
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:
Frequency of Known Mutations in Early-Onset Parkinson Disease
Roy N. Alcalay, Elise Caccappolo, Helen Mejia‐Santana, et al.
Archives of Neurology (2010) Vol. 67, Iss. 9
Open Access | Times Cited: 142
Roy N. Alcalay, Elise Caccappolo, Helen Mejia‐Santana, et al.
Archives of Neurology (2010) Vol. 67, Iss. 9
Open Access | Times Cited: 142
Showing 1-25 of 142 citing articles:
Parkinson disease
Werner Poewe, Klaus Seppi, Caroline M. Tanner, et al.
Nature Reviews Disease Primers (2017) Vol. 3, Iss. 1
Closed Access | Times Cited: 3800
Werner Poewe, Klaus Seppi, Caroline M. Tanner, et al.
Nature Reviews Disease Primers (2017) Vol. 3, Iss. 1
Closed Access | Times Cited: 3800
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
Christine Klein, Ana Westenberger
Cold Spring Harbor Perspectives in Medicine (2012) Vol. 2, Iss. 1, pp. a008888-a008888
Open Access | Times Cited: 1234
Metabolic control of cell death
Douglas R. Green, Lorenzo Galluzzi, Guido Kroemer
Science (2014) Vol. 345, Iss. 6203
Open Access | Times Cited: 583
Douglas R. Green, Lorenzo Galluzzi, Guido Kroemer
Science (2014) Vol. 345, Iss. 6203
Open Access | Times Cited: 583
Web-Based Genome-Wide Association Study Identifies Two Novel Loci and a Substantial Genetic Component for Parkinson's Disease
Joshua Shulman, Joyce Y. Tung, Elizabeth H. Dorfman, et al.
PLoS Genetics (2011) Vol. 7, Iss. 6, pp. e1002141-e1002141
Open Access | Times Cited: 514
Joshua Shulman, Joyce Y. Tung, Elizabeth H. Dorfman, et al.
PLoS Genetics (2011) Vol. 7, Iss. 6, pp. e1002141-e1002141
Open Access | Times Cited: 514
Autophagy in health and disease: A comprehensive review
Sarbari Saha, Debasna Pritimanjari Panigrahi, Shankargouda Patil, et al.
Biomedicine & Pharmacotherapy (2018) Vol. 104, pp. 485-495
Closed Access | Times Cited: 455
Sarbari Saha, Debasna Pritimanjari Panigrahi, Shankargouda Patil, et al.
Biomedicine & Pharmacotherapy (2018) Vol. 104, pp. 485-495
Closed Access | Times Cited: 455
Mitochondrial Quality Control and Disease: Insights into Ischemia-Reperfusion Injury
Anthony R. Anzell, Rita Maizy, Karin Przyklenk, et al.
Molecular Neurobiology (2017) Vol. 55, Iss. 3, pp. 2547-2564
Open Access | Times Cited: 315
Anthony R. Anzell, Rita Maizy, Karin Przyklenk, et al.
Molecular Neurobiology (2017) Vol. 55, Iss. 3, pp. 2547-2564
Open Access | Times Cited: 315
Roles of Autophagy in Oxidative Stress
Hyeong Rok Yun, Yong Hwa Jo, Ji‐Eun Kim, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 9, pp. 3289-3289
Open Access | Times Cited: 300
Hyeong Rok Yun, Yong Hwa Jo, Ji‐Eun Kim, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 9, pp. 3289-3289
Open Access | Times Cited: 300
The neuropathology of genetic Parkinson's disease
Markos Poulopoulos, Oren Levy, Roy N. Alcalay
Movement Disorders (2012) Vol. 27, Iss. 7, pp. 831-842
Open Access | Times Cited: 283
Markos Poulopoulos, Oren Levy, Roy N. Alcalay
Movement Disorders (2012) Vol. 27, Iss. 7, pp. 831-842
Open Access | Times Cited: 283
Cognitive performance of GBA mutation carriers with early-onset PD
Roy N. Alcalay, Elise Caccappolo, Helen Mejia‐Santana, et al.
Neurology (2012) Vol. 78, Iss. 18, pp. 1434-1440
Open Access | Times Cited: 251
Roy N. Alcalay, Elise Caccappolo, Helen Mejia‐Santana, et al.
Neurology (2012) Vol. 78, Iss. 18, pp. 1434-1440
Open Access | Times Cited: 251
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
Andreas Puschmann
Parkinsonism & Related Disorders (2013) Vol. 19, Iss. 4, pp. 407-415
Open Access | Times Cited: 232
Genetics and Pathogenesis of Parkinson's Syndrome
Hui Ye, Laurie Robak, Meigen Yu, et al.
Annual Review of Pathology Mechanisms of Disease (2022) Vol. 18, Iss. 1, pp. 95-121
Open Access | Times Cited: 213
Hui Ye, Laurie Robak, Meigen Yu, et al.
Annual Review of Pathology Mechanisms of Disease (2022) Vol. 18, Iss. 1, pp. 95-121
Open Access | Times Cited: 213
Autophagy in Neurodegenerative Diseases: From Mechanism to Therapeutic Approach
Jihoon Nah, Junying Yuan, Yong‐Keun Jung
Molecules and Cells (2015) Vol. 38, Iss. 5, pp. 381-389
Open Access | Times Cited: 206
Jihoon Nah, Junying Yuan, Yong‐Keun Jung
Molecules and Cells (2015) Vol. 38, Iss. 5, pp. 381-389
Open Access | Times Cited: 206
Neurodegenerative Diseases: Regenerative Mechanisms and Novel Therapeutic Approaches
Rashad Hussain, Hira Zubair, Sarah Pursell, et al.
