Peter Elfferich

1.6k citations

28 papers · 1.2k · h-index 17

Impact in

Physiology top 5%
- Tuberous Sclerosis Complex Research
- Histiocytic Disorders and Treatments
Genetics top 10%

Papers in

Genetics 9
- Virus-based gene therapy research 4
Molecular Biology 17
- RNA Research and Splicing 4
- Molecular Biology Techniques and Applications 3
- RNA modifications and cancer 3
- Genomics and Phylogenetic Studies 2

Co-authors: Mark D. Nellist (4 shared papers)Dicky J.J. Halley (2 shared papers)Anneke Maat‐Kievit (2 shared papers)Bernard A. Zonnenberg (2 shared papers)Senno Verhoef (1 shared paper)Miriam Goedbloed (1 shared paper)Ans van den Ouweland (1 shared paper)Ite A. Laird‐Offringa (2 shared papers)
Journals: Human Mutation (7 papers)Nucleic Acids Research (3 papers)Sexual Development (2 papers)European Journal of Human Genetics (2 papers)Neurogenetics (1 paper)
Partner nations: Netherlands United Kingdom United States

In The Last Decade

Peter Elfferich

28 papers receiving 1.2k citations

Peers

Countries citing papers authored by Peter Elfferich

Since Specialization

Citations

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

Fields of papers citing papers by Peter Elfferich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype – phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex European Journal of Human Genetics ·Őzgür Sancak, Mark D. Nellist, Miriam Goedbloed, Peter Elfferich, Anneke Maat‐Kievit, Bernard A. Zonnenberg, Senno Verhoef, Dicky J.J. Halley	2005	393
2	Comparison of viable cell counts and fluorescence in situ hybridization using specific rRNA-based probes for the quantification of human fecal bacteria FEMS Microbiology Letters ·Hermie J. M. Harmsen, Glenn R. Gibson, Peter Elfferich, G. C. Raangs, Alida C. M. Wildeboer-Veloo, A. Argaiz, Marcel B. Roberfroid, G.W. Welling	2000	180
3	Poly(A) Tail Shortening Is the Translation-Dependent Step in c- myc mRNA Degradation Molecular and Cellular Biology ·Ite A. Laird‐Offringa, Carla L. De Wit, Peter Elfferich, Alex J. van der Eb	1990	90
4	RET andGDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems Human Mutation ·Robert M.W. Hofstra, Ying Wu, Rein P. Stulp, Peter Elfferich, Jan Osinga, Saskia M Maas, Liesbeth Siderius, A S Brooks	2000	81
5	A DGGE system for comprehensive mutation screening ofBRCA1andBRCA2: application in a Dutch cancer clinic setting Human Mutation ·Annemarie H. van der Hout, Ans M.W. van den Ouweland, Rob B. van der Luijt, Daniëlle Bodmer, Hennie T. Brüggenwirth, Inge M. Mulder, Pieter van der Vlies, Peter Elfferich	2006	72
6	16S Ribosomal RNA-Targeted Oligonucleotide Probes for Monitoring of Intestinal Tract Bacteria Scandinavian Journal of Gastroenterology ·G.W. Welling, Peter Elfferich, G. C. Raangs, Alida C. M. Wildeboer-Veloo, Gijsbert J. Jansen, J. E. Degener	1997	45
7	Rapidc-mycmRNA degradation does not require (A + U)-rich sequences or complete translation of the mRNA Nucleic Acids Research ·Ite A. Laird‐Offringa, Peter Elfferich, A.J. van der Eb	1991	40
8	Web-accessible application for identifying pathogenic transcripts with RNA-seq: Increased sensitivity in diagnosis of neurodevelopmental disorders The American Journal of Human Genetics ·Jordy Dekker, Rachel Schot, Michiel Bongaerts, Walter G. de Valk, Monique M. van Veghel–Plandsoen, Kathryn Monfils, Hannie Douben, Peter Elfferich	2023	38
9	A 16S rRNA-targeted Probe for Detection of Lactobacilli and Enterococci in Faecal Samples by FluorescentIn SituHybridization Microbial Ecology in Health and Disease ·Hermie J. M. Harmsen, Peter Elfferich, Frits Schut, Gjalt W. Welling	1999	36
10	Mucopolysaccharidosis type IIID: 12 new patients and 15 novel mutations Human Mutation ·Marlies J. Valstar, Aida Maria Bertoli‐Avella, Marja W. Wessels, George J. G. Ruijter, Bianca de Graaf, Renske Olmer, Peter Elfferich, Sanne Neijs	2010	33
11	Heterogeneous clinical phenotypes and cerebral malformations reflected by rotatin cellular dynamics Brain ·Laura V. Vandervore, Rachel Schot, Esmee Kasteleijn, Renske Oegema, Katrien Stouffs, Alexander Gheldof, Martyna M. Grochowska, Marianne L. T. van der Sterre	2019	25
