Joanne Norton

9.9k total citations · 1 hit paper
40 papers, 2.6k citations indexed

About

Joanne Norton is a scholar working on Physiology, Molecular Biology and Neurology. According to data from OpenAlex, Joanne Norton has authored 40 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Physiology, 16 papers in Molecular Biology and 11 papers in Neurology. Recurrent topics in Joanne Norton's work include Alzheimer's disease research and treatments (21 papers), Amyotrophic Lateral Sclerosis Research (6 papers) and Neurological diseases and metabolism (5 papers). Joanne Norton is often cited by papers focused on Alzheimer's disease research and treatments (21 papers), Amyotrophic Lateral Sclerosis Research (6 papers) and Neurological diseases and metabolism (5 papers). Joanne Norton collaborates with scholars based in United States, United Kingdom and Colombia. Joanne Norton's co-authors include Alison Goate, John C. Morris, Sumi Chakraverty, Daniel W. McKeel, Carlos Cruchaga, Kevin H. Mayo, Mary A. Coats, Denise Levitch, Michael A. Gitcho and Nigel J. Cairns and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Joanne Norton

39 papers receiving 2.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Clinicopathologic Studies in Cognitively Healthy Aging and Alzheimer Disease

1998 546 citations Daniel W. McKeel, J. Philip Miller et al. Archives of Neurology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joanne Norton United States	21	1.4k	1.0k	703	630	545	40	2.6k
Yvonne S. Davidson United Kingdom	29	1.3k 1.0×	1.7k 1.7×	751 1.1×	557 0.9×	548 1.0×	63	2.8k
Anna Karydas United States	31	1.6k 1.2×	1.5k 1.5×	1.3k 1.8×	704 1.1×	838 1.5×	58	3.7k
Patrizia Rizzu Netherlands	22	1.4k 1.0×	1.2k 1.2×	1.0k 1.5×	519 0.8×	206 0.4×	44	2.5k
Pau Pástor Spain	36	1.2k 0.9×	2.2k 2.2×	952 1.4×	790 1.3×	341 0.6×	123	3.6k
Toshitaka Kawarai Canada	30	1.4k 1.0×	948 0.9×	1.2k 1.8×	824 1.3×	241 0.4×	75	3.2k
Richard Crook United States	34	2.5k 1.9×	1.1k 1.1×	1.4k 2.0×	627 1.0×	831 1.5×	73	3.9k
Claire E. Shepherd Australia	25	1.3k 1.0×	752 0.7×	802 1.1×	663 1.1×	402 0.7×	68	2.5k
Anna M. Karydas United States	18	849 0.6×	733 0.7×	514 0.7×	380 0.6×	493 0.9×	24	1.9k
Shunsuke Koga United States	31	1.2k 0.9×	1.9k 1.9×	614 0.9×	687 1.1×	267 0.5×	107	2.9k
Gilbert Ho United States	21	1.1k 0.8×	675 0.7×	686 1.0×	369 0.6×	380 0.7×	48	2.4k

Countries citing papers authored by Joanne Norton

Since Specialization

Citations

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

Fields of papers citing papers by Joanne Norton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joanne Norton

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

All Works

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20 of 20 papers shown

Beric, Aleksandra, Muhammad Ali, María Victoria Fernández, et al.. (2023). Cell-free RNA signatures predict Alzheimer’s disease. iScience. 26(12). 108534–108534. 3 indexed citations

Karch, Celeste M., Damián Hernández, Jen‐Chyong Wang, et al.. (2018). Human fibroblast and stem cell resource from the Dominantly Inherited Alzheimer Network. Alzheimer s Research & Therapy. 10(1). 69–69. 23 indexed citations

Fernández, María Victoria, John Budde, Jorge L. Del‐Aguila, et al.. (2018). Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease. Frontiers in Neuroscience. 12. 209–209. 18 indexed citations

Hsu, Simon, Brian A. Gordon, Russ C. Hornbeck, et al.. (2018). Discovery and validation of autosomal dominant Alzheimer’s disease mutations. Alzheimer s Research & Therapy. 10(1). 67–67. 27 indexed citations

