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Year Number of Results
2016 2
2017 8
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2019 2
2020 2
2021 2
2024 2

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Page 1
Defective ciliogenesis in INPP5E-related Joubert syndrome.
Hardee I, Soldatos A, Davids M, Vilboux T, Toro C, David KL, Ferreira CR, Nehrebecky M, Snow J, Thurm A, Heller T, Macnamara EF, Gunay-Aygun M, Zein WM, Gahl WA, Malicdan MCV. Hardee I, et al. Am J Med Genet A. 2017 Dec;173(12):3231-3237. doi: 10.1002/ajmg.a.38376. Epub 2017 Oct 20. Am J Med Genet A. 2017. PMID: 29052317 Free PMC article.
Cover Image, Volume 173A, Number 12, December 2017.
Hardee I, Soldatos A, Davids M, Vilboux T, Toro C, David KL, Ferreira CR, Nehrebecky M, Snow J, Thurm A, Heller T, Macnamara EF, Gunay-Aygun M, Zein WM, Gahl WA, Malicdan MCV. Hardee I, et al. Am J Med Genet A. 2017 Dec;173(12):i. doi: 10.1002/ajmg.a.38548. Am J Med Genet A. 2017. PMID: 29136352
The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease.
Ramoni RB, Mulvihill JJ, Adams DR, Allard P, Ashley EA, Bernstein JA, Gahl WA, Hamid R, Loscalzo J, McCray AT, Shashi V, Tifft CJ; Undiagnosed Diseases Network; Wise AL. Ramoni RB, et al. Am J Hum Genet. 2017 Feb 2;100(2):185-192. doi: 10.1016/j.ajhg.2017.01.006. Am J Hum Genet. 2017. PMID: 28157539 Free PMC article.
A Novel Risk Score to Guide the Evaluation of Acute Hematogenous Osteomyelitis in Children.
Stephan AM, Platt S, Levine DA, Qiu Y, Buchhalter L, Lyons TW, Gaines N, Cruz AT, Sudanagunta S, Hardee IJ, Eisenberg JR, Tamas V, McAneney C, Chinta SS, Yeung C, Root JM, Fant C, Dunnick J, Pifko E, Campbell C, Bruce M, Srivastava G, Pruitt CM, Hueschen LA, Ugalde IT, Becker C, Granda E, Klein EJ, Kaplan RL. Stephan AM, et al. Among authors: hardee ij. Pediatrics. 2024 Jan 1;153(2):e2023063153. doi: 10.1542/peds.2023-063153. Pediatrics. 2024. PMID: 38239108
At-home self-collection of saliva, oropharyngeal swabs and dried blood spots for SARS-CoV-2 diagnosis and serology: Post-collection acceptability of specimen collection process and patient confidence in specimens.
Valentine-Graves M, Hall E, Guest JL, Adam E, Valencia R, Shinn K, Hardee I, Sanchez T, Siegler AJ, Sullivan PS. Valentine-Graves M, et al. Among authors: hardee i. PLoS One. 2020 Aug 5;15(8):e0236775. doi: 10.1371/journal.pone.0236775. eCollection 2020. PLoS One. 2020. PMID: 32756585 Free PMC article.
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3.
Chao HT, Davids M, Burke E, Pappas JG, Rosenfeld JA, McCarty AJ, Davis T, Wolfe L, Toro C, Tifft C, Xia F, Stong N, Johnson TK, Warr CG; Undiagnosed Diseases Network; Yamamoto S, Adams DR, Markello TC, Gahl WA, Bellen HJ, Wangler MF, Malicdan MCV. Chao HT, et al. Am J Hum Genet. 2017 Jan 5;100(1):128-137. doi: 10.1016/j.ajhg.2016.11.018. Epub 2016 Dec 22. Am J Hum Genet. 2017. PMID: 28017372 Free PMC article.
17 results