Brain Sciences (2018) Vol. 8, Iss. 9, pp. 177-177
Open Access | Times Cited: 190
Rashad Hussain, Hira Zubair, Sarah Pursell, et al.
Brain Sciences (2018) Vol. 8, Iss. 9, pp. 177-177
Open Access | Times Cited: 190
Genetic predispositions of Parkinson’s disease revealed in patient-derived brain cells
Jenne Tran, Helena Targa Dias Anastacio, Cédric Bardy
npj Parkinson s Disease (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 143
Jenne Tran, Helena Targa Dias Anastacio, Cédric Bardy
npj Parkinson s Disease (2020) Vol. 6, Iss. 1
Open Access | Times Cited: 143
The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population
Yuwen Zhao, Lixia Qin, Hongxu Pan, et al.
Brain (2020) Vol. 143, Iss. 7, pp. 2220-2234
Open Access | Times Cited: 139
Yuwen Zhao, Lixia Qin, Hongxu Pan, et al.
Brain (2020) Vol. 143, Iss. 7, pp. 2220-2234
Open Access | Times Cited: 139
Depletion of dopamine in Parkinson's disease and relevant therapeutic options: A review of the literature
S Ramesh, Arosh S. Perera Molligoda Arachchige
AIMS neuroscience (2023) Vol. 10, Iss. 3, pp. 200-231
Open Access | Times Cited: 76
S Ramesh, Arosh S. Perera Molligoda Arachchige
AIMS neuroscience (2023) Vol. 10, Iss. 3, pp. 200-231
Open Access | Times Cited: 76
Parkinson’s disease variant detection and disclosure: PD GENEration, a North American study
Lola Cook, Jennifer Verbrugge, Tae‐Hwi Schwantes‐An, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2668-2679
Open Access | Times Cited: 21
Lola Cook, Jennifer Verbrugge, Tae‐Hwi Schwantes‐An, et al.
Brain (2024) Vol. 147, Iss. 8, pp. 2668-2679
Open Access | Times Cited: 21
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease
Margaux F. Keller, Mohamad Saad, José Brás, et al.
Human Molecular Genetics (2012) Vol. 21, Iss. 22, pp. 4996-5009
Open Access | Times Cited: 197
Margaux F. Keller, Mohamad Saad, José Brás, et al.
Human Molecular Genetics (2012) Vol. 21, Iss. 22, pp. 4996-5009
Open Access | Times Cited: 197
Systematic Review and UK‐Based Study of PARK2 (parkin), PINK1, PARK7 (DJ‐1) and LRRK2 in early‐onset Parkinson's disease
Laura L. Kilarski, Justin Pearson, Victoria Newsway, et al.
Movement Disorders (2012) Vol. 27, Iss. 12, pp. 1522-1529
Closed Access | Times Cited: 165
Laura L. Kilarski, Justin Pearson, Victoria Newsway, et al.
Movement Disorders (2012) Vol. 27, Iss. 12, pp. 1522-1529
Closed Access | Times Cited: 165
Age-specific penetrance ofLRRK2G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium
Karen Marder, Yuanjia Wang, Roy N. Alcalay, et al.
Neurology (2015) Vol. 85, Iss. 1, pp. 89-95
Open Access | Times Cited: 153
Karen Marder, Yuanjia Wang, Roy N. Alcalay, et al.
Neurology (2015) Vol. 85, Iss. 1, pp. 89-95
Open Access | Times Cited: 153
Association Between Early-Onset Parkinson Disease and 22q11.2 Deletion Syndrome
Nancy J. Butcher, Tim‐Rasmus Kiehl, Lili‐Naz Hazrati, et al.
JAMA Neurology (2013) Vol. 70, Iss. 11, pp. 1359-1359
Open Access | Times Cited: 146
Nancy J. Butcher, Tim‐Rasmus Kiehl, Lili‐Naz Hazrati, et al.
JAMA Neurology (2013) Vol. 70, Iss. 11, pp. 1359-1359
Open Access | Times Cited: 146
Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research
Selina Wray, Matthew W. Self, Patrick A. Lewis, et al.
PLoS ONE (2012) Vol. 7, Iss. 8, pp. e43099-e43099
Open Access | Times Cited: 138
Selina Wray, Matthew W. Self, Patrick A. Lewis, et al.
PLoS ONE (2012) Vol. 7, Iss. 8, pp. e43099-e43099
Open Access | Times Cited: 138
Understanding the susceptibility of dopamine neurons to mitochondrial stressors in Parkinson's disease
Dominik Haddad, Ken Nakamura
FEBS Letters (2015) Vol. 589, Iss. 24PartA, pp. 3702-3713
Open Access | Times Cited: 135
Dominik Haddad, Ken Nakamura
FEBS Letters (2015) Vol. 589, Iss. 24PartA, pp. 3702-3713
Open Access | Times Cited: 135
GBA-Associated Parkinson’s Disease and Other Synucleinopathies
Ziv Gan‐Or, Christopher Liong, Roy N. Alcalay
Current Neurology and Neuroscience Reports (2018) Vol. 18, Iss. 8
Closed Access | Times Cited: 129
Ziv Gan‐Or, Christopher Liong, Roy N. Alcalay
Current Neurology and Neuroscience Reports (2018) Vol. 18, Iss. 8
Closed Access | Times Cited: 129
Genetics of Parkinson disease
Aloysius Domingo, Christine Klein
Handbook of clinical neurology (2018), pp. 211-227
Closed Access | Times Cited: 128
Aloysius Domingo, Christine Klein
Handbook of clinical neurology (2018), pp. 211-227
Closed Access | Times Cited: 128