Margit Schraders

2.8k citations

32 papers · 1.5k indexed · 1 hit paper · h-index 20

Co-authors: Hannie Kremer Henricus P. M. Kunst Cor W. R. J. Cremers Jaap Oostrik Brandon G. Bentz Jean‐Pierre Bayley Jared Rutter Peter Devilee
Topics: Hearing, Cochlea, Tinnitus, Genetics (21 papers)Vestibular and auditory disorders (11 papers)Connexins and lens biology (6 papers)
Cited by: Sensory Systems Otorhinolaryngology Neurology
Journals: Science Nature Communications Blood
Partner nations: Netherlands Germany United States

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

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

#	Work	Indexed citations
1	De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment 2018 ·Human Genetics ·(unknown),Jaap Oostrik,Andy J. Beynon,Sarina G. Kant,(unknown),Liselotte J. C. Rotteveel,Jolien S. Klein Wassink‐Ruiter,Rolien H. Free,Saskia M. Maas,Jiddeke van de Kamp,Paul Merkus,Wouter Koole,Ilse Feenstra,R.J.C. Admiraal,Cris Lanting,Margit Schraders,Helger G. Yntema,Ronald J. E. Pennings,Hannie Kremer	25
2	Grxcr2 is required for stereocilia morphogenesis in the cochlea 2018 ·PLoS ONE ·Matthew R. Avenarius,(unknown),Charles Askew,Sherri M. Jones,Kristina L. Hunker,Héla Azaiez,Atteeq U. Rehman,Margit Schraders,Hossein Najmabadi,Hannie Kremer,Richard J. Smith,Gwenaëlle S. G. Géléoc,David F. Dolan,Yehoash Raphael,David C. Kohrman	11
3	Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment 2017 ·Hearing Research ·(unknown),Jiddeke M. van de Kamp,Erik F. Hensen,Margit Schraders,Jaap Oostrik,Helger G. Yntema,Ilse Feenstra,R.J.C. Admiraal,Henricus P. M. Kunst,Mustafa Tekin,Moien Kanaan,Hannie Kremer,Ronald J. E. Pennings	14
4	Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells 2015 ·European Journal of Human Genetics ·Celia Zazo Seco,Arnaud P. J. Giese,(unknown),Margit Schraders,Anne M.M. Oonk,(unknown),Jaap Oostrik,Tim M. Strom,Rashmi S. Hegde,Erwin van Wijk,Gregory I. Frolenkov,Maleeha Azam,Helger G. Yntema,Rolien H. Free,Saima Riazuddin,Joanne Verheij,R.J.C. Admiraal,Raheel Qamar,Zubair M. Ahmed,Hannie Kremer	22
5	Similar Phenotypes Caused by Mutations in OTOG and OTOGL 2014 ·Ear and Hearing ·Anne M.M. Oonk,(unknown),P.L.M. Huygen,Margit Schraders,Miguel Del Campo,Ignacio del Castillo,Mustafa Tekin,Ilse Feenstra,Andy J. Beynon,Henricus P. M. Kunst,A.F.M. Snik,Hannie Kremer,R.J.C. Admiraal,Ronald J. E. Pennings	18
6	Nonsyndromic Hearing Loss Caused by USH1G Mutations 2014 ·Ear and Hearing ·(unknown),Ramon A. C. van Huet,(unknown),Jaap Oostrik,Hanka Venselaar,Erwin van Wijk,Andy J. Beynon,Henricus P. M. Kunst,Carel B. Hoyng,Hannie Kremer,Margit Schraders,Ronald J. E. Pennings	20
7	Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families 2014 ·PLoS ONE ·(unknown),Saima Siddiqi,Margit Schraders,Jaap Oostrik,Humaira Ayub,(unknown),Muhammad Ajmal,(unknown),Tim M. Strom,Atika Mansoor,Kehkashan Mazhar,Syed Tahir Abbas Shah,Alamdar Hussain,Maleeha Azam,Hannie Kremer,Raheel Qamar	53
8	A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani family 2014 ·Journal of Human Genetics ·Saima Siddiqi,Muhammad Ismail,Jaap Oostrik,(unknown),Atika Mansoor,Hannie Kremer,Raheel Qamar,Margit Schraders	4
9	Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5 2014 ·European Journal of Human Genetics ·Celia Zazo Seco,Anne M.M. Oonk,(unknown),Jos Draaisma,Marta Gandía,Jaap Oostrik,Kornelia Neveling,Henricus P. M. Kunst,Lies H. Hoefsloot,Ignacio del Castillo,Ronald J. E. Pennings,Hannie Kremer,R.J.C. Admiraal,Margit Schraders	41
10	Novel mutation in AAA domain of BCS1L causing Bjornstad syndrome 2013 ·Journal of Human Genetics ·Saima Siddiqi,(unknown),Atika Mansoor,Jaap Oostrik,Nafees Ahmad,(unknown),Hannie Kremer,Raheel Qamar,Margit Schraders	15
