The DOI matches its Crossref record; 283 of the 290 references it cites were found in a registry or an index.
A review of quality of life after predictive testing for and earlier identification of neurodegenerative diseases
Open accessAbstract
The past decade has witnessed an explosion of evidence suggesting that many neurodegenerative diseases can be detected years, if not decades, earlier than previously thought. To date, these scientific advances have not provoked any parallel translational or clinical improvements. There is an urgency to capitalize on this momentum so earlier detection of disease can be more readily translated into improved health-related quality of life for families at risk for, or suffering with, neurodegenerative diseases. In this review, we discuss health-related quality of life (HRQOL) measurement in neurodegenerative diseases and the importance of these "patient reported outcomes" for all clinical research. Next, we address HRQOL following early identification or predictive genetic testing in some neurodegenerative diseases: Huntington disease, Alzheimer's disease, Parkinson's disease, Dementia with Lewy bodies, frontotemporal dementia, amyotrophic lateral sclerosis, prion diseases, hereditary ataxias, Dentatorubral-pallidoluysian atrophy and Wilson's disease. After a brief report of available direct-to-consumer genetic tests, we address the juxtaposition of earlier disease identification with assumed reluctance toward predictive genetic testing. Forty-one studies examining health-related outcomes following predictive genetic testing for neurodegenerative disease suggested that (a) extreme or catastrophic outcomes are rare; (b) consequences commonly include transiently increased anxiety and/or depression; (c) most participants report no regret; (d) many persons report extensive benefits to receiving genetic information; and (e) stigmatization and discrimination for genetic diseases are poorly understood and policy and laws are needed. Caution is appropriate for earlier identification of neurodegenerative diseases but findings suggest further progress is safe, feasible and likely to advance clinical care.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Principles of Biomedical Ethics
(2012) · Thieves of Virtue · doi:10.7551/mitpress/9079.003.0009 · Cited by 13,453
Amyloid oligomers exacerbate tau pathology in a mouse model of tauopathy
Selenica, M.-L. B., Brownlow, M., Jimenez, J. P., Lee, D. C., Pena, G., Dickey, C. A., Gordon, M. N., & Morgan, D. (2013) · Neurodegenerative Diseases · doi:10.1159/000337230 · Cited by 10,359
MACDONALD, M. (1993) · Cell · doi:10.1016/0092-8674(93)90585-e · Cited by 8,366
Finding the missing heritability of complex diseases
Manolio, T. A., Collins, F. S., Cox, N. J., Goldstein, D. B., Hindorff, L. A., Hunter, D. J., McCarthy, M. I., Ramos, E. M., Cardon, L. R., Chakravarti, A., et al. (2009) · Nature · doi:10.1038/nature08494 · Cited by 8,336
Cella, D., Riley, W., Stone, A., Rothrock, N., Reeve, B., Yount, S., Amtmann, D., Bode, R., Buysse, D., Choi, S., et al. (2010) · Journal of Clinical Epidemiology · doi:10.1016/j.jclinepi.2010.04.011 · Cited by 5,128
DeJesus-Hernandez, M., Mackenzie, I. R., Boeve, B. F., Boxer, A. L., Baker, M., Rutherford, N. J., Nicholson, A. M., Finch, N. A., Flynn, H., Adamson, J., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.011 · Cited by 4,936
Goate, A., Chartier-Harlin, M.-C., Mullan, M., Brown, J., Crawford, F., Fidani, L., Giuffra, L., Haynes, A., Irving, N., James, L., et al. (1991) · Nature · doi:10.1038/349704a0 · Cited by 4,659
The Sickness Impact Profile: Development and Final Revision of a Health Status Measure
Bergner, M., Bobbitt, R. A., Carter, W. B., & Gilson, B. S. (1981) · Medical Care · doi:10.1097/00005650-198108000-00001 · Cited by 4,619
Classificação Internacional de Funcionalidade (CIF)
