Generation and characterization of human-derived induced pluripotent stem cell line (IGIBi010-A) from a patient with neurodegenerative disease phenotype carrying mutation in SQSTM1... by Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, Mohammed Faruq

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Generation of two human induced pluripotent stem cell lines, IGIBi012-A and IGIBi013-A from Friedreich’s ataxia (FRDA) patients with homozygous GAA repeat expansion in FXN gene by Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, Mohammed Faruq

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Generation and characterization of two human iPSC lines, IGIBi014-A and IGIBi015-A, from Friedreich's ataxia (FRDA) patients with pathogenic (GAA/TTC)n repeat expansion in first in... by Istaq Ahmad, Himanshi Kapoor, Achal Kumar Srivastava, Mohammed Faruq

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The clinical diagnostic utility of array CGH in children with syndromic microcephaly by Manisha Goyal, Mohammed Faruq, Ashok Gupta, Divya Shrivastava, Uzma Shamim

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Microdeletion 12p12.1 involving SRY-related HMG-box 5 gene with developmental delay and autistic behavior: A rare case report by Manisha Goyal, Ashok Gupta, Rahul Gupta, Mohammed Faruq, Divya Shrivastava

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A novel CYP27A1 frameshift mutation causing cerebrotendinous xanthomatosis in an Indian family by Shilpi Shukla, Harshad Chovatiya, Uzma Shamim, Mohammed Faruq, Soaham Desai

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Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population by Divya Goel, Varun Suroliya, Uzma Shamim, Aradhna Mathur, Mohammed Faruq

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Manganism without Parkinsonism: Isolated Unilateral Upper Limb Tremor in a Welder by Shweta Prasad, Uzma Shamim, Akanksha Minj, Mohammed Faruq, Pramod Kumar Pal

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Infantile Onset Alexander Disease with Normal Head Circumference: A Genetically Proven Case Report by Manisha Goyal, Sumit Mehndiratta, Mohammed Faruq, Manish Kumar Dwivedi, Seema Kapoor

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Generation and characterization of iPSC lines from Friedreich’s ataxia patient (FRDA) with GAA.TTC repeat expansion in the Frataxin (FXN) gene’s first intron (IGIBi016-A) and a non... by Istaq Ahmad, Asangla Kamai, Sana Zahra, Himanshi Kapoor, Achal Kumar Srivastava, Mohammed Faruq

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Treating Hereditary Ataxias—Where Can We Help? by Ayush Agarwal, Divyani Garg, Mohammed Faruq, Roopa Rajan, Vinay Goyal, Achal Kumar Srivastava

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Identifying unstable CNG repeat loci in the human genome: a heuristic approach and implications for neurological disorders by Varun Suroliya, Bharathram Uppili, Manish Kumar, Vineet Jha, Achal K. Srivastava, Mohammed Faruq

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Generation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A) by Deepak Kumar, Ashaq Hussain, Achal K. Srivastava, Mitali Mukerji, Odity Mukherjee, Mohammed Faruq

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Generation of an Induced pluripotent stem cell (iPSC) line (IGIBi011-A) from a Spinocerebellar ataxia type 12 gait dominant patient by Sana Zahra, Himanshi Kapoor, Istaq Ahmad, Asangla Kamai, Achal Kumar Srivastava, Mohammed Faruq

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CRISPR/Cas9 technology in neurological disorders: An update for clinicians by Vishnu Swarup, Vikas Kumar, Mohammed Faruq, Himanshu N Singh, Inder Singh, Achal K Srivastava

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Lab resource: Single cell line generation and characterization of a human-derived induced pluripotent stem cell line (IGIBi005-A) from a patient with spastic paraplegia/ataxia/ALS... by Istaq Ahmad, Divya Goel, Anindita Ghosh, Himanshi Kapoor, Deepak Kumar, Achal K. Srivastava, Mohammed Faruq

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Clinical and genetic analysis of A father-son duo with monomelic amyotrophy: Case report by Shiffali Khurana, Abhishek Vats, Mandaville Gourie-Devi, Ankkita Sharma, Sagar Verma, Mohammed Faruq, Uma Dhawan, Vibha Taneja

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Molecular clues unveiling spinocerebellar ataxia type-12 pathogenesis by Manish Kumar, Shweta Sahni, Vivekanand A, Deepak Kumar, Neetu Kushwah, Divya Goel, Himanshi Kapoor, Achal K. Srivastava, Mohammed Faruq

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Generation of two induced pluripotent stem cell (iPSC) lines from patients with Duchenne muscular dystrophy (IGIBi006-A and IGIBi008-A) carrying exonic deletions in the dystrophin... by Istaq Ahmad, Divya Goel, Anindita Ghosh, Himanshi Kapoor, Deepak Kumar, Keerthi Ramesh, Berty Ashley, K Deepika, Arun Shastry, Mohammed Faruq

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Generation of induced pluripotent stem cell line (IGIBi007-A) from a patient with a novel acromesomelic dysplasia, PRKG2 type (AMDP) by Manish Kumar, Saruchi Wadhwa, Nishu Tyagi, Istaq Ahmad, Somesh Kumar, Shakti Sagar, Sana Zahra, Asangla Kamai, Uzma Shamim, Seema Kapoor, Mohammed Faruq

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