Items where Author is "Faruq, Mohammed"

Article

Singh, Swati ; Bhardwaj, Supriya ; Dandapath, Iman ; Singh, Jyotsna ; Das, Sumanta ; Mohan, Trishala ; Bora, Santanu Kumar ; Kedia, Shweta ; Suri, Ashish ; Sharma, Mehar Chand ; Sarkar, Chitra ; Faruq, Mohammed ; Suri, Vaishali (2024) Clinical utility of plasma cell-free DNA (cfDNA) in diffuse gliomas for the detection of IDH1 R132H mutation Pathology - Research and Practice, 263 . p. 155571. ISSN 0344-0338

Chakraborty, Samarpana ; Dakle, Pushkar ; Sinha, Anirban ; Vishweswaraiah, Sangeetha ; Nagori, Aditya ; Salimath, Shivalingaswamy ; Prakash, Y. S. ; Lodha, R. ; Kabra, S. K. ; Ghosh, Balaram ; Faruq, Mohammed ; Mahesh, P. A. ; Agrawal, Anurag (2019) Genetic variations in olfactory receptor gene OR2AG2 in a large multigenerational family with asthma Scientific Reports, 9 (1). ISSN 2045-2322

Kumari, Renu ; Kumar, Deepak ; Brahmachari, Samir K. ; Srivastava, Achal K. ; Faruq, Mohammed ; Mukerji, Mitali (2018) Paradigm for disease deconvolution in rare neurodegenerative disorders in Indian population: insights from studies in cerebellar ataxias Journal of Genetics, 97 (3). pp. 589-609. ISSN 0022-1333

Pathak, Pankaj ; Kumar, Anupam ; Jha, Prerana ; Purkait, Suvendu ; Faruq, Mohammed ; Suri, Ashish ; Suri, Vaishali ; Sharma, Mehar C. ; Sarkar, Chitra (2017) Genetic alterations related to BRAF‐FGFR genes and dysregulated MAPK/ERK/mTOR signaling in adult pilocytic astrocytoma Brain Pathology, 27 (5). pp. 580-589. ISSN 1015-6305

Singh, Inder ; Faruq, Mohammed ; Padma, Madakasira Vasantha ; Goyal, Vinay ; Behari, Madhuri ; Grover, Ashoo ; Mukerji, Mitali ; Srivastava, Achal K. (2015) Investigation of mitochondrial DNA variations among Indian Friedreich's ataxia (FRDA) patients Mitochondrion, 25 . pp. 1-5. ISSN 1567-7249

Kumar, Anupam ; Pathak, Pankaj ; Purkait, Suvendu ; Faruq, Mohammed ; Jha, Prerana ; Mallick, Supriya ; Suri, Vaishali ; Sharma, Mehar C. ; Suri, Ashish ; Sarkar, Chitra (2015) Oncogenic KIAA1549-BRAF fusion with activation of the MAPK/ERK pathway in pediatric oligodendrogliomas Cancer Genetics and Cytogenetics, 208 (3). pp. 91-95. ISSN 0165-4608

Faruq, Mohammed ; Srivastava, Achal Kumar ; Singh, Suman ; Gupta, Rohit ; Dada, Tanuj ; Garg, Ajay ; Behari, Madhuri ; Mukerji, Mitali (2015) Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population Indian Journal of Medical Research, 141 (2). pp. 187-198. ISSN 0019-5340

Pathak, Pankaj ; Jha, Prerana ; Purkait, Suvendu ; Sharma, Vikas ; Suri, Vaishali ; Sharma, Mehar C. ; Faruq, Mohammed ; Suri, Ashish ; Sarkar, Chitra (2014) Altered global histone-trimethylation code and H3F3A-ATRX mutation in pediatric GBM Journal of Neuro-Oncology, 121 (3). pp. 489-497. ISSN 0167-594X

Singh, Ankur ; Faruq, Mohammed ; Mukerji, Mitali ; Dwivedi, Manish Kumar ; Pruthi, Sumit ; Kapoor, Seema (2014) Infantile onset Spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases Journal of Child Neurology, 29 (1). pp. 139-144. ISSN 0883-0738

Singh, Inder ; Faruq, Mohammed ; Mukherjee, Odity ; Jain, Sanjeev ; Pal, Pramod Kumar ; Padma Srivastav, M. V. ; Behari, Madhuri ; Srivastava, Achal K. ; Mukerji, Mitali (2010) North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion Annals of Human Genetics, 74 (3). pp. 202-210. ISSN 0003-4800

Faruq, Mohammed ; Scaria, Vinod ; Singh, Inder ; Tyagi, Shivani ; Srivastava, Achal K. ; Mukerji, Mitali (2009) SCA-LSVD: A repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias Human Mutation, 30 (7). pp. 1037-1042. ISSN 1059-7794