Elizabeth Spriggs

1.3k total citations
25 papers, 888 citations indexed

About

Elizabeth Spriggs is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Elizabeth Spriggs has authored 25 papers receiving a total of 888 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Reproductive Medicine. Recurrent topics in Elizabeth Spriggs's work include Sperm and Testicular Function (7 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Elizabeth Spriggs is often cited by papers focused on Sperm and Testicular Function (7 papers), Chromosomal and Genetic Variations (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Elizabeth Spriggs collaborates with scholars based in Canada, United States and France. Elizabeth Spriggs's co-authors include Renée H. Martin, Alfred Rademaker, Edmund Ko, Cheryl R. Greenberg, Diane Allingham‐Hawkins, Brian J. Schmidt, Leona Barclay, Evelyn Ko, Qinghua Shi and L. Leigh Field and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gastroenterology and PLoS ONE.

In The Last Decade

Elizabeth Spriggs

25 papers receiving 849 citations

Peers

Elizabeth Spriggs

GENET

PPCH

Brigitte Benzacken France

Sandra Chantot‐Bastaraud France

Joseph Shen United States

J. O. Van Hemel Netherlands

Susana Fernandes Portugal

Sylvie Jaillard France

Arie P.T. Smits Netherlands

György Kosztolányi Hungary

Susana Kofman‐Alfaro Mexico

Thue Bryndorf Denmark

Brigitte Benzacken France

Elizabeth Spriggs

737 ×1.6

GENET

361 ×1.2

426 ×1.5

PPCH

462 ×1.6

156 ×0.7

Citations per year, relative to Elizabeth Spriggs Elizabeth Spriggs (= 1×) peers Brigitte Benzacken

Countries citing papers authored by Elizabeth Spriggs

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth Spriggs

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth Spriggs

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth Spriggs. A scholar is included among the top collaborators of Elizabeth Spriggs 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 Elizabeth Spriggs. Elizabeth Spriggs 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

Spriggs, Elizabeth, et al.. (2021). Prenatal hydrops fetalis associated with infantile free sialic acid storage disease due to a novel homozygous deletion in the SLC17A5 gene. Molecular Case Studies. 7(5). a006106–a006106. 2 indexed citations

Mhanni, Aizeddin A., et al.. (2020). Isolated sulfite oxidase deficiency: a founder mutation. Molecular Case Studies. 6(6). a005900–a005900. 5 indexed citations

Bernstein, Çharles N., Michael Sargent, Qin Kuang, et al.. (2019). Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease. PLoS ONE. 14(6). e0217846–e0217846. 18 indexed citations

Sargent, Michael, Qin Kuang, John Wei, et al.. (2017). Genome-Wide Analysis Identifies Rare Copy Number Variations Associated with Inflammatory Bowel Disease. Gastroenterology. 152(5). S984–S984. 1 indexed citations

Dawson, Angelika J., et al.. (2015). PWS/AS MS-MLPA Confirms Maternal Origin of 15q11.2 Microduplication. SHILAP Revista de lepidopterología. 2015. 1–3. 6 indexed citations

Chudley, Albert E., et al.. (2014). A Case of an Infant With Compound Heterozygous Mutations for Hypertrophic Cardiomyopathy Producing a Phenotype of Left Ventricular Noncompaction. Canadian Journal of Cardiology. 30(10). 1249.e1–1249.e3. 7 indexed citations

Spriggs, Elizabeth, et al.. (2014). Germline mosaicism in X-linked periventricular nodular heterotopia. BMC Neurology. 14(1). 125–125. 5 indexed citations

DeSimone, Michael, Elizabeth Spriggs, Jennifer Gass, et al.. (2012). Sexual Dysfunction in Female Cancer Survivors. American Journal of Clinical Oncology. 37(1). 101–106. 61 indexed citations

Mhanni, Aziz, et al.. (2011). Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder. Seizure. 20(9). 711–712. 3 indexed citations

10.

Charames, George S., Lily Ramyar, Terri Berk, et al.. (2008). A large novel deletion in the APC promoter region causes gene silencing and leads to classical familial adenomatous polyposis in a Manitoba Mennonite kindred. Human Genetics. 124(5). 535–541. 20 indexed citations

11.

Frosk, Patrick, et al.. (2007). The Use of Ancestral Haplotypes in the Molecular Diagnosis of Familial Breast Cancer. Genetic Testing. 11(3). 208–215. 4 indexed citations

12.

Andrew, Susan E., et al.. (2002). An Intronic Polymorphism of the hMLH1 Gene Contributes Toward Incomplete Genetic Testing for HNPCC. Genetic Testing. 6(4). 319–322. 3 indexed citations

13.

Shi, Qinghua, Elizabeth Spriggs, L. Leigh Field, et al.. (2002). Absence of Age Effect on Meiotic Recombination between Human X and Y Chromosomes. The American Journal of Human Genetics. 71(2). 254–261. 34 indexed citations

14.

Shi, Qinghua, Elizabeth Spriggs, L. Leigh Field, et al.. (2001). Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm. American Journal of Medical Genetics. 99(1). 34–38. 80 indexed citations

15.

Martin, Renée H., Elizabeth Spriggs, & Alfred Rademaker. (1996). Multicolor Fluorescence in Situ Hybridization Analysis of Aneuploidy and Diploidy Frequencies in 225 846 Sperm from 10 Normal Men1. Biology of Reproduction. 54(2). 394–398. 92 indexed citations

16.

Spriggs, Elizabeth, Alfred Rademaker, & Renée H. Martin. (1995). Aneuploidy in human sperm: results of two- and three-color fluorescence in situ hybridization using centromeric probes for chromosomes 1, 12, 15, 18, X, and Y. Cytogenetic and Genome Research. 71(1). 47–53. 99 indexed citations

17.

Martin, Renée H. & Elizabeth Spriggs. (1995). Sperm chromosome complements in a man heterozygous for a reciprocal translocation 46,XY,t(9;13)(q21.1;q21.2) and a review of the literature. Clinical Genetics. 47(1). 42–46. 42 indexed citations

18.

Martin, Renée H., Elizabeth Spriggs, Edmund Ko, & Alfred Rademaker. (1995). The relationship between paternal age, sex ratios, and aneuploidy frequencies in human sperm, as assessed by multicolor FISH.. PubMed. 57(6). 1395–9. 133 indexed citations

19.

Spriggs, Elizabeth, et al.. (1994). Aneuploidy in 165,330 human sperm; results of two- and three-colour fluorescence in situ hybridization for chromosomes 1, 12, 15, 18, X, and Y. The American Journal of Human Genetics. 55. 1 indexed citations

20.

Spriggs, Elizabeth, et al.. (1994). Analysis of segregation in a human male reciprocal translocation carrier, t(1;11) (p36.3;q13.1) by two‐colour fluorescence in situ hybridization. Molecular Reproduction and Development. 38(3). 247–250. 23 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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