Genetic analysis of an Indian family with members affected with Waardenburg syndrome and Duchenne muscular dystrophy

Por Kapoor, Saketh, Bindu, Parayil Sankaran, Taly, Arun B., Sinha, Sanjib, Gayathri, Narayanappa, Rani, S. Vasantha, Chandak, Giriraj Ratan, Kumar, Arun
Publicado em 2012

Mutation analysis of the SLC4A11 gene in Indian families with congenital hereditary endothelial dystrophy 2 and a review of the literature

Por Kodaganur, Srinivas Gopinath, Kapoor, Saketh, Veerappa, Avinash M., Tontanahal, Sagar Jagannath, Sarda, Astha, Yathish, S., Prakash, D. Ravi, Kumar, Arun
Publicado em 2013

Integrated Multi-Omic Analysis of Mycobacterium tuberculosis H37Ra Redefines Virulence Attributes

Por Pinto, Sneha M., Verma, Renu, Advani, Jayshree, Chatterjee, Oishi, Patil, Arun H., Kapoor, Saketh, Subbannayya, Yashwanth, Raja, Remya, Gandotra, Sheetal, Prasad, T. S. Keshava
Publicado no Front Microbiol (2018)

Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation

Por Netravathi, Manjunath, Kumari, Renu, Kapoor, Saketh, Dakle, Pushkar, Dwivedi, Manish Kumar, Roy, Sumitabho Deb, Pandey, Paritosh, Saini, Jitender, Ramakrishna, Anil, Navalli, Devaraddi, Satishchandra, Parthasarathy, Pal, Pramod Kumar, Kumar, Arun, Faruq, Mohammed
Publicado no BMC Med Genet (2015)

Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex

Por Kapoor, Saketh, Shah, Mohd Hussain, Singh, Nivedita, Rather, Mohammad Iqbal, Bhat, Vishwanath, Gopinath, Sindhura, Bindu, Parayil Sankaran, Taly, Arun B., Sinha, Sanjib, Nagappa, Madhu, Bharath, Rose Dawn, Mahadevan, Anita, Narayanappa, Gayathri, Chickabasaviah, Yasha T., Kumar, Arun
Publicado no PLoS One (2016)