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Plos One|January 16, 2020
Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemiaAvani Solanki, Aruna Rajendran, Sheila Mohan, et al.
Gene|July 13, 2013
Lowered expression levels of a tumor suppressor gene - caveolin-1 within dysregulated gene networks of Fanconi anemiaPavithra Shyamsunder, Prasanna Vidyasekar, Akshay Ranjan Shukla, et al.
Gene|September 17, 2013
Identification of novel target genes involved in Indian Fanconi anemia patients using microarrayPavithra Shyamsunder, Kripa S Ganesh, Prasanna Vidyasekar, et al.
Molecular Biology Reports|January 4, 2021
Severe telomere shortening in Fanconi anemia complementation group LAnjali Shah, Merin George, Somprakash Dhangar, et al.
Molecular Biology Reports|March 29, 2021
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemiaMerin George, Avani Solanki, Purvi Mohanty, et al.
Genomics|August 18, 2020
Defective cell proliferation is an attribute of overexpressed Notch1 receptor and impaired autophagy in Fanconi AnemiaBinita Zipporah E, Bamadeb Patra, Kavitha Govarthanan, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|April 25, 2007
Identification of the Fanconi anemia complementation group I gene, FANCIJosephine C Dorsman, Marieke Levitus, Davy Rockx, et al.
Human Mutation|September 29, 2021
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjectsMerin George, Avani Solanki, Niranjan Chavan, et al.
Human Mutation|September 13, 2019
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in IndiaFrank X Donovan, Avani Solanki, Minako Mori, et al.
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