Paul B. Vrana

1.6k total citations
37 papers, 1.2k citations indexed

About

Paul B. Vrana is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Paul B. Vrana has authored 37 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 16 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Paul B. Vrana's work include Genetic Syndromes and Imprinting (16 papers), Epigenetics and DNA Methylation (14 papers) and Prenatal Screening and Diagnostics (10 papers). Paul B. Vrana is often cited by papers focused on Genetic Syndromes and Imprinting (16 papers), Epigenetics and DNA Methylation (14 papers) and Prenatal Screening and Diagnostics (10 papers). Paul B. Vrana collaborates with scholars based in United States, United Kingdom and Canada. Paul B. Vrana's co-authors include Robert S. Ingram, S M Tilghman, Michael J. O’Neill, Ward C. Wheeler, S M Tilghman, Paul G. Matteson, Michael R. Felder, Tony del Rio, Rachel J. O’Neill and John Fossella and has published in prestigious journals such as Nature Genetics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Paul B. Vrana

37 papers receiving 1.2k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Paul B. Vrana United States	19	735	649	324	169	132	37	1.2k
Melissa A. Wilson United States	20	575 0.8×	449 0.7×	165 0.5×	104 0.6×	68 0.5×	69	1.4k
Benjamin M. Skinner United Kingdom	16	643 0.9×	571 0.9×	164 0.5×	56 0.3×	34 0.3×	32	1.2k
Irene Tiemann‐Boege Austria	16	487 0.7×	552 0.9×	122 0.4×	60 0.4×	91 0.7×	40	1.2k
R. V. Short United Kingdom	25	564 0.8×	264 0.4×	102 0.3×	126 0.7×	171 1.3×	48	1.7k
Alfredo Daniel Vitullo Argentina	22	438 0.6×	486 0.7×	81 0.3×	187 1.1×	201 1.5×	85	1.6k
Matthew D. Dean United States	25	936 1.3×	479 0.7×	42 0.1×	514 3.0×	256 1.9×	44	1.7k
Annie Orth France	23	759 1.0×	435 0.7×	150 0.5×	183 1.1×	336 2.5×	39	1.2k
L. Susan Pletscher United States	26	1.2k 1.7×	440 0.7×	74 0.2×	149 0.9×	87 0.7×	42	1.8k
Elina Immonen Sweden	23	418 0.6×	194 0.3×	79 0.2×	426 2.5×	176 1.3×	39	998
Michael G. Elliot Canada	12	238 0.3×	158 0.2×	167 0.5×	94 0.6×	61 0.5×	20	715

Countries citing papers authored by Paul B. Vrana

Since Specialization

Citations

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

Fields of papers citing papers by Paul B. Vrana

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul B. Vrana. 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 Paul B. Vrana. The network helps show where Paul B. Vrana may publish in the future.

Co-authorship network of co-authors of Paul B. Vrana

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

All Works

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20 of 20 papers shown

Strong, Alanna, Caoimhe McKenna, Karen Stals, et al.. (2025). Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay. American Journal of Medical Genetics Part A. 197(10). e64119–e64119. 1 indexed citations

Bustamante, Angela C., et al.. (2019). A high methyl donor diet affects physiology and behavior in Peromyscus polionotus. Physiology & Behavior. 209. 112615–112615. 6 indexed citations

Wiedmeyer, Charles E., Janet P. Crossland, Michael J. Dewey, et al.. (2014). Hematologic and serum biochemical values of 4 species of Peromyscus mice and their hybrids.. PubMed. 53(4). 336–43. 5 indexed citations

O’Neill, Rachel J., Paul B. Vrana, & Cheryl S. Rosenfeld. (2014). Maternal methyl supplemented diets and effects on offspring health. Frontiers in Genetics. 5. 289–289. 51 indexed citations

Kenney‐Hunt, Jane P., Travis C. Glenn, Olga V. Tsyusko, et al.. (2014). A genetic map of Peromyscus with chromosomal assignment of linkage groups (a Peromyscus genetic map). Mammalian Genome. 25(3-4). 160–179. 21 indexed citations

Crossland, Janet P., et al.. (2014). Natural Genetic Variation Underlying Differences in Peromyscus Repetitive and Social/Aggressive Behaviors. Behavior Genetics. 44(2). 126–135. 15 indexed citations

Crossland, Janet P., et al.. (2012). Peromyscusas a Mammalian Epigenetic Model. PubMed. 2012. 1–11. 27 indexed citations

Hong, Jenny H., Anne C. Ferguson‐Smith, Carol Moreno, et al.. (2011). Recent acquisition of imprinting at the rodent Sfmbt2 locus correlates with insertion of a large block of miRNAs. BMC Genomics. 12(1). 204–204. 46 indexed citations

Pryor, William, et al.. (2011). The biology and methodology of assisted reproduction in deer mice (Peromyscus maniculatus). Theriogenology. 77(2). 311–319. 18 indexed citations

10.

Oriel, Roxanne C., Christopher D. Wiley, Michael J. Dewey, & Paul B. Vrana. (2008). Adaptive genetic variation, stress and glucose regulation. Disease Models & Mechanisms. 1(4-5). 255–263. 7 indexed citations

11.

Vrana, Paul B., et al.. (2007). Retrieval of Mouse Oocytes. Journal of Visualized Experiments. 185–185. 9 indexed citations

12.

Vrana, Paul B., et al.. (2007). Retrieval of Mouse Oocytes. Journal of Visualized Experiments. 1 indexed citations

13.

Nguyen, Quang K., et al.. (2007). Mapping and identification of candidate loci responsible for Peromyscus hybrid overgrowth. Mammalian Genome. 18(1). 75–85. 29 indexed citations

14.

Sikandar, Shaheen S., Mavee Witherspoon, Diana Dizon, et al.. (2007). Impaired placental trophoblast lineage differentiation in Alkbh1^−/− mice. Developmental Dynamics. 237(2). 316–327. 71 indexed citations

15.

Wiley, Christopher D., et al.. (2005). Genetic evidence for a maternal effect locus controlling genomic imprinting and growth. genesis. 43(4). 155–165. 22 indexed citations

16.

Vrana, Paul B.. (2005). Assays to Determine Allelic Usage of Gene Expression in the Placenta. Humana Press eBooks. 121. 437–448. 2 indexed citations

17.

Vrana, Paul B., John Fossella, Paul G. Matteson, et al.. (2000). Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus. Nature Genetics. 25(1). 120–124. 146 indexed citations

18.

Vrana, Paul B., et al.. (1998). Genomic imprinting is disrupted in interspecific Peromyscus hybrids. Nature Genetics. 20(4). 362–365. 157 indexed citations

19.

Vrana, Paul B. & Ward C. Wheeler. (1996). Molecular Evolution and Phylogenetic Utility of the Polyubiquitin Locus in Mammals and Higher Vertebrates. Molecular Phylogenetics and Evolution. 6(2). 259–269. 11 indexed citations

20.

Vrana, Paul B., Michel C. Milinkovitch, Jeffrey R. Powell, & Ward C. Wheeler. (1994). Higher Level Relationships of the Arctoid Carnivora Based on Sequence Data and "Total Evidence". Molecular Phylogenetics and Evolution. 3(1). 47–58. 84 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.

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