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D. Bobbili · SciRah

Researcher profile · Semantic Scholar

D. Bobbili

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D. Bobbili — researcher profile on SciRah

h-index: 18
Works: 57
Citations: 1,283

Most-cited papers

Parkinson’s disease-associated alterations of the gut microbiome predict disease-relevant changes in metabolic functions
Federico Baldini, Johannes Hertel, E. Sandt, C. Thinnes +110 more
2020BMC Biology207 citations Open access
Semantic Scholar
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
R. Stevelink, C. Campbell, Si-Wei Chen, B. Abou-Khalil +315 more
2023Nature Genetics198 citations Open access
Semantic Scholar
Metformin reverses TRAP1 mutation‐associated alterations in mitochondrial function in Parkinson's disease
J. Fitzgerald, A. Zimprich, D. C. Carvajal Berrio, Kevin M Schindler +22 more
2017Brain : a journal of neurology90 citations Open access
Semantic Scholar
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study.
P. May, S. Girard, Merle Harrer, D. Bobbili +121 more
2018Lancet Neurology72 citations Open access
Semantic Scholar
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson’s Disease
Cloé Domenighetti, P. Sugier, A. A. Sreelatha, C. Schulte +75 more
2021Journal of Parkinson's Disease66 citations Open access
Semantic Scholar
A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease
D. Hartl, P. May, W. Gu, M. Mayhaus +18 more
2018Molecular Psychiatry65 citations Open access
Semantic Scholar
A patient-based model of RNA mis-splicing uncovers treatment targets in Parkinson’s disease
I. Boussaad, C. Obermaier, Zoé Hanss, D. Bobbili +30 more
2020Science Translational Medicine46 citations Open access
Semantic Scholar
Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study
Cloé Domenighetti, P. Sugier, Ashwin Ashok Kumar Sreelatha, C. Schulte +75 more
2022Movement Disorders38 citations Open access
Semantic Scholar
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease Evidence From the COURAGE-PD Consortium
Sandeep Grover, A. A. Sreelatha, L. Pihlstrøm, Cloé Domenighetti +78 more
38 citations
Semantic Scholar
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 +6 more
2021Genetics in Medicine33 citations Open access
Semantic Scholar
Integrating digital gait data with metabolomics and clinical data to predict outcomes in Parkinson’s disease
Cyril Brzenczek, Quentin Klopfenstein, T. Hähnel, H. Fröhlich +113 more
2024npj Digital Medicine32 citations Open access
Semantic Scholar
Age at onset as stratifier in idiopathic Parkinson’s disease – effect of ageing and polygenic risk score on clinical phenotypes
L. Pavelka, A. Rauschenberger, Z. Landoulsi, S. Pachchek +123 more
2022npj Parkinson's Disease32 citations Open access
Semantic Scholar
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence
E. Hassanin, I. Spier, D. Bobbili, R. Aldisi +14 more
2022BMC Medical Genomics32 citations Open access
Semantic Scholar
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease
Sandeep Grover, A. Kumar-Sreelatha, L. Pihlstrøm, Cloé Domenighetti +79 more
2022Neurology30 citations Open access
Semantic Scholar
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam
C. Campbell, M. McCormack, Sonn Patel, Caragh P. Stapleton +22 more
2022Epilepsia29 citations Open access
Semantic Scholar
Investigation of shared genetic risk factors between Parkinson’s disease and cancers
P. Sugier, E. Lucotte, Cloé Domenighetti, M. Law +90 more
2023Movement Disorders28 citations Open access
Semantic Scholar
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy
D. Bobbili, Dennis Lal, P. May, E. Reinthaler +20 more
2018European Journal of Human Genetics23 citations Open access
Semantic Scholar