Battistella, L. R., & de Brito, C. M. M. (2002) · Acta Fisiátrica · doi:10.5935/0104-7795.20020003 · Cited by 4,470
(1994) · Medical Entomology and Zoology · Cited by 4,156
Research works printed but not linked: 6
- Cassidy, 2008, Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's disease, Alzheimer's Dementia: J. Alzheimer's Assoc., 4, 406, 10.1016/j.jalz.2008.04.007 · DOI
- Cella, 2010, The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008, J. Clin. Epidemiol., 63, 1179, 10.1016/j.jclinepi.2010.04.011 · DOI · Paper page
- Huntington, 1872, On chorea, Med. Surg. Rep. Phila., 26, 317
- Patrick, 1988, What constitutes quality of life?. Concepts and dimensions, Clin. Nutr., 7, 53
- Rothstein, 2007, Genetic Information Nondiscirimination Act is a first step; won’t solve the problem, CCH Labor Law Rep., 950
- Wahlin, 1998, Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic status, Am. J. Med. Genet., 73, 356, 10.1002/(SICI)1096-8628(19971219)73:3<356::AID-AJMG24>3.0.CO;2-H · DOI
Cited by
Sorted by citations
Bao, H., Cao, J., Chen, M., Min, C., Chen, W., Chen, X., Chen, Y., Chen, Y., Chen, Y., Chen, Z., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-023-2305-0 · Cited by 402
Lewczuk, P., Riederer, P. F., O’Bryant, S. E., Verbeek, M. M., Dubois, B., Visser, P. J., Jellinger, K. A., Engelborghs, S., Ramírez, A., Parnetti, L., et al. (2017) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2017.1375556 · Cited by 318
Depression in neurodegenerative diseases: Common mechanisms and current treatment options
Galts, C., Bettio, L. E. B., Jewett, D. C., Yang, C. C., Brocardo, P. S., Rodrigues, A. L. S., Thacker, J. S., & Gil‐Mohapel, J. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.04.002 · Cited by 278
Multi-modality machine learning predicting Parkinson’s disease
Makarious, M. B., Leonard, H. L., Vitale, D., Iwaki, H., Sargent, L. J., Dadu, A., Violich, I., Hutchins, E. D., Saffo, D., Bandrés‐Ciga, S., et al. (2022) · npj Parkinson s Disease · doi:10.1038/s41531-022-00288-w · Cited by 194
Self-citationThe Patterns of Inheritance in Early-Onset Dementia
Jarmolowicz, A. I., Chen, H.-Y., & Panegyres, P. K. (2014) · American Journal of Alzheimer s Disease & Other Dementias® · doi:10.1177/1533317514545825 · Cited by 91
Self-citationCognitive and behavioral changes in Huntington disease before diagnosis
Paulsen, J. S., Miller, A. C., Hayes, T., & Shaw, E. E. (2017) · Handbook of clinical neurology · doi:10.1016/b978-0-12-801893-4.00006-7 · Cited by 83
Self-citationEpidemiology of mucopolysaccharidoses (MPS) in United States: challenges and opportunities
Puckett, Y., Mallorga-Hernández, A., & Montaño, A. M. (2021) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-021-01880-8 · Cited by 73
Wurcel, V., Cicchetti, A., Garrison, L. P., Kip, M. M. A., Koffijberg, H., Kolbe, A., Leeflang, M., Merlin, T., Mestre‐Ferrandiz, J., Oortwijn, W., et al. (2019) · Public Health Genomics · doi:10.1159/000501832 · Cited by 76
Ethics of genetic and biomarker test disclosures in neurodegenerative disease prevention trials
Kim, S. Y. H., Karlawish, J. H., & Berkman, B. E. (2015) · Neurology · doi:10.1212/wnl.0000000000001451 · Cited by 70
Vinther‐Jensen, T., Larsen, I. U., Hjermind, L. E., Budtz–Jørgensen, E., Nielsen, T. T., Nørremølle, A., Nielsen, J. E., & Vogel, A. (2014) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-014-0114-8 · Cited by 69
Considerations regarding a diagnosis of Alzheimer’s disease before dementia: a systematic review
van der Schaar, J., Visser, L. N. C., Bouwman, F. H., Ket, J. C. F., Scheltens, P., Bredenoord, A. L., & van der Flier, W. M. (2022) · Alzheimer s Research & Therapy · doi:10.1186/s13195-022-00971-3 · Cited by 74
Guan, D., Su, Y., Li, Y., Wu, C., Yi, M., Peng, X., & Cui, Y. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13161 · Cited by 66
Onset of Huntington's disease: Can it be purely cognitive?
