Ina Schanze

1.3k citations

19 papers · 295 indexed · h-index 11

Co-authors: Martin Zenker André Reis Denny Schanze Christiane Zweier Sabine Endele Juliane Hoyer Anita Rauch Bronwyn Kerr
Topics: Genetics and Neurodevelopmental Disorders (4 papers)Genomic variations and chromosomal abnormalities (3 papers)RNA regulation and disease (2 papers)
Cited by: Genetics Clinical Biochemistry Molecular Biology
Journals: Human Molecular Genetics Human Mutation Frontiers in Endocrinology
Partner nations: Germany Netherlands United Kingdom

In The Last Decade

Ina Schanze

18 papers receiving 291 citations

Peers

Countries citing papers authored by Ina Schanze

Since Specialization

Citations

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

Fields of papers citing papers by Ina Schanze

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ina Schanze

This figure shows the co-authorship network connecting the top 25 collaborators of Ina Schanze. A scholar is included among the top collaborators of Ina Schanze 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 Ina Schanze. Ina Schanze is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Intrafamilial phenotypic variability in autosomal recessive DOCK6-related Adams-Oliver syndrome 2022 ·European Journal of Medical Genetics ·Luz Consuelo Zepeda‐Romero,Martin Zenker,Denny Schanze,Ina Schanze,(unknown),(unknown),(unknown),(unknown),(unknown),Lucina Bobadilla‐Morales,Alfredo Corona‐Rivera,Jorge Román Corona‐Rivera	4
2	Integration of genomic analysis and transcript expression of ABCC8 and KCNJ11 in focal form of congenital hyperinsulinism 2022 ·Frontiers in Endocrinology ·Ilse Wieland,Ina Schanze,(unknown),Winfried Barthlen,Silke Vogelgesang,Klaus Mohnike,Martin Zenker	6
3	Correlation of PET-MRI, Pathology, LOH, and Surgical Success in a Case of CHI With Atypical Large Pancreatic Focus 2022 ·Journal of the Endocrine Society ·(unknown),Konrad Mohnike,Klaus Mohnike,Katharina Warncke,(unknown),Martin Zenker,Ilse Wieland,Ina Schanze,Julia Hoefele,Christine Förster,Winfried Barthlen,(unknown),(unknown)	1
4	Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation 2020 ·Human Mutation ·Simone Martinelli,Luca Pannone,Christina Lißewski,Julia Brinkmann,Elisabetta Flex,Denny Schanze,Paolo Calligari,Massimiliano Anselmi,Francesca Pantaleoni,(unknown),Francesca Clementina Radio,Adonis S. Ioannides,Nils Rahner,Ina Schanze,Dragana Josifova,Gianfranco Bocchinfuso,Mina Ryten,Lorenzo Stella,Marco Tartaglia,Martin Zenker	1
5	Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower Leg 2020 ·Anticancer Research ·Reinhard E. Friedrich,Christian Hagel,(unknown),Ina Schanze,Ilse Wieland,Martin Zenker	3
6	Variants in nuclear factor I genes influence growth and development 2019 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Martin Zenker,Jens Bunt,Ina Schanze,Denny Schanze,Michael Piper,Manuela Priolo,Erica H. Gerkes,Richard M. Gronostajski,Linda J. Richards,Julie Vogt,Marja W. Wessels,Raoul C. M. Hennekam	32
7	A 2q24.2 microdeletion containing TANK as novel candidate gene for intellectual disability 2019 ·American Journal of Medical Genetics Part A ·Ante Karoglan,Denny Schanze,(unknown),Petra Muschke,Martin Zenker,Ina Schanze	0
8	Sema3a plays a role in the pathogenesis of CHARGE syndrome 2018 ·Human Molecular Genetics ·Roser Ufartes,(unknown),(unknown),Christiane Neuhofer,Janika Möller,Peter Wehner,Conny M.A. van Ravenswaaij‐Arts,(unknown),Ina Schanze,Andreas Tzschach,Oliver Bartsch,Annette Borchers,Silke Pauli	20
9	Multicentre approach to epidemiological aspects of craniosynostosis in Germany 2018 ·British Journal of Oral and Maxillofacial Surgery ·(unknown),(unknown),Alexander W. Eckert,Raimund Firsching,(unknown),(unknown),Michael Haase,Gerhard Jorch,(unknown),Siegfried Kropf,(unknown),Ina Schanze,(unknown),Anke Rißmann	15
