Mari‐Anne Vals

592 total citations
14 papers, 177 citations indexed

About

Mari‐Anne Vals is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mari‐Anne Vals has authored 14 papers receiving a total of 177 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mari‐Anne Vals's work include Glycosylation and Glycoproteins Research (3 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (3 papers). Mari‐Anne Vals is often cited by papers focused on Glycosylation and Glycoproteins Research (3 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (3 papers). Mari‐Anne Vals collaborates with scholars based in Estonia, United States and Netherlands. Mari‐Anne Vals's co-authors include Katrin Õunap, Sander Pajusalu, Kai Muru, Tiina Kahre, Mart Kals, Karit Reinson, Reedik Mägi, Vallo Tillmann, Eve Õiglane‐Shlik and Dirk J. Lefeber and has published in prestigious journals such as Nature Communications, Acta Paediatrica and European Journal of Human Genetics.

In The Last Decade

Mari‐Anne Vals

13 papers receiving 161 citations

Peers

Countries citing papers authored by Mari‐Anne Vals

Since Specialization

Citations

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

Fields of papers citing papers by Mari‐Anne Vals

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mari‐Anne Vals. 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 Mari‐Anne Vals. The network helps show where Mari‐Anne Vals may publish in the future.

Co-authorship network of co-authors of Mari‐Anne Vals

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	ACTG2 -Related Visceral Myopathy: Case Reports with Phenotypic Variations and Review of the Previously Published Cases 2025 ·Fetal and Pediatric Pathology ·(unknown), (unknown), Mari‐Anne Vals, (unknown), Tiia Reimand, Kristiina Rull	0
2	Congenital disorder of glycosylation caused by starting site-specific variant in syntaxin-5 2021 ·Nature Communications ·Peter Linders, (unknown), Angel Ashikov, Mari‐Anne Vals, Rinse de Boer, Natalia H. Revelo, (unknown), (unknown), Fokje Zijlstra, Karin Huijben, Kimiyo Raymond, Kai Muru, (unknown), Sander Pajusalu, Katrin Õunap, Martin ter Beest, Dirk J. Lefeber, Geert van den Bogaart	16
3	The Estimated Prevalence of N-Linked Congenital Disorders of Glycosylation Across Various Populations Based on Allele Frequencies in General Population Databases 2021 ·Frontiers in Genetics ·Sander Pajusalu, Mari‐Anne Vals, (unknown), (unknown), Tiina Kahre, Katrin Õunap	13
4	A retrospective analysis of the prevalence of imprinting disorders in Estonia from 1998 to 2016 2019 ·European Journal of Human Genetics ·(unknown), Tiina Kahre, Riina Žordania, Karit Reinson, Rita Teek, Vallo Tillmann, Aleksandr Peet, Eve Õiglane‐Shlik, Sander Pajusalu, (unknown), Mari‐Anne Vals, (unknown), Monica H. Wojcik, Katrin Õunap	17
5	High incidence of low vitamin B12 levels in Estonian newborns 2018 ·Molecular Genetics and Metabolism Reports ·Karit Reinson, (unknown), (unknown), Mari‐Anne Vals, Kai Muru, Katrin Õunap	21
6	The Prevalence of PMM2-CDG in Estonia Based on Population Carrier Frequencies and Diagnosed Patients 2017 ·JIMD Reports ·Mari‐Anne Vals, Sander Pajusalu, Mart Kals, Reedik Mägi, Katrin Õunap	26
7	Three families with mild PMM2‐CDG and normal cognitive development 2017 ·American Journal of Medical Genetics Part A ·Mari‐Anne Vals, Éva Morava, (unknown), Riina Žordania, Sander Pajusalu, Dirk J. Lefeber, Katrin Õunap	15
8	The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver–Russell Syndrome and Beckwith–Wiedemann Syndrome 2015 ·Genetic Testing and Molecular Biomarkers ·Mari‐Anne Vals, (unknown), Tiina Kahre, (unknown), Kai Muru, Kairit Joost, Rita Teek, Lukas Soellner, Thomas Eggermann, Katrin Õunap	7
9	Familial 1.3-Mb 11p15.5p15.4 Duplication in Three Generations Causing Silver-Russell and Beckwith-Wiedemann Syndromes 2015 ·Molecular Syndromology ·Mari‐Anne Vals, Tiina Kahre, (unknown), Kai Muru, (unknown), Olga Žilina, Vallo Tillmann, Katrin Õunap	24
10	Coffin–Siris Syndrome with obesity, macrocephaly, hepatomegaly and hyperinsulinism caused by a mutation in the ARID1B gene 2014 ·European Journal of Human Genetics ·Mari‐Anne Vals, Eve Õiglane‐Shlik, Margit Nõukas, (unknown), Aleksandr Peet, Mart Kals, (unknown), Andres Metspalu, Katrin Õunap	15
11	Follow‐up study of 2‐year‐olds born at very low gestational age in Estonia 2012 ·Acta Paediatrica ·Liis Toome, Heili Varendi, Mairi Männamaa, Mari‐Anne Vals, (unknown), Anneli Kolk	16
12	AO-03. Gestational age-related morbidity and treatment procedures in newborns born between 32 0/7 and 36 6/7 gestational weeks in Estonia 2010 ·Early Human Development ·Mari‐Anne Vals, Liis Toome, (unknown), (unknown), Heili Varendi	1
13	181: Pre-existing neoplasms and risk for malignancy after heart transplantation. Data from the Spanish Post-Heart Transplant Tumors Registry 2007 ·The Journal of Heart and Lung Transplantation ·Juan F. Delgado, (unknown), L. Alonso Pulpón, José M. Arizón, Luís Almenar, Jesús Palomo, Nicolás Manito, Gregorio Rábago, E. Lage, (unknown), Eulàlia Roig, Domingo A. Pascual‐Figal, Teresa Blasco, Luis de la Fuente, Mari‐Anne Vals, Marta Campreciós, Javier Muñiz	4
14	224 2006 ·The Journal of Heart and Lung Transplantation ·María G. Crespo‐Leiro, L. Alonso Pulpón, José M. Arizón, Luís Almenar, Juan F. Delgado, Jesús Palomo, Nicolás Manito, Gregorio Rábago, E. Lage, Beatriz Díaz, Eulàlia Roig, Domingo A. Pascual‐Figal, Teresa Blasco, Luis de la Fuente, Mari‐Anne Vals, Marta Campreciós, (unknown)	2

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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