Julia E. VanderMeer

656 total citations
14 papers, 417 citations indexed

About

Julia E. VanderMeer is a scholar working on Molecular Biology, Developmental Biology and Genetics. According to data from OpenAlex, Julia E. VanderMeer has authored 14 papers receiving a total of 417 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Developmental Biology and 5 papers in Genetics. Recurrent topics in Julia E. VanderMeer's work include Congenital limb and hand anomalies (5 papers), Congenital heart defects research (4 papers) and Genomics and Chromatin Dynamics (4 papers). Julia E. VanderMeer is often cited by papers focused on Congenital limb and hand anomalies (5 papers), Congenital heart defects research (4 papers) and Genomics and Chromatin Dynamics (4 papers). Julia E. VanderMeer collaborates with scholars based in United States, Ireland and Canada. Julia E. VanderMeer's co-authors include Nadav Ahituv, Gill Bejerano, Aaron M. Wenger, Nicola Illing, Mandy K. Mason, Walter L. Eckalbar, Katherine S. Pollard, Bruce T. Schaar, Shoa L. Clarke and Tara Friedrich and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Development.

In The Last Decade

Julia E. VanderMeer

14 papers receiving 410 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Julia E. VanderMeer United States	13	307	124	96	54	45	14	417
Virginia Scott United States	9	232 0.8×	87 0.7×	24 0.3×	35 0.6×	58 1.3×	12	395
Gina M. Calabrese United States	14	215 0.7×	143 1.2×	8 0.1×	12 0.2×	7 0.2×	22	455
Ming Tu China	11	123 0.4×	124 1.0×	8 0.1×	5 0.1×	25 0.6×	26	320
Pieter Verdyck Belgium	12	128 0.4×	205 1.7×	9 0.1×	5 0.1×	69 1.5×	45	453
Neide Santos Brazil	13	145 0.5×	86 0.7×	6 0.1×	33 0.6×	129 2.9×	36	347
Brian Bunke United States	4	99 0.3×	173 1.4×	10 0.1×	3 0.1×	41 0.9×	4	207
Friedel Wenzel Switzerland	11	136 0.4×	164 1.3×	5 0.1×	11 0.2×	24 0.5×	21	341
Vicki J. Swier United States	12	106 0.3×	81 0.7×	13 0.1×	5 0.1×	59 1.3×	27	501
Andrew T. Major Australia	15	340 1.1×	348 2.8×	3 0.0×	10 0.2×	24 0.5×	28	637
Malcolm Ferguson-Smith United Kingdom	11	222 0.7×	312 2.5×	10 0.1×	5 0.1×	249 5.5×	16	548

Countries citing papers authored by Julia E. VanderMeer

Since Specialization

Citations

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

Fields of papers citing papers by Julia E. VanderMeer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julia E. VanderMeer. 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 Julia E. VanderMeer. The network helps show where Julia E. VanderMeer may publish in the future.

Co-authorship network of co-authors of Julia E. VanderMeer

This figure shows the co-authorship network connecting the top 25 collaborators of Julia E. VanderMeer. A scholar is included among the top collaborators of Julia E. VanderMeer 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 Julia E. VanderMeer. Julia E. VanderMeer 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

Friedrich, Tara, Mandy K. Mason, Julia E. VanderMeer, et al.. (2016). Bat Accelerated Regions Identify a Bat Forelimb Specific Enhancer in the HoxD Locus. PLoS Genetics. 12(3). e1005738–e1005738. 47 indexed citations

Eckalbar, Walter L., Stephen A. Schlebusch, Mandy K. Mason, et al.. (2016). Transcriptomic and epigenomic characterization of the developing bat wing. Nature Genetics. 48(5). 528–536. 56 indexed citations

VanderMeer, Julia E., Tonia C. Carter, Faith Pangilinan, et al.. (2016). Evaluation of proton‐coupled folate transporter (SLC46A1) polymorphisms as risk factors for neural tube defects and oral clefts. American Journal of Medical Genetics Part A. 170(4). 1007–1016. 5 indexed citations

VanderMeer, Julia E., et al.. (2014). Genome-wide identification of signaling center enhancers in the developing limb. Development. 141(21). 4194–4198. 15 indexed citations

VanderMeer, Julia E., Reymundo Lozano, Miao Sun, et al.. (2014). A Novel ZRS Mutation Leads to Preaxial Polydactyly Type 2 in a Heterozygous Form and Werner Mesomelic Syndrome in a Homozygous Form. Human Mutation. 35(8). 945–948. 24 indexed citations

Laurell, Tobias, Daniel Nilsson, Wolfgang Hofmeister, et al.. (2014). Identification of three novelFGF16mutations in X‐linked recessive fusion of the fourth and fifth metacarpals and possible correlation with heart disease. Molecular Genetics & Genomic Medicine. 2(5). 402–411. 14 indexed citations

Clarke, Shoa L., Julia E. VanderMeer, Aaron M. Wenger, et al.. (2012). Human Developmental Enhancers Conserved between Deuterostomes and Protostomes. PLoS Genetics. 8(8). e1002852–e1002852. 49 indexed citations

VanderMeer, Julia E., et al.. (2012). A novel ZRS mutation in a Balochi tribal family with triphalangeal thumb, pre‐axial polydactyly, post‐axial polydactyly, and syndactyly. American Journal of Medical Genetics Part A. 158A(8). 2031–2035. 12 indexed citations

Bacino, Carlos A., B. Stephens Richards, Christine M. Alvarez, et al.. (2012). Studies of TBX4 and chromosome 17q23.1q23.2: An uncommon cause of nonsyndromic clubfoot. American Journal of Medical Genetics Part A. 158A(7). 1620–1627. 33 indexed citations

10.

Laurell, Tobias, Julia E. VanderMeer, Aaron M. Wenger, et al.. (2012). A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb. Human Mutation. 33(7). 1063–1066. 28 indexed citations

11.

VanderMeer, Julia E. & Nadav Ahituv. (2011). cis‐regulatory mutations are a genetic cause of human limb malformations. Developmental Dynamics. 240(5). 920–930. 58 indexed citations

12.

Pangilinan, Faith, Adam Mitchell, Julia E. VanderMeer, et al.. (2010). Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects. Journal of Medical Genetics. 47(10). 677–685. 33 indexed citations

13.

Carter, Tonia C., Faith Pangilinan, James Troendle, et al.. (2010). Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population. American Journal of Medical Genetics Part A. 155(1). 14–21. 30 indexed citations

14.

Ganoza, M. Clelia, et al.. (1973). Mechanism of Protein Chain Termination: Further Characterization of a Mutant Defective in a New Protein Synthesis Factor. Proceedings of the National Academy of Sciences. 70(1). 31–35. 13 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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