Del‐Aguila, Jorge L., Daniel C. Koboldt, Kathleen Black, et al.. (2015). Alzheimer's disease: rare variants with large effect sizes. Current Opinion in Genetics & Development. 33. 49–55. 34 indexed citations

Benítez, Bruno A., Nigel J. Cairns, Robert E. Schmidt, et al.. (2015). Clinically early-stage CSPα mutation carrier exhibits remarkable terminal stage neuronal pathology with minimal evidence of synaptic loss. Acta Neuropathologica Communications. 3(1). 73–73. 19 indexed citations

Jin, Sheng Chih, Bruno A. Benítez, Celeste M. Karch, et al.. (2014). Coding variants in TREM2 increase risk for Alzheimer's disease. Human Molecular Genetics. 23(21). 5838–5846. 237 indexed citations

Ghoshal, Nupur, Arie Perry, Daniel W. McKeel, et al.. (2014). Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old. Alzheimer Disease & Associated Disorders. 29(2). 173–176. 6 indexed citations

Cruchaga, Carlos, Caroline Graff, Huei‐Hsin Chiang, et al.. (2011). Association of TMEM106B Gene Polymorphism With Age at Onset in Granulin Mutation Carriers and Plasma Granulin Protein Levels. Archives of Neurology. 68(5). 581–6. 114 indexed citations

10.

Norton, Joanne, N.J. Cairns, Sumitra Chakraverty, et al.. (2009). PRESENILIN1 G217R MUTATION LINKED TO ALZHEIMER DISEASE WITH COTTON WOOL PLAQUES. Neurology. 73(6). 480–482. 7 indexed citations

11.

Foláyan, Morẹ́nikẹ́ Oluwátóyìn, et al.. (2007). Cervical screening in under 25s: A high-risk young population. European Journal of Obstetrics & Gynecology and Reproductive Biology. 139(1). 86–89. 22 indexed citations

12.

Snider, B. Joy, Joanne Norton, Mary A. Coats, et al.. (2005). Novel Presenilin 1 Mutation (S170F) Causing Alzheimer Disease With Lewy Bodies in the Third Decade of Life. Archives of Neurology. 62(12). 1821–1821. 96 indexed citations

13.

Johnson, Janel, Lars Lannfelt, Anna Glaser, et al.. (2004). No evidence for tau duplications in frontal temporal dementia families showing genetic linkage to the tau locus in which tau mutations have not been found. Neuroscience Letters. 363(2). 99–101. 5 indexed citations

14.

Pástor, Pau, Mario Ezquerra, J. Christian Pérez, et al.. (2004). Novel haplotypes in 17q21 are associated with progressive supranuclear palsy. Annals of Neurology. 56(2). 249–258. 51 indexed citations

15.

Pástor, Pau, Catherine M. Roe, Andrés Villegas, et al.. (2003). Apolipoprotein Eε4 modifies Alzheimer's disease onset in an E280A PS1 kindred. Annals of Neurology. 54(2). 163–169. 139 indexed citations

16.

Ahmad, Nadeem, Allan J. Richards, Leonard M. Shapiro, et al.. (2002). Prevalence of mitral valve prolapse in Stickler syndrome. American Journal of Medical Genetics Part A. 116A(3). 234–237. 28 indexed citations

17.

Kwon, Jennifer M., Petra Nowotny, Sumi Chakraverty, et al.. (2000). Tau polymorphisms are not associated with Alzheimer's disease. Neuroscience Letters. 284(1-2). 77–80. 28 indexed citations

18.

McKeel, Daniel W., J. Philip Miller, Martha Storandt, et al.. (1998). Clinicopathologic Studies in Cognitively Healthy Aging and Alzheimer Disease. Archives of Neurology. 55(3). 326–326. 546 indexed citations breakdown →

19.

Lendon, Corinne, Timothy Lynch, Joanne Norton, et al.. (1998). Hereditary dysphasic disinhibition dementia A frontotemporal dementia linked to 17 q21‐‐22. Neurology. 50(6). 1546–1555. 111 indexed citations

20.

Marks, James F., Joanne Norton, & John S. Fordtran. (1966). Glucose-galactose malabsorption. The Journal of Pediatrics. 69(2). 225–228. 19 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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