Nivedita Singh

Employment

• National Institutes of Health Research Fellow
  2024 - Present
• National Eye Institute Visiting Fellow
  2018 - 2024

Education

• Indian Institute of Science PhD

Projects & Funding

Projects & funding information is unavailable.

Publications (13)

• Structural framework to address variant-gene relationship in primary open-angle glaucoma
  Vision Research 2025 DOI: 10.1016/J.VISRES.2024.108505
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• Genome wide profiling of promoter anchored chromatin interactions in the human trabecular meshwork cells
  Investigative Ophthalmology & Visual Science 2024
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• Loss of paired immunoglobin-like type 2 receptor B gene associated with age-related macular degeneration impairs photoreceptor function in mouse retina
  Human Molecular Genetics 2024 DOI: 10.1093/HMG/DDAE161
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• NRL-centered Rod Gene Regulatory Network identified by gene delivery in a patient iPSC-derived retinal organoid model of NRL-retinopathy
  Investigative Ophthalmology & Visual Science 2024
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• High-resolution genome topology of human retina uncovers super enhancer-promoter interactions at tissue-specific and multifactorial disease loci.
  Claire Marchal, Nivedita Singh, Zachary A. Batz +4 more
  Nature communications 2022 DOI: 10.1038/s41467-022-33427-1
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• HiCRes: a computational method to estimate and predict the genomic resolution of Hi-C libraries.
  Claire Marchal, Nivedita Singh, Ximena Corso‐Díaz +1 more
  Nucleic acids research 2022 DOI: 10.1093/nar/gkab1235
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• Aging of the Retina: Molecular and Metabolic Turbulences and Potential Interventions.
  Laura Campello, Nivedita Singh, Jayshree Advani

  +3 more

  • Anupam K. Mondal
  • Ximena Corso‐Díaz
  • Anand Swaroop
  Annual review of vision science 2021 DOI: 10.1146/annurev-vision-100419-114940
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• Exome sequencing and functional studies in zebrafish identify WDR8 as the causative gene for isolated Microspherophakia in Indian families.
  M. Madhangi, Debanjan Dutta, Sautan Show +8 more
  Human molecular genetics 2021 DOI: 10.1093/hmg/ddab061
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• Making Biological Sense of Genetic Studies of Age-Related Macular Degeneration.
  Advances in experimental medicine and biology 2021 DOI: 10.1007/978-3-030-66014-7_8
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• Genetic analysis of ATP7B in 102 south Indian families with Wilson disease.
  Nivedita Singh, Pradeep Kallollimath, Mohd Hussain Shah

  +8 more

  • Saketh Kapoor
  • Vishwanath Kumble Bhat
  • Lakshminarayanapuram Gopal Viswanathan
  • Madhu Nagappa
  • Parayil Sankaran Bindu
  • +3 more
  PloS one 2019 DOI: 10.1371/journal.pone.0215779
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• A homozygous mutation in TRIM36 causes autosomal recessive anencephaly in an Indian family.
  Human molecular genetics 2017 DOI: 10.1093/hmg/ddx020
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• Genetic Analysis of PLA2G6 in 22 Indian Families with Infantile Neuroaxonal Dystrophy, Atypical Late-Onset Neuroaxonal Dystrophy and Dystonia Parkinsonism Complex.
  Saketh Kapoor, Mohd Hussain Shah, Nivedita Singh

  +12 more

  • Mohammed Iqbal Rather
  • Vishwanath Kumble Bhat
  • Sindhura Gopinath
  • Parayil Sankaran Bindu
  • Arun B. Taly
  • +7 more
  PloS one 2016 DOI: 10.1371/journal.pone.0155605
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• Non-Wilsonian hepatolenticular degeneration: Clinical and MRI observations in four families from south India.
  Madhu Nagappa, Sanjib Sinha, Jitender S. Saini

  +5 more

  • Pradeep Kallollimath
  • Nivedita Singh
  • Arun Kumar
  • Parayil Sankaran Bindu
  • Arun B. Taly
  Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2016 DOI: 10.1016/j.jocn.2015.06.035
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