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Dheeraj Bobbili

Postdoctoral researcher

Faculté ou Centre Luxembourg Centre for Systems Biomedicine
Department Bioinformatics Core
Adresse postale Université du Luxembourg
2, Avenue de l'Université
L-4365 Esch-sur-Alzette
E-mail

Postdoctoral researcher in the Bioinformatics Core group (R. Schneider Lab)

Last updated on: mardi 04 mai 2021

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2021

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See detailAssessing the role of polygenic background on the penetrance of monogenic forms in Parkinson\textquoterights disease. 2021.06.06.21253270
Hassanin, Emadeldin; May, Patrick; Aldisi, Rana; Krawitz, Peter; Maj, Carlo; Bobbili, Dheeraj Reddy

E-print/Working paper (2021)

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See detailBreast and prostate cancer risk: the interplay of polygenic risk, high-impact monogenic variants, and family history 2021.06.04.21258277
Hassanin, Emadeldin; May, Patrick; Aldisi, Rana; Spier, Isabel; Forstner, Andreas J.; Nothen, Markus M.; Aretz, Stefan; Krawitz, Peter; Bobbili, Dheeraj Reddy; Maj, Carlo

E-print/Working paper (2021)

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2020

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See detailA rare loss-of function variant of ADAM17 is associated with late-onset familial Alzheimer disease
Hartl, Daniela; May, Patrick; Gu, Wei; Mayhaus, Manuel; Pichler, Sabrina; Spaniol, Christian; Glaab, Enrico; Bobbili, Dheeraj Reddy; Antony, Paul; Köglsberger, Sandra; Kurz, Alexander; Grimmer, Timo; Morgan, Kevin; Vardarajan, Badri N.; Reitz, Christiane; Hardy, John; Bras, Jose; Guerreiro, Rita; AESG; Balling, Rudi; Schneider, Jochen; Riemenschneider, Matthias

in Molecular Psychiatry (2020), 25(3), 629-639

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2019

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See detailIntestinal-Cell Kinase and Juvenile Myoclonic Epilepsy.
Lerche, Holger; Berkovic, Sam F.; Lowenstein, Daniel H.; EuroEPINOMICS-CoGIE; May, Patrick; Bobbili, Dheeraj Reddy; Krause, Roland; Balling, Rudi; EpiPGX consortium; Peter, Sarah; Epi4K Consortium/Epilepsy Phenome/Genome

in New England Journal of Medicine (2019), 380(16), 24

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2018

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See detailUNRAVELING THE COMPLEX GENETICS OF NEUROLOGICAL DISORDERS
Bobbili, Dheeraj Reddy

Doctoral thesis (2018)

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See detailExome-wide analysis of mutational burden in patients with typical and atypical Rolandic Epilepsy
Bobbili, Dheeraj Reddy; Lal, Dennis; May, Patrick; Reinthaler, Eva M.; Jabbari, Kamel; Thiele, Holger; Nothnagel, Michael; Jurkowski, Wiktor; EuroEPINOMICS COGIE Consortium; Balling, Rudi; Feucht, Martha; Nürnberg, Peter; Lerche, Holger; Zimprich, Fritz; Krause, Roland; Neubauer, Bernd A.

in European Journal of Human Genetics (2018)

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See detailReply: No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson’s disease
Fitzgerald, Julia C.; Zimprich, Alexander; Bobbili, Dheeraj Reddy; Sharma, Manu; May, Patrick; Krüger, Rejko

in Brain : A Journal of Neurology (2018)

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See detailRare gene deletions in genetic generalized and Rolandic epilepsies
Jabbari, Kamel; Bobbili, Dheeraj Reddy; Lal, Dennis; Reinthaler, Eva M.; Schubert, Julian; Wolking, Stefan; Sinha, Vishai; Motameny, Susanne; Thiele, Holger; Kawalla, Amit; Altmüller, Janine; Toliat, Mohammed Reza; Kraaij, Robert; van Rooij, Jeroen; Uitterlinden, André G.; Ikram, M. Arfam; EuroEPINOMICS CoGIE Consortium; Balling, Rudi; Zara, Federico; Lehesjoki, Anna-Elina; Krause, Roland; Zimprich, Fritz; Sander, Thomas; Neubauer, Bernd A.; May, Patrick; Lerche, Holger; Nürnberg, Peter

in PLoS ONE (2018)

