rothschild, Sebastian Eck, Elisabeth Graf, Rebecca Buchert, Guntram Borck, Arif B. Ekici, Felix F. Brockschmidt, Markus M. Nöthen, Arnold Münnich, Tim M. Strom, André Reis, Laurence Colleaux	167
15	Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation 2004 ·The American Journal of Human Genetics ·Marc Trimborn, Sandra Bell, (unknown), Yasmin Abdul Rashid, Hussain Jafri, Paul Griffiths, Luitgard M. Neumann, Alice Krebs, André Reis, Karl Sperling, Heidemarie Neitzel, Andrew P. Jackson	190
16	The Fanconi Anemia Group E Gene, FANCE, Maps to Chromosome 6p 1999 ·The American Journal of Human Genetics ·Quinten Waisfisz, Çiğdem Altay, Peter A. J. Leegwater, Johan P. de Winter, Kenshi Komatsu, D. Gareth Evans, Rolf‐Dieter Wegner, André Reis, Hans Joenje, Fré Arwert, Christopher G. Mathew, Jan C. Pronk, Kathrin Saar, Neil V. Morgan, Martin Digweed	41
17	Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome breakdown → 1998 ·Cell ·Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen Cerosaletti, Krystyńa Chrzańowska, Kathrin Saar, Georg Beckmann, E Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stümm, Corry M.R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed, André Rosenthal, Karl Sperling, Patrick Concannon, André Reis	811
18	Microsatellite Haplotypes of Polish Cystic Fibrosis Alleles: ΔF508 Chromosomes Demonstrate a North-South Haplotype Frequency Gradient 1996 ·Human Heredity ·Michał Witt, André Reis, Wojciech Cichy, (unknown)	4
19	Molecular and clinical heterogeneity in palmoplantar keratoderma (PPK) 1994 ·The American Journal of Human Genetics ·(unknown), (unknown), André Reis	1
20	The direct early diagnosis of cystic fibrosis by the detection of the deltaF508 CFTR gene mutation in a prematurely delivered boy 1991 ·Clinical Genetics ·Milan Maçek, Manfred Stuhrmann, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), André Reis, (unknown), Jörg Schmidtke	6

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.

Explore authors with similar magnitude of impact