标题
Genetic Testing in Parkinson's Disease
作者
关键词
-
出版物
MOVEMENT DISORDERS
Volume 38, Issue 8, Pages 1384-1396
出版商
Wiley
发表日期
2023-06-27
DOI
10.1002/mds.29500
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Parkinson Disease and Subthalamic Nucleus Deep Brain Stimulation: Cognitive Effects in GBA Mutation Carriers
- (2022) Gian Pal et al. ANNALS OF NEUROLOGY
- Reanalysis of genomic data: An overview of the mechanisms and complexities of clinical adoption
- (2022) Alan J. Robertson et al. GENETICS IN MEDICINE
- The Role of Genetic Testing for Parkinson’s Disease
- (2021) Lola Cook et al. Current Neurology and Neuroscience Reports
- Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review
- (2021) Ashley Crook et al. JOURNAL OF NEUROLOGY
- GP2 : The Global Parkinson's Genetics Program
- (2021) MOVEMENT DISORDERS
- Worldwide barriers to genetic testing for movement disorders
- (2021) Emilia M. Gatto et al. EUROPEAN JOURNAL OF NEUROLOGY
- Genotype-driven therapeutic developments in Parkinson’s disease
- (2021) Jannik Prasuhn et al. MOLECULAR MEDICINE
- Genotype–Phenotype Relations for the Atypical Parkinsonism Genes: MDSGene Systematic Review
- (2021) Christina Wittke et al. MOVEMENT DISORDERS
- Application of a framework to guide genetic testing communication across clinical indications
- (2021) Miranda L. G. Hallquist et al. Genome Medicine
- Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD
- (2021) Ashley Crook et al. ALZHEIMER DISEASE & ASSOCIATED DISORDERS
- Availability of Therapies and Services for Parkinson's Disease in Africa: A Continent‐Wide Survey
- (2021) Eman Hamid et al. MOVEMENT DISORDERS
- The commercial genetic testing landscape for Parkinson's disease
- (2021) Lola Cook et al. PARKINSONISM & RELATED DISORDERS
- Penetrance of Glucocerebrosidase ( GBA ) Mutations in Parkinson’s Disease: a Kin Cohort Study
- (2020) Roberta Balestrino et al. MOVEMENT DISORDERS
- Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study
- (2020) Jennifer Verbrugge et al. Journal of Genetic Counseling
- The Rostock International Parkinson's Disease ( ROPAD ) Study: Protocol and Initial Findings
- (2020) Volha Skrahina et al. MOVEMENT DISORDERS
- Patient Knowledge and Attitudes towards Genetic Testing in Parkinson’s Disease Subjects with Deep Brain Stimulation
- (2019) Avram Fraint et al. Parkinsons Disease
- Genetic Counseling in Huntington's Disease: Potential New Challenges on Horizon?
- (2019) Simone Migliore et al. Frontiers in Neurology
- Genetic testing for Parkinson disease: current practice, knowledge, and attitudes among US and Canadian movement disorders specialists
- (2019) Roy N. Alcalay et al. GENETICS IN MEDICINE
- Knowledge and attitudes of Parkinson’s disease risk in the Gaucher population
- (2019) Leah Zaretsky et al. Journal of Genetic Counseling
- Approach to Assessment of Parkinson Disease with Emphasis on Genetic Testing
- (2019) Katelyn Payne et al. MEDICAL CLINICS OF NORTH AMERICA
- The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials
- (2019) Anett Illés et al. Frontiers in Genetics
- Confidential genetic testing and electronic health records: A survey of current practices among Huntington disease testing centers
- (2019) Celeste C. Eno et al. Molecular Genetics & Genomic Medicine
- Interleukin-18 promoter polymorphisms and idiopathic Parkinson disease: an Egyptian study
- (2018) Ebtesam Fahmy et al. ACTA NEUROLOGICA BELGICA
- Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease
- (2018) B. Schormair et al. CLINICAL GENETICS
- Genetics of Movement Disorders and the Practicing Clinician; Who and What to Test for?
