Ann Jewell

584 total citations
15 papers, 393 citations indexed

About

Ann Jewell is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Ann Jewell has authored 15 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Physiology. Recurrent topics in Ann Jewell's work include Tuberous Sclerosis Complex Research (3 papers), Retinal Development and Disorders (3 papers) and RNA regulation and disease (2 papers). Ann Jewell is often cited by papers focused on Tuberous Sclerosis Complex Research (3 papers), Retinal Development and Disorders (3 papers) and RNA regulation and disease (2 papers). Ann Jewell collaborates with scholars based in United States, Canada and New Zealand. Ann Jewell's co-authors include Jonathan L. Haines, M. Priscilla Short, David J. Kwiatkowski, R.S. Kandt, M. Smith, Pamela Flodman, Allen D. Roses, J L Weber, S. A. Wall and R. J. M. Gardner and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Annals of the New York Academy of Sciences.

In The Last Decade

Ann Jewell

14 papers receiving 378 citations

Peers

Countries citing papers authored by Ann Jewell

Since Specialization

Citations

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

Fields of papers citing papers by Ann Jewell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ann Jewell

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	C21orf2 variants causing inherited retinal disease: A review of what we know and a report of two new suspected cases 2023 ·SHILAP Revista de lepidopterología ·(unknown), Ann Jewell, (unknown), (unknown)	7
2	Genotype-phenotype analysis of ocular findings in Rubinstein-Taybi syndrome – A case report and review of literature 2023 ·Ophthalmic Genetics ·(unknown), (unknown), Ann Jewell, (unknown)	2
3	THE ROLE OF GENETIC TESTING IN AVOIDING DIAGNOSTIC DELAYS IN INHERITED RETINAL DISEASE 2023 ·Retinal Cases & Brief Reports ·Arth H. Shah, (unknown), (unknown), Qingguo Xu, Ann Jewell, (unknown)	0
4	Occult Macular Dystrophy: a case report and major review 2022 ·Ophthalmic Genetics ·(unknown), Ann Jewell, Vikram Brar, (unknown)	4
5	Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review 2022 ·Ophthalmic Genetics ·(unknown), (unknown), Ann Jewell, (unknown), Amy Harper, (unknown), (unknown)	2
6	Prenatal Bowel Findings in Male Siblings With a Confirmed FOXP3 Mutation 2017 ·Journal of Ultrasound in Medicine ·(unknown), (unknown), (unknown), Ann Jewell	2
7	Lethal osteosclerotic osteochondrodysplasia with platyspondyly, metaphyseal widening, and intracellular inclusions in sibs 1998 ·American Journal of Medical Genetics ·Steven G. Brodie, Ralph S. Lachman, Ann Jewell, Carey L. Winkler, (unknown), William R. Wilcox	1
8	Strain differences in rat brain and liver σ binding: lack of cytochrome P450-2D1 involvement 1993 ·European Journal of Pharmacology ·Ann Jewell, Peter J. Wedlund, Linda P. Dwoskin	9
9	Linkage analysis in juvenile neuronal ceroid lipofuscinosis 1992 ·American Journal of Medical Genetics ·Jonathan L. Haines, (unknown), Rose‐Mary Boustany, Ann Jewell, Cécile Julier, Xandra O. Breakefield, James F. Gusella	9
10	Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease 1992 ·Nature Genetics ·R.S. Kandt, Jonathan L. Haines, M. Smith, Hope Northrup, R. J. M. Gardner, M. Priscilla Short, (unknown), E. Steve Roach, (unknown), S. A. Wall, Susan H. Blanton, Pamela Flodman, David J. Kwiatkowski, Ann Jewell, J L Weber, Allen D. Roses, Margaret A. Pericak‐Vance	248
11	Parental origin of chromosome 22 loss in sporadic and NF2 neuromas 1991 ·Genomics ·Bertrand Fontaine, Marc Sanson, Olivier Delattre, Anil G. Menon, Guy A. Rouleau, Bernd R. Seizinger, Ann Jewell, (unknown), Alain Aurias, Robert L. Martuza, James F. Gusella, Gilles Thomas	16
12	Molecular Genetics of Neurofibromatosis 2 and Related Tumors (Acoustic Neuroma and Meningioma)^a 1991 ·Annals of the New York Academy of Sciences ·Bertrand Fontaine, Guy A. Rouleau, Bernd R. Seizinger, (unknown), Ann Jewell, Robert L. Martuza, James F. Gusella	27
13	Clinical Findings and Linkage Studies in Familial Tuberous Sclerosis 1991 ·Annals of the New York Academy of Sciences ·M. Priscilla Short, Jess Haines, Ann Jewell, Bassem A. Bejjani, (unknown), (unknown), H MacFarlane, E. Andermann, (unknown), J. Amos	2
14	Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneity. 1991 ·PubMed ·Jonathan L. Haines, M. Priscilla Short, D J Kwiatkowski, Ann Jewell, E. Andermann, Bassem A. Bejjani, Chao Yang, James F. Gusella, J. Amos	53
15	Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprinting. 1990 ·PubMed ·Bertrand Fontaine, Guy A. Rouleau, Bernd R. Seizinger, Ann Jewell, (unknown), R L Martuza, James F. Gusella	11

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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