10	Expanding the mutational spectrum in Johanson‐Blizzard syndrome: identification of whole exon deletions and duplications in theUBR1gene by multiplex ligation‐dependent probe amplification analysis 2017 ·Molecular Genetics & Genomic Medicine ·Maja Sukalo,(unknown),Ina Schanze,David B. Everman,Nima Rezaei,Jesús Argente,Isabel Lorda‐Sánchez,Charu Deshpande,Tsutomu Takahashi,Alexander Kleger,Martin Zenker	7
11	Copy number variants including RAS pathway genes—How much RASopathy is in the phenotype? 2015 ·American Journal of Medical Genetics Part A ·Christina Lißewski,Sarina G. Kant,Zornitza Stark,Ina Schanze,Martin Zenker	12
12	Loss-of-function variants in HIVEP2 are a cause of intellectual disability 2015 ·European Journal of Human Genetics ·Siddharth Srivastava,Hartmut Engels,Ina Schanze,Kirsten Cremer,Thomas Wieland,Moritz Menzel,Max Schubach,Saskia Biskup,Martina Kreiß,Sabine Endele,Tim M. Strom,Dagmar Wieczorek,Martin Zenker,Siddharth Gupta,Julie S. Cohen,Alexander M. Zink,Sakkubai Naidu	31
13	Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors 2015 ·Molecular Syndromology ·Ron Hochstenbach,Beata Nowakowska,Marianne Volleth,(unknown),Anna Kutkowska‐Kaźmierczak,Ewa Obersztyn,(unknown),(unknown),Denny Schanze,Martin Zenker,Petra Muschke,Ina Schanze,Martin Poot,Thomas Liehr	10
14	HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disorders 2014 ·American Journal of Medical Genetics Part A ·Miriam S. Reuter,Jörn Oliver Sass,Thomas Leis,(unknown),Johannes A. Mayr,René G. Feichtinger,Manfred Rauh,Ina Schanze,(unknown),Regina Trollmann,Steffen Uebe,Arif B. Ekici,André Reis	28
15	AlteredGPM6A/M6Dosage Impairs Cognition and Causes Phenotypes Responsive to Cholesterol in Human andDrosophila 2014 ·Human Mutation ·Anne Gregor,Jamie M. Kramer,Monique van der Voet,Ina Schanze,Steffen Uebe,Rogier Donders,André Reis,Annette Schenck,Christiane Zweier	24
16	Deletions in the 3′ Part of theNFIXGene Including a Recurrent Alu-Mediated Deletion of Exon 6 and 7 Account for Previously Unexplained Cases of Marshall-Smith Syndrome 2014 ·Human Mutation ·Denny Schanze,(unknown),Valérie Cormier‐Daire,Marie-Ange Delrue,Anne Dieux‐Coëslier,Tomonobu Hasegawa,Eva Holmberg,Rainer Koenig,(unknown),Ina Schanze,E Seemanová,Adam Shaw,Julie Vogt,Marianne Volleth,André Reis,Peter Meinecke,Raoul C. M. Hennekam,Martin Zenker	23
17	Evaluation of Chromosome 11p Imbalances in Aniridia and Wilms Tumor Patients 2013 ·American Journal of Medical Genetics Part A ·Maike Busch,Barbara Leube,Anne Thiel,Ina Schanze,Manfred Beier,Brigitte Royer‐Pokora	2
18	Haploinsufficiency of SOX5, a member of the SOX (SRY-related HMG-box) family of transcription factors is a cause of intellectual disability 2012 ·European Journal of Medical Genetics ·Ina Schanze,Denny Schanze,Carlos A. Bacino,Sofia Douzgou,Bronwyn Kerr,Martin Zenker	31
19	In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of <b><i>SMARCA2</i></b> in Three Patients with Nicolaides-Baraitser Syndrome 2011 ·Molecular Syndromology ·(unknown),Sabine Endele,Silvia Azzarello‐Burri,Juliane Hoyer,Markus Zweier,Ina Schanze,Bernhard Schmitt,Anita Rauch,André Reis,Christiane Zweier	45

About Ina Schanze

Ina Schanze is a scholar working on Genetics, Molecular Biology and Virology, having authored 19 papers that have together received 295 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Genetics (146 citations), Clinical Biochemistry (21 citations) and Molecular Biology (201 citations). Ina Schanze has collaborated with scholars based in Germany, Netherlands and United Kingdom. Frequent co-authors include Martin Zenker, André Reis, Denny Schanze, Christiane Zweier, Sabine Endele, Juliane Hoyer, Anita Rauch, Bronwyn Kerr, Carlos A. Bacino and Silvia Azzarello‐Burri. Their work appears in journals such as Human Molecular Genetics, Human Mutation and Frontiers in Endocrinology.

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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