Peer Arts

4.7k citations

26 papers · 1.8k · 2 hit papers · h-index 12

Impact in

Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Immunology top 5%
- Immunodeficiency and Autoimmune Disorders
- Immune Response and Inflammation
- Immune Cell Function and Interaction

Papers in

Molecular Biology 12
- RNA modifications and cancer 5
- RNA Research and Splicing 2
- Congenital heart defects research 2
Genetics 9
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 3

Co-authors: Alexander Hoischen (14 shared papers)Christian Gilissen (8 shared papers)Joris A. Veltman (7 shared papers)Marloes Steehouwer (6 shared papers)Han G. Brunner (3 shared papers)Bart van Lier (2 shared papers)Nienke Wieskamp (3 shared papers)Mihai G. Netea (6 shared papers)
Journals: Blood (2 papers)Human Mutation (2 papers)The American Journal of Human Genetics (2 papers)iScience (1 paper)Nature Genetics (1 paper)
Partner nations: Netherlands Australia United States

In The Last Decade

Peer Arts

26 papers receiving 1.8k citations

Peer Arts's Hit Papers

align trajectories log scale

STAT1 Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis 2011 · 436 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2011 New England Journal of Medicine
2010 Nature Genetics

Peers

Countries citing papers authored by Peer Arts

Since Specialization

Citations

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

Fields of papers citing papers by Peer Arts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Peer Arts, 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 Peer Arts Line = papers co-authored together Peer Arts 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 26 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A de novo paradigm for mental retardation Nature Genetics ·Lisenka E.L.M. Vissers, Joep de Ligt, Christian Gilissen, Irene M. Janssen, Marloes Steehouwer, Petra de Vries, Bart van Lier, Peer Arts, Nienke Wieskamp, Marisol del Rosario, Bregje W.M. van Bon, Alexander Hoischen, Bert B.A. de Vries, Han G. Brunner, Joris A. Veltman Hit paper breakdown →	2010	526
2	STAT1 Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis New England Journal of Medicine ·Frank L. van de Veerdonk, Theo S. Plantinga, Alexander Hoischen, Sanne P. Smeekens, Leo A. B. Joosten, Christian Gilissen, Peer Arts, Diana C. Rosentul, Andrew Carmichael, Chantal A.A. Smits-van der Graaf, Bart Jan Kullberg, J.W.M. van der Meer, Desa Lilić, Joris A. Veltman, Mihai G. Netea Hit paper breakdown →	2011	436
3	Human TLR10 is an anti-inflammatory pattern-recognition receptor Proceedings of the National Academy of Sciences ·Marije Oosting, Shih‐Chin Cheng, Judith M. Bolscher, Rachel Vestering-Stenger, Theo S. Plantinga, Ineke Verschueren, Peer Arts, Anja Garritsen, Hans van Eenennaam, Patrick Sturm, Bart Jan Kullberg, Alexander Hoischen, Gosse J. Adema, J.W.M. van der Meer, Mihai G. Netea, Leo A. B. Joosten	2014	199
4	Exome Sequencing Identifies WDR35 Variants Involved in Sensenbrenner Syndrome The American Journal of Human Genetics ·Christian Gilissen, Heleen H. Arts, Alexander Hoischen, Liesbeth Spruijt, Dorus A. Mans, Peer Arts, Bart van Lier, Marloes Steehouwer, Jeroen van Reeuwijk, Sarina G. Kant, Ronald Roepman, Nine V.A.M. Knoers, Joris A. Veltman, Han G. Brunner	2010	197
