Alida Griffith

4.7k total citations · 1 hit paper
25 papers, 1.8k citations indexed

About

Alida Griffith is a scholar working on Neurology, Molecular Biology and Neurology. According to data from OpenAlex, Alida Griffith has authored 25 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Neurology, 9 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Alida Griffith's work include Parkinson's Disease Mechanisms and Treatments (18 papers), Neurological diseases and metabolism (7 papers) and RNA regulation and disease (5 papers). Alida Griffith is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (18 papers), Neurological diseases and metabolism (7 papers) and RNA regulation and disease (5 papers). Alida Griffith collaborates with scholars based in United States, United Kingdom and Greece. Alida Griffith's co-authors include Cyrus P. Zabetian, Ali Samii, John W. Roberts, Haydeh Payami, Denise M. Kay, Stewart A. Factor, John G. Nutt, Dora Yearout, Berta C. Leis and Jennifer S. Montimurro and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Alida Griffith

23 papers receiving 1.7k citations

Hit Papers

align trajectories

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.

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

2010 584 citations Taye H. Hamza, Cyrus P. Zabetian et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alida Griffith United States	16	1.3k	632	541	451	434	25	1.8k
Dora Yearout United States	18	1.3k 1.0×	624 1.0×	542 1.0×	487 1.1×	443 1.0×	24	1.8k
Julie P. Taylor United States	15	1.2k 1.0×	503 0.8×	425 0.8×	604 1.3×	377 0.9×	17	1.6k
Jennifer S. Montimurro United States	14	983 0.8×	442 0.7×	487 0.9×	396 0.9×	231 0.5×	16	1.4k
Mark S. Moehle United States	17	1.1k 0.8×	492 0.8×	568 1.0×	610 1.4×	399 0.9×	27	1.7k
Ayşe Ulusoy Germany	22	1.4k 1.1×	351 0.6×	808 1.5×	625 1.4×	415 1.0×	36	2.0k
Kelly M. Hinkle United States	15	759 0.6×	269 0.4×	329 0.6×	323 0.7×	372 0.9×	18	1.1k
Kateřina Venderová United States	13	574 0.4×	172 0.3×	436 0.8×	438 1.0×	227 0.5×	17	1.2k
Marie L. Schmidt United States	17	1.1k 0.9×	451 0.7×	496 0.9×	615 1.4×	1.3k 3.0×	22	2.0k
Isabella Russo Italy	22	692 0.5×	509 0.8×	438 0.8×	583 1.3×	514 1.2×	39	1.5k
Anthony DelleDonne United States	17	1.0k 0.8×	581 0.9×	446 0.8×	406 0.9×	790 1.8×	21	1.9k

Countries citing papers authored by Alida Griffith

Since Specialization

Citations

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

Fields of papers citing papers by Alida Griffith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alida Griffith

This figure shows the co-authorship network connecting the top 25 collaborators of Alida Griffith. A scholar is included among the top collaborators of Alida Griffith 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 Alida Griffith. Alida Griffith 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

Agarwal, Pinky, et al.. (2017). Optimizing Recruitment of Racial and Ethnic minority population in Clinical Trials in Parkinson’s Disease: Potential Barriers and Prospective Strategies (P4.010). Neurology. 88(16_supplement). 1 indexed citations

Seeberger, Lauren, et al.. (2011). Rasagiline. The Neurologist. 17(6). 318–324. 7 indexed citations

Hamza, Taye H., Cyrus P. Zabetian, Albert Tenesa, et al.. (2010). Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nature Genetics. 42(9). 781–785. 584 indexed citations breakdown →

Furlong, Clement E., Stephanie M. Suzuki, Richard Stevens, et al.. (2010). Human PON1, a biomarker of risk of disease and exposure. Chemico-Biological Interactions. 187(1-3). 355–361. 95 indexed citations

Hall, Deborah A., et al.. (2009). MOVEMENT DISORDERS ASSOCIATED WITH ARIPIPRAZOLE USE: A CASE SERIES. International Journal of Neuroscience. 119(12). 2274–2279. 15 indexed citations

Hutter, Carolyn M., Ali Samii, Stewart A. Factor, et al.. (2008). Lack of evidence for an association between UCHL1 S18Y and Parkinson’s disease. European Journal of Neurology. 15(2). 134–139. 25 indexed citations

Ross, Owen A., Cleanthe Spanaki, Alida Griffith, et al.. (2008). Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism. Parkinsonism & Related Disorders. 15(6). 466–467. 30 indexed citations

Kay, Denise M., Stewart A. Factor, Ali Samii, et al.. (2008). Genetic association between α‐synuclein and idiopathic parkinson's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1222–1230. 55 indexed citations

Mata, Ignácio F., Ali Samii, John W. Roberts, et al.. (2008). Glucocerebrosidase Gene Mutations. Archives of Neurology. 65(3). 379–82. 155 indexed citations

10.

Agarwal, Pinky & Alida Griffith. (2008). Restless legs syndrome: a unique case and essentials of diagnosis and treatment.. PubMed. 10(12). 296–296. 2 indexed citations

11.

McCulloch, Colin, Denise M. Kay, Stewart A. Factor, et al.. (2008). Exploring gene-environment interactions in Parkinson’s disease. Human Genetics. 123(3). 257–265. 72 indexed citations

12.

Powers, Karen M., Denise M. Kay, Stewart A. Factor, et al.. (2007). Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk. Movement Disorders. 23(1). 88–95. 105 indexed citations

13.

Zabetian, Cyrus P., Carolyn M. Hutter, Stewart A. Factor, et al.. (2007). Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease. Annals of Neurology. 62(2). 137–144. 113 indexed citations

14.

Samii, Ali, Carolyn M. Hutter, Alida Griffith, et al.. (2007). DBH −1021C→T does not modify risk or age at onset in Parkinson's disease. Annals of Neurology. 62(1). 99–101. 5 indexed citations

15.

Kay, Denise M., T. Bird, Cyrus P. Zabetian, et al.. (2006). Validity and Utility of a LRRK2 G2019S Mutation Test for the Diagnosis of Parkinson's Disease. Genetic Testing. 10(3). 221–227. 17 indexed citations

16.

Zabetian, Cyrus P., Carolyn M. Hutter, Dora Yearout, et al.. (2006). LRRK2 G2019S in Families with Parkinson Disease Who Originated from Europe and the Middle East: Evidence of Two Distinct Founding Events Beginning Two Millennia Ago. The American Journal of Human Genetics. 79(4). 752–758. 87 indexed citations

17.

Ishihara, Lianna, Liling Warren, Rachel A. Gibson, et al.. (2006). Clinical Features of Parkinson Disease Patients With Homozygous Leucine-Rich Repeat Kinase 2 G2019S Mutations. Archives of Neurology. 63(9). 1250–1250. 74 indexed citations

18.

Zabetian, Cyrus P., Hiroyuki Morino, Hiroshi Ujike, et al.. (2006). Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease. Neurology. 67(4). 697–699. 48 indexed citations

19.

Griffith, Alida, et al.. (2000). Exacerbation of Multiple Sclerosis Following Wasp Stings. Mayo Clinic Proceedings. 75(3). 317–318. 1 indexed citations

20.

Griffith, Alida, et al.. (2000). Exacerbation of Multiple Sclerosis Following Wasp Stings. Mayo Clinic Proceedings. 75(3). 317–318. 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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