Alexej Knaus

1.3k total citations
23 papers, 308 citations indexed

About

Alexej Knaus is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Alexej Knaus has authored 23 papers receiving a total of 308 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Genetics and 5 papers in Physiology. Recurrent topics in Alexej Knaus's work include Genomics and Rare Diseases (7 papers), Lysosomal Storage Disorders Research (5 papers) and Trypanosoma species research and implications (4 papers). Alexej Knaus is often cited by papers focused on Genomics and Rare Diseases (7 papers), Lysosomal Storage Disorders Research (5 papers) and Trypanosoma species research and implications (4 papers). Alexej Knaus collaborates with scholars based in Germany, United Kingdom and United States. Alexej Knaus's co-authors include Peter Krawitz, Stefan Mundlos, Peter Shaw, Denise Horn, Malte Spielmann, Maria Teschler‐Nicola, Ron Pinhasi, Taroh Kinoshita, Yoshiko Murakami and Manuel Holtgrewe and has published in prestigious journals such as Nucleic Acids Research, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Alexej Knaus

23 papers receiving 302 citations

Peers

Countries citing papers authored by Alexej Knaus

Since Specialization

Citations

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

Fields of papers citing papers by Alexej Knaus

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexej Knaus

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

#	Work	Indexed citations
1	Rare Genetic Developmental Disabilities: Mabry Syndrome (MIM 239300) Index Cases and Glycophosphatidylinositol (GPI) Disorders 2024 ·Genes ·Miles D. Thompson, Alexej Knaus	1
2	Occurrence of a paroxysmal nocturnal hemoglobinuria clone in an essential thrombocythemia: a link between <i>PIGV</i> and <i>MPL</i> 2022 ·Haematologica ·Alexej Knaus, François Vergez, Cédric Garcia, Hartmut Engels, (unknown), David Ribes, Laëtitia Largeaud, Suzanne Tavitian, Bernard Payrastre, Peter Krawitz, Stanislas Faguer, Agnès Ribes	3
3	CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graph 2021 ·NAR Genomics and Bioinformatics ·(unknown), (unknown), Alexander Schmid, Ashar Ahmad, Alexej Knaus, (unknown), (unknown), Birgit Zirn, Tobias B. Haack, Stephan Ossowski, Matias Wagner, Theresa Brunet, Nadja Ehmke, Magdalena Danyel, (unknown), Tom Kamphans, Guy Nadav, Nicole Fleischer, Holger Fröhlich, Peter Krawitz	15
4	TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19 2021 ·npj Genomic Medicine ·Axel Schmidt, Sophia Peters, Alexej Knaus, Hemmen Sabir, (unknown), Carlo Maj, Julia Fazaal, Sugirthan Sivalingam, (unknown), (unknown), Dirk Holzinger, Ulrich Neudorf, Andreas Müller, Kerstin U. Ludwig, Peter Krawitz, Hartmut Engels, Markus M. Nöthen, Soyhan Bağcı	28
5	A Novel Mutation in <b><i>PIGA</i></b> Associated with Multiple Congenital Anomalies-Hypotonia-Seizure Syndrome 2 (MCAHS2) in a Boy with a Combination of Severe Epilepsy and Gingival Hyperplasia 2020 ·Molecular Syndromology ·Christiane Neuhofer, (unknown), Bernd Wilken, Alexej Knaus, Janine Altmüller, Peter Nürnberg, Yun Li, Bernd Wollnik, Peter Burfeind, Silke Pauli	7
6	Adult Osteosclerotic Metaphyseal Dysplasia With Progressive Osteonecrosis of the Jaws and Abnormal Bone Resorption Pattern Due to a LRRK1 Splice Site Mutation 2020 ·Journal of Bone and Mineral Research ·(unknown), (unknown), Tim Rolvien, (unknown), (unknown), Alexej Knaus, Sebastian Böttger, Jozef Zustin, Sven Geißler, Ralf Oheim, Michael Amling, (unknown), Uwe Kornak	15
7	Evidence of the milder phenotypic spectrum of c.1582G>A PIGT variant: Delineation based on seven novel Polish patients 2020 ·Clinical Genetics ·Aleksandra Jezela‐Stanek, Elżbieta Szczepanik, Hanna Mierzewska, Małgorzata Rydzanicz, (unknown), Alexej Knaus, Robert Śmigiel, Iwona Stępniak, (unknown), (unknown), Peter Krawitz, Rafał Płoski	8
