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Late onset Pompe Disease in India - Beyond the Caucasian phenotype.
Neuromuscul Disord. 2021 May;31(5):431-441. doi: 10.1016/j.nmd.2021.02.013. Epub 2021 Feb 16.
Neuromuscul Disord. 2021.
PMID: 33741225
Computational biology insights into genotype-clinical phenotype-protein phenotype relationships between novel SLC26A2 variants identified in inherited skeletal dysplasias.
Biji IK, Yadav S, Kulshrestha S, Saxena R, Kohli S, Verma IC, Kumar B, Puri RD.
Biji IK, et al.
Eur J Med Genet. 2022 Oct;65(10):104595. doi: 10.1016/j.ejmg.2022.104595. Epub 2022 Aug 22.
Eur J Med Genet. 2022.
PMID: 36007841
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Genetic analysis of familial hypercholesterolemia in Asian Indians: A single-center study.
Setia N, Movva S, Balakrishnan P, Biji IK, Sawhney JPS, Puri R, Arora A, Puri RD, Saxena R, Mishra S, Apte S, Kulshrestha S, Ramprasad VL, Verma IC.
Setia N, et al. Among authors: biji ik.
J Clin Lipidol. 2020 Jan-Feb;14(1):35-45. doi: 10.1016/j.jacl.2019.12.010. Epub 2020 Jan 9.
J Clin Lipidol. 2020.
PMID: 32044282
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Fan beam CT image synthesis from cone beam CT image using nested residual UNet based conditional generative adversarial network.
Joseph J, Biji I, Babu N, Pournami PN, Jayaraj PB, Puzhakkal N, Sabu C, Patel V.
Joseph J, et al. Among authors: biji i.
Phys Eng Sci Med. 2023 Jun;46(2):703-717. doi: 10.1007/s13246-023-01244-5. Epub 2023 Mar 21.
Phys Eng Sci Med. 2023.
PMID: 36943626
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Antenatal Phenotype of Desbuquois Dysplasia.
Biji IK, Mahay SB, Saxena R, Verma I, Kumar B, Puri RD.
Biji IK, et al.
Indian J Pediatr. 2023 Jan;90(1):83-86. doi: 10.1007/s12098-022-04386-8. Epub 2022 Nov 4.
Indian J Pediatr. 2023.
PMID: 36331722
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