Phyllis Frosst

8.9k total citations · 2 hit papers
12 papers, 2.6k citations indexed

About

Phyllis Frosst is a scholar working on Rheumatology, Surgery and Molecular Biology. According to data from OpenAlex, Phyllis Frosst has authored 12 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Rheumatology, 5 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in Phyllis Frosst's work include Folate and B Vitamins Research (8 papers), Esophageal and GI Pathology (3 papers) and Metabolism and Genetic Disorders (3 papers). Phyllis Frosst is often cited by papers focused on Folate and B Vitamins Research (8 papers), Esophageal and GI Pathology (3 papers) and Metabolism and Genetic Disorders (3 papers). Phyllis Frosst collaborates with scholars based in United States, Canada and Netherlands. Phyllis Frosst's co-authors include Rima Rozen, Henk J. Blom, Lambertus P. van den Heuvel, Rima Rozen, Philippe Goyette, Régine P.M. Steegers‐Theunissen, Michelle Heyer, David S. Rosenblatt, T.K.A.B. Eskes and Edwin C.M. Mariman and has published in prestigious journals such as The Lancet, Circulation and The Journal of Cell Biology.

In The Last Decade

Phyllis Frosst

12 papers receiving 2.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1995 715 citations F. Trijbels, Lambertus P. van den Heuvel et al. The Lancet profile →
Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

1996 542 citations Leo A. J. Kluijtmans, Lambertus P. van den Heuvel et al. PubMed profile →

Peers

Countries citing papers authored by Phyllis Frosst

Since Specialization

Citations

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

Fields of papers citing papers by Phyllis Frosst

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Phyllis Frosst

This figure shows the co-authorship network connecting the top 25 collaborators of Phyllis Frosst. A scholar is included among the top collaborators of Phyllis Frosst 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 Phyllis Frosst. Phyllis Frosst 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:

12 of 12 papers shown

#	Work	Indexed citations
1	Karyopherin binding interactions and nuclear import mechanism of nuclear pore complex protein Tpr 2009 ·BMC Cell Biology ·Iris Ben‐Efraim, Phyllis Frosst, Larry Gerace	28
2	At-home genetic tests. 2006 ·PubMed ·Phyllis Frosst, (unknown)	2
3	The curly-tail (ct) mouse, an animal model of neural tube defects, displays altered homocysteine metabolism without folate responsiveness or a defect in Mthfr 2002 ·Molecular Genetics and Metabolism ·Pamela V. Tran, (unknown), Phyllis Frosst, Suzanne Lussier‐Cacan, Pamela J. Bagley, Jacob Selhub, Teodoro Bottiglieri, Rima Rozen	7
4	Tpr is localized within the nuclear basket of the pore complex and has a role in nuclear protein export 2002 ·The Journal of Cell Biology ·Phyllis Frosst, Tinglu Guan, (unknown), Klaus M. Hahn, Larry Gerace	143
5	Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR) 1998 ·Mammalian Genome ·Philippe Goyette, (unknown), (unknown), Phyllis Frosst, Pamela V. Tran, Zhoutao Chen, Manuel Chan, Rima Rozen	288
6	Correlation of a Common Mutation in the Methylenetetrahydrofolate Reductase Gene With Plasma Homocysteine in Patients With Premature Coronary Artery Disease 1997 ·Arteriosclerosis Thrombosis and Vascular Biology ·Benedicte Christensen, Phyllis Frosst, Suzanne Lussier‐Cacan, Jacob Selhub, Philippe Goyette, David S. Rosenblatt, Jacques Genest, Rima Rozen	199
7	The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse Chromosome 4 1996 ·Mammalian Genome ·Phyllis Frosst, (unknown), (unknown), Rima Rozen	10
8	Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. breakdown → 1996 ·PubMed ·Leo A. J. Kluijtmans, Lambertus P. van den Heuvel, G. H. J. Boers, Phyllis Frosst, (unknown), Bernard A. van Oost, Martin den Heijer, Frans J.M. Trijbels, Rima Rozen, Henk J. Blom	542
9	Methylenetetrahydrofolate Reductase Polymorphism, Plasma Folate, Homocysteine, and Risk of Myocardial Infarction in US Physicians 1996 ·Circulation ·Jing Ma, Meir J. Stampfer, Charles H. Hennekens, Phyllis Frosst, Jacob Selhub, (unknown), M.R. Malinow, Walter C. Willett, Rima Rozen	417
10	Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida breakdown → 1995 ·The Lancet ·(unknown), F. Trijbels, Lambertus P. van den Heuvel, Henk J. Blom, Régine P.M. Steegers‐Theunissen, T.K.A.B. Eskes, Edwin C.M. Mariman, Michelle Heyer, Phyllis Frosst, Rima Rozen	715
11	Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida [short report] 1995 ·N.M.J. van der Put, Régine P.M. Steegers‐Theunissen, Phyllis Frosst, J. M. F. Trijbels, T.K.A.B. Eskes, Michelle Heyer, Rima Rozen, Henk J. Blom	76
12	Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency. 1995 ·PubMed ·Philippe Goyette, Phyllis Frosst, David S. Rosenblatt, Rima Rozen	213

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