Oliver Brandau

3.9k total citations
38 papers, 1.9k citations indexed

About

Oliver Brandau is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Oliver Brandau has authored 38 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Cell Biology. Recurrent topics in Oliver Brandau's work include RNA regulation and disease (5 papers), Retinal Development and Disorders (5 papers) and Cell Adhesion Molecules Research (5 papers). Oliver Brandau is often cited by papers focused on RNA regulation and disease (5 papers), Retinal Development and Disorders (5 papers) and Cell Adhesion Molecules Research (5 papers). Oliver Brandau collaborates with scholars based in Germany, Sweden and Austria. Oliver Brandau's co-authors include Reinhard Fässler, Ernst B. Hunziker, Denitsa Docheva, Alfons Meindl, Attila Aszódi, Bernd Wissinger, Helene Achatz, Alison J. Hardcastle, Dietmar Vestweber and Thomas Meitinger and has published in prestigious journals such as Nature Genetics, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Oliver Brandau

38 papers receiving 1.9k citations

Peers

Countries citing papers authored by Oliver Brandau

Since Specialization

Citations

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

Fields of papers citing papers by Oliver Brandau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oliver Brandau

This figure shows the co-authorship network connecting the top 25 collaborators of Oliver Brandau. A scholar is included among the top collaborators of Oliver Brandau 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 Oliver Brandau. Oliver Brandau 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	A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature 2019 ·Journal of Applied Genetics ·(unknown), Tibor Kalmár, Nikoletta Nagy, (unknown), (unknown), Zoltán Maróti, Oliver Brandau, László Sztriha	15
2	Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD 2019 ·Journal of Human Genetics ·(unknown), Vijaya Ramachandran, (unknown), Arndt Rolfs, Oliver Brandau, Sabrina Eichler, Anil Kumar Bhalla, Dinesh Khullar, (unknown), (unknown), Vijay Kher, Jyotsna Verma, Sudha Kohli, Renu Saxena, Ishwar C. Verma	5
3	Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability 2018 ·European Journal of Human Genetics ·Aida M. Bertoli‐Avella, José María García-Aznar, Oliver Brandau, (unknown), Zafer Yüksel, Anett Marais, Nana‐Maria Grüning, Lia Abbasi Moheb, Omid Paknia, (unknown), Seham Alameer, (unknown), Fahd Al‐Mulla, Nouriya Al‐Sannaa, Arndt Rolfs, Peter Bauer	17
4	Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report 2018 ·BMC Medical Genetics ·(unknown), (unknown), Nirmala D. Sirisena, Nana‐Maria Grüning, Oliver Brandau, T. Kumanan‬, Casey Dagnall, Lisa J. McReynolds, Sharon A. Savage, Vajira H. W. Dissanayake	18
5	Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome 2017 ·Journal of Human Genetics ·Anju Shukla, Malavika Hebbar, Anshika Srivastava, Rajagopal Kadavigere, (unknown), (unknown), Oliver Brandau, Stephanie Bielas, Katta M. Girisha	47
6	A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis–lymphedema–telangiectasia syndrome by Whole Exome Sequencing 2015 ·Molecular and Cellular Probes ·(unknown), (unknown), Pratibha Nair, (unknown), (unknown), Mahmoud Taleb Al‐Ali, Oliver Brandau, Abdul Rezzak Hamzeh	13
7	Identification and molecular characterisation of a homozygous missense mutation in the ADAMTS10 gene in a patient with Weill–Marchesani syndrome 2014 ·European Journal of Human Genetics ·Hannes Steinkellner, Julia Etzler, (unknown), Jürgen Neesen, Eva Stifter, Oliver Brandau, Franco Laccone	11
