Follow
Lynne Krohn
Lynne Krohn
Verified email at mail.mcgill.ca
Title
Cited by
Cited by
Year
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
17592019
Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms
C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ...
Movement Disorders 34 (6), 866-875, 2019
3082019
Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
C Blauwendraat, X Reed, L Krohn, K Heilbron, S Bandres-Ciga, M Tan, ...
Brain 143 (1), 234-248, 2020
2022020
Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets
DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ...
JAMA neurology 78 (4), 464-472, 2021
1332021
Expanding Parkinson’s disease genetics: novel risk loci, genomic context, causal insights and heritable risk
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
BioRxiv, 388165, 2019
982019
System Genomics of Parkinson’s Disease Consortium; International Parkinson’s Disease Genomics Consortium. Identification of novel risk loci, causal insights, and heritable risk …
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
Lancet Neurol 18 (12), 1091-1102, 2019
972019
The Parkinson's disease genome‐wide association study locus browser
FP Grenn, JJ Kim, MB Makarious, H Iwaki, A Illarionova, K Brolin, ...
Movement Disorders 35 (11), 2056-2067, 2020
892020
Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies
L Krohn, TN Öztürk, B Vanderperre, B Ouled Amar Bencheikh, JA Ruskey, ...
Annals of neurology 87 (1), 139-153, 2020
882020
GBA variants in REM sleep behavior disorder: A multicenter study
L Krohn, JA Ruskey, U Rudakou, E Leveille, F Asayesh, MTM Hu, I Arnulf, ...
Neurology 95 (8), e1008-e1016, 2020
652020
Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score
H Iwaki, C Blauwendraat, MB Makarious, S Bandrés‐Ciga, HL Leonard, ...
Movement Disorders 35 (5), 774-780, 2020
652020
The genetic architecture of Parkinson disease in Spain: characterizing population‐specific risk, differential haplotype structures, and providing etiologic insight
S Bandres‐Ciga, S Ahmed, MS Sabir, C Blauwendraat, ...
Movement Disorders 34 (12), 1851-1863, 2019
592019
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson’s disease
H Leonard, C Blauwendraat, L Krohn, F Faghri, H Iwaki, G Ferguson, ...
Journal of medical genetics 57 (5), 331-338, 2020
572020
Parkinson’s disease genetics: identifying novel risk loci, providing causal insights and improving estimates of heritable risk
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
BioRxiv, 388165, 2018
542018
Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies
L Krohn, RYJ Wu, K Heilbron, JA Ruskey, SB Laurent, C Blauwendraat, ...
Annals of neurology 87 (4), 584-598, 2020
532020
Investigation of autosomal genetic sex differences in Parkinson's disease
C Blauwendraat, H Iwaki, MB Makarious, S Bandres‐Ciga, HL Leonard, ...
Annals of neurology 90 (1), 35-42, 2021
502021
Fine mapping of the HLA locus in Parkinson’s disease in Europeans
E Yu, A Ambati, MS Andersen, L Krohn, MA Estiar, P Saini, K Senkevich, ...
npj Parkinson's Disease 7 (1), 84, 2021
472021
Comprehensive assessment of PINK1 variants in Parkinson's disease
L Krohn, FP Grenn, MB Makarious, JJ Kim, S Bandres-Ciga, DA Roosen, ...
Neurobiology of aging 91, 168. e1-168. e5, 2020
472020
Heritability enrichment implicates microglia in Parkinson's disease pathogenesis
MS Andersen, S Bandres‐Ciga, RH Reynolds, J Hardy, M Ryten, L Krohn, ...
Annals of neurology 89 (5), 942-951, 2021
452021
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease
E Yu, U Rudakou, L Krohn, K Mufti, JA Ruskey, F Asayesh, MA Estiar, ...
Movement Disorders 36 (1), 178-187, 2021
432021
Targeted sequencing of Parkinson’s disease loci genes highlights SYT11, FGF20 and other associations
U Rudakou, E Yu, L Krohn, JA Ruskey, F Asayesh, Y Dauvilliers, ...
Brain 144 (2), 462-472, 2021
402021
The system can't perform the operation now. Try again later.
Articles 1–20