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Diagnostic Utility of Exome Sequencing for Kidney Disease.
N Engl J Med. 2019 Jan 10;380(2):142-151. doi: 10.1056/NEJMoa1806891. Epub 2018 Dec 26.
N Engl J Med. 2019.
PMID: 30586318
Free PMC article.
Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia.
Alkelai A, Shohat S, Greenbaum L, Schechter T, Draiman B, Chitrit-Raveh E, Rienstein S, Dagaonkar N, Hughes D, Aggarwal VS, Heinzen EL, Shifman S, Goldstein DB, Kohn Y.
Alkelai A, et al. Among authors: dagaonkar n.
J Hum Genet. 2021 Mar;66(3):339-343. doi: 10.1038/s10038-020-00846-1. Epub 2020 Sep 18.
J Hum Genet. 2021.
PMID: 32948840
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A comprehensive next-generation sequencing assay for the diagnosis of epidermolysis bullosa.
Lucky AW, Dagaonkar N, Lammers K, Husami A, Kissell D, Zhang K.
Lucky AW, et al. Among authors: dagaonkar n.
Pediatr Dermatol. 2018 Mar;35(2):188-197. doi: 10.1111/pde.13392. Epub 2018 Jan 15.
Pediatr Dermatol. 2018.
PMID: 29334134
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Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.
Niss O, Chonat S, Dagaonkar N, Almansoori MO, Kerr K, Rogers ZR, McGann PT, Quarmyne MO, Risinger M, Zhang K, Kalfa TA.
Niss O, et al. Among authors: dagaonkar n.
Blood Cells Mol Dis. 2016 Oct;61:4-9. doi: 10.1016/j.bcmd.2016.07.003. Epub 2016 Jul 17.
Blood Cells Mol Dis. 2016.
PMID: 27667160
Free PMC article.
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Hereditary xerocytosis: Diagnostic considerations.
Risinger M, Glogowska E, Chonat S, Zhang K, Dagaonkar N, Joiner CH, Quinn CT, Kalfa TA, Gallagher PG.
Risinger M, et al. Among authors: dagaonkar n.
Am J Hematol. 2018 Mar;93(3):E67-E69. doi: 10.1002/ajh.24996. Epub 2017 Dec 23.
Am J Hematol. 2018.
PMID: 29210095
Free PMC article.
No abstract available.
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The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA.
Chonat S, et al. Among authors: dagaonkar n.
Front Physiol. 2019 Jul 3;10:815. doi: 10.3389/fphys.2019.00815. eCollection 2019.
Front Physiol. 2019.
PMID: 31333484
Free PMC article.
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Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Chonat S, Risinger M, Sakthivel H, Niss O, Rothman JA, Hsieh L, Chou ST, Kwiatkowski JL, Khandros E, Gorman MF, Wells DT, Maghathe T, Dagaonkar N, Seu KG, Zhang K, Zhang W, Kalfa TA.
Chonat S, et al. Among authors: dagaonkar n.
Front Physiol. 2019 Oct 18;10:1331. doi: 10.3389/fphys.2019.01331. eCollection 2019.
Front Physiol. 2019.
PMID: 31736770
Free PMC article.
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