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K. Marder · SciRah

Researcher profile · Semantic Scholar

K. Marder

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K. Marder — researcher profile on SciRah

h-index: 109
Works: 456
Citations: 47K

Most-cited papers

Research criteria for the diagnosis of prodromal dementia with Lewy bodies
I. McKeith, T. Ferman, Alan J. Thomas, F. Blanc +26 more
2020Neurology639 citations Open access
Semantic Scholar
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R. Chia, M. Sabir, S. Bandres-Ciga, S. Saez-Atienzar +151 more
2021Nature Genetics373 citations Open access
Semantic Scholar
α-Synuclein-specific T cell reactivity is associated with preclinical and early Parkinson’s disease
Cecilia S. Lindestam Arlehamn, Rekha Dhanwani, J. Pham, R. Kuan +13 more
2020Nature Communications330 citations Open access
Semantic Scholar
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study
R. Guerreiro, O. Ross, Célia Kun-Rodrigues, D. Hernandez +61 more
2017Lancet Neurology244 citations Open access
Semantic Scholar
Penetrance estimate of LRRK2 p.G2019S Mutation in Individuals of Non-Ashkenazi Jewish Ancestry
Annie J. Lee, Yuan-Jia Wang, R. Alcalay, H. Mejia‐Santana +25 more
2017Movement Disorders158 citations Open access
Semantic Scholar
Progression in the LRRK2-Asssociated Parkinson Disease Population
R. Saunders-Pullman, A. Mirelman, R. Alcalay, Cui-Ling Wang +11 more
2018JAMA Neurology142 citations Open access
Semantic Scholar
Statistical Approaches to Longitudinal Data Analysis in Neurodegenerative Diseases: Huntington’s Disease as a Model
Tanya P. Garcia, K. Marder
2017Current Neurology and Neuroscience Reports126 citations Open access
Semantic Scholar
A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease
A. McGarry, M. McDermott, K. Kieburtz, E. D. de Blieck +56 more
2017Neurology125 citations Open access
Semantic Scholar
Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson’s Progression Markers Initiative (PPMI): a cross-sectional study
T. Simuni, Liz Uribe, H. Cho, C. Caspell-Garcia +129 more
2019Lancet Neurology121 citations Open access
Semantic Scholar
SMPD1 mutations, activity and α-synuclein accumulation in Parkinson’s disease
R. Alcalay, Victoria Mallett, Benoît Vanderperre, Omid Tavassoly +30 more
2019Movement Disorders112 citations Open access
Semantic Scholar
Elevated GM3 plasma concentration in idiopathic Parkinson’s disease: A lipidomic analysis
R. Chan, A. Perotte, Bowen Zhou, Christopher Liong +10 more
2017PLoS ONE100 citations Open access
Semantic Scholar
Safety and efficacy of pridopidine in patients with Huntington's disease (PRIDE-HD): a phase 2, randomised, placebo-controlled, multicentre, dose-ranging study.
R. Reilmann, A. McGarry, I. Grachev, J. Savola +115 more
2019Lancet Neurology87 citations
Semantic Scholar
Dietary Patterns, Physical Activity, Sleep, and Risk for Dementia and Cognitive Decline
Chen Zhao, J. Noble, K. Marder, Jacob S Hartman +2 more
2018Current nutrition reports83 citations Open access
Semantic Scholar
Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression
Robert Ortega, Cui-Ling Wang, D. Raymond, Nicole Bryant +11 more
2021JAMA Network Open79 citations Open access
Semantic Scholar
Alpha galactosidase A activity in Parkinson’s disease
R. Alcalay, Pavlina Wolf, O. Levy, U. Kang +17 more
2018Neurobiology of Disease72 citations Open access
Semantic Scholar
Increased yield of full GBA sequencing in Ashkenazi Jews with Parkinson’s disease
J. Ruskey, L. Greenbaum, L. Roncière, A. Alam +14 more
2018European Journal of Medical Genetics57 citations Open access
Semantic Scholar
Application of the Movement Disorder Society Prodromal Criteria in healthy G2019S-LRRK2 carriers
A. Mirelman, R. Saunders-Pullman, R. Alcalay, S. Shustak +13 more
2018Movement Disorders56 citations Open access
