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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1974 1
1975 3
1976 1
1978 1
1979 7
1980 1
1981 2
1982 2
1983 1
1984 2
1987 5
1988 3
1989 2
1990 1
1991 1
1992 1
1993 1
1994 1
1995 2
1997 2
2000 4
2001 4
2002 2
2003 1
2004 3
2005 5
2006 5
2007 1
2008 1
2009 1
2010 2
2011 5
2012 4
2013 2
2014 2
2015 1
2016 2
2017 1
2018 1
2020 2
2021 4
2022 4
2023 7
2024 3

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100 results

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Page 1
Genetic testing for unexplained perinatal disorders.
Hays T, Wapner RJ. Hays T, et al. Curr Opin Pediatr. 2021 Apr 1;33(2):195-202. doi: 10.1097/MOP.0000000000000999. Curr Opin Pediatr. 2021. PMID: 33605625 Free PMC article. Review.
Genetic testing for kidney disease of unknown etiology.
Hays T, Groopman EE, Gharavi AG. Hays T, et al. Kidney Int. 2020 Sep;98(3):590-600. doi: 10.1016/j.kint.2020.03.031. Epub 2020 Apr 24. Kidney Int. 2020. PMID: 32739203 Free PMC article. Review.
A Brief History of Research on Mitotic Mechanisms.
McIntosh JR, Hays T. McIntosh JR, et al. Among authors: hays t. Biology (Basel). 2016 Dec 21;5(4):55. doi: 10.3390/biology5040055. Biology (Basel). 2016. PMID: 28009830 Free PMC article. Review.
Childhood thrombosis.
Nuss R, Hays T, Manco-Johnson M. Nuss R, et al. Among authors: hays t. Pediatrics. 1995 Aug;96(2 Pt 1):291-4. Pediatrics. 1995. PMID: 7630687
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.
Ahram DF, Lim TY, Ke J, Jin G, Verbitsky M, Bodria M, Kil BH, Chatterjee D, Piva SE, Marasa M, Zhang JY, Cocchi E, Caridi G, Gucev Z, Lozanovski VJ, Pisani I, Izzi C, Savoldi G, Gnutti B, Capone VP, Morello W, Guarino S, Esposito P, Lambert S, Radhakrishnan J, Appel GB, Uy NS, Rao MK, Canetta PA, Bomback AS, Nestor JG, Hays T, Cohen DJ, Finale C, Wijk JAEV, La Scola C, Baraldi O, Tondolo F, Di Renzo D, Jamry-Dziurla A, Pezzutto A, Manca V, Mitrotti A, Santoro D, Conti G, Martino M, Giordano M, Gesualdo L, Zibar L, Masnata G, Bonomini M, Alberti D, La Manna G, Caliskan Y, Ranghino A, Marzuillo P, Kiryluk K, Krzemień G, Miklaszewska M, Lin F, Montini G, Scolari F, Fiaccadori E, Arapović A, Saraga M, McKiernan J, Alam S, Zaniew M, Szczepańska M, Szmigielska A, Sikora P, Drożdż D, Mizerska-Wasiak M, Mane S, Lifton RP, Tasic V, Latos-Bielenska A, Gharavi AG, Ghiggeri GM, Materna-Kiryluk A, Westland R, Sanna-Cherchi S. Ahram DF, et al. Among authors: hays t. J Am Soc Nephrol. 2023 Jun 1;34(6):1105-1119. doi: 10.1681/ASN.0000000000000132. Epub 2023 Mar 30. J Am Soc Nephrol. 2023. PMID: 36995132 Free article.
Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease.
Hays T, Hernan R, Disco M, Griffin EL, Goldshtrom N, Vargas D, Krishnamurthy G, Bomback M, Rehman AU, Wilson AT, Guha S, Phadke S, Okur V, Robinson D, Felice V, Abhyankar A, Jobanputra V, Chung WK. Hays T, et al. Circ Genom Precis Med. 2023 Oct;16(5):415-420. doi: 10.1161/CIRCGEN.122.004050. Epub 2023 Jul 7. Circ Genom Precis Med. 2023. PMID: 37417234 Free article.
The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction.
Brar BK, Blakemore K, Hertenstein C, Miller JL, Miller KA, Shamseldin H, Maddirevula S, Hays T, Lianoglou B, Dukhovny S, Baker LA, Sparks TN, Wapner R, Alkuraya FS, Norton ME, Jelin AC; Fetal Sequencing Consortium. Brar BK, et al. Among authors: hays t. Prenat Diagn. 2024 Feb;44(2):196-204. doi: 10.1002/pd.6425. Epub 2023 Aug 18. Prenat Diagn. 2024. PMID: 37594370
100 results