Oliver Brandau

3.9k citations

38 papers · 1.9k indexed · h-index 19

Orthopedics and Sports Medicine top 2%
Immunology and Allergy top 5%
- Cell Adhesion Molecules Research 5
Nephrology top 5%
Cell Biology top 5%
Ophthalmology top 5%
Molecular Biology
- RNA regulation and disease 5
- Retinal Development and Disorders 5
- Renal and related cancers 4
- Pluripotent Stem Cells Research 3
Cardiology and Cardiovascular Medicine
- Cardiomyopathy and Myosin Studies 4
Immunology
- Neutrophil, Myeloperoxidase and Oxidative Mechanisms 3
Genetics
- Connective tissue disorders research 3

Co-authors: Reinhard Fässler Ernst B. Hunziker Denitsa Docheva Alfons Meindl Attila Aszódi Bernd Wissinger Helene Achatz Alison J. Hardcastle
Cited by: Orthopedics and Sports Medicine Immunology and Allergy Nephrology
Journals: Nature Genetics (1 paper)The Journal of Experimental Medicine (1 paper)SHILAP Revista de lepidopterología (1 paper)
Partner nations: Germany Sweden Austria

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

The 25 scholars most cited alongside Oliver Brandau, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Oliver Brandau Line = papers co-authored together Oliver Brandau links everyone, so they are left out of the graph.