Semantic Scholar
Pepinemab antibody blockade of SEMA4D in early Huntington’s disease: a randomized, placebo-controlled, phase 2 trial
A. Feigin, E. Evans, T. Fisher, J. Leonard +47 more
2022Nature Medicine51 citations Open access
Semantic Scholar
Genetic Testing for Parkinson’s Disease: Current Practice, Knowledge and Attitudes among US and Canadian Movement Disorders Specialists
R. Alcalay, Caitlin M. Kehoe, Evan Shorr, Roseanna Battista +8 more
2019Genetics in Medicine49 citations Open access
Semantic Scholar
Challenges and opportunities for improving the landscape for Lewy body dementia clinical trials
Jennifer G. Goldman, L. Forsberg, B. Boeve, M. Armstrong +16 more
2020Alzheimer's Research & Therapy47 citations Open access
Semantic Scholar
Frequency of GBA variants in autopsy-proven multiple system atrophy
Miriam Sklerov, U. Kang, Christopher Liong, L. Clark +8 more
2017Movement Disorders Clinical Practice46 citations Open access
Semantic Scholar
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort
Eva-Juliane Vollstedt, S. Schaake, K. Lohmann, S. Padmanabhan +130 more
2023Movement Disorders44 citations Open access
Semantic Scholar
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease
Dong-Bing Lai, Babak Alipanahi, P. Fontanillas, Tae-Hwi Schwantes-An +57 more
2021Annals of Neurology42 citations Open access
Semantic Scholar
Plasma glucosylsphingosine in GBA1 mutation carriers with and without Parkinson disease
Matthew Surface, M. Balwani, C. Waters, Alexander Haimovich +8 more
2021Movement Disorders40 citations Open access
Semantic Scholar
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies
Tatiana Orme, D. Hernandez, O. Ross, Célia Kun-Rodrigues +48 more
2020Acta Neuropathologica Communications39 citations Open access
Semantic Scholar
The TCR repertoire of α-synuclein-specific T cells in Parkinson’s disease is surprisingly diverse
A. Singhania, J. Pham, Rekha Dhanwani, A. Frazier +10 more
2021Scientific Reports38 citations Open access
Semantic Scholar
Allele-specific DNA methylation is increased in cancers and its dense mapping in normal plus neoplastic cells increases the yield of disease-associated regulatory SNPs
Catherine Do, Emmanuel L. P. Dumont, Martha Salas, Angélica Castaño +22 more
2019Genome Biology38 citations Open access
Semantic Scholar
Developmental malformations in Huntington disease: neuropathologic evidence of focal neuronal migration defects in a subset of adult brains
R. Hickman, P. Faust, M. Rosenblum, K. Marder +2 more
2021Acta Neuropathologica36 citations Open access
Semantic Scholar
Heritability and genetic variance of dementia with Lewy bodies
R. Guerreiro, V. Escott-Price, D. Hernandez, Célia Kun-Rodrigues +66 more
2018bioRxiv36 citations Open access
Semantic Scholar
Low-dose Lithium treatment for agitation and psychosis in Alzheimer’s disease and Frontotemporal dementia: A case series
D. Devanand, G. Pelton, Kristina D’Antonio, Jesse G. Strickler +5 more
2017Alzheimer Disease and Associated Disorders35 citations Open access
Semantic Scholar
Sex differences in LRRK2 G2019S and idiopathic Parkinson's Disease
Marta San Luciano, Cui-Ling Wang, Robert Ortega, Nir Giladi +3 more
2017Annals of Clinical and Translational Neurology33 citations Open access
Semantic Scholar
Cancer Outcomes Among Parkinson’s Disease Patients with Leucine Rich Repeat Kinase 2 Mutations, Idiopathic Parkinson’s Disease Patients, and Nonaffected Controls
I. Agalliu, Robert Ortega, M. S. Luciano, A. Mirelman +21 more
2019Movement Disorders30 citations Open access
Semantic Scholar
DaT-SPECT assessment depicts dopamine depletion among asymptomatic G2019S LRRK2 mutation carriers
M. Artzi, E. Even-Sapir, Hedva Lerman Shacham, Avner Thaler +7 more
2017PLoS ONE28 citations Open access
Semantic Scholar
