Heleen H. Arts

3.7k citations

32 papers · 1.1k indexed · h-index 15

Genetics top 2%
- Genetic and Kidney Cyst Diseases 20
- Genetic Syndromes and Imprinting 6
- Genomics and Rare Diseases 3
Molecular Biology top 10%
- Renal and related cancers 8
- Epigenetics and DNA Methylation 6
- Hedgehog Signaling Pathway Studies 3
- Protist diversity and phylogeny 3
Cell Biology top 10%
Pediatrics, Perinatology and Child Health top 10%
- Fetal and Pediatric Neurological Disorders 4
Pathology and Forensic Medicine top 10%

Co-authors: Ronald Roepman Nine V.A.M. Knoers Nine Knoers Sylvia E. C. van Beersum Jeroen van Reeuwijk Frans P.M. Cremers Han G. Brunner Stef J.F. Letteboer
Cited by: Genetics Molecular Biology Cell Biology
Journals: Proceedings of the National Academy of Sciences (1 paper)Nature Genetics (1 paper)SHILAP Revista de lepidopterología (2 papers)
Partner nations: Netherlands Canada United States

In The Last Decade

Heleen H. Arts

32 papers receiving 1.1k citations

Peers

Countries citing papers authored by Heleen H. Arts

Since Specialization

Citations

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

Fields of papers citing papers by Heleen H. Arts

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Increased intracranial pressure in a patient with Congenital Heart Defect and Ectodermal Dysplasia (CHDED): Extension of phenotype and review of literature American Journal of Medical Genetics Part A ·Fahad A. Alghaith,Heleen H. Arts,Francois J. Plourde,Andrew Boswall,Partima Gulati,P. Daniel McNeely,Philip D. Acott,Kenny K. Wong,Sarah Dyack	2022	2
2	A 132 bp deletion affecting the KCNQ1OT1 gene associated with Silver-Russell syndrome clinical phenotype Journal of Medical Genetics ·Marie Véronique Gaudet,Éric P. Allain,Lynne M Gallant,Heleen H. Arts,Mouna Ben Amor	2022	1
3	Multisite verification of the accuracy of a multi-gene next generation sequencing panel for detection of mutations and copy number alterations in solid tumours PLoS ONE ·John M.S. Bartlett,Yutaka Amemiya,Heleen H. Arts,Jane Bayani,Barry Eng,Daria Grafodatskaya,Suzanne Kamel Reid,Mathieu Larivière,Bernard Lo,Rebecca F. McClure,Vinay Kumar Mittal,Bekim Sadiković,Seth Sadis,Arun Seth,Jeff Smith,Xiao Zhang,Harriet Feilotter	2021	7
4	Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease Orphanet Journal of Rare Diseases ·Joanna Walczak‐Sztulpa,Renata Posmyk,Ewelina Bukowska‐Olech,Anna Wawrocka,Aleksander Jamsheer,Machteld M. Oud,Miriam Schmidts,Heleen H. Arts,Anna Latos‐Bieleńska,Anna Wasilewska	2020	12
5	Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35 American Journal of Medical Genetics Part A ·Joanna Walczak‐Sztulpa,Anna Wawrocka,Beata Leszczyńska,Boyana Mikulska,Heleen H. Arts,Ewelina Bukowska‐Olech,Maria Daniel,M Krawczyński,Anna Latos‐Bieleńska,Ewa Obersztyn	2020	8
6	ATM whole gene deletion in an Italian family with hereditary pancreatic cancer: Challenges to cancer risk prediction associated with an 11q22.3 microdeletion Cancer Genetics ·Heleen H. Arts,Lorrie Lynch,Daria Grafodatskaya,Barry Eng,Lesley Malloy,John Duck,Robyn White,Crystal Woodside,Kathleen Bell,Kevin Zbuk,M. Elizabeth McCready	2019	2
7	The KOUNCIL Consortium: From Genetic Defects to Therapeutic Development for Nephronophthisis Frontiers in Pediatrics ·Kirsten Y. Renkema,Rachel H. Giles,Marc R. Liliën,Philip L. Beales,Ronald Roepman,Machteld M. Oud,Heleen H. Arts,Nine V.A.M. Knoers	2018	3
8	A truncating mutation in CEP55 is the likely cause of MARCH, a novel syndrome affecting neuronal mitosis Journal of Medical Genetics ·Patrick Frosk,Heleen H. Arts,Julien Philippe,Carter S Gunn,Emma Brown,Bernard Chodirker,Louise R. Simard,Jacek Majewski,Somayyeh Fahiminiya,Chad Russell,Yangfan P. Liu,(unknown),Robert A. Hegele,Nicholas Katsanis,Conrad Goerz,Marc R. Del Bigio,Erica E. Davis	2017	35