8	Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G > A (p.E1856K) with high interfamilial cardiac variability and putative anticipation 2014 ·Neuromuscular Disorders ·Josef Finsterer, Oliver Brandau, Claudia Stöllberger, William Wallefeld, Nigel G. Laing, Franco Laccone	10
9	Amniotic fluid stem cells to study mTOR signaling in differentiation 2012 ·Organogenesis ·Margit Rosner, Katharina Schipany, (unknown), Gert Lübec, Oliver Brandau, Markus Hengstschläger	2
10	Human amniotic fluid stem cells as a model for functional studies of genes involved in human genetic diseases or oncogenesis 2011 ·Oncotarget ·Margit Rosner, Helmut Dolznig, Katharina Schipany, Mario Mikula, Oliver Brandau, Markus Hengstschläger	23
11	Complete loss of murine Xin results in a mild cardiac phenotype with altered distribution of intercalated discs 2009 ·Cardiovascular Research ·Julia Otten, Peter F. M. van der Ven, Padmanabhan Vakeel, (unknown), Gregor Kirfel, Oliver Brandau, Michael Boesl, Jan W. Schrickel, Markus Linhart, Katrin Hayeß, Francisco J. Naya, Hendrik Milting, (unknown), Dieter O. Fürst	32
12	PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions☆ 2003 ·Experimental Cell Research ·Attila Braun, (unknown), Fabio Stanchi, Markus Moser, Günter Kostka, Elisabeth Ehler, Oliver Brandau, Reinhard Fässler	64
13	An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders 2002 ·Genomics ·Dawn L. Thiselton, Jennifer McDowall, Oliver Brandau, Juliane Ramser, Fabiana D’Esposito, Shomi S. Bhattacharya, Mark T. Ross, Alison J. Hardcastle, Alfons Meindl	72
14	Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis 2002 ·Gene ·Attila Braun, Attila Aszódi, Heide Hellebrand, Alejandro Berna‐Erro, Reinhard Fässler, Oliver Brandau	34
15	Stage-and tissue-specific expression of a Col2a1-Cre fusion gene in transgenic mice 2001 ·Matrix Biology ·Keiko Sakai, László Hiripi, Virpi Glumoff, Oliver Brandau, (unknown), Eero Vuorio, Zsuzsa Bösze, Reinhard Fässler, Attila Aszódi	84
16	The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein 2000 ·Nature Genetics ·Carsten M. Pusch, Christina Zeitz, Oliver Brandau, (unknown), Helene Achatz, Silke Feil, Curt Scharfe, Johannes Maurer, Frank Jacobi, A. Pinckers, Sten Andréasson, Alison J. Hardcastle, Bernd Wissinger, Wolfgang Berger, Alfons Meindl	187
17	Epstein--Barr Virus-Negative Boys With Non-Hodgkin Lymphoma Are Mutated in the Sh2D1A Gene, as Are Patients With X-Linked Lymphoproliferative Disease (XLP) 1999 ·Human Molecular Genetics ·Oliver Brandau, Volker Schuster, Michael Weiss, Heide Hellebrand, Franz Martin Fink, Alfons Kreczy, W Friedrich, Brigitte Strahm, Charlotte M. Niemeyer, B. H. Belohradsky, A Meindl	81
18	Mutation Screening of the BTK Gene in 56 Families With X-Linked Agammaglobulinemia (XLA): 47 Unique Mutations Without Correlation to Clinical Course 1998 ·PEDIATRICS ·Elke Holinski‐Feder, Michael Weiss, Oliver Brandau, Kerry Baldwin Jedele, Beston F. Nore, (unknown), Mauno Vihinen, Stevan R. Hubbard, Bernd H. Belohradsky, Smith Rjh, Alfons Meindl	87
19	UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2 1998 ·European Journal of Human Genetics ·Oliver Brandau, Gerald Nyakatura, Kerry Baldwin Jedele, Matthias Platzer, Helene Achatz, Mark T. Ross, Jan Murken, André Rosenthal, Alfons Meindl	6
20	Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets 1997 ·Genome Research ·Fiona Francis, Tim M. Strom, Steffen Hennig, Annett Böddrich, Bettina Lorenz, Oliver Brandau, Klaus Mohnike, (unknown), (unknown), Sven Klages, Katja Borzym, Thomas Pohl, C Oudet, Michael J. Econs, Peter Rowe, Richard Reinhardt, Thomas Meitinger, Hans Lehrach	129

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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