Fluid and Tissue Biomarkers of Lewy Body Dementia: Report of an LBDA Symposium
G. Scott, Moriah R. Arnold, T. Beach, C. Gibbons +41 more
2021Frontiers in Neurology27 citations Open access
Semantic Scholar
Providing Genetic Testing and Genetic Counseling for Parkinson's Disease to the Community.
L. Cook, J. Verbrugge, Tae-Hwi Schwantes-An, J. Schulze +11 more
2023Genetics in Medicine25 citations Open access
Semantic Scholar
The distribution and density of Huntingtin inclusions across the Huntington disease neocortex: regional correlations with Huntingtin repeat expansion independent of pathologic grade
R. Hickman, P. Faust, K. Marder, Ai Yamamoto +1 more
2022Acta Neuropathologica Communications25 citations Open access
Semantic Scholar
T Cell Responses to Neural Autoantigens Are Similar in Alzheimer’s Disease Patients and Age-Matched Healthy Controls
Rekha Dhanwani, J. Pham, A. Premlal, A. Frazier +9 more
2020Frontiers in Neuroscience25 citations Open access
Semantic Scholar
Safety and Tolerability of SRX246, a Vasopressin 1a Antagonist, in Irritable Huntington’s Disease Patients—A Randomized Phase 2 Clinical Trial
Michael J. Brownstein, Neal G. Simon, J. Long, Jon W. Yankey +62 more
2020Journal of Clinical Medicine25 citations Open access
Semantic Scholar
Selected Health and Life Style Factors, CAG Status and Phenoconversion in Huntington’s Disease
C. Tanner, K. Marder, S. Eberly, K. Biglan +2 more
2018Movement Disorders24 citations Open access
Semantic Scholar
The choice not to undergo genetic testing for Huntington disease: Results from the PHAROS study
K. Anderson, S. Eberly, K. Marder, D. Oakes +3 more
2019Clinical Genetics23 citations
Semantic Scholar
Genetic Testing in Parkinson's Disease
Gian Pal, L. Cook, J. Schulze, J. Verbrugge +23 more
2023Movement Disorders22 citations Open access
Semantic Scholar
Hierarchical Data-Driven Analysis of Clinical Symptoms Among Patients With Parkinson's Disease
T. Kozlovski, Alexis Mitelpunkt, Avner Thaler, T. Gurevich +10 more
2019Frontiers in Neurology21 citations Open access
Semantic Scholar
Quantifying postural control in premanifest and manifest Huntington’s disease using wearable sensors
Franchino Porciuncula, Paula Wasserman, K. Marder, A. Rao
2020Neurorehabilitation and Neural Repair20 citations Open access
Semantic Scholar
Patterns of TDP-43 Deposition in Brains with LRRK2 G2019S Mutations
Julian Agin-Liebes, R. Hickman, J. Vonsattel, P. Faust +9 more
2023Movement Disorders19 citations Open access
Semantic Scholar
Amyotrophic lateral sclerosis is over-represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion
R. Hickman, Ramita Dewan, Etty P. Cortes, B. Traynor +2 more
2021Acta Neuropathologica18 citations Open access
Semantic Scholar
A comprehensive screening of copy number variability in dementia with Lewy bodies
Célia Kun-Rodrigues, Tatiana Orme, Susana Carmona, D. Hernandez +64 more
2018Neurobiology of Aging18 citations Open access
Semantic Scholar
Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study
Hila Milo Rasouly, J. Wynn, M. Marasà, R. Reingold +34 more
2019Genetics in Medicine17 citations Open access
Semantic Scholar
Movement Disorders Rounds: A Case of Missing Pathology in a Patient with LRRK2 Parkinson’s Disease
Julian Agin-Liebes, Etty P. Cortes, J. Vonsattel, K. Marder +1 more
2019Parkinsonism & Related Disorders13 citations Open access
Semantic Scholar
International Genetic Testing and Counseling Practices for Parkinson’s Disease
R. Saunders-Pullman, D. Raymond, Robert Ortega, A. Shalash +25 more
2023Movement Disorders12 citations Open access
Semantic Scholar
Age of onset of Huntington’s disease in carriers of reduced penetrance alleles
Erin I. McDonnell, Yuan-Jia Wang, J. Goldman, K. Marder
2021Movement Disorders12 citations Open access
Semantic Scholar

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