Tessa van Dijk

619 total citations
18 papers, 320 citations indexed

About

Tessa van Dijk is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Tessa van Dijk has authored 18 papers receiving a total of 320 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 6 papers in Molecular Biology and 5 papers in Clinical Biochemistry. Recurrent topics in Tessa van Dijk's work include Fetal and Pediatric Neurological Disorders (6 papers), Metabolism and Genetic Disorders (5 papers) and Diet and metabolism studies (3 papers). Tessa van Dijk is often cited by papers focused on Fetal and Pediatric Neurological Disorders (6 papers), Metabolism and Genetic Disorders (5 papers) and Diet and metabolism studies (3 papers). Tessa van Dijk collaborates with scholars based in Netherlands, Chile and Canada. Tessa van Dijk's co-authors include Frank Baas, Bwee Tien Poll‐The, P. G. Barth, R. Berger, Dirk‐Jan Reijngoud, M. van Rijn, Liesbeth Reneman, H. S. A. Heymans, Francjan J. van Spronsen and Gerrit Smit and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and American Journal of Clinical Nutrition.

In The Last Decade

Tessa van Dijk

18 papers receiving 315 citations

Peers

Countries citing papers authored by Tessa van Dijk

Since Specialization

Citations

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

Fields of papers citing papers by Tessa van Dijk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tessa van Dijk. 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 Tessa van Dijk. The network helps show where Tessa van Dijk may publish in the future.

Co-authorship network of co-authors of Tessa van Dijk

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their child 2023 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), Tessa van Dijk, (unknown), Gepke Visser, Mirjam Langeveld, Lidewij Henneman	1
2	New Genetic Variant in the MYH7 Gene Associated With Hypoplastic Right Heart Syndrome and Hypertrophic Cardiomyopathy in the Same Family 2023 ·Circulation Genomic and Precision Medicine ·(unknown), Janine M. van Gils, J. Lauran Stöger, Philippine Kiès, Anastasia D. Egorova, Tamara T. Koopmann, Tessa van Dijk, Marco C. DeRuiter, Daniela Q.C.M. Barge‐Schaapveld, Monique R.M. Jongbloed	2
3	Parents’ views on accepting, declining, and expanding newborn bloodspot screening 2022 ·PLoS ONE ·Sylvia van der Pal, (unknown), (unknown), Tessa van Dijk, (unknown), C.P.B. van der Ploeg, Suze Jans, Stephan Kemp, (unknown), (unknown), Lidewij Henneman	11
4	Informing Parents about Newborn Screening: A European Comparison Study 2021 ·International Journal of Neonatal Screening ·(unknown), Tessa van Dijk, (unknown), Gerard Loeber, Viktor Kožich, Lidewij Henneman, Marleen E. Jansen	15
5	Primary Ovarian Failure in Addition to Classical Clinical Features of Coats Plus Syndrome in a Female Carrying 2 Truncating Variants of CTC1 2021 ·Hormone Research in Paediatrics ·(unknown), Sanami Takada, Tessa van Dijk, (unknown), Merel W. Boogaard, Hermine A. van Duyvenvoorde, Ingrid Pico‐Knijnenburg, Jan M. Wit, Mirjam van der Burg, Verónica Mericq, Monique Losekoot	3
6	Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder Perspective 2021 ·Frontiers in Pediatrics ·Tessa van Dijk, (unknown), Marleen E. Jansen, Wybo Dondorp, Maartje Blom, Stephan Kemp, Mirjam Langeveld, Martina C. Cornel, Sylvia van der Pal, Lidewij Henneman	15
7	Towards representative resilience: the power of culture to foster local resource representation 2021 ·Local Environment ·(unknown), Lummina Horlings, Tessa van Dijk, Henrike Rau	7
8	TSEN54 Pontocerebellar Hypoplasia 2020 ·Europe PMC (PubMed Central) ·Tessa van Dijk, Frank Baas	1
9	Postnatal Brain Growth Patterns in Pontocerebellar Hypoplasia 2020 ·Neuropediatrics ·Tessa van Dijk, P. G. Barth, Frank Baas, Liesbeth Reneman, Bwee Tien Poll‐The	6
10	Biallelic loss of function variants in COASY cause prenatal onset pontocerebellar hypoplasia, microcephaly, and arthrogryposis 2018 ·European Journal of Human Genetics ·Tessa van Dijk, Sacha Ferdinandusse, Jos P.N. Ruiter, Mariëlle Alders, Inge B. Mathijssen, Jillian S. Parboosingh, A. Micheil Innes, Hanne Meijers-Heijboer, Bwee Tien Poll‐The, François P. Bernier, Ronald J. A. Wanders, Ryan E. Lamont, Frank Baas	31
11	What’s new in pontocerebellar hypoplasia? An update on genes and subtypes 2018 ·Orphanet Journal of Rare Diseases ·Tessa van Dijk, Frank Baas, P. G. Barth, Bwee Tien Poll‐The	89
12	A SEPSECS mutation in a 23‐year‐old woman with microcephaly and progressive cerebellar ataxia 2018 ·Journal of Inherited Metabolic Disease ·Tessa van Dijk, Jan‐Dirk Vermeij, Silvana van Koningsbruggen, Phillis Lakeman, Frank Baas, Bwee Tien Poll‐The	11
13	A de novo missense mutation in the inositol 1,4,5‐triphosphate receptor type 1 gene causing severe pontine and cerebellar hypoplasia: Expanding the phenotype of ITPR1‐related spinocerebellar ataxia's 2016 ·American Journal of Medical Genetics Part A ·Tessa van Dijk, P. G. Barth, Liesbeth Reneman, (unknown), Frank Baas, Bwee Tien Poll‐The	30
14	RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy? 2016 ·JIMD Reports ·Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, Richard J. Rodenburg, (unknown), Merel van Maarle, Frank Baas, Nicole I. Wolf, Bwee Tien Poll‐The	13
15	Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1 2015 ·SHILAP Revista de lepidopterología ·Jessie C. Jacobsen, Emma Glamuzina, Juliet Taylor, (unknown), (unknown), Callum Wilson, Michael Fietz, Tessa van Dijk, (unknown), R. Sean Hill, (unknown), Donald R. Love, Stephen P. Robertson, Russell G. Snell, Klaus Lehnert	2
16	Recombinant human apolipoprotein-a-i prebeta-HDL (cer-001) promotes reverse cholesterol transport and reduces carotid wall thickness in patients with genetically-determined low HDL 2014 ·Atherosclerosis ·Ruud S. Kootte, Loek P. Smits, Fleur M. van der Valk, Jean‐Louis Dasseux, Constance Keyserling, Ronald Barbaras, John F. Paolini, G. Kees Hovingh, Tessa van Dijk, Aart J. Nederveen, J Kastelein, (unknown), Erik S.G. Stroes	3
17	Large daily fluctuations in plasma tyrosine in treated patients with phenylketonuria 1996 ·American Journal of Clinical Nutrition ·(unknown), Tessa van Dijk, (unknown), M. van Rijn, Dirk‐Jan Reijngoud, R. Berger, (unknown)	38
18	Plasma Phenylalanine and Tyrosine Responses to Different Nutritional Conditions (Fasting/Postprandial) in Patients With Phenylketonuria: Effect of Sample Timing 1993 ·PEDIATRICS ·Francjan J. van Spronsen, M. van Rijn, Tessa van Dijk, Gerrit Smit, Dirk‐Jan Reijngoud, R. Berger, H. S. A. Heymans	42

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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