8	VarFish: comprehensive DNA variant analysis for diagnostics and research 2020 ·Nucleic Acids Research ·Manuel Holtgrewe, (unknown), Mikko Nieminen, Stefan Mundlos, Alexej Knaus, Uwe Kornak, Dominik Seelow, (unknown), Malte Spielmann, Björn Fischer‐Zirnsak, Felix Boschann, Ute I. Scholl, Nadja Ehmke, Dieter Beule	33
9	Mutations in PIGU Impair the Function of the GPI Transamidase Complex, Causing Severe Intellectual Disability, Epilepsy, and Brain Anomalies 2019 ·The American Journal of Human Genetics ·Alexej Knaus, Fanny Kortüm, Tjitske Kleefstra, Asbjørg Stray‐Pedersen, (unknown), Yoshiko Murakami, Thorsten Gerstner, Hans van Bokhoven, Zafar Iqbal, Denise Horn, Taroh Kinoshita, Maja Hempel, Peter Krawitz	35
10	A post glycosylphosphatidylinositol (GPI) attachment to proteins, type 2 (PGAP2) variant identified in Mabry syndrome index cases: Molecular genetics of the prototypical inherited GPI disorder 2019 ·European Journal of Medical Genetics ·Miles D. Thompson, Alexej Knaus, Bruce A. Barshop, Almuth Caliebe, Hiltrud Muhle, Thi Tuyet Mai Nguyen, Nissan Baratang, Taroh Kinoshita, Maire E. Percy, Philippe M. Campeau, Yoshiko Murakami, David E.C. Cole, Peter Krawitz, C. Charlton Mabry	10
11	Familial Xp11.22 microdeletion including SHROOM4 and CLCN5 is associated with intellectual disability, short stature, microcephaly and Dent disease: a case report 2019 ·BMC Medical Genomics ·Magdalena Danyel, (unknown), (unknown), Jutta Gellermann, Alexej Knaus, Denise Horn	3
12	Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation 2018 ·Scientific Reports ·Manuel Holtgrewe, Alexej Knaus, (unknown), Jean Tori Pantel, (unknown), Kornelia Neveling, Jakob M. Goldmann, Max Schubach, Marten Jäger, Marie Coutelier, Stefan Mundlos, Dieter Beule, Karl Sperling, Peter Krawitz	22
13	A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia 2017 ·Molecular Syndromology ·Seval Türkmen, Malte Spielmann, Nilay Güneş, Alexej Knaus, Ricarda Flöttmann, Stefan Mundlos, Beyhan Tüysüz	10
14	Reduced cell surface levels of GPI-linked markers in a new case with PIGG loss of function 2017 ·Human Mutation ·Jin Zhao, Jonatan Halvardson, Alexej Knaus, Patrik Georgii‐Hemming, (unknown), Peter Krawitz, Ann‐Charlotte Thuresson, Lars Feuk	13
15	Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome 2016 ·Human Mutation ·Alexej Knaus, Tomonari Awaya, Ingo Helbig, Zaid Afawi, Manuela Pendziwiat, (unknown), Miles D. Thompson, David E.C. Cole, Steve A. Skinner, Fran Annese, Natalie Canham, Michal R. Schweiger, Peter N. Robinson, Stefan Mundlos, Taroh Kinoshita, Arnold Münnich, Yoshiko Murakami, Denise Horn, Peter Krawitz	35
16	A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation 2015 ·American Journal of Medical Genetics Part A ·Daniel M. Ibrahim, Naeimeh Tayebi, Alexej Knaus, Asita C. Stiege, (unknown), Jochen Hecht, Stefan Mundlos, Malte Spielmann	15
17	FGFR2 mutation in a patient without typical features of Pfeiffer syndrome – The emerging role of combined NGS and phenotype based strategies 2015 ·European Journal of Medical Genetics ·Ricarda Flöttmann, Alexej Knaus, Tomasz Żemojtel, Peter N. Robinson, Stefan Mundlos, Denise Horn, Malte Spielmann	5
18	Crowdsourced direct-to-consumer genomic analysis of a family quartet 2015 ·BMC Genomics ·Manuel Corpas, (unknown), Nazareth Torres, Bastian Greshake Tzovaras, Alain Coletta, Alexej Knaus, Andrew Harrison, Mike Cariaso, Federico Morán, Fiona Nielsen, Daniel Swan, David Solís, Peter Krawitz, Frank Schacherer, Peter Schols, (unknown), Pascal Borry, Gustavo Glusman, Peter N. Robinson	11
19	Cross-population analysis of the growth of long bones and the os coxae of three Early Medieval Austrian populations 2005 ·American Journal of Human Biology ·Ron Pinhasi, Maria Teschler‐Nicola, Alexej Knaus, Peter Shaw	22
20	Dermatoglyphics of two cases of X tetrasomy. 1969 ·PubMed ·J Sokołowski, Alexej Knaus, A. Kleczkowska	7

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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