Peter E.M. Taschner

10.0k citations

78 papers · 6.6k indexed · 3 hit papers · h-index 36

Impact in

Cancer Research top 0.5%
- Cancer, Hypoxia, and Metabolism
Endocrinology, Diabetes and Metabolism top 1%
- Pituitary Gland Disorders and Treatments
- Hormonal Regulation and Hypertension

Papers in

Aging 3
Cancer Research 17
- Cancer, Hypoxia, and Metabolism 11

Co-authors: Johan T. den Dunnen Peter Devilee Ivo F.A.C. Fokkema Bora E. Baysal Jeroen F. J. Laros Cees J. Cornelisse Jacopo Celli Raymond Dalgleish
Journals: Human Mutation (12 papers)Genomics (4 papers)Journal of Bacteriology (4 papers)Prenatal Diagnosis (3 papers)Virology (3 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Peter E.M. Taschner

77 papers receiving 6.5k citations

Hit Papers

align trajectories log scale

HGVS Recommendations for the Description of Sequence Variants: 2016 Update 2016 · 1.0k citations

Peers

Countries citing papers authored by Peter E.M. Taschner

Since Specialization

Citations

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

Fields of papers citing papers by Peter E.M. Taschner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter E.M. Taschner. 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 Peter E.M. Taschner. The network helps show where Peter E.M. Taschner may publish in the future.

