Natascia Anastasio

442 total citations
8 papers, 300 citations indexed

About

Natascia Anastasio is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Natascia Anastasio has authored 8 papers receiving a total of 300 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 3 papers in Rheumatology. Recurrent topics in Natascia Anastasio's work include Metabolism and Genetic Disorders (5 papers), Porphyrin Metabolism and Disorders (3 papers) and Folate and B Vitamins Research (3 papers). Natascia Anastasio is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Porphyrin Metabolism and Disorders (3 papers) and Folate and B Vitamins Research (3 papers). Natascia Anastasio collaborates with scholars based in Canada, United States and Qatar. Natascia Anastasio's co-authors include David S. Rosenblatt, David Watkins, Junhui Liu, Tomi Pastinen, Jordan Lerner‐Ellis, Chantal F. Morel, Brian Fowler, Martin Stucki, David Coelho and Scott Gurd and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Natascia Anastasio

7 papers receiving 296 citations

Peers

Countries citing papers authored by Natascia Anastasio

Since Specialization

Citations

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

Fields of papers citing papers by Natascia Anastasio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natascia Anastasio

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis 2024 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Natascia Anastasio, Jean‐Baptiste Rivière, (unknown), Paul Goodyer, Elena Torban, Thomas M. Kitzler	0
2	Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivity 2023 ·Journal of Neurosurgery Pediatrics ·Tenzin Gayden, (unknown), (unknown), Christine Saint‐Martin, Robert Eveleigh, Mirko S. Gilardino, Natascia Anastasio, Yannis Trakadis, Angelia V. Bassenden, Albert M. Berghuis, Nada Jabado, Roy Dudley	1
3	Mitochondrial Complex III Deficiency with Ketoacidosis and Hyperglycemia Mimicking Neonatal Diabetes 2016 ·JIMD Reports ·Natascia Anastasio, Maja Tarailo‐Graovac, Reem Al Khalifah, Laurent Legault, Britt I. Drögemöller, Colin J.D. Ross, Wyeth W. Wasserman, Clara van Karnebeek, Daniela Buhaş	5
4	Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene in patients with a non-classic phenotype 2011 ·Journal of Medical Genetics ·Ahmed Alfares, (unknown), Khalid Al‐Thihli, John J. Mitchell, S. Melançon, Natascia Anastasio, Kevin Ha, Jacek Majewski, David S. Rosenblatt, Nancy Braverman	35
5	Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome 2010 ·The American Journal of Human Genetics ·Natascia Anastasio, Tawfeg Ben‐Omran, Ahmad S. Teebi, Kevin Ha, Emilie Lalonde, Rehab Ali, Mariam Al‐Mureikhi, Vazken M. Der Kaloustian, Junhui Liu, David S. Rosenblatt, Jacek Majewski, Loydie A. Jerome‐Majewska	45
6	Positive newborn screen for methylmalonic aciduria identifies the first mutation in TCblR/CD320, the gene for cellular uptake of transcobalamin-bound vitamin B12 2010 ·Human Mutation ·Edward V. Quadros, (unknown), Yasumi Nakayama, Jeffrey M. Sequeira, Luciana Hannibal, Sihe Wang, Donald W. Jacobsen, Sergey N. Fedosov, (unknown), Renata C. Gallagher, Natascia Anastasio, David Watkins, David S. Rosenblatt	49
7	Epigenetic modification of the gene for the vitamin B12 chaperone MMACHC can result in increased tumorigenicity and methionine dependence 2009 ·Molecular Genetics and Metabolism ·(unknown), Kirsten M. Niles, Natascia Anastasio, David Watkins, Josée N. Lavoie, Jordan Lerner‐Ellis, Tomi Pastinen, Jacquetta M. Trasler, David S. Rosenblatt	20
8	Spectrum of mutations inMMACHC, allelic expression, and evidence for genotypeâphenotype correlations 2009 ·Human Mutation ·Jordan Lerner‐Ellis, Natascia Anastasio, Junhui Liu, David Coelho, Terttu Suormala, Martin Stucki, (unknown), Scott Gurd, Elin Grundberg, Chantal F. Morel, David Watkins, Matthias R. Baumgartner, Tomi Pastinen, David S. Rosenblatt, Brian Fowler	145

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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