Paulsen, J. S., & Long, J. D. (2014) · Movement Disorders · doi:10.1002/mds.25997 · Cited by 63
Self-citationLiao, L., Zhang, X. D., Li, J., Zhang, Z. W., Yang, C., Rao, C., Zhou, C., Zeng, L., Zhao, L., Fang, L., et al. (2017) · International Immunopharmacology · doi:10.1016/j.intimp.2017.05.036 · Cited by 63
Lycium barbarum polysaccharide protects against neurotoxicity via the Nrf2‑HO‑1 pathway
Cao, S., Du, J., & Hei, Q. (2017) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2017.5127 · Cited by 63
Jia, Z., Wei, Y., Li, X., Yang, L., Liu, H., Guo, C., Zhang, L., Li, N., Guo, S., Qian, Y., et al. (2018) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph15010160 · Cited by 62
P5 eHealth: An Agenda for the Health Technologies of the Future
Pravettoni, G., & Triberti, S. (2019) · Springer eBooks · doi:10.1007/978-3-030-27994-3 · Cited by 63
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)
Carlozzi, N. E., Schilling, S. G., Lai, J., Paulsen, J. S., Hahn, E. A., Perlmutter, J. S., Ross, C. A., Downing, N. R., Kratz, A. L., McCormack, M. K., et al. (2016) · Quality of Life Research · doi:10.1007/s11136-016-1386-3 · Cited by 58
Self-citationQuality of Life in Patients with Neurodegenerative Diseases
Batista, P., & Pereira, A. (2016) · Journal of Neurology and Neuroscience · doi:10.21767/2171-6625.100074 · Cited by 56
Shajari, S., Salahandish, R., Zare, A., Hassani, M., Moossavi, S., Munro, E., Rashid, R., Rosenegger, D., Bains, J. S., & Sanati Nezhad, A. (2023) · Advanced Science · doi:10.1002/advs.202204171 · Cited by 55
Patients' views on the ethical challenges of early Parkinson disease detection
Schaeffer, E., Rogge, A., Nieding, K., Helmker, V., Letsch, C., Hauptmann, B., & Berg, D. (2020) · Neurology · doi:10.1212/wnl.0000000000009400 · Cited by 49
Gautam, A. (2022) · ECS Sensors Plus · doi:10.1149/2754-2726/ac973e · Cited by 50
Genetic Testing and Counseling in the Diagnosis and Management of Young-Onset Dementias
Goldman, J. S. (2015) · Psychiatric Clinics of North America · doi:10.1016/j.psc.2015.01.008 · Cited by 52
Wang, R., Chen, Z., Fu, Y., Wei, X., Liao, J., Liu, X., He, B., Xu, Y., Zou, J., Yang, X., et al. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00026 · Cited by 50
Emerging roles for high‐density lipoproteins in neurodegenerative disorders
Bahrami, A., Barreto, G. E., Lombardi, G., Pirro, M., & Sahebkar, A. (2019) · BioFactors · doi:10.1002/biof.1541 · Cited by 50
siRNA Therapeutics: Future Promise for Neurodegenerative Diseases
Amiri, A., Barreto, G. E., Sathyapalan, T., & Sahebkar, A. (2021) · Current Neuropharmacology · doi:10.2174/1570159x19666210402104054 · Cited by 46
Crook, A., Williams, K. L., Adams, L., Blair, I. P., & Rowe, D. B. (2017) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.1080/21678421.2017.1332079 · Cited by 44
Application of Nanomedicine to the CNS Diseases
Carradori, D., Gaudin, A., Brambilla, D., & Andrieux, K. (2016) · International review of neurobiology · doi:10.1016/bs.irn.2016.06.002 · Cited by 39
Talebi, M., Talebi, M., Kakouri, E., Farkhondeh, T., Pourbagher‐Shahri, A. M., Tarantilis, P. Α., & Samarghandian, S. (2021) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.01.042 · Cited by 42
Risk Disclosure in Prodromal Parkinson's Disease
