Variation in Exon 29 of the NOS1 Gene Does Not Contribute to Parkinson’s Disease in the North Karnataka Population

por Bulagouda, Rudragouda, Hegde, Smita, Hegde, Rajat, Hiremath, Ashwini, Wali, G M, Kadakol, Gurushantappa S
Publicado 2023

Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing

por Kumar, Kishore R, Wali, G.M., Kamate, Mahesh, Wali, Gautam, Minoche, André E, Puttick, Clare, Pinese, Mark, Gayevskiy, Velimir, Dinger, Marcel E, Roscioli, Tony, Sue, Carolyn M., Cowley, Mark J
Publicado 2016

Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research

por Rajan, Roopa, Divya, K. P., Kandadai, Rukmini Mridula, Yadav, Ravi, Satagopam, Venkata P., Madhusoodanan, U. K., Agarwal, Pankaj, Kumar, Niraj, Ferreira, Teresa, Kumar, Hrishikesh, Sreeram Prasad, A. V., Shetty, Kuldeep, Mehta, Sahil, Desai, Soaham, Kumar, Suresh, Prashanth, L. K., Bhatt, Mohit, Wadia, Pettarusp, Ramalingam, Sudha, Wali, G. M., Pandey, Sanjay, Bartusch, Felix, Hannussek, Maximilian, Krüger, Jens, Kumar-Sreelatha, Ashwin, Grover, Sandeep, Lichtner, Peter, Sturm, Marc, Roeper, Jochen, Busskamp, Volker, Chandak, Giriraj R., Schwamborn, Jens, Seth, Pankaj, Gasser, Thomas, Riess, Olaf, Goyal, Vinay, Pal, Pramod Kumar, Borgohain, Rupam, Krüger, Rejko, Kishore, Asha, Sharma, Manu
Publicado 2020