Rare ABCA7 variants in 2 German families with Alzheimer disease

por May, Patrick, Pichler, Sabrina, Hartl, Daniela, Bobbili, Dheeraj R., Mayhaus, Manuel, Spaniol, Christian, Kurz, Alexander, Balling, Rudi, Schneider, Jochen G., Riemenschneider, Matthias
Publicado 2018

Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence

por Hassanin, Emadeldin, Spier, Isabel, Bobbili, Dheeraj R., Aldisi, Rana, Klinkhammer, Hannah, David, Friederike, Dueñas, Nuria, Hüneburg, Robert, Perne, Claudia, Brunet, Joan, Capella, Gabriel, Nöthen, Markus M., Forstner, Andreas J., Mayr, Andreas, Krawitz, Peter, May, Patrick, Aretz, Stefan, Maj, Carlo
Publicado 2023

Rare gene deletions in genetic generalized and Rolandic epilepsies

por Jabbari, Kamel, Bobbili, Dheeraj R., Lal, Dennis, Reinthaler, Eva M., Schubert, Julian, Wolking, Stefan, Sinha, Vishal, Motameny, Susanne, Thiele, Holger, Kawalia, Amit, Altmüller, Janine, Toliat, Mohammad Reza, Kraaij, Robert, van Rooij, Jeroen, Uitterlinden, André G., Ikram, M. Arfan, Zara, Federico, Lehesjoki, Anna-Elina, Krause, Roland, Zimprich, Fritz, Sander, Thomas, Neubauer, Bernd A., May, Patrick, Lerche, Holger, Nürnberg, Peter
Publicado 2018