Replication of a Novel Parkinson's Locus in a European Ancestry Population
S. Grover, A. Kumar-Sreelatha, D. Bobbili, P. May +7 more
2021Movement Disorders19 citations Open access
Semantic Scholar
Rare ABCA7 variants in 2 German families with Alzheimer disease
P. May, S. Pichler, D. Hartl, D. Bobbili +6 more
2018Neurology: Genetics17 citations Open access
Semantic Scholar
The interaction between HLA-DRB1 and smoking in Parkinson’s disease revisited
Cloé Domenighetti, Venceslas Douillard, P. Sugier, A. A. Sreelatha +76 more
2022Movement Disorders16 citations Open access
Semantic Scholar
Distinct gene-set burden patterns underlie common generalized and focal epilepsies
M. Koko, R. Krause, T. Sander, D. Bobbili +3 more
2021EBioMedicine16 citations Open access
Semantic Scholar
Community-Reviewed Biological Network Models for Toxicology and Drug Discovery Applications
A. Namasivayam, Alejandro Ferreiro Morales, Ángela María Fajardo Lacave, Aravind Tallam +25 more
2016Gene Regulation and Systems Biology16 citations Open access
Semantic Scholar
Polygenic Risk Scores Validated in Patient‐Derived Cells Stratify for Mitochondrial Subtypes of Parkinson's Disease
Giuseppe Arena, Z. Landoulsi, Dajana Grossmann, T. Payne +18 more
2023medRxiv14 citations Open access
Semantic Scholar
Genome-wide linkage analysis of families with primary hyperhidrosis
Andrea B Schote, F. Schiel, B. Schmitt, U. Winnikes +9 more
2020PLoS ONE14 citations Open access
Semantic Scholar
Dissecting genetics of spectrum of epilepsies with eyelid myoclonia by exome sequencing
A. Coppola, S. Krithika, M. Iacomino, D. Bobbili +31 more
2023Epilepsia13 citations Open access
Semantic Scholar
Association of ultra-rare coding variants with genetic generalized epilepsy: a case-control whole exome sequencing study
M. Koko, Joshua E. Motelow, Kate E. Stanley, D. Bobbili +2 more
2022Epilepsia12 citations Open access
Semantic Scholar
Penetrance of Parkinson’s disease in GBA1 carriers depends on variant severity and polygenic background
E. Hassanin, Z. Landoulsi, S. Pachchek, Geeta Acharya +112 more
2025npj Parkinson's Disease10 citations Open access
Semantic Scholar
Excess of singleton loss-of-function variants in Parkinson’s disease contributes to genetic risk
D. Bobbili, Peter Banda, Rejko Krüger, P. May
2020Journal of Medical Genetics10 citations Open access
Semantic Scholar
Multi-cohort machine learning identifies predictors of cognitive impairment in Parkinson’s disease
Rebecca Ting Jiin Loo, L. Pavelka, G. Mangone, F. Khoury +155 more
2025npj Digital Medicine9 citations Open access
Semantic Scholar
Trans-ancestry polygenic models for the prediction of LDL blood levels: an analysis of the United Kingdom Biobank and Taiwan Biobank
E. Hassanin, Ko-Han Lee, Tzung-Chien Hsieh, R. Aldisi +6 more
2023Frontiers in Genetics8 citations Open access
Semantic Scholar
Genetic landscape of Parkinson’s disease and related diseases in Luxembourg
Z. Landoulsi, S. Pachchek, D. Bobbili, L. Pavelka +2 more
2023Frontiers in Aging Neuroscience8 citations Open access
Semantic Scholar
Rare gene deletions in genetic generalized and Rolandic epilepsies
K. Jabbari, D. Bobbili, Dennis Lal, E. Reinthaler +21 more
2018PLoS ONE8 citations Open access
Semantic Scholar
Association of Body Mass Index and Parkinson Disease
Cloé Domenighetti, P. Sugier, Ashwin Ashok Kumar Sreelatha, C. Schulte +73 more
2024Neurology7 citations Open access
Semantic Scholar
Cardiovascular history and risk of idiopathic Parkinson’s disease: a cross-sectional observational study
Shubhra Acharya, A. Lumley, Yvan Devaux, Muhammad Ali +121 more
2024BMC Neuroscience6 citations Open access
Semantic Scholar
Assessing the performance of European-derived cardiometabolic polygenic risk scores in South-Asians and their interplay with family history
