Juliane Hoyer

5.7k total citations
43 papers, 1.9k citations indexed

About

Juliane Hoyer is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Juliane Hoyer has authored 43 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Genetics, 27 papers in Molecular Biology and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Juliane Hoyer's work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (10 papers) and BRCA gene mutations in cancer (8 papers). Juliane Hoyer is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (10 papers) and BRCA gene mutations in cancer (8 papers). Juliane Hoyer collaborates with scholars based in Germany, Switzerland and United States. Juliane Hoyer's co-authors include André Reis, Anita Rauch, Christiane Zweier, Cornelia Kraus, Arif B. Ekici, Christian T. Thiel, Martin Zenker, Ulrike Hüffmeier, Steffen Uebe and Georgia Vasileiou and has published in prestigious journals such as The American Journal of Human Genetics, International Journal of Cancer and Frontiers in Microbiology.

In The Last Decade

Juliane Hoyer

43 papers receiving 1.9k citations

Peers

Countries citing papers authored by Juliane Hoyer

Since Specialization

Citations

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

Fields of papers citing papers by Juliane Hoyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Juliane Hoyer

This figure shows the co-authorship network connecting the top 25 collaborators of Juliane Hoyer. A scholar is included among the top collaborators of Juliane Hoyer 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 Juliane Hoyer. Juliane Hoyer 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	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
2	Determinants Affecting the Clinical Implementation of a Molecularly Informed Molecular Tumor Board Recommendation: Experience from a Tertiary Cancer Center 2023 ·Cancers ·Lars Tögel, (unknown), Sebastian Lettmaier, Clemens Neufert, Juliane Hoyer, Kerstin Wolff, Evgeny A. Moskalev, Robert Stöhr, Abbas Agaimy, André Reis, Bernd Wullich, Andréas Mackensen, Marianne Pavel, Matthias W. Beckmann, Arndt Hartmann, Rainer Fietkau, Norbert Meidenbauer, Florian Haller, Silvia Spoerl	3
3	Familial acute aortic dissection associated with a novel ACTA2 germline variant 2022 ·Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·Thomas Strecker, (unknown), Sabine Rudnik‐Schöneborn, Juliane Hoyer, André Reis, Michael Weyand, Abbas Agaimy	2
4	What’s a Biofilm?—How the Choice of the Biofilm Model Impacts the Protein Inventory of Clostridioides difficile 2021 ·Frontiers in Microbiology ·(unknown), Christian Lassek, Christian Hinze, Juliane Hoyer, Dörte Becher, Dieter Jahn, Susanne Sievers, Katharina Riedel	12
5	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
6	Central nervous system anomalies in two females with Borjeson-Forssman-Lehmann syndrome 2017 ·Epilepsy & Behavior ·Burkhard S. Kasper, Arnd Dörfler, Nataliya Di Donato, Ekkehard M. Kasper, Dagmar Wieczorek, Juliane Hoyer, Christiane Zweier	7
7	Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling 2015 ·The American Journal of Human Genetics ·Georgia Vasileiou, Arif B. Ekici, Steffen Uebe, Christiane Zweier, Juliane Hoyer, Hartmut Engels, Jürgen Behrens, André Reis, Michel V. Hadjihannas	64
8	Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome 2014 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Christiane Zweier, Olaf Rittinger, Ingrid Bader, Siren Berland, Trevor Cole, Franziska Degenhardt, Nataliya Di Donato, Luitgard Graul‐Neumann, Juliane Hoyer, Sally Ann Lynch, (unknown), Dagmar Wieczorek	20
9	De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females 2014 ·European Journal of Human Genetics ·Bernt Popp, Svein I. Støve, Sabine Endele, Line M. Myklebust, Juliane Hoyer, Heinrich Sticht, Silvia Azzarello‐Burri, Anita Rauch, Thomas Arnesen, André Reis	63
10	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
11	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
12	De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability 2013 ·The American Journal of Human Genetics ·Anne Gregor, Martin Oti, Evelyn N. Kouwenhoven, Juliane Hoyer, Heinrich Sticht, Arif B. Ekici, Susanne Kjærgaard, Anita Rauch, H.G. Stunnenberg, Steffen Uebe, Georgia Vasileiou, André Reis, Huiqing Zhou, Christiane Zweier	112
13	7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B) 2011 ·European Journal of Medical Genetics ·(unknown), Jutta Becker, Raoul Heller, Odile Boute, Joris Andrieux, Juliane Hoyer, Arif B. Ekici, André Reis, Anita Rauch	7
14	Primary diagnosis of Wolfram syndrome in an adult patient — Case report and description of a novel pathogenic mutation 2010 ·Journal of the Neurological Sciences ·Anne Waschbisch, Bastian Volbers, Tobias Struffert, Juliane Hoyer, Stefan Schwab, Juergen Bardutzky	14
15	SMARCAL1 Mutations: A Cause of Prepubertal Idiopathic Steroid-resistant Nephrotic Syndrome 2009 ·Pediatric Research ·Miroslav Živičnjak, Doris Franke, Martin Zenker, Juliane Hoyer, Thomas Lücke, Lars Pape, J. H. H. Ehrich	19
16	Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin‐4 gene mutation 2009 ·Clinical Genetics ·Juliane Hoyer, Cornelia Kraus, G. Hammersen, (unknown), Anita Rauch	40
17	A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients 2009 ·European Journal of Human Genetics ·Hartmut Engels, Eva Wohlleber, Alexander M. Zink, Juliane Hoyer, Kerstin U. Ludwig, Felix F. Brockschmidt, Dagmar Wieczorek, Ute Moog, (unknown), Ruthild G. Weber, Lionel Willatt, Martina Kreiß‐Nachtsheim, Helen V. Firth, Anita Rauch	68
18	A de novo 7.6 Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay 2008 ·European Journal of Medical Genetics ·Christian T. Thiel, Helmuth‐Günther Dörr, Udo Trautmann, Juliane Hoyer, (unknown), Cornelia Kraus, Arif B. Ekici, André Reis, Anita Rauch	15
19	Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome) 2007 ·The American Journal of Human Genetics ·Christiane Zweier, Maarit Peippo, Juliane Hoyer, Sérgio B. Sousa, Armand Bottani, Jill Clayton‐Smith, William Reardon, Jorge Saraiva, (unknown), (unknown), Koenraad Devriendt, Thomy de Ravel, Emilia K. Bijlsma, Raoul C. M. Hennekam, Alfredo Orrico, Monika Cohen, Alexander Dreweke, André Reis, (unknown), Anita Rauch	215
20	Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays 2007 ·Journal of Medical Genetics ·Juliane Hoyer, Alexander Dreweke, C. Becker, Isabel Göhring, Christian T. Thiel, Maarit Peippo, Rami Rauch, Michael Hofbeck, Udo Trautmann, Christiane Zweier, Martin Zenker, Ulrike Hüffmeier, Cornelia Kraus, Arif B. Ekici, Franz Rüschendorf, Peter Nürnberg, André Reis, Anita Rauch	56

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