12	The N-terminal region of the adenovirus type 5 E1A proteins can repress expression of cellular genes via two distinct but overlapping domains Journal of Virology ·Josephine C. Dorsman, Bertine M. Hagmeyer, Jetty G. Veenstra, Peter Elfferich, N Nabben, Alt ZANTEMA, A.J. van der Eb	1995	25
13	Identification of a large rearrangement in CYLD as a cause of familial cylindromatosis Familial Cancer ·Ans M.W. van den Ouweland, Peter Elfferich, Roy J Lamping, Raoul van de Graaf, Monique M. van Veghel–Plandsoen, S. M. Franken, Arjan C. Houweling	2010	24
14	Comparison of the functional and structural characteristics of rare TSC2 variants with clinical and genetic findings Human Mutation ·Luiz Gustavo Dufner‐Almeida, Santoesha Nanhoe, Andrea Zonta, Mitra Hosseinzadeh, Regina Kom‐Gortat, Peter Elfferich, Gerben Schaaf, Annegien T. Kenter	2019	22
15	Improved mutation detection in GC-rich DNA fragments by combined DGGE and CDGE Nucleic Acids Research ·R. P. Stulp, Peter Elfferich, Joris A.J. Osinga, Charles H.C.M. Buys, Robert M.W. Hofstra +1 other	1999	20
16	Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations Neurogenetics ·Peter Elfferich, Marja C. T. Verleun-Mooijman, J A Maat-Kievit, Bart P.C. van de Warrenburg, Wilson Farid Abdo, Sylvia A. Eshuis, Klaus Leonhard Leenders, A. Hovestadt	2011	20
17	Altered AP-1/ATF complexes in adenovirus-E1-transformed cells due to EIA-dependent induction of ATF3. PubMed ·Bertine M. Hagmeyer, Monique C.A. Duyndam, Peter E. Angel, Rolf P. de Groot, M. Verlaan, Peter Elfferich, A.J. van der Eb, Alt ZANTEMA	1996	18
18	High‐yield identification of pathogenic NF1 variants by skin fibroblast transcriptome screening after apparently normal diagnostic DNA testing Human Mutation ·Hannie Douben, Mark D. Nellist, Leontine van Unen, Peter Elfferich, Esmee Kasteleijn, Marianne Hoogeveen‐Westerveld, Jesse Louwen, Monique van Veghel‐Plandsoen	2022	12
19	Functional and structural analyses of novel Smith-Kingsmore Syndrome-Associated MTOR variants reveal potential new mechanisms and predictors of pathogenicity PLoS Genetics ·Aaron D. Besterman, Thorsten Althoff, Peter Elfferich, Irma Gutierrez-Mejia, Joshua Sadik, Jonathan Adam Bernstein, Yvette van Ierland, Anja A. Kattentidt‐Mouravieva	2021	11
20	High level expression and secretion of truncated forms of herpes simplex virus type 1 and type 2 glycoprotein D by the methylotrophic yeast Pichia pastoris Protein Expression and Purification ·Adriaan van Kooij, Jeena Middel, Ferenc Jakab, Peter Elfferich, Danny G. A. M. Koedijk, Matty Feijlbrief, Albert Jan Scheffer, John E. Degener	2002	11

About Peter Elfferich

Peter Elfferich is a scholar working on Genetics, Molecular Biology, Oncology, Physiology and Neurology, having authored 28 papers that have together received 1.2k indexed citations. Recurring topics across this work include Tuberous Sclerosis Complex Research (4 papers), Virus-based gene therapy research (4 papers), RNA Research and Splicing (4 papers), Polyomavirus and related diseases (3 papers), Molecular Biology Techniques and Applications (3 papers), RNA modifications and cancer (3 papers), Histiocytic Disorders and Treatments (3 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Physiology (428 citations), Genetics (244 citations), Molecular Biology (523 citations), Food Science (123 citations) and Nutrition and Dietetics (94 citations). Peter Elfferich has collaborated with scholars based in Netherlands, United Kingdom and United States. Frequent co-authors include Mark D. Nellist, Dicky J.J. Halley, Anneke Maat‐Kievit, Bernard A. Zonnenberg, Senno Verhoef, Miriam Goedbloed, Ans van den Ouweland, Ite A. Laird‐Offringa, Hermie J. M. Harmsen and G.W. Welling. Their work appears in journals such as Human Mutation, Nucleic Acids Research, Sexual Development, European Journal of Human Genetics and Neurogenetics.

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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