Elizabeth Ives

2.5k total citations
28 papers, 1.5k citations indexed

About

Elizabeth Ives is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elizabeth Ives has authored 28 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elizabeth Ives's work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Prenatal Screening and Diagnostics (4 papers). Elizabeth Ives is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Prenatal Screening and Diagnostics (4 papers). Elizabeth Ives collaborates with scholars based in Canada, United States and Sweden. Elizabeth Ives's co-authors include Cheryl R. Greenberg, Michael R. Hayden, Berry Kremer, Susan E. Andrew, Jane Theilmann, Shelin Adam, Håkan Telenius, Jutta Zeisler, Y. Paul Goldberg and L. Clarke and has published in prestigious journals such as Nature Genetics, Genes & Development and Neurology.

In The Last Decade

Elizabeth Ives

26 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth Ives Canada 21 895 526 417 261 201 28 1.5k
R. J. M. Gardner New Zealand 18 766 0.9× 682 1.3× 126 0.3× 82 0.3× 356 1.8× 27 1.6k
Armand Bottani Switzerland 24 1.2k 1.4× 1.3k 2.5× 147 0.4× 178 0.7× 302 1.5× 62 2.2k
Sibel Kantarci United States 15 821 0.9× 1.0k 1.9× 142 0.3× 248 1.0× 385 1.9× 23 1.8k
Jean‐Pierre Fryns Belgium 21 1.2k 1.4× 909 1.7× 117 0.3× 206 0.8× 202 1.0× 25 2.0k
Bertrand Isidor France 26 1.3k 1.4× 908 1.7× 144 0.3× 157 0.6× 107 0.5× 112 2.1k
Brigitte Gilbert‐Dussardier France 19 636 0.7× 369 0.7× 118 0.3× 225 0.9× 63 0.3× 48 1.4k
Diana Baralle United Kingdom 24 1.8k 2.1× 761 1.4× 142 0.3× 106 0.4× 84 0.4× 84 2.7k
Jennifer L. Silhavy United States 16 1.1k 1.3× 976 1.9× 159 0.4× 96 0.4× 319 1.6× 21 1.6k
Elizabeth Roeder United States 21 1.2k 1.3× 972 1.8× 165 0.4× 216 0.8× 346 1.7× 37 1.9k
Julie Désir Belgium 19 676 0.8× 529 1.0× 72 0.2× 99 0.4× 119 0.6× 46 1.4k

Countries citing papers authored by Elizabeth Ives

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth Ives

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth Ives

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

All Works

20 of 20 papers shown
1.
Meijer, Inge A., Cynthia V. Bourassa, Nancy D. Merner, et al.. (2013). A VAMP1 Mutation Causes Chromosome 12p13 Hereditary Spastic Ataxia in Newfoundland Families (S43.002). Neurology. 80(7_supplement).
2.
Bourassa, Cynthia V., Inge A. Meijer, Nancy D. Merner, et al.. (2012). VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families. The American Journal of Human Genetics. 91(3). 548–552. 32 indexed citations
3.
Doucette, Lance P., Nancy D. Merner, Elizabeth Ives, et al.. (2008). Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15. European Journal of Human Genetics. 17(5). 554–564. 30 indexed citations
4.
Moore, S. Jo, H. Dawn Marshall, Leslie Steele, et al.. (2008). The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in Newfoundland. Clinical Genetics. 74(3). 213–222. 51 indexed citations
5.
Stefanelli, Mark, et al.. (2004). A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy. American Journal of Medical Genetics Part A. 131A(3). 249–254. 6 indexed citations
6.
Ahmed, Zubair M., Saima Riazuddin, Terry‐Lynn Young, et al.. (2004). Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan. BMC Medical Genetics. 5(1). 24–24. 28 indexed citations
7.
Meijer, Inge A., et al.. (2002). A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1,Maps to Chromosome 12p13. The American Journal of Human Genetics. 70(3). 763–769. 20 indexed citations
8.
Chong, Samuel S., E. Almqvist, H. Telenius, et al.. (1997). Contribution of DNA Sequence and CAG Size to Mutation Frequencies of Intermediate Alleles for Huntington Disease: Evidence from Single Sperm Analyses. Human Molecular Genetics. 6(2). 301–309. 92 indexed citations
9.
Ives, Elizabeth, Maryse Chalifoux, Sandra A. Farrell, et al.. (1996). Regional localization of an X-linked mental retardation gene to Xp21.1-Xp22.13 (MRX38). American Journal of Medical Genetics. 64(1). 89–96. 15 indexed citations
10.
Tonin, Patricia N., Roxana Moslehi, Roger Green, et al.. (1995). Linkage analysis of 26 Canadian breast and breast-ovarian cancer families. Human Genetics. 95(5). 545–50. 24 indexed citations
11.
Narod, Steven A., David E. Goldgar, Lisa Cannon‐Albright, et al.. (1995). Risk modifiers in carriers of brca1 mutations. International Journal of Cancer. 64(6). 394–398. 126 indexed citations
12.
Weber, Bernhard H. F., et al.. (1994). Sorsby's fundus dystrophy is genetically linked to chromosome 22q13–qter. Nature Genetics. 7(2). 158–161. 49 indexed citations
13.
Telenius, Håkan, Berry Kremer, Y. Paul Goldberg, et al.. (1994). Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm. Nature Genetics. 6(4). 409–414. 333 indexed citations
14.
Ives, Elizabeth, et al.. (1990). Monochorionic diamniotic minimally conjoined twins: A case report. American Journal of Medical Genetics. 37(4). 558–561. 20 indexed citations
15.
Stern, H., John M. Graham, Ralph S. Lachman, et al.. (1990). Atelosteogenesis type III: A distinct skeletal dysplasia with features overlapping atelosteogenesis and oto‐palato‐digital syndrome type II. American Journal of Medical Genetics. 36(2). 183–195. 30 indexed citations
16.
Hamilton, William K., Cecil C. Ewing, Elizabeth Ives, & Jean Carruthers. (1989). Sorsby's Fundus Dystrophy. Ophthalmology. 96(12). 1755–1762. 47 indexed citations
17.
Ryan, C. Anthony, Neil N. Finer, Elizabeth Ives, John M. Optiz, & James F. Reynolds. (1988). Discordance of signs in monozygotic twins concordant for the goldenhar anomaly. American Journal of Medical Genetics. 29(4). 755–761. 38 indexed citations
18.
Etches, Philip C., et al.. (1982). Familial congenital amputations. The Journal of Pediatrics. 101(3). 448–449. 36 indexed citations
19.
Ives, Elizabeth, C. Stuart Houston, & John M. Optiz. (1980). Autosomal recessive microcephaly and micromelia in Cree Indians. American Journal of Medical Genetics. 7(3). 351–360. 22 indexed citations
20.
Ives, Elizabeth. (1962). Thalidomide and Anal Abnormalities.. PubMed. 87(12). 670–2. 8 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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