Margit Schraders

2.8k total citations · 1 hit paper
32 papers, 1.5k citations indexed

About

Margit Schraders is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Margit Schraders has authored 32 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Sensory Systems, 17 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in Margit Schraders's work include Hearing, Cochlea, Tinnitus, Genetics (21 papers), Vestibular and auditory disorders (11 papers) and Connexins and lens biology (6 papers). Margit Schraders is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (21 papers), Vestibular and auditory disorders (11 papers) and Connexins and lens biology (6 papers). Margit Schraders collaborates with scholars based in Netherlands, Germany and United States. Margit Schraders's co-authors include Hannie Kremer, Henricus P. M. Kunst, Cor W. R. J. Cremers, Jaap Oostrik, Brandon G. Bentz, Jean‐Pierre Bayley, Jared Rutter, Peter Devilee, Oleh Khalimonchuk and Joshua D. Schiffman and has published in prestigious journals such as Science, Nature Communications and Blood.

In The Last Decade

Margit Schraders

32 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

SDH5 , a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma

2009 541 citations Huai‐Xiang Hao, Oleh Khalimonchuk et al. Science profile →

Peers

Margit Schraders

SURGE

NEURO

Hassan Chaı̈b United States

Chaim Jalas United States

Claudio Graziano Italy

Tiansheng Shen United States

Catherine B. Talmadge United States

Atsushi Shiga Japan

G. Lefèvre France

Laurence Delacroix Belgium

Véronique Paquis‐Flucklinger France

Tommaso Pippucci Italy

Hassan Chaı̈b United States

Margit Schraders

638 ×0.9

295 ×0.6

130 ×0.3

163 ×0.7

SURGE

94 ×0.4

NEURO

Citations per year, relative to Margit Schraders Margit Schraders (= 1×) peers Hassan Chaı̈b

Countries citing papers authored by Margit Schraders

Since Specialization

Citations

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

Fields of papers citing papers by Margit Schraders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Margit Schraders

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

All Works

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20 of 20 papers shown

Oostrik, Jaap, Andy J. Beynon, Sarina G. Kant, et al.. (2018). De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment. Human Genetics. 138(1). 61–72. 25 indexed citations

Avenarius, Matthew R., Charles Askew, Sherri M. Jones, et al.. (2018). Grxcr2 is required for stereocilia morphogenesis in the cochlea. PLoS ONE. 13(8). e0201713–e0201713. 11 indexed citations

Kamp, Jiddeke M. van de, Erik F. Hensen, Margit Schraders, et al.. (2017). Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment. Hearing Research. 347. 56–62. 14 indexed citations

Seco, Celia Zazo, Arnaud P. J. Giese, Margit Schraders, et al.. (2015). Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells. European Journal of Human Genetics. 24(4). 542–549. 22 indexed citations

Oonk, Anne M.M., P.L.M. Huygen, Margit Schraders, et al.. (2014). Similar Phenotypes Caused by Mutations in OTOG and OTOGL. Ear and Hearing. 35(3). e84–e91. 18 indexed citations

Huet, Ramon A. C. van, Jaap Oostrik, Hanka Venselaar, et al.. (2014). Nonsyndromic Hearing Loss Caused by USH1G Mutations. Ear and Hearing. 36(2). 205–211. 20 indexed citations

Siddiqi, Saima, Margit Schraders, Jaap Oostrik, et al.. (2014). Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families. PLoS ONE. 9(6). e100146–e100146. 53 indexed citations

Siddiqi, Saima, Muhammad Ismail, Jaap Oostrik, et al.. (2014). A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family. Journal of Human Genetics. 59(12). 683–686. 4 indexed citations

Seco, Celia Zazo, Anne M.M. Oonk, Jos Draaisma, et al.. (2014). Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5. European Journal of Human Genetics. 23(2). 189–194. 41 indexed citations

10.

Siddiqi, Saima, Atika Mansoor, Jaap Oostrik, et al.. (2013). Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome. Journal of Human Genetics. 58(12). 819–821. 15 indexed citations

11.

Huygen, P.L.M., et al.. (2011). Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family. Hearing Research. 282(1-2). 167–177. 12 indexed citations

12.

Lelli, Andrea, Margit Schraders, Kausik K. Ray, et al.. (2011). Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human. Nature Communications. 2(1). 201–201. 78 indexed citations

13.

Schraders, Margit, P.L.M. Huygen, Lies H. Hoefsloot, et al.. (2011). Audiometric characteristics of a Dutch family with Muckle-Wells syndrome. Hearing Research. 282(1-2). 243–251. 8 indexed citations

14.

Schraders, Margit, Jaap Oostrik, P.L.M. Huygen, et al.. (2011). Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations. Journal of the Association for Research in Otolaryngology. 12(6). 753–766. 67 indexed citations

15.

Schraders, Margit, Kwanghyuk Lee, Jaap Oostrik, et al.. (2010). Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment. The American Journal of Human Genetics. 86(2). 138–147. 50 indexed citations

16.

Collin, Rob W.J., P.L.M. Huygen, Margit Schraders, et al.. (2010). Progressive Sensorineural Hearing Loss and Normal Vestibular Function in a Dutch DFNB7/11 Family with a Novel Mutation in <i>TMC1</i>. Audiology and Neurotology. 16(2). 93–105. 34 indexed citations

17.

Schraders, Margit, Jaap Oostrik, P.L.M. Huygen, et al.. (2010). Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction. The American Journal of Human Genetics. 86(4). 604–610. 62 indexed citations

18.

Hao, Huai‐Xiang, Oleh Khalimonchuk, Margit Schraders, et al.. (2009). SDH5 , a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma. Science. 325(5944). 1139–1142. 541 indexed citations breakdown →

19.

Schraders, Margit, Simon V. van Reijmersdal, Eveline J. Kamping, et al.. (2009). High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage. Cancer Genetics and Cytogenetics. 191(1). 27–33. 23 indexed citations

20.

Schraders, Margit, Pedro Jares, Sı́lvia Beà, et al.. (2008). Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene‐dosage regulated candidate genes. British Journal of Haematology. 143(2). 210–221. 21 indexed citations

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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