Ann Harris

2.2k total citations
31 papers, 1.1k citations indexed

About

Ann Harris is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Ann Harris has authored 31 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 10 papers in Pulmonary and Respiratory Medicine and 9 papers in Genetics. Recurrent topics in Ann Harris's work include Cystic Fibrosis Research Advances (6 papers), Glycosylation and Glycoproteins Research (5 papers) and Cell Adhesion Molecules Research (5 papers). Ann Harris is often cited by papers focused on Cystic Fibrosis Research Advances (6 papers), Glycosylation and Glycoproteins Research (5 papers) and Cell Adhesion Molecules Research (5 papers). Ann Harris collaborates with scholars based in United Kingdom, United States and India. Ann Harris's co-authors include Colm J. Reid, Stephen J. Gould, John P. Russell, Nita H. Salzman, Ralph J. DeBerardinis, Charles Bevins, Eduardo D. Ruchelli, Susan H. Bernacki, Scott H. Randell and Andrew Nelson and has published in prestigious journals such as Journal of Biological Chemistry, Biochemical Journal and The American Journal of Human Genetics.

In The Last Decade

Ann Harris

31 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ann Harris United Kingdom 18 569 311 187 184 166 31 1.1k
Hassan Lemjabbar United States 11 440 0.8× 381 1.2× 184 1.0× 200 1.1× 80 0.5× 11 1.2k
RT Parmley United States 13 355 0.6× 86 0.3× 370 2.0× 111 0.6× 264 1.6× 23 974
Christine T. N. Pham United States 8 403 0.7× 219 0.7× 748 4.0× 123 0.7× 70 0.4× 11 1.5k
Jean Willems Belgium 15 658 1.2× 144 0.5× 705 3.8× 135 0.7× 210 1.3× 25 1.3k
Rosa Ten United States 20 390 0.7× 212 0.7× 741 4.0× 295 1.6× 105 0.6× 28 1.5k
Jonathan G. Lieber United States 11 477 0.8× 139 0.4× 469 2.5× 114 0.6× 54 0.3× 12 1.1k
L. Tarcsay Switzerland 11 648 1.1× 135 0.4× 401 2.1× 60 0.3× 53 0.3× 17 931
Nico Cerletti Switzerland 15 880 1.5× 113 0.4× 354 1.9× 46 0.3× 35 0.2× 25 1.3k
Jun‐ichi Mashimo Japan 12 700 1.2× 64 0.2× 298 1.6× 64 0.3× 42 0.3× 25 1.1k
J T Conary United States 14 662 1.2× 112 0.4× 256 1.4× 69 0.4× 15 0.1× 18 1.1k

Countries citing papers authored by Ann Harris

Since Specialization
Citations

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

Fields of papers citing papers by Ann Harris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ann Harris

This figure shows the co-authorship network connecting the top 25 collaborators of Ann Harris. A scholar is included among the top collaborators of Ann Harris 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 Ann Harris. Ann Harris 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.
Ott, Christopher J., et al.. (2009). Interaction of intestinal and pancreatic transcription factors in the regulation of CFTR gene expression. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1789(11-12). 709–718. 10 indexed citations
2.
3.
Broackes-Carter, Fiona, et al.. (2003). Alternative splicing of the ovine CFTR gene. Mammalian Genome. 14(11). 778–787. 3 indexed citations
4.
Williams, S. Henry, et al.. (2003). Evaluation of gene targeting by homologous recombination in ovine somatic cells. Molecular Reproduction and Development. 66(2). 115–125. 17 indexed citations
5.
Hefferon, Timothy, Fiona Broackes-Carter, Ann Harris, & Garry R. Cutting. (2002). Atypical 5′ Splice Sites Cause CFTR Exon 9 To Be Vulnerable to Skipping. The American Journal of Human Genetics. 71(2). 294–303. 34 indexed citations
6.
Mouchel, Nathalie, Scott J. Tebbutt, Fiona Broackes-Carter, et al.. (2001). The Sheep Genome Contributes to Localization of Control Elements in a Human Gene with Complex Regulatory Mechanisms. Genomics. 76(1-3). 9–13. 12 indexed citations
7.
Harris, Ann, Nita H. Salzman, John P. Russell, et al.. (1996). Human Enteric Defensins. Journal of Biological Chemistry. 271(8). 4038–4045. 239 indexed citations
8.
Davis, Connie L., David R. Gretch, James D. Perkins, et al.. (1995). Hepatitis c-associated glomerualar disease in liver transplant recipients. Liver Transplantation and Surgery. 1(3). 166–175. 25 indexed citations
9.
Boye, Eileen, Frances Flinter, Jing Zhou, et al.. (1995). Detection of 12 novel mutations in the collagenous domain of the COL4A5 gene in Alport syndrome patients. Human Mutation. 5(3). 197–204. 18 indexed citations
10.
Gieselmann, Volkmar, Joël Zlotogora, Ann Harris, David A. Wenger, & C. Phillip Morris. (1994). Molecular genetics of metachromatic leukodystrophy. Human Mutation. 4(4). 233–242. 81 indexed citations
11.
Vetrie, David, Elaine Kendall, Alison J. Coffey, et al.. (1994). A 6.5-Mb Yeast Artificial Chromosome Contig Incorporating 33 DNA Markers on the Human X Chromosome at Xq22. Genomics. 19(1). 42–47. 22 indexed citations
12.
Hull, Jeremy, Sue Shackleton, & Ann Harris. (1994). Analysis of mutations and alternative splicing patterns in the CFTR gene using mRNA derived from nasal epithelial cells. Human Molecular Genetics. 3(7). 1141–1146. 26 indexed citations
13.
Fensom, Anthony H., et al.. (1993). Missense mutations in the arylsulphatase A genes of metachromatic leukodystrophy patients. Human Molecular Genetics. 2(12). 2117–2121. 21 indexed citations
14.
Harris, Ann & Barry E. Argent. (1993). The cystic fibrosis and is product CFTR. PubMed. 4(1). 37–44. 15 indexed citations
15.
Vetrie, David, David Bentley, Martin Bobrow, & Ann Harris. (1993). Physical mapping shows close linkage between the ?-galactosidase A gene (GLA) and the DXS178 locus. Human Genetics. 92(1). 95–99. 10 indexed citations
16.
Walley, Andrew J. & Ann Harris. (1993). A novel point mutation (D380A) and a rare deletion (1255deI55) in the glucocerebrosidase gene causing Gaucher's disease. Human Molecular Genetics. 2(10). 1737–1738. 21 indexed citations
17.
Vetrie, David, Eileen Boye, Frances Flinter, Martin Bobrow, & Ann Harris. (1992). DNA rearrangements in the α5(IV) collagen gene (COL4A5) of individuals with alport syndrome: Further refinement using pulsed-field gel electrophoresis. Genomics. 14(3). 624–633. 17 indexed citations
18.
Vetrie, David, Frances Flinter, Martin Bobrow, & Ann Harris. (1992). Construction of a yeast artificial chromosome contig encompassing the human α5(IV) collagen gene (COL4A5). Genomics. 14(3). 634–642. 8 indexed citations
19.
Boye, Eileen, David Vetrie, Frances Flinter, et al.. (1991). Major rearrangements in the α5(IV) collagen gene in three patients with alport syndrome. Genomics. 11(4). 1125–1132. 43 indexed citations
20.
Harris, Ann, et al.. (1988). X‐linked lymphoproliferative disease: linkage studies using DNA probes. Clinical Genetics. 33(3). 162–168. 4 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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