Schaeffer, E., Toedt, I., Köhler, S., Rogge, A., & Berg, D. (2021) · Movement Disorders · doi:10.1002/mds.28723 · Cited by 37
Handels, R. L. H., Wimo, A. B., Dodel, R. C., Kramberger, M. G., Visser, P. J., Molinuevo, J. L., Verhey, F. R. J., & Winblad, B. G. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170324 · Cited by 39
Next Generation Sequencing Analysis in Early Onset Dementia Patients
Bonvicini, C., Initiative, A. D. N., Scassellati, C., Benussi, L., Maria, E. D., Maj, C., Ciani, M., Fostinelli, S., Mega, A., Bocchetta, M., et al. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-180482 · Cited by 37
Genetic counseling for prion disease: Updates and best practices
Goldman, J. S., & Vallabh, S. M. (2022) · Genetics in Medicine · doi:10.1016/j.gim.2022.06.003 · Cited by 37
Song, J., Cho, E., Lee, H., Lee, S., Kim, S., & Kim, J. (2025) · Biosensors · doi:10.3390/bios15020102 · Cited by 38
Self-citationCarlozzi, N. E., Miciura, A. L., Migliore, N., & Dayalu, P. (2014) · Journal of Huntington s Disease · doi:10.3233/jhd-140115 · Cited by 34
Self-citationScotti, L., & Scotti, L. (2015) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026615666150610143510 · Cited by 33
Acquarone, M., de Melo, T. M., Meireles, F., Brito‐Moreira, J., de Oliveira, G. M., Ferreira, S. T., Castro, N. G., Tovar-Moll, F. F., Houzel, J., & Rehen, S. K. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00097 · Cited by 32
Ursin, F., Timmermann, C., & Steger, F. (2021) · Diagnostics · doi:10.3390/diagnostics11030440 · Cited by 38
Activation of TrkB-Akt signaling rescues deficits in a mouse model of SCA6
Cook, A. A., Jayabal, S., Sheng, J., Fields, E., Leung, T. C. S., Quilez, S., McNicholas, E., Lau, L., Huang, S., & Watt, A. J. (2022) · Science Advances · doi:10.1126/sciadv.abh3260 · Cited by 32
The Many Facets of Unawareness in Huntington Disease
McCusker, E. A., & Loy, C. T. (2014) · PubMed Central · doi:10.7916/d8fj2fd3 · Cited by 31
Self-citationThe Arch Electrode: A Novel Dry Electrode Concept for Improved Wearing Comfort
Vasconcelos, B., Fiedler, P., Machts, R., Haueisen, J., & Fonseca, C. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.748100 · Cited by 30
Chekani, F., Bali, V., & Aparasu, R. R. (2015) · Research in Social and Administrative Pharmacy · doi:10.1016/j.sapharm.2015.09.007 · Cited by 30
Science and Suffering: Genetics and the Lived Experience of Illness
Halpin, M. (2017) · Social Problems · doi:10.1093/socpro/spw057 · Cited by 28
Crook, A., Jacobs, C., Newton-John, T. R. O., Richardson, E., & McEwen, A. (2021) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0000000000000458 · Cited by 27
Birolini, G., Valenza, M., Ottonelli, I., Talpo, F., Minoli, L., Cappelleri, A., Bombaci, M., Caccia, C., Canevari, C., Trucco, A., et al. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106823 · Cited by 28
Dommershuijsen, L. J., Darweesh, S. K. L., Luik, A. I., Kieboom, B. C. T., Koudstaal, P. J., Boon, A. J. W., Ikram, M. A., Ikram, M. K., & Bunnik, E. M. (2020) · Movement Disorders · doi:10.1002/mds.28262 · Cited by 25
Rostamzadeh, A., Schwegler, C., Gil‐Navarro, S., Rosende‐Roca, M., Romotzky, V., Ortega, G., Cañabate, P., Moreno, M., Schmitz‐Luhn, B., Boada, M., et al. (2021) · Journal of Alzheimer s Disease · doi:10.3233/jad-200484 · Cited by 25
