Nina Ishorst

583 total citations
8 papers, 115 citations indexed

About

Nina Ishorst is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Nina Ishorst has authored 8 papers receiving a total of 115 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Surgery. Recurrent topics in Nina Ishorst's work include Cleft Lip and Palate Research (5 papers), Craniofacial Disorders and Treatments (4 papers) and RNA modifications and cancer (2 papers). Nina Ishorst is often cited by papers focused on Cleft Lip and Palate Research (5 papers), Craniofacial Disorders and Treatments (4 papers) and RNA modifications and cancer (2 papers). Nina Ishorst collaborates with scholars based in Germany, Spain and Poland. Nina Ishorst's co-authors include Kerstin U. Ludwig, Michael Knapp, Álvaro Rada-Iglesias, Elisabeth Mangold, Augusto Rojas-Martı́nez, Miloš Nikolić, Khalid Aldhorae, Markus M. Nöthen, Nigel L. Hammond and Michael J. Dixon and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Journal of Dental Research.

In The Last Decade

Nina Ishorst

7 papers receiving 115 citations

Peers

Countries citing papers authored by Nina Ishorst

Since Specialization

Citations

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

Fields of papers citing papers by Nina Ishorst

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nina Ishorst

This figure shows the co-authorship network connecting the top 25 collaborators of Nina Ishorst. A scholar is included among the top collaborators of Nina Ishorst 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 Nina Ishorst. Nina Ishorst 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:

8 of 8 papers shown

#	Work	Indexed citations
1	Wie ist die Weiterbildungssituation der NaturwissenschaftlerInnen in der Humangenetik in Deutschland, und wie erreichen wir eine staatliche Anerkennung der Weiterbildung zur/zum FachhumangenetikerIn? 2023 ·Medizinische Genetik ·Yvonne Lisa Behrens, (unknown), Nina Ishorst, (unknown), Lisa Sindermann	0
2	Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations 2022 ·Human Genetics and Genomics Advances ·(unknown), Leonie Weinhold, Axel Schmidt, Manuel Holtgrewe, Stefan Juranek, (unknown), (unknown), (unknown), Elisabeth Mangold, Nina Ishorst, (unknown), (unknown), Dieter Beule, Katrin Paeschke, Peter Krawitz, Kerstin U. Ludwig	2
3	Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate 2021 ·SHILAP Revista de lepidopterología ·(unknown), Nigel L. Hammond, Miloš Nikolić, (unknown), Nina Ishorst, Elizabeth J. Leslie, Seth M. Weinberg, Terri H. Beaty, Mary L. Marazita, Elisabeth Mangold, Michael Knapp, Justin Cotney, Álvaro Rada-Iglesias, Michael J. Dixon, Kerstin U. Ludwig	13
4	MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration 2021 ·Journal of Dental Research ·(unknown), (unknown), Magdalena Laugsch, Lara M. Hochfeld, (unknown), Julia Schröder, (unknown), Nina Ishorst, (unknown), Leonie Weinhold, Timo Hess, Jan Gehlen, Adrianna Mostowska, Stefanie Heilmann‐Heimbach, Elisabeth Mangold, Álvaro Rada-Iglesias, Michael Knapp, Christian P. Schaaf, Kerstin U. Ludwig	9
5	Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene 2019 ·Genes ·Iris A.L.M. van Rooij, Kerstin U. Ludwig, (unknown), Nina Ishorst, (unknown), Tessel E. Galesloot, Edwin M. Ongkosuwito, Stefaan Bergé, Khalid Aldhorae, Augusto Rojas-Martı́nez, Lambertus A. Kiemeney, Joris Vermeesch, Han G. Brunner, Nel Roeleveld, Koenraad Devriendt, Titiaan Dormaar, Greet Hens, Michael Knapp, Carine Carels, Elisabeth Mangold	13
6	Imputation of Orofacial Clefting Data Identifies Novel Risk Loci and Sheds Light on the Genetic Background of Cleft Lip ± Cleft Palate and Cleft Palate Only. 2017 ·Human Molecular Genetics ·Kerstin U. Ludwig, Anne C. Böhmer, John Bowes, Miloš Nikolić, Nina Ishorst, (unknown), Nigel L. Hammond, Lina Gölz, (unknown), Sandra Barth, (unknown), (unknown), Malte Spielmann, Khalid Aldhorae, Augusto Rojas-Martı́nez, Markus M. Nöthen, Álvaro Rada-Iglesias, Michael J. Dixon, Michael Knapp, Elisabeth Mangold	66
7	Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse‐Sakati Syndrome: Report of a Family with Mutation in the C2orf37 Gene 2013 ·Pediatric Dermatology ·Arti Nanda, Sandra M. Pasternack, (unknown), Nina Ishorst, Ramón Grimalt, Regina C. Betz	10
8	Functional analysis of splice site mutations in the human hairless (HR) gene using a minigene assay 2011 ·British Journal of Dermatology ·(unknown), Sandra M. Pasternack, Britta Fiebig, (unknown), Nina Ishorst, Michael Ludwig, Markus M. Nöthen, Marieke M.B. Seyger, Ben C.J. Hamel, Regina C. Betz	2

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