Dheeraj Reddy Bobbili
Dheeraj Reddy Bobbili
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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
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
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
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
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
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), 2018
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
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
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
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
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
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
Rare gene deletions in genetic generalized and Rolandic epilepsies
K Jabbari, DR Bobbili, D Lal, EM Reinthaler, J Schubert, S Wolking, ...
Plos one 13 (8), e0202022, 2018
Genome-wide association and meta-analysis of age at onset in Parkinson disease: evidence from the COURAGE-PD consortium
S Grover, AAK Sreelatha, L Pihlstrom, C Domenighetti, C Schulte, ...
Neurology 99 (7), e698-e710, 2022
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
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
Intestinal-Cell Kinase and Juvenile Myoclonic Epilepsy.
H Lerche, SF Berkovic, DH Lowenstein
The New England Journal of Medicine 380 (16), e24-e24, 2019
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam
C Campbell, M McCormack, S Patel, C Stapleton, D Bobbili, R Krause, ...
Epilepsia, 2022
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, 103588, 2021
Reply: No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson’s disease
JC Fitzgerald, A Zimprich, D Reddy Bobbili, M Sharma, P May, R Krüger
Brain 141 (3), e17-e17, 2018
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