- (2018) Alessio Di Fonzo et al. Current Neurology and Neuroscience Reports
- The Promise and Pitfalls of Facebook Advertising: a Genetic Counselor’s Perspective
- (2018) Jennifer Verbrugge et al. Journal of Genetic Counseling
- Parkinson’s Disease: Patients’ Knowledge, Attitudes, and Interest in Genetic Counseling
- (2018) Kristin A. Maloney et al. Journal of Genetic Counseling
- Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin , PINK1 , DJ1: MDSGene Systematic Review
- (2018) Meike Kasten et al. MOVEMENT DISORDERS
- Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey
- (2018) Christoph Kessler et al. PARKINSONISM & RELATED DISORDERS
- Pipeline to gene discovery - Analysing familial Parkinsonism in the Queensland Parkinson's Project
- (2018) Steven R. Bentley et al. PARKINSONISM & RELATED DISORDERS
- Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders
- (2018) Solveig Montaut et al. JAMA Neurology
- Phase determination using chromosomal microarray and fluorescence in situ hybridization in a patient with early onset Parkinson disease and two deletions in PRKN
- (2018) Eli S. Williams et al. Molecular Genetics & Genomic Medicine
- Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease
- (2018) M.Z. Jankovic et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review
- (2018) Joanne Trinh et al. MOVEMENT DISORDERS
- Direct-To-Consumer Genetic Testing: Is the Public Ready for Simple, At-Home DNA Tests to Detect Disease Risk?
- (2018) Mary Bates IEEE Pulse
- MDSGene: Closing Data Gaps in Genotype-Phenotype Correlations of Monogenic Parkinson’s Disease
- (2018) Christine Klein et al. Journal of Parkinsons Disease
- Patients’ Opinions on Genetic Counseling on the Increased Risk of Parkinson Disease among Gaucher Disease Carriers
- (2017) Maureen Mulhern et al. Journal of Genetic Counseling
- The heterozygous R1441C mutation of leucine-rich repeat kinase 2 gene in a Chinese patient with Parkinson disease: A five-year follow-up and literatures review
- (2017) Fang Peng et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- The rise and fall and rise again of 23andMe
- (2017) Erika Check Hayden NATURE
- NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
- (2017) Cornelis Blauwendraat et al. NEUROBIOLOGY OF AGING
- GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia
- (2017) Valerija Dobričić et al. PARKINSONISM & RELATED DISORDERS
- Olfaction in Parkin carriers in Chinese patients with Parkinson disease
- (2017) Ying Wang et al. Brain and Behavior
- Additional rare variant analysis in Parkinson’s disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
- (2016) Steven J. Lubbe et al. HUMAN MOLECULAR GENETICS
- Genetic Mutation Analysis of Parkinson’s Disease Patients Using Multigene Next-Generation Sequencing Panels
- (2016) Ana Gorostidi et al. Molecular Diagnosis & Therapy
- Genetics of movement disorders in the next-generation sequencing era
- (2016) Simone Olgiati et al. MOVEMENT DISORDERS
- DNAJC6 mutations are not common causes of early onset Parkinson’s disease in Chinese Han population
- (2016) Changhe Shi et al. NEUROSCIENCE LETTERS
- Cognitive Impairments in LRRK2-Related Parkinson’s Disease: A Study in Chinese Individuals
- (2015) Yifan Zheng et al. BEHAVIOURAL NEUROLOGY
- The genetics of Parkinson's disease
- (2015) Stephen Mullin et al. BRITISH MEDICAL BULLETIN
- Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population
- (2015) Milena Z. Janković et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Disclosure of research results in genetic studies of Parkinson's disease caused byLRRK2mutations
- (2015) Claustre Pont-Sunyer et al. MOVEMENT DISORDERS
- Novel GCH1 variant in Dopa-responsive dystonia and Parkinson's disease
- (2015) A.J. Lewthwaite et al. PARKINSONISM & RELATED DISORDERS
- Usefulness of Genetic Testing in PD and PD Trials: A Balanced Review
- (2015) Thomas Gasser Journal of Parkinsons Disease
- Genetic mutations in early-onset Parkinson's disease Mexican patients: Molecular testing implications
- (2014) Nancy Monroy-Jaramillo et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Interest in Genetic Testing in Ashkenazi Jewish Parkinson’s Disease Patients and Their Unaffected Relatives
- (2014) Manisha Gupte et al. Journal of Genetic Counseling
- Genetic Diagnosis of Two Dopa-Responsive Dystonia Families by Exome Sequencing
- (2014) Zhan-fang Sun et al. PLoS One
- Genetic Movement Disorders in Patients of Jewish Ancestry
- (2014) Rivka Inzelberg et al. JAMA Neurology
- Knowledge of and Interest in Genetic Results Among Parkinson Disease Patients and Caregivers
- (2013) Karina Sakanaka et al. Journal of Genetic Counseling
- The CamPaIGN study of Parkinson's disease: 10-year outlook in an incident population-based cohort
- (2013) Caroline H Williams-Gray et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Comprehensive LRRK2 and GBA screening in Portuguese patients with Parkinson's disease: Identification of a new family with the LRRK2 p.Arg1441His mutation and novel missense variants
- (2013) Lei Zhang et al. PARKINSONISM & RELATED DISORDERS
- Genetic testing of LRRK2 in Parkinson's disease: is there a clinical role?
