Juliane Hoyer

5.7k citations

43 papers · 1.9k indexed · h-index 21

Genetics top 2%
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 10
- BRCA gene mutations in cancer 8
- Genomics and Rare Diseases 6
Molecular Biology top 10%
- Congenital heart defects research 7
- Chromatin Remodeling and Cancer 6
Cancer Research
- Cancer Genomics and Diagnostics 4
Developmental Neuroscience top 10%
Pathology and Forensic Medicine top 10%
- Genetic factors in colorectal cancer 4

Co-authors: André Reis Anita Rauch Christiane Zweier Cornelia Kraus Arif B. Ekici Christian T. Thiel Martin Zenker Ulrike Hüffmeier
Cited by: Genetics Molecular Biology Cancer Research
Journals: The American Journal of Human Genetics (4 papers)International Journal of Cancer (1 paper)Frontiers in Microbiology (1 paper)
Partner nations: Germany Switzerland United States

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

The 25 scholars most cited alongside Juliane Hoyer, 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 Juliane Hoyer Line = papers co-authored together Juliane Hoyer 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	Ex Vivo Chromosomal Radiosensitivity Testing in Patients with Pathological Germline Variants in Breast Cancer High-Susceptibility Genes BReast CAncer 1 and BReast CAncer 2 Current Issues in Molecular Biology ·T. Zuhair Kassem,Marius Wunderle,Lukas Kuhlmann,Matthias Ruebner,Hanna Huebner,Juliane Hoyer,André Reis,Peter A. Fasching,Matthias W. Beckmann,Carolin C. Hack,Rainer Fietkau,Luitpold Distel	2023	2
2	Determinants Affecting the Clinical Implementation of a Molecularly Informed Molecular Tumor Board Recommendation: Experience from a Tertiary Cancer Center Cancers ·Lars Tögel,Christoph Schubart,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	2023	3
3	Familial acute aortic dissection associated with a novel ACTA2 germline variant Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin ·Thomas Strecker,Felix Wiesmueller,Sabine Rudnik‐Schöneborn,Juliane Hoyer,André Reis,Michael Weyand,Abbas Agaimy	2022	2
4	What’s a Biofilm?—How the Choice of the Biofilm Model Impacts the Protein Inventory of Clostridioides difficile Frontiers in Microbiology ·Madita Brauer,Christian Lassek,Christian Hinze,Juliane Hoyer,Dörte Becher,Dieter Jahn,Susanne Sievers,Katharina Riedel	2021	12
5	Exome Pool-Seq in neurodevelopmental disorders European Journal of Human Genetics ·Bernt Popp,Arif B. Ekici,Christian T. Thiel,Juliane Hoyer,Antje Wiesener,Cornelia Kraus,André Reis,Christiane Zweier	2017	59
6	Central nervous system anomalies in two females with Borjeson-Forssman-Lehmann syndrome Epilepsy & Behavior ·Burkhard S. Kasper,Arnd Dörfler,Nataliya Di Donato,Ekkehard M. Kasper,Dagmar Wieczorek,Juliane Hoyer,Christiane Zweier	2017	7
7	Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling 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	2015	64
8	Females with de novo aberrations in PHF6: Clinical overlap of Borjeson–Forssman–Lehmann with Coffin–Siris syndrome 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,Ingrid Vlasak,Dagmar Wieczorek	2014	20
9	De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females 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	2014	63
10	Biallelic SEMA3A defects cause a novel type of syndromic short stature American Journal of Medical Genetics Part A ·Kristin Hofmann,Markus Zweier,Heinrich Sticht,Christiane Zweier,Wolfgang Wittmann,Juliane Hoyer,Steffen Uebe,Arie van Haeringen,Christian T. Thiel,Arif B. Ekici,André Reis,Anita Rauch	2013	9
11	A new face of Borjeson–Forssman–Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype 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	2013	32
12	De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability 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	2013	112
13	7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B) European Journal of Medical Genetics ·Kristin Hofmann,Jutta Becker,Raoul Heller,Odile Boute,Joris Andrieux,Juliane Hoyer,Arif B. Ekici,André Reis,Anita Rauch	2011	7
14	Primary diagnosis of Wolfram syndrome in an adult patient — Case report and description of a novel pathogenic mutation Journal of the Neurological Sciences ·Anne Waschbisch,Bastian Volbers,Tobias Struffert,Juliane Hoyer,Stefan Schwab,Juergen Bardutzky	2010	14
15	SMARCAL1 Mutations: A Cause of Prepubertal Idiopathic Steroid-resistant Nephrotic Syndrome Pediatric Research ·Miroslav Živičnjak,Doris Franke,Martin Zenker,Juliane Hoyer,Thomas Lücke,Lars Pape,J. H. H. Ehrich	2009	19
16	Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin‐4 gene mutation Clinical Genetics ·Juliane Hoyer,Cornelia Kraus,G. Hammersen,J‐P Geppert,Anita Rauch	2009	40
17	A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients European Journal of Human Genetics ·Hartmut Engels,Eva Wohlleber,Alexander M. Zink,Juliane Hoyer,Kerstin U. Ludwig,Felix F. Brockschmidt,Dagmar Wieczorek,Ute Moog,Birgit Hellmann-Mersch,Ruthild G. Weber,Lionel Willatt,Martina Kreiß‐Nachtsheim,Helen V. Firth,Anita Rauch	2009	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 European Journal of Medical Genetics ·Christian T. Thiel,Helmuth‐Günther Dörr,Udo Trautmann,Juliane Hoyer,Kristin Hofmann,Cornelia Kraus,Arif B. Ekici,André Reis,Anita Rauch	2008	15
19	Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome) The American Journal of Human Genetics ·Christiane Zweier,Maarit Peippo,Juliane Hoyer,Sérgio B. Sousa,Armand Bottani,Jill Clayton‐Smith,William Reardon,Jorge Saraiva,Alexandra Cabral,Ina Göhring,Koenraad Devriendt,Thomy de Ravel,Emilia K. Bijlsma,Raoul C. M. Hennekam,Alfredo Orrico,Monika Cohen,Alexander Dreweke,André Reis,Peter Nürnberg,Anita Rauch	2007	215
20	Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays 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	2007	56

About Juliane Hoyer

Juliane Hoyer is a scholar working on Genetics, Cancer Research and Molecular Biology, having authored 43 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (10 papers), BRCA gene mutations in cancer (8 papers), Congenital heart defects research (7 papers), Genomics and Rare Diseases (6 papers), Chromatin Remodeling and Cancer (6 papers), Cancer Genomics and Diagnostics (4 papers) and Genetic factors in colorectal cancer (4 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (1.1k citations) and Cancer Research (151 citations). Juliane Hoyer has collaborated with scholars based in Germany, Switzerland and United States. Frequent 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. Their work appears in journals such as The American Journal of Human Genetics, International Journal of Cancer and Frontiers in Microbiology.

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