| 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 | 92 | 2018 |
| 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 | 90 | 2017 |
| 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 | 61 | 2020 |
| 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 | 37 | 2022 |
| 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 | 33 | 2022 |
| 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 | 30 | 2020 |
| 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 | 29 | 2022 |
| 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 | 29 | 2018 |
| 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 | 24 | 2022 |
| GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Nature genetics 55 (9), 1471-1482, 2023 | 18 | 2023 |
| 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 | 18 | 2018 |
| 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 | 16 | 2023 |
| 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 | 16 | 2022 |
| 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 | 16 | 2016 |
| 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 | 15 | 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 | 12 | 2020 |
| 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 | 11 | 2022 |
| 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 | 11 | 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 | 11 | 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, 2021 | 11 | 2021 |
Patrick MayGenome Analysis, Bioinformatics Core, Luxembourg Centre for Systems Biomedicine在 uni.lu 的电子邮件经过验证