Lake, J., Storm, C. S., Makarious, M. B., & Bandrés‐Ciga, S. (2021) · Cells · doi:10.3390/cells10051030 · Cited by 24
The Views of Patients with Isolated Rapid Eye Movement Sleep Behavior Disorder on Risk Disclosure
Pérez‐Carbonell, L., Simonet, C., Chohan, H., Gill, A., Leschziner, G. D., Schrag, A. E., & Noyce, A. J. (2023) · Movement Disorders · doi:10.1002/mds.29403 · Cited by 24
Seyfizadeh, N., Seyfizadeh, N., Borzoueisileh, S., Elahimanesh, F., Hosseini, V., & Nouri, M. (2019) · Process Biochemistry · doi:10.1016/j.procbio.2019.06.025 · Cited by 24
Predictive Precision Medicine: Towards the Computational Challenge
Tuena, C., Semonella, M., Fernández‐Álvarez, J., Colombo, D., & Cipresso, P. (2019) · Springer eBooks · doi:10.1007/978-3-030-27994-3_5 · Cited by 23
Mozersky, J. T., Hartz, S. M., Linnenbringer, E. L., Levin, L., Streitz, M. L., Stock, K., Moulder, K. L., & Morris, J. C. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-200993 · Cited by 24
Into the Prodrome: Diagnosis, Disadvantage, and Biomedical Ambiguity
Halpin, M. (2020) · Society and Mental Health · doi:10.1177/2156869320912456 · Cited by 21
Health-Related Quality of Life Assessment in Children Followed in a Cardiomyopathy Clinic
Friess, M. R., Marino, B. S., Cassedy, A. E., Wilmot, I., Jefferies, J. L., & Lorts, A. (2014) · Pediatric Cardiology · doi:10.1007/s00246-014-1042-z · Cited by 21
Lee, D., Ko, W., Song, B.-K., Son, I., Kim, D.-W., Kang, D. G., Lee, H.-S., Oh, H., Jang, J., Kim, Y.-E., et al. (2016) · Molecular Medicine Reports · doi:10.3892/mmr.2016.5129 · Cited by 21
Birmann, P. T., Casaril, A. M., Hartwig, D., Jacob, R. G., Seixas, F. K., Collares, T. V., & Savegnago, L. (2020) · Brain Research · doi:10.1016/j.brainres.2020.146880 · Cited by 21
Ethical issues in susceptibility genetic testing for late‐onset neurodegenerative diseases
de Lara, A. M., Soto‐Gómez, L., Núñez‐Acosta, E., Zavala, G. S., & Rentería, M. E. (2018) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.32699 · Cited by 21
Yang, Z., Zhou, H., Srivastav, S., Shaffer, J. G., Abraham, K. T., Naandam, S. M., & Kakraba, S. (2025) · Data · doi:10.3390/data10010004 · Cited by 22
Managing Ethical Dilemmas in End-Stage Neurodegenerative Diseases
Low, J., & Ho, E. P. Y. (2017) · Geriatrics · doi:10.3390/geriatrics2010008 · Cited by 20
Prospective Evaluation of Predictive DNA Testing for Huntington's Disease in a Large German Center
Ibisler, A., Ocklenburg, S., Stemmler, S., Arning, L., Epplen, J. T., Carsten Saft, C., & Hoffjan, S. (2017) · Journal of Genetic Counseling · doi:10.1007/s10897-017-0085-8 · Cited by 20
Surampalli, A., Khare, M., Kubrussi, G., Wencel, M., Tanaja, J., Donkervoort, S. C., Osann, K., Simon, M. T., Wallace, D. C., Smith, C. D., et al. (2015) · Journal of Genetic Counseling · doi:10.1007/s10897-015-9819-7 · Cited by 20
Phosphatidylserine: An overview on functionality, processing techniques, patents, and prospects
Chen, J., Li, J., Xu, H., Li, J., Yuan, Y., Xu, X., & Bi, Y. (2023) · Grain & Oil Science and Technology · doi:10.1016/j.gaost.2023.11.001 · Cited by 19
Haile, Y. G., Nakhaei‐Nejad, M., Boakye, P. A., Baker, G. B., Smith, P. A., Murray, A. G., Giuliani, F., & Jahroudi, N. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119617 · Cited by 19