5	Next-Generation Sequencing of a 40 Mb Linkage Interval Reveals TSPAN12 Mutations in Patients with Familial Exudative Vitreoretinopathy The American Journal of Human Genetics ·Konstantinos Nikopoulos, Christian Gilissen, Alexander Hoischen, C. E. van Nouhuys, F. Nienke Boonstra, Ellen A.W. Blokland, Peer Arts, Nienke Wieskamp, Tim M. Strom, Carmen Ayuso, M. A. D. Tilanus, Sanne Bouwhuis, Arijit Mukhopadhyay, Hans Scheffer, Lies H. Hoefsloot, Joris A. Veltman, Frans P.M. Cremers, Rob W.J. Collin	2010	168
6	Massively parallel sequencing of ataxia genes after array-based enrichment Human Mutation ·Alexander Hoischen, Christian Gilissen, Peer Arts, Nienke Wieskamp, Walter van der Vliet, Sascha Vermeer, Marloes Steehouwer, Petra de Vries, Rowdy Meijer, Jorge Seiqueros, Nine V.A.M. Knoers, Michael F. Buckley, Hans Scheffer, Joris A. Veltman	2010	63
7	Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2 British Journal of Cancer ·Marjolijn J. L. Ligtenberg, Frans B.L. Hogervorst, H.W. Willems, Peer Arts, Gijs R. van den Brink, S. Hageman, Ermanno Bosgoed, Erica van der Looij, Matti A. Rookus, Peter Devilee, E M A W Vos, Gea Wigbout, Patrick Struycken, Fred H. Menko, Emiel J. Rutgers, Elisabeth H. Hoefsloot, Edwin C.M. Mariman, Han G. Brunner, Laura J. van’t Veer	1999	41
8	GATA2 deficiency syndrome: A decade of discovery Human Mutation ·Claire C. Homan, Parvathy Venugopal, Peer Arts, Nur Hezrin Shahrin, Simone Feurstein, Lesley Rawlings, David Lawrence, James Andrews, Sarah L. King‐Smith, Natasha L. Harvey, Anna Brown, Hamish S. Scott, Christopher N Hahn	2021	29
9	Quantification of differential gene expression by multiplexed targeted resequencing of cDNA Nature Communications ·Peer Arts, Jori van der Raadt, Sebastianus H. C. van Gestel, Marloes Steehouwer, Jay Shendure, Alexander Hoischen, Cornelis A. Albers	2017	18
10	Progressive multifocal leukoencephalopathy in an immunocompetent patient Annals of Clinical and Translational Neurology ·Nicolien M. van der Kolk, Peer Arts, Ingeborg W.M. van Uden, Alexander Hoischen, Frank L. van de Veerdonk, Mihai G. Netea, Brigit A. de Jong	2016	17
11	Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6 npj Genomic Medicine ·Alicia B. Byrne, Peer Arts, Steven W. Polyak, Jinghua Feng, Andreas Schreiber, Karin S. Kassahn, Christopher N Hahn, Dylan Mordaunt, Janice M. Fletcher, Jillian Lipsett, Drago Bratkovic, Grant W. Booker, Nicholas Smith, Hamish S. Scott	2019	16
12	Paternal mosaicism for a novel PBX1 mutation associated with recurrent perinatal death: Phenotypic expansion of the PBX1‐related syndrome American Journal of Medical Genetics Part A ·Peer Arts, Jessica Garland, Alicia B. Byrne, Tristan Hardy, Milena Babic, Jinghua Feng, Paul Wang, Thuong Ha, Sarah L. King‐Smith, Andreas Schreiber, April Crawford, Nick Manton, Lynette Moore, Christopher Barnett, Hamish S. Scott	2020	11
13	Introme accurately predicts the impact of coding and noncoding variants on gene splicing, with clinical applications Genome biology ·Patricia J. Sullivan, Velimir Gayevskiy, Ryan L. Davis, Marie Wong, Chelsea Mayoh, Amali Mallawaarachchi, Yvonne Hort, Mark J. McCabe, Sarah J. Beecroft, Matilda R. Jackson, Peer Arts, Andrew Dubowsky, Nigel G. Laing, Marcel E. Dinger, Hamish S. Scott, Emily C. Oates, Mark Pinese, Mark J. Cowley	2023	10
14	A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples Journal of the Neurological Sciences ·I.F.M. de Coo, T Gussinklo, Peer Arts, Bernard A. van Oost, Hubert J.M. Smeets	1997	10
