I. Snoeck

1.6k total citations
11 papers, 664 citations indexed

About

I. Snoeck is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, I. Snoeck has authored 11 papers receiving a total of 664 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in I. Snoeck's work include Fetal and Pediatric Neurological Disorders (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Mitochondrial Function and Pathology (2 papers). I. Snoeck is often cited by papers focused on Fetal and Pediatric Neurological Disorders (3 papers), Neurogenetic and Muscular Disorders Research (3 papers) and Mitochondrial Function and Pathology (2 papers). I. Snoeck collaborates with scholars based in Netherlands, Italy and Germany. I. Snoeck's co-authors include Arie van Haeringen, J. Motte, Johan T. den Dunnen, Stefano Ricci, Marjolein Kriek, V. des Portes, M.L. Moutard, Gijs W.E. Santen, Emmelien Aten and Isabelle Desguerre and has published in prestigious journals such as Nature Genetics, Journal of Bone and Joint Surgery and Human Molecular Genetics.

In The Last Decade

I. Snoeck

10 papers receiving 651 citations

Peers

I. Snoeck

MB

GENET

PPCH

CMN

DN

Sarah Wynn United Kingdom

Jessica A. Panzer United States

Julie T. Parke United States

David B. Everman United States

Connie Schrander‐Stumpel Netherlands

Alice Goldenberg France

Kazushi Aoto Japan

Darren T. Oystreck Saudi Arabia

Ivan F. M. Lo China

Laurence E. Walsh United States

Sarah Wynn United Kingdom

I. Snoeck

538 ×1.4

MB

181 ×1.0

GENET

35 ×0.3

PPCH

67 ×0.7

CMN

92 ×1.1

DN

Citations per year, relative to I. Snoeck I. Snoeck (= 1×) peers Sarah Wynn

Countries citing papers authored by I. Snoeck

Since Specialization

Citations

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

Fields of papers citing papers by I. Snoeck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. Snoeck

This figure shows the co-authorship network connecting the top 25 collaborators of I. Snoeck. A scholar is included among the top collaborators of I. Snoeck 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 I. Snoeck. I. Snoeck is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

1.

Verrips, Aad, Bwee Tien Poll‐The, Jan-Maarten Cobben, et al.. (2013). Clinical and mutational characteristics of spinal muscular atrophy with respiratory distress type 1 in the Netherlands. Neuromuscular Disorders. 23(6). 461–468. 10 indexed citations

2.

Coebergh, Jan, et al.. (2013). A new variable phenotype in spinocerebellar ataxia 27 (SCA 27) caused by a deletion in the FGF14 gene. European Journal of Paediatric Neurology. 18(3). 413–415. 40 indexed citations

3.

Santen, Gijs W.E., Emmelien Aten, Yu Sun, et al.. (2012). Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome. Nature Genetics. 44(4). 379–380. 235 indexed citations

4.

Valstar, M. J., et al.. (2010). Langdurige neonatale icterus met later ataxie,verticale blikparese en progressieve mentale achteruitgang: de ziekte van Niemann-Pick type C. Tijdschrift voor kindergeneeskunde. 78(2). 77–80.

5.

Cobben, Jan M., et al.. (2008). Survival in SMA type I: A prospective analysis of 34 consecutive cases. Neuromuscular Disorders. 18(7). 541–544. 46 indexed citations

6.

Vries, Maaike C. de, Richard J. Rodenburg, Éva Morava, et al.. (2006). Multiple oxidative phosphorylation deficiencies in severe childhood multi-system disorders due to polymerase gamma (POLG1) mutations. European Journal of Pediatrics. 166(3). 229–234. 59 indexed citations

7.

Vries, Maaike C. de, Richard J. Rodenburg, H. ter Laak, et al.. (2006). Multiple oxidative phosphorylation deficiencies in severe childhood multi-system disorders due to polymerase γ (POLG) mutations. Mitochondrion. 6(5). 17–17. 1 indexed citations

8.

Rijn, Ariadne M Roelants‐van, Peter G. J. Nikkels, Floris Groenendaal, et al.. (2002). Neonatal Diffusion-Weighted MR Imaging: Relation with Histopathology or Follow-Up MR Examination. Neuropediatrics. 32(6). 286–294. 47 indexed citations

9.

Valk, P. van der, I. Snoeck, Linda C. Meiners, et al.. (1999). Subcortical Laminar Heterotopia in Two Sisters and Their Mother: MRI, Clinical Findings and Pathogenesis. Neuropediatrics. 30(3). 155–160. 3 indexed citations

10.

Portes, V. des, Fiona Francis, J.-M. Pinard, et al.. (1998). Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH). Human Molecular Genetics. 7(7). 1063–1070. 209 indexed citations

11.

Vandertop, W. Peter, et al.. (1994). Aneurysmal bone cyst of the thoracic spine. Journal of Bone and Joint Surgery. 76(4). 608–611. 14 indexed citations

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.

Explore authors with similar magnitude of impact