Reconceptualizing Harms and Benefits in the Genomic Age
Prince, A. E. R., & Berkman, B. E. (2018) · Personalized Medicine · doi:10.2217/pme-2018-0022 · Cited by 19
Genetic Testing in Prion Disease: Psychological Consequences of the Decisions to Know or Not to Know
Schwartz, M., Brandel, J., Babonneau, M.-L., Boucher, C., Schaerer, É., Haı̈k, S., Laplanche, J., Gargiulo, M., & Dürr, A. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00895 · Cited by 18
Alvarado, C. X., Makarious, M. B., Weller, C. A., Vitale, D., Koretsky, M. J., Bandrés‐Ciga, S., Iwaki, H., Levine, K. S., Singleton, A., Faghri, F., et al. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2023.12.006 · Cited by 19
Tortajada-Pérez, J., Carranza, A. D. V., Río, C. T.-D., Collado-Pérez, M., Millán, J. M., García‐García, G., & Vázquez‐Manrique, R. P. (2025) · Antioxidants · doi:10.3390/antiox14010078 · Cited by 19
Carlozzi, N. E., Victorson, D. E., Sung, V., Beaumont, J. L., Cheng, W. Y., Gorin, B., Duh, M. S., Samuelson, D., Tulsky, D. S., Gutiérrez, S., et al. (2014) · Europe PMC (PubMed Central) · doi:10.7916/d8pn93nz · Cited by 18
Self-citationCarver, R. B., Fredheim, N. A. G., Mowinckel, A. M., Ebmeier, K. P., Friedman, B. B., Rosness, T. A., Drevon, C. A., Suri, S., Baaré, W. F. C., Zsoldos, E., et al. (2022) · Frontiers in Public Health · doi:10.3389/fpubh.2022.998302 · Cited by 17
Identification of Prodromal Parkinson Disease
Rees, R. N., Noyce, A. J., & Schrag, A. E. (2024) · Neurology · doi:10.1212/wnl.0000000000209394 · Cited by 18
Marković, F. N., Jovanović, L., Spalević, P., Kaljević, J., Zivkovic, M. Z., Šimić, V., Shaker, H., & Bačanin, N. (2025) · Neural Processing Letters · doi:10.1007/s11063-025-11735-z · Cited by 20
Understanding domains that influence perceived stigma in individuals with Huntington disease.
Boileau, N. R., Paulsen, J. S., Ready, R. E., Hahn, E. A., Lai, J., & Carlozzi, N. E. (2020) · Rehabilitation Psychology · doi:10.1037/rep0000311 · Cited by 16
Self-citationDratch, L., Owczarzak, J., Mu, W., Cousins, K. A. Q., Massimo, L. M., Grossman, M., & Erby, L. H. (2023) · Journal of Genetic Counseling · doi:10.1002/jgc4.1749 · Cited by 15
What ARE Parkinson disease? Non-motor features transform conception of the shaking palsy
Jain, S., & Goldstein, D. S. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.04.013 · Cited by 15
Sherman, C. W., Iyer, R. G., Abler, V., Antonelli, A., & Carlozzi, N. E. (2019) · Neuropsychological Rehabilitation · doi:10.1080/09602011.2018.1564675 · Cited by 14
Self-citationPerspectives of People At-Risk on Parkinson’s Prevention Research
Keavney, J. L., Mathur, S., Schroeder, K., Merrell, R., Castillo‐Torres, S. A., Gao, V., Crotty, G. F., Schwarzschild, M. A., & Poma, J. M. (2024) · Journal of Parkinson s Disease · doi:10.3233/jpd-230436 · Cited by 13
O’Neill, S. C., Tercyak, K. P., Baytop, C., Alford, S. H., & McBride, C. M. (2015) · Public Health Genomics · doi:10.1159/000370101 · Cited by 14
Mahmood, S., Law, S., & Bombard, Y. (2021) · Clinical Genetics · doi:10.1111/cge.14024 · Cited by 14
Victorson, D. E., Carlozzi, N. E., Frank, S., Beaumont, J. L., Cheng, W. Y., Gorin, B., Duh, M. S., Samuelson, D., Tulsky, D. S., Gutiérrez, S., et al. (2014) · Europe PMC (PubMed Central) · doi:10.7916/d8jw8bws · Cited by 14