15	Rare NOX3 Variants Confer Susceptibility to Agranulocytosis During Thyrostatic Treatment of Graves' Disease Clinical Pharmacology & Therapeutics ·Theo S. Plantinga, Peer Arts, GH Knarren, AH Mulder, I M M J Wakelkamp, AR Hermus, L.A.B. Joosten, M.G. Netea, PH Bisschop, WW de Herder, HJ Beijers, IJ de Bruin, Christian Gilissen, Joris A. Veltman, Alexander Hoischen, Johannes W. A. Smit, RT Netea‐Maier	2017	10
16	Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis Journal of Medical Genetics ·Alicia B. Byrne, Shuji Mizumoto, Peer Arts, Patrick Yap, Jinghua Feng, Andreas Schreiber, Milena Babic, Sarah L. King‐Smith, Christopher Barnett, Lynette Moore, Kazuyuki Sugahara, Hatice Mutlu Albayrak, Gen Nishimura, Jan Liebelt, Shuhei Yamada, Ravi Savarirayan, Hamish S. Scott	2020	9
17	Impact of rare and common genetic variation in the interleukin-1 pathway on human cytokine responses Genome Medicine ·Rosanne C. van Deuren, Peer Arts, Giulio Cavalli, Martin Jaeger, Marloes Steehouwer, Maartje van de Vorst, Christian Gilissen, Leo A. B. Joosten, Charles A. Dinarello, Musa M. Mhlanga, Vinod Kumar, Mihai G. Netea, Frank L. van de Veerdonk, Alexander Hoischen	2021	7
18	A missense mutation underlies defective SOCS4 function in a family with autoimmunity Journal of Internal Medicine ·Peer Arts, Theo S. Plantinga, J. Merlijn van den Berg, Christian Gilissen, Joris A. Veltman, A S Paul van Trotsenburg, Frank L. van de Veerdonk, Taco W. Kuijpers, Alexander Hoischen, Mihai G. Netea	2015	6
19	Compound heterozygous variants in LAMC3 in association with posterior periventricular nodular heterotopia BMC Medical Genomics ·Carla De Angelis, Alicia B. Byrne, Rebecca Morrow, Jinghua Feng, Thuong Ha, Paul Wang, Andreas Schreiber, Milena Babic, Ajay Taranath, Nick Manton, Sarah L. King‐Smith, Quenten Schwarz, Peer Arts, Hamish S. Scott, Christopher Barnett	2021	5
20	Mimicking Behçet's disease: GM-CSF gain of function mutation in a family suffering from a Behçet's disease-like disorder marked by extreme pathergy Clinical & Experimental Immunology ·Berenice Rösler, Bas Heinhuis, X Wang, Ricardo Silvestre, L.A.B. Joosten, M.G. Netea, Peer Arts, Tuomo Mantere, Dirk J. Lefeber, Alexander Hoischen, Frank L. van de Veerdonk	2020	4

About Peer Arts

Peer Arts is a scholar working on Molecular Biology, Genetics, Immunology, Rheumatology and Hematology, having authored 26 papers that have together received 1.8k indexed citations. Recurring topics across this work include RNA modifications and cancer (5 papers), Acute Myeloid Leukemia Research (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (3 papers), RNA Research and Splicing (2 papers), Immune Response and Inflammation (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (805 citations), Immunology (526 citations), Molecular Biology (732 citations), Cancer Research (158 citations) and Infectious Diseases (191 citations). Peer Arts has collaborated with scholars based in Netherlands, Australia and United States. Frequent co-authors include Alexander Hoischen, Christian Gilissen, Joris A. Veltman, Marloes Steehouwer, Han G. Brunner, Bart van Lier, Nienke Wieskamp, Mihai G. Netea, Theo S. Plantinga and J.W.M. van der Meer. Their work appears in journals such as Blood, Human Mutation, The American Journal of Human Genetics, iScience and Nature Genetics.

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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Peer Arts's Hit Papers

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About Peer Arts

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