11	Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family 2011 ·Hearing Research ·(unknown),P.L.M. Huygen,Margit Schraders,Hannie Kremer,Ronald J. E. Pennings,(unknown)	12
12	Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human 2011 ·Nature Communications ·(unknown),Andrea Lelli,Margit Schraders,Kausik K. Ray,Michael S. Hildebrand,Arabandi Ramesh,C. R. Srikumari Srisailapathy,Jaap Oostrik,R.J.C. Admiraal,Harold R. Neely,Joseph R. Latoche,Richard J. Smith,John K. Northup,Hannie Kremer,Jeffrey R. Holt,Konrad Noben‐Trauth	78
13	Audiometric characteristics of a Dutch family with Muckle-Wells syndrome 2011 ·Hearing Research ·(unknown),Margit Schraders,(unknown),(unknown),P.L.M. Huygen,Lies H. Hoefsloot,Jaap Oostrik,Ronald J. E. Pennings,Anna Simon,(unknown),Hannie Kremer,Henricus P. M. Kunst	8
14	Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations 2011 ·Journal of the Association for Research in Otolaryngology ·(unknown),Margit Schraders,Jaap Oostrik,P.L.M. Huygen,Tim M. Strom,(unknown),Ronald J. E. Pennings,Hanka Venselaar,Lies H. Hoefsloot,Mariet Elting,Cor W. R. J. Cremers,R.J.C. Admiraal,Hannie Kremer,Henricus P. M. Kunst	67
15	Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment 2010 ·The American Journal of Human Genetics ·Margit Schraders,Kwanghyuk Lee,Jaap Oostrik,P.L.M. Huygen,Ghazanfar Ali,Lies H. Hoefsloot,Joris A. Veltman,Frans P.M. Cremers,Sulman Basit,Muhammad Ansar,Cor W. R. J. Cremers,Henricus P. M. Kunst,Wasim Ahmad,R.J.C. Admiraal,Suzanne M. Leal,Hannie Kremer	50
16	Progressive Sensorineural Hearing Loss and Normal Vestibular Function in a Dutch DFNB7/11 Family with a Novel Mutation in <i>TMC1</i> 2010 ·Audiology and Neurotology ·(unknown),Rob W.J. Collin,P.L.M. Huygen,Margit Schraders,Jaap Oostrik,(unknown),Henricus P. M. Kunst,Hannie Kremer,Cor W. R. J. Cremers	34
17	Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction 2010 ·The American Journal of Human Genetics ·Margit Schraders,Jaap Oostrik,P.L.M. Huygen,Tim M. Strom,Erwin van Wijk,Henricus P. M. Kunst,Lies H. Hoefsloot,Cor W. R. J. Cremers,R.J.C. Admiraal,Hannie Kremer	62
18	SDH5 , a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paragangliomabreakdown → 2009 ·Science ·Huai‐Xiang Hao,Oleh Khalimonchuk,Margit Schraders,Noah Dephoure,Jean‐Pierre Bayley,Henricus P. M. Kunst,Peter Devilee,Cor W. R. J. Cremers,Joshua D. Schiffman,Brandon G. Bentz,Steven P. Gygi,Dennis R. Winge,Hannie Kremer,Jared Rutter	541
19	High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineage 2009 ·Cancer Genetics and Cytogenetics ·Margit Schraders,Simon V. van Reijmersdal,Eveline J. Kamping,J. Han van Krieken,Ad Geurts van Kessel,Patricia J.T.A. Groenen,Peter M. Hoogerbrugge,Roland P. Kuiper	23
20	Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene‐dosage regulated candidate genes 2008 ·British Journal of Haematology ·Margit Schraders,Pedro Jares,Sı́lvia Beà,Eric Schoenmakers,J. Han van Krieken,Elı́as Campo,Patricia J.T.A. Groenen	21

About Margit Schraders

Margit Schraders is a scholar working on Sensory Systems, Neurology and Otorhinolaryngology, having authored 32 papers that have together received 1.5k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (21 papers), Vestibular and auditory disorders (11 papers) and Connexins and lens biology (6 papers). The work is most often cited by research in Sensory Systems (528 citations), Otorhinolaryngology (151 citations) and Neurology (213 citations). Margit Schraders has collaborated with scholars based in Netherlands, Germany and United States. Frequent 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. Their work appears in journals such as Science, Nature Communications and Blood.

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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