E. Hassanin, C. Maj, H. Klinkhammer, P. Krawitz +2 more
2023BMC Medical Genomics6 citations Open access
Semantic Scholar
Mixed effects models but not t-tests or linear regression detect progression of apathy in Parkinson’s disease over seven years in a cohort: a comparative analysis
Anne-Marie Hanff, R. Krüger, C. McCrum, C. Ley +111 more
2024BMC Medical Research Methodology4 citations Open access
Semantic Scholar
Genome-wide association study of copy number variations in Parkinson’s disease
Z. Landoulsi, A. A. Sreelatha, Nicole Kuznetsov, C. Schulte +80 more
2024medRxiv2 citations Open access
Semantic Scholar
Trans-ancestry polygenic models for the prediction of LDL blood levels: An analysis of the UK Biobank and Taiwan Biobank
E. Hassanin, Ko-Han Lee, Tzung-Chien Hsieh, R. Aldisi +6 more
2023medRxiv2 citations Open access
Semantic Scholar
Data-driven clinical decision support tool for diagnosing mild cognitive impairment in Parkinson’s disease
Gabriel Martínez Tirado, Patricia Martins Conde, S. Sapienza, H. Fröhlich +111 more
2026npj Parkinson's Disease1 citations Open access
Semantic Scholar
Modifiable lifestyle factors and genetic risk of obesity in Indians
E. Hassanin, R. Kalapala, N. Jagtap, Ravi K. Vishnubhotla +11 more
2025Scientific Reports1 citations Open access
Semantic Scholar
Transferability of European-derived cardiometabolic polygenic risk scores in the South Asians and their interplay with family history
E. Hassanin, C. Maj, P. Krawitz, P. May +1 more
2023medRxiv1 citations Open access
Semantic Scholar
Publisher Correction: Age at onset as stratifier in idiopathic Parkinson’s disease – effect of ageing and polygenic risk score on clinical phenotypes
L. Pavelka, A. Rauschenberger, Z. Landoulsi, S. Pachchek +123 more
2022npj Parkinson's Disease1 citations Open access
Semantic Scholar
Ultra-rare constrained missense variants in the epilepsies: Shared and specific enrichment patterns in neuronal gene-sets
M. Koko, R. Krause, T. Sander, D. Bobbili +3 more
2021bioRxiv1 citations Open access
Semantic Scholar
Exome-wide analysis of mutational burden in patients with typical and atypical Rolandic epilepsy
D. Bobbili, Dennis Lal, P. May, E. Reinthaler +23 more
2018European Journal of Human Genetics1 citations Open access
Semantic Scholar
[P2–108]: IDENTIFICATION OF A RARE GENE VARIANT THAT IS ASSOCIATED WITH FAMILIAL ALZHEIMER DISEASE AND REGULATES APP EXPRESSION
D. Hartl, P. May, W. Gu, M. Mayhaus +10 more
20171 citations Open access
Semantic Scholar
Screening Luxembourg's older general population for probable REM sleep behaviour disorder with a nationwide online survey
Gloria A. Aguayo, Eduardo Rosales Jubal, Gilles van Cutsem, A. Schritz +128 more
2026Scientific Reports0 citations Open access
Semantic Scholar
Genome-wide association study of copy number variations in Parkinson’s disease
Z. Landoulsi, A. A. Sreelatha, Nicole Kuznetsov, C. Schulte +80 more
2026npj Parkinson's Disease0 citations Open access
Semantic Scholar
Genetic variation in antidiabetic drug targets: associations with Parkinson’s disease risk and age at onset
K. Vincze, Agnieszka Szwajda, Alexander Ploner, R. Karlsson +79 more
2026npj Parkinson's Disease0 citations Open access
Semantic Scholar
PGxRAG: A Retrieval Augmented Generation supported Pharmacogenomics Assistant
Dhanush Borishetty, Peter Banda, Nikhilesh Andhi, Aakash Desai +3 more
2025medRxiv0 citations
Semantic Scholar
An improved polygenic score for Parkinson's disease partly explains variable penetrance of genetic Parkinson's disease
S. Sendel, Z. Landoulsi, K. Lohmann, Björn-Hergen Laabs +33 more
2025medRxiv0 citations Open access
Semantic Scholar

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