OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Deciphering the role of heterozygous mutations in genes associated with parkinsonism
Christine Klein, K. Lohmann-Hedrich, Ekaterina Rogaeva, et al.
The Lancet Neurology (2007) Vol. 6, Iss. 7, pp. 652-662
Closed Access | Times Cited: 309

Showing 1-25 of 309 citing articles:

Parkinson's disease
Lorraine V. Kalia, Anthony E. Lang
The Lancet (2015) Vol. 386, Iss. 9996, pp. 896-912
Closed Access | Times Cited: 4810

Genetics of Parkinson's Disease
Christine Klein, Ana Westenberger
Cold Spring Harbor Perspectives in Medicine (2012) Vol. 2, Iss. 1, pp. a008888-a008888
Open Access | Times Cited: 1234

Epidemiology and etiology of Parkinson’s disease: a review of the evidence
Karin Wirdefeldt, Hans‐Olov Adami, Philip Cole, et al.
European Journal of Epidemiology (2011) Vol. 26, Iss. S1, pp. 1-58
Open Access | Times Cited: 1149

Parkinson's disease: from monogenic forms to genetic susceptibility factors
Suzanne Lesage, Alexis Brice
Human Molecular Genetics (2009) Vol. 18, Iss. R1, pp. R48-R59
Open Access | Times Cited: 916

Parkinson's Disease: Genetics and Pathogenesis
Joshua Shulman, Philip L. De Jager, Mel Β. Feany
Annual Review of Pathology Mechanisms of Disease (2011) Vol. 6, Iss. 1, pp. 193-222
Closed Access | Times Cited: 780

What Genetics Tells us About the Causes and Mechanisms of Parkinson's Disease
Olga Corti, Suzanne Lesage, Alexis Brice
Physiological Reviews (2011) Vol. 91, Iss. 4, pp. 1161-1218
Closed Access | Times Cited: 554

Mitochondrial Diseases of the Brain
Rajnish Kumar Chaturvedi, M. Flint Beal
Free Radical Biology and Medicine (2013) Vol. 63, pp. 1-29
Closed Access | Times Cited: 394

Mitochondrial function and morphology are impaired in parkin‐mutant fibroblasts
Heather Mortiboys, Kelly Jean Thomas Craig, Werner J.H. Koopman, et al.
Annals of Neurology (2008) Vol. 64, Iss. 5, pp. 555-565
Open Access | Times Cited: 336

The genetics of Parkinson's disease: Progress and therapeutic implications
Andrew Singleton, Matthew J. Farrer, Vincenzo Bonifati
Movement Disorders (2013) Vol. 28, Iss. 1, pp. 14-23
Open Access | Times Cited: 330

The interplay of aging, genetics and environmental factors in the pathogenesis of Parkinson’s disease
Shirley Yin-Yu Pang, Philip Wing‐Lok Ho, Huifang Liu, et al.
Translational Neurodegeneration (2019) Vol. 8, Iss. 1
Open Access | Times Cited: 306

Acid β‐glucosidase mutants linked to gaucher disease, parkinson disease, and lewy body dementia alter α‐synuclein processing
Valerie Cullen, S. Pablo Sardi, Juliana Ng, et al.
Annals of Neurology (2011) Vol. 69, Iss. 6, pp. 940-953
Open Access | Times Cited: 298

Monogenic Parkinson's disease and parkinsonism: Clinical phenotypes and frequencies of known mutations
Andreas Puschmann
Parkinsonism & Related Disorders (2013) Vol. 19, Iss. 4, pp. 407-415
Open Access | Times Cited: 232

Signaling pathways in Parkinson’s disease: molecular mechanisms and therapeutic interventions
Dong-Chen Xu, Yong Chen, Yang Xu, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 199

Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism
Max Borsche, Inke R. König, Sylvie Delcambre, et al.
Brain (2020) Vol. 143, Iss. 10, pp. 3041-3051
Open Access | Times Cited: 149

Characterization of PINK1 processing, stability, and subcellular localization
William Lin, Un Jung Kang
Journal of Neurochemistry (2008) Vol. 106, Iss. 1, pp. 464-474
Open Access | Times Cited: 233

Animal models of Parkinson’s disease progression
Gloria E. Meredith, Patricia K. Sonsalla, Marie‐Françoise Chesselet
Acta Neuropathologica (2008) Vol. 115, Iss. 4, pp. 385-398
Open Access | Times Cited: 221

The genetics of Parkinson's syndromes: a critical review
John Hardy, Patrick A. Lewis, Tamás Révész, et al.
Current Opinion in Genetics & Development (2009) Vol. 19, Iss. 3, pp. 254-265
Closed Access | Times Cited: 206

The effect of onset age on the clinical features of Parkinson’s disease
Mirdhu Wickremaratchi, Yoav Ben‐Shlomo, Huw R. Morris
European Journal of Neurology (2009) Vol. 16, Iss. 4, pp. 450-456
Closed Access | Times Cited: 176

DNAJC6Mutations Associated With Early‐Onset Parkinson's Disease
Simone Olgiati, Marialuisa Quadri, Mingyan Fang, et al.
Annals of Neurology (2015) Vol. 79, Iss. 2, pp. 244-256
Closed Access | Times Cited: 171

Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio)
Laura Flinn, Heather Mortiboys, Katrin Volkmann, et al.
Brain (2009) Vol. 132, Iss. 6, pp. 1613-1623
Open Access | Times Cited: 170

Milestones in PD genetics
Thomas Gasser, John Hardy, Yoshikuni Mizuno
Movement Disorders (2011) Vol. 26, Iss. 6, pp. 1042-1048
Closed Access | Times Cited: 165

Cancer and Neurodegeneration: Between the Devil and the Deep Blue Sea
Hélène Plun‐Favreau, Patrick A. Lewis, John Hardy, et al.
PLoS Genetics (2010) Vol. 6, Iss. 12, pp. e1001257-e1001257
Open Access | Times Cited: 163

Gene–environment interactions: Key to unraveling the mystery of Parkinson's disease
Hui‐Ming Gao, Jau‐Shyong Hong
Progress in Neurobiology (2011) Vol. 94, Iss. 1, pp. 1-19
Open Access | Times Cited: 162

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