Julia Parrish

2.1k citations

19 papers · 695 indexed · h-index 13

Impact in

Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
Molecular Biology
- RNA modifications and cancer
- RNA regulation and disease
- Genomics and Chromatin Dynamics

Papers in ⓘ

Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Genetic and rare skin diseases. 3
Molecular Biology 15
- RNA regulation and disease 4
- Genomics and Chromatin Dynamics 3
- RNA Research and Splicing 3
- Hedgehog Signaling Pathway Studies 2
- Nuclear Structure and Function 2

Co-authors: David L. Nelson (2 shared papers)Ben A. Oostra (1 shared paper)Aimee S. Spikes (1 shared paper)James B. Reynolds (1 shared paper)C. Sue Richards (1 shared paper)Annemieke J.M.H. Verkerk (1 shared paper)Lisa G. Shaffer (1 shared paper)Dan E. Wells (4 shared papers)
Journals: Genomics (5 papers)Human Molecular Genetics (4 papers)Human Mutation (2 papers)Nature Genetics (1 paper)Cytokine (1 paper)
Partner nations: United States Germany United Kingdom

In The Last Decade

Julia Parrish

19 papers receiving 678 citations

Peers

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-authors

The 25 scholars most cited alongside Julia Parrish, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Julia Parrish Line = papers co-authored together Julia Parrish links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE Nature Genetics ·Julia Parrish, Ben A. Oostra, Annemieke J.M.H. Verkerk, C. Sue Richards, James B. Reynolds, Aimee S. Spikes, Lisa G. Shaffer, David L. Nelson	1994	142
2	Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome Human Molecular Genetics ·H.-J. Lüdecke, M.J. Wagner, J. Nardmann, Biagio La Pillo, Julia Parrish, Patrick J. Willems, E Haan, Moshe Frydman, Guus Hamers, D. E.Weils, Bernhard Horsthemke	1995	95
3	Selection against mutant alleles in blood leukocytes is a consistent feature in Incontinentia Pigmenti type 2 Human Molecular Genetics ·Julia Parrish	1996	87
4	Human chromosome 8 linkage map based on short tandem repeat polymorphisms: Effect of genotyping errors Genomics ·James Tomfohrde, Stephen Wood, Michael Schertzer, Michael Wagner, Dan E. Wells, Julia Parrish, Lori A. Sadler, Susan H. Blanton, Stephen P. Daiger, Zhenyuan Wang, Patricia J. Wilkie, James L. Weber	1992	59
5	A muscle-specific DNase I-like gene in human Xq28 Human Molecular Genetics ·Julia Parrish, Alfredo Ciccodicola, Manfred Wehnert, Gerald F. Cox, Ellson Chen, David Lee Nelson	1995	48
6	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 ·Angus C. Wilson, Julia Parrish, Hillary F. Massa, David L. Nelson, Barbara J. Trask, Winship Herr	1995	40
7	A 4-Megabase YAC Contig That Spans the Langer-Giedion Syndrome Region on Human Chromosome 8q24.1: Use in Refining the Location of the Trichorhinophalangeal Syndrome and Multiple Exostoses Genes (TRPS1 and EXT1) Genomics ·Jiakai Hou, Julia Parrish, H.‐J. Lüdecke, M. Sapru, Y. Wang, Wen‐Shan Chen, April Hill, J. Siegel‐Bartelt, Hope Northrup, Frederick F.B. Elder, Craig Chinault, Bernhard Horsthemke, M.J. Wagner, Dan E. Wells	1995	39
8	Diagnostic utility of APOE, soluble CD40, CD40L, and Aβ1–40 levels in plasma in Alzheimer’s disease Cytokine ·Ghania Ait‐Ghezala, Laila Abdullah, Claude‐Henry Volmar, Daniel Paris, Cheryl A. Luis, Amita Quadros, Benoit Mouzon, Myles Mullan, Andrew P. Keegan, Julia Parrish, Fiona Crawford, Venkatarajan S. Mathura, Michael Mullan	2008	36