All Works

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

20 of 20 papers shown

#	Work
1	A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature Journal of Applied Genetics ·Melinda Zombor,Tibor Kalmár,Nikoletta Nagy,Marianne Berényi,Borbála Telcs,Zoltán Maróti,Oliver Brandau,László Sztriha	2019	15
2	Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD Journal of Human Genetics ·Shewata Pandita,Vijaya Ramachandran,Prahlad Balakrishnan,Arndt Rolfs,Oliver Brandau,Sabrina Eichler,Anil Kumar Bhalla,Dinesh Khullar,Vindu Amitabh,Sivaramakrishnan Ramanarayanan,Vijay Kher,Jyotsna Verma,Sudha Kohli,Renu Saxena,Ishwar C. Verma	2019	5
3	Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability European Journal of Human Genetics ·Aida M. Bertoli‐Avella,José María García-Aznar,Oliver Brandau,Fahad Al-Hakami,Zafer Yüksel,Anett Marais,Nana‐Maria Grüning,Lia Abbasi Moheb,Omid Paknia,Nahla Alshaikh,Seham Alameer,Makia J. Marafi,Fahd Al‐Mulla,Nouriya Al‐Sannaa,Arndt Rolfs,Peter Bauer	2018	17
4	Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report BMC Medical Genetics ·Vithiya Ratnasamy,Navaneethakrishnan Suganthan,Nirmala D. Sirisena,Nana‐Maria Grüning,Oliver Brandau,T. Kumanan‬,Casey Dagnall,Lisa J. McReynolds,Sharon A. Savage,Vajira H. W. Dissanayake	2018	18
5	Homozygous p.(Glu87Lys) variant in ISCA1 is associated with a multiple mitochondrial dysfunctions syndrome Journal of Human Genetics ·Anju Shukla,Malavika Hebbar,Anshika Srivastava,Rajagopal Kadavigere,Priyanka Upadhyai,Anil Kanthi,Oliver Brandau,Stephanie Bielas,Katta M. Girisha	2017	47
6	A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis–lymphedema–telangiectasia syndrome by Whole Exome Sequencing Molecular and Cellular Probes ·Fatma Bastaki,Madiha Mohamed,Pratibha Nair,Fatima Saif,Nafisa Tawfiq,Mahmoud Taleb Al‐Ali,Oliver Brandau,Abdul Rezzak Hamzeh	2015	13
7	Identification and molecular characterisation of a homozygous missense mutation in the ADAMTS10 gene in a patient with Weill–Marchesani syndrome European Journal of Human Genetics ·Hannes Steinkellner,Julia Etzler,Laura Gogoll,Jürgen Neesen,Eva Stifter,Oliver Brandau,Franco Laccone	2014	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 Neuromuscular Disorders ·Josef Finsterer,Oliver Brandau,Claudia Stöllberger,William Wallefeld,Nigel G. Laing,Franco Laccone	2014	10
9	Amniotic fluid stem cells to study mTOR signaling in differentiation Organogenesis ·Margit Rosner,Katharina Schipany,Bharanidharan Shanmugasundaram,Gert Lübec,Oliver Brandau,Markus Hengstschläger	2012	2
10	Human amniotic fluid stem cells as a model for functional studies of genes involved in human genetic diseases or oncogenesis Oncotarget ·Margit Rosner,Helmut Dolznig,Katharina Schipany,Mario Mikula,Oliver Brandau,Markus Hengstschläger	2011	23
11	Complete loss of murine Xin results in a mild cardiac phenotype with altered distribution of intercalated discs Cardiovascular Research ·Julia Otten,Peter F. M. van der Ven,Padmanabhan Vakeel,Stefan Eulitz,Gregor Kirfel,Oliver Brandau,Michael Boesl,Jan W. Schrickel,Markus Linhart,Katrin Hayeß,Francisco J. Naya,Hendrik Milting,Rainer Meyer,Dieter O. Fürst	2009	32
12	PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions☆ Experimental Cell Research ·Attila Braun,Randi Bordoy,Fabio Stanchi,Markus Moser,Günter Kostka,Elisabeth Ehler,Oliver Brandau,Reinhard Fässler	2003	64
13	An Integrated, Functionally Annotated Gene Map of the DXS8026–ELK1 Interval on Human Xp11.3–Xp11.23: Potential Hotspot for Neurogenetic Disorders Genomics ·Dawn L. Thiselton,Jennifer McDowall,Oliver Brandau,Juliane Ramser,Fabiana D’Esposito,Shomi S. Bhattacharya,Mark T. Ross,Alison J. Hardcastle,Alfons Meindl	2002	72
14	Genomic organization of profilin-III and evidence for a transcript expressed exclusively in testis Gene ·Attila Braun,Attila Aszódi,Heide Hellebrand,Alejandro Berna‐Erro,Reinhard Fässler,Oliver Brandau	2002	34
15	Stage-and tissue-specific expression of a Col2a1-Cre fusion gene in transgenic mice Matrix Biology ·Keiko Sakai,László Hiripi,Virpi Glumoff,Oliver Brandau,Riitta Eerola,Eero Vuorio,Zsuzsa Bösze,Reinhard Fässler,Attila Aszódi	2001	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 Nature Genetics ·Carsten M. Pusch,Christina Zeitz,Oliver Brandau,Katrin Pesch,Helene Achatz,Silke Feil,Curt Scharfe,Johannes Maurer,Frank Jacobi,A. Pinckers,Sten Andréasson,Alison J. Hardcastle,Bernd Wissinger,Wolfgang Berger,Alfons Meindl	2000	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) 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	1999	81
18	Mutation Screening of the BTK Gene in 56 Families With X-Linked Agammaglobulinemia (XLA): 47 Unique Mutations Without Correlation to Clinical Course PEDIATRICS ·Elke Holinski‐Feder,Michael Weiss,Oliver Brandau,Kerry Baldwin Jedele,Beston F. Nore,C. Magnus Bäckesjö,Mauno Vihinen,Stevan R. Hubbard,Bernd H. Belohradsky,Smith Rjh,Alfons Meindl	1998	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 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	1998	6
20	Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets Genome Research ·Fiona Francis,Tim M. Strom,Steffen Hennig,Annett Böddrich,Bettina Lorenz,Oliver Brandau,Klaus Mohnike,Michele Cagnoli,Christina Steffens,Sven Klages,Katja Borzym,Thomas Pohl,C Oudet,Michael J. Econs,Peter Rowe,Richard Reinhardt,Thomas Meitinger,Hans Lehrach	1997	129

About Oliver Brandau

Oliver Brandau is a scholar working on Immunology and Allergy, Equine and Cell Biology, having authored 38 papers that have together received 1.9k indexed citations. Recurring topics across this work include RNA regulation and disease (5 papers), Retinal Development and Disorders (5 papers), Cell Adhesion Molecules Research (5 papers), Cardiomyopathy and Myosin Studies (4 papers), Renal and related cancers (4 papers), Neutrophil, Myeloperoxidase and Oxidative Mechanisms (3 papers), Connective tissue disorders research (3 papers) and Pluripotent Stem Cells Research (3 papers). The work is most often cited by research in Orthopedics and Sports Medicine (350 citations), Immunology and Allergy (172 citations) and Nephrology (122 citations). Oliver Brandau has collaborated with scholars based in Germany, Sweden and Austria. Frequent 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. Their work appears in journals such as Nature Genetics, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

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