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Page 1
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.
Kaur M, Blair J, Devkota B, Fortunato S, Clark D, Lawrence A, Kim J, Do W, Semeo B, Katz O, Mehta D, Yamamoto N, Schindler E, Al Rawi Z, Wallace N, Wilde JJ, McCallum J, Liu J, Xu D, Jackson M, Rentas S, Tayoun AA, Zhe Z, Abdul-Rahman O, Allen B, Angula MA, Anyane-Yeboa K, Argente J, Arn PH, Armstrong L, Basel-Salmon L, Baynam G, Bird LM, Bruegger D, Ch'ng GS, Chitayat D, Clark R, Cox GF, Dave U, DeBaere E, Field M, Graham JM Jr, Gripp KW, Greenstein R, Gupta N, Heidenreich R, Hoffman J, Hopkin RJ, Jones KL, Jones MC, Kariminejad A, Kogan J, Lace B, Leroy J, Lynch SA, McDonald M, Meagher K, Mendelsohn N, Micule I, Moeschler J, Nampoothiri S, Ohashi K, Powell CM, Ramanathan S, Raskin S, Roeder E, Rio M, Rope AF, Sangha K, Scheuerle AE, Schneider A, Shalev S, Siu V, Smith R, Stevens C, Tkemaladze T, Toimie J, Toriello H, Turner A, Wheeler PG, White SM, Young T, Loomes KM, Pipan M, Harrington AT, Zackai E, Rajagopalan R, Conlin L, Deardorff MA, McEldrew D, Pie J, Ramos F, Musio A, Kline AD, Izumi K, Raible SE, Krantz ID. Kaur M, et al. Among authors: tayoun aa. Am J Med Genet A. 2023 Aug;191(8):2113-2131. doi: 10.1002/ajmg.a.63247. Epub 2023 Jun 28. Am J Med Genet A. 2023. PMID: 37377026
Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Li MM, Tayoun AA, DiStefano M, Pandya A, Rehm HL, Robin NH, Schaefer AM, Yoshinaga-Itano C; ACMG Professional Practice and Guidelines Committee. Electronic address: documents@acmg.net. Li MM, et al. Among authors: tayoun aa. Genet Med. 2022 Jul;24(7):1392-1406. doi: 10.1016/j.gim.2022.03.018. Epub 2022 May 10. Genet Med. 2022. PMID: 35802133 Free article.
Utility of clinical exome sequencing in a complex Emirati pediatric cohort.
Mahfouz NA, Kizhakkedath P, Ibrahim A, El Naofal M, Ramaswamy S, Harilal D, Qutub Y, Uddin M, Taylor A, Alloub Z, AlBanna A, Abuhammour W, Fathalla B, Tayoun AA. Mahfouz NA, et al. Among authors: tayoun aa. Comput Struct Biotechnol J. 2020 Apr 22;18:1020-1027. doi: 10.1016/j.csbj.2020.04.013. eCollection 2020. Comput Struct Biotechnol J. 2020. PMID: 32382396 Free PMC article.
Kawasaki disease (KD) and multisystem inflammatory syndrome in children (MIS-C) in a Middle Eastern patient cohort.
Yavuz L, AlHamdani S, Alasrawi S, Wafadari D, Al-Fraihat A, Bebars MA, Nath J, Arango D, Pallavidino M, Jain R, Yavuz S, AlAwadhi M, Alkhayat A, Tayoun AA, Abuhammour WM. Yavuz L, et al. Among authors: tayoun aa. Pediatr Rheumatol Online J. 2023 Jun 29;21(1):64. doi: 10.1186/s12969-023-00834-7. Pediatr Rheumatol Online J. 2023. PMID: 37386568 Free PMC article.
Clinical and epidemiological features and severity markers in children admitted with multisystem inflammatory syndrome in children (MISC) in a tertiary care center in the United Arab Emirates.
AboAlEla HH, Ali AY, Al-Sharif GA, Abuhammour W, Tayoun AA, Almoosa M, Uribe DA, Al-Fraihat A, Ho SB, Khamis AH, Popatia R, Yavuz L. AboAlEla HH, et al. Among authors: tayoun aa. Pediatr Pulmonol. 2023 Oct;58(10):2930-2940. doi: 10.1002/ppul.26614. Epub 2023 Aug 10. Pediatr Pulmonol. 2023. PMID: 37565706
32 results