9	Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy Human Molecular Genetics ·Sali M.K. Farhan,Kevin C. Nixon,Michelle Everest,Tara N. Edwards,S.P. Long,Dmitri Segal,Maria J. Knip,Heleen H. Arts,Rana Chakrabarti,Jian Wang,John F. Robinson,Donald Lee,Seyed M. Mirsattari,C. Anthony Rupar,Victoria Mok Siu,Michael O. Poulter,Robert A. Hegele,Jamie M. Kramer	2017	32
10	A mutation in IFT43 causes non-syndromic recessive retinal degeneration Human Molecular Genetics ·Pooja Biswas,Jacque L. Duncan,Muhammad Ali,Hiroko Matsui,Muhammad Asif Naeem,Pongali B. Raghavendra,Kelly A. Frazer,Heleen H. Arts,Sheikh Riazuddin,Javed Akram,J. Fielding Hejtmancik,Radha Ayyagari	2017	10
11	Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum Scientific Reports ·Maleeha Maria,Ideke J.C. Lamers,Miriam Schmidts,Muhammad Ajmal,Sulman Jaffar,Ehsan Ullah,Bilal Mustafa,Shakeel Ahmad,Katia Nazmutdinova,Bethan E. Hoskins,Erwin van Wijk,Linda Koster‐Kamphuis,Muhammad Imran Khan,Phil Beales,Frans P.M. Cremers,Ronald Roepman,Maleeha Azam,Heleen H. Arts,Raheel Qamar	2016	31
12	BARDET-BIEDL SYNDROME – CASE PRESENTATION SHILAP Revista de lepidopterología ·S I Iurian,Heleen H. Arts,Han G. Brunner,Dana Fîntînă	2015	2
13	Non-invasive sources of cells with primary cilia from pediatric and adult patients PubMed ·Henry Ajzenberg,Gisela G. Slaats,Marijn F. Stokman,Heleen H. Arts,Ive Logister,Hester Y. Kroes,Kirsten Y. Renkema,Mieke M. van Haelst,Pauline Terhal,Iris A.L.M. van Rooij,Mandy G. Keijzer‐Veen,Nine Knoers,Marc R. Liliën,Michael A.S. Jewett,Rachel H. Giles	2015	27
14	Sensenbrenner syndrome (Cranioectodermal dysplasia): Clinical and molecular analyses of 39 patients including two new patients American Journal of Medical Genetics Part A ·Angela E. Lin,Avram Z. Traum,Inderneel Sahai,Kim M. Keppler‐Noreuil,Mary K. Kukolich,Margaret P Adam,Sjirk J. Westra,Heleen H. Arts	2013	49
15	Current insights into renal ciliopathies: what can genetics teach us? Pediatric Nephrology ·Heleen H. Arts,Nine Knoers	2012	61
16	C14ORF179 encoding IFT43 is mutated in Sensenbrenner syndrome Journal of Medical Genetics ·Heleen H. Arts,Ernie M.H.F. Bongers,Dorus A. Mans,Sylvia E. C. van Beersum,M. M. Oud,Emine Bolat,Liesbeth Spruijt,Elisabeth A. M. Cornelissen,Janneke Schuurs-Hoeijmakers,Nicole de Leeuw,Valérie Cormier‐Daire,Han G. Brunner,Nine V.A.M. Knoers,Ronald Roepman	2011	102
17	Scrutinizing ciliopathies by unraveling ciliary interaction networks Human Molecular Genetics ·Jeroen van Reeuwijk,Heleen H. Arts,Ronald Roepman	2011	43
18	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
19	Focus on Molecules: RPGRIP1 Experimental Eye Research ·Heleen H. Arts,Frans P.M. Cremers,Nine V.A.M. Knoers,Ronald Roepman	2008	10
20	Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome Nature Genetics ·Heleen H. Arts,Dan Doherty,Sylvia E. C. van Beersum,Melissa A. Parisi,Stef J.F. Letteboer,Nicholas T. Gorden,Theo Peters,Tina Märker,Krysta Voesenek,Aileen Kartono,Hamìt Özyürek,Federico M. Farin,Hester Y. Kroes,Uwe Wolfrum,Han G. Brunner,Frans P.M. Cremers,Ian A. Glass,Nine V.A.M. Knoers,Ronald Roepman	2007	235

About Heleen H. Arts

Heleen H. Arts is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 32 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (20 papers), Renal and related cancers (8 papers), Genetic Syndromes and Imprinting (6 papers), Epigenetics and DNA Methylation (6 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genomics and Rare Diseases (3 papers), Hedgehog Signaling Pathway Studies (3 papers) and Protist diversity and phylogeny (3 papers). The work is most often cited by research in Genetics (914 citations), Molecular Biology (892 citations) and Cell Biology (159 citations). Heleen H. Arts has collaborated with scholars based in Netherlands, Canada and United States. Frequent co-authors include Ronald Roepman, Nine V.A.M. Knoers, Nine Knoers, Sylvia E. C. van Beersum, Jeroen van Reeuwijk, Frans P.M. Cremers, Han G. Brunner, Stef J.F. Letteboer, Dorus A. Mans and Liesbeth Spruijt. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

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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