Self-citationMcCusker, E. A., & Loy, C. T. (2017) · PubMed Central · doi:10.7916/d8pk0tdd · Cited by 13
Self-citationCohn‐Hokke, P. E., Swieten, J. C. V., Pijnenburg, Y. A. L., Tibben, A., Meijers-Heijboer, H. E. J., & Kievit, A. J. A. (2017) · Journal of Genetic Counseling · doi:10.1007/s10897-017-0195-3 · Cited by 15
Ahlgrim, N. S., Garza, K. M., Hoffman, C. A., & Rommelfanger, K. S. (2019) · eNeuro · doi:10.1523/eneuro.0439-18.2019 · Cited by 16
Shao, T., Xu, X., Wang, L., Shen, Y., Zhao, J., Li, H., Zhang, D., Du, W., Bai, H., Peng, B., et al. (2022) · Journal of Innovative Optical Health Sciences · doi:10.1142/s1793545822500390 · Cited by 12
Shih, P., Ding, P., Carter, S. M., Stanaway, F., Horvath, A. R., Langguth, D., Saad, M., John, A. S., & Bell, K. (2023) · BMJ Open · doi:10.1136/bmjopen-2023-074205 · Cited by 12
Poyraz, M., Poyraz, A. K., Doğan, Y., Gunes, S., Mir, H., Paul, J. K., Barua, P. D., Bayğın, M., Doğan, Ş., Tuncer, T., et al. (2025) · Cognitive Neurodynamics · doi:10.1007/s11571-025-10235-z · Cited by 12
The Clinical Spectrum of Young Onset Dementia Points to Its Stochastic Origins
Panegyres, P. K. (2021) · Journal of Alzheimer s Disease Reports · doi:10.3233/adr-210309 · Cited by 12
Self-citationLinden, I., Wolfs, C. A. G., Perry, M., Metsemakers, J. F. M., van der Weijden, T., de Vugt, M. E., Verhey, F. R. J., Handels, R. L. H., Rikkert, M. G. M. O., Dirksen, C. D., et al. (2021) · BMJ Open · doi:10.1136/bmjopen-2021-049322 · Cited by 11
Unlocking Access to Broad Molecular Profiling: Benefits, Barriers, and Policy Solutions
Thomas, D. M., Hackett, J. M., & Pleština, S. (2021) · Public Health Genomics · doi:10.1159/000520000 · Cited by 11
Health survey of adults with hereditary spastic paraparesis compared to population study controls
Fjermestad, K. W., Kanavin, O. J., Næss, E. E., Hoxmark, L. B., & Hummelvoll, G. (2016) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-016-0469-0 · Cited by 11
Research Participant Interest in Learning Results of Biomarker Tests for Alzheimer Disease
Goswami, S., Hartz, S. M., Oliver, A., Jackson, S., Ogungbenle, T., Evans, A., Linnenbringer, E. L., Moulder, K. L., Morris, J. C., & Mozersky, J. T. (2025) · JAMA Network Open · doi:10.1001/jamanetworkopen.2025.2919 · Cited by 10
Impacts of apolipoprotein E disclosure on healthy Asian older adults: a cohort study
Sng, W. T., Yeo, S. N., Lin, X. B., & Lee, T.-S. W. (2019) · International Psychogeriatrics · doi:10.1017/s1041610218002089 · Cited by 10
Liu, X., Yuan, Q., Li, G., Jia, C., Liu, J., Yang, Y., Wang, X., Hou, Y., & Wang, B. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/1457089 · Cited by 11
Ethical Issues Raised by Epigenetic Testing for Alcohol, Tobacco, and Cannabis
Erwin, C. J. (2015) · Behavioral Sciences & the Law · doi:10.1002/bsl.2204 · Cited by 10
Self-citationCompleted Suicide in An Autopsy-Confirmed Case of Early Onset Alzheimer’s Disease
Hartzell, J. W., Geary, R., Gyure, K. A., Chivukula, V. R., & Haut, M. W. (2018) · Neurodegenerative Disease Management · doi:10.2217/nmt-2017-0045 · Cited by 9
Morganti, F., Palena, N., Savoldelli, P., & Greco, A. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.01117 · Cited by 9