9	The influence of diagnosis, intra- and inter-person variability on serum and plasma Aβ levels Neuroscience Letters ·Laila Abdullah, Daniel Paris, Cheryl A. Luis, Amita Quadros, Julia Parrish, Luís Valdés, Andrew P. Keegan, Venkatarajan S. Mathura, Fiona Crawford, Michael Mullan	2007	32
10	MSG1(Melanocyte-Specific Gene 1): Mapping to Chromosome Xq13.1, Genomic Organization, and Promoter Analysis Genomics ·Martin Fenner, Julia Parrish, Yvonne Boyd, Vivienne Reed, Marcy E. MacDonald, David L. Nelson, Kurt J. Isselbacher, Toshi Shioda	1998	23
11	Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion syndrome Genomics ·Julia Parrish, Michael J. Wagner, Jacqueline T. Hecht, Charles I. Scott, Dan E. Wells	1991	23
12	High Serum Aβ and Vascular Risk Factors in First-Degree Relatives of Alzheimer’s Disease Patients Molecular Medicine ·Laila Abdullah, Cheryl A. Luis, Daniel Paris, Ghania Ait‐Ghezala, Benoit Mouzon, Elizabeth Allen, Julia Parrish, Myles Mullan, Scott Ferguson, Marcie Wood, Fiona Crawford, Michael Mullan	2009	15
13	Methods for finding genes a major rate-limiting step in positional cloning Genetic Analysis Biomolecular Engineering ·Julia Parrish, David L. Nelson	1993	15
14	Six novel mutations in the emerin gene causing X‐linked Emery‐Dreifuss muscular dystrophy Human Mutation ·K. Wulff, Julia Parrish, F. H. Herrmann, Manfred Wehnert	1997	12
15	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 ·Arnab Chatterjee, Toshihiro Tanaka, Julia Parrish, Gail E. Herman	1995	10
16	Regional assignment of 19 X-linked ESTs Human Molecular Genetics ·Julia Parrish, David L. Nelson	1993	10
17	Alignment of physical and genetic maps of human 8q23-qter using somatic cell hybrid mapping panel Somatic Cell and Molecular Genetics ·Julia Parrish, Yang Wang, Michael J. Wagner, Dan E. Wells	1994	6
18	Six novel mutations in the emerin gene causing X‐linked Emery‐Dreifuss muscular dystrophy Human Mutation ·K. Wulff, Julia Parrish, Falko H. Herrmann, Manfred Wehnert	1997	2
19	ABCL-312: Survival Outcomes of Primary Intraocular Lymphoma Clinical Lymphoma Myeloma & Leukemia ·Shehab Mohamed, Maliha Khan, Julia Parrish, Patricia Chevez Barrios, Bouthinia Dabaja, Nathan Fowler, Dan S. Gombos, Lei Feng, Saminathan Iyer	2021	1

About Julia Parrish

Julia Parrish is a scholar working on Genetics, Molecular Biology, Cell Biology, Neurology and Physiology, having authored 19 papers that have together received 695 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), RNA regulation and disease (4 papers), Alzheimer's disease research and treatments (3 papers), Genomics and Chromatin Dynamics (3 papers), RNA Research and Splicing (3 papers), Genetic and rare skin diseases. (3 papers), Hedgehog Signaling Pathway Studies (2 papers) and Nuclear Structure and Function (2 papers). The work is most often cited by research in Genetics (348 citations), Molecular Biology (414 citations), Oral Surgery (42 citations), Rheumatology (63 citations) and Cancer Research (55 citations). Julia Parrish has collaborated with scholars based in United States, Germany and United Kingdom. Frequent co-authors include David L. Nelson, Ben A. Oostra, Aimee S. Spikes, James B. Reynolds, C. Sue Richards, Annemieke J.M.H. Verkerk, Lisa G. Shaffer, Dan E. Wells, Manfred Wehnert and Bernhard Horsthemke. Their work appears in journals such as Genomics, Human Molecular Genetics, Human Mutation, Nature Genetics and Cytokine.

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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