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Dheeraj Reddy Bobbili
Dheeraj Reddy Bobbili
Wellytics | University of Luxembourg
Подтвержден адрес электронной почты в домене wellytics.health
Название
Процитировано
Процитировано
Год
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
P May, S Girard, M Harrer, DR Bobbili, J Schubert, S Wolking, F Becker, ...
The Lancet Neurology 17 (8), 699-708, 2018
872018
Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson’s disease
JC Fitzgerald, A Zimprich, DA Carvajal Berrio, KM Schindler, B Maurer, ...
Brain 140 (9), 2444-2459, 2017
832017
A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease
D Hartl, P May, W Gu, M Mayhaus, S Pichler, C Spaniol, E Glaab, ...
Molecular psychiatry 25 (3), 629-639, 2020
542020
Genome-wide association and meta-analysis of age at onset in Parkinson disease: evidence from the COURAGE-PD consortium
S Grover, AA Kumar Sreelatha, L Pihlstrom, C Domenighetti, C Schulte, ...
Neurology 99 (7), e698-e710, 2022
332022
Mendelian randomisation study of smoking, alcohol, and coffee drinking in relation to Parkinson’s disease
C Domenighetti, PE Sugier, AAK Sreelatha, C Schulte, S Grover, ...
Journal of Parkinson's disease 12 (1), 267-282, 2022
272022
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy
DR Bobbili, D Lal, P May, EM Reinthaler, K Jabbari, H Thiele, ...
European Journal of Human Genetics 26 (2), 258-264, 2018
262018
A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson’s disease
I Boussaad, CD Obermaier, Z Hanss, DR Bobbili, S Bolognin, E Glaab, ...
Science translational medicine 12 (560), eaau3960, 2020
252020
Breast and prostate cancer risk: The interplay of polygenic risk, rare pathogenic germline variants, and family history
E Hassanin, P May, R Aldisi, I Spier, AJ Forstner, MM Nöthen, S Aretz, ...
Genetics in Medicine 24 (3), 576-585, 2022
242022
Dairy intake and Parkinson's disease: a Mendelian randomization study
C Domenighetti, PE Sugier, A Ashok Kumar Sreelatha, C Schulte, ...
Movement Disorders 37 (4), 857-864, 2022
172022
Rare ABCA7 variants in 2 German families with Alzheimer disease
P May, S Pichler, D Hartl, DR Bobbili, M Mayhaus, C Spaniol, A Kurz, ...
Neurology: Genetics 4 (2), e224, 2018
172018
Community-reviewed biological network models for toxicology and drug discovery applications
AA Namasivayam, AF Morales, ÁMF Lacave, A Tallam, B Simovic, ...
Gene regulation and systems biology 10, GRSB. S39076, 2016
162016
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam
C Campbell, M McCormack, S Patel, C Stapleton, D Bobbili, R Krause, ...
Epilepsia 63 (6), 1563-1570, 2022
132022
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
E Hassanin, I Spier, DR Bobbili, R Aldisi, H Klinkhammer, F David, ...
BMC Medical Genomics 16 (1), 42, 2023
112023
Polygenic resilience modulates the penetrance of Parkinson disease genetic risk factors
H Liu, M Dehestani, C Blauwendraat, MB Makarious, H Leonard, JJ Kim, ...
Annals of neurology 92 (2), 270-278, 2022
112022
Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study
M Koko, JE Motelow, KE Stanley, DR Bobbili, RS Dhindsa, P May, ...
Epilepsia 63 (3), 723-735, 2022
112022
Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk
DR Bobbili, P Banda, R Krüger, P May
Journal of medical genetics 57 (9), 617-623, 2020
112020
Distinct gene-set burden patterns underlie common generalized and focal epilepsies
M Koko, R Krause, T Sander, DR Bobbili, M Nothnagel, P May, H Lerche, ...
EBioMedicine 72, 2021
102021
Replication of a novel Parkinson's locus in a European ancestry population
S Grover, AA Kumar‐Sreelatha, DR Bobbili, P May, C Domenighetti, ...
Movement Disorders 36 (7), 1689-1695, 2021
102021
Genome-wide linkage analysis of families with primary hyperhidrosis
AB Schote, F Schiel, B Schmitt, U Winnikes, N Frank, K Gross, MA Croyé, ...
Plos one 15 (12), e0244565, 2020
102020
The Interaction between HLA‐DRB1 and Smoking in Parkinson's Disease Revisited
C Domenighetti, V Douillard, PE Sugier, AAK Sreelatha, C Schulte, ...
Movement Disorders 37 (9), 1929-1937, 2022
92022
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