Risk disclosure in prodromal Parkinson's disease – A survey of neurologists
Kayiş, G., Yılmaz, R., Arda, B., & Akbostancı, M. C. (2022) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2022.105240 · Cited by 9
Predictors of Workplace Disability in a Premanifest Huntington’s Disease Cohort
Goh, A. M. Y., You, E., Perin, S., Clay, F. J., Loi, S., Ellis, K., Chong, T., Ames, D., & Lautenschlager, N. (2018) · The Journal of Neuropsychiatry and Clinical Neurosciences · doi:10.1176/appi.neuropsych.17040086 · Cited by 8
Self-citationWilkinson, B. E., & Arora, K. S. (2015) · The New Bioethics · doi:10.1179/2050287715z.00000000067 · Cited by 8
Prognoza: Parkinson’s Disease Prediction Using Classification Algorithms
Shivakoti, M., Medaramatla, S. C., Godavarthi, D., & Shivakoti, N. (2023) · EAI Endorsed Transactions on Pervasive Health and Technology · doi:10.4108/eetpht.9.3933 · Cited by 8
Steigerwald, C. G., Bertolini, C., McElhiney, M. C., Bergner, A. L., Harms, M. B., & Harrington, E. A. (2024) · Journal of Genetic Counseling · doi:10.1002/jgc4.1890 · Cited by 8
Metadata
- Authors
- Paulsen, J. S., Nance, M., Kim, J.-I., Carlozzi, N. E., Panegyres, P. K., Erwin, C., Goh, A., McCusker, E., & Williams, J. K.
- Affiliations
- University of Iowa (US)
- Park Nicollet Methodist Hospital (US)
- University of Michigan (US)
- The University of Texas Health Science Center at Houston (US)
- The Royal Melbourne Hospital (AU)
- The University of Sydney (AU)
- Corresponding author
- Paulsen, Jane S.
- ORCID
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2013-11
- Volume
- 110
- Pages
- 2-28
- ISSN
- 0301-0082 (ISSN-L)
- PMC
- PMC3833259
- OpenAlex
- W1980542254
- Cited by
- 168
- References
- 290
- Citations by year
- 2026: 8 · 2025: 16 · 2024: 18 · 2023: 10 · 2022: 18 · 2021: 21 · 2020: 10 · 2019: 14 · 2018: 9 · 2017: 14 · 2016: 8 · 2015: 11 · 2014: 10
- FWCI
- 0.98
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Progress in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Iowa Research Online (The University of Iowa) (submittedVersion)
- Funders
- National Institutes of Health (UL1TR000442)
- U.S. Public Health Service (NGHG003330)
- National Human Genome Research Institute (R01HG003330)
- National Institute of Neurological Disorders and Stroke (R01NS040068, R01NS077946, NS040068, R01NS054893, NS054893, NS077946)
- National Center for Advancing Translational Sciences
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Genetic Neurodegenerative Diseases
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Social Sciences › Economics, Econometrics and Finance › Economics and Econometrics › Health Systems, Economic Evaluations, Quality of Life
- Keywords
- health-related quality of life, predictive genetic testing, early diagnosis, neurodegenerative diseases, patient-reported outcomes, Huntington's disease, Alzheimer's disease, Parkinson's disease, dementia with Lewy bodies, frontotemporal dementia, amyotrophic lateral sclerosis, prion disease, hereditary ataxia, dentatorubral-pallidoluysian atrophy, Wilson's disease, direct-to-consumer genetic testing, regret, genetic discrimination, stigmatization
- MeSH terms
- Brain, Genetic Testing, Humans, Quality of Life, Neurodegenerative Diseases, Early Diagnosis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review