Dora Yearout

4.8k total citations · 1 hit paper
24 papers, 1.8k citations indexed

About

Dora Yearout is a scholar working on Neurology, Neurology and Cognitive Neuroscience. According to data from OpenAlex, Dora Yearout has authored 24 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 11 papers in Neurology and 5 papers in Cognitive Neuroscience. Recurrent topics in Dora Yearout's work include Parkinson's Disease Mechanisms and Treatments (17 papers), Neurological diseases and metabolism (10 papers) and Autism Spectrum Disorder Research (5 papers). Dora Yearout is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (17 papers), Neurological diseases and metabolism (10 papers) and Autism Spectrum Disorder Research (5 papers). Dora Yearout collaborates with scholars based in United States, Japan and Italy. Dora Yearout's co-authors include Cyrus P. Zabetian, Ali Samii, John W. Roberts, Alida Griffith, Haydeh Payami, Denise M. Kay, Stewart A. Factor, John G. Nutt, Jennifer S. Montimurro and Berta C. Leis and has published in prestigious journals such as Nature Genetics, Neurology and Annals of Neurology.

In The Last Decade

Dora Yearout

24 papers receiving 1.8k 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
Dora Yearout United States	18	1.3k	624	542	487	443	24	1.8k
Alida Griffith United States	16	1.3k 1.0×	632 1.0×	541 1.0×	451 0.9×	434 1.0×	25	1.8k
Hiroyuki Tomiyama Japan	23	1.3k 1.0×	549 0.9×	614 1.1×	513 1.1×	430 1.0×	43	2.0k
Hiroyo Yoshino Japan	26	1.7k 1.3×	706 1.1×	985 1.8×	741 1.5×	478 1.1×	62	2.3k
Hiroo Yamaguchi Japan	18	1.2k 1.0×	452 0.7×	753 1.4×	904 1.9×	657 1.5×	52	2.4k
Iria Carballo‐Carbajal Spain	13	1.2k 0.9×	375 0.6×	738 1.4×	923 1.9×	469 1.1×	15	2.1k
Roberto Di Maio United States	19	752 0.6×	266 0.4×	641 1.2×	796 1.6×	365 0.8×	35	1.8k
Andreas Puschmann Sweden	24	1.0k 0.8×	282 0.5×	530 1.0×	408 0.8×	379 0.9×	57	1.6k
Emily M. Rocha United States	16	1.2k 0.9×	358 0.6×	580 1.1×	664 1.4×	689 1.6×	23	2.0k
Reema Paudel United Kingdom	16	785 0.6×	320 0.5×	521 1.0×	401 0.8×	445 1.0×	20	1.4k
Ayşe Ulusoy Germany	22	1.4k 1.0×	351 0.6×	808 1.5×	625 1.3×	415 0.9×	36	2.0k

Countries citing papers authored by Dora Yearout

Since Specialization

Citations

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

Fields of papers citing papers by Dora Yearout

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dora Yearout

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

Velez‐Pardo, Carlos, Oswaldo Lorenzo‐Betancor, Marlene Jiménez-Del-Río, et al.. (2019). The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru. Parkinsonism & Related Disorders. 63. 204–208. 27 indexed citations

Costa‐Mallen, Paola, Cyrus P. Zabetian, Shu-Ching Hu, et al.. (2016). Smoking and haptoglobin phenotype modulate serum ferritin and haptoglobin levels in Parkinson disease. Journal of Neural Transmission. 123(11). 1319–1330. 8 indexed citations

Mata, Ignácio F., Marie Y. Davis, Michael O. Dorschner, et al.. (2016). The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(7). 925–930. 15 indexed citations

Costa‐Mallen, Paola, Cyrus P. Zabetian, Pinky Agarwal, et al.. (2015). Haptoglobin phenotype modifies serum iron levels and the effect of smoking on Parkinson disease risk. Parkinsonism & Related Disorders. 21(9). 1087–1092. 25 indexed citations

Chahine, Lana M., Judy Qiang, Dora Yearout, et al.. (2013). Clinical and Biochemical Differences in Patients Having Parkinson Disease With vs WithoutGBAMutations. JAMA Neurology. 70(7). 852–852. 102 indexed citations

Wan, Jia Y., Karen L. Edwards, Carolyn M. Hutter, et al.. (2013). Association mapping of the PARK10 region for Parkinson's disease susceptibility genes. Parkinsonism & Related Disorders. 20(1). 93–98. 18 indexed citations

Qiang, Judy, Yvette C. Wong, Andrew Siderowf, et al.. (2013). Plasma apolipoprotein A1 as a biomarker for Parkinson disease. Annals of Neurology. 74(1). 119–127. 106 indexed citations

Burns, Gully, Pritam Ganguly, Taye H. Hamza, et al.. (2012). A genetic basis for the variable effect of smoking/nicotine on Parkinson’s disease. The Pharmacogenomics Journal. 13(6). 530–537. 51 indexed citations

Snapinn, Katherine W., Eric B. Larson, Hideshi Kawakami, et al.. (2011). The UCHL1 S18Y polymorphism and Parkinson’s disease in a Japanese population. Parkinsonism & Related Disorders. 17(6). 473–475. 5 indexed citations

10.

Mata, Ignácio F., Dora Yearout, Victoria Álvarez, et al.. (2011). Replication of MAPT and SNCA, but not PARK16‐18, as susceptibility genes for Parkinson's disease. Movement Disorders. 26(5). 819–823. 59 indexed citations

11.

Shi, Min, Cyrus P. Zabetian, Aneeka M. Hancock, et al.. (2010). Significance and confounders of peripheral DJ-1 and alpha-synuclein in Parkinson's disease. Neuroscience Letters. 480(1). 78–82. 173 indexed citations

12.

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 →

13.

Poorkaj, Parvoneh, Wendy H. Raskind, James B. Leverenz, et al.. (2010). A novel X‐linked four‐repeat tauopathy with Parkinsonism and spasticity. Movement Disorders. 25(10). 1409–1417. 17 indexed citations

14.

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

15.

Zabetian, Cyrus P., Mitsutoshi Yamamoto, Hiroshi Ujike, et al.. (2009). LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease. Movement Disorders. 24(7). 1034–1041. 49 indexed citations

16.

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

17.

Mata, Ignácio F., Carlos Cosentino, Luis Torres, et al.. (2008). LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay. Parkinsonism & Related Disorders. 15(5). 370–373. 29 indexed citations

18.

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

19.

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

20.

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

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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