Julie D. Sharp

1.3k total citations
13 papers, 980 citations indexed

About

Julie D. Sharp is a scholar working on Physiology, Cell Biology and Molecular Biology. According to data from OpenAlex, Julie D. Sharp has authored 13 papers receiving a total of 980 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Physiology, 6 papers in Cell Biology and 4 papers in Molecular Biology. Recurrent topics in Julie D. Sharp's work include Lysosomal Storage Disorders Research (11 papers), Cellular transport and secretion (6 papers) and Glycosylation and Glycoproteins Research (3 papers). Julie D. Sharp is often cited by papers focused on Lysosomal Storage Disorders Research (11 papers), Cellular transport and secretion (6 papers) and Glycosylation and Glycoproteins Research (3 papers). Julie D. Sharp collaborates with scholars based in United Kingdom, Finland and United States. Julie D. Sharp's co-authors include Ruth B. Wheeler, Sara Mole, Ruth Williams, Roger A. Schultz, John M. Joslin, Hans H. Goebel, Liina Lonka, Anna‐Elina Lehesjoki, Susanna Ranta and Anne Messer and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Molecular Psychiatry.

In The Last Decade

Julie D. Sharp

13 papers receiving 937 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Julie D. Sharp United Kingdom	11	655	382	354	165	126	13	980
Erin Feeney United States	6	242 0.4×	76 0.2×	129 0.4×	80 0.5×	89 0.7×	8	511
Tam Quach France	15	95 0.1×	147 0.4×	373 1.1×	25 0.2×	22 0.2×	25	862
Ana Djarmati Germany	19	162 0.2×	121 0.3×	499 1.4×	30 0.2×	19 0.2×	29	1.3k
Tim Van Langenhove Belgium	11	339 0.5×	48 0.1×	316 0.9×	93 0.6×	10 0.1×	23	1.1k
Joseph Vithayathil United States	8	123 0.2×	90 0.2×	213 0.6×	12 0.1×	8 0.1×	12	473
Milena Laure‐Kamionowska Poland	13	103 0.2×	53 0.1×	342 1.0×	21 0.1×	12 0.1×	46	782
Fumihiko Fukamauchi Japan	14	66 0.1×	193 0.5×	380 1.1×	50 0.3×	19 0.2×	40	808
Hiroaki Kawasaki Japan	15	62 0.1×	40 0.1×	398 1.1×	102 0.6×	10 0.1×	43	766
Natalie Landeck Sweden	13	267 0.4×	205 0.5×	241 0.7×	11 0.1×	5 0.0×	18	919
Hendrik Luuk Estonia	17	91 0.1×	272 0.7×	318 0.9×	15 0.1×	6 0.0×	34	652

Countries citing papers authored by Julie D. Sharp

Since Specialization

Citations

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

Fields of papers citing papers by Julie D. Sharp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julie D. Sharp. 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 Julie D. Sharp. The network helps show where Julie D. Sharp may publish in the future.

Co-authorship network of co-authors of Julie D. Sharp

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

All Works

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13 of 13 papers shown

Mole, Sara, Grégoire Michaux, Sandra Codlin, et al.. (2004). CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein. Experimental Cell Research. 298(2). 399–406. 87 indexed citations

Sharp, Julie D., Ruth B. Wheeler, Keith A. Parker, et al.. (2003). Spectrum ofCLN6mutations in variant late infantile neuronal ceroid lipofuscinosis. Human Mutation. 22(1). 35–42. 60 indexed citations

Wheeler, Ruth B., Julie D. Sharp, Roger A. Schultz, et al.. (2002). The Gene Mutated in Variant Late-Infantile Neuronal Ceroid Lipofuscinosis (CLN6) and in nclf Mutant Mice Encodes a Novel Predicted Transmembrane Protein. The American Journal of Human Genetics. 70(2). 537–542. 151 indexed citations

Mitchell, Wayne, Ruth B. Wheeler, Julie D. Sharp, et al.. (2001). Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8. European Journal of Paediatric Neurology. 5. 21–27. 39 indexed citations

Sharp, Julie D., Ruth B. Wheeler, Roger A. Schultz, et al.. (2001). Analysis of candidate genes in the CLN6 critical regionusing in silico cloning. European Journal of Paediatric Neurology. 5. 29–31. 4 indexed citations

Curran, Sarah, Jonathan Mill, Eda Tahir Turanlı, et al.. (2001). Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples. Molecular Psychiatry. 6(4). 425–428. 125 indexed citations

Mill, Jonathan, Sarah Curran, Lindsey Kent, et al.. (2001). Attention deficit hyperactivity disorder (ADHD) and the dopamine D4 receptor gene: evidence of association but no linkage in a UK sample. Molecular Psychiatry. 6(4). 440–444. 59 indexed citations

Sharp, Julie D., et al.. (1999). Genetic and Physical Mapping of theCLN6Gene on Chromosome 15q21–23. Molecular Genetics and Metabolism. 66(4). 329–331. 18 indexed citations

Ranta, Susanna, Barbara Ross, Liina Lonka, et al.. (1999). The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Nature Genetics. 23(2). 233–236. 247 indexed citations

10.

Wheeler, Ruth B., Julie D. Sharp, Wayne Mitchell, et al.. (1999). A New Locus for Variant Late Infantile Neuronal Ceroid Lipofuscinosis—CLN7. Molecular Genetics and Metabolism. 66(4). 337–338. 43 indexed citations

11.

Goebel, Hans H. & Julie D. Sharp. (1998). The Neuronal Ceroid‐Lipofuscinoses. Recent Advances. Brain Pathology. 8(1). 151–162. 50 indexed citations

12.

Sharp, Julie D., Minna Savukoski, Ruth B. Wheeler, et al.. (1995). Linkage analysis of late‐infantile neuronal ceroid‐lipofuscinosis. American Journal of Medical Genetics. 57(2). 348–349. 5 indexed citations

13.

Savukoski, Minna, Marjo Kestilä, Irma Järvelä, et al.. (1994). Defined chromosomal assignment of CLN5 demonstrates that at least four genetic loci are involved in the pathogenesis of human ceroid lipofuscinoses.. PubMed. 55(4). 695–701. 92 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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