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See detailRare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
May, Patrick; Girard, Simon; Harrer, Merle; Bobbili, Dheeraj Reddy; Schubert, Julian; Wolking, Stefan; Becker, Felicitas; Lachance-Touchette, Pamela; Meloche, Caroline; Gravel, Micheline; Niturad, Christina E.; Knaus, Julia; De Kovel, Carolien; Toliat, Mohamad; Polvi, Anne; Iacomino, Michele; Guerrero-López, Rosa; Baulac, Stéphanie; Marini, Carla; Thiele, Holger; Altmüller, Janine; Jabbari, Kamel; Ruppert, Ann-Kathrin; Jurkowski, Wiktor; Lal, Dennis; Rusconi, Raffaella; Cestèle, Sandrine; Terragni, Benedetta; Coombs, Ian D.; Reid, Christopher A.; Striano, Pasquale; Caglayan, Hande; Siren, Auli; Everett, Kate; Møller, Rikke S.; Hjalgrim, Hille; Muhle, Hiltrud; Helbig, Ingo; Kunz, Wolfram S.; Weber, Yvonne G.; De Jonghe, Peter; Sisodiya, Sanjay M.; Nabbout, Rima; Franceschetti, Silvana; Coppola, Antonietta; Vari, Maria S.; Kasteleijn-Nolst Trenité, Dorothée; Baykan, Betul; Ozbek, Ugur; Bebek, Nerses; Klein, Karl M.; Rosenow, Felix; Nguyen, Dang K.; Dubeau, Francis; Carmant, Lionel; Lortie, Anne; Desbiens, Richard; Clément, Jean-François; Cieuta-Walti; Sills, Graeme J.; Auce, Pauls; Francin, Ben; Johnson, Michael R.; Berghuis, Bianca; Sander, Josemir W.; Avbersek, Andreja; McCormack, Mark; Cavalleri, Gianpiero L.; Delanty, Norman; Depondt, Chantal; Krenn, Martin; Zimprich, Fritz; Peter, Sarah; Nikanorova, Marina; Kraaij, Robert; van Rooij, Jeroen; Balling, Rudi; Ikram, M. Arfan; Uitterlinden, André G.; Avanzini, Giuliano; Schorge, Stephanie; Petrou, Steven; Mantegazza, Massimo; Sander, Thomas; LeGuern, Eric; Serratosa Jose M.; Koeleman, Bobby P.C.; Palotie, Aarno; Lehesjoki, Anna-Elina; Nothnagel, Michael; Nürnberg, Peter; Maljevic, Snezana; Zara, Federico; Cossette, Patrick; Krause, Roland; Lerche, Holger

in Lancet Neurology (2018), 17(8), 699-708

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See detailRare ABCA7 variants in 2 German families with Alzheimer disease
May, Patrick; Pichler, Sabrina; Hartl, Daniela; Bobbili, Dheeraj Reddy; Mayhaus, Manuel; Spaniol, Christian; Kurz, Alexander; Balling, Rudi; Schneider, Jochen; Riemenschneider, Matthias

in Neurology Genetics (2018), 4(2),

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2017

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See detailRare variant analysis of the PPMI dataset to uncover the complex genetic architecture of Parkinson’s disease
Bobbili, Dheeraj Reddy; May, Patrick; Krüger, Rejko

in Movement Disorders : Official Journal of the Movement Disorder Society (2017, June 02), 322(Supplement S2), 405

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See detailMetformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's disease
Fitzgerald, Julia C.; Zimprich, Alexander; Carvajal-Berrio, Daniel A.; Schindler, Kevin M.; Maurer, Brigitte; Schulte, Claudia; Bus, Christine; Hauser, Anne-Kathrin; Kübler, Manuela; Lewin, Rahel; Bobbili, Dheeraj Reddy; Schwarz, Lisa M.; Vartholomaiou, Evangela; Brockmann, Kathrin; Wüst, Richard; Madlung, Johannes; Nordheim, Alfred; Riess, Olaf; Martins, L. Miguel; Glaab, Enrico; May, Patrick; Schenke-Layland, Katja; Picard, Didier; Sharma, Manu; Gasser, Thomas; Krüger, Rejko

in Brain : A Journal of Neurology (2017), 140(9), 2444-2459

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See detailIDENTIFICATION OF A RARE GENE VARIANT THAT IS ASSOCIATED WITH FAMILIAL ALZHEIMER DISEASE AND REGULATES APP EXPRESSION
Hartl, Daniela; May, Patrick; Gu, Wei; Mayhaus, Manuel; Glaab, Enrico; Antony, Paul; Bobbili, Dheeraj Reddy; Köglsberger, Sandra; Pichler, Sabrina; Spaniol, Christian; Kurz, Alexander; Balling, Rudi; Schneider, Jochen; Riemenschneider, Matthias

in Alzheimer's and Dementia: the Journal of the Alzheimer's Association (2017), 13(7, Supplement), 648

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