E K Pivnick

628 total citations
14 papers, 422 citations indexed

About

E K Pivnick is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, E K Pivnick has authored 14 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Neurology. Recurrent topics in E K Pivnick's work include Genomic variations and chromosomal abnormalities (4 papers), RNA regulation and disease (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). E K Pivnick is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), RNA regulation and disease (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). E K Pivnick collaborates with scholars based in United States and India. E K Pivnick's co-authors include R. Sid Wilroy, Avirachan T. Tharapel, Gopalrao V.N. Velagaleti, Robert Tipton, Robert A. Kaufman, Susan R. Rose, M E Beth Smith, Mazin Β. Qumsiyeh, J. William Langston and John O. Glass and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Neuroradiology and Journal of Medical Genetics.

In The Last Decade

E K Pivnick

14 papers receiving 409 citations

Peers

E K Pivnick

GENET

NEURO

SURGE

EPIDE

Heather J. Stalker United States

Axel Bohring Germany

Lidia Pezzani Italy

Smita M. Purandare United States

E Tarantino Italy

N S Thomas United Kingdom

B C Davison United Kingdom

Duane Superneau United States

Mark J. Stephan United States

Donna L. Daentl United States

Heather J. Stalker United States

E K Pivnick

277 ×1.4

GENET

272 ×1.6

45 ×0.4

NEURO

78 ×0.9

SURGE

43 ×0.7

EPIDE

Citations per year, relative to E K Pivnick E K Pivnick (= 1×) peers Heather J. Stalker

Countries citing papers authored by E K Pivnick

Since Specialization

Citations

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

Fields of papers citing papers by E K Pivnick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E K Pivnick

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

Thompson, Jerome W., et al.. (2013). Imaging of Acute Invasive Fungal Rhinosinusitis in a Patient with Gorlin Syndrome and Acute Lymphocytic Leukemia. SHILAP Revista de lepidopterología. 2013. 1–4. 4 indexed citations

Steen, R. Grant, J S Taylor, J. William Langston, et al.. (2001). Prospective evaluation of the brain in asymptomatic children with neurofibromatosis type 1: relationship of macrocephaly to T1 relaxation changes and structural brain abnormalities.. American Journal of Neuroradiology. 22(5). 810–7. 60 indexed citations

Pivnick, E K, et al.. (1998). Infant with midline thoracoabdominal schisis and limb defects. Teratology. 58(5). 205–208. 41 indexed citations

Kaste, Sue C. & E K Pivnick. (1998). Bony orbital morphology in neurofibromatosis type 1 (NF1).. Journal of Medical Genetics. 35(8). 628–631. 12 indexed citations

Pivnick, E K, et al.. (1998). Infant with midline thoracoabdominal schisis and limb defects. Teratology. 58(5). 205–208. 4 indexed citations

Michaelis, Ron C., Gopalrao V.N. Velagaleti, Christopher T. Jones, et al.. (1998). Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B.. PubMed. 76(3). 222–8. 37 indexed citations

Pivnick, E K, et al.. (1998). Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation.. Journal of Medical Genetics. 35(4). 328–332. 31 indexed citations

Pivnick, E K, et al.. (1998). Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patients.. Journal of Medical Genetics. 35(10). 813–820. 57 indexed citations

Michaelis, Ron C., Gopalrao V.N. Velagaleti, Christopher T. Jones, et al.. (1998). Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B. American Journal of Medical Genetics. 76(3). 222–228. 34 indexed citations

10.

Pivnick, E K, et al.. (1996). Hypertrichosis, pigmentary retinopathy, and facial anomalies: A new syndrome?. American Journal of Medical Genetics. 62(4). 386–390. 10 indexed citations

11.

Pivnick, E K, R. Sid Wilroy, M E Beth Smith, et al.. (1996). Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.. Journal of Medical Genetics. 33(9). 772–778. 62 indexed citations

12.

Pivnick, E K, et al.. (1996). Gorlin syndrome associated with midline nasal dermoid cyst.. Journal of Medical Genetics. 33(8). 704–706. 7 indexed citations

13.

Pivnick, E K, et al.. (1992). Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesis. Human Genetics. 90(3). 308–10. 16 indexed citations

14.

Pivnick, E K, et al.. (1990). Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome.. Journal of Medical Genetics. 27(8). 523–526. 47 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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