Julia Parrish

2.1k total citations
19 papers, 695 citations indexed

About

Julia Parrish is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Julia Parrish has authored 19 papers receiving a total of 695 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Julia Parrish's work include Genomic variations and chromosomal abnormalities (6 papers), RNA regulation and disease (4 papers) and Alzheimer's disease research and treatments (3 papers). Julia Parrish is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), RNA regulation and disease (4 papers) and Alzheimer's disease research and treatments (3 papers). Julia Parrish collaborates with scholars based in United States, Germany and United Kingdom. Julia Parrish's co-authors include David L. Nelson, Lisa G. Shaffer, James B. Reynolds, Ben A. Oostra, Aimee S. Spikes, Annemieke J.M.H. Verkerk, C. Sue Richards, Dan E. Wells, Manfred Wehnert and Bernhard Horsthemke and has published in prestigious journals such as Nature Genetics, Human Molecular Genetics and Genomics.

In The Last Decade

Julia Parrish

19 papers receiving 678 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julia Parrish United States 13 414 348 71 63 57 19 695
Jennifer E. Posey United States 16 481 1.2× 394 1.1× 29 0.4× 41 0.7× 54 0.9× 61 813
Bianca Miterski Germany 14 299 0.7× 90 0.3× 73 1.0× 89 1.4× 160 2.8× 19 778
Véronique Geoffroy France 12 559 1.4× 510 1.5× 14 0.2× 58 0.9× 64 1.1× 17 775
Pauline Terhal Netherlands 18 574 1.4× 632 1.8× 33 0.5× 38 0.6× 79 1.4× 28 1.0k
Tadashi Kaname Japan 14 436 1.1× 249 0.7× 66 0.9× 36 0.6× 43 0.8× 96 729
Sahar Mansour United Kingdom 11 575 1.4× 288 0.8× 63 0.9× 65 1.0× 43 0.8× 15 854
Soo‐Mi Park United Kingdom 15 464 1.1× 258 0.7× 25 0.4× 27 0.4× 43 0.8× 39 794
Sigrid Fuchs Germany 16 584 1.4× 148 0.4× 75 1.1× 19 0.3× 69 1.2× 35 790
Nisha Patel Saudi Arabia 17 428 1.0× 267 0.8× 51 0.7× 43 0.7× 69 1.2× 39 727
Grace M. Hobson United States 23 851 2.1× 297 0.9× 39 0.5× 46 0.7× 85 1.5× 42 1.2k

Countries citing papers authored by Julia Parrish

Since Specialization
Citations

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

Fields of papers citing papers by Julia Parrish

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julia Parrish

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

All Works

19 of 19 papers shown
1.
Mohamed, Shehab, et al.. (2021). ABCL-312: Survival Outcomes of Primary Intraocular Lymphoma. Clinical Lymphoma Myeloma & Leukemia. 21. S389–S390. 1 indexed citations
2.
Abdullah, Laila, Cheryl A. Luis, Daniel Paris, et al.. (2009). High Serum Aβ and Vascular Risk Factors in First-Degree Relatives of Alzheimer’s Disease Patients. Molecular Medicine. 15(3-4). 95–100. 15 indexed citations
3.
Ait‐Ghezala, Ghania, Laila Abdullah, Claude‐Henry Volmar, et al.. (2008). Diagnostic utility of APOE, soluble CD40, CD40L, and Aβ1–40 levels in plasma in Alzheimer’s disease. Cytokine. 44(2). 283–287. 36 indexed citations
4.
Abdullah, Laila, Daniel Paris, Cheryl A. Luis, et al.. (2007). The influence of diagnosis, intra- and inter-person variability on serum and plasma Aβ levels. Neuroscience Letters. 428(2-3). 53–58. 32 indexed citations
5.
Fenner, Martin, Julia Parrish, Yvonne Boyd, et al.. (1998). MSG1(Melanocyte-Specific Gene 1): Mapping to Chromosome Xq13.1, Genomic Organization, and Promoter Analysis. Genomics. 51(3). 401–407. 23 indexed citations
6.
Wulff, K., Julia Parrish, F. H. Herrmann, & Manfred Wehnert. (1997). Six novel mutations in the emerin gene causing X‐linked Emery‐Dreifuss muscular dystrophy. Human Mutation. 9(6). 526–530. 12 indexed citations
7.
Wulff, K., Julia Parrish, Falko H. Herrmann, & Manfred Wehnert. (1997). Six novel mutations in the emerin gene causing X‐linked Emery‐Dreifuss muscular dystrophy. Human Mutation. 9(6). 526–530. 2 indexed citations
8.
Parrish, Julia. (1996). Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti type 2. Human Molecular Genetics. 5(11). 1777–1783. 87 indexed citations
9.
10.
Wilson, Angus C., Julia Parrish, Hillary F. Massa, et al.. (1995). The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney. Genomics. 25(2). 462–468. 40 indexed citations
11.
Chatterjee, Arnab, Toshihiro Tanaka, Julia Parrish, & Gail E. Herman. (1995). Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X Chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions. Mammalian Genome. 6(11). 802–804. 10 indexed citations
12.
Lüdecke, H.-J., M.J. Wagner, Julia Parrish, et al.. (1995). Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome. Human Molecular Genetics. 4(1). 31–36. 95 indexed citations
13.
Parrish, Julia, Alfredo Ciccodicola, Manfred Wehnert, et al.. (1995). A muscle-specific DNase I-like gene in human Xq28. Human Molecular Genetics. 4(9). 1557–1564. 48 indexed citations
14.
Parrish, Julia, Ben A. Oostra, Annemieke J.M.H. Verkerk, et al.. (1994). Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE. Nature Genetics. 8(3). 229–235. 142 indexed citations
15.
Parrish, Julia, Yang Wang, Michael J. Wagner, & Dan E. Wells. (1994). Alignment of physical and genetic maps of human 8q23-qter using somatic cell hybrid mapping panel. Somatic Cell and Molecular Genetics. 20(2). 143–146. 6 indexed citations
16.
Parrish, Julia & David L. Nelson. (1993). Regional assignment of 19 X-linked ESTs. Human Molecular Genetics. 2(11). 1901–1905. 10 indexed citations
17.
Parrish, Julia & David L. Nelson. (1993). Methods for finding genes a major rate-limiting step in positional cloning. Genetic Analysis Biomolecular Engineering. 10(2). 29–41. 15 indexed citations
18.
Tomfohrde, James, Stephen Wood, Michael Schertzer, et al.. (1992). Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors. Genomics. 14(1). 144–152. 59 indexed citations
19.
Parrish, Julia, Michael J. Wagner, Jacqueline T. Hecht, Charles I. Scott, & Dan E. Wells. (1991). Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome. Genomics. 11(1). 54–61. 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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