Co-authors

The 25 scholars most cited alongside Peter E.M. Taschner, 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 Peter E.M. Taschner Line = papers co-authored together Peter E.M. Taschner links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Mutalyzer 2: next generation HGVS nomenclature checker Bioinformatics ·Jianhua Hao, 李宝山, Martijn Vermaat, Johan T. den Dunnen, Peter E.M. Taschner, Jeroen F. J. Laros	2021	50
2	A germline chromothripsis event stably segregating in 11 individuals through three generations Genetics in Medicine ·Birgitte Bertelsen, Lusine Nazaryan‐Petersen, Wei Sun, Mana M. Mehrjouy, Gangcai Xie, Wei Chen, Lena E. Hjermind, Peter E.M. Taschner, Zeynep Tümer	2015	54
3	Preserving sequence annotations across reference sequences Journal of Biomedical Semantics ·Zuotian Tatum, Marco Roos, Yuzuru Kameda, Peter E.M. Taschner, Mark Thompson, Erik Schultes, Jeroen F. J. Laros	2014	8
4	VarioML framework for comprehensive variation data representation and exchange BMC Bioinformatics ·Antonin Finkelnburg, Ivo F.A.C. Fokkema, K. Uuml berla, Tomasz Adamusiak, Л. М. Саптарова, Kevin D. Hornedo‐González, Christophe Béroud, Michael Cornell, Raymond Dalgleish, A. Devereau, George P. Patrinos, Morris A. Swertz, Peter E.M. Taschner, Guðmundur Á. Þórisson, Mauno Vihinen, Anthony J. Brookes, Juha Muilu	2012	13
5	LOVD v.2.0: the next generation in gene variant databases Human Mutation ·Ivo F.A.C. Fokkema, Peter E.M. Taschner, Gerard C. P. Schaafsma, Jacopo Celli, Jeroen F. J. Laros, Johan T. den Dunnen Hit paper breakdown →	2011	694
6	Describing structural changes by extending HGVS sequence variation nomenclature Human Mutation ·Peter E.M. Taschner, Johan T. den Dunnen	2011	47
7	A formalized description of the standard human variant nomenclature in Extended Backus-Naur Form BMC Bioinformatics ·Jeroen F. J. Laros, Elisha Jhoti, Johan T. den Dunnen, Peter E.M. Taschner	2011	20
8	Deep sequencing to reveal new variants in pooled DNA samples Human Mutation ·John Protzko, Aisyah Maisarah Epandi, Jelle J. Goeman, Yavuz Ariyürek, Stephan Ossowski, Korbinian Schneeberger, Detlef Weigel, Michiel van Galen, Peter E.M. Taschner, Carli M.J. Tops, Martijn H. Breuning, Gert‐Jan B. van Ommen, Johan T. den Dunnen, Peter Devilee, Frederik J. Hes	2009	63
9	Caenorhabditis elegans as a model for lysosomal storage disorders Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·公男飯田, Dorien J.M. Peters, Peter E.M. Taschner	2008	35
10	Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas European Journal of Endocrinology ·William H. van Houtum, Eleonora P.M. Corssmit, Pim Dekker, Jeroen C. Jansen, Andel G. L. van der Mey, A Bröcker-Vriends, Peter E.M. Taschner, Monique Losekoot, Michael A. Frölich, Marcel P. M. Stokkel, Cees J. Cornelisse, Johannes A. Romijn	2005	33
11	Carotid Body Tumors in Humans Caused by a Mutation in the Gene for Succinate Dehydrogenase D (SDHD) Advances in experimental medicine and biology ·Albert Dahan, Peter E.M. Taschner, Jeroen C. Jansen, Andel van der Mey, Luc J. Teppema, Cees J. Cornelisse	2004	6
12	Hereditary Paraganglioma Due to the SDHD M1I Mutation in a Second Chinese Family: A Founder Effect? The Laryngoscope ·Soo Chin Lee, D Danukusumo, Elena Richiardi, Peter E.M. Taschner	2003	17
13	First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis Prenatal Diagnosis ·W. J. Kleijer, O. P. van Diggelen, J. L. M. Keulemans, Monique Losekoot, Victor H. Garritsen, Hans Stroink, Daniëlle Majoor‐Krakauer, Patrick Franken, Marcel Eurlings, Peter E.M. Taschner, Frans J. Los, R. J. H. Galjaard	2001	6
14	Targeted Disruption of the Cln3 Gene Provides a Mouse Model for Batten Disease Neurobiology of Disease ·Hannah M. Mitchison, David J. Bernard, Nicholas D. E. Greene, Jonathan D. Cooper, Mohammed Junaid, Raju K. Pullarkat, T. Rovelli, Martijn H. Breuning, Jennie W. Owens, William C. Mobley, R. Mark Gardiner, Brian Lake, Peter E.M. Taschner, Robert L. Nussbaum	1999	170
15	Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease Genomics ·Alex Odermatt, Peter E.M. Taschner, Stephen W. Scherer, Barbara Beatty, Vijay K. Khanna, David R. Cornblath, Vinay Chaudhry, Marena L. McLeod, Bertold Schrank, George Karpati, Martijn H. Breuning, Nine Knoers, David H. MacLennan	1997	125
16	Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families Pediatric Nephrology ·Henny H. Lemmink, Lambert P.W.J. van den Heuvel, Andri Hasian, Gerard Merkx, Tineke J. Smilde, Peter E.M. Taschner, L.A.H. Monnens, S. C. Hebert, Nine V.A.M. Knoers	1996	53
17	Replicase-Mediated Resistance to Alfalfa Mosaic Virus Virology ·Frans Th. Brederode, Peter E.M. Taschner, C. Nekula, John F. Bol	1995	42
18	Application of chromosome 16 markers in the differential diagnosis of neuronal ceroid‐lipofuscinosis American Journal of Medical Genetics ·Peter E.M. Taschner, T. Rovelli, Coriene E. Catsman‐Berrevoets, Sjoerd G. van Duinen, Dick Lindhout, Martijn H. Breuning	1995	4
19	Complementation and disruption of viral processes in transgenic plants Philosophical Transactions of the Royal Society B Biological Sciences ·John F. Bol, Frans Th. Brederode, Lyda Neeleman, Peter E.M. Taschner, Nilgun E. Tumer	1993	1
20	Replication of an incomplete alfalfa mosaic virus genome in plants transformed with viral replicase genes Virology ·Peter E.M. Taschner, Antoinette C. van der Kuyl, Lyda Neeleman, John F. Bol	1991	86

About Peter E.M. Taschner

Peter E.M. Taschner is a scholar working on Aging, Cancer Research, Genetics, Physiology and Physiology, having authored 78 papers that have together received 6.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (25 papers), Genomics and Rare Diseases (14 papers), Adrenal and Paraganglionic Tumors (13 papers), Genomics and Phylogenetic Studies (11 papers), Cancer, Hypoxia, and Metabolism (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Trypanosoma species research and implications (8 papers) and Glycosylation and Glycoproteins Research (6 papers). The work is most often cited by research in Cancer Research (1.9k citations), Endocrinology, Diabetes and Metabolism (1.1k citations), Genetics (1.6k citations), Molecular Biology (3.2k citations) and Physiology (1.0k citations). Peter E.M. Taschner has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Johan T. den Dunnen, Peter Devilee, Ivo F.A.C. Fokkema, Bora E. Baysal, Jeroen F. J. Laros, Cees J. Cornelisse, Jacopo Celli, Raymond Dalgleish, Gerard C. P. Schaafsma and Wendy S. Rubinstein. Their work appears in journals such as Human Mutation, Genomics, Journal of Bacteriology, Prenatal Diagnosis and Virology.

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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