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Page 1
Profiling PIK3CA variants in disorders of somatic mosaicism.
Mojarad BA, Hernandez PV, Evenson MJ, Corliss MM, Stein SL, Theos A, Coughlin CC, Sisk B, Menezes M, Schroeder MC, Heusel JW, Neidich JA, Cao Y. Mojarad BA, et al. Among authors: neidich ja. Genet Med Open. 2023 May 6;1(1):100815. doi: 10.1016/j.gimo.2023.100815. eCollection 2023. Genet Med Open. 2023. PMID: 39669231 Free PMC article.
Homozygous, Intragenic Tandem Duplication of SFTPB Causes Neonatal Respiratory Failure.
Wambach JA, Wegner DJ, Kitzmiller J, White FV, Heins HB, Yang P, Paul AJ, Granadillo JL, Eghtesady P, Kuklinski C, Turner T, Fairman K, Stone K, Wilson T, Breman A, Smith J, Schroeder MC, Neidich JA, Whitsett JA, Cole FS. Wambach JA, et al. Among authors: neidich ja. Am J Respir Cell Mol Biol. 2024 Jan;70(1):78-80. doi: 10.1165/rcmb.2023-0156LE. Am J Respir Cell Mol Biol. 2024. PMID: 38156804 Free PMC article. No abstract available.
SARS-CoV-2 Screening Testing in Schools for Children with Intellectual and Developmental Disabilities.
Sherby MR, Walsh T, Lai AM, Neidich JA, Balls-Berry JE, Morris SM, Head R, Prener C, Newland JG, Gurnett CA; COMPASS-T Study Group. Sherby MR, et al. Among authors: neidich ja. Res Sq [Preprint]. 2021 Jul 20:rs.3.rs-700296. doi: 10.21203/rs.3.rs-700296/v1. Res Sq. 2021. Update in: J Neurodev Disord. 2021 Sep 1;13(1):31. doi: 10.1186/s11689-021-09376-z PMID: 34312616 Free PMC article. Updated. Preprint.
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.
Vaseghi P, Habibi L, Neidich JA, Cao Y, Fattahi N, Rashidi-Nezhad R, Salehnezhad T, Dalili H, Rahimi Sharbaf F, Zarkesh MR, Malekian M, Mokhberdezfuli M, Mehrtash A, Ardeshirdavani A, Kariminejad R, Ghorbansabagh V, Sadeghimoghadam P, Naddaf A, Esmaeilnia Shirvany T, Mosayebi Z, Sahebdel B, Golshahi F, Shirazi M, Shamel S, Moeini R, Heidari A, Daneshmand MA, Ghasemi R, Akrami SM, Rashidi-Nezhad A. Vaseghi P, et al. Among authors: neidich ja. Eur J Hum Genet. 2024 Oct;32(10):1238-1249. doi: 10.1038/s41431-024-01533-x. Epub 2024 Jan 26. Eur J Hum Genet. 2024. PMID: 38278869
Clinical whole-genome sequencing and FISH identify two different fusion partners for NUP98 in a patient with acute myeloid leukemia: A case report.
Mojarad BA, Crees ZD, Schroeder MC, Xiang Z, Vader J, Sina J, Jacoby M, Frater JL, Duncavage EJ, Spencer DH, Lavine K, Neidich JA, Amarillo I. Mojarad BA, et al. Among authors: neidich ja. Cancer Genet. 2024 Jan;280-281:1-5. doi: 10.1016/j.cancergen.2023.11.001. Epub 2023 Nov 29. Cancer Genet. 2024. PMID: 38056049
36 results