- (2013) Donna Mae Lyn Buhat et al. PARKINSONISM & RELATED DISORDERS
- Clinicians' Attitudes toward General Screening of the Ashkenazi-Jewish Population for Prevalent Founder BRCA1/2 and LRRK2 Mutations
- (2013) S. Shkedi-Rafid et al. Public Health Genomics
- Genetics of Parkinson's Disease
- (2013) C. Klein et al. Cold Spring Harbor Perspectives in Medicine
- Next-Generation Phenotyping Using theParkinExample
- (2013) Anne Grünewald et al. JAMA Neurology
- Recommendations for the predictive genetic test in Huntington's disease
- (2012) R MacLeod et al. CLINICAL GENETICS
- EFNS/MDS-ES recommendations for the diagnosis of Parkinson's disease
- (2012) A. Berardelli et al. EUROPEAN JOURNAL OF NEUROLOGY
- “Trust is not something you can reclaim easily”: patenting in the field of direct-to-consumer genetic testing
- (2012) Sigrid Sterckx et al. GENETICS IN MEDICINE
- Age-specific Parkinson disease risk in GBA mutation carriers: information for genetic counseling
- (2012) Huma Q. Rana et al. GENETICS IN MEDICINE
- Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers
- (2012) M. Anheim et al. NEUROLOGY
- Genetics of Parkinson's Disease
- (2012) Kishore Kumar et al. SEMINARS IN NEUROLOGY
- Parkinson disease: Insights in clinical, genetic and pathological features of monogenic disease subtypes
- (2011) David Crosiers et al. JOURNAL OF CHEMICAL NEUROANATOMY
- Genetic Testing and Parkinson Disease: Assessment of Patient Knowledge, Attitudes, and Interest
- (2011) Dana Clay Falcone et al. Journal of Genetic Counseling
- Fighting the risk of developing Parkinson's disease; clinical counseling for first degree relatives of patients with Parkinson's disease
- (2011) Nir Giladi et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Genetic testing in Parkinson disease—who should be assessed?
- (2011) Christine Klein et al. Nature Reviews Neurology
- LRRK2 G2019S mutation does not contribute to Parkinson′s disease in South India
- (2011) Asha Kishore et al. NEUROLOGY INDIA
- Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson’s disease
- (2011) Soraya Bardien et al. PARKINSONISM & RELATED DISORDERS
- Genetic variants in Sporadic Parkinson's Disease: East vs West
- (2011) Tasneem Peeraully et al. PARKINSONISM & RELATED DISORDERS
- The Parkinson Progression Marker Initiative (PPMI)
- (2011) Kenneth Marek et al. PROGRESS IN NEUROBIOLOGY
- Frequency of Known Mutations in Early-Onset Parkinson Disease
- (2010) Roy N. Alcalay et al. ARCHIVES OF NEUROLOGY
- Clinical implications of gene discovery in Parkinson's disease and parkinsonism
- (2010) Christian Wider et al. MOVEMENT DISORDERS
- Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain)
- (2010) Javier Ruiz-Martínez et al. MOVEMENT DISORDERS
- LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort
- (2010) Soreya Belarbi et al. PARKINSONISM & RELATED DISORDERS
- Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India
- (2009) M. Vinish et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Mutation analysis for DJ-1 in sporadic and familial parkinsonism: Screening strategy in parkinsonism
- (2009) Hiroyuki Tomiyama et al. NEUROSCIENCE LETTERS
- Genetic screening for mutations in the Nrdp1 gene in Parkinson disease patients in a Chinese population
- (2009) Xiaoyun Mo et al. PARKINSONISM & RELATED DISORDERS
- The GIGYF2 variants are not associated with Parkinson's disease in the mainland Chinese population
- (2009) L. Cao et al. PARKINSONISM & RELATED DISORDERS
- Genetic diagnostics of functional variants of the human dopamine D2 receptor gene
- (2009) Alexandra Doehring et al. PSYCHIATRIC GENETICS
- Is the G2019S LRRK2 mutation common in all southern European populations?
- (2008) Spiridon Papapetropoulos et al. JOURNAL OF CLINICAL NEUROSCIENCE
- High-Throughput Homogeneous Mass Cleave Assay Technology for the Diagnosis of Autosomal Recessive Parkinson's Disease
- (2008) Christopher Schroeder et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
- (2008) Daniel G Healy et al. LANCET NEUROLOGY
- Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy
- (2008) Anna De Rosa et al. PARKINSONISM & RELATED DISORDERS
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